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C12orf42

chromosome 12 open reading frame 42

HCNC Approved Symbol
C12orf42 (HGNC:24729)
Genomic Coordinates
: - (12q23.2)
Synonyms
FLJ25323
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 are 3 patients* with variant(s) predicted to be damaging.*2 of the patients have been diagnosed with a variant in another gene.

C12orf42 - Gene browser | 3billion