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

IMPG2 Gene

protein-coding   GIFtS: 51
GCID: GC03M100944

Interphotoreceptor Matrix Proteoglycan 2

  See related diseases
at  

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
About This Section

Aliases
Interphotoreceptor Matrix Proteoglycan 21 2     RP562 5
IPM2002 3 5     SPACRCAN2
Interphotoreceptor Matrix Proteoglycan Of 200 KDa2 3     Interphotoreceptor Matrix Proteoglycan IPM 2002
Sialoprotein Associated With Cones And Rods Proteoglycan2 3     Spacrcan3
IPM 2002 3     

External Ids:    HGNC: 183621   Entrez Gene: 509392   Ensembl: ENSG000000811487   OMIM: 6070565   UniProtKB: Q9BZV33   

Export aliases for IMPG2 gene to outside databases

Previous GC identifers: GC03M097598 GC03M100372 GC03M102226 GC03M102266 GC03M102428 GC03M098313


(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 IMPG2 Gene:
The protein encoded by this gene binds chondroitin sulfate and hyaluronan and is a proteoglycan. The encoded
protein plays a role in the organization of the interphotoreceptor matrix and may promote the growth and
maintenance of the light-sensitive photoreceptor outer segment. Defects in this gene are a cause of retinitis
pigmentosa type 56 and maculopathy, IMPG2-related.(provided by RefSeq, Mar 2011)

GeneCards Summary for IMPG2 Gene: 
IMPG2 (interphotoreceptor matrix proteoglycan 2) is a protein-coding gene. Diseases associated with IMPG2 include maculopathy, impg2-related, and impg2-related retinitis pigmentosa, and among its related super-pathways are FAK1 Signaling and MAPK Signaling. GO annotations related to this gene include heparin binding and hyaluronic acid binding. An important paralog of this gene is IMPG1.

UniProtKB/Swiss-Prot: IMPG2_HUMAN, Q9BZV3
Function: Chondroitin sulfate- and hyaluronan-binding proteoglycan involved in the organization of
interphotoreceptor matrix; may participate in the maturation and maintenance of the light-sensitive photoreceptor
outer segment. Binds heparin




(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 73), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000003.11  NC_018914.2  NT_005612.16  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the IMPG2 gene promoter:
         Oct-B1   E2F-3a   E2F-4   E2F-5   oct-B2   E2F-2   E2F   E2F-1   POU2F1   POU2F1a   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidIMPG2 promoter sequence
   Search SABiosciences Chromatin IP Primers for IMPG2

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat IMPG2


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

Entrez Gene cytogenetic band: 3q12.2-q12.3   Ensembl cytogenetic band:  3q12.3   HGNC cytogenetic band: 3q12.2-q12.3

IMPG2 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
IMPG2 gene location

GeneLoc information about chromosome 3         GeneLoc Exon Structure

GeneLoc location for GC03M100944:  view genomic region     (about GC identifiers)

Start:
100,941,390 bp from pter      End:
101,039,419 bp from pter
Size:
98,030 bases      Orientation:
minus strand

(According to UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MAXQB 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 Cloud-Clone Corp.,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Cloud-Clone Corp., Ontologies according to Gene Ontology Consortium 01 Oct 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, and/or Cloud-Clone Corp.)
About This Section

UniProtKB/Swiss-Prot: IMPG2_HUMAN, Q9BZV3 (See protein sequence)
Recommended Name: Interphotoreceptor matrix proteoglycan 2 precursor  
Size: 1241 amino acids; 138621 Da
Subcellular location: Membrane; Single-pass type I membrane protein (Potential)
Secondary accessions: A8MWT5 Q9UKD4 Q9UKK5

Explore the universe of human proteins at neXtProt for IMPG2: NX_Q9BZV3

Explore proteomics data for IMPG2 at MOPED 

Post-translational modifications:

  • UniProtKB: Highly glycosylated (N- and O-linked carbohydrates)
  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q9BZV3

  • IMPG2 Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    IMPG2 Protein Expression
    REFSEQ proteins: NP_057331.2  
    ENSEMBL proteins: 
     ENSP00000193391  

    Human Recombinant Protein Products for IMPG2: 
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    Cloud-Clone Corp. Proteins for IMPG2 

