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C2orf42

chromosome 2 open reading frame 42

HCNC Approved Symbol
C2orf42 (HGNC:26056)
Genomic Coordinates
: - (2p13.3)
Synonyms
FLJ20558
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.