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

SLAIN1 Gene

protein-coding   GIFtS: 45
GCID: GC13P078272

SLAIN motif family, member 1

(Previous name: chromosome 13 open reading frame 32 )
(Previous symbol: C13orf32)
  Search for SLAIN1
in our new
 Human Malady Compendium 
Biological research products
for SLAIN1
    

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

Aliases
SLAIN Motif Family, Member 11 2
C13orf321 2 3
FLJ300461
Chromosome 13 Open Reading Frame 321
SLAIN Motif-Containing Protein 12

External Ids:    HGNC: 263871   Entrez Gene: 1220602   Ensembl: ENSG000001397377   OMIM: 6104915   UniProtKB: Q8ND833   

Export aliases for SLAIN1 gene to outside databases

Previous GC identifers: GC13P077170 GC13P058971


(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_000013.10  NC_018924.1  NT_024524.14  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the SLAIN1 gene promoter:
         Egr-3   C/EBPbeta   Sox5   AML1a   HOXA3   FOXD1   LCR-F1   Roaz   S8   En-1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidSLAIN1 promoter sequence
   Search SABiosciences Chromatin IP Primers for SLAIN1

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat SLAIN1


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

Entrez Gene cytogenetic band: 13q22.3   Ensembl cytogenetic band:  13q22.3   HGNC cytogenetic band: 13q22.3

SLAIN1 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SLAIN1 gene location

GeneLoc information about chromosome 13         GeneLoc Exon Structure

GeneLoc location for GC13P078272:  view genomic region     (about GC identifiers)

Start:
78,272,023 bp from pter      End:
78,338,377 bp from pter
Size:
66,355 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: SLAI1_HUMAN, Q8ND83 (See protein sequence)
Recommended Name: SLAIN motif-containing protein 1  
Size: 568 amino acids; 60595 Da
Sequence caution: Sequence=AAI11498.1; Type=Erroneous initiation; Sequence=CAD39000.2; Type=Erroneous initiation;
Sequence=CAI12505.1; Type=Erroneous gene model prediction; Sequence=CAI12509.1; Type=Erroneous gene model prediction;
Secondary accessions: A8K0Z9 B7Z209 Q5T6P4 Q5T6P7 Q8ND10 Q96NV0
Alternative splicing: 4 isoforms:  Q8ND83-1   Q8ND83-2   Q8ND83-3   Q8ND83-4   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for SLAIN1: NX_Q8ND83

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q8ND83

  • SLAIN1 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins (6 alternative transcripts): 
    NP_001035243.2  NP_001229797.1  NP_001229798.1  NP_001229799.1  NP_001229800.1  NP_653196.1  

    ENSEMBL proteins: 
     ENSP00000389195   ENSP00000419730   ENSP00000403049   ENSP00000393990   ENSP00000418707  
     ENSP00000366444   ENSP00000267219   ENSP00000403056   ENSP00000420320   ENSP00000420619  
     ENSP00000419436   ENSP00000418053   ENSP00000351507   ENSP00000400921   ENSP00000314546  
     ENSP00000314443  

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    Uscn Proteins for SLAIN1


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    Uscn ELISAs and CLIAs for SLAIN1


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

    SLAIN1 for domains           About GeneDecksing

    1 InterPro domain/family:
     IPR026179 Slain

    Graphical View of Domain Structure for InterPro Entry Q8ND83

    ProtoNet protein and cluster: Q8ND83

    UniProtKB/Swiss-Prot: SLAI1_HUMAN, Q8ND83
    Similarity: Belongs to the SLAIN motif-containing 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

    miRNA
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    hsa-miR-301a hsa-miR-218 hsa-miR-519a hsa-miR-373* hsa-miR-548l hsa-miR-7-1* hsa-miR-130b hsa-miR-626
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    Inhib. RNA
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    Animal Models:
         1 MGI mutant phenotype (inferred from 2 alleles(MGI details for Slain1):
     no phenotypic analysis 

