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

CNTF Gene

protein-coding   GIFtS: 61
GCID: GC11P058390

ciliary neurotrophic factor

 Explore 77 diseases affiliated with
CNTF via our new
 Human Malady Compendium 
Biological research products
for CNTF
    

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

Aliases
Ciliary Neurotrophic Factor1 2
HCNTF1 2

External Ids:    HGNC: 21691   Entrez Gene: 12702   Ensembl: ENSG000002426897   OMIM: 1189455   UniProtKB: P264413   

Export aliases for CNTF gene to outside databases

Previous GC identifers: GC11P060741 GC11P059903 GC11P058641 GC11P058165 GC11P058146 GC11P054738


(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 CNTF:
The protein encoded by this gene is a polypeptide hormone whose actions appear to be restricted to the nervous system
where it promotes neurotransmitter synthesis and neurite outgrowth in certain neuronal populations. The protein is a
potent survival factor for neurons and oligodendrocytes and may be relevant in reducing tissue destruction during
inflammatory attacks. A mutation in this gene, which results in aberrant splicing, leads to ciliary neurotrophic
factor deficiency, but this phenotype is not causally related to neurologic disease. A read-through transcript variant
composed of the upstream ZFP91 gene and CNTF sequence has been identified, but it is thought to be non-coding.
Read-through transcription of ZFP91 and CNTF has also been observed in mouse. (provided by RefSeq, Oct 2010)

UniProtKB/Swiss-Prot: CNTF_HUMAN, P26441
Function: CNTF is a survival factor for various neuronal cell types. Seems to prevent the degeneration of motor axons
after axotomy

Gene Wiki entry for CNTF (Ciliary neurotrophic factor)


(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_000011.9  NC_018922.1  NT_167190.1  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the CNTF gene promoter:
         CREB   PPAR-gamma1   deltaCREB   MyoD   PPAR-gamma2   NF-kappaB1   
         Other transcription factors

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

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


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

Entrez Gene cytogenetic band: 11q12.2   Ensembl cytogenetic band:  11q12.1   HGNC cytogenetic band: 11q12

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

GeneLoc information about chromosome 11         GeneLoc Exon Structure

GeneLoc location for GC11P058390:  view genomic region     (about GC identifiers)

Start:
58,390,146 bp from pter      End:
58,393,206 bp from pter
Size:
3,061 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: CNTF_HUMAN, P26441 (See protein sequence)
Recommended Name: Ciliary neurotrophic factor  
Size: 200 amino acids; 22931 Da
Subunit: Homodimer
Subcellular location: Cytoplasm
1 PDB 3D structure from and Proteopedia for CNTF:
1CNT (3D)    
Secondary accessions: B2RAB2

Explore the universe of human proteins at neXtProt for CNTF: NX_P26441

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_P26441

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

    REFSEQ proteins: NP_000605.1  
    ENSEMBL proteins: 
     ENSP00000355370  

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    ProSpec Recombinant Protein for CNTF
    Uscn Proteins for CNTF

    Gene Ontology (GO): 5/9 cellular component terms (GO ID links to tree view) (see all 9):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005615extracellular space IC12643274
    GO:0005634nucleus ----
    GO:0005737cytoplasm IEA--
    GO:0005829cytosol ----
    GO:0030424axon ----


    CNTF for ontologies           About GeneDecksing



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    Uscn ELISAs and CLIAs for CNTF


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

    CNTF for domains           About GeneDecksing

    3 InterPro domains/families:
     IPR012351 4_helix_cytokine_core
     IPR000151 Ciliary_neurotrophic_fac_CNTF
     IPR009079 4_helix_cytokine-like_core

    Graphical View of Domain Structure for InterPro Entry P26441

    ProtoNet protein and cluster: P26441

    1 Blocks protein family: IPB000151 Ciliary neurotrophic factor

    UniProtKB/Swiss-Prot: CNTF_HUMAN, P26441
    Similarity: Belongs to the CNTF 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

    Function Summary:

         UniProtKB/Swiss-Prot: CNTF_HUMAN, P26441
    Function: CNTF is a survival factor for various neuronal cell types. Seems to prevent the degeneration of motor axons
    after axotomy

