APOL6

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Apolipoprotein L6 is a protein that in humans is encoded by the APOL6 gene.[5][6][7]

AliasesAPOL6, APOL-VI, APOLVI, apolipoprotein L6
End35,668,404 bp[1]
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APOL6
Identifiers
AliasesAPOL6, APOL-VI, APOLVI, apolipoprotein L6
External IDsOMIM: 607256; MGI: 1919189; HomoloGene: 49940; GeneCards: APOL6; OMA:APOL6 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_030641

NM_001163621
NM_028010

RefSeq (protein)

NP_085144

n/a

Location (UCSC)Chr 22: 35.65 – 35.67 MbChr 15: 76.93 – 76.94 Mb
PubMed search[3][4]
Wikidata
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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]

References

Further reading

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