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C22orf31

chromosome 22 open reading frame 31

HCNC Approved Symbol
C22orf31 (HGNC:26931)
Genomic Coordinates
: - (22q12.1)
Synonyms
HS747E2A, bK747E2.1
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.

C22orf31 - Gene browser | 3billion