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C3orf38

chromosome 3 open reading frame 38

HCNC Approved Symbol
C3orf38 (HGNC:28384)
Genomic Coordinates
: - (3p11.1)
Synonyms
MGC26717
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.

C3orf38 - Gene browser | 3billion