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

HOXC9 Gene

protein-coding   GIFtS: 48
GCID: GC12P054388

homeobox C9

(Previous name: homeo box C9 )
(Previous symbols: HOX3, HOX3B)
 Explore 6 diseases affiliated with
HOXC9 via
MalaCards
our new
 Human Malady Compendium 
Biological research products
for HOXC9    

Aliases
for HOXC9 gene

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section
Aliases
Homeobox C91 2
HOX3B1 2 3 5
HOX31 2
Homeo Box C91 2
Homeobox Protein Hox-3B2 3
Homeobox Protein Hox-C92

External Ids:    HGNC: 51301   Entrez Gene: 32252   Ensembl: ENSG000001808067   OMIM: 1429715   UniProtKB: P312743   

Export aliases for HOXC9 gene to outside databases

Previous GC identifers: GC12M054413 GC12P054506 GC12P054110 GC12P052680 GC12P054393 GC12P051432


Summaries
for HOXC9 gene

(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 HOXC9:
This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription
factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar
homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11
genes arranged in tandem. This gene is one of several homeobox HOXC genes located in a cluster on chromosome 12.
(provided by RefSeq, Jul 2008)

UniProtKB/Swiss-Prot: HXC9_HUMAN, P31274
Function: Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells
with specific positional identities on the anterior-posterior axis

Gene Wiki entry for HOXC9


Genomic Views
for HOXC9 gene

(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_000012.11  NC_018923.1  NT_029419.12  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the HOXC9 gene promoter:
         RORalpha1   E2F-5   Sp1   Hand1   E47   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmid: HOXC9 promoter sequence
   Search SABiosciences Chromatin IP Primers for HOXC9

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat HOXC9


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

Entrez Gene cytogenetic band: 12q13.3   Ensembl cytogenetic band:  12q13.13   HGNC cytogenetic band: 12q13.13

HOXC9 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
HOXC9 gene location

GeneLoc information about chromosome 12         GeneLoc Exon Structure

GeneLoc location for GC12P054388:  view genomic region     (about GC identifiers)

Start:
 54,388,679 bp from pter      End:
 54,397,121 bp from pter
Size:
 8,443 bases      Orientation:
 plus strand

Proteins
for HOXC9 gene

(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: HXC9_HUMAN, P31274 (See protein sequence)
Recommended Name: Homeobox protein Hox-C9  
Size: 260 amino acids; 29248 Da
Subunit: Interacts with Geminin/GMNN, which inhibits transcriptional activity
Subcellular location: Nucleus
1 PDB 3D structure from and Proteopedia for HOXC9:
2LP0 (3D)    
Secondary accessions: B2RCN7 Q9H1I0

Explore the universe of human proteins at neXtProt for HOXC9: NX_P31274

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_P31274

    • HOXC9 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_008828.1  
    ENSEMBL proteins: 
     ENSP00000423861   ENSP00000302836  

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    Novus Biologicals HOXC9 Protein
    Novus Biologicals HOXC9 Lysate
    Browse Sino Biological Recombinant Proteins
    Browse ProSpec Recombinant Proteins
    Uscn Proteins for HOXC9

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005634nucleus IEA--


    HOXC9 for ontologies           About GeneDecksing



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    Uscn ELISAs and CLIAs for HOXC9

    Protein Domains /
    Families
    for HOXC9 gene

    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    HOXC9 for domains           About GeneDecksing

    5/6 InterPro domains/families (see all 6):
     IPR020479 Homeobox_metazoa
     IPR006711 Hox9_activation_N
     IPR017112 Homeobox_Hox9
     IPR017970 Homeobox_CS
     IPR001356 Homeodomain

    Graphical View of Domain Structure for InterPro Entry P31274

    ProtoNet protein and cluster: P31274

    2 Blocks protein families:
    IPB000047 Lambda and other repressor helix-turn-helix signature
    IPB006711 Hox9 activation region


    UniProtKB/Swiss-Prot: HXC9_HUMAN, P31274
    Similarity: Belongs to the Abd-B homeobox family
    Similarity: Contains 1 homeobox DNA-binding domain


    Function
    for HOXC9 gene

    (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
    Function Summary:

         UniProtKB/Swiss-Prot: HXC9_HUMAN, P31274
    Function: Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells
    with specific positional identities on the anterior-posterior axis

