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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

LPA Gene

protein-coding   GIFtS: 62
GCID: GC06M160952

lipoprotein, Lp(a)


(Previous symbol: LP)
 Explore 104 diseases affiliated with
LPA via our new
 Human Malady Compendium 
Biological research products
for LPA
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Aliases
Lipoprotein, Lp(A)1 2     Lp(A)1
LP1 2     Apo(A)1
AK382     EC 3.4.21.-3
APOA2     Lp(A)1
Antiangiogenic AK38 Protein2     EC 3.4.218
Apo(A)1     EC 3.4.21.78
Apolipoprotein(A)1     

External Ids:    HGNC: 66671   Entrez Gene: 40182   Ensembl: ENSG000001986707   OMIM: 1522005   UniProtKB: P085193   

Export aliases for LPA gene to outside databases

Previous GC identifers: GC06U990074 GC06M160826 GC06M160707 GC06M160861 GC06M160844 GC06M160872 GC06M158427


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for LPA:
The protein encoded by this gene is a serine proteinase that inhibits the activity of tissue-type plasminogen activator
I. The encoded protein constitutes a substantial portion of lipoprotein(a) and is proteolytically cleaved, resulting
in fragments that attach to atherosclerotic lesions and promote thrombogenesis. Elevated plasma levels of this protein
are linked to atherosclerosis. Depending on the individual, the encoded protein contains 2-43 copies of kringle-type
domains. The allele represented here contains 15 copies of the kringle-type repeats and corresponds to that found in
the reference genome sequence. (provided by RefSeq, Dec 2009)

UniProtKB/Swiss-Prot: APOA_HUMAN, P08519
Function: Apo(a) is the main constituent of lipoprotein(a) (Lp(a)). It has serine proteinase activity and is able of
autoproteolysis. Inhibits tissue-type plasminogen activator 1. Lp(a) may be a ligand for megalin/Gp 330

Gene Wiki entry for LPA (Lipoprotein(a))


(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000006.11  NC_018917.1  NT_025741.15  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the LPA gene promoter:
         CREB   PPAR-gamma1   ATF-2   deltaCREB   c-Jun   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmids (see all 2): LPA promoter sequence
   Search SABiosciences Chromatin IP Primers for LPA

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat LPA


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 6q26   Ensembl cytogenetic band:  6q26   HGNC cytogenetic band: 6q25-q26

LPA Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
LPA gene location

GeneLoc information about chromosome 6         GeneLoc Exon Structure

GeneLoc location for GC06M160952:  view genomic region     (about GC identifiers)

Start:
160,952,515 bp from pter      End:
161,087,407 bp from pter
Size:
134,893 bases      Orientation:
minus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: APOA_HUMAN, P08519 (See protein sequence)
Recommended Name: Apolipoprotein(a) precursor  
Size: 4548 amino acids; 501319 Da
Subunit: Disulfide-linked to apo-B100. Binds to fibronectin and decorin
Miscellaneous: Apo(a) is known to be proteolytically cleaved, leading to the formation of the so-called mini-Lp(a).
Apo(a) fragments accumulate in atherosclerotic lesions, where they may promote thrombogenesis. O-glycosylation may
limit the extent of proteolytic fragmentation. Homology with plasminogen kringles IV and V is thought to underlie the
atherogenicity of the protein, because the fragments are competing with plasminogen for fibrin(ogen) binding
6 PDB 3D structures from and Proteopedia for LPA:
1I71 (3D)        1JFN (3D)        1KIV (3D)        2FEB (3D)        3KIV (3D)        4KIV (3D)    
Secondary accessions: Q5VTD7 Q9UD88

Explore the universe of human proteins at neXtProt for LPA: NX_P08519

Post-translational modifications:

  • N- and O-glycosylated. The N-glycans are complex biantennary structures present in either a mono- or disialylated
  • state. The O-glycans are mostly (80%) represented by the monosialylated core type I structure,
    NeuNAcalpha2-3Galbeta1-3GalNAc, with smaller amounts of disialylated and non-sialylated O-glycans also detected1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_P08519

