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General Information



Gene_Symbol Gene_ID Gene_Name Chromosome Alias
APOE 348 Apolipoprotein E  19AD2; LPG; LDLCQ5 







  • Evidence
  • Gene
  • mRNA
  • CDS
  • Protein
  • PTM
  • Enzyme
  • PPi
  • Pathway
  • Structural
  • Domain
  • Ontology
  • SNP
  • Drug
  • External Links



Evidence Information


Pubmed ID Year Sample Information Techniques Mechanism Fold Change Remark
15817610   2005Cell line : -

Source : Kaiser Permanente Medical Care Program of Northern California (KPMCP), the state of Utah, and the Twin City metropolitan area of Minnesota.

Sample Type : Population based case-control study

No. of Sample : Colon cancer (1556 cases and 1948 controls) and rectal cancer (777 cases and 988 controls)

Stage : -

GenotypingMutation-ApoE genotypes that do not include the e3 allele, the same genotypes that are associated with increased risk of coronary heart disease, may influence development of colon cancer among those who are older at diagnosis.

22799385   2012Cell line : -

Source : Department of Gastrointestinal Surgery, Guangdong Provincial People Hospital.

Sample Type : CRC tumor and Normal tissue

No. of Sample : 13

Stage : -

2-D Gelelectrophoresis and MALDI-TOF mass spectrometry.Up-regulation-This Gene differentially expressed and analysed by 2-D Gel Electrophoresis.


Gene Details



Chromosome: 19; NC_000019.9 (45409039..45412650)

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Gene Type protein coding
Gene Family Apolipoproteins
Description Chylomicron remnants and very low density lipoprotein (VLDL) remnants are rapidly removed from the circulation by receptor-mediated endocytosis in the liver. Apolipoprotein E, a main apoprotein of the chylomicron, binds to a specific receptor on liver cells and peripheral cells. ApoE is essential for the normal catabolism of triglyceride-rich lipoprotein constituents. The APOE gene is mapped to chromosome 19 in a cluster with APOC1 and APOC2. Defects in apolipoprotein E result in familial dysbetalipoproteinemia, or type III hyperlipoproteinemia (HLP III), in which increased plasma cholesterol and triglycerides are the consequence of impaired clearance of chylomicron and VLDL remnants. [provided by RefSeq, Jul 2008]  
Chromosome 19
Location 19q13.2
Start 44905749  
End 44909395  
Strand +  
Gene Sequence

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Length 3647  
OMIM ID 107741   
HGNC ID HGNC:613   
Unigene ID Hs.654439    
Ensembl ID ENSG00000130203   
PharmGKB ID PA55   

mRNA Information


mRNA ID NM_001302688.1
Exon join(1..175,854..919,2012..2204,2785..3647)  
mRNA Sequence

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Length 1223  



CDS Information


   
Locationjoin(121..175,854..919,2012..2204,2785..3502)
CDS Sequence

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CCDS ID -



Protein Information


      
Protein IDNP_000032.1
Protein NameApolipoprotein E
Molecular Wt. (Da)34237
Protein Sequence

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Length 317  
Uniprot IDQ99541
Ensembl Protein ID ENSP00000276914  



Post-translational Modification Information (Source : HPRD)


Residue Type site
TGlycosylation212
LProteolytic Cleavage286
MProteolytic Cleavage290
KGlycation93
SPhosphorylation147
SPhosphorylation241

Enzyme Information


No matching records could be found.

PPi Information


(Click to view network : Source STRING)      View   

                                                                           
Interactant Gene ID (Source: HPRD) Gene Symbol HPRD ID Ref Seq ID Technique References
2A2M72NP_000005.2in vitro;in vivo9831625   
213ALB62NP_000468.1in vitro8063017   
351APP100NP_000475.1in vitro10559559   
1270CNTF347NP_000605.1in vitro9236223   
4137MAPT1142NP_001116538.1in vitro;in vivo914   740   875   666   529   000   000   


Pathway Information


      
Pathway Name Pathway ID
Alzheimer's disease hsa05010


Structure Information


No matching records could be found.

Domain Information




ID Location Description
pfam01442104-299  Apolipoprotein
pfam0144261-186  Apolipoprotein
pfam1212865-278  DUF3584


Ontology Information


   
HPRD ID57
Molecular ClassTransport/cargo protein
Molecular FunctionLipid transporter activity (GO:0005319)
Biological ProcessLipid storage (GO:0019915); Lipid transport (GO:0006869)  



SNP Information


View SNP Geneview Report   

Drug Information


Uniprot ID DrugBank ID Name Type
P02649DB00062Human Serum AlbuminBiotechDrug
P02649DB00064Serum albumin iodonatedBiotechDrug

External Links


                                 
ArrayExpressGO
ICGCGO
Cancer3DGO
COSMICGO
NCGGO
TSGeneGO
Tumor Gene Family of DatabasesGO
CCDBGO
G2SBCGO
Osteosarcoma DatabaseGO
RCDBGO