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
RS2491561874 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491562057 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491562436 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491577146 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491577168 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491577873 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491580027 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491580504 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491774580 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491774628 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491842094 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491842475 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491842486 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491842520 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491873704 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491976646 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491976835 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2491976875 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492005762 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492005783 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492005812 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492006068 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492006345 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492009076 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492009169 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492010569 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492013977 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492014077 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492015710 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492027730 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492092129 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492093854 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492095273 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492120101 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492123085 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492124610 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492202628 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492236593 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492236950 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492237494 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492237648 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492237807 Health Risk Pathogenic
RS2492239255 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492241039 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492277833 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492278870 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492279007 Health Risk Pathogenic
RS2492346869 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492347008 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
RS2492347312 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
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