|
41
|
|
|
VPS53 subunit of GARP complex |
HCCS1, PCH2E, hVps53L, pp13624 |
Cerebellar atrophy, Cerebral atrophy, Developmental delay, Dwarfism, Hypoplasia of corpus callosum, Mental retardation, Hypotonia, Osteoporosis, Pontoneocerebellar hypoplasia, Progressive cerebello-cerebral atrophy, Prostate cancer, Scoliosis, Spastic quadriplegia |
|
42
|
|
|
Vanin 3, pseudogene |
HSA238982, VNN3 |
|
|
43
|
|
|
Vezatin, adherens junctions transmembrane protein |
VEZATIN |
|
|
44
|
|
|
VAC14 component of PIKFYVE complex |
ArPIKfyve, TAX1BP2, TRX |
Agenesis of corpus callosum, Arrhinencephaly, Atrial septal defect, Basal ganglia degeneration syndrome, Cardiomyopathy, Cataract, Cerebellar hypoplasia, Congenital microcephaly, Craniofacial dystonia, Cryptorchidism, Defect of skull ossification, Developmental delay, Developmental regression, Dolichocephaly, Dwarfism, Dysphagia, Gingival recession, Glossoptosis, Hydrocephalus, Hydrops fetalis, Hypertension, Hypertrophy of clitoris, Hypospadias, Malignant neoplasm, Metastatic prostate carcinoma, Micrognathism, Microphthalmos, Neuropathy, Pachygyria, Penis agenesis, Proptosis, Pulmonary arterial hypertension, Renal artery stenosis, Sclerocornea, Scleroderma, Striatonigral degeneration, Syndactyly, Tetralogy of fallot, Thumb aplasia, Ventricular septal defect, Vertical talus, Yunis varon syndromeView all (27 more) |
|
45
|
|
|
VPS35 retromer complex component |
MEM3, PARK17 |
Akinesia, Cerebral cortical atrophy, Dementia, Dyskinetic syndrome, Dysphagia, Dyssomnia, Hereditary parkinson`s disease, Mental depression, Parkinson disease, Schizophrenia, Sleep disorders |
|
46
|
|
|
VPS11 core subunit of CORVET and HOPS complexes |
DYT32, END1, HLD12, HLD12; DYT32, PEP5, RNF108, hVPS11 |
Central visual impairment, Cerebellar atrophy, Coronary artery disease, Developmental delay, Dysautonomia, Dyscognitive seizures, Dysphagia, Febrile seizures, Hearing loss, Hypomyelinating leukodystrophy, Hypoplasia of corpus callosum, Leukodystrophy, Leukoencephalopathy, Mental retardation, Microcephaly, Neurogenic urinary bladder, Optic atrophy, Oromotor apraxia, Seizure, StrabismusView all (5 more) |
|
47
|
|
|
VPS35 endosomal protein sorting factor like |
C16orf62, EC97, RTSC3 |
|
|
48
|
|
|
Valyl-tRNA synthetase 2, mitochondrial |
COXPD20, VALRS, VARS2L, VARSL |
|
|
49
|
|
|
VANGL planar cell polarity protein 2 |
LPP1, LTAP, STB1, STBM, STBM1 |
Acrania, Addison`s disease, Anencephaly, Cervical spina bifida aperta, Cervical spina bifida cystica, Cervicothoracic spina bifida, Craniorachischisis, Diastematomyelia, Hydrocephalus, Isolated anencephaly, Isolated exencephaly, Lipoma, Lumbosacral spina bifida aperta, Lumbosacral spina bifida cystica, Meningomyelocele, Multiple lipomata, Neural tube defect, Neurenteric cyst, Primary tethered cord syndrome, Rachischisis, Sacral agenesis, Spina bifida, Spina bifida cystica, Spina bifida occulta, Spinal cord myelodysplasia, Status dysraphicus, Thoracolumbosacral spina bifida aperta, Thoracolumbosacral spina bifida cystica, Upper thoracic spina bifida aperta, Upper thoracic spina bifida cysticaView all (15 more) |
|
50
|
|
|
VPS18 core subunit of CORVET and HOPS complexes |
PEP3 |
|
