261
|
|
|
Vanin 3, pseudogene |
HSA238982, VNN3 |
Curated: N/A
Unreviewed: Congestive Heart Failure, Palmoplantar Pustules, Psoriasis, ST Segment Elevation Myocardial Infarction
|
262
|
|
|
VOPP1 WW domain binding protein |
ECOP, GASP, WBP1L2 |
Curated: Myeloid leukemia
Unreviewed: Asthma, Atrial Fibrillation, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Carcinoma, Esophageal squamous cell carcinoma, Glioblastoma, Hepatocellular carcinoma, Hereditary breast and ovarian cancer syndrome, Leukemia, Lymphoma, Malignant Neoplasm, Mammary Neoplasms, Mitochondrial disease, Myeloid Leukemia, Myocardial Infarction, Neoplasms, Septicemia, Squamous cell carcinoma, Stomach neoplasms
|
263
|
|
|
VOPP1 divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|
264
|
|
|
VOPP family member 2, pseudogene |
- |
Curated: N/A
Unreviewed: N/A
|
265
|
|
|
V-set pre-B cell surrogate light chain 1 |
CD179a, IGI, IGVPB, VPREB |
Curated: Alzheimer disease
Unreviewed: Autoimmune Diseases, Blast phase chronic myelogenous leukemia, Burkitt`s Lymphoma, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Diabetic Retinopathy, Down Syndrome, Hematologic neoplasm, Hematopoietic Neoplasms, Immune System Diseases, Leukemia, Lupus Erythematosus, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoid leukemia, Multiple myeloma, Myeloid Leukemia, Neoplasms, Rheumatoid arthritis, Systemic lupus erythematosus
|
266
|
|
|
V-set pre-B cell surrogate light chain 3 |
8HS20, N27C7-2 |
Curated: N/A
Unreviewed: B-Cell Lymphoma, Burkitt lymphoma, Burkitt`s Lymphoma, Conn Syndrome, Diffuse Lymphoma, Lymphoma, Multiple myeloma, Neoplasms
|
267
|
|
|
VPS11 core subunit of CORVET and HOPS complexes |
DYT32, END1, HLD12, HLD12; DYT32, PEP5, RNF108, hVPS11 |
Curated: Coronary artery disease, Dystonia, Gallstones, Hypomyelinating leukodystrophy, Diabetes mellitus type 2, VPS11-related neurological disorder
Unreviewed: Blindness, Breast Cancer, Breast Carcinoma, Central Visual Impairment, Cerebellar atrophy, Demyelinating diseases, Developmental Delay, Developmental disability, Dysautonomia, Dyscognitive seizures, Dysphagia, Ectrodactyly, Endometriosis, Enterocolitis, Febrile seizures, Glioblastoma, Hearing Loss, Hypertension, Hypertrophic cardiomyopathy, Hypomyelinating Leukodystrophy, Hypoplasia Of Corpus Callosum, Hypoxia, Left Ventricular Hypertrophy, Leukodystrophy, Leukoencephalopathy, Mental retardation, Microcephaly, Necrotizing Enterocolitis, Neoplasms, Neurogenic Urinary Bladder, Optic Atrophy, Oromotor apraxia, Parkinson disease, Seizure, Seizures, Strabismus, Xeroderma Pigmentosum
|
268
|
|
|
VPS11 divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|
269
|
|
|
Vacuolar protein sorting 13 homolog A |
BLTP5A, CHAC, CHOREIN |
Curated: Benign hereditary chorea, Chorea, Choreoacanthocytosis, Congenital neurologic anomalies, Vascular dementia, Mood disorder
Unreviewed: Abetalipoproteinemia, Anxiety Disorder, Atrophy, Attention Deficit Hyperactivity Disorder, Autism, Cataract, Cerebral cortical atrophy, Cognition disorder, Cohen syndrome, Colorectal Cancer, Developmental regression, Distal Muscular Atrophy, Dwarfism, Dysarthria, Dysgraphia, Dysphagia, Dyssomnia, Epilepsy, Head and neck neoplasm, Hyperkalemia, Hyperkinesia, Hypertrophic cardiomyopathy, Ischemic stroke, Liver failure, Lymphatic metastasis, Malabsorption Syndrome, McLeod neuroacanthocytosis syndrome, Mitochondrial disease, Mood Disorder, Mood swings, Movement Disorders, Myopathy, Nervous System Diseases, Neurodegenerative disorder, Neurodegenerative Disorders, Nystagmus, Orofacial dyskinesia, Parkinson Disease, Psychosis, Rhabdomyosarcoma, Secondary parkinson disease, Seizures, Sensory neuropathy, Sleep Disorders, Spinal muscular atrophy, Stomach Neoplasms, Stroke, Syndromic microphthalmia, Temporal lobe epilepsy, Tourette syndrome, Vasculitis
|
270
|
|
|
VPS13A antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|