271
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|
|
Vacuolar protein sorting 13 homolog B |
BLTP5B, CHS1, COH1 |
Curated: Attention deficit hyperactivity disorder, Autism, Central nervous system cancer, Cholecystolithiasis, Ciliary dyskinesia, Cohen syndrome, Congenital neurologic anomalies, Dental caries, Endometriosis, Long qt syndrome, Glioblastoma, Glioma, Global developmental delay, Intellectual developmental disorder, Lung cancer, Meniere disease, Myopia, Pituitary stalk interruption syndrome, Retinitis pigmentosa, Schizophrenia, Squamous cell carcinoma, Urolithiasis
Unreviewed: Anhidrosis, Aphthous Ulcer, Arachnodactyly, Attention Deficit Hyperactivity Disorder, Autism Spectrum Disorder, Brain disease, Breast Cancer, Camptodactyly of fingers, Cerebellar Hypoplasia, Chediak-Higashi Syndrome, Chorioretinal dystrophy, Cognitive disorder, Cohen Syndrome, Cone-rod dystrophy, Congenital Coloboma Of Iris, Congenital Neutropenia, Congenital Pectus Excavatum, Corpus callosum agenesis, Cryptorchidism, Cubitus valgus, Development Disorder, Developmental and epileptic encephalopathy, Developmental Delay, Developmental disability, Dubowitz syndrome, Dwarfism, Dysmorphic Features, Facial dysmorphism, Growth disorder, Hearing Loss, Hypoplasia of the maxilla, Hypotonia, Impaired Cognition, Ischemic stroke, Isolated Somatotropin Deficiency, Laryngomalacia, Leukemia, Leukopenia, Lung carcinoma, Lymphohistiocytosis, Lymphoma, Lymphoproliferative Syndrome, X-Linked, Macrodontia, Major depressive disorder, Mental Depression, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Mitral Valve Prolapse, Motor delay, Movement Disorders, Neurodevelopmental Disorders, Neutropenia, Nyctalopia, Nystagmus, Obesity, Oculocutaneous albinism, Oligospermia, Optic Atrophy, Osteoporosis, Retinal detachment, Retinal Diseases, Retinal Dystrophy, Scoliosis, Secondary parkinson disease, Small cell lung carcinoma, Somatotropin Deficiency, Speech Disorders, Strabismus, Syndactyly of fingers, Trichohepatoenteric Syndrome, Ventricular septal defect, Visual disorder
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272
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|
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VPS13B divergent transcript |
OLC8 |
Curated: N/A
Unreviewed: Stomach Carcinoma, Stomach Neoplasms
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273
|
|
|
Vacuolar protein sorting 13 homolog C |
BLTP5C, PARK23 |
Curated: Parkinson disease, Bipolar disorder, Diabetic retinopathy, Hemiparkinsonism, Major depressive disorder, Metabolic syndrome, Oligodendroglioma, Alzheimer disease, Schizophrenia, Thyroid hemiagenesis, Diabetes mellitus type 2
Unreviewed: Abnormal Male Sexual Function, Akinesia, Anxiety Disorder, Cerebral cortical atrophy, Cohen syndrome, Dementia, Dementia Of Frontal Lobe, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 2, Dysautonomia, Dyskinetic Syndrome, Female sexual dysfunction, Gastroparesis, Hallucinations, Hypoglycemia, Impaired Cognition, Lewy Body Disease, Male sexual dysfunction, Melanoma, Mental Depression, Movement Disorders, Multiple myeloma, Neoplasms, Neurodegenerative disorder, Obesity, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Panic Disorder, Parkinsonian disease, Restless Legs Syndrome, Secondary parkinson disease, Social Communication Disorder, Systemic lupus erythematosus
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274
|
|
|
VPS13C divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|
275
|
|
|
Vacuolar protein sorting 13 homolog D |
BLTP5D, SCA24, SCAR4, SCASI |
Curated: Arthrogryposis multiplex congenita, Spinocerebellar ataxia, Cerebellar ataxia, Central nervous system cancer, Cholecystolithiasis, Glioblastoma, Glioma, Non-immune hydrops fetalis, Leigh syndrome, Neurodevelopmental disorder, Pena-shokeir syndrome , Psychiatric disorders
Unreviewed: Asthma, Ataxia, Atrophy, Cataract, Chorea, Distal amyotrophy, Dysarthria, Dystonia, Hereditary spastic paraplegia, Hyperkinesia, Left Bundle-Branch Block, Movement disorder, Movement Disorders, Nervous System Disorder, Nystagmus, Paraplegia, Peripheral arterial disease, Peripheral axonal neuropathy, Spastic ataxia, Spinocerebellar Ataxia
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276
|
|
|
VPS16 core subunit of CORVET and HOPS complexes |
DYT30, hVPS16 |
Curated: Autism, Dystonia, Metabolic syndrome, Peripheral neuropathy, Scoliosis, Diabetes mellitus type 2
Unreviewed: Choreoathetosis, Hepatocellular carcinoma, Parkinson disease
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277
|
|
|
VPS18 core subunit of CORVET and HOPS complexes |
PEP3 |
Curated: Leukodystrophy
Unreviewed: Autism, Autism Spectrum Disorder, Colorectal Cancer, Melanoma, Neoplasms
|
278
|
|
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Vacuolar protein sorting 25 homolog |
DERP9, EAP20, FAP20 |
Curated: N/A
Unreviewed: Cholangiocarcinoma, Squamous cell carcinoma
|
279
|
|
|
VPS25 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
280
|
|
|
VPS26 retromer complex component A |
HB58, Hbeta58, PEP8A, VPS26 |
Curated: Diabetes mellitus type 2, Diabetic retinopathy, Psoriasis
Unreviewed: Alzheimer disease, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic Retinopathy, Gestational diabetes, Hepatocellular carcinoma, Myocardial infarction, Obesity, Pancreatic neoplasm, Parkinson disease
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