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C16orf92

chromosome 16 open reading frame 92

HCNC Approved Symbol
C16orf92 (HGNC:26346)
Genomic Coordinates
16:30,023,198 - 30,027,736 (16p11.2)
Synonyms
FLJ25404, FIMP
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
There are no patients* with variants predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

C16orf92 - Gene browser | 3billion