Homo sapiens Gene: NPAP1
Summary
InnateDB Gene IDBG-4183.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol NPAP1
Gene Name nuclear pore associated protein 1
Synonyms C15orf2
Species Homo sapiens
Ensembl Gene ENSG00000185823
Encoded Proteins
chromosome 15 open reading frame 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
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]
Gene Information
Type Protein coding
Genomic Location Chromosome 15:24675868-24683393
Strand Forward strand
Band q11.2
Transcripts
ENST00000329468 ENSP00000333735
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
Biological Process
GO:0007275 multicellular organismal development
GO:0007283 spermatogenesis
GO:0030154 cell differentiation
Cellular Component
GO:0005637 nuclear inner membrane
GO:0005654 nucleoplasm
GO:0070062 extracellular vesicular exosome
Orthologs
No orthologs found for this gene
Cross-References
SwissProt Q9NZP6
TrEMBL
UniProt Splice Variant
Entrez Gene 23742
UniGene Hs.649663
RefSeq NM_018958
HUGO HGNC:1190
OMIM 610922
CCDS CCDS10015
HPRD
IMGT
EMBL AC100720 AF179681
GenPept AAF72107
RNA Seq Atlas 23742