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MAGI2

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

MAGI2

Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 also known as membrane-associated guanylate kinase inverted 2 (MAGI-2) and atrophin-1-interacting protein 1 (AIP-1) is an enzyme that in humans is encoded by the MAGI2 gene.[5][6][7]

Quick Facts Available structures, PDB ...
MAGI2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesMAGI2, ACVRIP1, AIP-1, AIP1, ARIP1, MAGI-2, SSCAM, membrane associated guanylate kinase, WW and PDZ domain containing 2, NPHS15
External IDsOMIM: 606382; MGI: 1354953; HomoloGene: 8189; GeneCards: MAGI2; OMA:MAGI2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001301128
NM_012301

NM_001170745
NM_001170746
NM_015823

RefSeq (protein)

NP_001288057
NP_036433

NP_001164216
NP_001164217
NP_056638

Location (UCSC)Chr 7: 78.02 – 79.45 MbChr 5: 19.43 – 20.91 Mb
PubMed search[3][4]
Wikidata
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Function

The protein encoded by this gene interacts with atrophin-1. Atrophin-1 contains a polyglutamine repeat, expansion of which is responsible for dentatorubral-pallidoluysian atrophy. This encoded protein is characterized by two WW domains, a guanylate kinase-like domain, and multiple PDZ domains. It has structural similarity to the membrane-associated guanylate kinase homologue (MAGUK) family.[7]

Interactions

MAGI2 has been shown to interact with ATN1[8] and PTEN (gene).

References

Further reading

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