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

ZNF135 Gene

protein-coding   GIFtS: 57
GCID: GC19P058587

Zinc Finger Protein 135

(Previous names: zinc finger protein 61, zinc finger protein 135 (clone pHZ-17))
(Previous symbols: ZNF61, ZNF78L1)
  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

This gene clusters with an RNA gene
Subcategory (RNA class): lncRNA

Quality score for the ORGUL clustered with this gene is 3

Aliases
Zinc Finger Protein 1351 2     pHZ-172
Zinc Finger Protein 611 2 3     pT32
ZNF611 2 3     Zinc Finger Protein 78-Like 1 (PT3)2
ZNF78L11 2 3     Zinc Finger Protein 78-Like 13
Zinc Finger Protein 135 (Clone PHZ-17)1 2     

External Ids:    HGNC: 129191   Entrez Gene: 76942   Ensembl: ENSG000001762937   OMIM: 6040775   UniProtKB: P527423   
ORGUL members:         
NONCODE14:n338971 n335909      

Export aliases for ZNF135 gene to outside databases

Previous GC identifers: GC19P059476 GC19P059025 GC19P063246 GC19P063263 GC19P063060 GC19P063264 GC19P058571 GC19P054881 GC19P058573 GC19P058577


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

GeneCards Summary for ZNF135 Gene: 
ZNF135 (zinc finger protein 135) is a protein-coding gene, and is affiliated with the lncRNA class. Diseases associated with ZNF135 include renal pelvis carcinoma, and glottis carcinoma, and among its related super-pathways are Gene Expression. GO annotations related to this gene include DNA binding and sequence-specific DNA binding transcription factor activity. An important paralog of this gene is ZNF420.

UniProtKB/Swiss-Prot: ZN135_HUMAN, P52742
Function: Plays a role in the regulation of cell morphology and cytoskeletal organization. May be involved in
transcriptional regulation




(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_000019.9  NT_011109.16  NC_018930.2  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the ZNF135 gene promoter:
         Elk-1   p53   Pax-2   Pax-2a   AREB6   Pax-2b   HOXA5   ARP-1   Zic3   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidZNF135 promoter sequence
   Search SABiosciences Chromatin IP Primers for ZNF135

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat ZNF135


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

Entrez Gene cytogenetic band: 19q13.4   Ensembl cytogenetic band:  19q13.43   HGNC cytogenetic band: 19q13.4

ZNF135 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
ZNF135 gene location

GeneLoc information about chromosome 19         GeneLoc Exon Structure

GeneLoc location for GC19P058587:  view genomic region     (about GC identifiers)

Start:
58,570,607 bp from pter      End:
58,597,677 bp from pter
Size:
27,071 bases      Orientation:
plus strand
ORGUL member locations:
Legend (see complete legend)

ORGUL Member Locations for ZNF135

(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: ZN135_HUMAN, P52742 (See protein sequence)
Recommended Name: Zinc finger protein 135  
Size: 658 amino acids; 75261 Da
Subcellular location: Nucleus (Potential)
Sequence caution: Sequence=AAC50254.1; Type=Frameshift; Positions=207, 558, 563;
Secondary accessions: B4DHH9 E9PEV2 F5GYY9 I3L0B3 Q5U5L3 Q8N1I7
Alternative splicing: 4 isoforms:  P52742-1   P52742-2   P52742-3   P52742-4   (Gene prediction based on EST data)

Explore the universe of human proteins at neXtProt for ZNF135: NX_P52742

Explore proteomics data for ZNF135 at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_P52742

  • ZNF135 Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    ZNF135 Protein Expression
    REFSEQ proteins (5 alternative transcripts): 
    NP_001157999.1  NP_001158001.1  NP_001158002.1  NP_003427.3  NP_009065.1  

    ENSEMBL proteins: 
     ENSP00000369437   ENSP00000441410   ENSP00000321406   ENSP00000422074   ENSP00000427691  
     ENSP00000471344   ENSP00000444828  
    Reactome Protein details: P52742
    Human Recombinant Protein Products for ZNF135: 
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    Cloud-Clone Corp. Proteins for ZNF135 

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005622intracellular ----
    GO:0005634nucleus NAS7557990

