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 1170 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1091
Mitochondrially encoded ATP synthase 6
ATPase6, MTATP6
Ataxia with polyneuropathy, Bicuspid aortic valve, Cardiomyopathy, Cerebellar ataxia, Cerebellar atrophy, Charcot-marie-tooth disease, Cleft palate and bilateral cleft lip, Diabetes mellitus, Gonadal dysgenesis, Hypertrophy, Systemic lupus erythematosus, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis
View all (8 more)

1092
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Ataxia with polyneuropathy, Bicuspid aortic valve, Cardiomyopathy, Cerebellar ataxia, Cerebellar atrophy, Charcot-marie-tooth disease, Cleft palate and bilateral cleft lip, Diabetes mellitus, Gonadal dysgenesis, Hypertrophy, Systemic lupus erythematosus, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis
View all (8 more)

1093
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Ataxia with polyneuropathy, Bicuspid aortic valve, Cardiomyopathy, Cerebellar ataxia, Cerebellar atrophy, Charcot-marie-tooth disease, Cleft palate and bilateral cleft lip, Diabetes mellitus, Gonadal dysgenesis, Hypertrophy, Systemic lupus erythematosus, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis
View all (8 more)

1094
ATPase H+ transporting accessory protein 1
16A, ATP6IP1, ATP6S1, Ac45, CF2, VATPS1, XAP-3, XAP3
Congenital disorder of glycosylation, Immunodeficiency, Lymphoma, Intellectual developmental disorder, x-linked

1095
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

1096
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

1097
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

1098
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

1099
ATPase H+ transporting V0 subunit b
ATP6F, HATPL, VMA16
Schizophrenia

1100
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