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FAM193A

family with sequence similarity 193 member A

HCNC Approved Symbol
FAM193A (HGNC:16822)
Genomic Coordinates
4:2,535,375 - 2,732,573 (4p16.3)
Synonyms
RES4-22, C4orf8
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 8 patients* with variant(s) predicted to be damaging.*3 of the patients have been diagnosed with a variant in another gene.

FAM193A - Gene browser | 3billion