AP1M1

AP1M1
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	1W63, 4EMZ, 4EN2, 4HMY, 4P6Z
Identifiers
Aliases	AP1M1, AP47, CLAPM2, CLTNM, MU-1A, adaptor related protein complex 1 mu 1 subunit, adaptor related protein complex 1 subunit mu 1, mu1A
External IDs	OMIM: 603535; MGI: 102776; HomoloGene: 4017; GeneCards: AP1M1; OMA:AP1M1 - orthologs
Gene location (Human)
Chr.	Chromosome 19 (human)
End	16,245,906 bp
Gene location (Mouse)
Chr.	Chromosome 8 (mouse)
End	73,011,229 bp
RNA expression pattern
	Top expressed in
	granulocyte; ; right lobe of liver; ; left testis; ; right testis; ; stromal cell of endometrium; ; prefrontal cortex; ; mucosa of ileum; ; monocyte; ; ganglionic eminence; ; right coronary artery;
	Top expressed in
	seminiferous tubule; ; internal carotid artery; ; external carotid artery; ; granulocyte; ; facial motor nucleus; ; endothelial cell of lymphatic vessel; ; neural layer of retina; ; Rostral migratory stream; ; ganglionic eminence; ; vas deferens;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	protein binding;
Cellular component	cytosol; clathrin-coated endocytic vesicle membrane; Golgi apparatus; trans-Golgi network membrane; membrane; Golgi membrane; lysosomal membrane; clathrin-coated vesicle membrane; extracellular exosome; cytoplasmic vesicle membrane; cytoplasmic vesicle; clathrin adaptor complex; plasma membrane; specific granule membrane;
Biological process	antigen processing and presentation of exogenous peptide antigen via MHC class II; mitigation of host defenses by virus; melanosome organization; endosome to melanosome transport; protein transport; intracellular protein transport; vesicle-mediated transport; viral process; neutrophil degranulation; transport;
	Sources:Amigo / QuickGO
Orthologs
	8907
	11767
	ENSG00000072958
	ENSMUSG00000003033
	Q9BXS5
	P35585
	NM_001130524; NM_032493
	NM_007456
	NP_001123996; NP_115882
	NP_031482
	Wikidata
View/Edit Human	View/Edit Mouse

AP-1 complex subunit mu-1 is a protein that in humans is encoded by the AP1M1 gene.