adaptor related protein complex 2 subunit mu 1

Summary
Gene Symbol
  • AP2M1
Organism
Homo sapiens (human)
NCBI Gene
1173
PubChem
1173
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Cell membrane
  • Coated pit
  • Disease variant
  • Endocytosis
  • Epilepsy
  • Intellectual disability
  • Lipid-binding
  • Phosphoprotein
  • Protein transport
  • Proteomics identification
  • Reference proteome
Proteins
Displaying all 3 entries
UniProt Protein Name
Q96CW1
  • AP-2 mu chain
  • Adaptin-mu2
  • Adaptor protein complex AP-2 subunit mu
  • Adaptor-related protein complex 2 subunit mu
  • Clathrin assembly protein complex 2 mu medium chain
  • Clathrin coat assembly protein AP50
  • Clathrin coat-associated protein AP50
  • HA2 50 kDa subunit
  • Plasma membrane adaptor AP-2 50 kDa protein
E9PFW3
B4DNB9
  • AP-2 mu chain
  • Clathrin assembly protein complex 2 mu medium chain
  • Clathrin coat assembly protein AP50
  • Clathrin coat-associated protein AP50
  • Plasma membrane adaptor AP-2 50 kDa protein
Gene Ontology (GO)
GO Hierarchy
Displaying entries 1 - 5 of 20 in total
GO Term Evidence Code PMID
lysosomal membrane
cytosol
plasma membrane
plasma membrane
clathrin-coated pit
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
complex, subunit
Functional Category
  • E: Amino acid transport and metabolism
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0060307 autosomal dominant intellectual developmental disorder

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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