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C16orf86

chromosome 16 open reading frame 86

HCNC Approved Symbol
C16orf86 (HGNC:33755)
Genomic Coordinates
: - (16q22.1)
Synonyms
FLJ41802
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.

C16orf86 - Gene browser | 3billion