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C15orf39

chromosome 15 open reading frame 39

HCNC Approved Symbol
C15orf39 (HGNC:24497)
Genomic Coordinates
: - (15q24.2)
Synonyms
DKFZP434H132, FLJ46337
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.*1 of the patient has been diagnosed with a variant in another gene.

C15orf39 - Gene browser | 3billion