IGSF9
immunoglobulin superfamily member 9
Summary
Predicted to enable cell-cell adhesion mediator activity. Predicted to be involved in axon guidance; dendrite self-avoidance; and homophilic cell adhesion via plasma membrane adhesion molecules. Predicted to act upstream of or within dendrite development and regulation of synapse organization. Predicted to be located in dendrite and inhibitory synapse. Predicted to be active in axon; glutamatergic synapse; and postsynaptic density membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants83 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs749791904 | 1:159,897,208 | C/T | — | uncertain significance |
| rs368508741 | 1:159,897,256 | G/A | — | uncertain significance |
| rs1215766939 | 1:159,897,280 | G/A | — | uncertain significance |
| rs775565374 | 1:159,897,580 | G/A | — | uncertain significance |
| rs536701343 | 1:159,897,582 | G/C | missense variant | — |
| rs1650795174 | 1:159,897,598 | G/C | — | uncertain significance |
| rs1320302566 | 1:159,897,970 | G/A | — | uncertain significance |
| rs889265929 | 1:159,898,234 | G/A | — | uncertain significance |
| rs1242718842 | 1:159,898,251 | G/T | — | uncertain significance |
| rs138505943 | 1:159,898,269 | G/A | — | likely benign |
| rs772497737 | 1:159,898,300 | G/A | — | uncertain significance |
| rs779951492 | 1:159,898,302 | C/T | — | uncertain significance |
| rs1571209760 | 1:159,898,404 | T/C | — | uncertain significance |
| rs949883242 | 1:159,898,416 | C/T | — | uncertain significance |
| rs376174475 | 1:159,898,450 | G/A | — | uncertain significance |
| rs1281489711 | 1:159,898,473 | T/A | — | uncertain significance |
| rs2525208299 | 1:159,898,494 | G/T | — | uncertain significance |
| rs1384317554 | 1:159,898,495 | G/T | — | uncertain significance |
| rs369389237 | 1:159,898,537 | C/T | — | uncertain significance |
| rs781183381 | 1:159,898,584 | C/T | — | likely benign |
| rs760663053 | 1:159,898,627 | C/T | — | uncertain significance |
| rs778205242 | 1:159,898,662 | G/C | — | uncertain significance |
| rs775389533 | 1:159,898,690 | G/C | — | uncertain significance |
| rs764000599 | 1:159,898,693 | G/T | — | uncertain significance |
| rs1249050859 | 1:159,898,717 | C/T | — | uncertain significance |
| rs373574698 | 1:159,898,774 | C/A | — | uncertain significance |
| rs1268863205 | 1:159,898,779 | C/G | — | uncertain significance |
| rs769499549 | 1:159,899,171 | A/G | — | uncertain significance |
| rs778769134 | 1:159,899,484 | C/G | — | likely benign |
| rs200969104 | 1:159,899,485 | C/T | — | uncertain significance |
| rs771421838 | 1:159,899,571 | G/A | — | uncertain significance |
| rs1325016540 | 1:159,899,592 | T/C | — | uncertain significance |
| rs761248889 | 1:159,899,704 | T/C | — | uncertain significance |
| rs1339963371 | 1:159,899,731 | G/A | — | uncertain significance |
| rs1245702945 | 1:159,899,741 | C/T | — | uncertain significance |
| rs1395473337 | 1:159,899,758 | A/G | — | uncertain significance |
| rs376264039 | 1:159,900,028 | G/C | — | likely benign |
| rs2525214713 | 1:159,900,095 | G/T | — | uncertain significance |
| rs1480973609 | 1:159,900,134 | G/A | — | uncertain significance |
| rs2525214932 | 1:159,900,169 | G/A | — | uncertain significance |
| rs774572392 | 1:159,900,196 | G/A | — | uncertain significance |
| rs776567601 | 1:159,900,491 | C/G | — | uncertain significance |
| rs757758969 | 1:159,900,545 | C/G | — | uncertain significance |
| rs140900410 | 1:159,900,552 | C/G | — | uncertain significance |
| rs139085517 | 1:159,900,580 | G/C | — | uncertain significance |
| rs147025620 | 1:159,900,593 | G/A | — | uncertain significance |
| rs144356235 | 1:159,900,605 | C/T | — | uncertain significance |
| rs758486657 | 1:159,900,640 | C/T | — | uncertain significance |
| rs755205713 | 1:159,900,649 | C/T | — | uncertain significance |
| rs771632078 | 1:159,901,019 | C/G | — | uncertain significance |
| rs200623535 | 1:159,901,386 | C/T | — | uncertain significance |
| rs2101876751 | 1:159,901,622 | G/A | — | uncertain significance |
| rs767110567 | 1:159,901,640 | C/A | — | uncertain significance |
| rs376059608 | 1:159,901,663 | C/T | — | uncertain significance |
| rs781687802 | 1:159,901,674 | T/G | — | uncertain significance |
| rs2525219865 | 1:159,901,679 | A/C | — | uncertain significance |
| rs759417456 | 1:159,901,696 | C/T | — | uncertain significance |
| rs561289172 | 1:159,901,718 | C/G | — | uncertain significance |
| rs111438240 | 1:159,902,335 | G/A | — | likely benign |
| rs200923422 | 1:159,902,337 | C/T | — | uncertain significance |
| rs145285329 | 1:159,902,414 | C/G | missense variant | — |
| rs116177033 | 1:159,902,438 | G/A | — | likely benign |
| rs773805413 | 1:159,904,045 | G/A | — | uncertain significance |
| rs759854785 | 1:159,904,072 | T/C | — | uncertain significance |
| rs755929234 | 1:159,904,102 | T/C | — | uncertain significance |
| rs373829879 | 1:159,904,317 | G/A | — | likely benign |
| rs35702833 | 1:159,904,539 | A/G | — | benign |
| rs774440380 | 1:159,904,609 | G/A | — | uncertain significance |
| rs573730997 | 1:159,906,293 | G/A | — | uncertain significance |
| rs2525234414 | 1:159,906,672 | G/A | — | uncertain significance |
| rs766563398 | 1:159,907,506 | T/C | — | uncertain significance |
| rs763972792 | 1:159,907,527 | T/C | — | uncertain significance |
| rs143630342 | 1:159,907,548 | C/G | — | uncertain significance |
| rs374768980 | 1:159,907,585 | A/G | — | likely benign |
| rs757719031 | 1:159,912,773 | C/T | — | uncertain significance |
| rs759146489 | 1:159,912,842 | T/G | — | uncertain significance |
| rs767227752 | 1:159,912,845 | A/G | — | uncertain significance |
| rs146918168 | 1:159,912,851 | G/A | — | uncertain significance |
| rs1267489789 | 1:159,912,861 | C/T | — | uncertain significance |
| rs970250853 | 1:159,912,867 | G/A | — | uncertain significance |
| rs369566514 | 1:159,912,917 | G/A | — | uncertain significance |
| rs754997577 | 1:159,912,938 | C/T | — | uncertain significance |
| rs2525252583 | 1:159,913,216 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.