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

ZMYND8 Gene

protein-coding   GIFtS: 54
GCID: GC20M045837

Zinc Finger, MYND-Type Containing 8

(Previous name: protein kinase C binding protein 1)
(Previous symbol: PRKCBP1)
  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
Zinc Finger, MYND-Type Containing 81 2     CTCL Tumor Antigen Se14-32
PRKCBP11 2 3     Predicted Protein Of HQ28932
Cutaneous T-Cell Lymphoma-Associated Antigen Se14-32 3     Protein Kinase C-Binding Protein 12
Zinc Finger MYND Domain-Containing Protein 82 3     KIAA11253
RACK72 3     Rack73
Protein Kinase C Binding Protein 11     CTCL-Associated Antigen Se14-33
PRO28932     

External Ids:    HGNC: 93971   Entrez Gene: 236132   Ensembl: ENSG000001010407   UniProtKB: Q9ULU43   

Export aliases for ZMYND8 gene to outside databases

Previous GC identifers: GC20M045272 GC20M042581


(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 ZMYND8 Gene:
The protein encoded by this gene is a receptor for activated C-kinase (RACK) protein. The encoded protein has been
shown to bind in vitro to activated protein kinase C beta I. In addition, this protein is a cutaneous T-cell
lymphoma-associated antigen. Finally, the protein contains a bromodomain and two zinc fingers, and is thought to
be a transcriptional regulator. Multiple transcript variants encoding several different isoforms have been found
for this gene. (provided by RefSeq, Jul 2008)

GeneCards Summary for ZMYND8 Gene: 
ZMYND8 (zinc finger, MYND-type containing 8) is a protein-coding gene. Diseases associated with ZMYND8 include cutaneous t cell lymphoma, and breast cancer. GO annotations related to this gene include RNA polymerase II transcription corepressor activity and repressing transcription factor binding. An important paralog of this gene is ZMYND11.

Gene Wiki entry for ZMYND8 Gene


(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_000020.10  NT_011362.10  NC_018931.2  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the ZMYND8 gene promoter:
         USF1   Bach2   Olf-1   E47   C/EBPalpha   CBF-B   FOXJ2 (long isoform)   USF-1   FOXJ2   CBF(2)   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidZMYND8 promoter sequence
   Search SABiosciences Chromatin IP Primers for ZMYND8

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat ZMYND8


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

Entrez Gene cytogenetic band: 20q13.12   Ensembl cytogenetic band:  20q13.12   HGNC cytogenetic band: 20q13.12

ZMYND8 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
ZMYND8 gene location

GeneLoc information about chromosome 20         GeneLoc Exon Structure

GeneLoc location for GC20M045837:  view genomic region     (about GC identifiers)

Start:
45,837,859 bp from pter      End:
45,985,567 bp from pter
Size:
147,709 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: PKCB1_HUMAN, Q9ULU4 (See protein sequence)
Recommended Name: Protein kinase C-binding protein 1  
Size: 1186 amino acids; 131692 Da
Subunit: Interacts in vitro with PRKCB1
Sequence caution: Sequence=AAC72244.1; Type=Frameshift; Positions=816; Sequence=BAA86439.1; Type=Erroneous
initiation; Note=Translation N-terminally shortened;
Secondary accessions: B7Z680 E1P5U5 Q13517 Q2HXV2 Q2HXV7 Q2HXV8 Q2HXW0 Q2HXW1 Q2HXW2 Q4JJ94
Q4JJ95 Q5TH09 Q6MZM1 Q8WXC5 Q9H1F3 Q9H1F4 Q9H1F5 Q9H1L8 Q9H1L9 Q9H2G5 Q9NYN3 Q9UIX6
Alternative splicing: 14 isoforms:  Q9ULU4-1   Q9ULU4-2   Q9ULU4-3   Q9ULU4-4   Q9ULU4-5   Q9ULU4-6   Q9ULU4-7   Q9ULU4-8   
Q9ULU4-9   Q9ULU4-10   Q9ULU4-11   Q9ULU4-12   Q9ULU4-13   Q9ULU4-14   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for ZMYND8: NX_Q9ULU4

Explore proteomics data for ZMYND8 at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q9ULU4

  • ZMYND8 Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    ZMYND8 Protein Expression
    REFSEQ proteins (18 alternative transcripts): 
    NP_001268698.1  NP_001268700.1  NP_001268701.1  NP_001268702.1  NP_001268703.1  NP_001268704.1  NP_001268705.1  NP_001268706.1  
    NP_001268707.1  NP_001268708.1  NP_001268709.1  NP_001268710.1  NP_001268711.1  NP_001268712.1  NP_001268713.1  NP_036540.3  
    NP_898868.1  NP_898869.1  

