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 1170 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1101
ATPase H+ transporting V0 subunit d2
ATP6D2, VMA6
Ehlers-danlos syndrome, Oligodendroglioma, Ovarian cysts, Scoliosis, Stomach neoplasms

1102
ATPase H+ transporting V0 subunit e1
ATP6H, ATP6V0E, M9.2, Vma21, Vma21p
Color vision deficiency

1103
ATPase H+ transporting V0 subunit e2
ATP6V0E2L, C7orf32
Alzheimer disease, Scoliosis

1104
ATPase H+ transporting V1 subunit A
ARCL2D, ATP6A1, ATP6V1A1, DEE93, HO68, IECEE3, VA68, VPP2, Vma1
Cutis laxa, Accessory skin tag, Cyclin-dependent kinase-like 5 deficiency, Developmental and epileptic encephalopathy, Developmental disability, Benign pemphigus, Darier disease, Rothmund-thomson syndrome

1105
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

1106
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

1107
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

1108
ATPase H+ transporting V1 subunit C2
ATP6C2, VMA5
Dementia, Distal renal tubular acidosis

1109
ATPase H+ transporting V1 subunit D
ATP6M, VATD, VMA8
Liver cirrhosis

1110
ATPase H+ transporting V1 subunit E1
ARCL2C, ATP6E, ATP6E2, ATP6V1E, P31, Vma4
Cutis laxa, Accessory skin tag, Benign pemphigus, Darier disease, Rothmund-thomson syndrome