ADGRD1
adhesion G protein-coupled receptor D1
Summary
The adhesion G-protein-coupled receptors (GPCRs), including GPR133, are membrane-bound proteins with long N termini containing multiple domains. GPCRs, or GPRs, contain 7 transmembrane domains and transduce extracellular signals through heterotrimeric G proteins (summary by Bjarnadottir et al., 2004 [PubMed 15203201]).[supplied by OMIM, Nov 2010]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs760240145 | 12:131,451,023 | C/T | — | uncertain significance |
| rs139456901 | 12:131,451,245 | C/T | regulatory region variant | — |
| rs4759815 | 12:131,455,253 | G/A | — | — |
| rs772967898 | 12:131,456,074 | G/A | — | uncertain significance |
| rs779512562 | 12:131,456,113 | T/C | — | uncertain significance |
| rs11061269 | 12:131,456,449 | G/A | intron variant | — |
| rs749318936 | 12:131,466,489 | C/T | — | uncertain significance |
| rs757972258 | 12:131,466,539 | G/A | — | uncertain significance |
| rs2548059432 | 12:131,466,586 | G/T | — | uncertain significance |
| rs755255484 | 12:131,471,642 | C/G | — | uncertain significance |
| rs200124958 | 12:131,471,743 | T/G | — | likely benign |
| rs201045213 | 12:131,471,758 | G/T | — | uncertain significance |
| rs1566003438 | 12:131,471,790 | A/G | — | uncertain significance |
| rs949956077 | 12:131,476,809 | A/G | — | uncertain significance |
| rs764392187 | 12:131,476,909 | C/T | — | uncertain significance |
| rs118097151 | 12:131,478,398 | T/G | coding sequence variant | — |
| rs776250054 | 12:131,487,733 | A/G | — | uncertain significance |
| rs780445686 | 12:131,487,812 | C/T | — | uncertain significance |
| rs747288448 | 12:131,487,823 | G/A | — | likely benign |
| rs1876787185 | 12:131,488,748 | A/C | — | likely benign |
| rs748754881 | 12:131,488,782 | G/A | — | uncertain significance |
| rs374575404 | 12:131,490,534 | G/A | — | uncertain significance |
| rs2548107302 | 12:131,490,571 | A/G | — | uncertain significance |
| rs3847687 | 12:131,525,053 | C/T | intron variant | — |
| rs144913560 | 12:131,529,643 | C/T | intron variant | — |
| rs7312364 | 12:131,539,571 | G/C | intron variant | — |
| rs775648550 | 12:131,561,349 | C/T | — | uncertain significance |
| rs771771921 | 12:131,561,363 | T/G | — | uncertain significance |
| rs752379247 | 12:131,561,386 | G/A | — | uncertain significance |
| rs144706021 | 12:131,569,097 | G/A | synonymous variant | — |
| rs544054620 | 12:131,569,126 | C/T | — | uncertain significance |
| rs2541169770 | 12:131,569,141 | C/T | — | uncertain significance |
| rs1480166089 | 12:131,569,170 | A/G | — | uncertain significance |
| rs774424301 | 12:131,569,184 | C/T | — | uncertain significance |
| rs2541170094 | 12:131,569,185 | C/A | — | uncertain significance |
| rs1569019 | 12:131,576,191 | C/T | — | — |
| rs1976930 | 12:131,576,445 | C/T | regulatory region variant | — |
| rs781596943 | 12:131,593,408 | A/G | — | uncertain significance |
| rs76234479 | 12:131,597,524 | G/T | intron variant | — |
| rs777129872 | 12:131,602,950 | A/C | — | uncertain significance |
| rs749141449 | 12:131,602,971 | A/G | — | uncertain significance |
| rs758656001 | 12:131,605,409 | C/T | — | uncertain significance |
| rs147677454 | 12:131,606,354 | C/T | regulatory region variant | — |
| rs1264466026 | 12:131,616,331 | A/G | — | uncertain significance |
| rs767106366 | 12:131,616,352 | G/A | — | uncertain significance |
| rs755095947 | 12:131,620,587 | C/T | — | uncertain significance |
| rs144814859 | 12:131,620,643 | G/A | — | uncertain significance |
| rs61746588 | 12:131,620,650 | C/T | missense variant | — |
| rs574429603 | 12:131,620,658 | G/A | — | uncertain significance |
| rs885389 | 12:131,621,762 | A/G | regulatory region variant | — |
| rs779854618 | 12:131,622,740 | G/A | — | uncertain significance |
| rs749166666 | 12:131,622,742 | A/G | — | uncertain significance |
| rs144740398 | 12:131,622,753 | G/A | — | likely benign |
| rs2541426380 | 12:131,623,743 | A/G | — | uncertain significance |
| rs2541426540 | 12:131,623,766 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.