Mus musculus Gene: Apoc2
Summary
InnateDB Gene IDBG-151996.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Apoc2
Gene Name apolipoprotein C-II
Synonyms
Species Mus musculus
Ensembl Gene ENSMUSG00000002992
Encoded Proteins
apolipoprotein C-II
apolipoprotein C-II
apolipoprotein C-II
apolipoprotein C-II
apolipoprotein C-II
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000224916:
This gene encodes a lipid-binding protein belonging to the apolipoprotein gene family. The protein is thought to play a role in lipid metabolism. Polymorphisms in this gene may influence circulating lipid levels and may be associated with coronary artery disease risk. This gene is present in a cluster with other related apolipoprotein genes on chromosome 19. Naturally occurring read-through transcription exists between this gene and the neighboring downstream apolipoprotein C-II (APOC2) gene. [provided by RefSeq, Mar 2011] This gene encodes a lipid-binding protein belonging to the apolipoprotein gene family. The protein is secreted in plasma where it is a component of very low density lipoprotein. This protein activates the enzyme lipoprotein lipase, which hydrolyzes triglycerides and thus provides free fatty acids for cells. Mutations in this gene cause hyperlipoproteinemia type IB, characterized by hypertriglyceridemia, xanthomas, and increased risk of pancreatitis and early atherosclerosis. This gene is present in a cluster with other related apolipoprotein genes on chromosome 19. Naturally occurring read-through transcription exists between this gene and the neighboring upstream apolipoprotein C-IV (APOC4) gene. [provided by RefSeq, Mar 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome 7:19671579-19681423
Strand Reverse strand
Band A3
Transcripts
ENSMUST00000003074 ENSMUSP00000003074
ENSMUST00000142352 ENSMUSP00000115173
ENSMUST00000134116 ENSMUSP00000118291
ENSMUST00000150569 ENSMUSP00000114512
ENSMUST00000127648 ENSMUSP00000118305
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 4 interaction(s) predicted by orthology.
Predicted by orthology
Total 4 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0008047 enzyme activator activity
GO:0008289 lipid binding
GO:0016004 phospholipase activator activity
GO:0042803 protein homodimerization activity
GO:0043274 phospholipase binding
GO:0055102 lipase inhibitor activity
GO:0060230 lipoprotein lipase activator activity
Biological Process
GO:0006629 lipid metabolic process
GO:0006869 lipid transport
GO:0010518 positive regulation of phospholipase activity
GO:0010898 positive regulation of triglyceride catabolic process
GO:0010916 negative regulation of very-low-density lipoprotein particle clearance
GO:0016042 lipid catabolic process
GO:0032375 negative regulation of cholesterol transport
GO:0033344 cholesterol efflux
GO:0033700 phospholipid efflux
GO:0034382 chylomicron remnant clearance
GO:0034384 high-density lipoprotein particle clearance
GO:0042493 response to drug
GO:0042953 lipoprotein transport
GO:0043086 negative regulation of catalytic activity
GO:0045723 positive regulation of fatty acid biosynthetic process
GO:0045833 negative regulation of lipid metabolic process
GO:0048261 negative regulation of receptor-mediated endocytosis
GO:0051006 positive regulation of lipoprotein lipase activity
GO:0060697 positive regulation of phospholipid catabolic process
GO:0070328 triglyceride homeostasis
Cellular Component
GO:0005576 extracellular region
GO:0005829 cytosol
GO:0034361 very-low-density lipoprotein particle
GO:0034362 low-density lipoprotein particle
GO:0034363 intermediate-density lipoprotein particle
GO:0034366 spherical high-density lipoprotein particle
GO:0042627 chylomicron
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Disease pathway
Retinoid metabolism and transport pathway
HDL-mediated lipid transport pathway
Metabolism pathway
Metabolism of lipids and lipoproteins pathway
Lipid digestion, mobilization, and transport pathway
Chylomicron-mediated lipid transport pathway
Lipoprotein metabolism pathway
Visual phototransduction pathway
Signal Transduction pathway
Diseases associated with visual transduction pathway
KEGG
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Retinoid metabolism and transport pathway
HDL-mediated lipid transport pathway
Chylomicron-mediated lipid transport pathway
Metabolism of lipids and lipoproteins pathway
Signal Transduction pathway
Diseases associated with visual transduction pathway
Visual phototransduction pathway
Lipoprotein metabolism pathway
Metabolism pathway
Lipid digestion, mobilization, and transport pathway
Disease pathway
Chylomicron-mediated lipid transport pathway
Retinoid metabolism and transport pathway
Lipoprotein metabolism pathway
Visual phototransduction pathway
HDL-mediated lipid transport pathway
Signal Transduction pathway
Diseases associated with visual transduction pathway
Metabolism of lipids and lipoproteins pathway
Metabolism pathway
Disease pathway
Lipid digestion, mobilization, and transport pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt Q05020
TrEMBL D3YXE8 Q3UJG0
UniProt Splice Variant
Entrez Gene 11813
UniGene Mm.483990
RefSeq NM_001277944 NM_009695
OMIM
CCDS CCDS39801
HPRD
IMGT
MGI ID MGI:88054
MGI Symbol Apoc2
EMBL AC149282 AK146468 BC024697 BC106108 CH466639 Z15090 Z22216 Z22217
GenPept AAH24697 AAI06109 BAE27195 CAA78804 CAA80220 EDL23171
RNA Seq Atlas 11813