GRID2IP
Grid2 interacting protein
Summary
Glutamate receptor delta-2 (GRID2; MIM 602368) is predominantly expressed at parallel fiber-Purkinje cell postsynapses and plays crucial roles in synaptogenesis and synaptic plasticity. GRID2IP1 interacts with GRID2 and may control GRID2 signaling in Purkinje cells (Matsuda et al., 2006 [PubMed 16835239]).[supplied by OMIM, Mar 2008]
Known Variants123 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs759983756 | 7:6,537,416 | G/C | — | uncertain significance |
| rs1786298455 | 7:6,537,436 | C/A | — | uncertain significance |
| rs759958693 | 7:6,537,708 | A/T | — | uncertain significance |
| rs2534231005 | 7:6,537,717 | G/A | — | uncertain significance |
| rs1461983429 | 7:6,537,727 | C/T | — | uncertain significance |
| rs540580671 | 7:6,537,817 | C/G | — | uncertain significance |
| rs61734441 | 7:6,541,448 | G/A | — | likely benign |
| rs537810167 | 7:6,541,697 | G/C | — | uncertain significance |
| rs763199065 | 7:6,541,723 | C/T | — | likely benign |
| rs1300663174 | 7:6,542,666 | G/T | — | uncertain significance |
| rs373500827 | 7:6,542,741 | G/A | — | likely benign |
| rs1003837078 | 7:6,543,197 | G/C | — | likely benign |
| rs763777860 | 7:6,543,225 | G/C | — | uncertain significance |
| rs1016991126 | 7:6,543,230 | A/T | — | uncertain significance |
| rs1211604985 | 7:6,543,273 | T/C | — | uncertain significance |
| rs920201178 | 7:6,544,484 | C/G | — | uncertain significance |
| rs1261496751 | 7:6,545,454 | C/A | — | uncertain significance |
| rs1470273928 | 7:6,545,517 | C/T | — | uncertain significance |
| rs530515112 | 7:6,545,535 | C/T | — | uncertain significance |
| rs564393205 | 7:6,547,659 | C/T | — | uncertain significance |
| rs1312592096 | 7:6,547,713 | C/G | — | uncertain significance |
| rs1320361100 | 7:6,547,714 | G/A | — | uncertain significance |
| rs1052029105 | 7:6,547,726 | G/A | — | uncertain significance |
| rs1255382415 | 7:6,547,741 | C/T | — | uncertain significance |
| rs1398231328 | 7:6,547,758 | G/A | — | uncertain significance |
| rs867834456 | 7:6,547,812 | G/A | — | likely benign |
| rs2534254477 | 7:6,547,818 | G/C | — | uncertain significance |
| rs958434719 | 7:6,547,827 | C/T | — | uncertain significance |
| rs536138132 | 7:6,547,845 | C/T | — | uncertain significance |
| rs897429366 | 7:6,547,889 | T/G | — | likely benign |
| rs184043502 | 7:6,547,908 | G/C | — | uncertain significance |
| rs2534254883 | 7:6,547,918 | G/T | — | uncertain significance |
| rs1161236078 | 7:6,547,932 | G/C | — | uncertain significance |
| rs1028434330 | 7:6,547,962 | C/T | — | uncertain significance |
| rs868318942 | 7:6,548,022 | T/C | — | uncertain significance |
| rs187045506 | 7:6,548,601 | G/A | — | likely benign |
| rs934248348 | 7:6,548,605 | T/A | — | uncertain significance |
| rs930018775 | 7:6,548,632 | G/C | — | uncertain significance |
| rs542032303 | 7:6,548,639 | G/A | — | uncertain significance |
| rs914939297 | 7:6,548,687 | G/A | — | uncertain significance |
| rs1786682990 | 7:6,548,699 | G/A | — | uncertain significance |
| rs564137288 | 7:6,548,710 | G/A | — | uncertain significance |
| rs997648976 | 7:6,548,719 | T/C | — | uncertain significance |
| rs757837390 | 7:6,548,726 | G/C | — | uncertain significance |
| rs866975715 | 7:6,548,734 | G/A | — | uncertain significance |
| rs755538872 | 7:6,548,737 | C/T | — | uncertain significance |
| rs765612081 | 7:6,548,743 | G/C | — | uncertain significance |
