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C22orf23

chromosome 22 open reading frame 23

HCNC Approved Symbol
C22orf23 (HGNC:18589)
Genomic Coordinates
22:37,943,050 - 37,953,669 (22q13.1)
Synonyms
FLJ32787, EVG1, LOC84645
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.

C22orf23 - Gene browser | 3billion