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|---|---|---|---|---|---|---|
48f143ea44d0acfb1a0a66d9814ae0227f198665 | wikidoc | ABHD6 | ABHD6
alpha/beta-Hydrolase domain containing 6 (ABHD6), also known as monoacylglycerol lipase ABHD6 or 2-arachidonoylglycerol hydrolase is an enzyme that in humans is encoded by the ABHD6 gene.
# Function
ABHD6 is a serine hydrolyzing enzyme that possesses typical α/β-hydrolase family domains. ABHD6 was first studied ... | ABHD6
alpha/beta-Hydrolase domain containing 6 (ABHD6), also known as monoacylglycerol lipase ABHD6 or 2-arachidonoylglycerol hydrolase is an enzyme that in humans is encoded by the ABHD6 gene.
# Function
ABHD6 is a serine hydrolyzing enzyme that possesses typical α/β-hydrolase family domains. ABHD6 was first studied... | https://www.wikidoc.org/index.php/ABHD6 | |
8d416bc2e41bb50535a71612375a220674b69542 | wikidoc | ACAA2 | ACAA2
3-Ketoacyl-CoA thiolase, mitochondrial also known as acetyl-Coenzyme A acyltransferase 2 is an enzyme that in humans is encoded by the ACAA2 gene.
Acetyl-Coenzyme A acyltransferase 2 is an acetyl-CoA C-acyltransferase enzyme.
# Structure
The ACAA2 gene encodes a 41.9 kDa protein that is composed of 397 amino aci... | ACAA2
3-Ketoacyl-CoA thiolase, mitochondrial also known as acetyl-Coenzyme A acyltransferase 2 is an enzyme that in humans is encoded by the ACAA2 gene.[1][2]
Acetyl-Coenzyme A acyltransferase 2 is an acetyl-CoA C-acyltransferase enzyme.
# Structure
The ACAA2 gene encodes a 41.9 kDa protein that is composed of 397 am... | https://www.wikidoc.org/index.php/ACAA2 | |
0a284d677f7f10c12a6f11c384504b6b01a8a7b5 | wikidoc | ACACB | ACACB
Acetyl-CoA carboxylase 2 also known as ACC-beta or ACC2 is an enzyme that in humans is encoded by the ACACB gene.
# Function
Acetyl-CoA carboxylase (ACC) is a complex multifunctional enzyme system. ACC is a biotin-containing enzyme which catalyzes the carboxylation of acetyl-CoA to malonyl-CoA, the rate-limiting... | ACACB
Acetyl-CoA carboxylase 2 also known as ACC-beta or ACC2 is an enzyme that in humans is encoded by the ACACB gene.[1][2]
# Function
Acetyl-CoA carboxylase (ACC) is a complex multifunctional enzyme system. ACC is a biotin-containing enzyme which catalyzes the carboxylation of acetyl-CoA to malonyl-CoA, the rate-l... | https://www.wikidoc.org/index.php/ACACB | |
dc63cb8127047adfe58fd5c86379cbde6313d2ae | wikidoc | ACAD8 | ACAD8
Isobutyryl-CoA dehydrogenase, mitochondrial is an enzyme that in humans is encoded by the ACAD8 gene on chromosome 11.
The protein encoded by ACAD8 is a mitochondrial protein belongs to the acyl-CoA dehydrogenase family of enzymes, which function to catalyze the dehydrogenation of acyl-CoA derivatives in the meta... | ACAD8
Isobutyryl-CoA dehydrogenase, mitochondrial is an enzyme that in humans is encoded by the ACAD8 gene on chromosome 11.[1][2]
The protein encoded by ACAD8 is a mitochondrial protein belongs to the acyl-CoA dehydrogenase family of enzymes, which function to catalyze the dehydrogenation of acyl-CoA derivatives in t... | https://www.wikidoc.org/index.php/ACAD8 | |
fd67c5f13345be2355ae4b996073f6254f838c1b | wikidoc | ACAD9 | ACAD9
Acyl-CoA dehydrogenase family member 9, mitochondrial is an enzyme that in humans is encoded by the ACAD9 gene. Mitochondrial Complex I Deficiency with varying clinical manifestations has been associated with mutations in ACAD9.
# Structure
The ACAD9 gene contains an open reading frame of 1866 base pairs; this g... | ACAD9
Acyl-CoA dehydrogenase family member 9, mitochondrial is an enzyme that in humans is encoded by the ACAD9 gene.[1][2] Mitochondrial Complex I Deficiency with varying clinical manifestations has been associated with mutations in ACAD9.[3]
# Structure
The ACAD9 gene contains an open reading frame of 1866 base pai... | https://www.wikidoc.org/index.php/ACAD9 | |
beda98a1337f8df310d37d8f20f94d478624dbcb | wikidoc | ACADL | ACADL
Acyl-CoA dehydrogenase, long chain is a protein that in humans is encoded by the ACADL gene.
ACADL is a gene that encodes LCAD - acyl-CoA dehydrogenase, long chain - which is a member of the acyl-CoA dehydrogenase family. The acyl-CoA dehydrogenase family is primarily responsible for beta-oxidation of fatty acids... | ACADL
Acyl-CoA dehydrogenase, long chain is a protein that in humans is encoded by the ACADL gene.[1]
ACADL is a gene that encodes LCAD - acyl-CoA dehydrogenase, long chain - which is a member of the acyl-CoA dehydrogenase family. The acyl-CoA dehydrogenase family is primarily responsible for beta-oxidation of fatty a... | https://www.wikidoc.org/index.php/ACADL | |
3cfa5e72e0be2c3a9d49006a885cacf9496d4483 | wikidoc | ACADM | ACADM
ACADM (acyl-Coenzyme A dehydrogenase, C-4 to C-12 straight chain) is a gene that provides instructions for making an enzyme called acyl-coenzyme A dehydrogenase that is important for breaking down (degrading) a certain group of fats called medium-chain fatty acids.
These fatty acids are found in foods such as mil... | ACADM
ACADM (acyl-Coenzyme A dehydrogenase, C-4 to C-12 straight chain) is a gene that provides instructions for making an enzyme called acyl-coenzyme A dehydrogenase that is important for breaking down (degrading) a certain group of fats called medium-chain fatty acids.
These fatty acids are found in foods such as mi... | https://www.wikidoc.org/index.php/ACADM | |
c684adfa181f209a1af99b17ada2d728d20469cc | wikidoc | ACADS | ACADS
Acyl-CoA dehydrogenase, C-2 to C-3 short chain is an enzyme that in humans is encoded by the ACADS gene. This gene encodes a tetrameric mitochondrial flavoprotein, which is a member of the acyl-CoA dehydrogenase family. This enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway... | ACADS
Acyl-CoA dehydrogenase, C-2 to C-3 short chain is an enzyme that in humans is encoded by the ACADS gene.[1] This gene encodes a tetrameric mitochondrial flavoprotein, which is a member of the acyl-CoA dehydrogenase family. This enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pat... | https://www.wikidoc.org/index.php/ACADS | |
afb93843293f432abc6d3723110b570885bb77f7 | wikidoc | ACAT1 | ACAT1
Acetyl-CoA acetyltransferase, mitochondrial, also known as acetoacetyl-CoA thiolase, is an enzyme that in humans is encoded by the ACAT1 (Acetyl-Coenzyme A acetyltransferase 1) gene.
Acetyl-Coenzyme A acetyltransferase 1 is an acetyl-CoA C-acetyltransferase enzyme.
# Structure
The gene spans approx. 27 kb and co... | ACAT1
Acetyl-CoA acetyltransferase, mitochondrial, also known as acetoacetyl-CoA thiolase, is an enzyme that in humans is encoded by the ACAT1 (Acetyl-Coenzyme A acetyltransferase 1) gene.[1]
Acetyl-Coenzyme A acetyltransferase 1 is an acetyl-CoA C-acetyltransferase enzyme.
# Structure
The gene spans approx. 27 kb an... | https://www.wikidoc.org/index.php/ACAT1 | |
328e5eba9e65386e8bf488d238162edce796b6a6 | wikidoc | ACER1 | ACER1
Alkaline ceramidase 1 also known as ACER1 is a ceramidase enzyme which in humans is encoded by the ACER1 gene.
# Function
ACER1 mediates cellular differentiation by controlling the generation of sphingosine (SPH) and sphingosine-1-phosphate (S1P).
# Model organisms
Model organisms have been used in the study of... | ACER1
Alkaline ceramidase 1 also known as ACER1 is a ceramidase enzyme which in humans is encoded by the ACER1 gene.[1]
# Function
ACER1 mediates cellular differentiation by controlling the generation of sphingosine (SPH) and sphingosine-1-phosphate (S1P).[1]
# Model organisms
Model organisms have been used in the s... | https://www.wikidoc.org/index.php/ACER1 | |
fee2415110deeef485bfc3f4d6639b50e69b2418 | wikidoc | ACKR3 | ACKR3
Atypical chemokine receptor 3 also known as C-X-C chemokine receptor type 7 (CXCR-7) and G-protein coupled receptor 159 (GPR159) is a protein that in humans is encoded by the ACKR3 gene.
This gene encodes a member of the G protein-coupled receptor family. This protein was earlier thought to be a receptor for vaso... | ACKR3
Atypical chemokine receptor 3 also known as C-X-C chemokine receptor type 7 (CXCR-7) and G-protein coupled receptor 159 (GPR159) is a protein that in humans is encoded by the ACKR3 gene.[1][2]
This gene encodes a member of the G protein-coupled receptor family. This protein was earlier thought to be a receptor f... | https://www.wikidoc.org/index.php/ACKR3 | |
88fc28fde85b8e8beb9f6545f73e4208ad760f4b | wikidoc | ACOT1 | ACOT1
Acyl-CoA thioesterase 1 is a protein that in humans is encoded by the ACOT1 gene.
