CLEC4F
C-type lectin domain family 4 member F
Summary
Predicted to enable galactose binding activity; glycolipid binding activity; and pattern recognition receptor activity. Predicted to be involved in immune response. Predicted to act upstream of or within NK T cell activation. Predicted to be located in plasma membrane. Predicted to be active in external side of plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2465954385 | 2:71,036,464 | G/A | — | uncertain significance |
| rs1403143830 | 2:71,036,473 | A/G | — | uncertain significance |
| rs567197497 | 2:71,036,481 | C/A | — | uncertain significance |
| rs1553393557 | 2:71,036,483 | T/C | — | uncertain significance |
| rs35001900 | 2:71,036,931 | C/T | — | conflicting classifications of pathogenicity |
| rs2465958068 | 2:71,036,933 | C/G | — | uncertain significance |
| rs782441312 | 2:71,036,953 | A/G | — | uncertain significance |
| rs782211960 | 2:71,036,968 | T/C | — | likely benign |
| rs782399642 | 2:71,036,971 | T/C | — | uncertain significance |
| rs373253086 | 2:71,039,608 | G/T | — | uncertain significance |
| rs200559066 | 2:71,039,655 | T/C | — | uncertain significance |
| rs1275208157 | 2:71,039,703 | C/T | — | uncertain significance |
| rs780710942 | 2:71,040,896 | A/G | — | — |
| rs150215912 | 2:71,042,216 | C/T | upstream gene variant | — |
| rs782797954 | 2:71,043,182 | C/A | — | uncertain significance |
| rs552472152 | 2:71,043,192 | C/T | — | uncertain significance |
| rs368089929 | 2:71,043,308 | G/C | — | uncertain significance |
| rs782375075 | 2:71,043,326 | C/T | — | likely benign |
| rs34318515 | 2:71,043,407 | A/G | — | benign |
| rs1346792062 | 2:71,043,417 | T/C | — | uncertain significance |
| rs782531692 | 2:71,043,777 | T/C | — | uncertain significance |
| rs78458500 | 2:71,043,809 | G/A | — | likely benign |
| rs782778887 | 2:71,043,849 | C/T | — | uncertain significance |
| rs201869143 | 2:71,043,896 | T/C | — | uncertain significance |
| rs782576049 | 2:71,043,915 | A/T | — | uncertain significance |
| rs2466004945 | 2:71,043,960 | C/T | — | uncertain significance |
| rs2466005045 | 2:71,043,976 | C/G | — | uncertain significance |
| rs61754946 | 2:71,044,076 | T/C | — | benign |
| rs782182562 | 2:71,044,119 | T/C | — | uncertain significance |
| rs2466006803 | 2:71,044,131 | C/G | — | uncertain significance |
| rs2466008057 | 2:71,044,221 | C/T | — | likely benign |
| rs2466020781 | 2:71,046,570 | T/G | — | uncertain significance |
| rs147008752 | 2:71,046,913 | C/G | — | uncertain significance |
| rs782745688 | 2:71,046,967 | C/T | — | uncertain significance |
| rs782468764 | 2:71,046,973 | C/T | — | likely benign |
| rs200287098 | 2:71,047,009 | C/T | — | uncertain significance |
| rs375805423 | 2:71,047,628 | T/C | — | uncertain significance |
| rs111692180 | 2:71,047,637 | G/C | — | uncertain significance |
| rs202048172 | 2:71,047,642 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.