Human
NPAP1 - Nuclear Pore Associated Protein 1
Alias:
C15orf2
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]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Models
Reference
NPAP1 Genetics information (+)
GRCh38
Chr : -
Sequence Homology
Selected Gene:
Human：NPAP1
Disease & Mutation
#
Disease
Anatomical Category
Score
Count
Transcripts & Proteins
Table View
Tile View
#
Transcript
Length(nt)
Exon Count
CDS(bp)
Protein
Length(aa)
* This data comes from NCBI.
Gene Expression
Tissue-specific RNA expression
Organ
Expression
Alphabetical
Cell-specific RNA expression
Organ
Expression
Alphabetical
Protein Interaction
Acting
Regulation
Detail
Mechanism
Target
Residues
Reference
Score
Related Models
Type
Name
MGI
Strain of Origin
Publications
Drugs
Name
CAS Number
Status
Phase
Link
References
Title
PMID
Journal
Year
IF
