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C17orf113

chromosome 17 open reading frame 113

HCNC Approved Symbol
C17orf113 (HGNC:53437)
Genomic Coordinates
: - (17q21.2)
Synonyms
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.*2 of the patients have been diagnosed with a variant in another gene.

C17orf113 - Gene browser | 3billion