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C16orf89

chromosome 16 open reading frame 89

HCNC Approved Symbol
C16orf89 (HGNC:28687)
Genomic Coordinates
: - (16p13.3)
Synonyms
MGC45438
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.

C16orf89 - Gene browser | 3billion