Homo sapiens Gene: APOL5
Summary
InnateDB Gene IDBG-5559.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol APOL5
Gene Name apolipoprotein L, 5
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000128313
Encoded Proteins
apolipoprotein L, 5
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 22:35717872-35729483
Strand Forward strand
Band q12.3
Transcripts
ENST00000249044 ENSP00000249044
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0008035 high-density lipoprotein particle binding
GO:0008289 lipid binding
Biological Process
GO:0006629 lipid metabolic process
GO:0006869 lipid transport
GO:0042157 lipoprotein metabolic process
Cellular Component
GO:0005575 cellular_component
GO:0005576 extracellular region
GO:0005737 cytoplasm
Orthologs
No orthologs found for this gene
Cross-References
SwissProt Q9BWW9
TrEMBL
UniProt Splice Variant
Entrez Gene 80831
UniGene Hs.326561
RefSeq NM_030642
HUGO HGNC:14869
OMIM 607255
CCDS CCDS13920
HPRD
IMGT
EMBL AL049748 AY014878
GenPept AAK07723
RNA Seq Atlas 80831