VPS13B Chromosome 8

Vacuolar protein sorting 13 homolog B
976 variants 976 Health Risk

Upload your DNA to see your personal genotypes for variants in VPS13B.

What This Gene Does
This gene encodes a potential transmembrane protein that may function in vesicle-mediated transport and sorting of proteins within the cell. This protein may play a role in the development and the function of the eye, hematological system, and central nervous system. Mutations in this gene have been associated with Cohen syndrome. Multiple splice variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Bridge-like lipid transfer protein family
Locus Type
gene with protein product
Location
8q22.2
Ensembl
ENSG00000132549
Associated Conditions (34)
Cohen syndrome
Inborn genetic diseases
VPS13B-related disorder
Abnormal brain morphology
Intellectual disability
Ovarian serous cystadenocarcinoma
Thyroid cancer
nonmedullary
1
Lung cancer
Gastric cancer
Adrenocortical carcinoma
hereditary
Early onset severe obesity
Familial cancer of breast
Malignant tumor of urinary bladder
Chronic lymphocytic leukemia/small lymphocytic lymphoma
High myopia
early-onset
Ovarian cancer
+14 more conditions
Key Variants
RS1019355776
Conflicting classifications of pathogenicity
Cohen syndrome, Inborn genetic diseases, Cohen syndrome
Health Risk
RS1046756662
Conflicting classifications of pathogenicity
Cohen syndrome, VPS13B-related disorder, Cohen syndrome
Health Risk
RS1057519183
Conflicting classifications of pathogenicity
Cohen syndrome, Cohen syndrome
Health Risk
RS1060499779
Conflicting classifications of pathogenicity
Abnormal brain morphology, Cohen syndrome, Abnormal brain morphology
Health Risk
RS112634620
Conflicting classifications of pathogenicity
Cohen syndrome, Inborn genetic diseases, VPS13B-related disorder
Health Risk
RS116546060
Conflicting classifications of pathogenicity
Cohen syndrome, Inborn genetic diseases, Cohen syndrome
Health Risk
RS117148013
Conflicting classifications of pathogenicity
Cohen syndrome, Inborn genetic diseases, VPS13B-related disorder
Health Risk
RS1178600682
Conflicting classifications of pathogenicity
Cohen syndrome, Inborn genetic diseases, Cohen syndrome
Health Risk
RS117934093
Conflicting classifications of pathogenicity
Cohen syndrome, VPS13B-related disorder, Cohen syndrome
Health Risk
RS1180933570
Conflicting classifications of pathogenicity
Cohen syndrome, Inborn genetic diseases, Cohen syndrome
Health Risk
RS118158347
Conflicting classifications of pathogenicity
Cohen syndrome, Inborn genetic diseases, VPS13B-related disorder
Health Risk
RS1225418115
Conflicting classifications of pathogenicity
Cohen syndrome, Inborn genetic diseases, Cohen syndrome
Health Risk
All Variants (976)
RSID Category Clinical Significance Conditions
RS2132481787 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2132497770 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2132497933 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2132498049 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2132516120 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2132555225 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2132556766 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2132581182 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2132581276 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2132581325 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2132663525 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2132727940 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2132728101 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2132728144 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2132728269 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2132728587 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2132994876 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133295344 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133312597 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133312718 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133312827 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133412405 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133412472 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133510569 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133510708 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133510772 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133511511 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133609624 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133609831 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133626786 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133637853 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133764725 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133808512 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133932364 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2133932487 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2488084191 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2488267195 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2488267313 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2488267977 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2488268134 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2488605060 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2488637479 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2488672432 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2488680476 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2488710351 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2488710723 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2488760578 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2488762498 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2488762701 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2488786625 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
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