GIPR
gastric inhibitory polypeptide receptor
Summary
This gene encodes a G-protein coupled receptor for gastric inhibitory polypeptide (GIP), which was originally identified as an activity in gut extracts that inhibited gastric acid secretion and gastrin release, but subsequently was demonstrated to stimulate insulin release in the presence of elevated glucose. Mice lacking this gene exhibit higher blood glucose levels with impaired initial insulin response after oral glucose load. Defect in this gene thus may contribute to the pathogenesis of diabetes. [provided by RefSeq, Oct 2011]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11671664 | 19:46,172,278 | G/A | regulatory region variant | — |
| rs374247187 | 19:46,172,800 | C/G | — | uncertain significance |
| rs1975427515 | 19:46,172,812 | C/G | — | uncertain significance |
| rs1326368872 | 19:46,172,825 | G/A | — | uncertain significance |
| rs750443279 | 19:46,172,827 | G/A | — | uncertain significance |
| rs1283579295 | 19:46,172,846 | C/G | — | uncertain significance |
| rs769250990 | 19:46,173,912 | C/A | — | uncertain significance |
| rs1031532803 | 19:46,173,921 | A/G | — | uncertain significance |
| rs773456016 | 19:46,173,927 | A/C | — | uncertain significance |
| rs13306401 | 19:46,174,378 | C/A | regulatory region variant | — |
| rs143490173 | 19:46,174,567 | A/T | — | uncertain significance |
| rs35560038 | 19:46,175,046 | A/G | — | — |
| rs2513591022 | 19:46,176,159 | C/G | — | uncertain significance |
| rs769461739 | 19:46,177,334 | C/A | — | uncertain significance |
| rs764416244 | 19:46,177,366 | T/C | — | uncertain significance |
| rs2238691 | 19:46,179,043 | G/A | downstream gene variant | — |
| rs756277634 | 19:46,180,355 | T/A | — | uncertain significance |
| rs201980985 | 19:46,180,969 | T/C | — | uncertain significance |
| rs143430880 | 19:46,180,976 | A/G | missense variant | — |
| rs777065585 | 19:46,181,011 | C/T | — | uncertain significance |
| rs373040041 | 19:46,181,024 | T/G | — | uncertain significance |
| rs376471889 | 19:46,181,026 | A/G | — | uncertain significance |
| rs1800437 | 19:46,181,392 | G/C | missense variant | — |
| rs1600311531 | 19:46,181,399 | T/C | — | uncertain significance |
| rs777826805 | 19:46,181,440 | C/A | — | uncertain significance |
| rs10423928 | 19:46,182,304 | T/A | downstream gene variant | — |
| rs766119961 | 19:46,185,002 | C/A | — | uncertain significance |
| rs1466887239 | 19:46,185,023 | C/T | — | uncertain significance |
| rs1967252905 | 19:46,185,035 | A/G | — | uncertain significance |
| rs200958147 | 19:46,185,036 | G/T | — | uncertain significance |
| rs199871847 | 19:46,185,131 | T/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.