SIRPG
signal regulatory protein gamma
Summary
The protein encoded by this gene is a member of the signal-regulatory protein (SIRP) family, and also belongs to the immunoglobulin superfamily. SIRP family members are receptor-type transmembrane glycoproteins known to be involved in the negative regulation of receptor tyrosine kinase-coupled signaling processes. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1048055 | 20:1,610,062 | A/C | upstream gene variant | — |
| rs2281807 | 20:1,610,201 | C/T | upstream gene variant | — |
| rs2281808 | 20:1,610,551 | T/C | upstream gene variant | benign |
| rs34442420 | 20:1,610,918 | T/A | — | benign |
| rs3746722 | 20:1,610,939 | G/A | synonymous variant | — |
| rs747232069 | 20:1,610,950 | G/A | — | uncertain significance |
| rs6043405 | 20:1,615,544 | T/G | — | — |
| rs547634798 | 20:1,615,915 | G/C | — | uncertain significance |
| rs2515423592 | 20:1,616,077 | C/T | — | uncertain significance |
| rs145447195 | 20:1,616,101 | G/A | — | uncertain significance |
| rs1024803591 | 20:1,616,179 | T/C | — | uncertain significance |
| rs548420665 | 20:1,616,213 | T/C | — | uncertain significance |
| rs747718268 | 20:1,616,836 | C/T | — | uncertain significance |
| rs2515428574 | 20:1,616,864 | C/T | — | uncertain significance |
| rs2515428837 | 20:1,616,887 | G/T | — | uncertain significance |
| rs148726891 | 20:1,616,920 | C/G | — | uncertain significance |
| rs775904582 | 20:1,616,932 | G/T | — | uncertain significance |
| rs570506979 | 20:1,616,959 | C/T | — | uncertain significance |
| rs746356323 | 20:1,616,974 | A/T | — | uncertain significance |
| rs2515429616 | 20:1,616,980 | T/C | — | uncertain significance |
| rs763718809 | 20:1,617,053 | C/T | — | likely benign |
| rs748421244 | 20:1,617,092 | C/T | — | uncertain significance |
| rs373555109 | 20:1,617,134 | C/T | — | uncertain significance |
| rs188141382 | 20:1,628,254 | A/G | coding sequence variant | — |
| rs2515465824 | 20:1,629,721 | G/A | — | uncertain significance |
| rs895636620 | 20:1,629,722 | G/C | — | uncertain significance |
| rs1335190516 | 20:1,629,749 | G/A | — | uncertain significance |
| rs200195769 | 20:1,629,752 | T/C | — | uncertain significance |
| rs1410520246 | 20:1,629,770 | C/T | — | uncertain significance |
| rs370269730 | 20:1,629,809 | T/C | — | uncertain significance |
| rs2091920607 | 20:1,629,862 | G/T | — | uncertain significance |
| rs2091920904 | 20:1,629,892 | T/C | — | likely benign |
| rs2091921079 | 20:1,629,910 | C/A | — | uncertain significance |
| rs143978848 | 20:1,629,967 | G/A | — | uncertain significance |
| rs2515468149 | 20:1,629,980 | T/C | — | uncertain significance |
| rs137982961 | 20:1,645,089 | A/G | downstream gene variant | — |
| rs117726277 | 20:1,646,513 | G/A | upstream gene variant | — |
| rs140840556 | 20:1,654,074 | G/C | downstream gene variant | — |
| rs6034368 | 20:1,658,258 | C/T | upstream gene variant | — |
| rs202554 | 20:1,658,700 | A/T | — | — |
| rs140315941 | 20:1,667,343 | T/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.