ITGA9
integrin subunit alpha 9
Summary
This gene encodes an alpha integrin. Integrins are heterodimeric integral membrane glycoproteins composed of an alpha chain and a beta chain that mediate cell-cell and cell-matrix adhesion. The protein encoded by this gene, when bound to the beta 1 chain, forms an integrin that is a receptor for VCAM1, cytotactin and osteopontin. Expression of this gene has been found to be upregulated in small cell lung cancers. [provided by RefSeq, Jul 2008]
Known Variants108 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs901587692 | 3:37,493,885 | C/G | — | uncertain significance |
| rs773014872 | 3:37,493,891 | G/A | — | uncertain significance |
| rs1029542671 | 3:37,493,899 | A/C | — | likely benign |
| rs1579032732 | 3:37,493,930 | T/G | — | uncertain significance |
| rs566237028 | 3:37,512,539 | C/G | — | uncertain significance |
| rs17036383 | 3:37,512,606 | C/A | — | benign |
| rs757641250 | 3:37,514,854 | G/T | — | uncertain significance |
| rs143806524 | 3:37,514,860 | C/T | — | likely benign |
| rs376199202 | 3:37,514,944 | G/A | — | uncertain significance |
| rs197770 | 3:37,515,827 | A/G | intron variant | — |
| rs2212020 | 3:37,517,462 | C/T | intron variant | — |
| rs189897 | 3:37,518,545 | T/A | intron variant | — |
| rs1380559036 | 3:37,522,987 | C/T | — | uncertain significance |
| rs967909532 | 3:37,522,988 | G/A | — | uncertain significance |
| rs775857944 | 3:37,523,013 | C/T | — | likely benign |
| rs760915010 | 3:37,523,014 | G/A | — | uncertain significance |
| rs1698555180 | 3:37,523,035 | T/C | — | uncertain significance |
| rs536240710 | 3:37,531,225 | C/T | — | — |
| rs2507940 | 3:37,535,984 | C/G | — | benign |
| rs2507941 | 3:37,536,056 | C/T | — | benign |
| rs267517 | 3:37,539,090 | G/C | — | — |
| rs149428936 | 3:37,544,736 | C/A | — | uncertain significance |
| rs1053181052 | 3:37,544,742 | A/G | — | uncertain significance |
| rs145968481 | 3:37,547,501 | G/A | — | benign |
| rs185553001 | 3:37,547,505 | G/A | — | uncertain significance |
| rs144367808 | 3:37,547,553 | C/T | — | uncertain significance |
| rs547761591 | 3:37,550,072 | G/A | — | uncertain significance |
| rs77438539 | 3:37,550,168 | T/A | — | benign |
| rs778182709 | 3:37,555,273 | C/T | — | uncertain significance |
| rs774729146 | 3:37,555,283 | C/G | — | uncertain significance |
| rs746058456 | 3:37,555,284 | G/A | — | uncertain significance |
| rs1215683751 | 3:37,555,302 | G/T | — | uncertain significance |
| rs755517251 | 3:37,555,350 | A/G | — | uncertain significance |
| rs141618223 | 3:37,555,387 | G/A | — | uncertain significance |
| rs373673092 | 3:37,559,014 | T/C | — | uncertain significance |
| rs150482056 | 3:37,559,040 | A/G | — | benign |
| rs780254896 | 3:37,559,087 | T/A | — | uncertain significance |
| rs2470632470 | 3:37,560,781 | A/C | — | uncertain significance |
| rs3733139 | 3:37,560,819 | G/A | — | likely benign |
| rs61751646 | 3:37,560,842 | A/G | — | benign |
| rs155524 | 3:37,562,141 | G/A | intron variant | — |
| rs155525 | 3:37,563,713 | G/A | intron variant | — |
| rs577107713 | 3:37,565,042 | C/A | — | uncertain significance |
| rs544515716 | 3:37,565,046 | G/A | — | uncertain significance |
| rs368707385 | 3:37,567,538 | T/C | — | uncertain significance |
| rs7427249 | 3:37,572,489 | G/C | — | — |