    SLAIN1 for phenotypes           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 SLAIN1

    (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 SLAIN1
    Search CenterWatch for drugs/clinical trials and news about SLAIN1 / SLAI1 

    (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, 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 SLAIN1 gene (6 alternative transcripts): 
    NM_001040153.3  NM_001242868.1  NM_001242869.1  NM_001242870.1  NM_001242871.1  NM_144595.3  

    Unigene Cluster for SLAIN1:

    SLAIN motif family, member 1
    Hs.349955  [show with all ESTs]
    Unigene Representative Sequence: NM_001242868
    17 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000422114 ENST00000466548(uc001vkk.2) ENST00000446759 ENST00000442759
    ENST00000488699 ENST00000377236 ENST00000267219 ENST00000465831 ENST00000441784
    ENST00000462234 ENST00000496045 ENST00000474663 ENST00000481614 ENST00000358679
    ENST00000418532(uc010thy.1) ENST00000351546(uc010thz.1 uc001vkl.1 uc010aex.1 uc010aey.1 uc001vkm.2)
    ENST00000314070

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    8/22 QIAGEN miScript miRNA Assays for microRNAs that regulate SLAIN1 (see all 22):
    hsa-miR-301a hsa-miR-218 hsa-miR-519a hsa-miR-373* hsa-miR-548l hsa-miR-7-1* hsa-miR-130b hsa-miR-626
    SwitchGear 3'UTR luciferase reporter plasmidSLAIN1 3' UTR sequence
    Inhib. RNA
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    OriGene siRNA: SLAIN1
    QIAGEN FlexiTube/FlexiPlate siRNA for gene silencing in human, mouse, rat SLAIN1
    Clone
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    Additional cDNA sequence: 

    AK054608.1 AK094337.1 AK289600.1 AK289714.1 AK294201.1 AK295423.1 AL834203.1 AL834332.1 
    BC045177.1 BC111497.1 

    10 DOTS entries:

    DT.100674073  DT.92433022  DT.100741650  DT.100022594  DT.92433017  DT.120780565  DT.40132759  DT.213893 
    DT.120780587  DT.92433023 

    24/113 AceView cDNA sequences (see all 113):

    BU191358 AA476671 AA974487 AI459104 BU183003 AK094337 CK904607 BM721521 
    BP347995 BU180065 BG392851 BM677151 T32870 Z45095 BM702624 AA446625 
    AV718254 BP348647 AV705265 AL834332 AL834203 AI341345 AA931158 AI423737 

    GeneLoc Exon Structure

    5/9 Alternative Splicing Database (ASD) splice patterns (SP) for SLAIN1 (see all 9)    About this scheme

    ExUns: 1a · 1b ^ 2 ^ 3a · 3b ^ 4 ^ 5 ^ 6a · 6b ^ 7 ^ 8a · 8b · 8c ^ 9 ^ 10a · 10b · 10c ^ 11
    SP1:                                -     -     -     -                                                         
    SP2:                                                                                                            
    SP3:              -     -     -     -     -     -     -                                                         
    SP4:                    -     -     -     -                                                                     
    SP5:                                -     -                                                                     


    ECgene alternative splicing isoforms for SLAIN1

    (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

    SLAIN1 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: AGCTCATTGC

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

    About this image

    SLAIN1 expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    1 LifeMap In Vivo Development Anatomical Compartment/Cell 
    Tissue Anatomical Compartment CellCategory (developmental path)
    OvaryOvigerous CordOvarian Somatic CellsOvary
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization
    Stem Cell Differentiation: 1 LifeMap Cell 
    NameCategory
    Line H9 (WA09) (Embryonic Stem Cell)Early Embryo, Inner Cell Mass

    See SLAIN1 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for SLAIN1

    SOURCE GeneReport for Unigene cluster: Hs.349955

    UniProtKB/Swiss-Prot: SLAI1_HUMAN, Q8ND83
    Tissue specificity: Expressed in embryonic stem cells

