Skip to Content
Merck
CN

NPAP1

nuclear pore associated protein 1

Synonyms:
C15orf2
Species:
UniProtKB ID:
Gene ID:
  • Human(23742) Summary: This gene is located in the Prader-Willi syndrome region on chromosome 15. This gene is biallelically expressed in adult testis and brain but is paternally imprinted in fetal brain. Defects in this gene may be associated with Prader-Willi syndrome. [provided by RefSeq, Aug 2012]

Custom & Knockdown Gene Products

esiRNA

Product Number
Description
Species
MISSION® esiRNA, targeting human NPAP1,
Species
human