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

ZNF138 Gene

protein-coding   GIFtS: 51
GCID: GC07P064254

Zinc Finger Protein 138

(Previous name: zinc finger protein 138 (clone pHZ-32))
  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 1381 2
Zinc Finger Protein 138 (Clone PHZ-32)1 2
pHZ-322

External Ids:    HGNC: 129221   Entrez Gene: 76972   Ensembl: ENSG000001970087   OMIM: 6040805   UniProtKB: P527443   
ORGUL members:         
NONCODE14:n334440 n407951 n407952      

Export aliases for ZNF138 gene to outside databases

Previous GC identifers: GC07P062894 GC07P063652 GC07P063684 GC07P063085 GC07P063698 GC07P063892 GC07P060636


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

GeneCards Summary for ZNF138 Gene: 
ZNF138 (zinc finger protein 138) is a protein-coding gene, and is affiliated with the lncRNA class. Diseases associated with ZNF138 include alagille syndrome, and thyroid adenoma, 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 ZNF85.

UniProtKB/Swiss-Prot: ZN138_HUMAN, P52744
Function: May be involved in transcriptional regulation as a repressor




(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_000007.13  NC_018918.2  NT_007933.15  NT_079593.2  
Regulatory elements:
   Search SABiosciences Regulatory transcription factor binding sites for ZNF138
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmids (see all 2): ZNF138 promoter sequence
   Search SABiosciences Chromatin IP Primers for ZNF138

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat ZNF138


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

Entrez Gene cytogenetic band: 7q11.21   Ensembl cytogenetic band:  7q11.21   HGNC cytogenetic band: 7q11.21

ZNF138 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
ZNF138 gene location

GeneLoc information about chromosome 7         GeneLoc Exon Structure

GeneLoc location for GC07P064254:  view genomic region     (about GC identifiers)

Start:
64,254,766 bp from pter      End:
64,294,054 bp from pter
Size:
39,289 bases      Orientation:
plus strand

1 alternative location:
Chr7+,CRA_TCAG 63,592,365-63,631,620     
ORGUL member locations:
Legend (see complete legend)

ORGUL Member Locations for ZNF138

(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: ZN138_HUMAN, P52744 (See protein sequence)
Recommended Name: Zinc finger protein 138  
Size: 262 amino acids; 30592 Da
Subcellular location: Nucleus (Potential)
Secondary accessions: B4DFX2 B4DP87 E9PHI7 E9PHK7
Alternative splicing: 3 isoforms:  P52744-1   P52744-2   P52744-3   (No experimental confirmation available. Ref.1 (BAG60499) sequence is in conflict in position: 33:M->V)

Explore the universe of human proteins at neXtProt for ZNF138: NX_P52744

Explore proteomics data for ZNF138 at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_P52744

  • ZNF138 Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    ZNF138 Protein Expression
    REFSEQ proteins (7 alternative transcripts): 
    NP_001153655.1  NP_001258566.1  NP_001258567.1  NP_001258568.1  NP_001258569.1  NP_001258578.1  NP_006515.2  

    ENSEMBL proteins: 
     ENSP00000303533   ENSP00000419197   ENSP00000407262   ENSP00000415995   ENSP00000399528  
     ENSP00000352770   ENSP00000380325  
    Reactome Protein details: P52744
    Human Recombinant Protein Products for ZNF138: 
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    Cloud-Clone Corp. Proteins for ZNF138 

    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

    ZNF138 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

    3 InterPro protein domains:
     IPR015880 Znf_C2H2-like
     IPR013087 Znf_C2H2/integrase_DNA-bd
     IPR007087 Znf_C2H2

    Graphical View of Domain Structure for InterPro Entry P52744

    ProtoNet protein and cluster: P52744

    UniProtKB/Swiss-Prot: ZN138_HUMAN, P52744
    Similarity: Belongs to the krueppel C2H2-type zinc-finger protein family
    Similarity: Contains 6 C2H2-type zinc fingers


    ZNF138 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: ZN138_HUMAN, P52744
    Function: May be involved in transcriptional regulation as a repressor

         Genatlas biochemistry entry for ZNF138:
    zinc finger protein 138 (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--
         
    ZNF138 for ontologies           About GeneDecksing


    Phenotypes:
         3 GenomeRNAi human phenotypes for ZNF138:
     Decreased NANOG protein expres  Decreased OCT4 protein express  Decreased POU5F1-GFP protein e 

