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

INIP Gene

protein-coding   GIFtS: 36
GCID: GC09M115449

INTS3 And NABP Interacting Protein

(Previous name: chromosome 9 open reading frame 80)
(Previous symbol: C9orf80)
  Search for INIP
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
INTS3 And NABP Interacting Protein1 2     hSSBIP12 3
C9orf801 2 3 5     INTS3- And NABP-Interacting Protein2 3
Sensor Of Single-Strand DNA Complex Subunit C1 2 3     SSB-Interacting Protein 12 3
HSSB-Interacting Protein 11 2     SOSSC2 5
Minute INTS3/HSSB-Associated Element1 2     Chromosome 9 Open Reading Frame 801
Sensor Of SsDNA Subunit C2 3     HSPC0432
Single-Stranded DNA-Binding Protein-Interacting Protein 12 3     MISE2
SOSS-C2 3     SOSS Complex Subunit C2
SSBIP12 3     

External Ids:    HGNC: 249941   Entrez Gene: 584932   Ensembl: ENSG000001481537   OMIM: 6132735   UniProtKB: Q9NRY23   

Export aliases for INIP gene to outside databases


(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 INIP Gene:
SOSSC is a subunit of single-stranded DNA (ssDNA)-binding complexes involved in the maintenance of genome
stability (Huang et al., 2009) (PubMed 19683501).(supplied by OMIM, Feb 2010)

GeneCards Summary for INIP Gene: 
INIP (INTS3 and NABP interacting protein) is a protein-coding gene. GO annotations related to this gene include protein binding.

UniProtKB/Swiss-Prot: SOSSC_HUMAN, Q9NRY2
Function: Component of the SOSS complex, a multiprotein complex that functions downstream of the MRN complex to
promote DNA repair and G2/M checkpoint. The SOSS complex associates with single-stranded DNA at DNA lesions and
influences diverse endpoints in the cellular DNA damage response including cell-cycle checkpoint activation,
recombinational repair and maintenance of genomic stability. Required for efficient homologous
recombination-dependent repair of double-strand breaks (DSBs) and ATM-dependent signaling pathways




(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_000009.11  NC_018920.2  NT_008470.19  
Regulatory elements:
   Search SABiosciences Regulatory transcription factor binding sites for INIP
         Other transcription factors

Browse SwitchGear Promoter luciferase reporter plasmids
   Search SABiosciences Chromatin IP Primers for INIP

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


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

Entrez Gene cytogenetic band: 9q32   Ensembl cytogenetic band:  9q32   HGNC cytogenetic band: 9q32

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

GeneLoc information about chromosome 9         GeneLoc Exon Structure

GeneLoc location for GC09M115449:  view genomic region     (about GC identifiers)

Start:
115,446,206 bp from pter      End:
115,480,516 bp from pter
Size:
34,311 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: SOSSC_HUMAN, Q9NRY2 (See protein sequence)
Recommended Name: SOSS complex subunit C  
Size: 104 amino acids; 11425 Da
Subunit: Component of the SOSS complex, composed of SOSS-B (SOSS-B1/NABP2 or SOSS-B2/NABP1), SOSS-A/INTS3 and
SOSS-C/INIP. SOSS complexes containing SOSS-B1/NABP2 are more abundant than complexes containing SOSS-B2/NABP1.
Interacts with INTS3; the interaction is direct
Subcellular location: Nucleus. Note=Localizes to nuclear foci following DNA damage
Sequence caution: Sequence=AAF28969.1; Type=Erroneous initiation; Sequence=AAH13097.1; Type=Erroneous initiation;
Sequence=CAH71934.1; Type=Erroneous gene model prediction;
Secondary accessions: Q5VWJ7 Q96E04 Q9P090
Alternative splicing: 2 isoforms:  Q9NRY2-1   Q9NRY2-2   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for INIP: NX_Q9NRY2

Explore proteomics data for INIP at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q9NRY2

