CD5
CD5 molecule
Summary
This gene encodes a member of the scavenger receptor cysteine-rich (SRCR) superfamily. Members of this family are secreted or membrane-anchored proteins mainly found in cells associated with the immune system. This protein is a type-I transmembrane glycoprotein found on the surface of thymocytes, T lymphocytes and a subset of B lymphocytes. The encoded protein contains three SRCR domains and may act as a receptor to regulate T-cell proliferation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2016]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs113883719 | 11:60,860,554 | G/A | intergenic variant | — |
| rs175134 | 11:60,861,380 | A/T | — | — |
| rs556412774 | 11:60,863,882 | G/C | — | — |
| rs529459761 | 11:60,869,878 | T/C | — | — |
| rs17155674 | 11:60,875,906 | T/C | intron variant | — |
| rs75448191 | 11:60,883,942 | G/C | — | — |
| rs111909354 | 11:60,884,278 | A/T | — | — |
| rs1166109568 | 11:60,885,667 | C/T | — | uncertain significance |
| rs746175908 | 11:60,885,677 | C/T | — | uncertain significance |
| rs769667296 | 11:60,885,715 | G/A | — | uncertain significance |
| rs182453573 | 11:60,885,725 | T/A | — | uncertain significance |
| rs562627397 | 11:60,885,754 | T/G | — | uncertain significance |
| rs755184614 | 11:60,885,799 | C/T | — | uncertain significance |
| rs759135823 | 11:60,885,853 | C/T | — | uncertain significance |
| rs139537878 | 11:60,886,423 | C/T | — | uncertain significance |
| rs1861007945 | 11:60,886,432 | C/A | — | uncertain significance |
| rs186723877 | 11:60,886,666 | C/T | intron variant | — |
| rs765315855 | 11:60,886,759 | G/A | — | uncertain significance |
| rs773426771 | 11:60,886,761 | G/T | — | likely benign |
| rs2241002 | 11:60,886,913 | T/C | — | benign |
| rs1213239041 | 11:60,886,946 | T/C | — | uncertain significance |
| rs199815445 | 11:60,886,965 | C/G | — | uncertain significance |
| rs200152277 | 11:60,887,035 | C/G | — | uncertain significance |
| rs181830818 | 11:60,888,507 | C/T | intron variant | — |
| rs757676838 | 11:60,889,119 | G/A | — | uncertain significance |
| rs1343140592 | 11:60,889,125 | G/C | — | uncertain significance |
| rs2539421267 | 11:60,889,145 | G/A | — | uncertain significance |
| rs143050269 | 11:60,889,260 | G/A | — | likely benign |
| rs201940040 | 11:60,889,290 | G/A | — | uncertain significance |
| rs2539423145 | 11:60,890,387 | C/G | — | uncertain significance |
| rs757219518 | 11:60,890,447 | C/G | — | uncertain significance |
| rs1416998289 | 11:60,891,374 | G/A | — | uncertain significance |
| rs139956085 | 11:60,892,516 | G/A | — | uncertain significance |
| rs145264378 | 11:60,892,525 | C/T | — | uncertain significance |
| rs147612862 | 11:60,892,558 | C/T | — | uncertain significance |
| rs200669351 | 11:60,892,569 | G/A | — | uncertain significance |
| rs1310670219 | 11:60,892,590 | C/T | — | uncertain significance |
| rs368583552 | 11:60,892,617 | T/C | — | uncertain significance |
| rs922697611 | 11:60,893,228 | G/A | — | uncertain significance |
| rs2229177 | 11:60,893,235 | C/T | — | benign |
| rs200138022 | 11:60,893,298 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.