    Animal Models:
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    1 QIAGEN miScript miRNA Assays for microRNA that regulate ZNF138:
    hsa-miR-629*
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    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 ZNF138 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 ZNF138
        Generic Transcription Pathway
    Gene Expression



    ZNF138 for pathways           About GeneDecksing

    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for ZNF138

    Gene Ontology (GO): 2 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

    ZNF138 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 ZNF138 (ZN138)

    Search CenterWatch for drugs/clinical trials and news about ZNF138 / ZN138

    (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 ZNF138 gene (7 alternative transcripts): 
    NM_001160183.2  NM_001271637.1  NM_001271638.1  NM_001271639.1  NM_001271640.1  NM_001271649.1  NM_006524.3  

    Unigene Cluster for ZNF138:

    Zinc finger protein 138
    Hs.184080  [show with all ESTs]
    Unigene Representative Sequence: NM_001160183
    8 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000307355 ENST00000494380 ENST00000440155 ENST00000440598 ENST00000437743(uc010kzs.3)
    ENST00000430838 ENST00000359735(uc011kdp.2 uc003ttg.3 uc011kdq.2 uc003tth.3)
    ENST00000397136
    miRNA
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    1 QIAGEN miScript miRNA Assays for microRNA that regulate ZNF138:
    hsa-miR-629*
    SwitchGear 3'UTR luciferase reporter plasmidZNF138 3' UTR sequence
    Inhib. RNA
    Products:
         
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    Clone
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                         Customized lentivirus expression plasmids for stable overexpression of ZNF138 
    Primer
    Products:
        
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      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat ZNF138
      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat ZNF138

    Additional mRNA sequence: 

    AK027335.1 AK055644.1 AK294302.1 AK298230.1 BC017945.1 BC037426.1 BC047786.1 BC131762.1 
    BC141847.1 NR_073389.1 NR_073391.1 U09847.1 

    9 DOTS entries:

    DT.423532  DT.101980138  DT.95291270  DT.121053135  DT.100684886  DT.100742918  DT.430330  DT.95307496 
    DT.121053122 

    24/43 AceView cDNA sequences (see all 43):

    AL601377 AK055644 R10020 AI537986 CD675666 CB997873 CA336222 H27785 
    AA678008 AU100551 BC067817 BC037426 AA988400 AU153406 NM_006524 AA983922 
    BU171453 AK027335 AL597519 BX642497 BM995520 U09847 CB995414 BG611334 

    GeneLoc Exon Structure

    2 Alternative Splicing Database (ASD) splice patterns (SP) for ZNF138    About this scheme

    ExUns: 1 ^ 2 ^ 3
    SP1:                  
    SP2:                  


    ECgene alternative splicing isoforms for ZNF138

    (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

    ZNF138 expression in normal human tissues (normalized intensities)      ZNF138 embryonic expression: see
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: CAGGAGAGAA
    ZNF138 Expression
    About this image


    ZNF138 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database 
     5/1 selected tissues (see all 1) fully expand
     
     Gut Tube (Gastrointestinal Tract)
             Definitive endoderm-like cells ( A scalable, suspension protocol for derivation of...

    See ZNF138 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for ZNF138

    SOURCE GeneReport for Unigene cluster: Hs.184080
        SABiosciences Custom PCR Arrays for ZNF138
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for ZNF138

    (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 ZNF138 gene from 1/3 species (see all 3)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    lizard
    (Anolis carolinensis)
    Reptilia --
    Uncharacterized protein
    11(a)
    1 → many
    GL343733.1(125230-159240)
            Species with no ortholog for ZNF138

    ENSEMBL Gene Tree for ZNF138 (if available)
    TreeFam Gene Tree for ZNF138 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for ZNF138 gene
    ZNF852  ZNF4862  ZNF1952  ZNF7272  ZNF922  ZNF1002  ZNF7322  ZNF6752  
    ZNF5062  ZNF662  ZNF2732  ZNF6952  ZNF6262  ZNF6802  ZNF4792  ZNF2532  
    ZNF6822  ZNF4922  ZNF6762  ZNF6812  ZNF1412  ZNF7362  ZNF6792  ZNF2572  
    ZNF2672  ZNF2542  ZNF7372  ZNF982  ZNF7162  ZNF7142  ZNF5192  ZNF4302  
    ZNF7302  ZNF7082  ZNF1172  ZNF4312  ZNF902  ZNF7262  ZNF7282  
    18/482 SIMAP similar genes for ZNF138 using alignment to 5 protein entries:     ZN138_HUMAN (see all proteins) (see all similar genes):
    MGC12518    ZNF738    ZNF415    ZNF554    ZNF78L1    ZNF85
    ZNF675    ZFS-1    ZFS-6    ZNF208    ZNF117    ZNF761
    ZNF257    ZNF813    ZNF92    ZNF492    ZNF737    ZNF724P