  • 4/36 DME Specific Peptides for LPA (P08519) (see all 36)
     KLFDYCD  CYITGWG  PHWHQRT  CRNPDGD 

    LPA Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_005568.2  
    ENSEMBL proteins: 
     ENSP00000321334   ENSP00000395608  
    Reactome Protein details: P08519
    Human Recombinant Protein Products: 
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    Browse Proteins at Uscn

    Gene Ontology (GO): 2 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005576extracellular region TAS--
    GO:0034358plasma lipoprotein particle IDA2531657


    LPA for ontologies           About GeneDecksing



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    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section

    LPA for domains           About GeneDecksing

    5/7 InterPro domains/families (see all 7):
     IPR001314 Peptidase_S1A
     IPR018056 Kringle_CS
     IPR001254 Peptidase_S1
     IPR018114 Peptidase_S1_AS
     IPR000001 Kringle

    Graphical View of Domain Structure for InterPro Entry P08519

    ProtoNet protein and cluster: P08519

    3 Blocks protein families:
    IPB000001 Kringle
    IPB001254 Serine protease
    IPB001314 Chymotrypsin serine protease family (S1) signature


    UniProtKB/Swiss-Prot: APOA_HUMAN, P08519
    Similarity: Belongs to the peptidase S1 family. Plasminogen subfamily
    Similarity: Contains 38 kringle domains
    Similarity: Contains 1 peptidase S1 domain


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Function Summary:

         UniProtKB/Swiss-Prot: APOA_HUMAN, P08519
    Function: Apo(a) is the main constituent of lipoprotein(a) (Lp(a)). It has serine proteinase activity and is able of
    autoproteolysis. Inhibits tissue-type plasminogen activator 1. Lp(a) may be a ligand for megalin/Gp 330

         Genatlas biochemistry entry for LPA:
    lipoprotein,Lp(a),tightly linked (50k6) and highly homologous to PLG,susceptibility gene for IDDM8

    Enzyme Numbers (IUBMB): EC 3.4.212 EC 3.4.21.72 EC 3.4.21.-1

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    Gene Ontology (GO): 5 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0001968fibronectin binding IPI2531657
    GO:0004252serine-type endopeptidase activity IDA2531657
    GO:0004866endopeptidase inhibitor activity TAS8047165
    GO:0008201heparin binding NAS2531657
    GO:0034185apolipoprotein binding IPI9269765


    LPA for ontologies           About GeneDecksing


    2 GenomeRNAi human phenotypes for LPA:
     Increased Salmonella enterica   Increased Salmonella enterica  


    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
    About This Section

    Unified GeneCards pathways  About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Lipoprotein metabolism
    Lipoprotein metabolism1.00
    Lipid digestion, mobilization, and transport0.56
    2Metabolism
    Metabolism1.00
    Metabolism of lipids and lipoproteins0.34
    3Selected targets of HNF1
    Selected targets of HNF11.00
    4amb2 Integrin signaling
    amb2 Integrin signaling1.00
    5LDL-mediated lipid transport
    LDL-mediated lipid transport1.00

    Pathway sources
    See GeneCards unified pathways
    Show all pathways

    1 EMD Millipore Pathway for LPA
        Selected targets of HNF1


    1 BioSystems Pathway for LPA 
        amb2 Integrin signaling

    5        Reactome Pathways for LPA
        Lipid digestion, mobilization, and transport
    Metabolism
    Lipoprotein metabolism
    LDL-mediated lipid transport
    Metabolism of lipids and lipoproteins



    LPA for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for LPA

    STRING Interaction Network Preview (showing 5 interactants - click image to see 13)

    5/17 Interacting proteins for LPA (P085193 ENSP000003213344) via UniProtKB, MINT, STRING, and/or I2D (see all 17)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    FGBP026753, ENSP000003060994I2D: score=2 STRING: ENSP00000306099
    FN1P027513, ENSP000003468394I2D: score=2 STRING: ENSP00000346839
    FBLN5Q9UBX53, ENSP000003450084I2D: score=1 STRING: ENSP00000345008
    CANXP278243, ENSP000002474614I2D: score=2 STRING: ENSP00000247461
    APOHP027493, ENSP000002059484I2D: score=2 STRING: ENSP00000205948
    About this table