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

    INIP Protein Expression
    REFSEQ proteins: NP_067041.1  
    ENSEMBL proteins: 
     ENSP00000363360   ENSP00000363353   ENSP00000363351   ENSP00000363355  

    Human Recombinant Protein Products for INIP: 
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    OriGene Protein Over-expression Lysate for INIP
    OriGene MassSpec for INIP 
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    GenScript Custom Purified and Recombinant Proteins Services for INIP
    Novus Biologicals INIP Protein
    Novus Biologicals INIP Lysate
    Browse Sino Biological Recombinant Proteins
    Browse Sino Biological Cell Lysates 
    Browse ProSpec Recombinant Proteins
    Browse Proteins at Cloud-Clone Corp. 

    Gene Ontology (GO): 3 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus IDA--
    GO:0005730NOT nucleolus IDA--
    GO:0070876SOSS complex IDA18449195

    INIP for ontologies           About GeneDecksing



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    Abcam antibodies for INIP
    Browse Antibodies at Cloud-Clone Corp. 
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    Search LSBio for Antibodies for INIP 

    Assay Products for INIP: 
    Browse Kits and Assays available from EMD Millipore
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    Browse Enzo Life Sciences for kits & assays
    Browse ELISAs at Cloud-Clone Corp. 
    Browse CLIAs at Cloud-Clone Corp.


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

    ProtoNet protein and cluster: Q9NRY2

    UniProtKB/Swiss-Prot: SOSSC_HUMAN, Q9NRY2
    Similarity: Belongs to the SOSS-C family


    (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: SOSSC_HUMAN, Q9NRY2
    Function: Component of the SOSS complex, a multiprotein complex that functions downstream of the MRN complex to
    promote DNA repair and G2/M checkpoint. The SOSS complex associates with single-stranded DNA at DNA lesions and
    influences diverse endpoints in the cellular DNA damage response including cell-cycle checkpoint activation,
    recombinational repair and maintenance of genomic stability. Required for efficient homologous
    recombination-dependent repair of double-strand breaks (DSBs) and ATM-dependent signaling pathways

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005515protein binding IPI19683501
         
    INIP for ontologies           About GeneDecksing


    Phenotypes:
         1 GenomeRNAi human phenotype for INIP:
     Increased S DNA content 

    Animal Models:
       inGenious Targeting Laboratory - Custom generated mouse model solutions for INIP 
       inGenious Targeting Laboratory - Custom generated inducible mouse model solutions for INIP

       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for INIP 
       genOway customized Knockin model: humanization, point mutation, expression monitoring, etc. for INIP 

    miRNA
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    QIAGEN Custom miScript Target Protector blocks miRNA-binding site of human, mouse, rat INIP
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    SwitchGear 3'UTR luciferase reporter plasmidINIP 3' UTR sequence
    Inhib. RNA
    Products:
        
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    Gene Editing
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    Clone
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    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat INIP
    Sirion Biotech Customized lentivirus for stable overexpression of INIP 
                         Customized lentivirus expression plasmids for stable overexpression of INIP 

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    In Situ Assay
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for INIP


    (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



    Interactions:

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

    STRING Interaction Network Preview (showing 3 interactants - click image to see more details)

    3 Interacting proteins for INIP (ENSP000003633604) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    INTS3ENSP000003186414STRING: ENSP00000318641
    NABP1ENSP000004036834STRING: ENSP00000403683
    NABP2ENSP000002670234STRING: ENSP00000267023
    About this table

    Gene Ontology (GO): 3 biological process terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006281DNA repair IMP19605351
    GO:0006974response to DNA damage stimulus IMP19683501
    GO:0010212response to ionizing radiation IMP19605351

    INIP 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 INIP (SOSSC)

    Search CenterWatch for drugs/clinical trials and news about INIP / SOSSC

    (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 INIP gene: 
    NM_021218.1  

    Unigene Cluster for INIP:

