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 |
---|---|---|---|---|---|
OMIM IDMIM:610922 Ensembl IDEnsembl:ENSG00000185823 HGNC IDHGNC:HGNC:1190 PHARMGKB IDPA25519 Map Location15q11.2 |
Gene Categories:
TRANSPORTERGO 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 |
Gene expression in normal tissue: NPAP1
Gene-model tissue-cancer distribution: Bubble Plot
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
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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No matching records found |