# Structure
The ACOT1 gene is located on the 14th chromosome, with its specific localization being 14q24.3. It contains 7 exons.
The protein encoded by this gene contains 410 amino acids, and forms a homodimer with another chain. T... | ACOT1
Acyl-CoA thioesterase 1 is a protein that in humans is encoded by the ACOT1 gene.[1]
# Structure
The ACOT1 gene is located on the 14th chromosome, with its specific localization being 14q24.3. It contains 7 exons.[1]
The protein encoded by this gene contains 410 amino acids, and forms a homodimer with another c... | https://www.wikidoc.org/index.php/ACOT1 | |
9825d9a21f95c15d7e1dde92dca3114ac0a5105c | wikidoc | ACOT2 | ACOT2
Acyl-CoA thioesterase 2, also known as ACOT2, is an enzyme which in humans is encoded by the ACOT2 gene.
Acyl-CoA thioesterases, such as ACOT2, are a group of enzymes that hydrolyze Coenzyme A (CoA) esters, such as acyl-CoAs, bile CoAs, and CoA esters of prostaglandins, to the corresponding free acid and CoA. ACO... | ACOT2
Acyl-CoA thioesterase 2, also known as ACOT2, is an enzyme which in humans is encoded by the ACOT2 gene.[1][2][3]
Acyl-CoA thioesterases, such as ACOT2, are a group of enzymes that hydrolyze Coenzyme A (CoA) esters, such as acyl-CoAs, bile CoAs, and CoA esters of prostaglandins, to the corresponding free acid an... | https://www.wikidoc.org/index.php/ACOT2 | |
1f5b247c1628ed06f6275331c6931cd8b3d99cdb | wikidoc | ACOT4 | ACOT4
Acyl-coenzyme A thioesterase 4 is an enzyme that in humans is encoded by the ACOT4 gene.
# Function
The protein encoded by the ACOT4 gene is part of a family of Acyl-CoA thioesterases, which catalyze the hydrolysis of various Coenzyme A esters of various molecules to the free acid plus CoA. These enzymes have al... | ACOT4
Acyl-coenzyme A thioesterase 4 is an enzyme that in humans is encoded by the ACOT4 gene.[1][2][3]
# Function
The protein encoded by the ACOT4 gene is part of a family of Acyl-CoA thioesterases, which catalyze the hydrolysis of various Coenzyme A esters of various molecules to the free acid plus CoA. These enzym... | https://www.wikidoc.org/index.php/ACOT4 | |
7cea8166c80b6c8f86b4b792e3b327222fd3cf18 | wikidoc | ACOT6 | ACOT6
Acyl-CoA thioesterase 6 is a protein that in humans is encoded by the ACOT6 gene. The protein, also known as C14orf42, is an enzyme with thioesterase activity.
# Function
The protein encoded by the ACOT1 gene is part of a family of Acyl-CoA thioesterases, which catalyze the hydrolysis of various Coenzyme A ester... | ACOT6
Acyl-CoA thioesterase 6 is a protein that in humans is encoded by the ACOT6 gene.[1] The protein, also known as C14orf42, is an enzyme with thioesterase activity.[1]
# Function
The protein encoded by the ACOT1 gene is part of a family of Acyl-CoA thioesterases, which catalyze the hydrolysis of various Coenzyme ... | https://www.wikidoc.org/index.php/ACOT6 | |
42ce2593a3c22b18cd05d39f0743b0fabed6a3e2 | wikidoc | ACRRM | ACRRM
ACRRM is the Australian College of Rural and Remote Medicine. It has a current membership of around 2,500 including fellows, registrars, practitioners and students.
# History
ACRRM was established in 1997
ACRRM received initial accreditation from the Australian Medical Council (AMC) in February 2007, and was in... | ACRRM
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ACRRM is the Australian College of Rural and Remote Medicine. It has a current membership of around 2,500 including fellows, registrars, practitioners and students.[1]
# History
ACRRM was established in 1997
ACRRM received initial accreditation from the Australian Medical Council (AMC) ... | https://www.wikidoc.org/index.php/ACRRM | |
83c452fed6276326421b02b2a3d62be3c5d211ad | wikidoc | ACSF3 | ACSF3
Acyl-CoA synthetase family member 3 is an enzyme that in humans is encoded by the ACSF3 gene.
# Structure
The ACSF3 gene is located on the 16th chromosome, with its specific location being 16q24.3. The gene contains 17 exons. ASCL4 encodes a 64.1 kDa protein that is composed of 576 amino acids; 20 peptides have ... | ACSF3
Acyl-CoA synthetase family member 3 is an enzyme that in humans is encoded by the ACSF3 gene.[1]
# Structure
The ACSF3 gene is located on the 16th chromosome, with its specific location being 16q24.3. The gene contains 17 exons.[1] ASCL4 encodes a 64.1 kDa protein that is composed of 576 amino acids; 20 peptide... | https://www.wikidoc.org/index.php/ACSF3 | |
dba1bf4067e914a31441effb1638b5a21a66ca86 | wikidoc | ACSL1 | ACSL1
Long-chain-fatty-acid—CoA ligase 1 is an enzyme that in humans is encoded by the ACSL1 gene.
# Structure
## Gene
The ACSL4 gene is located on the 4th chromosome, with its specific location being 4q35.1. The gene contains 28 exons.
The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenz... | ACSL1
Long-chain-fatty-acid—CoA ligase 1 is an enzyme that in humans is encoded by the ACSL1 gene.[1][2][3]
# Structure
## Gene
The ACSL4 gene is located on the 4th chromosome, with its specific location being 4q35.1. The gene contains 28 exons.[3]
The protein encoded by this gene is an isozyme of the long-chain fat... | https://www.wikidoc.org/index.php/ACSL1 | |
2fc6468b62b7cb224e2fcfba5ab6b255e03ac4b4 | wikidoc | ACSL4 | ACSL4
Long-chain-fatty-acid—CoA ligase 4 is an enzyme that in humans is encoded by the ACSL4 gene.
The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this fa... | ACSL4
Long-chain-fatty-acid—CoA ligase 4 is an enzyme that in humans is encoded by the ACSL4 gene.[1][2][3]
The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes ... | https://www.wikidoc.org/index.php/ACSL4 | |
c3b286aa6dcde1c48be602690c07591ce1f735ae | wikidoc | ACSS2 | ACSS2
Acyl-coenzyme A synthetase short-chain family member 2 is an enzyme that in humans is encoded by the ACSS2 gene.
# Function
This gene encodes a cytosolic enzyme that catalyzes the activation of acetate for use in lipid synthesis and energy generation. The protein acts as a monomer and produces acetyl-CoA from ac... | ACSS2
Acyl-coenzyme A synthetase short-chain family member 2 is an enzyme that in humans is encoded by the ACSS2 gene.[1][2]
# Function
This gene encodes a cytosolic enzyme that catalyzes the activation of acetate for use in lipid synthesis and energy generation. The protein acts as a monomer and produces acetyl-CoA ... | https://www.wikidoc.org/index.php/ACSS2 | |
28b454407af68fd025251fd0b707fa1e116625c7 | wikidoc | ACTA2 | ACTA2
Alpha-actin-2 also known as actin, aortic smooth muscle or alpha smooth muscle actin (α-SMA, SMactin, alpha-SM-actin, ASMA) is a protein that in humans is encoded by the ACTA2 gene located on 10q22-q24.
Actin alpha 2, the human aortic smooth muscle actin gene, is one of six different actin isoforms which have bee... | ACTA2
Alpha-actin-2 also known as actin, aortic smooth muscle or alpha smooth muscle actin (α-SMA, SMactin, alpha-SM-actin, ASMA) is a protein that in humans is encoded by the ACTA2 gene located on 10q22-q24.[1][2]
Actin alpha 2, the human aortic smooth muscle actin gene, is one of six different actin isoforms which h... | https://www.wikidoc.org/index.php/ACTA2 | |
8c5729886aff96f5d457d934660fdc2fcae6a55f | wikidoc | ACTC1 | ACTC1
ACTC1 encodes cardiac muscle alpha actin. This isoform differs from the alpha actin that is expressed in skeletal muscle, ACTA1. Alpha cardiac actin is the major protein of the thin filament in cardiac sarcomeres, which are responsible for muscle contraction and generation of force to support the pump function of... | ACTC1
ACTC1 encodes cardiac muscle alpha actin.[1][2] This isoform differs from the alpha actin that is expressed in skeletal muscle, ACTA1. Alpha cardiac actin is the major protein of the thin filament in cardiac sarcomeres, which are responsible for muscle contraction and generation of force to support the pump func... | https://www.wikidoc.org/index.php/ACTC1 | |
ab6042d27a520592f131257291b80a6dbab3301a | wikidoc | ACTG1 | ACTG1
Gamma-actin is a protein that in humans is encoded by the ACTG1 gene. Gamma-actin is widely expressed in cellular cytoskeletons of many tissues; in adult striated muscle cells, gamma-actin is localized to Z-discs and costamere structures, which are responsible for force transduction and transmission in muscle cel... | ACTG1
Gamma-actin is a protein that in humans is encoded by the ACTG1 gene.[1] Gamma-actin is widely expressed in cellular cytoskeletons of many tissues; in adult striated muscle cells, gamma-actin is localized to Z-discs and costamere structures, which are responsible for force transduction and transmission in muscle... | https://www.wikidoc.org/index.php/ACTG1 | |
5d453e6e78ce51bc11af6fbc45c8d43f8f8a707c | wikidoc | ACVR1 | ACVR1
Activin A receptor, type I (ACVR1) is a protein which in humans is encoded by the ACVR1 gene; also known as ALK-2 (activin receptor-like kinase-2). ACVR1 has been linked to the 2q23-24 region of the genome. This protein is important in the bone morphogenic protein (BMP) pathway which is responsible for the devel... | ACVR1
Activin A receptor, type I (ACVR1) is a protein which in humans is encoded by the ACVR1 gene; also known as ALK-2 (activin receptor-like kinase-2).[1] ACVR1 has been linked to the 2q23-24 region of the genome.[2] This protein is important in the bone morphogenic protein (BMP) pathway which is responsible for th... | https://www.wikidoc.org/index.php/ACVR1 | |
ed350c1dff2c2accfd068e7c2ba2cb5f0f86b1ae | wikidoc | AD-36 | AD-36
AD-36 is one of 51 types of adenoviruses known to infect humans. It was first shown to be associated with obesity in chickens by Dr. Nikhil Dhurandhar.
