LRCH4
leucine rich repeats and calponin homology domain containing 4
Summary
This gene encodes a protein that contains leucine-rich repeats (LRR) at its amino terminus and that is known to be involved in ligand binding. The carboxyl terminus may act as a membrane anchor. Identified structural elements suggest that the encoded protein resembles a receptor. [provided by RefSeq, Jul 2008]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1448957294 | 7:100,172,734 | G/C | — | uncertain significance |
| rs369773140 | 7:100,172,747 | G/A | — | uncertain significance |
| rs144934792 | 7:100,172,774 | T/C | — | uncertain significance |
| rs780059053 | 7:100,172,791 | A/C | — | uncertain significance |
| rs766041503 | 7:100,172,815 | G/C | — | uncertain significance |
| rs770400987 | 7:100,172,827 | G/A | — | uncertain significance |
| rs369534057 | 7:100,172,845 | C/T | — | uncertain significance |
| rs370810162 | 7:100,172,875 | C/T | — | uncertain significance |
| rs996091876 | 7:100,172,884 | C/T | — | likely benign |
| rs201734399 | 7:100,172,885 | G/A | — | uncertain significance |
| rs1801311287 | 7:100,172,903 | G/A | — | uncertain significance |
| rs745577563 | 7:100,172,904 | A/T | — | uncertain significance |
| rs2485911976 | 7:100,173,502 | G/A | — | uncertain significance |
| rs746804965 | 7:100,173,534 | G/A | — | uncertain significance |
| rs953096811 | 7:100,173,541 | G/T | — | uncertain significance |
| rs1801355071 | 7:100,173,883 | T/A | — | uncertain significance |
| rs759535697 | 7:100,173,910 | C/G | — | uncertain significance |
| rs150672994 | 7:100,174,340 | C/T | — | uncertain significance |
| rs764193242 | 7:100,174,561 | G/A | — | uncertain significance |
| rs148780206 | 7:100,174,700 | G/A | — | benign |
| rs769820187 | 7:100,174,731 | C/T | — | likely benign |
| rs753379286 | 7:100,174,908 | G/A | — | uncertain significance |
| rs765196008 | 7:100,174,912 | C/A | — | uncertain significance |
| rs749358816 | 7:100,174,921 | C/T | — | uncertain significance |
| rs776051139 | 7:100,174,944 | C/T | — | uncertain significance |
| rs764615072 | 7:100,174,950 | C/T | — | uncertain significance |
| rs201757672 | 7:100,174,951 | G/A | — | uncertain significance |
| rs1801410858 | 7:100,175,151 | C/T | — | uncertain significance |
| rs1011724577 | 7:100,175,166 | C/T | — | uncertain significance |
| rs759557651 | 7:100,175,300 | C/T | — | uncertain significance |
| rs200805374 | 7:100,175,335 | G/T | — | uncertain significance |
| rs139516267 | 7:100,175,342 | A/G | — | uncertain significance |
| rs762557450 | 7:100,175,477 | C/T | — | uncertain significance |
| rs1268975152 | 7:100,175,498 | G/A | — | uncertain significance |
| rs2485938138 | 7:100,175,528 | T/C | — | uncertain significance |
| rs776255264 | 7:100,176,076 | C/A | — | uncertain significance |
| rs1801440917 | 7:100,176,134 | C/T | — | likely benign |
| rs762977065 | 7:100,176,317 | C/A | — | uncertain significance |
| rs52833865 | 7:100,176,362 | C/T | — | benign |
| rs1287025294 | 7:100,176,364 | C/T | — | uncertain significance |
| rs149828516 | 7:100,179,411 | G/A | — | uncertain significance |
| rs756995516 | 7:100,179,699 | G/C | — | uncertain significance |
| rs746531511 | 7:100,179,971 | C/T | — | uncertain significance |
| rs377324041 | 7:100,180,059 | C/T | — | uncertain significance |
| rs531092089 | 7:100,182,747 | T/C | — | — |
| rs149959065 | 7:100,183,609 | C/T | — | uncertain significance |
| rs377121985 | 7:100,183,650 | G/C | — | uncertain significance |
| rs1801734761 | 7:100,183,653 | C/T | — | uncertain significance |
| rs1380778082 | 7:100,183,672 | C/T | — | uncertain significance |
| rs1801737415 | 7:100,183,702 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.