LINGO2
leucine rich repeat and Ig domain containing 2
Summary
Predicted to act upstream of or within positive regulation of synapse assembly. Predicted to be located in membrane. Predicted to be active in several cellular components, including extracellular space; glutamatergic synapse; and synaptic membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs62541086 | 9:27,943,037 | T/G | coding sequence variant | — |
| rs2489132517 | 9:27,948,922 | G/A | — | uncertain significance |
| rs772866502 | 9:27,948,940 | A/G | — | uncertain significance |
| rs776045242 | 9:27,948,946 | T/C | — | uncertain significance |
| rs113646467 | 9:27,948,975 | C/T | — | likely benign |
| rs200696442 | 9:27,949,076 | T/C | — | uncertain significance |
| rs201237761 | 9:27,949,137 | C/T | — | likely benign |
| rs764089619 | 9:27,949,232 | T/C | — | uncertain significance |
| rs750277332 | 9:27,949,321 | C/G | — | uncertain significance |
| rs145458168 | 9:27,949,504 | C/T | — | uncertain significance |
| rs1823528558 | 9:27,949,573 | A/G | — | uncertain significance |
| rs902461834 | 9:27,949,666 | G/C | — | uncertain significance |
| rs144743055 | 9:27,949,697 | C/G | — | benign |
| rs1188062764 | 9:27,949,762 | T/C | — | uncertain significance |
| rs1587509733 | 9:27,949,789 | G/C | — | uncertain significance |
| rs1317035058 | 9:27,950,028 | G/C | — | uncertain significance |
| rs775438948 | 9:27,950,184 | G/T | — | uncertain significance |
| rs920114694 | 9:27,950,243 | T/G | — | uncertain significance |
| rs540601601 | 9:27,950,293 | G/A | — | uncertain significance |
| rs879488252 | 9:27,950,312 | C/G | — | uncertain significance |
| rs1040309410 | 9:27,950,338 | C/T | — | uncertain significance |
| rs376791650 | 9:27,950,362 | T/C | — | uncertain significance |
| rs761477487 | 9:27,950,386 | T/C | — | uncertain significance |
| rs143274692 | 9:27,950,494 | G/A | — | uncertain significance |
| rs1451741510 | 9:27,950,617 | A/C | — | uncertain significance |
| rs754215724 | 9:27,950,656 | G/A | — | uncertain significance |
| rs150391726 | 9:27,950,658 | C/T | — | likely benign |
| rs12057050 | 9:27,957,175 | G/A | intron variant | — |
| rs12683422 | 9:27,969,440 | C/T | intron variant | — |
| rs10968280 | 9:28,011,645 | T/A | intron variant | — |
| rs548787624 | 9:28,037,702 | G/T | — | — |
| rs184726399 | 9:28,144,135 | A/G | upstream gene variant | — |
| rs1319535 | 9:28,181,085 | C/A | — | — |
| rs16912725 | 9:28,359,782 | C/A | intron variant | — |
| rs10968562 | 9:28,402,043 | A/G | intron variant | — |
| rs13285209 | 9:28,410,903 | T/C | intron variant | — |
| rs17770163 | 9:28,411,264 | T/G | — | — |
| rs7857323 | 9:28,412,227 | A/T | — | — |
| rs2383766 | 9:28,412,500 | G/T | intron variant | — |
| rs10968576 | 9:28,414,339 | A/G | intron variant | — |
| rs17770336 | 9:28,414,625 | C/T | intron variant | — |
| rs10968577 | 9:28,415,512 | C/T | intron variant | — |
| rs13288841 | 9:28,418,511 | G/A | intron variant | — |
| rs1412239 | 9:28,425,515 | C/G | — | — |
| rs62555197 | 9:28,433,953 | A/G | — | — |
| rs73439357 | 9:28,493,041 | T/C | intron variant | — |
| rs58662928 | 9:28,577,294 | T/C | intron variant | — |
| rs2891316 | 9:28,587,994 | G/A | intron variant | — |
| rs12348435 | 9:28,600,142 | A/C | upstream gene variant | — |
| rs12344656 | 9:28,604,268 | G/A | upstream gene variant | — |
| rs10968719 | 9:28,685,167 | T/A | — | — |
| rs1438480 | 9:28,717,112 | A/C | intergenic variant | — |
| rs824248 | 9:28,772,700 | A/T | intergenic variant | — |
| rs531114053 | 9:28,790,405 | A/C | — | — |
| rs4879286 | 9:28,935,868 | C/T | intergenic variant | — |
| rs4879287 | 9:28,935,926 | A/G | intergenic variant | — |
| rs13299788 | 9:28,941,459 | C/G | intergenic variant | — |
| rs7470946 | 9:28,948,308 | G/T | intergenic variant | — |
| rs1418351 | 9:29,067,934 | G/C | intergenic variant | — |
| rs13288108 | 9:29,089,437 | C/A | intergenic variant | — |
| rs182835395 | 9:29,196,676 | T/C | intergenic variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.