11
|
|
|
VPS37A subunit of ESCRT-I |
HCRP1, PQBP2, SPG53 |
|
12
|
|
|
Vesicle transport through interaction with t-SNAREs 1A |
MMDS3, MVti1, VTI1RP2, Vti1-rp2 |
Adenocarcinoma, Carcinoma, Central nervous system neoplasms, Colonic neoplasms, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Glioma, Lung carcinoma, Lung adenocarcinoma, Lung cancer |
13
|
|
|
Von Willebrand factor A domain containing 3A |
- |
|
14
|
|
|
Versican |
CSPG2, ERVR, GHAP, PG-M, WGN, WGN1 |
Adenocarcinoma, Cataract, Chorioretinal atrophy, Disorder of eye, Endometrioma, Endometriosis, Glaucoma, Laryngeal carcinoma, Myopia, Optic atrophy, Polycystic ovary syndrome, Salivary gland neoplasm, Malignant neoplasm of salivary gland, Thoracic aortic aneurysm and aortic dissection, Vitreoretinal degeneration, Wagner syndromeView all (1 more) |
15
|
|
|
Vacuolar protein sorting 13 homolog B |
BLTP5B, CHS1, COH1 |
Cubitus valgus, Aphthous ulcer, Arachnodactyly, Attention deficit hyperactivity disorder, Breast cancer, Camptodactyly of fingers, Cerebellar hypoplasia, Chorioretinal dystrophy, Cohen syndrome, Congenital coloboma of iris, Congenital pectus excavatum, Cryptorchidism, Developmental delay, Dwarfism, Dysmorphic features, Hearing loss, Hypoplasia of the maxilla, Isolated somatotropin deficiency, Laryngomalacia, Leukopenia, Macrodontia, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Mitral valve prolapse, Motor delay, Movement disorders, Myopia, Hypotonia, Neutropenia, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinal dystrophy, Scoliosis, Somatotropin deficiency, Speech disorders, Strabismus, Syndactyly of fingers, Ventricular septal defectView all (27 more) |
16
|
|
|
V-set and transmembrane domain containing 4 |
C10orf72 |
|
17
|
|
|
Von Willebrand factor A domain containing 3B |
SCAR22 |
|
18
|
|
|
Vacuolar ATPase assembly factor VMA21 |
MEAX, XMEA |
|
19
|
|
|
Vascular endothelial growth factor D |
FIGF, VEGF-D |
|
20
|
|
|
Von Willebrand factor A domain containing 8 |
KIAA0564, P7BP2, RP97 |
|