NPAP1

GENE INFORMATION

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Gene name

NPAP1 (HGNC Symbol)

Synonyms

C15orf2

Description

Nuclear pore associated protein 1 (HGNC Symbol)

Entrez gene 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]

Chromosome

15

Cytoband

q11.2

Chromosome location (bp)

24675868 - 24683393

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000185823 (version 78.38)

Entrez gene

23742

UniProt

Q9NZP6 (UniProt - Evidence at protein level)

neXtProt

NX_Q9NZP6

Antibodypedia

NPAP1 antibodies
 

PROTEIN VIEW

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NPAP1-001
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

NPAP1-001 ENSP00000333735
ENST00000329468
Q9NZP6
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