         Genatlas biochemistry entry for CNTF:
    ciliary neurotrophic factor,interleukin-6 cytokine family member,cytosolic protein,expressed in myelinating Schwann
    cells and astrocyte subpopulation,involved in axon out growth in retinal ganglion cells and in the spinal cord,with
    decreased expression in the lateral corticospinal tract of amyotrophic lateral sclerosis (ALS)

         Summary:  
    During embryonic development, CNTF as signaling molecule
    affects the following cells: Late Retinal Progenitor Cells in Neuroblastic Layer

    CNTF as growth factor is involved in stem cell differentiation protocols towards the derivation of the following cells: Motor neuron-like cells, Schwann-like cells (see all 4).

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    Gene Ontology (GO): 4 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005125cytokine activity ----
    GO:0005127ciliary neurotrophic factor receptor binding TAS1714745
    GO:0005138interleukin-6 receptor binding IPI12643274
    GO:0008083growth factor activity IDA12643274


    CNTF for ontologies           About GeneDecksing


    1 GenomeRNAi human phenotype for CNTF:
     Decreased Hepatitis C virus re 

    Animal Models:
         Mouse knock-outs for CNTF: Cntftm1Gdy Cntftm1Mpin
         8 MGI mutant phenotypes (inferred from 4 alleles(MGI details for Cntf):
     behavior/neurological  cellular  hematopoietic system  homeostasis/metabolism  immune system 
     muscle  nervous system  no phenotypic analysis 

    CNTF 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

    Unified GeneCards pathways  About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Development_CNTF receptor signaling
    Development CNTF receptor signaling1.00
    Development_CNTF receptor signaling1.00
    2CNTF Signaling
    CNTF Signaling1.00
    3Jak-STAT signaling pathway
    Jak-STAT signaling pathway1.00
    4Notch Signaling Pathway
    Delta-Notch Signaling Pathway0.27
    5PEDF Induced Signaling
    Cytokine-cytokine receptor interaction0.26

    Pathway sources
    See GeneCards unified pathways
    Show all pathways

    1 EMD Millipore Pathway for CNTF
        Development CNTF receptor signaling

    1 Downloadable PowerPoint Slide of QIAGEN Pathway Central Maps for CNTF
        CNTF Signaling

    1 GeneGo (Thomson Reuters) Pathway for CNTF
        Development CNTF receptor signaling

    1 BioSystems Pathway for CNTF 
        Delta-Notch Signaling Pathway


    2         Kegg Pathways  (Kegg details for CNTF):
        Cytokine-cytokine receptor interaction
    Jak-STAT signaling pathway


    CNTF for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for CNTF

    STRING Interaction Network Preview (showing 5 interactants - click image to see 10)

    5/11 Interacting proteins for CNTF (P264411, 2, 3 ENSP000003553704) via UniProtKB, MINT, STRING, and/or I2D (see all 11)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    IL6STP401892, 3, ENSP000003387994MINT-62479 MINT-62480 I2D: score=2 STRING: ENSP00000338799
    STK16O757161, 3, ENSP000003799644EBI-1050897,EBI-749295 I2D: score=2 STRING: ENSP00000379964
    VHLP403371, 3EBI-1050897,EBI-301246 I2D: score=2 
    LIFRP427022, 3, ENSP000002634094MINT-62474 MINT-62473 I2D: score=3 STRING: ENSP00000263409
    EXT2Q930631, 3, ENSP000003426564EBI-1050897,EBI-1047761 I2D: score=2 STRING: ENSP00000342656
    About this table

    Gene Ontology (GO): 5/22 biological process terms (GO ID links to tree view) (see all 22):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0007165signal transduction NAS1840538
    GO:0007259JAK-STAT cascade ----
    GO:0007399nervous system development ----
    GO:0008284positive regulation of cell proliferation IEA--
    GO:0014068positive regulation of phosphatidylinositol 3-kinase cascade ----


