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CC2D1B

coiled-coil and C2 domain containing 1B

HCNC Approved Symbol
CC2D1B (HGNC:29386)
Genomic Coordinates
: - (1p32.3)
Synonyms
KIAA1836, Freud-2, Lgd1
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 3 patients* with variant(s) predicted to be damaging.*2 of the patients have been diagnosed with a variant in another gene.

CC2D1B - Gene browser | 3billion