ABCG5

ABCG5
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	5DO7
Identifiers
Aliases	ABCG5, STSL, ATP binding cassette subfamily G member 5, STSL2
External IDs	OMIM: 605459; MGI: 1351659; HomoloGene: 31909; GeneCards: ABCG5; OMA:ABCG5 - orthologs
Gene location (Human)
Chr.	Chromosome 2 (human)
End	43,838,865 bp
Gene location (Mouse)
Chr.	Chromosome 17 (mouse)
End	84,990,439 bp
RNA expression pattern
	Top expressed in
	jejunal mucosa; ; right lobe of liver; ; duodenum; ; mucosa of ileum; ; gallbladder; ; gonad; ; prefrontal cortex; ; Brodmann area 9; ; islet of Langerhans; ; kidney;
	Top expressed in
	intestinal villus; ; jejunum; ; duodenum; ; ileum; ; epithelium of small intestine; ; crypt of lieberkuhn of small intestine; ; left lobe of liver; ; choroidal fissure; ; Paneth cell; ; left colon;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	nucleotide binding; ATPase activity; protein binding; ATP binding; cholesterol transfer activity; protein heterodimerization activity; ATPase-coupled transmembrane transporter activity; metal ion binding; xenobiotic transmembrane transporter activity;
Cellular component	integral component of membrane; membrane; ATP-binding cassette (ABC) transporter complex; receptor complex; apical part of cell; plasma membrane; integral component of plasma membrane; apical plasma membrane;
Biological process	response to ionizing radiation; excretion; response to nutrient; negative regulation of intestinal phytosterol absorption; intestinal cholesterol absorption; negative regulation of intestinal cholesterol absorption; cholesterol homeostasis; xenobiotic transmembrane transport; lipid transport; cholesterol efflux; transmembrane transport;
	Sources:Amigo / QuickGO
Orthologs
	64240
	27409
	ENSG00000138075
	ENSMUSG00000040505
	Q9H222
	Q99PE8
	NM_022436
	NM_031884
	NP_071881
	NP_114090
	Wikidata
View/Edit Human	View/Edit Mouse

ATP-binding cassette sub-family G member 5 is a protein that in humans is encoded by the ABCG5 gene.