Homo sapiens Gene: APOL6
Summary
InnateDB Gene IDBG-281551.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol APOL6
Gene Name apolipoprotein L, 6
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000221963
Encoded Proteins
apolipoprotein L, 6
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary 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. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 22:35648395-35668409
Strand Forward strand
Band q12.3
Transcripts
ENST00000409652 ENSP00000386280
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0008289 lipid binding
Biological Process
GO:0006869 lipid transport
GO:0042157 lipoprotein metabolic process
Cellular Component
GO:0005576 extracellular region
GO:0005737 cytoplasm
Orthologs
Species
Mus musculus
Gene ID
Gene Order
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.257352 Hs.636032
RefSeq NM_030641
HUGO
OMIM
CCDS CCDS13919
HPRD 06266
IMGT
EMBL
GenPept
RNA Seq Atlas