CLEC18B
C-type lectin domain family 18 member B
Summary
Predicted to enable polysaccharide binding activity. Predicted to be located in Golgi apparatus; endosome; and sarcoplasmic reticulum. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1241712023 | 16:74,442,917 | C/T | — | likely benign |
| rs76072921 | 16:74,442,924 | G/A | — | likely benign |
| rs1200167226 | 16:74,442,938 | T/C | — | uncertain significance |
| rs1342844334 | 16:74,443,489 | T/G | — | uncertain significance |
| rs566819716 | 16:74,444,892 | A/G | — | uncertain significance |
| rs765021041 | 16:74,444,920 | C/A | — | uncertain significance |
| rs150933152 | 16:74,445,632 | C/T | missense variant | — |
| rs762109492 | 16:74,446,076 | C/T | — | uncertain significance |
| rs753379322 | 16:74,446,108 | C/T | — | uncertain significance |
| rs759144388 | 16:74,446,685 | C/T | — | uncertain significance |
| rs777864675 | 16:74,446,739 | T/C | — | uncertain significance |
| rs770433083 | 16:74,446,991 | C/T | — | uncertain significance |
| rs369764401 | 16:74,447,018 | T/C | — | uncertain significance |
| rs772439400 | 16:74,447,556 | T/C | — | uncertain significance |
| rs1178077414 | 16:74,451,974 | A/G | — | uncertain significance |
| rs747577194 | 16:74,451,983 | T/G | — | uncertain significance |
| rs1555503698 | 16:74,451,992 | A/G | — | uncertain significance |
| rs146242972 | 16:74,452,003 | G/A | — | uncertain significance |
| rs376806221 | 16:74,452,004 | C/T | — | uncertain significance |
| rs199857045 | 16:74,452,015 | C/T | — | likely benign |
| rs1474275453 | 16:74,452,094 | C/A | — | uncertain significance |
| rs555823564 | 16:74,452,123 | G/A | — | uncertain significance |
| rs754190860 | 16:74,452,154 | C/T | — | uncertain significance |
| rs1237835795 | 16:74,452,163 | C/T | — | uncertain significance |
| rs1363279226 | 16:74,454,409 | A/G | — | uncertain significance |
| rs1336219782 | 16:74,454,446 | G/A | — | uncertain significance |
| rs1487124880 | 16:74,455,087 | C/T | — | uncertain significance |
| rs375542401 | 16:74,455,109 | G/C | — | likely benign |
| rs756726066 | 16:74,455,150 | A/G | — | uncertain significance |
| rs62056018 | 16:74,455,311 | A/G | regulatory region variant | — |
| rs199895842 | 16:74,456,717 | T/G | — | — |
| rs77199494 | 16:74,458,445 | T/G | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.