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NPAP1

Official Full Name
nuclear pore associated protein 1
Organism
Homo sapiens
GeneID
23742
Background
This intronless retrogene is located in the Prader-Willi syndrome region on chromosome 15. This gene exhibits tissue-specific imprinting. Expression in adult testis and brain is biallelic, while expression in fetal brain is monoallelic and only from the paternal chromosome. The encoded protein is associated with the nuclear pore complex. [provided by RefSeq, Mar 2021]
Synonyms
C15orf2;

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