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C21orf58

chromosome 21 open reading frame 58

HCNC Approved Symbol
C21orf58 (HGNC:1300)
Genomic Coordinates
: - (21q22.3)
Synonyms
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 is 1 patient* with variant(s) predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

C21orf58 - Gene browser | 3billion