IPW gene

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]

From NCBI Gene:

• Prader-Willi syndrome

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 109.20191205, GRCh38.p13) (NCBI)

• NCRNA00002