C15orf2
Contents
Annotation
Name
C15orf2
Alias
NA
Disease
Disease: angelman syndrome (PMID:17337158)
Dysfunction type: expression
Description: C15orf2 and a novel noncoding transcript from the Prader-Willi/Angelman syndrome region show monoallelic expression in fetal brain.
Function
Function Mechanism: NA (PMID:17337158)
Biological Process: pathogenic process
Description: NA
