NOS1AP

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Nitric oxide synthase 1 adaptor protein (NOS1AP) also known as carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein (CAPON) is a protein that in humans is encoded by the NOS1AP gene.[3][4][5]

AliasesNOS1AP, 6330408P19Rik, CAPON, nitric oxide synthase 1 adaptor protein, NPHS22
End162,370,475 bp[1]
Quick facts Identifiers, Aliases ...
NOS1AP
Identifiers
AliasesNOS1AP, 6330408P19Rik, CAPON, nitric oxide synthase 1 adaptor protein, NPHS22
External IDsOMIM: 605551; HomoloGene: 136252; GeneCards: NOS1AP; OMA:NOS1AP - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_014697
NM_001126060
NM_001164757

n/a

RefSeq (protein)

NP_001119532
NP_001158229
NP_055512

n/a

Location (UCSC)Chr 1: 162.07 – 162.37 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human
Close

This gene encodes a cytosolic protein that binds to the signaling molecule, neuronal nitric oxide synthase (nNOS). This protein has a C-terminal PDZ-binding domain that mediates interactions with nNOS and an N-terminal phosphotyrosine binding (PTB) domain that binds to the small monomeric G protein, Dexras1. Studies of the related mouse and rat proteins have shown that this protein functions as an adapter protein linking nNOS to specific targets, such as Dexras1 and the synapsins.[5] NOS1AP polymorphisms has been associated with the QT interval length.[6]

Interactions

NOS1AP has been shown to interact with:

References

Further reading

Related Articles

Wikiwand AI