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FAM47B

family with sequence similarity 47 member B

HCNC Approved Symbol
FAM47B (HGNC:26659)
Genomic Coordinates
: - (Xp21.1)
Synonyms
FLJ35782
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 9 patients* with variant(s) predicted to be damaging.*4 of the patients have been diagnosed with a variant in another gene.

FAM47B - Gene browser | 3billion