There has been a positive correlation between body fat and the presence of AD-36 antibodies in the blood. Previous research showed that chicken or mice injected w... | AD-36
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AD-36 is one of 51 types of adenoviruses know... | https://www.wikidoc.org/index.php/AD-36 | |
89701d60762d7c644e68c989a353b620ed53b904 | wikidoc | PSEN2 | PSEN2
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Presenilin-2 is a protein that in humans is encoded by the PSEN2 gene.
# Function
Alzheimer's disease (AD) patients with an inherited form of the disease carry mutations in the presenilin proteins (PSEN1; PSEN2) or the amyloid precu... | PSEN2
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Presenilin-2 is a protein that in humans is encoded by the PSEN2 gene.[1]
# Function
Alzheimer's disease (AD) patients with an inherited form of the disease carry mutations in the presenilin proteins (PSEN1; PSEN2) or the amyloid p... | https://www.wikidoc.org/index.php/AD4 | |
f383a3b36c6fda1c1b9cb7c82f6a49647ecbc8d9 | wikidoc | ADAM7 | ADAM7
Disintegrin and metalloproteinase domain-containing protein 7 is a protein that in humans is encoded by the ADAM7 gene. ADAM7 is an 85-kDa enzyme that is a member of the transmembrane ADAM (A Disintegrin and Metalloprotease) protein family. Members of this family are membrane-anchored proteins structurally relat... | ADAM7
Disintegrin and metalloproteinase domain-containing protein 7 is a protein that in humans is encoded by the ADAM7 gene.[1] ADAM7 is an 85-kDa enzyme that is a member of the transmembrane ADAM (A Disintegrin and Metalloprotease) protein family. Members of this family are membrane-anchored proteins structurally r... | https://www.wikidoc.org/index.php/ADAM7 | |
65b262a7637b6e92401d333fccdbb2b07fcae891 | wikidoc | ADCK3 | ADCK3
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aarF domain containing kinase 3 is a protein that in humans is encoded by the ADCK3 gene.
This gene encodes a mitochondrial protein similar to yeast ABC1, which functions in an electron-transferring membrane protein... | ADCK3
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aarF domain containing kinase 3 is a protein that in humans is encoded by the ADCK3 gene.[1]
This gene encodes a mitochondrial protein similar to yeast ABC1, which functions in an electron-transferring membrane pro... | https://www.wikidoc.org/index.php/ADCK3 | |
08c8f7aa1347740c18c135be3dfe6bc8322657ea | wikidoc | ADCY1 | ADCY1
Adenylyl cyclase type 1 is an enzyme that in humans is encoded by the ADCY1 gene.
This gene encodes a form of adenylyl cyclase expressed in brain. A similar protein in mice is involved in pattern formation of the brain.
# Function
ADCY1 is a calmodulin-sensitive adenylyl cyclase. In terms of function, It may be ... | ADCY1
Adenylyl cyclase type 1 is an enzyme that in humans is encoded by the ADCY1 gene.[1][2]
This gene encodes a form of adenylyl cyclase expressed in brain. A similar protein in mice is involved in pattern formation of the brain.[2]
# Function
ADCY1 is a calmodulin-sensitive adenylyl cyclase. In terms of function, ... | https://www.wikidoc.org/index.php/ADCY1 | |
4b19ff836bff6154671b1fe6930e702909cba6fd | wikidoc | ADCY2 | ADCY2
Adenylyl cyclase type 2 is an enzyme typically expressed in the brain of humans, that is encoded by the ADCY2 gene. It belongs to the adenylyl cyclase class-3 or guanylyl cyclase family because it contains two guanylate cyclase domains. ADCY2 is one of ten different mammalian isoforms of adenylyl cyclases. ADCY2 ... | ADCY2
Adenylyl cyclase type 2 is an enzyme typically expressed in the brain of humans, that is encoded by the ADCY2 gene.[1][2] It belongs to the adenylyl cyclase class-3 or guanylyl cyclase family because it contains two guanylate cyclase domains.[3] ADCY2 is one of ten different mammalian isoforms of adenylyl cyclas... | https://www.wikidoc.org/index.php/ADCY2 | |
7273bc8797a819a58d07f43329e94fc738752e79 | wikidoc | ADCY3 | ADCY3
Adenylyl cyclase type 3 is an enzyme that in humans is encoded by the ADCY3 gene.
# Function
This gene encodes adenylyl cyclase 3, which is a membrane-associated enzyme and catalyzes the formation of the secondary messenger cyclic adenosine monophosphate (cAMP).
The ADCY3 subtype likely mediates odorant detectio... | ADCY3
Adenylyl cyclase type 3 is an enzyme that in humans is encoded by the ADCY3 gene.[1][2]
# Function
This gene encodes adenylyl cyclase 3, which is a membrane-associated enzyme and catalyzes the formation of the secondary messenger cyclic adenosine monophosphate (cAMP).[2]
The ADCY3 subtype likely mediates odoran... | https://www.wikidoc.org/index.php/ADCY3 | |
5959137ea0dbc793147301e117b7a72c7f80f25d | wikidoc | ADH1B | ADH1B
Alcohol dehydrogenase 1B is an enzyme that in humans is encoded by the ADH1B gene.
The protein encoded by this gene is a member of the alcohol dehydrogenase family. Members of this enzyme family metabolize a wide variety of substrates, including ethanol (beverage alcohol), retinol, other aliphatic alcohols, hydro... | ADH1B
Alcohol dehydrogenase 1B is an enzyme that in humans is encoded by the ADH1B gene.[1][2]
The protein encoded by this gene is a member of the alcohol dehydrogenase family. Members of this enzyme family metabolize a wide variety of substrates, including ethanol (beverage alcohol), retinol, other aliphatic alcohols... | https://www.wikidoc.org/index.php/ADH1B | |
04db6d8238badbc669ebd2f3126eec676cae29f2 | wikidoc | ADRM1 | ADRM1
Proteasomal ubiquitin receptor ADRM1 is a protein that in humans is encoded by the ADRM1 gene. Recent evidences on proteasome complex structure confirmed that the protein encoded by gene ADRM1, also known as 26S Proteasome regulatory subunit Rpn13 (systematic nomenclature for proteasome subunits), is a subunit of... | ADRM1
Proteasomal ubiquitin receptor ADRM1 is a protein that in humans is encoded by the ADRM1 gene.[1][2] Recent evidences on proteasome complex structure confirmed that the protein encoded by gene ADRM1, also known as 26S Proteasome regulatory subunit Rpn13 (systematic nomenclature for proteasome subunits), is a sub... | https://www.wikidoc.org/index.php/ADRM1 | |
cb6efc5ae63f794a2aa294bfffdc5c44fd6f3711 | wikidoc | AEBP2 | AEBP2
Adipocyte Enhancer-Binding Protein is a zinc finger protein that in humans is encoded by the evolutionarily well-conserved gene AEBP2. It was initially identified due to its binding capability to the promoter of the adipocyte P2 gene, and was therefore named Adipocyte Enhancer Binding Protein 2. AEBP2 is a potent... | AEBP2
Adipocyte Enhancer-Binding Protein is a zinc finger protein that in humans is encoded by the evolutionarily well-conserved gene AEBP2. It was initially identified due to its binding capability to the promoter[1] of the adipocyte P2 gene, and was therefore named Adipocyte Enhancer Binding Protein 2. AEBP2 is a po... | https://www.wikidoc.org/index.php/AEBP2 | |
b83057b11563347c4286f4cc8d7115f245554c4e | wikidoc | AGG01 | AGG01
AGG01 is the tentative name of a new Penicillin-class antibiotic, recently discovered in the breast milk of the Tammar Wallaby, reportedly one hundred times more powerful than penicillin.
This compound was found to be effective against MRSA, E. coli, Streptococci, Salmonella, Bacillus subtilis, Pseudomonas spp.,... | AGG01
AGG01 is the tentative name of a new Penicillin-class antibiotic, recently discovered in the breast milk[1] of the Tammar Wallaby, reportedly one hundred times more powerful than penicillin.
This compound was found to be effective against MRSA, E. coli, Streptococci, Salmonella, Bacillus subtilis, Pseudomonas s... | https://www.wikidoc.org/index.php/AGG01 | |
4bedb3e0559030555cd954252b622801436f7927 | wikidoc | AGGF1 | AGGF1
Angiogenic factor with G patch and FHA domains 1 is a protein that in humans is encoded by the AGGF1 gene.
AGGF1 is a human gene that functions as an angiogenic factor with a G-patch and forkhead-associated domain. This gene is predominantly expressed in activated, plump endothelial cells and acts to regulate ang... | AGGF1
Angiogenic factor with G patch and FHA domains 1 is a protein that in humans is encoded by the AGGF1 gene.[1][2][3]
AGGF1 is a human gene that functions as an angiogenic factor with a G-patch and forkhead-associated domain.[4] This gene is predominantly expressed in activated, plump endothelial cells and acts to... | https://www.wikidoc.org/index.php/AGGF1 | |
759e5b3f4f11c5c693a8933bea764c26bdfc2802 | wikidoc | AIFM1 | AIFM1
Apoptosis-inducing factor 1, mitochondrial is a protein that in humans is encoded by the AIFM1 gene on the X chromosome. This protein localizes to the mitochondria, as well as the nucleus, where it carries out nuclear fragmentation as part of caspase-independent apoptosis.