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005578proteinaceous extracellular matrix TAS10702256
    GO:0016021integral to membrane IEA--

    IMPG2 for ontologies           About GeneDecksing



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    Cloud-Clone Corp. CLIAs for IMPG2


    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    3 InterPro protein domains:
     IPR000742 EG-like_dom
     IPR000082 SEA_dom
     IPR013032 EGF-like_CS

    Graphical View of Domain Structure for InterPro Entry Q9BZV3

    ProtoNet protein and cluster: Q9BZV3

    1 Blocks protein domain: IPB000082 SEA domain

    UniProtKB/Swiss-Prot: IMPG2_HUMAN, Q9BZV3
    Similarity: Contains 2 EGF-like domains
    Similarity: Contains 2 SEA domains


    IMPG2 for domains           About GeneDecksing


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory, genOway,
    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, Sirion Biotech, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, Vector BioLabs, and Sirion Biotech, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Oct 2013 via Entrez Gene.)
    About This Section

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: IMPG2_HUMAN, Q9BZV3
    Function: Chondroitin sulfate- and hyaluronan-binding proteoglycan involved in the organization of
    interphotoreceptor matrix; may participate in the maturation and maintenance of the light-sensitive photoreceptor
    outer segment. Binds heparin

         Gene Ontology (GO): 4 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005201extracellular matrix structural constituent TAS10702256
    GO:0005515protein binding ----
    GO:0005540hyaluronic acid binding TAS10702256
    GO:0008201heparin binding IEA--
         
    IMPG2 for ontologies           About GeneDecksing


    Phenotypes:
         1 GenomeRNAi human phenotype for IMPG2:
     Decreased POU5F1-GFP protein e 

    Animal Models:
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    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Sino Biological, 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 Oct 2013 via Entrez Gene).
    About This Section

    SuperPaths for IMPG2 About                                                                                                See pathways by source

    SuperPathContained pathways About
    1Integrin Pathway
    Integrin Pathway0.67
    UPA-UPAR Pathway0.56
    FAK1 Signaling0.67
    Inhibition of Angiogenesis by TSP10.50
    GnRH Signaling0.56
    Transendothelial Migration of Leukocytes0.38
    2Rho Family GTPases
    Rho Family GTPases0.61
    Molecular Mechanisms of Cancer0.51
    ERK Signaling0.61
    ILK Signaling0.49
    MAPK Signaling0.58
    3PTEN Pathway
    PTEN Pathway0.56
    Phospholipase-C Pathway0.56

    5/13 Downloadable PowerPoint Slides of QIAGEN Pathway Central Maps for IMPG2 (see all 13)
        MAPK Signaling
    Molecular Mechanisms of Cancer
    PTEN Pathway
    Transendothelial Migration of Leukocytes
    UPA-UPAR Pathway


    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for IMPG2

    1 Interacting protein for IMPG2 (Q9BZV33) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    PPP2CAP677753I2D: score=1 
    About this table

    Gene Ontology (GO): 1 biological process term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0007601visual perception TAS10702256

    IMPG2 for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section
    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for IMPG2

    1 HMDB Compound for IMPG2    About this table
    CompoundSynonyms CAS #PubMed Ids
    Hyaluronanhyaluronic acid (see all 13)9004-61-9--

    Search CenterWatch for drugs/clinical trials and news about IMPG2

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 236 Homo sapiens; Apr 25 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    Conferences by KenesGroup, 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, Sirion Biotech, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for IMPG2 gene: 
    NM_016247.3  

    Unigene Cluster for IMPG2:

    Interphotoreceptor matrix proteoglycan 2
    Hs.209249  [show with all ESTs]
    Unigene Representative Sequence: NM_016247
    1 Ensembl transcript including schematic representation, and UCSC links where relevant:
    ENST00000193391(uc011bhe.2 uc003duq.2 uc010hpj.1)
    miRNA
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    8/52 QIAGEN miScript miRNA Assays for microRNAs that regulate IMPG2 (see all 52):
    hsa-miR-607 hsa-miR-520e hsa-miR-302d hsa-miR-136 hsa-let-7d hsa-miR-488 hsa-miR-570 hsa-let-7g
    SwitchGear 3'UTR luciferase reporter plasmidIMPG2 3' UTR sequence
    Inhib. RNA
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    Additional mRNA sequence: 

