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FAM177B

family with sequence similarity 177 member B

HCNC Approved Symbol
FAM177B (HGNC:34395)
Genomic Coordinates
: - (1q41)
Synonyms
RP11-452F19.2, FLJ43505
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 2 patients* with variant(s) predicted to be damaging.*2 of the patients have been diagnosed with a variant in another gene.

FAM177B - Gene browser | 3billion