    Gene Ontology (GO): 5/8 biological process terms (GO ID links to tree view) (see all 8):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006508proteolysis IEA--
    GO:0006629lipid metabolic process TAS--
    GO:0006869lipid transport IEA--
    GO:0006898receptor-mediated endocytosis TAS--
    GO:0008015blood circulation TAS8047165


    LPA for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section

    LPA for compounds           About GeneDecksing

    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for LPA

    1 DrugBank Compound for LPA    About this table
    CompoundSynonyms CAS #TypeActionsPubMed Ids
    Aminocaproic Acid6-aminohexanoic acid (see all 7)60-32-2targetother17139284 17016423 15287725

    10/68 Novoseek chemical compound relationships for LPA gene (see all 68)    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    cholesterol 83.8 281 1531990 (3), 16092061 (3), 16375584 (3), 8461626 (2) (see all 99)
    lipid 75.3 123 9029226 (4), 9542772 (2), 12380908 (2), 11165958 (2) (see all 99)
    fibrinogen 59 41 17669712 (3), 16125536 (3), 10102473 (2), 9169895 (2) (see all 28)
    cholesterol ester 54.1 3 12679198 (1), 18187430 (1), 17211855 (1)
    homocysteine 48.1 25 14977830 (3), 16125536 (3), 16103723 (1), 12297895 (1) (see all 16)
    fenofibrate 48 3 12017210 (1), 1588829 (1)
    mspi 47.4 2 1968792 (1)
    epsilon aminocaproic acid 46.1 8 8845377 (2), 1838924 (2), 9837867 (1)
    lovastatin 45.3 5 8026027 (1), 7654731 (1), 7981178 (1), 10532693 (1)
    gemfibrozil 31.6 1 9006811 (1)

    Search CenterWatch for drugs/clinical trials and news about LPA / APOA 

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for LPA gene: 
    NM_005577.2  

    Unigene Cluster for LPA:

    Lipoprotein, Lp(a)
    Hs.520120  [show with all ESTs]
    Unigene Representative Sequence: X06290
    3 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000316300 ENST00000484276 ENST00000447678(uc003qtl.3)

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    Inhib. RNA
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    Additional cDNA sequence: 

    AY039748.1 X06290.1 

    5 DOTS entries:

    DT.95162934  DT.91880191  DT.92414811  DT.453211  DT.95162941 

    4 AceView cDNA sequences:

    CD620865 AY039748 NM_005577 X06290 

    GeneLoc Exon Structure


    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
    About This Section

    LPA expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: --

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)

    About this image

    LPA expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    Stem Cell Differentiation: 1 LifeMap Cell 
    NameCategory
    Embryoid bodies (Two-step protocol fo...)
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization

    See LPA Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for LPA

    SOURCE GeneReport for Unigene cluster: Hs.520120
        SABiosciences Expression via Pathway-Focused PCR Array including LPA: 
              Atherosclerosis in human mouse rat

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    In Situ
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for LPA

    (Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
    About This Section

    This gene was present in the common ancestor of animals.

    Orthologs for LPA gene from 4/12 species (see all 12)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves F1NWX6_CHICK6
    Uncharacterized protein
    48(a)
    1 → many
    3(47263284-47284746)
    lizard
    (Anolis carolinensis)
    Reptilia --
    --
    49(a)
    1 → many
    1(211782122-211817166)
    zebrafish
    (Danio rerio)
    Actinopterygii plg6
    plasminogen
    47(a)
    1 → many
    20(42720219-42734615)
    honey bee
    (Apis mellifera)
    Insecta --
    --
    9(a)
    possible ortholog
    GroupUn.841(30640-42833)


