2191
|
|
|
ATPase H+ transporting V0 subunit a2 |
A2, ARCL, ARCL2A, ATP6A2, ATP6N1D, J6B7, RTF, STV1, TJ6, TJ6M, TJ6S, VPH1, WSS, a2V |
Curated: 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, autosomal recessive cutis laxa type 2A
Unreviewed: Acquired Kyphoscoliosis, Alopecia, Arteriosclerosis, Atherosclerosis, Bicuspid aortic valve, Bone Disease, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Cerebellar Ataxia, Cerebellar Hypoplasia, Congenital Clubfoot, Congenital Epicanthus, Congenital Exomphalos, Congenital kyphoscoliosis, Congenital Pectus Excavatum, Cortical development malformation, Crohn Disease, Cryptorchidism, Cutis Laxa, Dandy-Walker Syndrome, Dementia, Developmental Delay, Developmental dysplasia of the hip, Diabetic Retinopathy, Dwarfism, Ehlers-Danlos Syndrome, Encephalitis, Epilepsy, Frontal bossing, Geroderma Osteodysplastica, Glioblastoma, Glioma, Hemochromatosis, Hemorrhagic disease, Hepatitis c, High palate, Hypertension, Intracranial Aneurysm, Lipodystrophy, Liver cirrhosis, Lung Diseases, Lung neoplasms, Male infertility, Malignant Osteopetrosis, Mental retardation, Microcephaly, Microdontia, Microstomia, Mixed connective tissue disease, Motor delay, Myopia, Neoplasms, Osteopenia, Osteosclerosis, Ovarian neoplasm, Pachygyria, Polymicrogyria, Pulmonary Emphysema, Rheumatoid arthritis, Scoliosis, Skin abnormalities, Status Epilepticus, Strabismus, Uterine neoplasm, von Willebrand disorder, Woodhouse Sakati Syndrome, Wrinkly Skin Syndrome
|
2192
|
|
|
ATPase H+ transporting V0 subunit a4 |
A4, ATP6N1B, ATP6N2, DRTA3, RDRTA2, RTA1C, RTADR, STV1, VPH1, VPP2 |
Curated: Distal renal tubular acidosis, Color vision deficiency, Hearing loss
Unreviewed: Astrocytoma, Breast neoplasm, Cutis Laxa, Deafness, Diabetes mellitus, Diabetic neuropathy, Distal Renal Tubular Acidosis, Encephalitis, Fanconi syndrome, Growth disorder, Hearing Loss, Kidney disease, Kidney stone, Nephrocalcinosis, Nephrolithiasis, Renal Carcinoma, Renal Tubular Acidosis, Renal Tubular Acidosis with Sensorineural Hearing Loss, Sensorineural hearing loss, Venous thromboembolism
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2193
|
|
|
ATPase H+ transporting V0 subunit b |
ATP6F, HATPL, VMA16 |
Curated: Schizophrenia
Unreviewed: Breast Cancer, Bronchopulmonary dysplasia, Hepatocellular carcinoma
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2194
|
|
|
ATPase H+ transporting V0 subunit c |
ATP6C, ATP6L, ATPL, EPEO3, VATL, VPPC, Vma3 |
Curated: Childhood-onset epilepsy syndrome, Developmental and epileptic encephalopathy, Early onset epilepsy with developmental delay
Unreviewed: Ataxia telangiectasia, Cardiovascular abnormalities, Colorectal Cancer, Corpus callosum agenesis, Developmental disability, Epilepsy, Esophageal Carcinoma, Esophageal neoplasm, Esophagus Neoplasm, Hypoxia, Intellectual developmental disorder, Liver carcinoma, Malignant Neoplasm, Microcephaly, Myoclonic epilepsy, Neoplasms, Osteopetrosis, Prostate cancer, Prostatic neoplasm, Seizures
|
2195
|
|
|
ATPase H+ transporting V0 subunit c pseudogene 1 |
ATCD1 |
Curated: N/A
Unreviewed: N/A
|
2196
|
|
|
ATPase H+ transporting V0 subunit c pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
2197
|
|
|
ATPase H+ transporting V0 subunit c pseudogene 3 |
- |
Curated: N/A
Unreviewed: Squamous cell carcinoma
|
2198
|
|
|
ATPase H+ transporting V0 subunit c pseudogene 4 |
- |
Curated: N/A
Unreviewed: N/A
|
2199
|
|
|
ATPase H+ transporting V0 subunit d1 |
ATP6D, ATP6DV, P39, VATX, VMA6, VPATPD |
Curated: N/A
Unreviewed: Age-related macular degeneration, Alzheimer disease, Carcinoma, Choriocarcinoma, Neoplasms, Pancreatic cancer, Pancreatic carcinoma, Schizophrenia, Syndromic microphthalmia
|
2200
|
|
|
ATP6V0D1 divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|