NPAP1


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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Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
Map Location

Gene Categories:

TRANSPORTER

GO terms in NPAP1


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Term Type
Evidence Type
GO Term ID
GO Des.
MF ND GO:0003674 molecular_function
MF IBA GO:0008139 nuclear localization sequence binding
MF IBA GO:0017056 structural constituent of nuclear pore
CC IEA GO:0005637 nuclear inner membrane
CC IBA GO:0005643 nuclear pore
CC IEA GO:0005654 nucleoplasm
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Gene expression in normal tissue: NPAP1

Gene-model tissue-cancer distribution: Bubble Plot

undefinetissue: undefine cancer: undefined model num: 0undefinedtissue: undefined cancer: ADENOCARCINOMA model num: 10undefinedtissue: undefined cancer: PANCAN model num: 52undefinedtissue: undefined cancer: NON_SMALL_CELL_CARCINOMA model num: 5LUNtissue: LUN cancer: LUNG model num: 0LUNGtissue: LUNG cancer: undefined model num: 30BOWEtissue: BOWE cancer: BOWEL model num: 0BOWELtissue: BOWEL cancer: undefined model num: 2

Gene-drug pathway distribution

Pathways in NPAP1


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Database
Pathway ID
Pathway Des.
wikipathways WP3998 Prader-Willi and Angelman Syndrome
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD562 Navitoclax 4
iGMDRD441 TW 37 2
iGMDRD52 Rotenone 2
iGMDRD138 PX 12 3
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in NPAP1

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
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