EPN1

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

Epsin-1 is a protein that in humans is encoded by the EPN1 gene.[5][6][7]

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EPN1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesEPN1, epsin 1
External IDsOMIM: 607262; MGI: 1333763; HomoloGene: 32172; GeneCards: EPN1; OMA:EPN1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001130071
NM_001130072
NM_013333
NM_001321263

NM_001252454
NM_010147

RefSeq (protein)

NP_001123543
NP_001123544
NP_001308192
NP_037465

NP_001239383
NP_034277
NP_001359429

Location (UCSC)Chr 19: 55.68 – 55.71 MbChr 7: 5.08 – 5.1 Mb
PubMed search[3][4]
Wikidata
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EPN1 is an endocytic accessory protein that interacts with EPS15 (MIM 600051), the alpha subunit of the clathrin adaptor AP2 (AP2A1; MIM 601026), and clathrin (see MIM 118960), as well as with other accessory proteins for the endocytosis of clathrin-coated vesicles.[supplied by OMIM][7]

Interactions

EPN1 has been shown to interact with REPS2,[6] AP2A2[5] and EPS15.[5]

References

Further reading

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