    ENSEMBL Gene Tree for LPA (if available)
    TreeFam Gene Tree for LPA (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for LPA gene
    KREMEN12  KREMEN22  PLAT2  PLG2  HGFAC2  PLAU2  HABP22  MST12  
    F122  MST1L2  HGF2  
    18/54 SIMAP similar genes for LPA using alignment to 2 protein entries:     APOA_HUMAN (see all proteins) (see all similar genes):
    APOA    LPAL2    PLG    MGC52282    DKFZp586F0824    ELANE
    PROC1    CELA3B    PROC    PRSS38    AZU1    CELA2A
    CELA3A    CTRB1    ELA3A    PRSS27    PRTN3    TRY6

    LPA for paralogs           About GeneDecksing


    4 Pseudogenes.org Pseudogenes for LPA
    PGOHUM00000250193 PGOHUM00000250194 PGOHUM00000250195 PGOHUM00000243843


    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    UniProtKB/Swiss-Prot: APOA_HUMAN, P08519
    Polymorphism: The reference genome sequence encodes a variant that contains 16 Kringle domains and that lack residues
    533 to 3040. Depending on the individual, the encoded protein contains 2-43 copies of kringle-type domains. The allele
    represented here contains 38 copies of the kringle-type repeats


    10/2501 NCBI SNPs in LPA are shown (see all 2501    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 6 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1428281891,2
    --160952125(+) TAAAAA/TAGGAT 1 -- ds50010--------
    rs1928436681,2
    --160952137(+) AGTTCA/GTGTCC 1 -- ds50010--------
    rs412663851,2
    C,F,--160952333(-) ATTTCT/GTTTAG 1 -- ds50013Minor allele frequency- G:0.03NS NA 212
    rs412663831,2
    C,--160952490(-) TTCAAA/CATTTT 1 -- ds50014Minor allele frequency- C:0.08NS WA 210
    rs1848614101,2
    --160952499(+) AAGACC/TAAAAC 1 -- ds50010--------
    rs1901497331,2
    --160952508(+) ACCAAA/GATTAA 1 -- ds50010--------
    rs412663811,2
    C,--160952621(-) ATTTTT/GGGTAT 1 -- ut312Minor allele frequency- G:0.01NS 92
    rs730122731,2
    --160952667(+) GTCTTC/GGTTTG 1 -- ut310--------
    rs1120384941,2
    F--160952754(+) TCTCCC/TGTCCA 1 -- ut311Minor allele frequency- T:0.50CSA 4
    rs1864139381,2
    C,--160952780(+) TCATTC/TCCTCA 2 E G mis11Minor allele frequency- T:0.00EU 1323

    HapMap Linkage Disequilibrium report for LPA (160952515 - 161087407 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 18 variations for LPA
         15/17 CNVs (see all 17): 36470 4514 8530 99781 36472 0604 69640 94142 6521 9552 31306 36469 7542 3648 81677
         1 Indel: 43715
    Human Gene Mutation Database (HGMD): LPA

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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Novoseek, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

    LPA for disorders           About GeneDecksing

    OMIM gene information: 152200    OMIM disorders: --

    20/104 diseases for LPA (see all 104):    About MalaCards
    lpa deficiency, congenital    hyperlipoproteinemia type iii    atherosclerosis    lipoprotein lipase deficiency
    retinol binding protein    hyperlipoproteinemia    aortic valve stenosis    myocardial infarction
    growth hormone deficiency    abdominal aortic aneurysm    peripheral vascular disease    acute myocardial infarction
    nonalcoholic steatohepatitis    type 2 diabetes mellitus    aortic aneurysm    coronary stenosis
    hdl deficiency    coronary heart disease    diabetes mellitus    alagille syndrome

    11 diseases from the University of Copenhagen DISEASES database for LPA:
    Atherosclerosis     Tangier disease     Coronary heart disease     Diabetes mellitus
    Myocardial infarction     Familial hyperlipidemia     Norum disease     Hypertension
    Cerebrovascular accident     Kidney failure     Nephrotic syndrome