         Genatlas biochemistry entry for HOXC9:
    homeo box C9(3B),homologous to mouse Hox-3.2,Drosophila abd-B,involved in mouse posterior limb patterning,expressed in
    posterior limb

    miRNA
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    QIAGEN Custom miScript Target Protector blocks miRNA-binding site of human, mouse, rat HOXC9
    8/33 QIAGEN miScript miRNA Assays for microRNAs that regulate HOXC9 (see all 33):
    hsa-miR-21* hsa-miR-3164 hsa-miR-193a-3p hsa-miR-200a hsa-let-7a-2* hsa-miR-141 hsa-miR-23a hsa-miR-3148
    SwitchGear 3'UTR luciferase reporter plasmid: HOXC9 3' UTR sequence
    Inhib. RNA
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    OriGene 29mer shRNA kits in GFP-retroviral vector in human, mouse, rat for HOXC9 (see all 4)
    OriGene shRNA RFP: HOXC9
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    Gene Editing
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    Clone
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    Cell Line
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    In Situ Assay
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    Gene Ontology (GO): 2 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003700sequence-specific DNA binding transcription factor activity IEA--
    GO:0043565sequence-specific DNA binding IEA--


    HOXC9 for ontologies           About GeneDecksing


    Animal Models:
         Mouse knock-outs for HOXC9: Hoxc9tm1Hsu Hoxc9tm1Mrc
         3 MGI mutant phenotypes (inferred from 2 alleles) (MGI details for Hoxc9):
     growth/size  limbs/digits/tail  skeleton 

    HOXC9 for phenotypes           About GeneDecksing


    Pathways & Interactions
    for HOXC9 gene

    (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 HOXC9

    STRING Interaction Network Preview (showing 5 interactants - click image to see 16)

    5/16 Interacting proteins for HOXC9 (P312743 ENSP000003028364) via UniProtKB, MINT, STRING, and/or I2D (see all 16)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    GTF2A1LQ9UNN43, ENSP000003845974I2D: score=1 STRING: ENSP00000384597
    HOXD9P283563, ENSP000002494994I2D: score=1 STRING: ENSP00000249499
    IRF9Q009783, ENSP000003800734I2D: score=1 STRING: ENSP00000380073
    NMIQ132873, ENSP000002433464I2D: score=1 STRING: ENSP00000243346
    PCGF2P352273, ENSP000003540334I2D: score=1 STRING: ENSP00000354033
    About this table

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006351transcription, DNA-dependent IEA--
    GO:0007275multicellular organismal development ----
    GO:0009952anterior/posterior pattern specification IEA--
    GO:0048704embryonic skeletal system morphogenesis IEA--
    GO:0048706embryonic skeletal system development ----


    HOXC9 for ontologies           About GeneDecksing



    Drugs & Compounds
    for HOXC9 gene

    (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 HOXC9
    Search CenterWatch for drugs/clinical trials and news about HOXC9 / HXC9 

    Transcripts
    for HOXC9 gene

    (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 HOXC9 gene: 
    NM_006897.1  

    Unigene Cluster for HOXC9:

    Homeobox C9
    Hs.658823  [show with all ESTs]
    Unigene Representative Sequence: NM_006897
    3 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000504557 ENST00000508190 ENST00000303450(uc001seq.3)

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    8/33 QIAGEN miScript miRNA Assays for microRNAs that regulate HOXC9 (see all 33):
    hsa-miR-21* hsa-miR-3164 hsa-miR-193a-3p hsa-miR-200a hsa-let-7a-2* hsa-miR-141 hsa-miR-23a hsa-miR-3148
    SwitchGear 3'UTR luciferase reporter plasmid: HOXC9 3' UTR sequence
    Inhib. RNA
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    OriGene 29mer shRNA kits in GFP-retroviral vector in human, mouse, rat for HOXC9 (see all 4)
    OriGene shRNA RFP: HOXC9
    OriGene siRNA: HOXC9
    QIAGEN FlexiTube/FlexiPlate siRNA for gene silencing in human, mouse, rat HOXC9
    Clone
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    Primer
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      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat HOXC9
      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat HOXC9

    Additional cDNA sequence: 

    AK000445.1 AK315194.1 BC021265.1 BC032769.1 BC053894.1 

    3 DOTS entries:

    DT.99957565  DT.208892  DT.99935637 

    24/51 AceView cDNA sequences (see all 51):

