Entrez Gene ID | 90627 |
---|---|
Official Gene Symbol | STARD13 (GeneCards) |
Full name | StAR related lipid transfer domain containing 13 |
Location | 13q13.1-q13.2 |
Other ids | Vega : OTTHUMG00000016708 MIM : 609866 HGNC : HGNC:19164 Ensembl : ENSG00000133121 |
Other names | DLC2, GT650, ARHGAP37, LINC00464 |
Summary | This gene encodes a protein which contains an N-terminal sterile alpha motif (SAM) for protein-protein interactions, followed by an ATP/GTP-binding motif, a GTPase-activating protein (GAP) domain, and a C-terminal STAR-related lipid transfer (START) domain. It may be involved in regulation of cytoskeletal reorganization, cell proliferation, and cell motility, and acts as a tumor suppressor in hepatoma cells. The gene is located in a region of chromosome 13 that is associated with loss of heterozygosity in hepatocellular carcinomas. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011] |
Found 9 variants in this database.
Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
---|---|---|---|---|---|---|---|
17377 | 90627 | STARD13 | 13 | 34355533 | 34355533 | Asymptomatic | HiSeq X Ten |
17391 | 90627 | STARD13 | 13 | 34258116 | 34258116 | Asymptomatic | HiSeq X Ten |
17491 | 90627 | STARD13 | 13 | 34100247 | 34100247 | Asymptomatic | HiSeq X Ten |
17534 | 90627 | STARD13 | 13 | 33755855 | 33755855 | Asymptomatic | HiSeq X Ten |
17820 | 90627 | STARD13 | 13 | 34053429 | 34053429 | Cockayne syndrome | HiSeq X Ten |
17841 | 90627 | STARD13 | 13 | 33761756 | 33761756 | Cockayne syndrome | HiSeq X Ten |
17933 | 90627 | STARD13 | 13 | 33783787 | 33783787 | Xeroderma Pigmentosum | HiSeq X Ten |
17958 | 90627 | STARD13 | 13 | 34243226 | 34243226 | Xeroderma Pigmentosum | HiSeq X Ten |
27611 | 90627 | STARD13 | 13 | 34056342 | 34056342 | Asymptomatic | HiSeq X Ten Single cell Sequencing Cell cloning |