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C18orf21

chromosome 18 open reading frame 21

HCNC Approved Symbol
C18orf21 (HGNC:28802)
Genomic Coordinates
: - (18q12.2)
Synonyms
PNAS-131, PNAS-124, HsT3108
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.

C18orf21 - Gene browser | 3billion