| rs1056993195 | 7:6,548,749 | G/A | — | uncertain significance |
| rs777628997 | 7:6,548,765 | C/G | — | uncertain significance |
| rs996821641 | 7:6,548,774 | T/G | — | uncertain significance |
| rs745606092 | 7:6,548,822 | T/C | — | uncertain significance |
| rs2534258391 | 7:6,548,831 | G/T | — | uncertain significance |
| rs1480441940 | 7:6,548,844 | G/T | — | uncertain significance |
| rs992416103 | 7:6,548,909 | C/T | — | uncertain significance |
| rs376075699 | 7:6,550,000 | C/T | — | uncertain significance |
| rs377432495 | 7:6,550,018 | T/G | — | uncertain significance |
| rs1306424266 | 7:6,550,249 | G/T | — | uncertain significance |
| rs938281164 | 7:6,550,290 | G/A | — | uncertain significance |
| rs1304975824 | 7:6,550,329 | C/T | — | uncertain significance |
| rs557860503 | 7:6,550,551 | C/T | — | likely benign |
| rs756306500 | 7:6,550,554 | C/T | — | uncertain significance |
| rs2534263481 | 7:6,550,569 | A/G | — | uncertain significance |
| rs769125927 | 7:6,550,580 | C/T | — | uncertain significance |
| rs1001140787 | 7:6,550,581 | G/A | — | uncertain significance |
| rs61732374 | 7:6,550,584 | A/G | — | benign |
| rs760171894 | 7:6,550,613 | C/T | — | uncertain significance |
| rs2534263984 | 7:6,550,645 | C/T | — | likely benign |
| rs1040071568 | 7:6,554,017 | G/A | — | uncertain significance |
| rs377023958 | 7:6,554,036 | C/T | — | uncertain significance |
| rs867008247 | 7:6,554,068 | T/C | — | uncertain significance |
| rs370600166 | 7:6,554,141 | C/T | — | uncertain significance |
| rs1289507716 | 7:6,554,153 | C/T | — | uncertain significance |
| rs368368440 | 7:6,560,212 | T/C | — | uncertain significance |
| rs761869402 | 7:6,560,228 | C/T | — | uncertain significance |
| rs1297739806 | 7:6,560,243 | C/G | — | uncertain significance |
| rs994387676 | 7:6,560,251 | C/T | — | uncertain significance |
| rs374250279 | 7:6,560,277 | C/T | — | likely benign |
| rs964173113 | 7:6,560,332 | G/A | — | uncertain significance |
| rs757776305 | 7:6,560,341 | T/C | — | uncertain significance |
| rs753939121 | 7:6,561,075 | C/T | — | uncertain significance |
| rs768992075 | 7:6,561,562 | T/G | — | uncertain significance |
| rs34905002 | 7:6,563,922 | G/C | intron variant | — |
| rs2534298323 | 7:6,565,918 | T/C | — | uncertain significance |
| rs1003510252 | 7:6,566,170 | C/T | — | uncertain significance |
| rs1205444520 | 7:6,566,171 | C/G | — | uncertain significance |
| rs1010926303 | 7:6,566,186 | C/T | — | uncertain significance |
| rs1779514197 | 7:6,566,194 | G/A | — | uncertain significance |
| rs565082275 | 7:6,566,225 | G/T | — | uncertain significance |
| rs1159003126 | 7:6,566,227 | C/G | — | uncertain significance |
| rs966114587 | 7:6,566,246 | G/A | — | uncertain significance |
| rs910093641 | 7:6,566,291 | G/C | — | uncertain significance |
| rs1409101454 | 7:6,566,314 | G/A | — | uncertain significance |
| rs1779520089 | 7:6,566,317 | C/G | — | uncertain significance |
| rs1366390616 | 7:6,566,326 | C/G | — | uncertain significance |
| rs747169421 | 7:6,579,361 | A/C | — | uncertain significance |
| rs761390675 | 7:6,579,391 | G/A | — | likely benign |
| rs78338870 | 7:6,579,403 | G/A | — | benign |
| rs769649909 | 7:6,579,455 | C/T | — | uncertain significance |
| rs1257458613 | 7:6,579,456 | G/C | — | uncertain significance |
| rs895471814 | 7:6,579,493 | A/C | — | uncertain significance |
Showing 100 of 123 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.