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CCDC168

coiled-coil domain containing 168

HCNC Approved Symbol
CCDC168 (HGNC:26851)
Genomic Coordinates
: - (13q33.1)
Synonyms
FLJ40176, C13orf40
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 11 patients* with variant(s) predicted to be damaging.*8 of the patients have been diagnosed with a variant in another gene.

CCDC168 - Gene browser | 3billion