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C21orf91

chromosome 21 open reading frame 91

HCNC Approved Symbol
C21orf91 (HGNC:16459)
Genomic Coordinates
: - (21q21.1)
Synonyms
YG81, EURL, CSSG1, BTG3-7:1, C21orf38, C21orf14
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.

C21orf91 - Gene browser | 3billion