ITGA11
integrin subunit alpha 11
Summary
This gene encodes an alpha integrin. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. This protein contains an I domain, is expressed in muscle tissue, dimerizes with beta 1 integrin in vitro, and appears to bind collagen in this form. Therefore, the protein may be involved in attaching muscle tissue to the extracellular matrix. Alternative transcriptional splice variants have been found for this gene, but their biological validity is not determined. [provided by RefSeq, Jul 2008]
Known Variants103 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs374029863 | 15:68,596,129 | A/G | — | uncertain significance |
| rs757047260 | 15:68,596,150 | C/T | — | uncertain significance |
| rs200576562 | 15:68,596,162 | C/A | — | uncertain significance |
| rs7174755 | 15:68,597,127 | T/G | — | — |
| rs761739603 | 15:68,599,690 | C/T | — | uncertain significance |
| rs1051082097 | 15:68,599,747 | G/A | — | uncertain significance |
| rs187377240 | 15:68,599,748 | C/T | — | uncertain significance |
| rs752004974 | 15:68,603,346 | G/A | — | uncertain significance |
| rs199548438 | 15:68,603,349 | G/A | — | uncertain significance |
| rs372902171 | 15:68,603,369 | G/T | — | uncertain significance |
| rs200056013 | 15:68,603,375 | C/T | — | uncertain significance |
| rs909209671 | 15:68,603,384 | G/C | — | uncertain significance |
| rs759923280 | 15:68,603,411 | G/A | — | uncertain significance |
| rs769198042 | 15:68,603,669 | C/T | — | uncertain significance |
| rs572985908 | 15:68,603,720 | G/A | — | uncertain significance |
| rs757895032 | 15:68,605,121 | C/G | — | uncertain significance |
| rs781603389 | 15:68,605,125 | T/C | — | uncertain significance |
| rs2505547263 | 15:68,605,135 | C/A | — | likely benign |
| rs267604299 | 15:68,605,160 | G/A | — | uncertain significance |
| rs372085965 | 15:68,605,179 | C/T | — | uncertain significance |
| rs200995747 | 15:68,606,120 | G/A | — | uncertain significance |
| rs1893548743 | 15:68,608,028 | A/G | — | uncertain significance |
| rs765252460 | 15:68,609,686 | T/C | — | uncertain significance |
| rs112547535 | 15:68,612,531 | T/A | — | uncertain significance |
| rs2505571918 | 15:68,612,557 | G/A | — | uncertain significance |
| rs1893752048 | 15:68,612,584 | T/C | — | uncertain significance |
| rs573730343 | 15:68,612,643 | C/G | — | uncertain significance |
| rs61729760 | 15:68,612,677 | G/A | — | uncertain significance |
| rs145852498 | 15:68,613,762 | G/C | — | uncertain significance |
| rs575269180 | 15:68,613,819 | T/A | — | uncertain significance |
| rs2505586404 | 15:68,617,483 | T/C | — | uncertain significance |
| rs768158251 | 15:68,617,495 | C/T | — | uncertain significance |
| rs200856232 | 15:68,617,496 | G/A | — | likely benign |
| rs375239763 | 15:68,617,539 | T/C | — | uncertain significance |
| rs758259065 | 15:68,617,540 | C/T | — | uncertain significance |
| rs2505587051 | 15:68,617,576 | T/G | — | uncertain significance |
| rs202203467 | 15:68,618,997 | C/T | — | uncertain significance |
| rs767175041 | 15:68,619,108 | C/T | — | uncertain significance |
| rs370530712 | 15:68,619,112 | C/T | — | uncertain significance |
| rs373273567 | 15:68,619,113 | A/G | — | uncertain significance |
| rs781200956 | 15:68,619,120 | C/T | — | uncertain significance |
| rs562059147 | 15:68,620,475 | G/T | — | uncertain significance |
| rs374681501 | 15:68,620,521 | G/T | — | uncertain significance |
| rs373351885 | 15:68,623,362 | T/C | — | likely benign |
| rs745366518 | 15:68,623,376 | T/C | — | uncertain significance |
| rs765594455 | 15:68,623,388 | T/C | — | uncertain significance |
