2211
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ATP6V1B1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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2212
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ATPase H+ transporting V1 subunit B2 |
ATP6B1B2, ATP6B2, DOOD, HO57, VATB, VPP3, Vma2, ZLS2 |
Curated: 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
Unreviewed: Anonychia, Aplasia Cutis Congenita, Arthritis, Brachydactyly, Cataract, Cognition disorder, Congenital abnormalities, Deafness, Deafness-Onychodystrophy Syndrome, Developmental disability, Dolichocephaly, Dwarfism, Epilepsy, Hearing Loss, Hidrotic Ectodermal Dysplasia, High palate, Hypodontia, Hypoplasia Of Thumb, Impaired Cognition, Intellectual developmental disorder, Macroglossia, Macrostomia, Mental Depression, Mental retardation, Micrognathism, Nail Diseases, Nail dystrophy, Oligodontia, Osteoarthrosis Deformans, Spinal Muscular Atrophy, Syndactyly Of The Toes, Synophrys, Zimmerman Laband Syndrome
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2213
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|
|
ATPase H+ transporting V1 subunit C1 |
ATP6C, ATP6D, VATC, Vma5 |
Curated: Digitrenocerebral syndrome, Gout, Juvenile idiopathic arthritis, Neurodevelopmental disorder, Obstructive sleep apnea syndrome, Small vessel stroke
Unreviewed: Breast Cancer, Breast Carcinoma, Breast neoplasm, Deafness with congenital onychodystrophy, Hepatocellular carcinoma, Lip and Oral Cavity Carcinoma, Malignant Neoplasm, Malignant neoplasm of mouth, Neoplasms, Skin Erosion, Squamous cell carcinoma, Stomach neoplasms
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2214
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|
|
ATPase H+ transporting V1 subunit C2 |
ATP6C2, VMA5 |
Curated: Dementia, Distal renal tubular acidosis
Unreviewed: Glioma, Osteosarcoma
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2215
|
|
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ATPase H+ transporting V1 subunit D |
ATP6M, VATD, VMA8 |
Curated: N/A
Unreviewed: Alzheimer disease, Chronic Obstructive Pulmonary Disease
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2216
|
|
|
ATPase H+ transporting V1 subunit E1 |
ARCL2C, ATP6E, ATP6E2, ATP6V1E, P31, Vma4 |
Curated: Cutis laxa, Accessory skin tag, Benign pemphigus, Darier disease, Rothmund-thomson syndrome, autosomal recessive cutis laxa type 2C
Unreviewed: Acquired Kyphoscoliosis, Alzheimer disease, Aortic Valve Insufficiency, Atrial Septal Defect, Biventricular hypertrophy, Bundle Branch Block, Carcinoma, Cat Eye Syndrome, Cerebellar Hypoplasia, Colorectal Cancer, Congenital Clubfoot, Congenital kyphoscoliosis, Cryptorchidism, Cutis Laxa, Dandy-Walker Syndrome, Dementia, Developmental Delay, Developmental dysplasia of the hip, Diabetes Mellitus, Dwarfism, Entropion, Hepatocellular carcinoma, High palate, Imperforate anus, Laryngomalacia, Lipodystrophy, Lung Cancer, Lung carcinoma, Malignant Neoplasm, Mesothelioma, Mitral Valve Prolapse, Motor delay, Myopia, Nasopharyngeal Carcinoma, Nystagmus, Osteosarcoma, Pachygyria, Polymicrogyria, Strabismus, Tricuspid Valve Insufficiency
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2217
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|
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ATPase H+ transporting V1 subunit E1 pseudogene 1 |
ATP6EP1, ATP6V1EP1 |
Curated: N/A
Unreviewed: N/A
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2218
|
|
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ATPase H+ transporting V1 subunit E1 pseudogene 2 |
ATP6EP2, ATP6V1EP2 |
Curated: N/A
Unreviewed: N/A
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2219
|
|
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ATPase H+ transporting V1 subunit E1 pseudogene 3 |
ATP6EL1, ATP6V1EL1 |
Curated: N/A
Unreviewed: N/A
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2220
|
|
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ATPase H+ transporting V1 subunit E2 |
ATP6E1, ATP6EL2, ATP6V1EL2, VMA4 |
Curated: N/A
Unreviewed: Bipolar Disorder, Schizoaffective Disorder, Schizophrenia
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