ATRNL1
attractin like 1
Summary
Predicted to enable Notch binding activity. Predicted to act upstream of or within G protein-coupled receptor signaling pathway. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants74 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1225588168 | 10:116,853,561 | G/A | — | uncertain significance |
| rs782142614 | 10:116,853,622 | A/C | — | uncertain significance |
| rs146316685 | 10:116,853,646 | A/G | — | uncertain significance |
| rs1377082565 | 10:116,853,750 | T/A | — | uncertain significance |
| rs371156017 | 10:116,853,757 | C/T | — | uncertain significance |
| rs782126275 | 10:116,880,028 | G/A | — | uncertain significance |
| rs377021159 | 10:116,881,536 | G/A | — | uncertain significance |
| rs782768109 | 10:116,881,554 | G/A | — | uncertain significance |
| rs782731288 | 10:116,889,197 | T/C | — | likely benign |
| rs201213434 | 10:116,889,228 | G/A | — | uncertain significance |
| rs566145462 | 10:116,889,247 | A/C | — | uncertain significance |
| rs1845130024 | 10:116,889,289 | G/A | — | uncertain significance |
| rs561376146 | 10:116,908,048 | A/G | — | — |
| rs2493374221 | 10:116,919,808 | T/A | — | uncertain significance |
| rs2493374238 | 10:116,919,809 | T/C | — | uncertain significance |
| rs936319452 | 10:116,919,834 | A/C | — | uncertain significance |
| rs782535012 | 10:116,919,972 | T/C | — | uncertain significance |
| rs2493399520 | 10:116,925,394 | G/T | — | uncertain significance |
| rs141967868 | 10:116,930,870 | A/G | — | benign |
| rs782347663 | 10:116,930,874 | A/G | — | uncertain significance |
| rs375963014 | 10:116,930,957 | A/G | — | uncertain significance |
| rs533092732 | 10:116,961,434 | T/C | — | — |
| rs2493595558 | 10:116,975,486 | A/T | — | uncertain significance |
| rs2493595668 | 10:116,975,503 | G/A | — | uncertain significance |
| rs1554896061 | 10:116,975,514 | C/T | — | uncertain significance |
| rs193156959 | 10:116,975,590 | A/G | — | uncertain significance |
| rs201880985 | 10:116,975,620 | A/G | — | uncertain significance |
| rs782508057 | 10:116,975,626 | A/G | — | uncertain significance |
| rs782381575 | 10:117,001,424 | A/G | — | uncertain significance |
| rs4328149 | 10:117,015,421 | G/T | — | — |
| rs142082253 | 10:117,024,687 | A/G | — | uncertain significance |
| rs1554910187 | 10:117,024,703 | A/G | — | uncertain significance |
| rs114220247 | 10:117,024,753 | G/A | — | uncertain significance |
| rs2493160430 | 10:117,026,321 | T/G | — | uncertain significance |
| rs752358215 | 10:117,026,322 | C/G | — | uncertain significance |
| rs142789674 | 10:117,026,339 | C/T | — | uncertain significance |
| rs201368972 | 10:117,026,446 | A/G | — | uncertain significance |
| rs1215149445 | 10:117,026,458 | A/G | — | uncertain significance |
| rs1341813361 | 10:117,059,587 | A/G | — | uncertain significance |
| rs145512153 | 10:117,059,641 | C/T | — | uncertain significance |
| rs147589789 | 10:117,059,653 | A/G | — | uncertain significance |
| rs1212010006 | 10:117,059,702 | A/T | — | uncertain significance |
| rs2493382942 | 10:117,061,374 | A/C | — | uncertain significance |
| rs202112185 | 10:117,061,389 | C/T | — | uncertain significance |
| rs1853487027 | 10:117,061,394 | A/G | — | uncertain significance |
| rs200013099 | 10:117,061,465 | C/G | — | uncertain significance |
| rs781941172 | 10:117,061,497 | A/G | — | uncertain significance |
| rs2493459184 | 10:117,075,075 | C/T | — | uncertain significance |
| rs140980345 | 10:117,075,142 | G/A | — | uncertain significance |
| rs782579538 | 10:117,075,150 | A/G | — | uncertain significance |
| rs782644929 | 10:117,075,165 | A/G | — | uncertain significance |
| rs1953758 | 10:117,075,175 | A/G | — | benign |
| rs1290872269 | 10:117,093,891 | G/C | — | uncertain significance |
| rs1844202477 | 10:117,154,254 | A/G | — | likely benign |
| rs199578378 | 10:117,226,720 | A/G | — | uncertain significance |
| rs1421045338 | 10:117,228,700 | A/G | — | uncertain significance |
| rs201735786 | 10:117,228,721 | A/G | — | uncertain significance |
| rs2494407874 | 10:117,228,722 | G/T | — | uncertain significance |
| rs138513096 | 10:117,228,756 | T/A | — | uncertain significance |
| rs144016778 | 10:117,228,762 | A/G | — | uncertain significance |
| rs371534050 | 10:117,228,763 | A/G | — | uncertain significance |
| rs10885721 | 10:117,228,794 | A/G | — | benign |
| rs7911480 | 10:117,241,931 | A/G | intron variant | — |
| rs150729224 | 10:117,278,792 | A/G | — | uncertain significance |
| rs369790974 | 10:117,278,809 | G/A | — | uncertain significance |
| rs782368586 | 10:117,486,821 | G/C | — | uncertain significance |
| rs375473778 | 10:117,486,849 | T/G | — | uncertain significance |
| rs10490919 | 10:117,512,588 | T/C | — | — |
| rs782287060 | 10:117,607,487 | C/A | — | uncertain significance |
| rs2960659 | 10:117,633,587 | T/A | — | — |
| rs190322680 | 10:117,684,300 | T/G | intron variant | — |
| rs782691849 | 10:117,704,177 | A/G | — | uncertain significance |
| rs2494867926 | 10:117,704,204 | C/G | — | uncertain significance |
| rs782748547 | 10:117,704,246 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.