    INTS3 and NABP interacting protein
    Hs.658575  [show with all ESTs]
    Unigene Representative Sequence: AK000637
    7 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000374242(uc004bgg.3 uc010muk.3) ENST00000497712 ENST00000374236
    ENST00000481146 ENST00000374234 ENST00000476599 ENST00000374238
    miRNA
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    Search QIAGEN for miScript miRNA Assays for microRNAs that regulate INIP
    SwitchGear 3'UTR luciferase reporter plasmidINIP 3' UTR sequence
    Inhib. RNA
    Products:
         
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    OriGene RNAi products in human, mouse, rat for INIP
    QIAGEN FlexiTube/FlexiPlate siRNA for gene silencing in human, mouse, rat INIP
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    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat INIP
    Sirion Biotech Customized lentivirus for stable overexpression of INIP 
                         Customized lentivirus expression plasmids for stable overexpression of INIP 
    Primer
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    OriGene qPCR primer pairs and template standards for INIP
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    Search SABiosciences RT2 qPCR Primer Assays in human, mouse, rat INIP
      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat INIP
      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat INIP

    Additional mRNA sequence: 

    AF161409.1 AF161411.2 AK000637.1 AK310007.1 BC013097.1 BC014881.1 BC065210.1 

    13 DOTS entries:

    DT.107326  DT.92423494  DT.100783163  DT.121152785  DT.100783161  DT.100783160  DT.100783164  DT.121152768 
    DT.121265258  DT.92423493  DT.95372374  DT.40315703  DT.86848052 

    24/128 AceView cDNA sequences (see all 128):

    BU608858 CA943261 NM_021218 AI027245 BU552857 BI255785 BM682030 BE885982 
    BP366108 BQ722175 BX100148 BU188550 CR607302 BC014881 BG681333 AA463558 
    BM729100 AI969189 BE867698 AI478656 BX427876 BF699454 AW337708 BG113794 

    GeneLoc Exon Structure

    5/7 Alternative Splicing Database (ASD) splice patterns (SP) for INIP (see all 7)    About this scheme

    ExUns: 1a · 1b · 1c · 1d · 1e · 1f · 1g ^ 2 ^ 3a · 3b ^ 4 ^ 5 ^ 6a · 6b · 6c · 6d · 6e · 6f · 6g
    SP1:                                                        -                                                         
    SP2:                                                  -     -                                                         
    SP3:                                                                    -                                             
    SP4:                                            -     -     -                                                         
    SP5:                                                  -     -           -                                             


    ECgene alternative splicing isoforms for INIP

    (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

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


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

    SOURCE GeneReport for Unigene cluster: Hs.658575
        SABiosciences Custom PCR Arrays for INIP
    Primer
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for INIP

    (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 INIP gene from 5/13 species (see all 13)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Inip1 , 5 RIKEN cDNA 1110054O05 gene5
    INTS3 and NABP interacting protein1
    90.38(n)1
    96.15(a)1
      4 (32.81 cM)5
    662091  NM_001013577.11  NP_001013595.11 
     597696375 
    chicken
    (Gallus gallus)
    Aves INIP1 chromosome Z open reading frame, human C9orf80 84.79(n)
    93.2(a)
      427331  NM_001006585.1  NP_001006585.1 
    lizard
    (Anolis carolinensis)
    Reptilia INIP6
    INTS3 and NABP interacting protein
    78(a)
    1 ↔ 1
    2(57819432-57844407)
    African clawed frog
    (Xenopus laevis)
    Amphibia hspc043-A-prov2 HSPC043 protein, MGC52783 protein 76.57(n)    BC041246.1 
    zebrafish
    (Danio rerio)
    Actinopterygii zgc562592 similar to HSPC043 protein 78.16(n)   393188  BC046030.1 