    ENSEMBL proteins: 
     ENSP00000312237   ENSP00000354166   ENSP00000392964   ENSP00000418495   ENSP00000262975  
     ENSP00000420095   ENSP00000335537   ENSP00000418210   ENSP00000413727   ENSP00000394379  
     ENSP00000393806   ENSP00000361093   ENSP00000443086   ENSP00000439800   ENSP00000379577  
     ENSP00000348246   ENSP00000396725  

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    Novus Biologicals ZMYND8 Protein
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    Cloud-Clone Corp. Proteins for ZMYND8 

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus ISS--

    ZMYND8 for ontologies           About GeneDecksing



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    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    HGNC Gene Families: 
    ZMYND: Zinc fingers, MYND-type
    PHF: Zinc fingers, PHD-type

    5/9 InterPro protein domains (see all 9):
     IPR002893 Znf_MYND
     IPR021931 DUF3544
     IPR019786 Zinc_finger_PHD-type_CS
     IPR001965 Znf_PHD
     IPR001487 Bromodomain

    Graphical View of Domain Structure for InterPro Entry Q9ULU4

    ProtoNet protein and cluster: Q9ULU4

    4 Blocks protein domains:
    IPB000313 PWWP domain
    IPB001487 Bromodomain signature
    IPB001965 Zn-finger-like
    IPB002893 Zn-finger


    UniProtKB/Swiss-Prot: PKCB1_HUMAN, Q9ULU4
    Similarity: Contains 1 bromo domain
    Similarity: Contains 1 MYND-type zinc finger
    Similarity: Contains 1 PHD-type zinc finger
    Similarity: Contains 1 PWWP domain


    ZMYND8 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

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0001106RNA polymerase II transcription corepressor activity ISS--
    GO:0005515protein binding IPI15095401
    GO:0008270zinc ion binding IEA--
    GO:0016301kinase activity ----
    GO:0070491repressing transcription factor binding ISS--
         
    ZMYND8 for ontologies           About GeneDecksing


    Phenotypes:
         2 GenomeRNAi human phenotypes for ZMYND8:
     Gemcitabine induced cell-death  Increased cell death HMECs cel 

         1 MGI phenotypic allele for Zmynd8 (no phenotypes)

    ZMYND8 for phenotypes           About GeneDecksing

    Animal Models:
       inGenious Targeting Laboratory - Custom generated mouse model solutions for ZMYND8 
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       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for ZMYND8 
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    hsa-miR-30c hsa-miR-323-3p hsa-miR-142-3p hsa-miR-3607-3p hsa-let-7a-2* hsa-miR-30d hsa-miR-30a hsa-miR-204
    SwitchGear 3'UTR luciferase reporter plasmidZMYND8 3' UTR sequence
    Inhib. RNA
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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 ZMYND8 About                                                                                                See pathways by source

    SuperPathContained pathways About
    1Integrated Breast Cancer Pathway
    Integrated Breast Cancer Pathway


    1 BioSystems Pathway for ZMYND8
        Integrated Breast Cancer Pathway


    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for ZMYND8

    STRING Interaction Network Preview (showing 5 interactants - click image to see 17)

    5/18 Interacting proteins for ZMYND8 (Q9ULU41, 2, 3 ENSP000004182104) via UniProtKB, MINT, STRING, and/or I2D (see all 18)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    REREQ9P2R62, 3, ENSP000003386294MINT-2871418 I2D: score=3 STRING: ENSP00000338629
    CSNK1EP496742, 3, ENSP000003529294MINT-8252835 I2D: score=2 STRING: ENSP00000352929
    ZFYVE9O954052, 3MINT-62049 I2D: score=3 
    ATN1P542592, 3, ENSP000003490764MINT-2871399 I2D: score=3 STRING: ENSP00000349076
    USP7Q930092, 3, ENSP000003435354MINT-2871437 I2D: score=3 STRING: ENSP00000343535
    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:0000122negative regulation of transcription from RNA polymerase II promoter ISS--

    ZMYND8 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 ZMYND8 (PKCB1)

    Search CenterWatch for drugs/clinical trials and news about ZMYND8 / PKCB1

    (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 ZMYND8 gene (18 alternative transcripts): 
    NM_001281769.1  NM_001281771.1  NM_001281772.1  NM_001281773.1  NM_001281774.1  NM_001281775.1  NM_001281776.1  NM_001281777.1  
    NM_001281778.1  NM_001281779.1  NM_001281780.1  NM_001281781.1  NM_001281782.1  NM_001281783.1  NM_001281784.1  NM_012408.4  
    NM_183047.2  NM_183048.2  

