IGSF11
immunoglobulin superfamily member 11
Summary
IGSF11 is an immunoglobulin (Ig) superfamily member that is preferentially expressed in brain and testis. It shares significant homology with coxsackievirus and adenovirus receptor (CXADR; MIM 602621) and endothelial cell-selective adhesion molecule (ESAM).[supplied by OMIM, Apr 2005]
Known Variants25 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1433486003 | 3:118,621,410 | G/C | — | uncertain significance |
| rs2472464803 | 3:118,621,416 | G/A | — | uncertain significance |
| rs781293570 | 3:118,621,423 | T/A | — | uncertain significance |
| rs757452341 | 3:118,621,476 | G/A | — | uncertain significance |
| rs753921823 | 3:118,621,569 | A/G | — | uncertain significance |
| rs1483889670 | 3:118,621,605 | T/A | — | uncertain significance |
| rs1416562846 | 3:118,621,623 | A/T | — | uncertain significance |
| rs769386891 | 3:118,621,689 | T/C | — | uncertain significance |
| rs374674136 | 3:118,621,704 | C/T | — | uncertain significance |
| rs759822063 | 3:118,621,786 | A/C | — | uncertain significance |
| rs2472468367 | 3:118,621,806 | T/C | — | uncertain significance |
| rs143587839 | 3:118,623,547 | A/G | — | uncertain significance |
| rs1341947543 | 3:118,623,600 | C/T | — | uncertain significance |
| rs779100034 | 3:118,624,539 | G/A | — | uncertain significance |
| rs764460197 | 3:118,647,521 | G/A | — | uncertain significance |
| rs369148066 | 3:118,647,539 | T/C | — | uncertain significance |
| rs2472602648 | 3:118,649,035 | G/A | — | uncertain significance |
| rs4687833 | 3:118,676,492 | T/C | intron variant | — |
| rs2160050 | 3:118,745,936 | T/C | intron variant | — |
| rs554488208 | 3:118,753,386 | G/A | — | uncertain significance |
| rs776367713 | 3:118,753,417 | G/A | — | uncertain significance |
| rs774885432 | 3:118,753,426 | T/G | — | uncertain significance |
| rs145868254 | 3:118,766,796 | C/T | intron variant | — |
| rs6773865 | 3:118,817,571 | G/C | regulatory region variant | — |
| rs149982219 | 3:118,865,618 | G/A | missense variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.