From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
Apolipoprotein L6 is a protein that in humans is encoded by the APOL6 gene .[ 5] [ 6] [ 7]
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 .[ 7]
^ a b c GRCh38: Ensembl release 89: ENSG00000221963 – Ensembl , May 2017
^ a b c GRCm38: Ensembl release 89: ENSMUSG00000033576 – Ensembl , May 2017
^ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ Page NM, Butlin DJ, Lomthaisong K, Lowry PJ (May 2001). "The human apolipoprotein L gene cluster: identification, classification, and sites of distribution". Genomics . 74 (1): 71–8. doi :10.1006/geno.2001.6534 . PMID 11374903 .
^ Liu Z, Lu H, Jiang Z, Pastuszyn A, Hu CA (Jan 2005). "Apolipoprotein l6, a novel proapoptotic Bcl-2 homology 3-only protein, induces mitochondria-mediated apoptosis in cancer cells" . Mol Cancer Res . 3 (1): 21–31. doi :10.1158/1541-7786.21.3.1 . PMID 15671246 . S2CID 2545675 .
^ a b "Entrez Gene: APOL6 apolipoprotein L, 6" .
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