    Unigene Clusters for ZMYND8:

    Zinc finger, MYND-type containing 8
    Hs.446240  [show with all ESTs], Hs.658553  [show with all ESTs], Hs.668465  [show with all ESTs]
    Unigene Representative Sequences: NM_183047, AF144233, AK098067
    18 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000311275(uc002xsu.1 uc002xsv.1 uc002xsw.1 uc002xsx.1 uc002xta.1 uc010zxy.1 uc002xtb.1 uc002xss.2 uc002xtc.1 uc002xte.1 uc010zya.1 uc002xtf.1)
    ENST00000360911(uc002xsr.1 uc010ghq.1 uc010ghr.1 uc002xst.1 uc002xsy.1 uc002xsz.1 uc010zxz.1 uc002xtd.1)
    ENST00000458360 ENST00000467200 ENST00000262975(uc002xth.3) ENST00000471951
    ENST00000352431 ENST00000461685 ENST00000468376(uc002xtg.3 uc010ghs.2)
    ENST00000435836 ENST00000446894 ENST00000441977 ENST00000372023 ENST00000540497
    ENST00000536340 ENST00000396281 ENST00000355972 ENST00000446994
    miRNA
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    hsa-miR-30c hsa-miR-323-3p hsa-miR-142-3p hsa-miR-3607-3p hsa-let-7a-2* hsa-miR-30d hsa-miR-30a hsa-miR-204
    SwitchGear 3'UTR luciferase reporter plasmidZMYND8 3' UTR sequence
    Inhib. RNA
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    Additional mRNA sequence: 

    AK098067.1 BC047609.1 

    24/44 DOTS entries (see all 44):

    DT.95118374  DT.91791034  DT.91747769  DT.120796799  DT.449137  DT.101984841  DT.100031543  DT.100789643 
    DT.100789639  DT.92003694  DT.100789644  DT.311950  DT.120796814  DT.87077800  DT.100789645  DT.75101056 
    DT.102836771  DT.75139609  DT.91664452  DT.120796912  DT.40116061  DT.40113726  DT.95118344  DT.91663821 

    24/415 AceView cDNA sequences (see all 415):

    BU171749 BU183213 AA464811 CD515288 AA635563 BQ776249 CB993991 BG472281 
    AI250888 Z40347 BM803189 BC030721 BQ777527 CN479810 AK000275 BU685833 
    BM979656 AI420219 T31925 AA236395 AA236410 NM_183048 AK001175 AA226843 

    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

    ZMYND8 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: ACAACTGGAA
    ZMYND8 Expression
    About this image


    See ZMYND8 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for ZMYND8

    SOURCE GeneReport for Unigene clusters: Hs.446240 Hs.658553 Hs.668465

    UniProtKB/Swiss-Prot: PKCB1_HUMAN, Q9ULU4
    Tissue specificity: Expressed in all tissues examined with highest expression in brain, lung, pancreas, and
    placenta. Expressed in cutaneous T-cell lymphomas (CTCL)

        SABiosciences Expression via Pathway-Focused PCR Array including ZMYND8: 
              Epigenetic Chromatin Remodeling Factors in human mouse rat

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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for ZMYND8

    (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 ZMYND8 gene from 6/15 species (see all 15)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Zmynd81 , 5 zinc finger, MYND-type containing 81, 5 86.7(n)1
    91.03(a)1
      2 (85.98 cM)5
    2288801  NM_027230.41  NP_081506.31 
     1657841555 
    chicken
    (Gallus gallus)
    Aves ZMYND81 zinc finger, MYND-type containing 8 80.27(n)
    88.83(a)
      419207  XM_417384.3  XP_417384.3 
    lizard
    (Anolis carolinensis)
    Reptilia ZMYND86
    Uncharacterized protein
    81(a)
    1 ↔ 1
    4(145055248-145107144)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.189462 Xenopus laevis transcribed sequences 81.86(n)    CA973379.1 
    zebrafish
    (Danio rerio)
    Actinopterygii wufb99d122 wufb99d12 76.07(n)   323479  BC058064.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG18151 CG1815 41.5(n)
    30.48(a)
      43730  NM_170562.1  NP_733441.2 


