CLEC3B Chromosome 3

C-type lectin domain family 3 member B
1 variant 1 Health Risk

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What This Gene Does
Enables calcium ion binding activity; heparin binding activity; and kringle domain binding activity. Involved in bone mineralization. Located in cytoplasm; extracellular space; and granular component. Implicated in osteoarthritis and retinal macular dystrophy 4. [provided by Alliance of Genome Resources, Jul 2025]
Gene Info
Gene Group
C-type lectin domain containing
Locus Type
gene with protein product
Location
3p21.31
Ensembl
ENSG00000163815
Associated Conditions (3)
Macular dystrophy
retinal
4
Key Variants
All Variants (1)
RSID Category Clinical Significance Conditions
RS2530665810 Health Risk Pathogenic Macular dystrophy, retinal, 4
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