Homo sapiens Gene: NPAP1 | |||||||
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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
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Protein Structure |
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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] |
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Gene Information | |||||||
Type | Protein coding | ||||||
Genomic Location | Chromosome 15:24675868-24683393 | ||||||
Strand | Forward strand | ||||||
Band | q11.2 | ||||||
Transcripts |
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Interactions | |||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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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 | ||||||