    NM_006897 CR600750 CR617045 AL556826 X99682 AI361560 AK000445 AA227902 
    AI522164 BE786336 CA446202 BC053894 AI949325 CA429963 AI333355 AI085613 
    AI934382 AA227856 BU621618 BQ015349 BU616567 CB125288 AI332412 AA719162 

    GeneLoc Exon Structure


    Expression
    for HOXC9 gene

    (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

    HOXC9 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: TACGGCTCGC

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

    HOXC9 expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    10 LifeMap In Vivo Development Anatomical Compartments/Cells 
    Tissue Anatomical Compartment CellCategory (developmental path)
    LimbLimb BudLimb Bud Mesenchyme CellsMesoderm
    SomiteThoracic Mesenchymal SclerotomeThoracic Sclerotome CellsBone, Cartilage, Tendons & Ligaments
    Spinal CordPreganglionic ColumnPreganglionic Motor NeuronsMotor Neurons
    AdiposeBody Subcutaneous White AdiposeSubcutaneous White AdipocytesAdipose
    AdiposeCranial Subcutaneous White AdiposeSubcutaneous White AdipocytesAdipose
    AdiposeFacial Subcutaneous White AdiposeSubcutaneous White AdipocytesAdipose
    AdiposeSubcutaneous White AdiposeBrown-like Adipocyte CellsAdipose
    AdiposeSubcutaneous White AdiposeSubcutaneous White AdipocytesAdipose
    AdiposeVisceral White AdiposeBrown-like Adipocyte CellsAdipose
    LimbLimb BudLimb
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization
    Stem Cell Differentiation: 5 LifeMap Cells 
    NameCategory
    mK3 (Cell line)Kidney
    mK4 (Cell line)Kidney
    PureStem™ progenitor SK17 (Embryonic Progenitor Cell)
    PureStem™ progenitor W8 (Embryonic Progenitor Cell)
    CD31, CD144 positive cells (Two-step protocol fo...)

    See HOXC9 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for HOXC9

    SOURCE GeneReport for Unigene cluster: Hs.658823
        SABiosciences Expression via Pathway-Focused PCR Arrays including HOXC9: 
              Stem Cell Transcription Factors in human mouse rat
              Homeobox (HOX) Genes in human mouse rat

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    In Situ
    Assay Products:     
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    Orthologs
    for HOXC9 gene

    (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 animals.

    Orthologs for HOXC9 gene from 5/9 species (see all 9)    About this table
    Organism Taxonomic
    classification    		 Gene Description Human
    Similarity    		 Orthology
    Type    		 Details
    mouse
    (Mus musculus)    		 Mammalia Hoxc95 homeobox C9   --   15 (58.04 cM) 102976439 
    chicken
    (Gallus gallus)    		 Aves HOXC91 homeobox C9 75.93(n)
    84.17(a)    		   425723  XM_423451.3  XP_423451.2 
    lizard
    (Anolis carolinensis)    		 Reptilia HOXD96
    		 --
    		 23(a)
    		 possible ortholog
    		 GL343356.1(518262-536480)
    zebrafish
    (Danio rerio)    		 Actinopterygii hoxc9a2 homeo box C9a 77.69(n)   58043  NM_131528.1 
    worm
    (Caenorhabditis elegans)    		 Secernentea nob-16
    		 kNOB-like posterior (NO Backside) family member (n...
    		 17(a)
    		 1 → many
    		 III(12077688-12084220)


    ENSEMBL Gene Tree for HOXC9 (if available)
    TreeFam Gene Tree for HOXC9 (if available) 

    Paralogs
    for HOXC9 gene

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for HOXC9 gene
    HOXA92  HOXA132  HOXD112  HOXC122  ENSG000002571842  HOXB132  HOXD102  HOXC112  
    HOXA112  HOXD132  HOXC132  HOXB92  HOXC102  HOXD92  HOXD122  HOXA102  
    11 SIMAP similar genes for HOXC9 using alignment to 3 protein entries:     HXC9_HUMAN (see all proteins):
    HOX B6    HOXB1    HOXA-9    HOXA9    HOXB9    HOXA6
    HOXD9    HOXC10    HOXD8    HOXA10    HOXC5

