Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "A"
1101 to 1110 of 1165 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1101
ATPase H+ transporting V1 subunit B1
ATP6B1, DRTA2, RTA1B, VATB, VMA2, VPP3
Distal renal tubular acidosis, Gout, Hearing impairment, Nephrolithiasis, Polydactyly, Scoliosis, Urogenital abnormalities, Usher syndrome

1102
ATPase H+ transporting V1 subunit B2
ATP6B1B2, ATP6B2, DOOD, HO57, VATB, VPP3, Vma2, ZLS2
Deafness-onychodystrophy syndrome, Bipolar disorder, Deafness with congenital onychodystrophy, Developmental and epileptic encephalopathy, Digitrenocerebral syndrome, Doors syndrome, Lymphoma, Major depressive disorder, Neurodevelopmental disorder, Osteoarthritis, Schizophrenia, Zimmermann-laband syndrome

1103
ATPase H+ transporting V1 subunit C1
ATP6C, ATP6D, VATC, Vma5
Digitrenocerebral syndrome, Gout, Juvenile idiopathic arthritis, Neurodevelopmental disorder, Obstructive sleep apnea syndrome, Small vessel stroke

1104
ATPase H+ transporting V1 subunit C2
ATP6C2, VMA5
Dementia, Distal renal tubular acidosis

1105
ATPase H+ transporting V1 subunit E1
ARCL2C, ATP6E, ATP6E2, ATP6V1E, P31, Vma4
Cutis laxa, Accessory skin tag, Benign pemphigus, Darier disease, Rothmund-thomson syndrome

1106
ATPase H+ transporting V1 subunit G1
ATP6G, ATP6G1, ATP6GL, ATP6J, Vma10
Oligodendroglioma

1107
ATPase H+ transporting V1 subunit G2
ATP6G, ATP6G2, NG38, VMA10
Myasthenia gravis, Myositis, Rheumatoid arthritis, Diabetes mellitus type 1

1108
ATPase H+ transporting V1 subunit G3
ATP6G3, Vma10
Bipolar disorder, Crohn disease, Hyperthyroidism, Inflammatory bowel disease, Insomnia, Obsessive-compulsive disorder, Optic atrophy, Rheumatoid arthritis, Systemic lupus erythematosus, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitis

1109
ATPase H+ transporting V1 subunit H
CGI-11, MSTP042, NBP1, SFD, SFDalpha, SFDbeta, VMA13
Astrocytoma, Bipolar disorder

1110
ATPase copper transporting alpha
DSMAX, HMNX, MK, MNK, SMAX3
Anemia, Aortic rupture, Ataxia, Au-kline syndrome, Charcot-marie-tooth disease, Colonic neoplasms, Cutis laxa, Ehlers-danlos syndrome, Growth disorder, Hemolysis, Hereditary motor and sensory neuropathies, Hirschsprung disease, Pulmonary hypertension, Distal hereditary motor neuropathy, Paralysis
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