    AB593127.1 AF157624.1 AF173155.1 AF319972.1 BC144092.1 

    5 DOTS entries:

    DT.101955084  DT.97839976  DT.95189990  DT.425499  DT.100739143 

    24/35 AceView cDNA sequences (see all 35):

    BM799621 BX953412 BX510203 AA364834 AA736980 AF157624 BX953286 NM_016247 
    BX954997 AL713046 BX509854 BX953550 AA721009 AF319972 BX491222 AL712421 
    BU167472 BM929973 AA815118 BX953290 AF173155 AA744481 BX283908 BX642541 

    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

    IMPG2 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: GAGAAGTCTG
    IMPG2 Expression
    About this image


    See IMPG2 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for IMPG2

    SOURCE GeneReport for Unigene cluster: Hs.209249

    UniProtKB/Swiss-Prot: IMPG2_HUMAN, Q9BZV3
    Tissue specificity: Expressed in the retina. Expressed by photoreceptors of the interphotoreceptor matrix (IPM)
    surrounding both rods and cones. IPM occupies the subretinal space between the apices of the retinal pigment
    epithelium and the neural retina. Detected in the pineal gland

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    In Situ
    Assay Products:
     

     
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    (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 chordates.

    Orthologs for IMPG2 gene from 4/10 species (see all 10)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Impg21 , 5 interphotoreceptor matrix proteoglycan 21, 5 81.46(n)1
    72.73(a)1
      16 (33.91 cM)5
    2242241  NM_174876.31  NP_777365.21 
     562043135 
    chicken
    (Gallus gallus)
    Aves IMPG21 interphotoreceptor matrix proteoglycan 2 61.76(n)
    52.41(a)
      418393  NM_001044639.1  NP_001038104.1 
    lizard
    (Anolis carolinensis)
    Reptilia IMPG26
    Uncharacterized protein
    43(a)
    1 ↔ 1
    3(173699472-173771539)
    zebrafish
    (Danio rerio)
    Actinopterygii IMPG2 (4 of 4)6
    IMPG2 (1 of 4)6
    (see all 4)
    interphotoreceptor matrix proteoglycan 2
    (see all 4)
    65(a)
    36(a)
    (see all 4)
    many → 1
    many → 1
    (see all 4)
    22(30302867-30339587)
    9(31228036-31230873)


    ENSEMBL Gene Tree for IMPG2 (if available)
    TreeFam Gene Tree for IMPG2 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for IMPG2 gene
    IMPG12  
    1 SIMAP similar gene for IMPG2 using alignment to 3 protein entries:     IMPG2_HUMAN (see all proteins):
    DKFZp686K0887

    IMPG2 for paralogs           About GeneDecksing



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, 4UniProtKB, 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

    10/1922 SNPs in IMPG2 are shown (see all 1922)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 3 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    VAR_0643364
    Maculopathy, IMPG2-related (MACLP-IMPG2)4--see VAR_0643362 F L mis40--------
    rs2018935451,2
    Cpathogenic1100990410(+) CCAAAA/GAGTCC 2 L F mis10--------
    rs729324681,2
    C,F--98352665(+) TTGTAT/CGGAAC 1 -- int12Minor allele frequency- C:0.03WA 120
    rs3776335821,2
    C--98398029(+) GTCTC-/AAAAAAA
    AAAAAAAAA
    AAAAA
    1 -- int10--------
    rs2000399611,2
    C--98399480(+) TATAC-/AAAAAA 1 -- int10--------
    rs360909401,2
    C--98404553(+) GGTGG-/GCATT 
    ATAAATGG
    TCATG
    1 -- int11Minor allele frequency- GCATTATAAATGG:0.00NA 2
    rs105405431,2
    C--98407612(+) AATAA-/AGTAGTAT 1 -- int10--------
    rs1895105011,2
    C--98407613(+) ATAAAA/G/TTAGTA 1 -- int10--------
    rs1918329911,2
    --100908300(+) TGTTTA/TTTTCT 1 -- ds50010--------
    rs1167137081,2
    C,F--100908302(+) TTTATT/GTCTTC 1 -- ds50011Minor allele frequency- G:0.04WA 118

