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

SLFN12 Gene

protein-coding   GIFtS: 40
GCID: GC17M033738

schlafen family member 12

  Search for SLFN12
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(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Aliases
Schlafen Family Member 121 2
FLJ102601
SLFN32

External Ids:    HGNC: 255001   Entrez Gene: 551062   Ensembl: ENSG000001721237   OMIM: 6149555   UniProtKB: Q8IYM23   

Export aliases for SLFN12 gene to outside databases

Previous GC identifers: GC17M030763 GC17M029923


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

  --

(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_000017.10  NC_018928.1  NT_010799.15  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the SLFN12 gene promoter:
         AhR   ISGF-3   RFX1   Lmo2   CUTL1   C/EBPalpha   Arnt   CREB   deltaCREB   HSF2   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidSLFN12 promoter sequence
   Search SABiosciences Chromatin IP Primers for SLFN12

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat SLFN12


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

Entrez Gene cytogenetic band: 17q12   Ensembl cytogenetic band:  17q12   HGNC cytogenetic band: 17q12

SLFN12 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SLFN12 gene location

GeneLoc information about chromosome 17         GeneLoc Exon Structure

GeneLoc location for GC17M033738:  view genomic region     (about GC identifiers)

Start:
33,738,079 bp from pter      End:
33,760,302 bp from pter
Size:
22,224 bases      Orientation:
minus 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: SLN12_HUMAN, Q8IYM2 (See protein sequence)
Recommended Name: Schlafen family member 12  
Size: 578 amino acids; 66972 Da
Secondary accessions: A8K711 Q9NP47

Explore the universe of human proteins at neXtProt for SLFN12: NX_Q8IYM2

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q8IYM2

  • SLFN12 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_060512.3  
    ENSEMBL proteins: 
     ENSP00000378063   ENSP00000302077   ENSP00000394903   ENSP00000398315   ENSP00000404175  

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    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section

    SLFN12 for domains           About GeneDecksing

    1 InterPro domain/family:
     IPR007421 ATPase_AAA-4

    Graphical View of Domain Structure for InterPro Entry Q8IYM2

    ProtoNet protein and cluster: Q8IYM2

    UniProtKB/Swiss-Prot: SLN12_HUMAN, Q8IYM2
    Similarity: Belongs to the Schlafen family


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

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005524ATP binding IEA--


    SLFN12 for ontologies           About GeneDecksing



    (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:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for SLFN12

    (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
    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for SLFN12
    Search CenterWatch for drugs/clinical trials and news about SLFN12 / SLN12 

    (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,
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    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 SLFN12 gene: 
    NM_018042.3  

    Unigene Cluster for SLFN12:

    Schlafen family member 12
    Hs.663548  [show with all ESTs]
    Unigene Representative Sequence: BX647081
    8 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000394562(uc002hjj.4 uc010cts.3) ENST00000304905(uc002hji.4)
    ENST00000452764 ENST00000460530 ENST00000479326 ENST00000447040 ENST00000445092
    ENST00000428476

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    Additional cDNA sequence: 

    AK001122.1 AK291826.1 BC035605.1 BX647081.1 

    6 DOTS entries:

    DT.203232  DT.100713816  DT.121004671  DT.99984644  DT.102829485  DT.40281717 

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

    CA434585 AA279089 AI419354 BQ227558 BE464669 BQ219120 AA279134 AU120577 
    AA761531 AA278409 CB215217 BI520035 AI798759 BG574411 NM_018042 BC035605 
    BF508339 AL708760 BF356869 BX647081 AK001122 BX472393 AI224532 BU853689 

    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

    SLFN12 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: --

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)

    About this image
    See SLFN12 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for SLFN12

    SOURCE GeneReport for Unigene cluster: Hs.663548
        SABiosciences Custom PCR Arrays for SLFN12
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SLFN12

    (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
      --

    ENSEMBL Gene Tree for SLFN12 (if available)
    TreeFam Gene Tree for SLFN12 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for SLFN12 gene
    SLFN132  SLFN142  SLFN12L2  SLFN112  SLFN52  
    5 SIMAP similar genes for SLFN12 using alignment to 3 protein entries:     SLN12_HUMAN (see all proteins):
    SLFN12L    SLFN11    SLFN14    SLFN13    SLFN5

    SLFN12 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

    10/494 NCBI SNPs in SLFN12 are shown (see all 494    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 17 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs620809991,2
    --33737595(+) GTATCC/TCACTC 1 -- ds50012Minor allele frequency- T:0.02NA 122
    rs1125619261,2
    F,--33737615(+) TCATCT/CTGGTC 1 -- ds50013Minor allele frequency- C:0.06CSA WA 122
    rs1847510231,2
    --33737653(+) ATGCCA/GGACCC 1 -- ds50010--------
    rs620810001,2
    F,--33737687(+) GAAAAC/GTCTCG 1 -- ds50011Minor allele frequency- G:0.02NA 120
    rs1892633021,2
    --33737692(+) CTCTCA/GTTGTC 1 -- ds50010--------
    rs1452586481,2
    C,--33737746(+) TAGTT-/AAGAGA 1 -- ds50010--------
    rs345407211,2
    C,F,--33737769(+) TTTTGT/ACATCT 1 -- ds500111Minor allele frequency- A:0.15NA WA CSA EA 551
    rs1169289261,2
    --33737777(+) TCTCAC/TGCTTC 1 -- ds50011Minor allele frequency- T:0.01EA 120
    rs1453164581,2
    --33737871(+) ACAACC/TCTTCC 1 -- ds50010--------
    rs1476065181,2
    --33737900(+) TAGCTC/TAAGAA 1 -- ds50010--------

    HapMap Linkage Disequilibrium report for SLFN12 (33738079 - 33760302 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 2 variations for SLFN12
         2 CNVs: 49846 53288

    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, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

    SLFN12 for disorders           About MalaCards

    SLFN12 for disorders           About GeneDecksing

    OMIM gene information: 614955    OMIM disorders: --


    Export disorders for SLFN12 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 SLFN12 gene integrated from 9 sources:
    (articles sorted by number of sources associating them with SLFN12)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. 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)
    2. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    3. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. (PubMed id 12477932)1, 3 Strausberg R.L....Marra M.A. (2002)
    4. Schlafen, a new family of growth regulatory genes that affect thymocyte development. (PubMed id 9846487)1 Schwarz D.A....Hedrick S.M. (1998)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Free Text  

      Query String
    PubMed
    OMIM
    NCBI Bookshelf
      (Note: In FireFox, select the above section and copy using Ctrl-C)

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 55106 HGNC: 25500 AceView: FLJ10260 Ensembl:ENSG00000172123 euGenes: HUgn55106
    ECgene: SLFN12 H-InvDB: SLFN12

    (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 SLFN12 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 SLFN12 gene:
    Search GeneIP for patents involving SLFN12

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



    (Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Uscn, Thermo Fisher Scientific, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript and LifeMap BioReagents, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences),
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    GeneCards Homepage - Last full update: 19 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 26 Apr 2013

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