2201
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ATPase H+ transporting V0 subunit d2 |
ATP6D2, VMA6 |
Curated: Ehlers-danlos syndrome, Oligodendroglioma, Ovarian cysts, Scoliosis, Stomach neoplasms
Unreviewed: Bone resorption, Breast neoplasm, Cardiovascular disease, Coronary artery disease, Corpus Luteum Cyst, Cutis Laxa, Esophageal neoplasm, Gastric Cancer, Hepatocellular carcinoma, Idiopathic pulmonary fibrosis, Malignant Neoplasm, Melanoma, Neoplasms, Osteopenia, Osteopetrosis, Ovarian Cysts, Renal cell carcinoma, Rheumatoid arthritis, Stomach Neoplasms
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2202
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ATPase H+ transporting V0 subunit e1 |
ATP6H, ATP6V0E, M9.2, Vma21, Vma21p |
Curated: Color vision deficiency
Unreviewed: Rheumatoid arthritis
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2203
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ATPase H+ transporting V0 subunit e1 pseudogene 1 |
- |
Curated: N/A
Unreviewed: Leukemia
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2204
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ATPase H+ transporting V0 subunit e1 pseudogene 2 |
- |
Curated: N/A
Unreviewed: Multiple myeloma
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2205
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ATPase H+ transporting V0 subunit e1 pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
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2206
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ATPase H+ transporting V0 subunit e1 pseudogene 4 |
- |
Curated: N/A
Unreviewed: N/A
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2207
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ATPase H+ transporting V0 subunit e2 |
ATP6V0E2L, C7orf32 |
Curated: Alzheimer disease, Scoliosis
Unreviewed: Pituitary neoplasm
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2208
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|
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ATP6V0E2 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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2209
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ATPase H+ transporting V1 subunit A |
ARCL2D, ATP6A1, ATP6V1A1, DEE93, HO68, IECEE3, VA68, VPP2, Vma1 |
Curated: Cutis laxa, Accessory skin tag, Cyclin-dependent kinase-like 5 deficiency, Developmental and epileptic encephalopathy, Developmental disability, Benign pemphigus, Darier disease, Rothmund-thomson syndrome, autosomal recessive cutis laxa type 2D
Unreviewed: Alzheimer disease, Atrial Septal Defect, Atrophy, Attention Deficit Hyperactivity Disorder, Autism, Blepharophimosis, Brain disease, Breast neoplasm, Bundle Branch Block, Cardiovascular abnormalities, Cataract, Cerebellar atrophy, Cerebellar Hypoplasia, Cerebral Atrophy, Colorectal Cancer, Congenital Camptodactyly, Congenital Clubfoot, Congenital Coloboma Of Iris, Congenital disorder of glycosylation, Congestive Heart Failure, Cryptorchidism, Cutis Laxa, Dandy-Walker Syndrome, Dementia, Developmental Delay, Developmental dysplasia of the hip, Developmental regression, Dwarfism, Dyskinetic Syndrome, Endometriosis, Entropion, Epilepsy, Epileptic encephalopathy, Gastroesophageal Reflux Disease, Graves ophthalmopathy, Growth disorder, High palate, Hyperopia, Hypertrophic cardiomyopathy, Hypodontia, Hypoplasia Of Corpus Callosum, Hypoxia, Intellectual developmental disorder, Lipodystrophy, Macrotia, Mental retardation, Microcephaly, Motor delay, Myopia, Non-Specifi Epileptic Encephalopathy, Nystagmus, Optic Atrophy, Pachygyria, Partial epilepsy, Penis Agenesis, Polymicrogyria, Ptosis, Renal cell carcinoma, Schizophrenia, Spastic tetraparesis, Squamous cell carcinoma, Status Epilepticus, Stomach Carcinoma, Stomach Neoplasms, Strabismus, Strawberry Nevus Of Skin, Visual disorder
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2210
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ATPase H+ transporting V1 subunit B1 |
ATP6B1, DRTA2, RTA1B, VATB, VMA2, VPP3 |
Curated: Distal renal tubular acidosis, Gout, Hearing loss, Nephrolithiasis, Polydactyly, Scoliosis, Urogenital abnormalities, Usher syndrome, renal tubular acidosis, distal, 2, with progressive sensorineural hearing loss
Unreviewed: Breast neoplasm, Deafness, Distal Renal Tubular Acidosis, Dysmorphic Features, Epithelial ovarian carcinoma, Fanconi syndrome, Growth disorder, Hearing Loss, Hepatoblastoma, Hypoxia, Kidney disease, Kidney stone, Multiple Congenital Anomalies, Nephritis, Nephrocalcinosis, Osteopetrosis, Ovarian neoplasm, Renal Tubular Acidosis, Renal Tubular Acidosis, Distal, With Progressive Nerve Deafness
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