    10/71 Novoseek disease relationships for LPA gene (see all 71)    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    atherosclerosis 72.6 59 15631881 (3), 19230958 (2), 12679978 (2), 10984073 (2) (see all 43)
    dyslipoproteinemia 71.1 2 10155712 (1), 8503411 (1)
    hyperlipoproteinemia type iii 69.7 3 15369733 (1), 12929622 (1), 1730728 (1)
    coronary heart disease 65.6 21 10817252 (2), 8989507 (1), 12891257 (1), 16297766 (1) (see all 15)
    hypertriglyceridemia 64.4 5 11740190 (1), 1531990 (1), 9179544 (1)
    endogenous hypertriglyceridemia 62.4 3 12575193 (1), 17680536 (1), 12600077 (1)
    hypercholesterolemia 57.6 6 7826229 (1), 7981178 (1), 12842838 (1), 9179544 (1) (see all 5)
    hyperlipidemia 57.5 1 1731853 (1)
    cardiovascular diseases 56.7 15 7857388 (1), 9693262 (1), 10751199 (1), 1345006 (1) (see all 15)
    coronary artery disease 53.5 16 1531990 (2), 9915664 (1), 1684707 (1), 1527895 (1) (see all 14)

    Genatlas disease: LPA
    coronary atherosclerosis,premature,with high Lpa

    Genetic Association Database (GAD): LPA
    Human Genome Epidemiology (HuGE) Navigator: LPA (128 documents)

    Export disorders for LPA gene to outside databases

    (in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
    About This Section

    PubMed articles for LPA gene, integrated from 9 sources (see all 647):
    (articles sorted by number of sources associating them with LPA)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. cDNA sequence of human apolipoprotein(a) is homologous to plasminogen. (PubMed id 3670400)1, 2, 3 McLean J.W.... Lawn R.M. (1987)
    2. Lp(a) and apoE polymorphisms in young South African Indians with myocardial infarction. (PubMed id 15258620)1, 4, 9 Ranjith N....Naidoo D.P. (2004)
    3. Apolipoprotein(a) gene polymorphisms (TTTTA)n and G/A-914 affect Lp(a) levels in ischemic heart disease patients from Serbia. (PubMed id 16053196)1, 4 Dincic D....Alavantic D. (2005)
    4. Association of polymorphisms of the apolipoprotein(a) gene with lipoprotein(a) levels and myocardial infarction. (PubMed id 12578871)1, 4 Holmer S.R....Schunkert H. (2003)
    5. APO(a) variants and lipoprotein(a) in men with or without myocardial infarction. (PubMed id 12127051)1, 4 Chimienti G....Pepe G. (2002)
    6. Apolipoprotein molecular variation in Moroccan Berbers: pentanucleotide (TTTTA)n repeat in the LPA gene and APOE-C1-C2 gene cluster. (PubMed id 12220441)1, 4 Harich N....Moral P. (2002)
    7. Possible association between genetic variability at the apolipoprotein(a) locus and Alzheimer's disease in apolipoprotein E2 carriers. (PubMed id 12359323)1, 4 Compton D....Hardy J. (2002)
    8. Multi-locus interactions predict risk for post-PTCA restenosis: an approach to the genetic analysis of common complex disease. (PubMed id 12082592)1, 4 Zee R.Y....Lindpainter K. (2002)
    9. Genetic effect of two APOA repeat polymorphisms (kringle 4 and pentanucleotide repeats) on plasma Lp(a) levels in American Samoans. (PubMed id 11332648)1, 4 DePrince K....Kamboh M.I. (2001)
    10. Genetic evaluation of lipoprotein(a) in intracranial aneurysm disease. (PubMed id 11440434)1, 4 Roberts G.A....Collins P.B. (2001)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Disorders
    Free Text  

      Query String
    PubMed
    OMIM
    NCBI Bookshelf
      (Note: In FireFox, select the above section and copy using Ctrl-C)

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 4018 HGNC: 6667 AceView: LPA Ensembl:ENSG00000198670 euGenes: HUgn4018
    ECgene: LPA H-InvDB: LPA

    (According to HUGE)
    About This Section
      --

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
    Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
    About This Section
    NameDescription
    PharmGKB entry for LPA Pharmacogenomics, SNPs, Pathways
    SHMPDhttp://shmpd.bii.a-star.edu.sg/gene.php?genestart=A&genename=APOA

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for LPA gene:
    Search GeneIP for patents involving LPA

    GeneCards and IP:
    Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



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