    ZNF138 for paralogs           About GeneDecksing


    5/14 Pseudogenes.org Pseudogenes for ZNF138 (see all 14)
    PGOHUM00000257944 PGOHUM00000248283 PGOHUM00000247691 PGOHUM00000235026 PGOHUM00000234233


    (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

    10/1598 SNPs in ZNF138 are shown (see all 1598)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 7 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs58845461,2
    C--64252807(+) TTTTTT/-GGAGA 11 -- us2k1 trp31Minor allele frequency- -:0.50NA 2
    rs1425319531,2
    --64252846(+) ACCACC/TCAGGC 11 -- us2k10--------
    rs69760521,2
    C,F,A,H--64252851(+) ccaggG/Ctgaag 11 -- us2k110Minor allele frequency- C:0.38NA WA CSA EA 371
    rs1460090531,2
    --64252977(+) TTTTTA/GTTTTT 11 -- us2k10--------
    rs1399643551,2
    C--64252999(+) TTTTTA/TATTTT 11 -- us2k10--------
    rs1493350121,2
    C--64253015(+) AGACGC/GAGTCT 11 -- us2k10--------
    rs1444407501,2
    --64253067(+) CTCACG/TGCAAG 11 -- us2k10--------
    rs1920376991,2
    --64253138(+) TTTTTA/CGTAGA 11 -- us2k10--------
    rs1839188461,2
    --64253207(+) CTCCTC/TGGCCT 11 -- us2k10--------
    rs1887142361,2
    C--64253217(+) TCCCAA/GAGTGC 11 -- us2k10--------

    HapMap Linkage Disequilibrium report for ZNF138 (64254766 - 64294054 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 10/13 variations for ZNF138 (see all 13):    About this table     
    Variant IDTypeSubtypePubMed ID
    esv2675483CNV Deletion23128226
    dgv1147e201CNV Deletion23290073
    esv2677316CNV Deletion23128226
    esv2734581CNV Deletion23290073
    esv2422405CNV Duplication17116639
    esv2478591CNV Insertion19546169
    nsv888281CNV Loss21882294
    nsv888279CNV Loss21882294
    nsv508457CNV Loss20534489
    dgv7308n71CNV Gain21882294

    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: 604080    OMIM disorders: --

    5 diseases for ZNF138:    About MalaCards
    alagille syndrome    thyroid adenoma    beckwith-wiedemann syndrome    adenoma
    thyroiditis

    1 disease from the University of Copenhagen DISEASES database for ZNF138:
    Alagille syndrome

    ZNF138 for disorders           About GeneDecksing

    Genetic Association Database (GAD): ZNF138
    Human Genome Epidemiology (HuGE) Navigator: ZNF138 (1 document)

    Export disorders for ZNF138 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 ZNF138 gene integrated from 9 sources:
    (articles sorted by number of sources associating them with ZNF138)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. (PubMed id 20379614)1, 4 Rose J.E....Uhl G.R. (2010)
    2. Genome-wide and candidate gene association study of cigarette smoking behaviors. (PubMed id 19247474)1, 4 Caporaso N....Bergen A.W. (2009)
    3. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    4. 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 Tommerup N. and Vissing H. (1995)
    5. 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)
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    7. The DNA sequence of human chromosome 7. (PubMed id 12853948)2 Hillier L.W.... Wilson R.K. (2003)
    8. 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)
    9. Generation and analysis of 280,000 human expressed sequence tags. (PubMed id 8889549)1 Hillier L.D....Marra M. (1996)

    (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: 7697 HGNC: 12922 AceView: ZNF138 Ensembl:ENSG00000197008 euGenes: HUgn7697
    ECgene: ZNF138 H-InvDB: ZNF138

    (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 ZNF138 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 ZNF138 gene:
    Search GeneIP for patents involving ZNF138

    GeneCards and IP:
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