The C22orf25 gene is located on the long arm (q) of chromosome 22 in region 1, band 1, and sub-band 2 (22q11.21) starting at 20,008,631
base pairs and ending at 20,053,447 base pairs. 22q11.2 deletion syndrome has a vast array of
phenotypes and is not attributed to the loss of a single gene. The vast phenotypes arise from deletions of not only DiGeorge Syndrome Critical Region (DGCR) genes and disease genes but other unidentified genes as well. C22orf25 is in close proximity to DGCR8 as well as other genes known to play a part in DiGeorge Syndrome such as armadillo repeat gene deleted in Velocardiofacial syndrome (
ARVCF), Cathechol-O-methyltransferase (
COMT) and T-box 1 (
TBX1). == Predicted mRNA features ==