NTM
neurotrimin
Summary
This gene encodes a member of the IgLON (LAMP, OBCAM, Ntm) family of immunoglobulin (Ig) domain-containing glycosylphosphatidylinositol (GPI)-anchored cell adhesion molecules. The encoded protein may promote neurite outgrowth and adhesion via a homophilic mechanism. This gene is closely linked to a related family member, opioid binding protein/cell adhesion molecule-like (OPCML), on chromosome 11. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2009]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7481514 | 11:131,291,963 | A/T | — | — |
| rs1550976 | 11:131,320,070 | T/C | intron variant | — |
| rs11601906 | 11:131,325,246 | C/T | intron variant | — |
| rs992564 | 11:131,336,074 | G/C | — | — |
| rs12421680 | 11:131,350,968 | G/C | — | — |
| rs412486 | 11:131,404,677 | G/A | coding sequence variant | — |
| rs187798970 | 11:131,406,834 | G/T | intron variant | — |
| rs12788343 | 11:131,452,912 | T/A | — | — |
| rs4936139 | 11:131,459,065 | G/T | — | — |
| rs10750486 | 11:131,463,916 | G/A | intron variant | — |
| rs75269996 | 11:131,468,913 | C/T | intron variant | — |
| rs71483681 | 11:131,469,205 | T/C | intron variant | — |
| rs1506660 | 11:131,472,232 | C/G | — | — |
| rs1506662 | 11:131,477,247 | G/T | — | — |
| rs4936141 | 11:131,478,970 | G/T | — | — |
| rs554309481 | 11:131,507,411 | C/T | — | — |
| rs376930803 | 11:131,781,428 | C/G | — | uncertain significance |
| rs767842712 | 11:131,781,470 | G/T | — | uncertain significance |
| rs201935214 | 11:131,781,500 | T/C | — | uncertain significance |
| rs75710163 | 11:131,781,519 | G/T | — | benign |
| rs1334919413 | 11:131,781,528 | G/C | — | uncertain significance |
| rs12098973 | 11:131,807,171 | A/G | intron variant | — |
| rs188290902 | 11:131,868,501 | A/G | intron variant | — |
| rs74863301 | 11:131,877,419 | T/C | intron variant | — |
| rs1940033 | 11:131,882,807 | C/G | — | — |
| rs6590611 | 11:131,900,557 | T/A | — | — |
| rs11222869 | 11:131,901,748 | A/T | — | — |
| rs11222875 | 11:131,907,305 | C/T | intron variant | — |
| rs1790165 | 11:131,928,971 | C/A | intron variant | — |
| rs1015053 | 11:131,933,511 | A/T | intron variant | — |
| rs4468361 | 11:132,010,117 | T/C | regulatory region variant | — |
| rs533353213 | 11:132,016,183 | A/G | — | uncertain significance |
| rs190818488 | 11:132,016,296 | G/A | — | benign |
| rs2540134909 | 11:132,016,298 | A/C | — | uncertain significance |
| rs772770138 | 11:132,081,933 | G/A | — | uncertain significance |
| rs1449435 | 11:132,088,917 | G/A | intron variant | — |
| rs3099797 | 11:132,121,386 | C/T | intron variant | — |
| rs116031926 | 11:132,153,347 | G/A | upstream gene variant | — |
| rs375999981 | 11:132,177,579 | G/A | — | likely benign |
| rs368362251 | 11:132,177,682 | C/T | — | uncertain significance |
| rs775322072 | 11:132,184,482 | C/G | — | uncertain significance |
| rs756339914 | 11:132,184,549 | G/A | — | uncertain significance |
| rs1839316 | 11:132,188,871 | C/A | intron variant | — |
| rs201653643 | 11:132,200,049 | G/A | — | likely benign |
| rs147788695 | 11:132,204,964 | G/A | — | likely benign |
| rs139579932 | 11:132,204,976 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.