C18orf32 - Gene browser

C18orf32

chromosome 18 open reading frame 32

HCNC Approved Symbol: C18orf32 (HGNC:31690)
Genomic Coordinates: 18:49,477,243 - 49,487,234 (18q21.1)
Synonyms: FLJ23458
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

0Patient

There are no patients diagnosed with a variant in the C18orf32 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results