|
51
|
|
|
Vesicle amine transport 1 like |
- |
|
|
52
|
|
|
VPS52 subunit of GARP complex |
ARE1, SAC2, SACM2L, dJ1033B10.5 |
|
|
53
|
|
|
VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog |
C14orf133, SPE-39, SPE39, VIPAR, VPS16B, hSPE-39 |
Arthrogryposis multiplex congenita, Arthrogryposis, renal dysfunction, and cholestasis, Cholestatic liver disease, Conjugated hyperbilirubinemia, Developmental delay, Ichthyosis, Kidney disease, Microcephaly, Nephrocalcinosis, Ventricular hypertrophy, Ventricular septal defect |
|
54
|
|
|
VPS33A core subunit of CORVET and HOPS complexes |
MPSPS |
Anemia, Developmental dysplasia of the hip, Congenital epicanthus, Congenital pectus carinatum, Congenital pectus excavatum, Developmental delay, Glomerulosclerosis, Hypertrophic cardiomyopathy, Macroglossia, Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders, Mucopolysaccharidosis-plus syndrome, Optic atrophy, Patent ductus arteriosus, Pfaundler-hurler syndrome, Synophrys |
|
55
|
|
|
Vesicle associated membrane protein 1 |
CMS25, SAX1, SPAX1, SYB1, VAMP-1 |
Acquired kyphoscoliosis, Amyotrophy, Arthrogryposis multiplex congenita, Ataxia, Bulbar palsy, Developmental dysplasia of the hip, Congenital kyphoscoliosis, Myasthenic syndrome, Congenital pectus carinatum, Distal amyotrophy, Dysarthria, Dysphagia, Esotropia, Gastroesophageal reflux disease, Hearing loss, High palate, Mental retardation, Motor delay, Myasthenia gravis, Myopathy, Nystagmus, Polyneuropathy, Ptosis, Scoliosis, Sleep apnea, Spastic ataxia, Spastic paraplegia, Strabismus, Sudden episodic apneaView all (14 more) |
|
56
|
|
|
Vesicle associated membrane protein 2 |
NEDHAHM, SYB2, VAMP-2 |
|
|
57
|
|
|
Vesicle associated membrane protein 7 |
SYBL1, TI-VAMP, TIVAMP, VAMP-7 |
46, xy partial gonadal dysgenesis, Ambiguous genitalia, Azoospermia, Carcinoma of the head and neck, Cryptorchidism, Gonadal dysgenesis, Gynecomastia, Hypertrophy of clitoris, Hypogonadism, Hypoplasia of vagina, Hypospadias, Nephroblastoma, Nephrotic syndrome, Osteoporosis, Ovarian gonadoblastoma, Penis agenesis, Physiologic amenorrhea, Streak ovary, Testicular gonadoblastoma, Testicular regression syndromeView all (5 more) |
|
58
|
|
|
Vacuolar protein sorting 72 homolog |
CFL1, Swc2, TCFL1, YL-1, YL1 |
|
|
59
|
|
|
Valyl-tRNA synthetase 1 |
G7A, NDMSCA, VARS, VARS2 |
Astigmatism, Cerebellar atrophy, Cerebral cortical atrophy, Combined oxidative phosphorylation deficiency, Developmental delay, Dysphagia, Epileptic encephalopathy, Hypoplasia of corpus callosum, Micrognathism, Myopia, Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy, Rheumatoid arthritis, Sarcoidosis |
|
60
|
|
|
Vav guanine nucleotide exchange factor 1 |
VAV |
|