| rs767369353 | 15:68,623,422 | C/A | — | uncertain significance |
| rs374711695 | 15:68,624,225 | C/T | — | likely benign |
| rs749667260 | 15:68,624,232 | C/T | — | uncertain significance |
| rs1032771262 | 15:68,624,236 | G/T | — | uncertain significance |
| rs765073756 | 15:68,624,283 | C/T | — | uncertain significance |
| rs2505609729 | 15:68,624,387 | T/C | — | uncertain significance |
| rs759310949 | 15:68,624,707 | C/T | — | uncertain significance |
| rs1480653704 | 15:68,624,753 | C/T | — | uncertain significance |
| rs201176891 | 15:68,624,762 | C/T | — | uncertain significance |
| rs372539285 | 15:68,624,768 | C/T | — | uncertain significance |
| rs369751022 | 15:68,624,771 | C/T | — | uncertain significance |
| rs28672317 | 15:68,625,689 | T/G | intron variant | — |
| rs72743231 | 15:68,626,471 | G/A | regulatory region variant | — |
| rs61729766 | 15:68,628,072 | C/T | — | conflicting classifications of pathogenicity |
| rs764516782 | 15:68,628,145 | G/A | — | uncertain significance |
| rs2306022 | 15:68,628,163 | C/T | missense variant | — |
| rs201105280 | 15:68,631,868 | C/T | — | uncertain significance |
| rs771247508 | 15:68,631,895 | G/A | — | uncertain significance |
| rs745968066 | 15:68,631,907 | C/T | — | uncertain significance |
| rs562286619 | 15:68,631,913 | C/T | — | uncertain significance |
| rs377427762 | 15:68,631,921 | G/A | — | uncertain significance |
| rs1244039226 | 15:68,631,937 | C/G | — | uncertain significance |
| rs200299485 | 15:68,631,953 | G/C | — | benign |
| rs368295467 | 15:68,631,957 | C/T | — | uncertain significance |
| rs368905309 | 15:68,641,200 | A/C | — | uncertain significance |
| rs2504989859 | 15:68,641,218 | A/G | — | uncertain significance |
| rs774914585 | 15:68,643,054 | C/T | — | uncertain significance |
| rs767641088 | 15:68,643,057 | T/C | — | uncertain significance |
| rs768867198 | 15:68,643,616 | C/T | — | uncertain significance |
| rs761902509 | 15:68,643,628 | C/T | — | uncertain significance |
| rs377301043 | 15:68,643,629 | G/A | — | likely benign |
| rs61729770 | 15:68,643,659 | G/A | — | likely benign |
| rs772882181 | 15:68,643,664 | C/T | — | uncertain significance |
| rs762884478 | 15:68,643,732 | G/A | — | uncertain significance |
| rs2505001466 | 15:68,649,508 | A/C | — | uncertain significance |
| rs375757460 | 15:68,649,517 | G/A | — | uncertain significance |
| rs200247746 | 15:68,649,574 | C/T | — | uncertain significance |
| rs376261838 | 15:68,649,588 | T/C | — | uncertain significance |
| rs768044608 | 15:68,649,607 | C/T | — | uncertain significance |
| rs753154822 | 15:68,649,609 | A/G | — | uncertain significance |
| rs377444249 | 15:68,650,900 | C/T | — | likely benign |
| rs770568289 | 15:68,650,901 | G/C | — | uncertain significance |
| rs148886354 | 15:68,653,946 | C/T | — | likely benign |
| rs1240966637 | 15:68,653,949 | T/A | — | uncertain significance |
| rs775833316 | 15:68,654,030 | G/A | — | uncertain significance |
| rs760770453 | 15:68,657,089 | G/T | — | uncertain significance |
| rs201928196 | 15:68,657,116 | C/T | — | uncertain significance |
| rs151266879 | 15:68,661,541 | G/T | — | uncertain significance |
| rs995830321 | 15:68,661,546 | C/T | — | uncertain significance |
| rs781506557 | 15:68,661,596 | G/A | — | uncertain significance |
| rs368518553 | 15:68,661,609 | C/T | — | uncertain significance |
| rs761425876 | 15:68,695,268 | A/T | — | uncertain significance |
| rs746813861 | 15:68,695,326 | A/G | — | uncertain significance |
| rs754238550 | 15:68,695,362 | G/A | — | uncertain significance |
Showing 100 of 103 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.