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    In Situ
    Assay Products:
     

     
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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 SLAIN1 gene from 4/12 species (see all 12)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves SLAIN11 SLAIN motif family, member 1 76.15(n)
    79.32(a)
      418807  XM_417002.3  XP_417002.3 
    lizard
    (Anolis carolinensis)
    Reptilia SLAIN16
    --
    81(a)
    1 ↔ 1
    3(86179555-86209940)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.24292 Xenopus laevis transcribed sequences 77.05(n)    BG410030.1 
    zebrafish
    (Danio rerio)
    Actinopterygii slain1b6
    slain1a6
    SLAIN motif family, member 1a
    50(a)
    34(a)
    1 ↔ many
    1 ↔ many
    6(59671251-59696160)
    9(17864963-17902674)


    ENSEMBL Gene Tree for SLAIN1 (if available)
    TreeFam Gene Tree for SLAIN1 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for SLAIN1 gene
    SLAIN22  
    1 SIMAP similar gene for SLAIN1 using alignment to 9 protein entries:     SLAI1_HUMAN (see all proteins):
    SLAIN2

    SLAIN1 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

    10/1067 NCBI SNPs in SLAIN1 are shown (see all 1067    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 13 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1910199381,2
    --78270224(+) GCATCC/TGCCAC 1 -- us2k10--------
    rs1469721081,2
    --78270337(+) GATATA/GCCGAA 1 -- us2k10--------
    rs801889911,2
    C,--78270340(+) ATACCA/GAAACT 1 -- us2k10--------
    rs1828493901,2
    --78270388(+) GGCTAC/GCAAGC 1 -- us2k10--------
    rs1408793041,2
    --78270449(+) TGGAAA/GCGCTC 1 -- us2k10--------
    rs767555821,2
    --78270451(+) GAAGCA/GCTCAC 1 -- us2k10--------
    rs1875335741,2
    --78270494(+) ACACAC/GAAGCT 1 -- us2k10--------
    rs1931585171,2
    --78270526(+) AGAAGA/GTACAA 1 -- us2k10--------
    rs1386563781,2
    --78270842(+) CGTTTG/TCCAAG 1 -- us2k10--------
    rs38611331,2
    C,F,A,H,--78270954(+) ACTTAC/TACATT 1 -- us2k122Minor allele frequency- T:0.44NS EA NA WA CSA 2344

    HapMap Linkage Disequilibrium report for SLAIN1 (78272023 - 78338377 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 1 variation for SLAIN1
         1 CNV: 66489

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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

    SLAIN1 for disorders           About MalaCards

    SLAIN1 for disorders           About GeneDecksing

    OMIM gene information: 610491    OMIM disorders: --


    Export disorders for SLAIN1 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 SLAIN1 gene integrated from 9 sources:
    (articles sorted by number of sources associating them with SLAIN1)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Transcriptional profiling of mouse and human ES cells identifies SLAIN1, a novel stem cell gene. (PubMed id 16546155)1, 2, 3 Hirst C.E....Elefanty A.G. (2006)
    2. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    3. Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions. (PubMed id 19690332)2 Mayya V.... Han D.K. (2009)
    4. The full-ORF clone resource of the German cDNA consortium. (PubMed id 17974005)2 Bechtel S.... Schupp I. (2007)
    5. 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)
    6. The DNA sequence and analysis of human chromosome 13. (PubMed id 15057823)2 Dunham A.... Ross M.T. (2004)
    7. 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)
    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)

    (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: 122060 HGNC: 26387 AceView: FLJ30046 Ensembl:ENSG00000139737 euGenes: HUgn122060
    ECgene: SLAIN1 H-InvDB: SLAIN1

    (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 SLAIN1 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 SLAIN1 gene:
    Search GeneIP for patents involving SLAIN1

    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),
    In Situ Hybridization Assays from
    Advanced Cell Diagnostics
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    GeneCards Homepage - Last full update: 18 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 26 Apr 2013

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