| rs267567 | 3:37,574,024 | G/T | — | — |
| rs781488596 | 3:37,574,806 | G/A | — | uncertain significance |
| rs759465761 | 3:37,574,846 | C/T | — | uncertain significance |
| rs150327524 | 3:37,574,847 | G/A | — | likely benign |
| rs547246502 | 3:37,574,911 | G/A | — | uncertain significance |
| rs267561 | 3:37,574,951 | A/G | — | benign |
| rs267540 | 3:37,581,843 | G/A | intron variant | — |
| rs2470668473 | 3:37,583,936 | G/A | — | uncertain significance |
| rs17827605 | 3:37,584,049 | A/G | — | benign |
| rs750899922 | 3:37,584,053 | C/T | — | uncertain significance |
| rs145528100 | 3:37,584,054 | G/A | — | likely benign |
| rs9850581 | 3:37,584,061 | T/C | — | benign |
| rs147277452 | 3:37,584,086 | C/T | — | benign |
| rs166508 | 3:37,590,435 | T/C | intron variant | — |
| rs9825420 | 3:37,604,012 | T/G | intron variant | — |
| rs61751189 | 3:37,670,679 | G/A | — | benign |
| rs369282174 | 3:37,670,693 | G/A | — | uncertain significance |
| rs145334938 | 3:37,670,698 | C/T | — | likely benign |
| rs766654628 | 3:37,670,708 | G/A | — | uncertain significance |
| rs138705453 | 3:37,670,749 | A/G | — | likely benign |
| rs114129792 | 3:37,670,752 | G/A | — | likely benign |
| rs777228206 | 3:37,670,774 | C/G | — | uncertain significance |
| rs746352590 | 3:37,670,792 | T/G | — | uncertain significance |
| rs2282485 | 3:37,670,876 | G/C | — | benign |
| rs779583800 | 3:37,695,227 | G/C | — | uncertain significance |
| rs769056713 | 3:37,695,277 | T/C | — | uncertain significance |
| rs143960385 | 3:37,695,288 | C/T | — | likely benign |
| rs73070742 | 3:37,703,568 | G/C | intron variant | — |
| rs372970747 | 3:37,725,349 | G/T | — | likely benign |
| rs146299367 | 3:37,725,370 | C/T | — | uncertain significance |
| rs538062566 | 3:37,725,432 | G/A | — | uncertain significance |
| rs754167910 | 3:37,725,445 | A/G | — | uncertain significance |
| rs139900262 | 3:37,725,466 | A/G | — | uncertain significance |
| rs146939332 | 3:37,725,482 | C/T | — | likely benign |
| rs142726080 | 3:37,774,225 | A/G | — | benign |
| rs917137238 | 3:37,774,231 | T/A | — | uncertain significance |
| rs145449301 | 3:37,774,284 | T/A | — | uncertain significance |
| rs142025172 | 3:37,778,407 | G/A | — | likely benign |
| rs923830335 | 3:37,778,434 | G/A | — | uncertain significance |
| rs2470539879 | 3:37,778,468 | C/T | — | uncertain significance |
| rs112785572 | 3:37,778,480 | G/T | — | likely benign |
| rs1118148 | 3:37,778,481 | G/C | — | benign |
| rs200735233 | 3:37,778,482 | G/C | — | likely benign |
| rs373225022 | 3:37,783,235 | G/A | — | uncertain significance |
| rs148785471 | 3:37,783,261 | C/G | — | uncertain significance |
| rs140716372 | 3:37,785,454 | G/A | — | likely benign |
| rs201925616 | 3:37,785,460 | G/A | — | uncertain significance |
| rs1181751894 | 3:37,818,923 | C/T | — | uncertain significance |
| rs962348254 | 3:37,818,955 | A/G | — | uncertain significance |
| rs777183871 | 3:37,819,003 | G/A | — | uncertain significance |
| rs76424398 | 3:37,819,040 | G/A | — | benign |
| rs75329080 | 3:37,821,466 | G/A | — | benign |
| rs751300551 | 3:37,826,494 | G/A | — | uncertain significance |
| rs147528488 | 3:37,826,500 | C/T | — | likely benign |
Showing 100 of 108 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.