LRRTM4
leucine rich repeat transmembrane neuronal 4
Summary
Predicted to enable heparan sulfate proteoglycan binding activity. Predicted to be involved in regulation of synapse assembly. Predicted to act upstream of or within AMPA glutamate receptor clustering; positive regulation of synapse assembly; and regulation of presynaptic membrane organization. Predicted to be located in postsynaptic membrane. Predicted to be part of AMPA glutamate receptor complex. Predicted to be active in several cellular components, including GABA-ergic synapse; photoreceptor ribbon synapse; and postsynaptic density membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1672736841 | 2:76,975,867 | G/A | — | uncertain significance |
| rs538522228 | 2:76,975,900 | A/C | — | uncertain significance |
| rs200328327 | 2:76,975,931 | G/C | — | uncertain significance |
| rs191264264 | 2:77,134,793 | A/T | intron variant | — |
| rs2178574 | 2:77,152,610 | A/G | intron variant | — |
| rs4853283 | 2:77,156,402 | A/G | intron variant | — |
| rs1470506 | 2:77,223,938 | C/T | intron variant | — |
| rs55985303 | 2:77,224,951 | G/A | intron variant | — |
| rs1446702 | 2:77,235,470 | A/T | intron variant | — |
| rs6547115 | 2:77,246,331 | A/T | — | — |
| rs72807203 | 2:77,292,600 | C/T | intron variant | — |
| rs148102408 | 2:77,318,982 | A/C | — | — |
| rs138799955 | 2:77,319,073 | A/T | — | — |
| rs62168766 | 2:77,332,735 | C/G | — | — |
| rs58449464 | 2:77,334,916 | T/C | intron variant | — |
| rs72809129 | 2:77,475,663 | C/A | intron variant | — |
| rs5832276 | 2:77,582,084 | A/G | — | — |
| rs185525572 | 2:77,638,066 | A/G | intron variant | — |
| rs11679943 | 2:77,724,624 | G/A | intron variant | — |
| rs6761838 | 2:77,730,997 | A/T | intron variant | — |
| rs1480832253 | 2:77,745,506 | C/T | — | uncertain significance |
| rs751743214 | 2:77,745,551 | G/T | — | uncertain significance |
| rs376246457 | 2:77,745,626 | G/C | — | uncertain significance |
| rs765681974 | 2:77,745,661 | A/G | — | uncertain significance |
| rs941094225 | 2:77,745,664 | T/C | — | uncertain significance |
| rs371191395 | 2:77,745,782 | A/T | — | uncertain significance |
| rs770128588 | 2:77,745,875 | C/G | — | uncertain significance |
| rs1679347960 | 2:77,745,953 | C/T | — | uncertain significance |
| rs367742060 | 2:77,745,962 | T/C | — | uncertain significance |
| rs765145008 | 2:77,746,123 | T/C | — | uncertain significance |
| rs2466102993 | 2:77,746,148 | T/C | — | uncertain significance |
| rs2466103756 | 2:77,746,225 | T/C | — | uncertain significance |
| rs1246990076 | 2:77,746,245 | C/A | — | uncertain significance |
| rs565553855 | 2:77,746,475 | T/C | — | uncertain significance |
| rs2466106036 | 2:77,746,578 | G/T | — | uncertain significance |
| rs2466106048 | 2:77,746,579 | T/G | — | uncertain significance |
| rs761625528 | 2:77,746,619 | T/C | — | uncertain significance |
| rs757583021 | 2:77,746,701 | G/A | — | likely benign |
| rs76327576 | 2:77,746,839 | G/C | — | likely benign |
| rs2466108297 | 2:77,746,910 | C/T | — | uncertain significance |
| rs377371374 | 2:77,746,957 | C/T | — | uncertain significance |
| rs1425430443 | 2:77,746,961 | T/C | — | uncertain significance |
| rs374244906 | 2:77,748,834 | C/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.