    HapMap Linkage Disequilibrium report for IMPG2 (100941390 - 101039419 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 2 variations for IMPG2:    About this table     
    Variant IDTypeSubtypePubMed ID
    nsv508232CNV Loss20534489
    nsv877222CNV Gain21882294


    Human Gene Mutation Database (HGMD): IMPG2

    Locus Specific Mutation Databases (LSDB): IMPG2
    SABiosciences Cancer Mutation PCR Assays
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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Conferences by KenesGroup, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section
    OMIM gene information: 607056   
    OMIM disorders: 613581  
    UniProtKB/Swiss-Prot: IMPG2_HUMAN, Q9BZV3
  • Retinitis pigmentosa 56 (RP56) [MIM:613581]: A retinal dystrophy belonging to the group of pigmentary
    retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination
    and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically
    have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose
    their far peripheral visual field and eventually central vision as well. Note=The disease is caused by mutations
    affecting the gene represented in this entry
  • Maculopathy, IMPG2-related (MACLP-IMPG2) [MIM:613581]: A mild maculopathy characterized by full-field
    electroretinogram responses within normal limits, normal color vision, elevation of the photoreceptor layer in
    the foveal region and mild nuclear sclerosis. Note=The disease is caused by mutations affecting the gene
    represented in this entry

  • 9 diseases for IMPG2:    About MalaCards
    maculopathy, impg2-related    impg2-related retinitis pigmentosa    rhyns syndrome    pigmentary retinopathy
    retinitis pigmentosa    age related macular degeneration    macular degeneration    retinitis
    blindness


    IMPG2 for disorders           About GeneDecksing

    Genetic Association Database (GAD): IMPG2
    Human Genome Epidemiology (HuGE) Navigator: IMPG2 (1 document)

    Export disorders for IMPG2 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)
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    PubMed articles for IMPG2 gene integrated from 9 sources:
    (articles sorted by number of sources associating them with IMPG2)
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    1. Molecular characterization and genomic mapping of human IPM 200, a second member of a novel family of proteoglycans. (PubMed id 10542133)1, 2, 3 Kuehn M.H. and Hageman G.S. (1999)
    2. SPACRCAN, a novel human interphotoreceptor matrix hyaluronan-binding proteoglycan synthesized by photoreceptors and pinealocytes. (PubMed id 10702256)1, 2, 9 Acharya S.... Hollyfield J.G. (2000)
    3. Organization of the human IMPG2 gene and its evaluation as a candidate gene in age-related macular degeneration and other retinal degenerative disorders. (PubMed id 11726612)1, 2, 9 Kuehn M.H.... Hageman G.S. (2001)
    4. Mutations in IMPG2, encoding interphotoreceptor matri x proteoglycan 2, cause autosomal-recessive retinitis pigmentosa. (PubMed id 20673862)1, 2 Bandah-Rozenfeld D....den Hollander A.I. (2010)
    5. Full-length transcriptome analysis of human retina-derived cell lines ARPE-19 and Y79 using the vector-capping method. (PubMed id 21697133)1 Oshikawa M.... Kato S. (2011)
    6. The DNA sequence, annotation and analysis of human chromosome 3. (PubMed id 16641997)2 Muzny D.M....Gibbs R.A. (2006)
    7. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. (PubMed id 12477932)1 Strausberg R.L....Marra M.A. (2002)
    8. Normalization and subtraction: two approaches to facilitate gene discovery. (PubMed id 8889548)1 Bonaldo M.F.... Soares M.B. (1996)
    9. Retinitis Pigmentosa Overvi ew (PubMed id 20301590)1 Pagon R.A. and Daiger S.P. (1993)
    10. SPACRCAN in the interphotoreceptor matrix of the mouse retina: molecular, developmental and promoter analysis. (PubMed id 12589770)9 Chen Q....Hollyfield J.G. (2003)

    (in PubMed, OMIM, and NCBI Bookshelf)
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
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    Entrez Gene: 50939 HGNC: 18362 AceView: IMPG2 Ensembl:ENSG00000081148 euGenes: HUgn50939
    ECgene: IMPG2 H-InvDB: IMPG2

    (According to HUGE)
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      --

    (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 IMPG2 Pharmacogenomics, SNPs, Pathways

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for IMPG2 gene:
    Search GeneIP for patents involving IMPG2

    GeneCards and IP:
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