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

DSPP Gene

protein-coding   GIFtS: 50
GCID: GC04P088529

dentin sialophosphoprotein


(Previous symbols: DFNA39, DGI1)
 Explore 85 diseases affiliated with
DSPP via our new
 Human Malady Compendium 
Biological research products
for DSPP
    

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

Aliases
Dentin Sialophosphoprotein1 2     DSP2
DFNA391 2 5     Dentin Phosphophoryn2
DGI11 2 5     Dentin Phosphoprotein2
DMP31 2     Dentin Phosphoryn2
DPP2 5     Dentin Sialoprotein2
DTDP22 5     

External Ids:    HGNC: 30541   Entrez Gene: 18342   Ensembl: ENSG000001525917   OMIM: 1254855   UniProtKB: Q9NZW43   

Export aliases for DSPP gene to outside databases

Previous GC identifers: GC04P088687 GC04P088831 GC04P088988 GC04P088886 GC04P084275


(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 DSPP:
This gene encodes two principal proteins of the dentin extracellular matrix of the tooth. The preproprotein is secreted
by odontoblasts and cleaved into dentin sialoprotein and dentin phosphoprotein. Dentin phosphoprotein is thought to be
involved in the biomineralization process of dentin. Mutations in this gene have been associated with dentinogenesis
imperfecta-1; in some individuals, dentinogenesis imperfecta occurs in combination with an autosomal dominant form of
deafness. Allelic differences due to repeat polymorphisms have been found for this gene. (provided by RefSeq, Jul
2008)

UniProtKB/Swiss-Prot: DSPP_HUMAN, Q9NZW4
Function: DSP may be an important factor in dentinogenesis. DPP may bind high amount of calcium and facilitate initial
mineralization of dentin matrix collagen as well as regulate the size and shape of the crystals

Gene Wiki entry for DSPP (Dentin sialophosphoprotein)


(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_000004.11  NC_018915.1  NT_016354.19  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the DSPP gene promoter:
         c-Fos   S8   AP-1   Pax-6   ATF-2   c-Jun   FOXL1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidDSPP promoter sequence
   Search SABiosciences Chromatin IP Primers for DSPP

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


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

Entrez Gene cytogenetic band: 4q21.3   Ensembl cytogenetic band:  4q22.1   HGNC cytogenetic band: 4q21.3

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

GeneLoc information about chromosome 4         GeneLoc Exon Structure

GeneLoc location for GC04P088529:  view genomic region     (about GC identifiers)

Start:
88,529,681 bp from pter      End:
88,538,062 bp from pter
Size:
8,382 bases      Orientation:
plus 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: DSPP_HUMAN, Q9NZW4 (See protein sequence)
Recommended Name: Dentin sialophosphoprotein precursor  
Size: 1301 amino acids; 131151 Da
Subunit: Interacts with FBLN7 (By similarity)
Subcellular location: Secreted, extracellular space, extracellular matrix
Secondary accessions: A8MUI0 O95815

Explore the universe of human proteins at neXtProt for DSPP: NX_Q9NZW4

Post-translational modifications:

  • DSP is glycosylated1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q9NZW4

  • DSPP Protein expression data from MOPED and PaxDb:    About this image 
    DSPP Protein Expression
    REFSEQ proteins: NP_055023.2  
    ENSEMBL proteins: 
     ENSP00000282478   ENSP00000382213  

    Human Recombinant Protein Products for DSPP: 
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    Uscn Proteins for DSPP

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005578proteinaceous extracellular matrix IEA--

    DSPP 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

    ProtoNet protein and cluster: Q9NZW4


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase, shRNA from OriGene, Sirion Biotech, 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, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, Sirion Biotech, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: DSPP_HUMAN, Q9NZW4
    Function: DSP may be an important factor in dentinogenesis. DPP may bind high amount of calcium and facilitate initial
    mineralization of dentin matrix collagen as well as regulate the size and shape of the crystals

         Genatlas biochemistry entry for DSPP:
    dentin sialophosphoprotein,precursor of dentin sialoprotein (DSP) and dentin phosphoprotein,non collagenous components
    of the dentin extra-cellular matrix,tooth specific,encoded by a bicistronic transcript

