IPW gene
imprinted in Prader-Willi syndrome
The information on this page was automatically extracted from online scientific databases.
From NCBI Gene:
This gene is non-protein coding, is expressed exclusively from the paternal allele, and may play a role in the imprinting process. Mutations in this gene are associated with Prader-Willi syndrome. [provided by RefSeq, May 2010]
Related Information
From NCBI Gene:
- Prader-Willi syndrome
Related Information
Cytogenetic Location: 15q11.2, which is the long (q) arm of chromosome 15 at position 11.2
Molecular Location: base pairs 25,116,545 to 25,122,476 on chromosome 15 (Homo sapiens Updated Annotation Release 109.20190905, GRCh38.p13) (NCBI)

Credit: Genome Decoration Page/NCBI
Related Information
- NCRNA00002