# Structure
AIFM1 is expressed as a 613... | AIFM1
Apoptosis-inducing factor 1, mitochondrial is a protein that in humans is encoded by the AIFM1 gene on the X chromosome.[1][2] This protein localizes to the mitochondria, as well as the nucleus, where it carries out nuclear fragmentation as part of caspase-independent apoptosis.[3]
# Structure
AIFM1 is expresse... | https://www.wikidoc.org/index.php/AIFM1 | |
b559a7156015e46daafad1706121dace76129bf9 | wikidoc | AIFM2 | AIFM2
Apoptosis-inducing factor 2 (AIFM2), also known as apoptosis-inducing factor-homologous mitochondrion-associated inducer of death (AMID), is a protein that in humans is encoded by the AIFM2 gene, also known as p53-responsive gene 3 (PRG3), on chromosome 10.
This gene encodes a flavoprotein oxidoreductase that bin... | AIFM2
Apoptosis-inducing factor 2 (AIFM2), also known as apoptosis-inducing factor-homologous mitochondrion-associated inducer of death (AMID), is a protein that in humans is encoded by the AIFM2 gene, also known as p53-responsive gene 3 (PRG3), on chromosome 10.[1][2][3][4]
This gene encodes a flavoprotein oxidoreduc... | https://www.wikidoc.org/index.php/AIFM2 | |
d6d3d4280911901315e363152b9611a57664f964 | wikidoc | AKAP4 | AKAP4
A-kinase anchor protein 4 is a scaffold protein that in humans is encoded by the AKAP4 gene. It involves in the intracellular signalling of protein kinase -A. AKAP4 is called as cancer /testis antigen (CTA), it belongs to a class of tumour linked antigens categories by high expression in germ cells and cancer tha... | AKAP4
A-kinase anchor protein 4 is a scaffold protein that in humans is encoded by the AKAP4 gene.[1][2][3] It involves in the intracellular signalling of protein kinase -A.[4] AKAP4 is called as cancer /testis antigen (CTA), it belongs to a class of tumour linked antigens categories by high expression in germ cells a... | https://www.wikidoc.org/index.php/AKAP4 | |
5be74977c93a981a430c8ed88a089c720435dadf | wikidoc | AKAP6 | AKAP6
A-kinase anchor protein 6 is an enzyme that in humans is encoded by the AKAP6 gene.
The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins, which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations wi... | AKAP6
A-kinase anchor protein 6 is an enzyme that in humans is encoded by the AKAP6 gene.[1][2][3]
The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins, which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete lo... | https://www.wikidoc.org/index.php/AKAP6 | |
64fa07626fbc5fc405e07ba4c0650978c2c2303c | wikidoc | AKAP9 | AKAP9
A-kinase anchor protein 9 is a protein that in humans is encoded by the AKAP9 gene. AKAP9 is also known as Centrosome- and Golgi-localized protein kinase N-associated protein (CG-NAP) or AKAP350 or AKAP450
# Function
The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins which have th... | AKAP9
A-kinase anchor protein 9 is a protein that in humans is encoded by the AKAP9 gene.[1][2][3] AKAP9 is also known as Centrosome- and Golgi-localized protein kinase N-associated protein (CG-NAP) or AKAP350 or AKAP450 [4]
# Function
The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins ... | https://www.wikidoc.org/index.php/AKAP9 | |
5f0db789f2cd7d21016cf84729581f1e9b72a23d | wikidoc | AKTIP | AKTIP
AKT-interacting protein is a protein that in humans is encoded by the AKTIP gene.
The mouse homolog of this gene produces fused toes and thymic hyperplasia in heterozygous mutant animals while homozygous mutants die in early development. This gene may play a role in apoptosis as these morphological abnormalities ... | AKTIP
AKT-interacting protein is a protein that in humans is encoded by the AKTIP gene.[1][2][3]
The mouse homolog of this gene produces fused toes and thymic hyperplasia in heterozygous mutant animals while homozygous mutants die in early development. This gene may play a role in apoptosis as these morphological abno... | https://www.wikidoc.org/index.php/AKTIP | |
ce59a684caaba95f08594b74c0b3d11c1a8c99cd | wikidoc | ALARA | ALARA
See also: radiation protection
# Overview
ALARA is an acronym for an important principle in radiation protection and stands for "As Low As Reasonably Achievable". The aim is to minimize the risk of radioactive exposure or amount of dose while keeping in mind that some exposure may be acceptable in order to furth... | ALARA
See also: radiation protection
# Overview
ALARA is an acronym for an important principle in radiation protection and stands for "As Low As Reasonably Achievable". The aim is to minimize the risk of radioactive exposure or amount of dose while keeping in mind that some exposure may be acceptable in order to furt... | https://www.wikidoc.org/index.php/ALARA | |
6f40b9fd5ce4b775835e896d8b6f5be51a17ed9b | wikidoc | ALAS2 | ALAS2
Delta-aminolevulinate synthase 2 also known as ALAS2 is a protein that in humans is encoded by the ALAS2 gene. ALAS2 is an aminolevulinic acid synthase.
The product of this gene specifies an erythroid-specific mitochondrially located enzyme. The encoded protein catalyzes the first step in the heme biosynthetic pa... | ALAS2
Delta-aminolevulinate synthase 2 also known as ALAS2 is a protein that in humans is encoded by the ALAS2 gene.[1][2][3] ALAS2 is an aminolevulinic acid synthase.
The product of this gene specifies an erythroid-specific mitochondrially located enzyme. The encoded protein catalyzes the first step in the heme biosy... | https://www.wikidoc.org/index.php/ALAS2 | |
52b7db9c6f685bb9bdc38a07417446890ececd4e | wikidoc | ALCAM | ALCAM
CD166 antigen is a 100-105 kD typeI transmembrane glycoprotein that is a member of the immunoglobulin superfamily of proteins. In humans it is encoded by the ALCAM gene. It is also called CD166 (cluster of differentiation 166), MEMD, SC-1/DM-GRASP/BEN in the chicken, and KG-CAM in the rat.
Some literature sources... | ALCAM
CD166 antigen is a 100-105 kD typeI transmembrane glycoprotein that is a member of the immunoglobulin superfamily of proteins. In humans it is encoded by the ALCAM gene.[1][2] It is also called CD166 (cluster of differentiation 166), MEMD,[3] SC-1/DM-GRASP/BEN in the chicken, and KG-CAM in the rat.
Some literatu... | https://www.wikidoc.org/index.php/ALCAM | |
dbbc87c629fedc8ded03ecf6b36ebbbca1df7c9a | wikidoc | ALDH2 | ALDH2
Aldehyde dehydrogenase, mitochondrial is an enzyme that in humans is encoded by the ALDH2 gene located on chromosome 12. This protein belongs to the aldehyde dehydrogenase family of enzymes. Aldehyde dehydrogenase is the second enzyme of the major oxidative pathway of alcohol metabolism. Two major liver isoforms... | ALDH2
Aldehyde dehydrogenase, mitochondrial is an enzyme that in humans is encoded by the ALDH2 gene located on chromosome 12.[1][2] This protein belongs to the aldehyde dehydrogenase family of enzymes. Aldehyde dehydrogenase is the second enzyme of the major oxidative pathway of alcohol metabolism. Two major liver i... | https://www.wikidoc.org/index.php/ALDH2 | |
cb90994b3ad40554c268aab56b192c2ffe3e86ee | wikidoc | ALMS1 | ALMS1
Alstrom syndrome 1 also known as ALMS1 is a protein which in humans is encoded by the ALMS1 gene.
# Molecular biology
The gene is located on the short arm of chromosome 2 (2p13.2) on the plus (Watson) strand. It is 224,161 bases in length organised into 23 exons. The encoded protein has 4,167 amino acids and mol... | ALMS1
Alstrom syndrome 1 also known as ALMS1 is a protein which in humans is encoded by the ALMS1 gene.[1][2]
# Molecular biology
The gene is located on the short arm of chromosome 2 (2p13.2) on the plus (Watson) strand. It is 224,161 bases in length organised into 23 exons. The encoded protein has 4,167 amino acids ... | https://www.wikidoc.org/index.php/ALMS1 | |
20e90ac84f8c4514711e1f6a5cddf538e5d252bd | wikidoc | AMELX | AMELX
Amelogenin, X isoform is a protein that in humans is encoded by the AMELX (amelogenin, X isoform) gene.
The protein Amelogenin, X isoform is an isoform of amelogenin that comes from the X chromosome. The protein Amelogenin is a type of extracellular matrix protein, and is involved in the process of amelogenesis, ... | AMELX
Amelogenin, X isoform is a protein that in humans is encoded by the AMELX (amelogenin, X isoform) gene.[1]
The protein Amelogenin, X isoform is an isoform of amelogenin that comes from the X chromosome.[2][3] The protein Amelogenin is a type of extracellular matrix protein, and is involved in the process of amel... | https://www.wikidoc.org/index.php/AMELX | |
f0b6069a768a0f9a7035bedbeb050e62c3ecc01f | wikidoc | AMPD3 | AMPD3
AMP deaminase 3 is an enzyme that in humans is encoded by the AMPD3 gene.
