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CLEC12B

C-type lectin domain family 12 member B

HCNC Approved Symbol
CLEC12B (HGNC:31966)
Genomic Coordinates
12:10,006,209 - 10,018,800 (12p13.2)
Synonyms
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there are 8 patients* with variant(s) predicted to be damaging.*5 of the patients have been diagnosed with a variant in another gene.

CLEC12B - Gene browser | 3billion