    ENSEMBL Gene Tree for ZMYND8 (if available)
    TreeFam Gene Tree for ZMYND8 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for ZMYND8 gene
    ZMYND112  
    5 SIMAP similar genes for ZMYND8 using alignment to 13 protein entries:     PKCB1_HUMAN (see all proteins):
    PRKCBP1    DKFZp564P1772    AIRE    ZMYND11    CBFA2T1

    ZMYND8 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

    10/3180 SNPs in ZMYND8 are shown (see all 3180)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 20 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs45553991,2
    C,F,A,H--45837896(+) GTAAAG/AAAATC 3 -- ds50019Minor allele frequency- A:0.26NS EA NA 664
    rs1176960791,2
    F--45837922(+) GGTGGG/AGGAAG 3 -- ds50011Minor allele frequency- A:0.03EA 120
    rs113509731,2
    C--45838101(+) GGCTA-/TTTTTT 3 -- ds5001 trp32Minor allele frequency- T:0.25NA CSA 4
    rs1171018141,2
    C,F--45838134(+) AAATGT/CTCTTT 3 -- ds50011Minor allele frequency- C:0.02EA 120
    rs1449639471,2
    C--45838161(+) TAATA-/CTCTCTT 3 -- ds50010--------
    rs105525901,2
    C--45838166(+) CTCTC-/TTATTTC 3 -- ds50010--------
    rs1425992501,2
    --45838176(+) TCTTCG/TCTAAT 3 -- ds50010--------
    rs1886577561,2
    --45838380(+) CGTAGA/TGTACG 3 -- ds50010--------
    rs1910828431,2
    --45838381(+) GTAGTA/GTACGG 3 -- ut310--------
    rs1825232121,2
    --45838445(+) AAAAAC/TGTGAA 3 -- ut310--------

    HapMap Linkage Disequilibrium report for ZMYND8 (45837859 - 45985567 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 3 variations for ZMYND8:    About this table     
    Variant IDTypeSubtypePubMed ID
    esv2663936CNV Deletion23128226
    esv990338CNV Deletion20482838
    esv33497CNV Loss17666407

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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
    2 diseases for ZMYND8:    About MalaCards
    cutaneous t cell lymphoma    breast cancer


    ZMYND8 for disorders           About GeneDecksing

    Genetic Association Database (GAD): ZMYND8
    Human Genome Epidemiology (HuGE) Navigator: ZMYND8 (4 documents)

    Export disorders for ZMYND8 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 ZMYND8 gene, integrated from 9 sources (see all 41):
    (articles sorted by number of sources associating them with ZMYND8)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Identification and characterization of PRKCBP1, a candidate RACK-like protein. (PubMed id 11003709)1, 2, 9 Fossey S.C....Bowden D.W. (2000)
    2. Variation at the NFATC2 locus increases the risk of t hiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipr il and rosiglitazone Medication (DREAM) study. (PubMed id 20628086)1, 4 Bailey S.D....Anand S. (2010)
    3. Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. (PubMed id 17081983)1, 2 Olsen J.V....Mann M. (2006)
    4. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    5. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1, 2 Gerhard D.S....Malek J. (2004)
    6. The DNA sequence and comparative analysis of human chromosome 20. (PubMed id 11780052)1, 2 Deloukas P....Rogers J. (2001)
    7. Serological detection of cutaneous T-cell lymphoma-associated antigens. (PubMed id 11149944)1, 2 Eichmueller S....Schadendorf D. (2001)
    8. Characterization of cDNA clones selected by the GeneMark analysis from size-fractionated cDNA libraries from human brain. (PubMed id 10574461)1, 2 Hirosawa M.... Ohara O. (1999)
    9. Identification of FHOD1-binding proteins and mechanisms of FHOD1-regulated actin dynamics. (PubMed id 15095401)1, 9 Westendorf J.J. and Koka S. (2004)
    10. The SOX2-interactome in brain cancer cells identifies the requirement of MSI2 and USP9X for the growth of brain tumor cells. (PubMed id 23667531)1 Cox J.L....Rizzino A. (2013)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
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      Query String
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 23613 HGNC: 9397 AceView: PRKCBP1 Ensembl:ENSG00000101040 euGenes: HUgn23613
    ECgene: ZMYND8 H-InvDB: ZMYND8

    (According to HUGE)
    About This Section
    HUGE: KIAA1125

    (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 ZMYND8 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 ZMYND8 gene:
    Search GeneIP for patents involving ZMYND8

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



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    GeneCards Homepage - Last full update: 23 Oct 2013 - Incrementals: 4 Nov 2013 , 7 Nov 2013 , 23 Jan 2014

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