This gene encodes a member of the AMP deaminase gene family. The encoded protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate cat... | AMPD3
AMP deaminase 3 is an enzyme that in humans is encoded by the AMPD3 gene.[1][2]
This gene encodes a member of the AMP deaminase gene family. The encoded protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenyl... | https://www.wikidoc.org/index.php/AMPD3 | |
0cccd89db3b20e94857ab59ad5ce707d2e3c029f | wikidoc | ANKK1 | ANKK1
Ankyrin repeat and kinase domain containing 1 (ANKK1) also known as protein kinase PKK2 or sugen kinase 288 (SgK288) is an enzyme that in humans is encoded by the ANKK1 gene. The ANKK1 is a member of an extensive family of the Ser/Thr protein kinase family, and protein kinase superfamily involved in signal tran... | ANKK1
Ankyrin repeat and kinase domain containing 1 (ANKK1) also known as protein kinase PKK2 or sugen kinase 288 (SgK288) is an enzyme that in humans is encoded by the ANKK1 gene. The ANKK1 is a member of an extensive family of the Ser/Thr protein kinase family, and protein kinase superfamily involved in signal tra... | https://www.wikidoc.org/index.php/ANKK1 | |
0d27ccaa03298c0c9834085823053ee949083589 | wikidoc | Aorta | Aorta
The aorta (generally pronounced eɪˈɔːtə or "ay-orta") is the largest artery in the human body, originating from the left ventricle of the heart and bringing oxygenated blood to all parts of the body in the systemic circulation.
# The course of the aorta
The aorta is usually divided into five segments/sections ... | Aorta
Template:Infobox Artery
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]
The aorta (generally pronounced eɪˈɔːtə or "ay-orta") is the largest artery in the human body, originating from the left ventricle of the heart and bringing oxygenated blood to all ... | https://www.wikidoc.org/index.php/AO | |
6ebe1c7d534e531e98412ca96c40c49a7382fb25 | wikidoc | AP1S1 | AP1S1
AP-1 complex subunit sigma-1A is a protein that in humans is encoded by the AP1S1 gene.
# Function
The protein encoded by this gene is part of the clathrin coat assembly complex which links clathrin to receptors in coated vesicles. These vesicles are involved in endocytosis and Golgi processing. This protein, as... | AP1S1
AP-1 complex subunit sigma-1A is a protein that in humans is encoded by the AP1S1 gene.[1][2][3]
# Function
The protein encoded by this gene is part of the clathrin coat assembly complex which links clathrin to receptors in coated vesicles. These vesicles are involved in endocytosis and Golgi processing. This p... | https://www.wikidoc.org/index.php/AP1S1 | |
ba9f0c4641f0bc73fe3fa327279bc59dbaf2b1ab | wikidoc | AP2M1 | AP2M1
AP-2 complex subunit mu is a protein that in humans is encoded by the AP2M1 gene.
# Function
This gene encodes a subunit of the heterotetrameric coat assembly protein complex 2 (AP2), which belongs to the adaptor complexes medium subunits family. The encoded protein is required for the activity of a vacuolar ATP... | AP2M1
AP-2 complex subunit mu is a protein that in humans is encoded by the AP2M1 gene.[1]
# Function
This gene encodes a subunit of the heterotetrameric coat assembly protein complex 2 (AP2), which belongs to the adaptor complexes medium subunits family. The encoded protein is required for the activity of a vacuolar... | https://www.wikidoc.org/index.php/AP2M1 | |
ebc4683b3a2d225f1a0689654a6047c60d3c0998 | wikidoc | AP4B1 | AP4B1
AP-4 complex subunit beta-1 is a protein that in humans is encoded by the AP4B1 gene.
# Function
The heterotetrameric adaptor protein (AP) complexes sort integral membrane proteins at various stages of the endocytic and secretory pathways. AP4 is composed of 2 large chains, beta-4 (AP4B1, this protein) and epsil... | AP4B1
AP-4 complex subunit beta-1 is a protein that in humans is encoded by the AP4B1 gene.[1][2]
# Function
The heterotetrameric adaptor protein (AP) complexes sort integral membrane proteins at various stages of the endocytic and secretory pathways. AP4 is composed of 2 large chains, beta-4 (AP4B1, this protein) an... | https://www.wikidoc.org/index.php/AP4B1 | |
da619021ba1993593e4b7a3fc6d2651983ff5814 | wikidoc | AP4E1 | AP4E1
AP-4 complex subunit epsilon-1 is a protein that in humans is encoded by the AP4E1 gene.
# Function
The heterotetrameric adaptor protein (AP) complexes sort integral membrane proteins at various stages of the endocytic and secretory pathways. AP4 is composed of 2 large chains, beta-4 (AP4B1) and epsilon-4 (AP4E1... | AP4E1
AP-4 complex subunit epsilon-1 is a protein that in humans is encoded by the AP4E1 gene.[1]
# Function
The heterotetrameric adaptor protein (AP) complexes sort integral membrane proteins at various stages of the endocytic and secretory pathways. AP4 is composed of 2 large chains, beta-4 (AP4B1) and epsilon-4 (A... | https://www.wikidoc.org/index.php/AP4E1 | |
f7b7f2b98ebc47996a104db3cd609f467bbe40bd | wikidoc | AP4M1 | AP4M1
AP-4 complex subunit mu-1 is a protein that in humans is encoded by the AP4M1 gene.
# Function
This gene encodes a subunit of the heterotetrameric AP-4 complex. The encoded protein belongs to the adaptor complexes medium subunits family. This AP-4 complex is involved in the recognition and sorting of cargo prote... | AP4M1
AP-4 complex subunit mu-1 is a protein that in humans is encoded by the AP4M1 gene.[1][2][3]
# Function
This gene encodes a subunit of the heterotetrameric AP-4 complex. The encoded protein belongs to the adaptor complexes medium subunits family. This AP-4 complex is involved in the recognition and sorting of c... | https://www.wikidoc.org/index.php/AP4M1 | |
c3491476d52901086f075cde81d50a3255217485 | wikidoc | AP4S1 | AP4S1
AP-4 complex subunit sigma-1 is a protein that in humans is encoded by the AP4S1 gene.
# Function
The heterotetrameric adaptor protein (AP) complexes sort integral membrane proteins at various stages of the endocytic and secretory pathways. AP4 is composed of 2 large chains, beta-4 (AP4B1) and epsilon-4 (AP4E1),... | AP4S1
AP-4 complex subunit sigma-1 is a protein that in humans is encoded by the AP4S1 gene.[1]
# Function
The heterotetrameric adaptor protein (AP) complexes sort integral membrane proteins at various stages of the endocytic and secretory pathways. AP4 is composed of 2 large chains, beta-4 (AP4B1) and epsilon-4 (AP4... | https://www.wikidoc.org/index.php/AP4S1 | |
f1a610bf3ad9cfb9986c48ac48bae45dede82dd1 | wikidoc | APAF1 | APAF1
Apoptotic protease activating factor 1, also known as APAF1, is a human homolog of C. elegans CED-4 gene.
# Function
This gene encodes a cytoplasmic protein that forms one of the central hubs in the apoptosis regulatory network. This protein contains (from the N terminal) a caspase recruitment domain (CARD), an ... | APAF1
Apoptotic protease activating factor 1, also known as APAF1, is a human homolog of C. elegans CED-4 gene.[1][2][3]
# Function
This gene encodes a cytoplasmic protein that forms one of the central hubs in the apoptosis regulatory network. This protein contains (from the N terminal) a caspase recruitment domain (... | https://www.wikidoc.org/index.php/APAF1 | |
8072302a93b6286009eec176733c04a7ec081e5e | wikidoc | APBA1 | APBA1
Amyloid beta A4 precursor protein-binding family A member 1 is a protein that in humans is encoded by the APBA1 gene.
# Function
The protein encoded by this gene is a member of the X11 protein family. It is a neuronal adaptor protein that interacts with the Alzheimer's disease amyloid precursor protein (APP). It... | APBA1
Amyloid beta A4 precursor protein-binding family A member 1 is a protein that in humans is encoded by the APBA1 gene.[1][2][3]
# Function
The protein encoded by this gene is a member of the X11 protein family. It is a neuronal adaptor protein that interacts with the Alzheimer's disease amyloid precursor protein... | https://www.wikidoc.org/index.php/APBA1 | |
1fa7154648f7884e230cd3b6f477bc15ed3e03d4 | wikidoc | APBA2 | APBA2
Amyloid beta A4 precursor protein-binding family A member 2 is a protein that in humans is encoded by the APBA2 gene.
# Function
The protein encoded by this gene is a member of the X11 protein family. It is a neuronal adaptor protein that interacts with the Alzheimer's disease amyloid precursor protein (APP). It... | APBA2
Amyloid beta A4 precursor protein-binding family A member 2 is a protein that in humans is encoded by the APBA2 gene.[1][2]
# Function
The protein encoded by this gene is a member of the X11 protein family. It is a neuronal adaptor protein that interacts with the Alzheimer's disease amyloid precursor protein (A... | https://www.wikidoc.org/index.php/APBA2 | |
d7a4ef6d4f33af386b765743ac13103c278ac0b4 | wikidoc | APBB1 | APBB1
Amyloid beta A4 precursor protein-binding family B member 1 is a protein that in humans is encoded by the APBB1 gene.
# Function
The protein encoded by this gene is a member of the Fe65 protein family. It is an adaptor protein localized in the nucleus. It interacts with the Alzheimer's disease amyloid precursor ... | APBB1
Amyloid beta A4 precursor protein-binding family B member 1 is a protein that in humans is encoded by the APBB1 gene.[1][2][3]
# Function
The protein encoded by this gene is a member of the Fe65 protein family. It is an adaptor protein localized in the nucleus. It interacts with the Alzheimer's disease amyloid ... | https://www.wikidoc.org/index.php/APBB1 | |
745fae0441078c2e3de67e15736b2df4e40d02a2 | wikidoc | APEX1 | APEX1
DNA-(apurinic or apyrimidinic site) lyase is an enzyme that in humans is encoded by the APEX1 gene.
