SCARA5
scavenger receptor class A member 5
Summary
Predicted to enable ferritin receptor activity. Predicted to be involved in several processes, including intracellular iron ion homeostasis; iron ion transmembrane transport; and protein homotrimerization. Predicted to act upstream of or within cellular response to heat. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants63 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs574772914 | 8:27,732,376 | G/A | — | — |
| rs138268936 | 8:27,737,212 | A/G | — | uncertain significance |
| rs771356304 | 8:27,737,235 | G/A | — | uncertain significance |
| rs11774576 | 8:27,740,417 | C/A | — | — |
| rs191109927 | 8:27,748,397 | C/T | regulatory region variant | — |
| rs372068788 | 8:27,762,301 | C/T | — | uncertain significance |
| rs189041471 | 8:27,763,492 | C/T | upstream gene variant | — |
| rs2486866994 | 8:27,764,679 | A/C | — | uncertain significance |
| rs768360891 | 8:27,764,713 | C/T | — | uncertain significance |
| rs764145315 | 8:27,764,752 | C/T | — | uncertain significance |
| rs1022398722 | 8:27,764,755 | C/T | — | uncertain significance |
| rs138456340 | 8:27,764,937 | A/G | upstream gene variant | — |
| rs754297792 | 8:27,767,254 | G/A | — | uncertain significance |
| rs140062457 | 8:27,778,614 | T/C | intron variant | — |
| rs1163661724 | 8:27,779,174 | A/G | — | uncertain significance |
| rs763964092 | 8:27,779,205 | C/T | — | uncertain significance |
| rs765044292 | 8:27,779,216 | C/G | — | uncertain significance |
| rs746653643 | 8:27,779,226 | G/A | — | uncertain significance |
| rs374738537 | 8:27,779,232 | C/T | — | uncertain significance |
| rs1483956668 | 8:27,779,258 | C/T | — | likely benign |
| rs1322486058 | 8:27,779,330 | C/T | — | uncertain significance |
| rs772210832 | 8:27,779,385 | C/T | — | uncertain significance |
| rs367893127 | 8:27,779,402 | C/T | — | uncertain significance |
| rs1415805449 | 8:27,779,437 | C/A | — | uncertain significance |
| rs368216809 | 8:27,779,438 | T/C | — | uncertain significance |
| rs747072623 | 8:27,779,486 | C/T | — | uncertain significance |
| rs772083997 | 8:27,779,517 | T/C | — | uncertain significance |
| rs776277770 | 8:27,779,531 | G/T | — | uncertain significance |
| rs781198035 | 8:27,779,561 | C/T | — | uncertain significance |
| rs775439485 | 8:27,779,571 | C/T | — | uncertain significance |
| rs1200559056 | 8:27,779,577 | C/T | — | uncertain significance |
| rs764943123 | 8:27,779,586 | G/T | — | uncertain significance |
| rs61737292 | 8:27,779,612 | G/A | missense variant | — |
| rs777920347 | 8:27,779,633 | T/C | — | uncertain significance |
| rs373848299 | 8:27,779,639 | G/A | — | uncertain significance |
| rs1807606226 | 8:27,779,643 | G/T | — | uncertain significance |
| rs751272418 | 8:27,779,715 | T/G | — | uncertain significance |
| rs118019452 | 8:27,779,717 | C/T | — | uncertain significance |
| rs142301969 | 8:27,800,243 | G/C | intron variant | — |
| rs2726950 | 8:27,806,764 | A/G | intron variant | — |
| rs2685417 | 8:27,807,434 | G/T | — | — |
| rs11994699 | 8:27,808,239 | G/T | — | — |
| rs2685416 | 8:27,808,489 | C/A | intron variant | — |
| rs4395853 | 8:27,808,770 | C/A | — | — |
| rs2685414 | 8:27,810,384 | C/A | — | — |
| rs2685412 | 8:27,810,603 | C/A | — | — |
| rs148071375 | 8:27,814,943 | C/G | intron variant | — |
| rs2726944 | 8:27,816,065 | C/T | intron variant | — |
| rs144992125 | 8:27,819,003 | T/C | intron variant | — |
| rs11783561 | 8:27,820,015 | C/T | — | — |
| rs10087301 | 8:27,820,792 | A/G | regulatory region variant | — |
| rs1305203716 | 8:27,823,943 | A/G | — | uncertain significance |
| rs767400860 | 8:27,823,948 | C/A | — | uncertain significance |
| rs371870933 | 8:27,824,000 | G/C | — | uncertain significance |
| rs760484926 | 8:27,824,027 | A/G | — | uncertain significance |
| rs539920202 | 8:27,824,044 | C/T | — | uncertain significance |
| rs562802872 | 8:27,827,726 | G/C | — | — |
| rs1340374424 | 8:27,845,062 | A/G | — | uncertain significance |
| rs2486503411 | 8:27,845,087 | T/C | — | uncertain significance |
| rs372626124 | 8:27,845,102 | C/T | — | uncertain significance |
| rs980492789 | 8:27,845,120 | C/T | — | uncertain significance |
| rs141394036 | 8:27,845,125 | T/C | — | uncertain significance |
| rs147766672 | 8:27,849,159 | A/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.