CLEC4D
C-type lectin domain family 4 member D
Summary
This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region. [provided by RefSeq, Jul 2008]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs570085152 | 12:8,665,069 | C/T | coding sequence variant | — |
| rs4534636 | 12:8,666,801 | T/A | upstream gene variant | — |
| rs4304840 | 12:8,667,897 | A/G | — | benign |
| rs773508170 | 12:8,667,913 | C/A | — | uncertain significance |
| rs1940406668 | 12:8,670,775 | T/C | — | uncertain significance |
| rs199672302 | 12:8,670,808 | A/G | — | uncertain significance |
| rs138087450 | 12:8,670,815 | G/A | — | likely benign |
| rs1157606562 | 12:8,670,835 | G/T | — | uncertain significance |
| rs776374879 | 12:8,670,837 | A/G | — | uncertain significance |
| rs111618025 | 12:8,670,856 | T/C | — | uncertain significance |
| rs1251648957 | 12:8,671,619 | T/G | — | uncertain significance |
| rs768461079 | 12:8,671,665 | C/A | — | uncertain significance |
| rs774176768 | 12:8,671,683 | C/T | — | uncertain significance |
| rs760000016 | 12:8,671,702 | G/C | — | uncertain significance |
| rs376236409 | 12:8,671,748 | G/A | — | uncertain significance |
| rs774598446 | 12:8,672,849 | C/T | — | uncertain significance |
| rs750089630 | 12:8,672,895 | A/G | — | uncertain significance |
| rs200185442 | 12:8,672,916 | C/T | — | likely benign |
| rs557801945 | 12:8,673,163 | G/T | — | — |
| rs775811730 | 12:8,673,728 | A/G | — | uncertain significance |
| rs1037179933 | 12:8,673,729 | T/A | — | uncertain significance |
| rs368418350 | 12:8,673,815 | G/T | — | uncertain significance |
| rs144228025 | 12:8,673,821 | T/C | — | likely benign |
| rs191199396 | 12:8,673,835 | A/G | — | uncertain significance |
| rs73045775 | 12:8,674,905 | T/C | 3 prime UTR variant | — |
| rs181721198 | 12:8,675,933 | T/C | downstream gene variant | — |
| rs191028249 | 12:8,679,786 | G/C | downstream gene variant | — |
| rs12302046 | 12:8,683,721 | A/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.