    CNTF for ontologies           About GeneDecksing



    (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

    CNTF for compounds           About GeneDecksing

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

    Browse Tocris compounds for CNTF
    10/59 Novoseek chemical compound relationships for CNTF gene (see all 59)    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    gp 130 94.3 225 17448148 (4), 9287306 (4), 12765290 (3), 7500350 (3) (see all 99)
    axokine 85.3 9 12861475 (1), 17971763 (1), 12610837 (1), 15340100 (1) (see all 6)
    tyrosine 56.8 53 12941469 (4), 9242633 (2), 9285712 (2), 7512571 (2) (see all 34)
    il 11 54 1 8605875 (1)
    choline 52.7 30 8034640 (3), 9476208 (2), 7760021 (2), 7891074 (2) (see all 13)
    quinolinic acid 49 14 12427308 (3), 8692996 (1), 9588602 (1), 9121555 (1) (see all 5)
    octadecaneuropeptide 48.8 2 15146610 (1), 15107726 (1)
    bupropion 20 3 16859393 (1), 17033290 (1), 17971763 (1)
    acetylcholine 16 13 9476208 (2), 9157328 (1), 19830843 (1), 12932444 (1) (see all 7)
    glutamate 12.6 21 11095495 (4), 1360545 (4), 10619557 (2), 19865482 (1) (see all 9)

    Search CenterWatch for drugs/clinical trials and news about CNTF 

    (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 CNTF gene: 
    NM_000614.3  

    Unigene Cluster for CNTF:

    Ciliary neurotrophic factor
    Hs.524920  [show with all ESTs]
    Unigene Representative Sequence: NM_053023
    1 Ensembl transcript including schematic representation, and UCSC links where relevant:
    ENST00000361987(uc001nna.4)

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    Additional cDNA sequence: 

    AB056107.1 AF310246.1 AJ270692.1 AK025502.1 AK128303.1 AK295700.1 AK314118.1 BC051743.1 
    BC068030.1 BC069167.1 BC074963.2 BC074964.2 NR_024091.1 S72921.1 

    21 DOTS entries:

    DT.95331869  DT.452558  DT.455066  DT.99962886  DT.99933507  DT.307724  DT.65286271  DT.100038803 
    DT.102837608  DT.92417425  DT.101958415  DT.95331866  DT.120748508  DT.75129424  DT.91966022  DT.95331872 
    DT.97763497  DT.120748532  DT.121024439  DT.121025771  DT.87017426 

    24/493 AceView cDNA sequences (see all 493):

    CK299809 BX383320 AA831592 BM548840 CA425830 N62831 BU788935 AW275211 
    AA765534 AA179521 AW516345 AI858235 N72280 BM667429 AA629762 BU619425 
    AI949929 AI281008 BM789867 BM670734 BC074964 BM470986 CA336703 D31537 

    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

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

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

    About this image

    CNTF expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table

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

    SOURCE GeneReport for Unigene cluster: Hs.524920

    UniProtKB/Swiss-Prot: CNTF_HUMAN, P26441
    Tissue specificity: Nervous system

        SABiosciences Expression via Pathway-Focused PCR Arrays including CNTF: 
              Neurotrophins & Receptors in human mouse rat
              Obesity in human mouse rat
              Cytokines & Chemokines in human mouse rat
              Common Cytokines in human mouse rat

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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for CNTF

    (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 CNTF gene from 3/8 species (see all 8)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Cntf1 , 5 ciliary neurotrophic factor1, 5 84.97(n)1
    83.42(a)1
      19 (8.73 cM)5
    128031  NM_170786.21  NP_740756.11 
     127636605 
    chicken
    (Gallus gallus)
    Aves CNTF1 ciliary neurotrophic factor 56.16(n)
    45.11(a)
      396488  NM_205492.1  NP_990823.1 
    lizard
    (Anolis carolinensis)
    Reptilia CNTF6
    --
    45(a)
    1 ↔ 1
    1(91266272-91271164)