         Gene Ontology (GO): 3 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005201extracellular matrix structural constituent TAS8995371
    GO:0005509calcium ion binding TAS9879917
    GO:0005518collagen binding TAS9879917
         
    DSPP for ontologies           About GeneDecksing


    Phenotypes:
         1 GenomeRNAi human phenotype for DSPP:
     Increased gamma-H2AX phosphory 

         1 MGI mutant phenotype (inferred from 1 allele(MGI details for Dspp):
     craniofacial 

    DSPP for phenotypes           About GeneDecksing

    Animal Models:
       inGenious Targeting Laboratory - Customizable classic, inducible, and humanized mouse model solutions for DSPP 

    miRNA
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    miRTarBase miRNAs that target DSPP:
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    (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



    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for DSPP

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0001501skeletal system development TAS8995371
    GO:0001503ossification TAS9879917
    GO:0007275multicellular organismal development TAS8995371
    GO:0031214biomineral tissue development IEA--
    GO:0071460cellular response to cell-matrix adhesion IEA--

    DSPP 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

    DSPP for compounds           About GeneDecksing

    Browse Small Molecules at EMD Millipore
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    Browse Tocris compounds for DSPP

    1 HMDB Compound for DSPP    About this table
    CompoundSynonyms CAS #PubMed Ids
    CalciumCa (see all 2)7440-70-2--
    10/143 Novoseek chemical compound relationships for DSPP gene (see all 143)    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    scotchbond 94.9 185 15575443 (3), 19683377 (3), 8600009 (3), 7499591 (3) (see all 99)
    gluma 93.4 165 15986959 (5), 7865421 (4), 11764114 (4), 1524756 (3) (see all 99)
    syntac 93 99 15851937 (2), 8600007 (2), 9545895 (2), 11572290 (2) (see all 69)
    phosphoric acid 91.2 505 12001244 (7), 11203785 (6), 1524738 (5), 17563100 (5) (see all 99)
    scotchbond 2 90.1 52 1901813 (4), 1813345 (3), 1819937 (2), 1524740 (2) (see all 35)
    dentsply 86 45 15272658 (2), 1401449 (1), 16752698 (1), 14528776 (1) (see all 33)
    calcium hydroxide 86 136 14600695 (4), 15322647 (3), 12540209 (3), 17212082 (3) (see all 74)
    copalite 84 9 2367241 (1), 7993602 (1), 7576386 (1), 9002794 (1) (see all 7)
    vivadent 83.5 25 15810477 (2), 18800947 (1), 1291387 (1), 1288602 (1) (see all 16)
    vitrebond 82.7 30 2200818 (4), 1991864 (3), 15851937 (2), 1901813 (2) (see all 21)

    Search CenterWatch for drugs/clinical trials and news about DSPP 

    (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, Sirion Biotech, 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 DSPP gene: 
    NM_014208.3  

    Unigene Cluster for DSPP:

    Dentin sialophosphoprotein
    Hs.678914
    Unigene Representative Sequence: NM_014208
    2 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000282478 ENST00000399271(uc003hqu.3)

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    1 QIAGEN miScript miRNA Assays for microRNA that regulate DSPP:
    hsa-miR-186
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    Inhib. RNA
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    1 DOTS entry:

    DT.121243912 

    1 AceView cDNA sequence:

    NM_014208 

    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

    DSPP expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: TTCTGAAAAT
    DSPP Expression
    About this image
    See DSPP Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for DSPP

    SOURCE GeneReport for Unigene cluster: Hs.678914

    UniProtKB/Swiss-Prot: DSPP_HUMAN, Q9NZW4
    Tissue specificity: Expressed in teeth. DPP is synthesized by odontoblast and transiently expressed by pre-ameloblasts

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    In Situ
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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 animals and fungi.