Apurinic/apyrimidinic (AP) sites (also called "abasic sites") occur frequently in DNA molecules by spontaneous hydrolysis, by DNA damaging agents or by DNA glycosylases that remove specific abnormal bases. AP sites... | APEX1
DNA-(apurinic or apyrimidinic site) lyase is an enzyme that in humans is encoded by the APEX1 gene.
Apurinic/apyrimidinic (AP) sites (also called "abasic sites") occur frequently in DNA molecules by spontaneous hydrolysis, by DNA damaging agents or by DNA glycosylases that remove specific abnormal bases. AP site... | https://www.wikidoc.org/index.php/APEX1 | |
89387e3ef551ed6d68f6dd5f16fd1ac97221bbac | wikidoc | APLP1 | APLP1
Amyloid-like protein 1, also known as APLP1, is a protein that in humans is encoded by the APLP1 gene. APLP1 along with APLP2 are important modulators of glucose and insulin homeostasis.
# Function
This gene encodes a member of the highly conserved amyloid precursor protein gene family. The encoded protein is a ... | APLP1
Amyloid-like protein 1, also known as APLP1, is a protein that in humans is encoded by the APLP1 gene.[1][2] APLP1 along with APLP2 are important modulators of glucose and insulin homeostasis.[3]
# Function
This gene encodes a member of the highly conserved amyloid precursor protein gene family. The encoded pro... | https://www.wikidoc.org/index.php/APLP1 | |
d674b8c6bb7644dd51885557c32581353a712e99 | wikidoc | APLP2 | APLP2
Amyloid-like protein 2, also known as APLP2, is a protein that in humans is encoded by the APLP2 gene. APLP2 along with APLP1 are important modulators of glucose and insulin homeostasis.
# Gene location
The human APLP2 gene is located on the long (q) arm of chromosome 11 at region 2 band 4, from base pair 130, 0... | APLP2
Amyloid-like protein 2, also known as APLP2, is a protein that in humans is encoded by the APLP2 gene.[1][2] APLP2 along with APLP1 are important modulators of glucose and insulin homeostasis.[3]
# Gene location
The human APLP2 gene is located on the long (q) arm of chromosome 11 at region 2 band 4, from base p... | https://www.wikidoc.org/index.php/APLP2 | |
98a6685cff9798175ebcaadf815e49d9d447227b | wikidoc | APOA2 | APOA2
Apolipoprotein A-II is a protein that in humans is encoded by the APOA2 gene.
# Function
This gene encodes apolipoprotein (apo-) A-II, which is the second most abundant protein of the high density lipoprotein particles. The protein is found in plasma as a monomer, homodimer, or heterodimer with apolipoprotein D.... | APOA2
Apolipoprotein A-II is a protein that in humans is encoded by the APOA2 gene.[1]
# Function
This gene encodes apolipoprotein (apo-) A-II, which is the second most abundant protein of the high density lipoprotein particles. The protein is found in plasma as a monomer, homodimer, or heterodimer with apolipoprotei... | https://www.wikidoc.org/index.php/APOA2 | |
656cf6deb89b3c1480e45ef8c95f3e26629aef9e | wikidoc | APOA4 | APOA4
Apolipoprotein A-IV (also known as apoA-IV, apoAIV, or apoA4) is plasma protein that is the product of the human gene APOA4.
# Gene
APOA4 resides on chromosome 11 in close linkage to APOA1 and APOC3. APOA4 contains 3 exons separated by two introns, and is polymorphic, although most of the reported sequence polym... | APOA4
Apolipoprotein A-IV (also known as apoA-IV, apoAIV, or apoA4) is plasma protein that is the product of the human gene APOA4.[1][2]
# Gene
APOA4 resides on chromosome 11 in close linkage to APOA1 and APOC3. APOA4 contains 3 exons separated by two introns, and is polymorphic, although most of the reported sequenc... | https://www.wikidoc.org/index.php/APOA4 | |
e61e1a91b0844bcabf9fec165e59a4958220f476 | wikidoc | APOA5 | APOA5
Apolipoprotein A-V is a protein that in humans is encoded by the APOA5 gene on chromosome 11. It is significantly expressed in liver. The protein encoded by this gene is an apolipoprotein and an important determinant of plasma triglyceride levels, a major risk factor for coronary artery disease. It is a component... | APOA5
Apolipoprotein A-V is a protein that in humans is encoded by the APOA5 gene on chromosome 11.[1][2][3] It is significantly expressed in liver.[4] The protein encoded by this gene is an apolipoprotein and an important determinant of plasma triglyceride levels, a major risk factor for coronary artery disease. It i... | https://www.wikidoc.org/index.php/APOA5 | |
4e460bf1b91d44b0e0cdefc15bc872b07770208f | wikidoc | APOL2 | APOL2
Apolipoprotein L2 is a protein that in humans is encoded by the APOL2 gene.
This gene is a member of the apolipoprotein L gene family and protein in this family are lipid-binding proteins. This gene encodes a 37.1 kDa protein and The protein sequence contains 337bp. Localization of this protein is mainly found i... | APOL2
Apolipoprotein L2 is a protein that in humans is encoded by the APOL2 gene.[1][2][3]
This gene is a member of the apolipoprotein L gene family and protein in this family are lipid-binding proteins. This gene encodes a 37.1 kDa protein and The protein sequence contains 337bp. Localization of this protein is main... | https://www.wikidoc.org/index.php/APOL2 | |
a4378e172d8244338464c28cd686ed0212871bd6 | wikidoc | APPL1 | APPL1
Adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1 (APPL1), or DCC-interacting protein 13-alpha (DIP13alpha), is a protein that in humans is encoded by the APPL1 gene. APPL1 contains several key interactory domains: pleckstrin homology (PH) domain, phosphotyrosine-binding (PTB) domai... | APPL1
Adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1 (APPL1), or DCC-interacting protein 13-alpha (DIP13alpha), is a protein that in humans is encoded by the APPL1 gene.[1][2][3] APPL1 contains several key interactory domains: pleckstrin homology (PH) domain, phosphotyrosine-binding (... | https://www.wikidoc.org/index.php/APPL1 | |
e39485878eb113c1d6e7211c9142fbf00745888b | wikidoc | APPL2 | APPL2
DCC-interacting protein 13-beta is a protein that in humans is encoded by the APPL2 gene.
# Model organisms
Model organisms have been used in the study of APPL2 function. A conditional knockout mouse line, called Appl2tm1a(KOMP)Wtsi was generated as part of the International Knockout Mouse Consortium program — a... | APPL2
DCC-interacting protein 13-beta is a protein that in humans is encoded by the APPL2 gene.[1][2][3]
# Model organisms
Model organisms have been used in the study of APPL2 function. A conditional knockout mouse line, called Appl2tm1a(KOMP)Wtsi[8][9] was generated as part of the International Knockout Mouse Consor... | https://www.wikidoc.org/index.php/APPL2 | |
606ad5a6888825aad746cbcbbcaf82c5d590d47d | wikidoc | ARID2 | ARID2
AT-rich interactive domain-containing protein 2 (ARID2) is a protein that in humans is encoded by the ARID2 gene.
# Function
ARID2 is a subunit of the PBAF chromatin-remodeling complex, which facilitates ligand-dependent transcriptional
activation by nuclear receptors.
# Structure
The ARID2 protein contains tw... | ARID2
AT-rich interactive domain-containing protein 2 (ARID2) is a protein that in humans is encoded by the ARID2 gene.[1]
# Function
ARID2 is a subunit of the PBAF chromatin-remodeling complex, which facilitates ligand-dependent transcriptional
activation by nuclear receptors.[1]
# Structure
The ARID2 protein cont... | https://www.wikidoc.org/index.php/ARID2 | |
32ceb3c59ae48dcb26ca53aab3424408bff2c915 | wikidoc | ARL4D | ARL4D
ADP-ribosylation factor-like protein 4D is a protein that in humans is encoded by the ARL4D gene.
# Function
ADP-ribosylation factor 4D is a member of the ADP-ribosylation factor family of GTP-binding proteins. ARL4D is closely similar to ARL4A and ARL4C and each has a nuclear localization signal and an unusuall... | ARL4D
ADP-ribosylation factor-like protein 4D is a protein that in humans is encoded by the ARL4D gene.[1][2]
# Function
ADP-ribosylation factor 4D is a member of the ADP-ribosylation factor family of GTP-binding proteins. ARL4D is closely similar to ARL4A and ARL4C and each has a nuclear localization signal and an u... | https://www.wikidoc.org/index.php/ARL4D | |
f7a90ce8b937f98ae8b9e422208fdb4170f690b5 | wikidoc | ARMC6 | ARMC6
The human gene ARMC6 encodes a protein called Armadillo repeat-containing protein 6.
The function of this gene's protein product has not been determined. A related protein in mouse suggests that this protein has a conserved function.
The protein is characterized by the presence of armadillo repeats in its amino a... | ARMC6
The human gene ARMC6 encodes a protein called Armadillo repeat-containing protein 6.[1][2]
The function of this gene's protein product has not been determined. A related protein in mouse suggests that this protein has a conserved function.[2]
The protein is characterized by the presence of armadillo repeats in i... | https://www.wikidoc.org/index.php/ARMC6 | |
491c229bb839877d427a91c106988f8868547657 | wikidoc | ARPC4 | ARPC4
Actin-related protein 2/3 complex subunit 4 is a protein that in humans is encoded by the ARPC4 gene.
