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C13orf42

chromosome 13 open reading frame 42

HCNC Approved Symbol
C13orf42 (HGNC:42693)
Genomic Coordinates
: - (13q14.3)
Synonyms
LINC00371
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.

C13orf42 - Gene browser | 3billion