TIMD4
T cell immunoglobulin and mucin domain containing 4
Summary
Predicted to enable phosphatidylserine binding activity. Predicted to be involved in apoptotic cell clearance and cytoskeletal rearrangement involved in phagocytosis, engulfment. Predicted to be located in extracellular region and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7731575 | 5:156,346,512 | C/T | — | benign |
| rs1225994470 | 5:156,347,506 | T/C | — | uncertain significance |
| rs763351424 | 5:156,349,125 | C/A | — | uncertain significance |
| rs779642915 | 5:156,349,172 | A/G | — | uncertain significance |
| rs7700944 | 5:156,366,181 | G/A | intron variant | — |
| rs74531909 | 5:156,369,474 | C/T | intron variant | — |
| rs10475851 | 5:156,370,404 | T/A | — | — |
| rs111394708 | 5:156,372,584 | A/G | intron variant | — |
| rs28581508 | 5:156,374,014 | A/C | intron variant | — |
| rs768395434 | 5:156,376,665 | T/G | — | uncertain significance |
| rs537749572 | 5:156,377,832 | G/C | — | — |
| rs2479985035 | 5:156,378,528 | G/T | — | uncertain significance |
| rs146696975 | 5:156,378,585 | G/A | — | uncertain significance |
| rs191810286 | 5:156,378,624 | G/A | — | uncertain significance |
| rs184214058 | 5:156,378,646 | T/C | — | uncertain significance |
| rs61744066 | 5:156,378,666 | G/A | — | benign |
| rs55920848 | 5:156,378,688 | C/T | — | benign |
| rs61743250 | 5:156,378,693 | G/T | — | benign |
| rs199980573 | 5:156,378,729 | C/T | — | uncertain significance |
| rs1384302006 | 5:156,378,747 | G/C | — | uncertain significance |
| rs753614328 | 5:156,378,762 | C/T | — | uncertain significance |
| rs373429027 | 5:156,378,789 | G/A | — | uncertain significance |
| rs10475859 | 5:156,379,053 | C/T | intron variant | — |
| rs141557472 | 5:156,381,444 | G/T | — | uncertain significance |
| rs767048599 | 5:156,381,557 | A/C | — | uncertain significance |
| rs1257003344 | 5:156,381,609 | C/T | — | uncertain significance |
| rs762338504 | 5:156,381,654 | G/C | — | uncertain significance |
| rs2479994995 | 5:156,381,657 | C/G | — | uncertain significance |
| rs1007738482 | 5:156,381,722 | C/T | — | uncertain significance |
| rs2862059 | 5:156,384,515 | G/C | intron variant | — |
| rs6873413 | 5:156,385,708 | C/T | intron variant | — |
| rs191283819 | 5:156,389,582 | C/T | intron variant | — |
| rs6882076 | 5:156,390,297 | T/C | upstream gene variant | — |
| rs4704826 | 5:156,392,082 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.