HMCN2
hemicentin 2
Summary
Predicted to enable axon guidance receptor activity. Predicted to be involved in homophilic cell adhesion via plasma membrane adhesion molecules and synapse organization. Located in collagen-containing extracellular matrix. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs549118533 | 9:133,028,096 | G/T | — | — |
| rs7870070 | 9:133,039,461 | A/T | — | — |
| rs186759152 | 9:133,039,468 | C/A | intergenic variant | — |
| rs138675727 | 9:133,041,757 | G/A | intergenic variant | — |
| rs150947458 | 9:133,048,596 | A/C | — | benign |
| rs140949717 | 9:133,057,898 | C/G | intron variant | — |
| rs555194710 | 9:133,061,568 | G/A | — | likely benign |
| rs1554935048 | 9:133,065,194 | G/C | — | likely benign |
| rs200362767 | 9:133,069,174 | T/C | — | likely benign |
| rs75330437 | 9:133,072,861 | G/T | downstream gene variant | — |
| rs772343403 | 9:133,223,954 | C/T | — | likely benign |
| rs200403870 | 9:133,224,056 | G/A | — | likely benign |
| rs753404073 | 9:133,224,448 | T/C | — | likely benign |
| rs553024377 | 9:133,228,450 | C/G | — | likely benign |
| rs368161226 | 9:133,228,484 | C/T | missense variant | — |
| rs533832066 | 9:133,230,229 | C/T | — | likely benign |
| rs758538948 | 9:133,230,274 | G/A | — | likely benign |
| rs142117460 | 9:133,230,319 | C/T | — | likely benign |
| rs199703083 | 9:133,233,839 | G/C | — | likely benign |
| rs571492167 | 9:133,238,337 | G/A | — | likely benign |
| rs575084282 | 9:133,240,814 | G/A | — | — |
| rs1034226626 | 9:133,243,743 | C/T | — | likely benign |
| rs576559505 | 9:133,257,472 | T/C | — | — |
| rs61734919 | 9:133,260,148 | C/T | — | likely benign |
| rs763936875 | 9:133,260,339 | T/A | — | — |
| rs35565324 | 9:133,261,639 | G/C | — | — |
| rs551741312 | 9:133,266,691 | G/A | — | likely benign |
| rs147050620 | 9:133,268,190 | T/C | intron variant | — |
| rs116972695 | 9:133,270,719 | C/T | — | likely benign |
| rs543084802 | 9:133,271,638 | C/T | — | likely benign |
| rs748735294 | 9:133,278,177 | C/T | — | likely benign |
| rs1029040969 | 9:133,280,269 | C/T | — | likely benign |
| rs112661203 | 9:133,285,969 | G/A | — | likely benign |
| rs368328308 | 9:133,294,224 | C/T | missense variant | — |
| rs529187161 | 9:133,294,306 | G/A | — | likely benign |
| rs147034490 | 9:133,300,194 | C/T | — | likely benign |
| rs748690966 | 9:133,302,752 | G/A | — | likely benign |
| rs2491700018 | 9:133,305,065 | C/T | — | likely benign |
| rs542658004 | 9:133,305,894 | C/T | — | likely benign |
| rs545237452 | 9:133,305,978 | C/T | — | likely benign |
| rs547989442 | 9:133,308,762 | C/T | — | likely benign |
| rs1006615 | 9:133,308,780 | C/A | synonymous variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.