PTGDR
prostaglandin D2 receptor
Summary
This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor (GPCR) superfamily. The receptors are seven-pass transmembrane proteins that respond to extracellular cues and activate intracellular signal transduction pathways. This protein is reported to be a receptor for prostaglandin D2, which is a mediator of allergic inflammation and allergic airway inflammation in asthma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs778655103 | 14:52,734,549 | A/T | — | uncertain significance |
| rs41311442 | 14:52,734,551 | C/T | — | benign |
| rs762884945 | 14:52,734,564 | C/T | — | uncertain significance |
| rs1005575850 | 14:52,734,686 | C/T | — | uncertain significance |
| rs747403014 | 14:52,734,719 | A/G | — | likely benign |
| rs769135378 | 14:52,734,815 | G/A | — | uncertain significance |
| rs141737848 | 14:52,734,822 | C/T | — | likely benign |
| rs768633584 | 14:52,735,016 | G/A | — | uncertain significance |
| rs142969446 | 14:52,735,046 | G/A | — | uncertain significance |
| rs570093208 | 14:52,735,103 | G/A | — | uncertain significance |
| rs571881468 | 14:52,735,128 | A/T | — | uncertain significance |
| rs150949412 | 14:52,735,242 | G/A | — | uncertain significance |
| rs2502536493 | 14:52,735,272 | G/A | — | uncertain significance |
| rs200415919 | 14:52,735,275 | C/T | — | uncertain significance |
| rs144706723 | 14:52,735,290 | C/G | — | likely benign |
| rs759247647 | 14:52,735,328 | C/A | — | uncertain significance |
| rs752252951 | 14:52,735,340 | A/G | — | uncertain significance |
| rs755199226 | 14:52,735,360 | G/A | — | uncertain significance |
| rs41312488 | 14:52,740,434 | T/C | intron variant | — |
| rs708486 | 14:52,740,971 | A/G | intron variant | — |
| rs762781041 | 14:52,741,475 | G/T | — | uncertain significance |
| rs142932547 | 14:52,741,530 | C/T | — | uncertain significance |
| rs2033392612 | 14:52,741,590 | G/C | — | uncertain significance |
| rs41312506 | 14:52,741,597 | A/G | — | likely benign |
| rs201662277 | 14:52,741,657 | C/T | — | uncertain significance |
| rs200003498 | 14:52,741,665 | A/G | — | likely benign |
| rs2502549660 | 14:52,741,666 | T/C | — | uncertain significance |
| rs2033396440 | 14:52,741,674 | A/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.