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C1orf122

chromosome 1 open reading frame 122

HCNC Approved Symbol
C1orf122 (HGNC:24789)
Genomic Coordinates
: - (1p34.3)
Synonyms
FLJ45459
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.

C1orf122 - Gene browser | 3billion