    HOXC9 for paralogs           About GeneDecksing



    Genomic Variants
    for HOXC9 gene

    (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

    10/85 NCBI SNPs in HOXC9 are shown (see all 85)     About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance    		Chr 12 posSequence#AA
    Chg    		TypeMore#Allele
    freq    		PopTotal
    sample    		More
    ----------
    rs1920860091,2
    		--54392122(+) CTTTCC/TTCCCC 1 -- us2k10--------
    rs1130504911,2
    		--54392170(+) TCTCCT/ACCCCA 1 -- us2k11Minor allele frequency- A:0.00CSA 1
    rs22419381,2
    		C,F,H,--54392449(-) GTGAAA/GCCCCC 1 -- us2k110Minor allele frequency- G:0.16EA NS WA NA 2274
    rs1841337621,2
    		--54392495(+) TGCCCC/TCTCTT 1 -- us2k10--------
    rs1869516491,2
    		--54392529(+) TACTTA/GACTAA 1 -- us2k10--------
    rs1150664151,2
    		C,F,--54392540(+) AGCCCC/TCCTTT 1 -- us2k11Minor allele frequency- T:0.03WA 118
    rs1431887021,2
    		--54392739(+) CGTTGC/TTTTTT 1 -- us2k10--------
    rs733131791,2
    		C,--54392816(+) CTCATA/TAAAAT 1 -- us2k11Minor allele frequency- T:0.01WA 118
    rs1150061651,2
    		F,--54393338(+) GCTGCT/ACCTGA 1 -- us2k11Minor allele frequency- A:0.03WA 118
    rs1913904111,2
    		--54393614(+) GGGGAA/GGCCAT 1 -- us2k10--------

    HapMap Linkage Disequilibrium report for HOXC9 (54388679 - 54397121 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 1 variation for HOXC9
         1 CNV: 3890

    SABiosciences Cancer Mutation PCR Assays
    QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing HOXC9
    DNA2.0 Custom Variant and Variant Library Synthesis for HOXC9

    Disorders / Diseases
    for HOXC9 gene

    (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
    HOXC9 for disorders           About GeneDecksing

    OMIM gene information: 142971    OMIM disorders: --

    6 diseases for HOXC9:    About MalaCards
    lung carcinoma    astrocytoma    lung cancer    neuroblastoma
    carcinoma    neuronitis


    Export disorders for HOXC9 gene to outside databases

    Publications
    for HOXC9 gene

    (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 HOXC9 gene, integrated from 9 sources (see all 23):
    (articles sorted by number of sources associating them with HOXC9)    		    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. Complete mutation analysis panel of the 39 human HOX genes. (PubMed id 11857506)1, 2 Kosaki K.... Matsuo N. (2002)
    4. Nomenclature for human homeobox genes. (PubMed id 1973146)1, 3 McAlpine P.J. and Shows T.B. (1990)
    5. Organization of human class I homeobox genes. (PubMed id 2576652)1, 2 Boncinelli E.... Simeone A. (1989)
    6. Homeobox C9 is not potentially related to congenital h eart disease in Chinese patients. (PubMed id 22106857)1 Sun L....Ma X. (2012)
    7. Structural basis for homeodomain recognition by the ce ll-cycle regulator Geminin. (PubMed id 22615398)2 Zhou B....Zhu G. (2012)
    8. HOXC9 links cell-cycle exit and neuronal differentiat ion and is a prognostic marker in neuroblastoma. (PubMed id 21507931)1 Mao L....Ding H.F. (2011)
    9. The transcription factor HOXC9 regulates endothelial cell quiescence and vascular morphogenesis in zebrafish via inhibition of inter leukin 8. (PubMed id 21493894)1 Stoll S.J....Kroll J. (2011)
    10. An atlas of combinatorial transcriptional regulation in mouse and man. (PubMed id 20211142)1 Ravasi T....Hayashizaki Y. (2010)

    External Searches for HOXC9 gene

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
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    Genome Databases showing HOXC9 gene

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 3225 HGNC: 5130 AceView: HOXC9 Ensembl:ENSG00000180806 euGenes: HUgn3225
    ECgene: HOXC9 H-InvDB: HOXC9

    Other Databases showing HOXC9 gene

    (According to HUGE)
    About This Section
    		   --

    Specialized Databases showing HOXC9 gene

    (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 HOXC9 Pharmacogenomics, SNPs, Pathways

    Intellectual Property
    for HOXC9 gene

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    		Patent Information for HOXC9 gene:
    Search GeneIP for patents involving HOXC9

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



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