ADGRG5
adhesion G protein-coupled receptor G5
Summary
This gene encodes a member of the adhesion family of G-protein coupled receptors. Members of this family are characterized by long N-termini and multiple functional domains. They may play a role in the immune system as well as in the central nervous system. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4784821 | 16:57,573,366 | C/T | — | — |
| rs4783993 | 16:57,573,729 | C/A | — | — |
| rs9931050 | 16:57,578,966 | G/A | intron variant | — |
| rs4783994 | 16:57,580,229 | G/A | intron variant | — |
| rs2404450 | 16:57,584,932 | C/T | intron variant | — |
| rs201729290 | 16:57,596,017 | T/G | — | uncertain significance |
| rs115266147 | 16:57,596,063 | A/G | — | benign |
| rs369916884 | 16:57,597,005 | A/G | — | uncertain significance |
| rs747653288 | 16:57,597,805 | G/A | — | uncertain significance |
| rs371259029 | 16:57,597,836 | G/A | — | uncertain significance |
| rs1324928240 | 16:57,597,878 | C/A | — | uncertain significance |
| rs146649312 | 16:57,598,947 | A/G | — | uncertain significance |
| rs2543768633 | 16:57,598,952 | A/G | — | uncertain significance |
| rs143828233 | 16:57,598,979 | G/A | — | uncertain significance |
| rs146807848 | 16:57,599,008 | C/A | — | uncertain significance |
| rs2543769293 | 16:57,599,061 | T/G | — | uncertain significance |
| rs2543773638 | 16:57,600,517 | T/C | — | uncertain significance |
| rs201845314 | 16:57,600,566 | G/C | — | uncertain significance |
| rs200838029 | 16:57,600,568 | G/C | — | uncertain significance |
| rs140617670 | 16:57,600,571 | G/A | — | uncertain significance |
| rs376486358 | 16:57,600,589 | T/G | — | uncertain significance |
| rs201524707 | 16:57,600,592 | C/T | — | uncertain significance |
| rs143632938 | 16:57,600,604 | C/G | — | uncertain significance |
| rs748490296 | 16:57,601,389 | C/T | — | uncertain significance |
| rs371516015 | 16:57,601,428 | C/T | — | uncertain significance |
| rs754328864 | 16:57,601,458 | C/G | — | uncertain significance |
| rs115719809 | 16:57,601,844 | C/G | — | benign |
| rs371454277 | 16:57,601,853 | G/A | — | uncertain significance |
| rs370454204 | 16:57,601,901 | G/A | — | uncertain significance |
| rs749931320 | 16:57,604,330 | G/C | — | uncertain significance |
| rs753724552 | 16:57,604,351 | T/G | — | uncertain significance |
| rs371947307 | 16:57,604,407 | G/A | — | likely benign |
| rs534912690 | 16:57,604,411 | G/A | — | uncertain significance |
| rs767544968 | 16:57,608,737 | C/T | — | uncertain significance |
| rs138832095 | 16:57,608,753 | A/G | — | uncertain significance |
| rs369909191 | 16:57,608,833 | C/T | — | uncertain significance |
| rs756923591 | 16:57,608,842 | C/T | — | uncertain significance |
| rs868663716 | 16:57,608,875 | T/C | — | uncertain significance |
| rs570246683 | 16:57,608,953 | G/A | — | likely benign |
| rs2543817614 | 16:57,609,381 | G/C | — | uncertain significance |
| rs781294748 | 16:57,609,389 | G/A | — | likely benign |
| rs769880817 | 16:57,609,404 | C/A | — | uncertain significance |
| rs2543818053 | 16:57,609,439 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.