    ZNF135 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: 
    ZNF: Zinc fingers, C2H2-type

    4 InterPro protein domains:
     IPR015880 Znf_C2H2-like
     IPR001909 Krueppel-associated_box
     IPR013087 Znf_C2H2/integrase_DNA-bd
     IPR007087 Znf_C2H2

    Graphical View of Domain Structure for InterPro Entry P52742

    ProtoNet protein and cluster: P52742

    1 Blocks protein domain: IPB007086 C2H2-type zinc finger signature

    UniProtKB/Swiss-Prot: ZN135_HUMAN, P52742
    Similarity: Belongs to the krueppel C2H2-type zinc-finger protein family
    Similarity: Contains 16 C2H2-type zinc fingers
    Similarity: Contains 1 KRAB domain


    ZNF135 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: ZN135_HUMAN, P52742
    Function: Plays a role in the regulation of cell morphology and cytoskeletal organization. May be involved in
    transcriptional regulation

         Genatlas biochemistry entry for ZNF135:
    zinc finger protein 135 (C2H2 type,Kruppel-like)

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003676nucleic acid binding ----
    GO:0003677DNA binding IEA--
    GO:0003700sequence-specific DNA binding transcription factor activity NAS7557990
    GO:0008270zinc ion binding ----
    GO:0046872metal ion binding IEA--
         
    ZNF135 for ontologies           About GeneDecksing


    Phenotypes:
         1 GenomeRNAi human phenotype for ZNF135:
     Increased G1 DNA content 

    Animal Models:
       inGenious Targeting Laboratory - Custom generated mouse model solutions for ZNF135 
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    2 QIAGEN miScript miRNA Assays for microRNAs that regulate ZNF135:
    hsa-miR-345 hsa-miR-29b-1*
    SwitchGear 3'UTR luciferase reporter plasmidZNF135 3' UTR sequence
    Inhib. RNA
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for ZNF135


    (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 ZNF135 About                                                                                                See pathways by source

    SuperPathContained pathways About
    1Generic Transcription Pathway
    Generic Transcription Pathway0.47
    Gene Expression0.47

    Pathways by source                                                                                                                                                                 See SuperPaths
    Show all pathways


    2        Reactome Pathways for ZNF135
        Generic Transcription Pathway
    Gene Expression



    ZNF135 for pathways           About GeneDecksing

    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for ZNF135

    STRING Interaction Network Preview (showing 1 interactants - click image to see more details)

    5/7 Interacting proteins for ZNF135 (P527422, 3 ENSP000003214064) via UniProtKB, MINT, STRING, and/or I2D (see all 7)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    ANXA7P200732, 3MINT-8248981 I2D: score=1 
    CDKN1AP389362, 3MINT-8252494 I2D: score=1 
    GADD45AP245222, 3MINT-8256140 I2D: score=1 
    GSK3BP498412, 3MINT-8257856 I2D: score=1 
    RAP1BP612242, 3MINT-8268185 I2D: score=1 
    About this table

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006351transcription, DNA-dependent IEA--
    GO:0006355regulation of transcription, DNA-dependent NAS7557990
    GO:0007010cytoskeleton organization IMP--
    GO:0022604regulation of cell morphogenesis IMP--

    ZNF135 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 ZNF135 (ZN135)

    Search CenterWatch for drugs/clinical trials and news about ZNF135 / ZN135

    (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 ZNF135 gene (5 alternative transcripts): 
    NM_001164527.1  NM_001164529.1  NM_001164530.1  NM_003436.3  NM_007134.1  

    Unigene Cluster for ZNF135:

    Zinc finger protein 135
    Hs.85863  [show with all ESTs]
    Unigene Representative Sequence: AL157426
    7 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000359978(uc002qrd.2) ENST00000401053(uc010yhq.2 uc010yhr.2 uc021vcu.1 uc002qrg.3)
    ENST00000313434(uc002qre.3) ENST00000511556 ENST00000506786(uc002qrf.3)
    ENST00000515535 ENST00000439855(uc021vct.1)
    miRNA
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    2 QIAGEN miScript miRNA Assays for microRNAs that regulate ZNF135:
    hsa-miR-345 hsa-miR-29b-1*
    SwitchGear 3'UTR luciferase reporter plasmidZNF135 3' UTR sequence
    Inhib. RNA
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      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat ZNF135