# Function
This gene encodes one of seven subunits of the human Arp2/3 protein complex. The Arp2/3 protein complex has been implicated in the control of actin polymerization in cells and has been conserved throu... | ARPC4
Actin-related protein 2/3 complex subunit 4 is a protein that in humans is encoded by the ARPC4 gene.[1][2][3]
# Function
This gene encodes one of seven subunits of the human Arp2/3 protein complex. The Arp2/3 protein complex has been implicated in the control of actin polymerization in cells and has been conse... | https://www.wikidoc.org/index.php/ARPC4 | |
f7bb55095853cfd14a65d2d55217bdef9712e258 | wikidoc | ARVD1 | ARVD1
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 1;
# Overview
# Pathophysiology
The pathogenesis of ARVD involves apoptosis with fatty and fibro-fatty infiltration of the right ventricular free wall leading to heart failure and ventricular arrhythmias.
## Genetics
There is an autosomal d... | ARVD1
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 1;
# Overview
# Pathophysiology
The pathogenesis of ARVD involves apoptosis with fatty and fibro-fatty infiltration of the right ventricular free wall leading to heart failure and ventricul... | https://www.wikidoc.org/index.php/ARVD1 | |
4748c76184435cfdc7a7f48bfcd5cca12714a0f8 | wikidoc | ARVD2 | ARVD2
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 2; arrhythmogenic right ventricular cardiomyopathy 2; ARVC2
# Overview
Arrhythmogenic right ventricular dysplasia type 2 is a "concealed form" of ARVD. There is no change in heart size. There are no EKG changes on the resting electrocardiogr... | ARVD2
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 2; arrhythmogenic right ventricular cardiomyopathy 2; ARVC2
# Overview
Arrhythmogenic right ventricular dysplasia type 2 is a "concealed form" of ARVD. There is no change in heart size. The... | https://www.wikidoc.org/index.php/ARVD2 | |
702216162266344bdcf36f2e16e1e87bbcde1982 | wikidoc | ARVD3 | ARVD3
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 3; arrhythmogenic right ventricular cardiomyopathy 3; ARVC3
# Overview
# Pathophysiology
The pathogenesis of ARVD involves apoptosis with fatty and fibro-fatty infiltration of the right ventricular free wall leading to heart failure and ven... | ARVD3
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 3; arrhythmogenic right ventricular cardiomyopathy 3; ARVC3
# Overview
# Pathophysiology
The pathogenesis of ARVD involves apoptosis with fatty and fibro-fatty infiltration of the right ve... | https://www.wikidoc.org/index.php/ARVD3 | |
f62060e139e3537875c2685b9faa1621b976c786 | wikidoc | ARVD4 | ARVD4
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 4; arrhythmogenic right ventricular cardiomyopathy 4; ARVC4
# Overview
Arrhythmogenic right ventricular dysplasia is a type of nonischemic cardiomyopathy that involves primarily the right ventricle. It is characterized by hypokinetic areas ... | ARVD4
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 4; arrhythmogenic right ventricular cardiomyopathy 4; ARVC4
# Overview
Arrhythmogenic right ventricular dysplasia is a type of nonischemic cardiomyopathy that involves primarily the right v... | https://www.wikidoc.org/index.php/ARVD4 | |
d902137a991586333058cff5e44e3bbae48b115f | wikidoc | ARVD5 | ARVD5
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 5; arrhythmogenic right ventricular cardiomyopathy 5; ARVC5
# Overview
Arrhythmogenic right ventricular dysplasia is a type of nonischemic cardiomyopathy that involves primarily the right ventricle. It is characterized by hypokinetic areas ... | ARVD5
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 5; arrhythmogenic right ventricular cardiomyopathy 5; ARVC5
# Overview
Arrhythmogenic right ventricular dysplasia is a type of nonischemic cardiomyopathy that involves primarily the right v... | https://www.wikidoc.org/index.php/ARVD5 | |
8799bca506727ec3db67332ac982d18325e1cf93 | wikidoc | ARVD6 | ARVD6
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 6; arrhythmogenic right ventricular cardiomyopathy 6; ARVC6
# Overview
Arrhythmogenic right ventricular dysplasia is a type of nonischemic cardiomyopathy that involves primarily the right ventricle. It is characterized by hypokinetic areas ... | ARVD6
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 6; arrhythmogenic right ventricular cardiomyopathy 6; ARVC6
# Overview
Arrhythmogenic right ventricular dysplasia is a type of nonischemic cardiomyopathy that involves primarily the right v... | https://www.wikidoc.org/index.php/ARVD6 | |
b9072c0114c5e5da7ea305f78f971905edb4243c | wikidoc | ARVD7 | ARVD7
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 7; arrhythmogenic right ventricular cardiomyopathy 7; ARVC7
# Overview
Arrhythmogenic right ventricular dysplasia is a type of nonischemic cardiomyopathy that involves primarily the right ventricle. It is characterized by hypokinetic areas ... | ARVD7
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 7; arrhythmogenic right ventricular cardiomyopathy 7; ARVC7
# Overview
Arrhythmogenic right ventricular dysplasia is a type of nonischemic cardiomyopathy that involves primarily the right v... | https://www.wikidoc.org/index.php/ARVD7 | |
8360b4c65a1306f893cccc844b102b2b432fa101 | wikidoc | ARVD8 | ARVD8
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 8; arrhythmogenic right ventricular cardiomyopathy 8; ARVC8
# Overview
Arrhythmogenic right ventricular dysplasia is a type of nonischemic cardiomyopathy that involves primarily the right ventricle. It is characterized by hypokinetic areas ... | ARVD8
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 8; arrhythmogenic right ventricular cardiomyopathy 8; ARVC8
# Overview
Arrhythmogenic right ventricular dysplasia is a type of nonischemic cardiomyopathy that involves primarily the right v... | https://www.wikidoc.org/index.php/ARVD8 | |
40cc8486f3b31b782e6ac912714e99dd313941d0 | wikidoc | ARVD9 | ARVD9
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 9; arrhythmogenic right ventricular cardiomyopathy 9; ARVC9
# Overview
Arrhythmogenic right ventricular dysplasia is a type of nonischemic cardiomyopathy that involves primarily the right ventricle. It is characterized by hypokinetic areas ... | ARVD9
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Arrhythmogenic right ventricular dysplasia type 9; arrhythmogenic right ventricular cardiomyopathy 9; ARVC9
# Overview
Arrhythmogenic right ventricular dysplasia is a type of nonischemic cardiomyopathy that involves primarily the right v... | https://www.wikidoc.org/index.php/ARVD9 | |
9f004512ea6e84f2a24c88829c1bafe7c8ce3850 | wikidoc | ASCL1 | ASCL1
Achaete-scute homolog 1 is a protein that in humans is encoded by the ASCL1 gene. Because it was discovered subsequent to studies on its homolog in Drosophila, the Achaete-scute complex, it was originally named MASH-1 for mammalian achaete scute homolog-1.
# Function
This gene encodes a member of the basic helix... | ASCL1
Achaete-scute homolog 1 is a protein that in humans is encoded by the ASCL1 gene.[1][2] Because it was discovered subsequent to studies on its homolog in Drosophila, the Achaete-scute complex, it was originally named MASH-1 for mammalian achaete scute homolog-1.[3]
# Function
This gene encodes a member of the b... | https://www.wikidoc.org/index.php/ASCL1 | |
4a6e13ac60eb664f5ec56c323fc2b210887ea1a1 | wikidoc | ASF1A | ASF1A
Histone chaperone ASF1A is a protein that in humans is encoded by the ASF1A gene.
# Function
This gene encodes a member of the H3/H4 family of histone chaperone proteins and is similar to the anti-silencing function-1 gene in yeast. The protein is a key component of a histone donor complex that functions in nucl... | ASF1A
Histone chaperone ASF1A is a protein that in humans is encoded by the ASF1A gene.[1][2][3]
# Function
This gene encodes a member of the H3/H4 family of histone chaperone proteins and is similar to the anti-silencing function-1 gene in yeast. The protein is a key component of a histone donor complex that functio... | https://www.wikidoc.org/index.php/ASF1A | |
aaea02cc4f41bbf56ff3fee5e6948964706ae1da | wikidoc | ASF1B | ASF1B
Histone chaperone ASF1B is a protein that in humans is encoded by the ASF1B gene.
# Function
This gene encodes a member of the H3/H4 family of histone chaperone proteins and is similar to the anti-silencing function-1 gene in yeast. The encoded protein is the substrate of the tousled-like kinase family of cell c... | ASF1B
Histone chaperone ASF1B is a protein that in humans is encoded by the ASF1B gene.[1][2][3]
# Function
This gene encodes a member of the H3/H4 family of histone chaperone proteins and is similar to the anti-silencing function-1 gene in yeast. The encoded protein is the substrate of the tousled-like kinase family... | https://www.wikidoc.org/index.php/ASF1B | |
ce8cde148f95fa34787bb493c20c6d82861f8a4f | wikidoc | ASH1L | ASH1L
ASH1L (also called huASH1, ASH1, ASH1L1, ASH1-like, or KMT2H) is a histone-lysine N-methyltransferase enzyme encoded by the ASH1L gene located at chromosomal band 1q22. ASH1L is the human homolog of Drosophila Ash1 (absent, small, or homeotic-like).
# Gene
Ash1 was discovered as a gene causing an imaginal disc ... | ASH1L
ASH1L (also called huASH1, ASH1, ASH1L1, ASH1-like, or KMT2H) is a histone-lysine N-methyltransferase enzyme encoded by the ASH1L gene located at chromosomal band 1q22. ASH1L is the human homolog of Drosophila Ash1 (absent, small, or homeotic-like).
