ADGRF5

adhesion G protein-coupled receptor F5

Summary

Predicted to enable G protein-coupled receptor activity. Predicted to be involved in several processes, including adenylate cyclase-activating G protein-coupled receptor signaling pathway; energy reserve metabolic process; and fat cell differentiation. Predicted to act upstream of or within several processes, including glomerular filtration; negative regulation of macrophage activation; and pharyngeal arch artery morphogenesis. Located in cell surface and cytoplasmic vesicle. [provided by Alliance of Genome Resources, Apr 2025]

Known Variants78 total

rsidPosition (GRCh37)AllelesClassClinVar
rs7695080376:46,821,745G/Tlikely benign
rs1471481776:46,821,769G/Auncertain significance
rs11725880666:46,821,778G/Auncertain significance
rs4759916:46,822,349A/C
rs7721326416:46,823,724C/Auncertain significance
rs13211525546:46,825,904C/Guncertain significance
rs1456504056:46,825,978A/Guncertain significance
rs7654209446:46,826,068A/Guncertain significance
rs25329612836:46,826,108G/Cuncertain significance
rs14877474516:46,826,180C/Tuncertain significance
rs1468063216:46,826,183G/Auncertain significance
rs17693202666:46,826,222G/Auncertain significance
rs7647109506:46,826,227C/Auncertain significance
rs3680078456:46,826,251A/Guncertain significance
rs1405327056:46,826,315G/Auncertain significance
rs7546466776:46,826,342C/Tuncertain significance
rs14838158226:46,826,390T/Auncertain significance
rs1383318436:46,826,393T/Guncertain significance
rs1492151086:46,826,400T/Cuncertain significance
rs1433649716:46,826,407C/Tlikely benign
rs7510802496:46,826,426C/Tuncertain significance
rs13977081756:46,826,518A/Guncertain significance
rs7552420886:46,826,596A/Guncertain significance
rs13732118116:46,826,621G/Tuncertain significance
rs7764577706:46,826,649C/Auncertain significance
rs1392217286:46,826,789C/Tlikely benign
rs3776259526:46,826,809T/Cuncertain significance
rs5296573536:46,826,845G/Alikely benign
rs1433447366:46,826,860G/Auncertain significance
rs9306291386:46,826,902A/Cuncertain significance
rs6117796:46,826,910G/Csynonymous variant
rs14385375736:46,826,954A/Cuncertain significance
rs7741860436:46,827,058C/Tuncertain significance
rs2002701766:46,827,257C/Tuncertain significance
rs6873836:46,828,159G/Aintron variant
rs3685678376:46,828,455C/Tuncertain significance
rs14050943386:46,828,497A/Tuncertain significance
rs9095440996:46,828,562C/Guncertain significance
rs7561666026:46,828,592T/Cuncertain significance
rs25329836786:46,828,620C/Auncertain significance
rs7604851616:46,830,688C/Guncertain significance
rs1996583596:46,830,690G/Tuncertain significance
rs1479755266:46,830,725A/Guncertain significance
rs4763746:46,831,060C/A
rs7742744016:46,832,917T/Cuncertain significance
rs1500032166:46,834,694G/Auncertain significance
rs10168349656:46,834,707C/Guncertain significance
rs5452520296:46,834,841G/Auncertain significance
rs3729579446:46,836,685G/Cuncertain significance
rs15817681866:46,836,799G/Auncertain significance
rs12909071256:46,836,825A/Tuncertain significance
rs13465520886:46,839,622C/Tuncertain significance
rs3752867946:46,839,672G/Auncertain significance
rs14124582366:46,846,025T/Cuncertain significance
rs2206676:46,846,825A/Gintron variant
rs2014688826:46,847,563C/Auncertain significance
rs25331180786:46,847,654T/Cuncertain significance
rs3679819256:46,847,678G/Auncertain significance
rs14454473356:46,847,746A/Cuncertain significance
rs11588046586:46,849,221T/Cuncertain significance
rs25331308326:46,849,259T/Guncertain significance
rs3713403986:46,849,840C/Tuncertain significance
rs17727331456:46,851,355C/Guncertain significance
rs1509599516:46,851,366C/Tuncertain significance
rs7536866066:46,851,402T/Auncertain significance
rs7803322406:46,851,841G/Auncertain significance
rs17727965096:46,851,853G/Tuncertain significance
rs1385166756:46,851,913G/Auncertain significance
rs1455807816:46,851,949G/Auncertain significance
rs25331540546:46,851,951G/Auncertain significance
rs1439992326:46,851,982A/Guncertain significance
rs1431072636:46,856,105T/Cuncertain significance
rs7509178226:46,856,132G/Auncertain significance
rs11949874746:46,856,162T/Cuncertain significance
rs14726727796:46,867,801G/Alikely benign
rs11823863656:46,867,811C/Guncertain significance
rs12341226:46,872,994A/Gsplice region variant
rs77660606:46,895,073C/Gregulatory region variant

Gene information from NCBI Gene. Variant classifications from ClinVar.