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

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for INIP gene

    INIP for paralogs           About GeneDecksing


    1 Pseudogenes.org Pseudogene for INIP
    PGOHUM00000246069


    (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

    10/671 SNPs in INIP are shown (see all 671)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 9 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs7869661,2
    C,F,A,H--115448341(+) AAATAT/GTGACC 1 -- int114Minor allele frequency- G:0.12NS EA NA WA 1888
    rs1821193081,2
    --115448440(+) ACTGTA/GTCTGT 1 -- int10--------
    rs1114164711,2
    F--115448565(+) ACGAAC/AATCTG 1 -- int11Minor allele frequency- A:0.50CSA 2
    rs1446818991,2
    --115448689(+) CCCCAC/GATACT 1 -- int10--------
    rs1853755101,2
    C--115448762(+) GAGCTC/TGACTT 1 -- int10--------
    rs7869671,2
    C,F,A,H--115448879(+) tcaagC/Tgattc 1 -- ut314Minor allele frequency- T:0.36NA CSA 11
    rs1418369691,2
    --115448917(+) GATTAC/TAGGCG 1 -- ut310--------
    rs7869681,2
    C,F,A,H--115449110(-) GTTCTG/ATTTTC 1 -- ut31 ese320Minor allele frequency- A:0.12EA MN NA NS CSA WA 2390
    rs1995976861,2
    C--115449120(-) AGTTTA/GTGTGG 1 -- ut310--------
    rs7869691,2
    C,F,O,A,H--115449556(+) GTTCAC/GAGTCT 1 -- ut31 ese314Minor allele frequency- G:0.11MN NA NS EA CSA WA 979

    HapMap Linkage Disequilibrium report for INIP (115446206 - 115480516 bp)

    Structural Variations
          Database of Genomic Variants (DGV) variations for INIP: --
    SABiosciences Cancer Mutation PCR Assays
    SeqTarget long-range PCR primers for resequencing INIP
    DNA2.0 Custom Variant and Variant Library Synthesis for INIP

    (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

    INIP for disorders           About MalaCards
    OMIM gene information: 613273    OMIM disorders: --


    INIP for disorders           About GeneDecksing


    Export disorders for INIP 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 INIP gene, integrated from 9 sources (see all 14):
    (articles sorted by number of sources associating them with INIP)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells. (PubMed id 11042152)1, 2, 3 Zhang Q.-H.... Chen Z. (2000)
    2. hSSB1 and hSSB2 form similar multiprotein complexes that participate in DNA damage response. (PubMed id 19605351)1, 2 Li Y.... Wang W. (2009)
    3. SOSS complexes participate in the maintenance of genomic stability. (PubMed id 19683501)1, 2 Huang J.... Chen J. (2009)
    4. 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)
    5. DNA sequence and analysis of human chromosome 9. (PubMed id 15164053)1, 2 Humphray S.J.... Dunham I. (2004)
    6. Bcl2-associated Athanogene 3 Interactome Analysis Reve als a New Role in Modulating Proteasome Activity. (PubMed id 23824909)1 Chen Y....Ge F. (2013)
    7. A census of human soluble protein complexes. (PubMed id 22939629)1 Havugimana P.C....Emili A. (2012)
    8. Interactions of pathological hallmark proteins: tubul in polymerization promoting protein/p25, beta-amyloid, and alpha-synuclein. (PubMed id 21832049)1 OlA!h J....OvA!di J. (2011)
    9. A proteome-wide, quantitative survey of in vivo ubiqui tylation sites reveals widespread regulatory roles. (PubMed id 21890473)1 Wagner S.A....Choudhary C. (2011)
    10. Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach. (PubMed id 19413330)2 Gauci S....Mohammed S. (2009)

    (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: 58493 HGNC: 24994 AceView: C9orf80 Ensembl:ENSG00000148153 euGenes: HUgn58493
    ECgene: INIP H-InvDB: INIP

    (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 INIP 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 INIP gene:
    Search GeneIP for patents involving INIP

    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, Cloud-Clone Corp., Thermo Fisher Scientific, LSBio, Gene Editing from DNA2.0 and Sirion Biotech, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Sirion Biotech, 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
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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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