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FAM162A

family with sequence similarity 162 member A

HCNC Approved Symbol
FAM162A (HGNC:17865)
Genomic Coordinates
3:122,384,182 - 122,412,334 (3q21.1)
Synonyms
E2IG5, HGTD-P, C3orf28
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 is 1 patient* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.