    Additional mRNA sequence: 

    AK094202.1 AK095796.1 AK098011.1 AK295110.1 AK297226.1 AL157426.1 AL833637.1 BC046434.1 
    BX647775.1 U09413.1 X65231.1 

    21 DOTS entries:

    DT.91775293  DT.100673715  DT.109676  DT.101981444  DT.95273940  DT.95273948  DT.75168482  DT.441381 
    DT.121438340  DT.121438298  DT.100000454  DT.99936969  DT.121438333  DT.107819  DT.121304337  DT.97777811 
    DT.121438337  DT.121438349  DT.95321894  DT.95364045  DT.99962472 

    24/67 AceView cDNA sequences (see all 67):

    BG678919 BM683265 AA436237 AI684767 AK094202 AK095796 CA450496 N67262 
    BX642404 BX454973 BP368295 BM720171 BX642405 BG541687 CN479421 BC046434 
    NM_003436 BX118276 AI288798 AI333583 BF347790 BE696848 AA436236 BM993886 

    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

    ZNF135 expression in normal human tissues (normalized intensities)      ZNF135 embryonic expression: see
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: GGGAAACTCC
    ZNF135 Expression
    About this image


    ZNF135 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database 
     5/33 selected tissues (see all 33) fully expand
     
     Brain (Nervous System)    fully expand to see all 5 entries
             Cerebral Cortex
             cortex   
     
     Epithelium
             cervix, uterine ; squamous epithelial cells   
     
     Uterus
             uterus, post-menopause ; glandular cells   
     
     Testis (Reproductive System)    fully expand to see all 4 entries
             Leydig Cells Testis Interstitium
             seminal vesicle ; glandular cells   
     
     Colon (Gastrointestinal Tract)    fully expand to see all 4 entries
             colon ; peripheral nerve/ganglion   

    See ZNF135 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for ZNF135

    SOURCE GeneReport for Unigene cluster: Hs.85863
        SABiosciences Custom PCR Arrays for ZNF135
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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 chordates.

    Orthologs for ZNF135 gene from 2/7 species (see all 7)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    dog
    (Canis familiaris)
    Mammalia --
    --
    48(a)
    possible ortholog
    1(106520300-106536984)
    lizard
    (Anolis carolinensis)
    Reptilia ZNF486
    --
    Uncharacterized protein
    39(a)
    38(a)
    1 ↔ many
    possible ortholog
    GL343516.1(205193-231700)
    2(194885249-194899810)


    ENSEMBL Gene Tree for ZNF135 (if available)
    TreeFam Gene Tree for ZNF135 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for ZNF135 gene
    ZNF4202  ZNF780A2  ZNF6652  ZNF724P2  ZNF72  ZNF232  ZNF4322  ZNF33A2  
    ZNF2342  ZNF302  ZNF5732  ZNF4292  ZNF5402  ZNF2512  ZNF6052  ZNF842  
    ZNF1892  ZNF5712  ZNF6302  ZNF932  ZNF162  ZNF2832  ZNF3472  ZNF4842  
    ZNF1842  ZNF585B2  ZNF412  ZNF6152  ZNF5692  ZNF4702  
    18/549 SIMAP similar genes for ZNF135 using alignment to 4 protein entries:     ZN135_HUMAN (see all proteins) (see all similar genes):
    ZNF78L1    ZNF818P    DKFZp313M0722    ZNF323    ZFP41    ZNF826P
    DKFZp686H10254    ZNF56    ZNF852    ZSCAN16    ZSCAN21    DKFZp666C237
    HZF36    ZFS-1    ZFS-6    ZNF146    ZNF167    ZNF345

    ZNF135 for paralogs           About GeneDecksing


    5 Pseudogenes.org Pseudogenes for ZNF135
    PGOHUM00000256878 PGOHUM00000256899 PGOHUM00000240826 PGOHUM00000233477 PGOHUM00000257273