    Orthologs for DSPP gene from 4/16 species (see all 16)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    African clawed frog
    (Xenopus laevis)
    Amphibia BJ071618.12   -- 67.6(n)    BJ071618.1 
    zebrafish
    (Danio rerio)
    Actinopterygii stm1 starmaker 35.62(n)
    32.65(a)
      386700  NM_198817.2  NP_942112.2 
    mosquito
    (Anopheles gambiae)
    Insecta AgaP_AGAP0108461 AGAP010846-PA 32.42(n)
    26.38(a)
      3291186  XM_564089.3  XP_564089.3 
    baker's yeast
    (Saccharomyces cerevisiae)
    Saccharomycetes DDR481 Ddr48p 39.83(n)
    39.5(a)
      855210   NP_013897.1 


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

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for DSPP gene
    DMP12  

    DSPP for paralogs           About GeneDecksing



    (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

    10/263 NCBI SNPs in DSPP are shown (see all 263    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 4 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs360944641,2
    C,Fpathogenic88533540(+) GAGGAA/TGGCAA 2 R W mis112Minor allele frequency- T:0.08EU NS NA WA CSA EA 2440
    rs1119072641,2
    C--88527754(+) ATTTCC/TCTCAT 1 -- us2k12Minor allele frequency- T:0.06WA 120
    rs758079671,2
    F--88527761(+) TCATTA/TGTCTG 1 -- us2k11Minor allele frequency- T:0.15EA 120
    rs1911942281,2
    --88527981(+) TTAGTA/GCTATA 1 -- us2k10--------
    rs1502121761,2
    --88528016(+) GTGACA/TTCCCA 1 -- us2k10--------
    rs1834968671,2
    --88528063(+) CCCATA/TTATTT 1 -- us2k10--------
    rs1128150261,2
    --88528142(+) ACTTGC/GGGTTT 1 -- us2k13Minor allele frequency- G:0.04CSA WA NA 240
    rs1883445971,2
    --88528202(+) TAAACA/CTAATT 1 -- us2k10--------
    rs1141202831,2
    C--88528213(+) TGTACA/GACTTG 1 -- us2k10--------
    rs1415022121,2
    --88528332(+) AAGTCA/GTCTGT 1 -- us2k10--------

    HapMap Linkage Disequilibrium report for DSPP (88529681 - 88538062 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 1 variation for DSPP
         1 CNV: 98788
    Human Gene Mutation Database (HGMD): DSPP

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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

    DSPP for disorders           About GeneDecksing

    OMIM gene information: 125485   
    OMIM disorders: 125490  605594  125500  125420  
    UniProtKB/Swiss-Prot: DSPP_HUMAN, Q9NZW4
  • Defects in DSPP are the cause of deafness autosomal dominant type 39 with dentinogenesis imperfecta 1
  • (DFNA39/DGI1) [MIM:605594]. Affected individuals present DGI1 associated with early onset progressive sensorineural
    high-frequency hearing loss
  • Defects in DSPP are the cause of dentinogenesis imperfecta type 1 (DGI1) [MIM:125490]; also known as
  • dentinogenesis imperfecta Shields type 2 (DGI2). DGI1 is an autosomal dominant disorder in which both the primary and
    the permanent teeth are affected. It occurs with an incidence of 1:8000 live births. The teeth are amber and
    opalescent, the pulp chamber being obliterated by abnormal dentin. The enamel, although unaffected, tends to fracture,
    which makes dentin undergo rapid attrition, leading to shortening of the teeth
  • Defects in DSPP are a cause of dentinogenesis imperfecta Shields type 3 (DGI3) [MIM:125500]. Patients with
  • DGI3 do not have stigmata of osteogenesis imperfecta. The finding that a single defects in the DSPP gene causes both
    phenotypic patterns of DGI2 and DGI3 strongly supports the conclusion that these two disorders are not separate
    diseases but rather the phenotypic variation of a single genetic defect
  • Defects in DSPP are the cause of dentin dysplasia type 2 (DTDP2) [MIM:125420]; also known as dentin dysplasia
  • Shields type 2. DTDP2 is an autosomal dominant disorder in which mineralization of the dentine of the primary teeth is
    abnormal. On the basis of the phenotypic overlap between, and shared chromosomal location with DGI2 it has been
    proposed that DTDP2 and DGI2 are allelic. From the results of recent studies, it is clear that different types of
    mutations in DSPP lead to the two different phenotypes

    20/85 diseases for DSPP (see all 85):    About MalaCards
    dentinogenesis imperfecta    dentinogenesis imperfecta 1    tricho-dento-osseous syndrome    deafness, autosomal dominant 36
    deafness, autosomal dominant 36, with dentinogenesis    ehlers-danlos syndrome    dentinogenesis imperfecta shields type 3    dentin dysplasia, type ii
    odontoma    dentin dysplasia    amelogenesis imperfecta    root caries
    dental pulp calcification    osteogenesis imperfecta    tooth resorption    dental enamel hypoplasia
    tooth erosion    gastroesophageal reflux disease    dental caries    cleft lip/palate

