AP-2 complex subunit mu

Summary
UniProt ID
Q96CW1
Gene Symbol
AP2M1 CLAPM1 KIAA0109
Gene ID
1173
Organism
Homo sapiens (human)
GlyGen
Q96CW1
PubChem
Q96CW1
The Human Metabolome Database
HMDBP14128
RaftProt
Q96CW1
Re-Glyco
Q96CW1
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
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
Sequence
MIGGLFIYNHKGEVLISRVYRDDIGRNAVDAFRVNVIHARQQVRSPVTNIARTSFFHVKRSNIWLAAVTKQNVNAAMVFEFLYKMCDVMAAYFGKISEENIKNNFVLIYELLDEILDFGYPQNSETGALKTFITQQGIKSQHQTKEEQSQITSQVTGQIGWRREGIKYRRNELFLDVLESVNLLMSPQGQVLSAHVSGRVVMKSYLSGMPECKFGMNDKIVIEKQGKGTADETSKSGKQSIAIDDCTFHQCVRLSKFDSERSISFIPPDGEFELMRYRTTKDIILPFRVIPLVREVGRTKLEVKVVIKSNFKPSLLAQKIEVRIPTPLNTSGVQVICMKGKAKYKASENAIVWKIKRMAGMKESQISAEIELLPTNDKKKWARPPISMNFEVPFAPSGLKVRYLKVFEPKLNYSDHDVIKWVRYIGRSGIYETRC
Glycosylation Sites
Displaying 1 entry
Position Description PubMed ID GlyTouCan ID Source
412
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Disease
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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Last updated: April 6, 2026