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C10orf88

chromosome 10 open reading frame 88

HCNC Approved Symbol
C10orf88 (HGNC:25822)
Genomic Coordinates
10:122,930,901 - 122,954,227 (10q26.13)
Synonyms
FLJ13490, Em:AC073585.5, PAAT
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.

C10orf88 - Gene browser | 3billion