PTGDR2
prostaglandin D2 receptor 2
Summary
This gene encodes a G-protein-coupled receptor that is preferentially expressed in CD4+ effector T helper 2 (Th2) cells. This protein is a prostaglandin D2 receptor that mediates the pro-inflammatory chemotaxis of eosinophils, basophils, and Th2 lymphocytes generated during allergic inflammation. Single nucleotide polymorphisms in the 3' UTR of this gene have been associated with asthma susceptibility.[provided by RefSeq, Mar 2011]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs41530751 | 11:60,617,993 | G/T | downstream gene variant | — |
| rs545659 | 11:60,619,657 | T/A | — | — |
| rs754566001 | 11:60,620,085 | C/G | — | uncertain significance |
| rs1855288024 | 11:60,620,110 | T/G | — | uncertain significance |
| rs571515921 | 11:60,620,160 | A/T | — | uncertain significance |
| rs983635490 | 11:60,620,195 | C/T | — | uncertain significance |
| rs773277258 | 11:60,620,202 | C/G | — | uncertain significance |
| rs762879192 | 11:60,620,217 | G/T | — | uncertain significance |
| rs1855292027 | 11:60,620,231 | A/G | — | uncertain significance |
| rs368130260 | 11:60,620,247 | G/A | — | uncertain significance |
| rs1855293866 | 11:60,620,274 | A/C | — | uncertain significance |
| rs966032658 | 11:60,620,345 | C/T | — | uncertain significance |
| rs1236541796 | 11:60,620,355 | G/A | — | likely benign |
| rs763575164 | 11:60,620,372 | T/C | — | uncertain significance |
| rs575311239 | 11:60,620,384 | C/T | — | uncertain significance |
| rs1304891210 | 11:60,620,407 | G/T | — | uncertain significance |
| rs979811922 | 11:60,620,431 | G/T | — | uncertain significance |
| rs1409036697 | 11:60,620,456 | A/G | — | uncertain significance |
| rs760275552 | 11:60,620,501 | C/A | — | uncertain significance |
| rs2496114052 | 11:60,620,568 | T/C | — | uncertain significance |
| rs2496114301 | 11:60,620,637 | G/C | — | uncertain significance |
| rs758293056 | 11:60,620,655 | T/C | — | uncertain significance |
| rs142523235 | 11:60,620,742 | A/C | — | uncertain significance |
| rs56067229 | 11:60,620,753 | G/A | — | uncertain significance |
| rs945653182 | 11:60,620,762 | A/C | — | uncertain significance |
| rs571378284 | 11:60,620,792 | C/G | — | uncertain significance |
| rs950681359 | 11:60,620,831 | A/G | — | uncertain significance |
| rs2496115246 | 11:60,620,955 | A/T | — | likely benign |
| rs2496115517 | 11:60,621,042 | C/G | — | likely benign |
| rs1478468727 | 11:60,621,155 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.