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"
1091 to 1100 of 1165 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1091
ATPase H+ transporting accessory protein 2
(P)RR, APT6M8-9, ATP6IP2, ATP6M8-9, CDG2R, ELDF10, HT028, M8-9, MRXE, MRXSH, MSTP009, PRR, RENR, XMRE, XPDS
Congenital disorder of glycosylation, Craniofacial abnormalities, Intellectual developmental disorder, x-linked, Parkinsonism with spasticity, x-linked, X-linked intellectual disability, X-linked parkinsonism-spasticity syndrome

1092
ATPase H+ transporting V0 subunit a1
ATP6N1, ATP6N1A, DEE104, NEDEBA, Stv1, VPP1, Vph1, a1
Asthma, Autism, Cerebellar ataxia, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Esophageal atresia, Global developmental delay, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Seizures

1093
ATPase H+ transporting V0 subunit a2
A2, ARCL, ARCL2A, ATP6A2, ATP6N1D, J6B7, RTF, STV1, TJ6, TJ6M, TJ6S, VPH1, WSS, a2V
Alzheimer disease, Cutis laxa, Accessory skin tag, Congenital disorder of glycosylation, Desbuquois syndrome, Aplasia of the vermis, Benign pemphigus, Darier disease, Meckel-gruber syndrome, Rothmund-thomson syndrome, Wrinkly skin syndrome

1094
ATPase H+ transporting V0 subunit a4
A4, ATP6N1B, ATP6N2, DRTA3, RDRTA2, RTA1C, RTADR, STV1, VPH1, VPP2
Distal renal tubular acidosis, Color vision deficiency, Hearing loss

1095
ATPase H+ transporting V0 subunit b
ATP6F, HATPL, VMA16
Schizophrenia

1096
ATPase H+ transporting V0 subunit c
ATP6C, ATP6L, ATPL, EPEO3, VATL, VPPC, Vma3
Childhood-onset epilepsy syndrome, Developmental and epileptic encephalopathy, Early onset epilepsy with developmental delay

1097
ATPase H+ transporting V0 subunit d2
ATP6D2, VMA6
Ehlers-danlos syndrome, Oligodendroglioma, Ovarian cysts, Scoliosis, Stomach neoplasms

1098
ATPase H+ transporting V0 subunit e1
ATP6H, ATP6V0E, M9.2, Vma21, Vma21p
Color vision deficiency

1099
ATPase H+ transporting V0 subunit e2
ATP6V0E2L, C7orf32
Alzheimer disease, Scoliosis

1100
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