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C22orf15

chromosome 22 open reading frame 15

HCNC Approved Symbol
C22orf15 (HGNC:15558)
Genomic Coordinates
: - (22q11.23)
Synonyms
FLJ36561, N27C7-3
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 is 1 patient* with variant(s) predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

C22orf15 - Gene browser | 3billion