    7 diseases from the University of Copenhagen DISEASES database for DSPP:
    Dentinogenesis imperfecta     Dentin dysplasia     Vaginal discharge     Dental pulp calcification
    Dental enamel hypoplasia     Endometritis     Tooth agenesis

    10/95 Novoseek disease relationships for DSPP gene (see all 95)    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    dentinogenesis imperfecta 89.4 141 11116156 (3), 10371252 (3), 17686168 (2), 18797159 (2) (see all 65)
    dentin dysplasia 89.2 110 9493074 (7), 1785908 (4), 19417880 (4), 1891231 (3) (see all 48)
    dentin sensitivity 89.2 82 2285881 (4), 1508870 (3), 1650304 (3), 1819929 (3) (see all 43)
    dgi-ii 85 35 10765957 (4), 20146806 (2), 8006116 (2), 11175779 (2) (see all 14)
    hereditary opalescent dentin 81.7 19 19927739 (3), 19186872 (2), 9780905 (2), 15573663 (2) (see all 9)
    teeth endodontically treated 81.4 38 16399275 (2), 15318256 (2), 18021825 (2), 18718775 (2) (see all 30)
    dgi-iii 75.2 9 15690376 (3), 10371253 (1), 17452557 (1)
    root caries 74.2 23 8054192 (2), 10522203 (2), 14674495 (2), 10575804 (1) (see all 17)
    collagen fibril 73.1 90 15769538 (3), 15846504 (2), 16973251 (2), 9736372 (2) (see all 65)
    pulpless teeth 71.8 12 1402574 (4), 1432755 (2), 7853252 (1), 17655074 (1) (see all 5)

    Human Genome Epidemiology (HuGE) Navigator: DSPP (2 documents)

    Export disorders for DSPP 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 DSPP gene, integrated from 9 sources (see all 2073):
    (articles sorted by number of sources associating them with DSPP)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Molecular cloning of a human dentin sialophosphoprotein gene. (PubMed id 10706475)1, 2, 9 Gu K.... Rutherford R.B. (2000)
    2. Dentin phosphoprotein and dentin sialoprotein are cleavage products expressed from a single transcript coded by a gene on human chromosome 4. Dentin phosphoprotein DNA sequence determination. (PubMed id 8995371)1, 3, 9 MacDougall M....Gu T.T. (1997)
    3. DSPP mutation in dentinogenesis imperfecta Shields type II. (PubMed id 11175779)1, 2, 9 Zhang X.... Shen Y. (2001)
    4. Human dentin phosphophoryn nucleotide and amino acid sequence. (PubMed id 9879917)1, 2, 9 Gu K....Ritchie H.H. (1998)
    5. DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis. (PubMed id 17033625)1, 2 Lorenz-Depiereux B.... Strom T.M. (2006)
    6. Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP. (PubMed id 11175790)1, 2 Xiao S.... Kong X. (2001)
    7. Assignment of dentin sialophosphoprotein (DSPP) to the critical DGI2 locus on human chromosome 4 band q21.3 by in situ hybridization. (PubMed id 9533027)1, 3 MacDougall M....DuPont B.R. (1997)
    8. Dentin sialophosphoprotein (DSPP) is cleaved into its two natural dentin matrix products by three isoforms of bone morphogenetic pro tein-1 (BMP1). (PubMed id 20079836)1, 9 von Marschall Z. and Fisher L.W. (2010)
    9. Dentin phosphoprotein frameshift mutations in hereditary dentin disorders and their variation patterns in normal human population. (PubMed id 18456718)1, 9 Song Y.L....Bian Z. (2008)
    10. Dentin sialoprotein and dentin phosphoprotein overexpression during amelogenesis. (PubMed id 16014627)1, 9 Paine M.L....Snead M.L. (2005)

    (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)
    About This Section
    Entrez Gene: 1834 HGNC: 3054 AceView: DSPP Ensembl:ENSG00000152591 euGenes: HUgn1834
    ECgene: DSPP H-InvDB: DSPP

    (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 DSPP Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for DSPP Genetics and Cytogenetics in Oncology and Haematology

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

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



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