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FAM117B

family with sequence similarity 117 member B

HCNC Approved Symbol
FAM117B (HGNC:14440)
Genomic Coordinates
: - (2q33.2)
Synonyms
FLJ38771, ALS2CR13
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.* None of the patients have been diagnosed with a variant in another gene.

FAM117B - Gene browser | 3billion