# Gene
Ash1 was discovered as a gene causing an imaginal disc... | https://www.wikidoc.org/index.php/ASH1L | |
edc73eb6f6688b4e6efa39e7d3ea132398a0bc81 | wikidoc | ASIC1 | ASIC1
Acid-sensing ion channel 1 (ASIC1) also known as amiloride-sensitive cation channel 2, neuronal (ACCN2) or brain sodium channel 2 (BNaC2) is a protein that in humans is encoded by the ASIC1 gene. The ASIC1 gene is one of the five paralogous genes that encode proteins that form trimeric acid-sensing ion channels ... | ASIC1
Acid-sensing ion channel 1 (ASIC1) also known as amiloride-sensitive cation channel 2, neuronal (ACCN2) or brain sodium channel 2 (BNaC2) is a protein that in humans is encoded by the ASIC1 gene. The ASIC1 gene is one of the five paralogous genes that encode proteins that form trimeric acid-sensing ion channels... | https://www.wikidoc.org/index.php/ASIC1 | |
db2d0963af6260ee3a21a56fedce4b5183d23e69 | wikidoc | ASIC2 | ASIC2
Acid-sensing ion channel 2 (ASIC2) also known as amiloride-sensitive cation channel 1, neuronal (ACCN1) or brain sodium channel 1 (BNaC1) is a protein that in humans is encoded by the ASIC2 gene. The ASIC2 gene is one of the five paralogous genes that encode proteins that form trimeric acid-sensing ion channels ... | ASIC2
Acid-sensing ion channel 2 (ASIC2) also known as amiloride-sensitive cation channel 1, neuronal (ACCN1) or brain sodium channel 1 (BNaC1) is a protein that in humans is encoded by the ASIC2 gene. The ASIC2 gene is one of the five paralogous genes that encode proteins that form trimeric acid-sensing ion channels... | https://www.wikidoc.org/index.php/ASIC2 | |
f4961b7ba1b42bb85d860e1855c29efafbf6ba96 | wikidoc | ASIC3 | ASIC3
Acid-sensing ion channel 3 (ASIC3) also known as amiloride-sensitive cation channel 3 (ACCN3) or testis sodium channel 1 (TNaC1) is a protein that in humans is encoded by the ASIC3 gene. The ASIC3 gene is one of the five paralogous genes that encode proteins that form trimeric acid-sensing ion channels (ASICs) in... | ASIC3
Acid-sensing ion channel 3 (ASIC3) also known as amiloride-sensitive cation channel 3 (ACCN3) or testis sodium channel 1 (TNaC1) is a protein that in humans is encoded by the ASIC3 gene. The ASIC3 gene is one of the five paralogous genes that encode proteins that form trimeric acid-sensing ion channels (ASICs) i... | https://www.wikidoc.org/index.php/ASIC3 | |
d5acc51787dd95dda11c5b4945a8ccb2de136c82 | wikidoc | ASIC4 | ASIC4
Acid-sensing ion channel 4 (ASIC4) also known as amiloride-sensitive cation channel 4 (ACCN4) is a protein that in humans is encoded by the ASIC4 gene. The ASIC4 gene is one of the five paralogous genes that encode proteins that form trimeric acid-sensing ion channels (ASICs) in mammals. The cDNA of this gene was... | ASIC4
Acid-sensing ion channel 4 (ASIC4) also known as amiloride-sensitive cation channel 4 (ACCN4) is a protein that in humans is encoded by the ASIC4 gene. The ASIC4 gene is one of the five paralogous genes that encode proteins that form trimeric acid-sensing ion channels (ASICs) in mammals.[1] The cDNA of this gene... | https://www.wikidoc.org/index.php/ASIC4 | |
321c59487cfe1eca3327c14c7e830f82768c162c | wikidoc | ASK-1 | ASK-1
Apoptosis signal-regulating kinase 1, ASK-1, is part of the mitogen-activated protein kinase (MAPK) cascade. In humans it is also known as "mitogen-activated protein kinase kinase kinase 5", abbreviated as "MAP3K5".
Mitogen-activated protein kinase (MAPK) signaling cascades include MAPK or extracellular signal-re... | ASK-1
Apoptosis signal-regulating kinase 1, ASK-1, is part of the mitogen-activated protein kinase (MAPK) cascade. In humans it is also known as "mitogen-activated protein kinase kinase kinase 5", abbreviated as "MAP3K5".
Mitogen-activated protein kinase (MAPK) signaling cascades include MAPK or extracellular signal-r... | https://www.wikidoc.org/index.php/ASK-1 | |
8c456498786bc38f6a39727da533be6435e7ff58 | wikidoc | ASXL1 | ASXL1
Putative Polycomb group protein ASXL1 is a protein that in humans is encoded by the ASXL1 gene.
In Drosophila, the Additional sex combs (Asx) gene encodes a chromatin-binding protein required for normal determination of segment identity in the developing embryo. The protein is a member of the Polycomb group of pr... | ASXL1
Putative Polycomb group protein ASXL1 is a protein that in humans is encoded by the ASXL1 gene.[1][2]
In Drosophila, the Additional sex combs (Asx) gene encodes a chromatin-binding protein required for normal determination of segment identity in the developing embryo. The protein is a member of the Polycomb grou... | https://www.wikidoc.org/index.php/ASXL1 | |
71d7916a3231b390c4c30df7b108ab3645755f71 | wikidoc | ATG12 | ATG12
Autophagy-related protein 12 is a protein that in humans is encoded by the ATG12 gene.
Autophagy is a process of bulk protein degradation in which cytoplasmic components, including organelles, are enclosed in double-membrane structures called autophagosomes and delivered to lysosomes or vacuoles for degradation. ... | ATG12
Autophagy-related protein 12 is a protein that in humans is encoded by the ATG12 gene.[1][2]
Autophagy is a process of bulk protein degradation in which cytoplasmic components, including organelles, are enclosed in double-membrane structures called autophagosomes and delivered to lysosomes or vacuoles for degrad... | https://www.wikidoc.org/index.php/ATG12 | |
628e5390be4428d9b02032dc6beefb9a9610c68c | wikidoc | ATG4B | ATG4B
Cysteine protease ATG4B is an enzyme that in humans is encoded by the ATG4B gene.
# Function
Autophagy is the process by which endogenous proteins and damaged organelles are destroyed intracellularly. Autophagy is postulated to be essential for cell homeostasis and cell remodeling during differentiation, metamor... | ATG4B
Cysteine protease ATG4B is an enzyme that in humans is encoded by the ATG4B gene.[1][2]
# Function
Autophagy is the process by which endogenous proteins and damaged organelles are destroyed intracellularly. Autophagy is postulated to be essential for cell homeostasis and cell remodeling during differentiation, ... | https://www.wikidoc.org/index.php/ATG4B | |
deee5073aeba1128afe83658d4670ad0c2b91014 | wikidoc | ATG4D | ATG4D
The human ATG4D gene encodes the protein Autophagy related 4D, cysteine peptidase.
# Function
Autophagy is the process by which endogenous proteins and damaged organelles are destroyed intracellularly. Autophagy is postulated to be essential for cell homeostasis and cell remodeling during differentiation, metamo... | ATG4D
The human ATG4D gene encodes the protein Autophagy related 4D, cysteine peptidase.[1]
# Function
Autophagy is the process by which endogenous proteins and damaged organelles are destroyed intracellularly. Autophagy is postulated to be essential for cell homeostasis and cell remodeling during differentiation, me... | https://www.wikidoc.org/index.php/ATG4D | |
20796e0e844682c9d3742ae52cbec398223e8571 | wikidoc | ATOX1 | ATOX1
ATOX1 is a copper metallochaperone protein that is encoded by the ATOX1 gene in humans. In mammals, ATOX1 plays a key role in copper homeostasis as it delivers copper from the cytosol to transporters ATP7A and ATP7B. Homologous proteins are found in a wide variety of eukaryotes, including Saccharomyces cerevisiae... | ATOX1
ATOX1 is a copper metallochaperone protein that is encoded by the ATOX1 gene in humans.[1][2] In mammals, ATOX1 plays a key role in copper homeostasis as it delivers copper from the cytosol to transporters ATP7A and ATP7B.[3][4][5] Homologous proteins are found in a wide variety of eukaryotes, including Saccharo... | https://www.wikidoc.org/index.php/ATOX1 | |
9d07674e9d1fec6e32cc7e02f29ff0a07a7311f2 | wikidoc | ATP5D | ATP5D
ATP synthase subunit delta, mitochondrial, also known as ATP synthase F1 subunit delta or F-ATPase delta subunit is an enzyme that in humans is encoded by the ATP5F1D (formerly ATP5D) gene. This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an ... | ATP5D
ATP synthase subunit delta, mitochondrial, also known as ATP synthase F1 subunit delta or F-ATPase delta subunit is an enzyme that in humans is encoded by the ATP5F1D (formerly ATP5D) gene.[1][2][3] This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, uti... | https://www.wikidoc.org/index.php/ATP5D | |
2b9c2d0a93e421cfe7ede4fbf01bd7fbe4d86901 | wikidoc | ATP5E | ATP5E
ATP synthase F1 subunit epsilon, mitochondrial is an enzyme that in humans is encoded by the ATP5F1E gene. The protein encoded by ATP5F1E is a subunit of ATP synthase, also known as Complex V. Variations of this gene have been associated with mitochondrial complex V deficiency, nuclear 3 (MC5DN3) and Papillary Th... | ATP5E
ATP synthase F1 subunit epsilon, mitochondrial is an enzyme that in humans is encoded by the ATP5F1E gene.[1][2] The protein encoded by ATP5F1E is a subunit of ATP synthase, also known as Complex V. Variations of this gene have been associated with mitochondrial complex V deficiency, nuclear 3 (MC5DN3) and Papil... | https://www.wikidoc.org/index.php/ATP5E | |
36f0e442da9a4348e626080d0b65ac11f2c7c816 | wikidoc | ATP5H | ATP5H
The human gene ATP5PD encodes subunit d of the peripheral stalk part of the enzyme mitochondrial ATP synthase.
Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit... | ATP5H
The human gene ATP5PD encodes subunit d of the peripheral stalk part of the enzyme mitochondrial ATP synthase.[1][2]
Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-... | https://www.wikidoc.org/index.php/ATP5H |
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