APOL6

APOL6
Identifiers
Aliases	APOL6, APOL-VI, APOLVI, apolipoprotein L6
External IDs	OMIM: 607256; MGI: 1919189; HomoloGene: 49940; GeneCards: APOL6; OMA:APOL6 - orthologs
Gene location (Human)
Chr.	Chromosome 22 (human)
End	35,668,404 bp
Gene location (Mouse)
Chr.	Chromosome 15 (mouse)
End	76,941,306 bp
RNA expression pattern
	Top expressed in
	pericardium; ; pylorus; ; sperm; ; buccal mucosa cell; ; monocyte; ; epithelium of colon; ; epithelium of nasopharynx; ; human penis; ; vena cava; ; cardia;
	Top expressed in
	white adipose tissue; ; subcutaneous adipose tissue; ; soleus muscle; ; brown adipose tissue; ; muscle of thigh; ; mammary gland; ; zygote; ; skeletal muscle tissue; ; intercostal muscle; ; thoracic diaphragm;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	lipid binding;
Cellular component	extracellular region; cytoplasm;
Biological process	lipoprotein metabolic process; lipid transport;
	Sources:Amigo / QuickGO
Orthologs
	80830
	71939
	ENSG00000221963
	ENSMUSG00000033576
	Q9BWW8
	n/a
	NM_030641
	NM_001163621; NM_028010
	NP_085144
	n/a
	Wikidata
View/Edit Human	View/Edit Mouse

Apolipoprotein L6 is a protein that in humans is encoded by the APOL6 gene.

This gene is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles.