LRRC4C
leucine rich repeat containing 4C
Summary
NGL1 is a specific binding partner for netrin G1 (NTNG1; MIM 608818), which is a member of the netrin family of axon guidance molecules (Lin et al., 2003 [PubMed 14595443]).[supplied by OMIM, Mar 2008]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs565418856 | 11:40,136,033 | G/A | — | uncertain significance |
| rs369448332 | 11:40,136,072 | C/T | — | uncertain significance |
| rs143371171 | 11:40,136,111 | C/T | — | uncertain significance |
| rs201412968 | 11:40,136,116 | G/A | — | uncertain significance |
| rs142620688 | 11:40,136,163 | G/A | — | likely benign |
| rs762086751 | 11:40,136,396 | C/T | — | uncertain significance |
| rs1855301305 | 11:40,136,405 | G/A | — | uncertain significance |
| rs1237120953 | 11:40,136,425 | T/A | — | uncertain significance |
| rs202214030 | 11:40,136,506 | G/A | — | uncertain significance |
| rs372777321 | 11:40,136,614 | G/A | — | uncertain significance |
| rs763416398 | 11:40,136,638 | C/T | — | uncertain significance |
| rs752236880 | 11:40,136,650 | G/A | — | uncertain significance |
| rs560815816 | 11:40,136,752 | T/C | — | uncertain significance |
| rs202082491 | 11:40,136,878 | G/A | — | uncertain significance |
| rs1855356004 | 11:40,136,970 | A/T | — | uncertain significance |
| rs769415358 | 11:40,136,980 | G/A | — | uncertain significance |
| rs1167879704 | 11:40,137,020 | C/T | — | uncertain significance |
| rs760514279 | 11:40,137,064 | C/T | — | uncertain significance |
| rs1314592573 | 11:40,137,077 | G/T | — | uncertain significance |
| rs373740831 | 11:40,137,113 | G/A | — | uncertain significance |
| rs190972515 | 11:40,137,145 | G/A | — | uncertain significance |
| rs769728836 | 11:40,137,167 | G/T | — | uncertain significance |
| rs1855386979 | 11:40,137,349 | G/A | — | uncertain significance |
| rs1855388780 | 11:40,137,369 | G/T | — | uncertain significance |
| rs183119791 | 11:40,137,428 | T/C | — | uncertain significance |
| rs1855393098 | 11:40,137,439 | C/T | — | uncertain significance |
| rs745329871 | 11:40,137,623 | T/C | — | uncertain significance |
| rs201688769 | 11:40,137,741 | T/A | — | uncertain significance |
| rs144974170 | 11:40,137,835 | T/G | — | likely benign |
| rs114169058 | 11:40,210,371 | A/T | — | — |
| rs140691861 | 11:40,264,616 | T/C | intron variant | — |
| rs10742539 | 11:40,358,180 | C/T | intron variant | — |
| rs6485210 | 11:40,664,224 | T/C | intron variant | — |
| rs189511601 | 11:40,770,036 | A/G | intron variant | — |
| rs4611189 | 11:40,837,713 | G/A | intron variant | — |
| rs78015633 | 11:40,876,586 | T/C | intron variant | — |
| rs11511923 | 11:41,090,930 | C/T | intron variant | — |
| rs2862035 | 11:41,225,433 | C/A | — | — |
| rs980952 | 11:41,225,954 | T/G | intron variant | — |
| rs2939756 | 11:41,436,297 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.