    (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

    10/377 SNPs in ZNF135 are shown (see all 377)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 19 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs2017244431,2
    --58568630(+) AAAGA-/TTTTTT 5 -- us2k10--------
    rs1923882911,2
    C--58568639(+) TTTTTA/TAAAGG 5 -- us2k10--------
    rs1492313871,2
    --58568814(+) ATGGTC/GGGGGG 5 -- us2k10--------
    rs1147029691,2
    C,F--58568884(+) AGCCAA/GGAAGG 5 -- us2k11Minor allele frequency- G:0.01WA 118
    rs116674821,2
    C,F,A,H--58568958(+) GGCACT/CGGAGT 5 -- us2k116Minor allele frequency- C:0.50NS NA WA CSA EA 608
    rs1843993771,2
    --58568995(+) GTAGAA/GTGTTA 5 -- us2k10--------
    rs9741831,2
    C,F,H--58569118(-) GGGTCG/CTGCGG 5 -- us2k114Minor allele frequency- C:0.35EA NS NA WA 862
    rs730718741,2
    C,F--58569169(+) AGCCCG/ACCCCT 5 -- us2k11Minor allele frequency- A:0.02NA 120
    rs1424534971,2
    --58569176(+) CCCTGA/CAAAAG 5 -- us2k10--------
    rs1896879771,2
    --58569190(+) GTACGA/GTTTAG 5 -- us2k10--------

    HapMap Linkage Disequilibrium report for ZNF135 (58570607 - 58597677 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 6 variations for ZNF135:    About this table     
    Variant IDTypeSubtypePubMed ID
    nsv912533CNV Loss21882294
    nsv912535CNV Loss21882294
    nsv912534CNV Loss21882294
    nsv833885CNV Loss17160897
    nsv828656CNV Gain20364138
    nsv458836CNV Gain19166990

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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: 604077    OMIM disorders: --

    10 diseases for ZNF135:    About MalaCards
    renal pelvis carcinoma    glottis carcinoma    hydronephrosis    gallbladder cancer
    esophageal cancer    thyroid cancer    esophagitis    renal cell carcinoma
    thyroiditis    colorectal cancer

    9 diseases from the University of Copenhagen DISEASES database for ZNF135:
    Carcinoma     Prostate cancer     Urinary bladder cancer     Renal cell carcinoma
    Ureteral benign neoplasm     Gallbladder cancer     Colorectal cancer     Renal pelvis carcinoma
    Esophageal cancer

    ZNF135 for disorders           About GeneDecksing

    Genetic Association Database (GAD): ZNF135

    Export disorders for ZNF135 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 ZNF135 gene, integrated from 9 sources (see all 15):
    (articles sorted by number of sources associating them with ZNF135)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Isolation and fine mapping of 16 novel human zinc finger-encoding cDNAs identify putative candidate genes for developmental and malignant disorders. (PubMed id 7557990)1, 2, 3 Tommerup N. and Vissing H. (1995)
    2. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    3. Clustering of C2-H2 zinc finger motif sequences within telomeric and fragile site regions of human chromosomes. (PubMed id 1505991)1, 3 Lichter P....Ward D.C. (1992)
    4. Methods for quantification of in vivo changes in prote in ubiquitination following proteasome and deubiquitinase inhibition. (PubMed id 22505724)1 Udeshi N.D....Carr S.A. (2012)
    5. Identification and characterization of a set of conserved and new regulators of cytoskeletal organisation, cell morphology and migration. (PubMed id 21834987)2 Bai S.W.... Ridley A.J. (2011)
    6. A directed protein interaction network for investigat ing intracellular signal transduction. (PubMed id 21900206)1 Vinayagam A....Wanker E.E. (2011)
    7. Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. (PubMed id 17903300)4 Fox C.S....Atwood L.D. (2007)
    8. A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. (PubMed id 17903292)4 Hwang S.J....Fox C.S. (2007)
    9. Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. (PubMed id 16344560)1 Kimura K.... Sugano S. (2006)
    10. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)2 Gerhard D.S....Malek J. (2004)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 7694 HGNC: 12919 AceView: ZNF135 Ensembl:ENSG00000176293 euGenes: HUgn7694
    ECgene: ZNF135 H-InvDB: ZNF135

    (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 ZNF135 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 ZNF135 gene:
    Search GeneIP for patents involving ZNF135

    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: 3 Nov 2013 , 7 Nov 2013 , 23 Jan 2014

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