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FAM171A1

family with sequence similarity 171 member A1

HCNC Approved Symbol
FAM171A1 (HGNC:23522)
Genomic Coordinates
: - (10p13)
Synonyms
FLJ12884, APCN, C10orf38
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 13 patients* with variant(s) predicted to be damaging.*8 of the patients have been diagnosed with a variant in another gene.

FAM171A1 - Gene browser | 3billion