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CFAP97D2

CFAP97 domain containing 2

HCNC Approved Symbol
CFAP97D2 (HGNC:53789)
Genomic Coordinates
: - (13q34)
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.
There are no patients* with variants predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

CFAP97D2 - Gene browser | 3billion