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C1orf167

chromosome 1 open reading frame 167

HCNC Approved Symbol
C1orf167 (HGNC:25262)
Genomic Coordinates
: - (1p36.22)
Synonyms
DKFZp434E1410, RP11-56N19.2
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 5 patients* with variant(s) predicted to be damaging.*2 of the patients have been diagnosed with a variant in another gene.

C1orf167 - Gene browser | 3billion