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

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

    (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

    10/118 NCBI SNPs in CNTF are shown (see all 118    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 11 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs25077621,2
    C,--54736563(+) AAGAAG/AAAAAA 1 -- us2k12Minor allele frequency- A:0.04WA 120
    rs1133198351,2
    C,--54736726(+) CAGGTG/-GTTAA 1 -- us2k11Minor allele frequency- -:0.50CSA 2
    rs744101961,2
    --54737412(+) TACCTA/TCCTCC 1 -- us2k10--------
    rs746705431,2
    C,F,--54737500(+) TTACCT/CTTAAA 1 -- us2k11Minor allele frequency- C:0.09WA 118
    rs784096521,2
    F,--54737754(+) GATCAA/GATGGA 1 -- us2k11Minor allele frequency- G:0.02WA 118
    rs768356161,2
    --54738114(+) GGCACA/GAAAAT 1 -- us2k10--------
    rs1113894921,2
    F--54738160(+) GCAGGG/ACGTGG 1 -- us2k11Minor allele frequency- A:0.50CSA 6
    rs341315861,2
    C--54738411(+) ATCCTA/GTGTAA 2 Y C mis13Minor allele frequency- G:0.01NA 78
    rs1857361881,2
    C,--54738800(+) TAGGAA/GGAGTA 1 -- int10--------
    rs171527761,2
    C,F,--54738874(+) CTTTTA/GGTATT 1 -- int14Minor allele frequency- G:0.02NA WA 260

    HapMap Linkage Disequilibrium report for CNTF (58390146 - 58393206 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for CNTF: --
    Human Gene Mutation Database (HGMD): CNTF

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

    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Novoseek, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

    CNTF for disorders           About GeneDecksing

    OMIM gene information: 118945    OMIM disorders: --

    20/77 diseases for CNTF (see all 77):    About MalaCards
    spinal cord injury    charcot-marie-tooth disease    neurologic diseases    amyotrophic lateral sclerosis
    wallerian degeneration    chronic inflammatory demyelinating polyneuropathy    amyotrophic lateral sclerosis (als)    demyelinating polyneuropathy
    plasmodium falciparum malaria    motor neuronopathy    lateral sclerosis    acute disseminated encephalomyelitis
    status epilepticus    polyneuropathy    learning disability    neuronitis
    motor neuron disease    muscular atrophy    retinitis pigmentosa    pituitary adenoma

    3 diseases from the University of Copenhagen DISEASES database for CNTF:
    Amyotrophic lateral sclerosis     Retinal degeneration     Huntington's disease

    10/57 Novoseek disease relationships for CNTF gene (see all 57)    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    leukemia 79.6 326 8187629 (6), 18240017 (5), 8034640 (5), 10362299 (3) (see all 99)
    amyotrophic lateral sclerosis 70.5 63 15266526 (4), 8971830 (3), 8543936 (2), 14656696 (2) (see all 31)
    motor neuron disease 66.4 30 8759781 (5), 8053649 (3), 7818257 (2), 9398466 (1) (see all 17)
    neurodegenerative diseases 55 11 8543936 (1), 14631864 (1), 9106250 (1), 7838303 (1) (see all 8)
    retinal degeneration 53.1 14 16505355 (2), 10235570 (2), 20209167 (2), 17325188 (1) (see all 8)
    huntington disease 50.5 27 9121555 (3), 8692996 (2), 9171158 (2), 14697316 (2) (see all 14)
    retinitis pigmentosa 46.3 10 17325188 (2), 16143329 (1), 17508034 (1), 18830926 (1) (see all 7)
    neurodegeneration 43.6 22 7585948 (1), 7585015 (1), 1641039 (1), 9171158 (1) (see all 11)
    response acute phase 43.5 7 8109896 (2), 12773095 (1), 8681311 (1), 8075593 (1) (see all 5)
    neurological disorders 40.6 10 8764576 (2), 7520198 (1), 8075647 (1), 15694712 (1) (see all 6)

    Genetic Association Database (GAD): CNTF
    Human Genome Epidemiology (HuGE) Navigator: CNTF (29 documents)

    Export disorders for CNTF 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 CNTF gene, integrated from 9 sources (see all 668):
    (articles sorted by number of sources associating them with CNTF)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Sequence and structural organization of the human gene encoding ciliary neurotrophic factor. (PubMed id 1840538)1, 2, 3, 9 Lam A....Cordell B. (1991)
    2. The relationship between ciliary neurotrophic factor (CNTF) genotype and motor unit physiology: preliminary studies. (PubMed id 16181490)1, 4, 9 Conwit R.A....Metter E.J. (2005)
    3. Association of a null mutation in the CNTF gene with early onset of multiple sclerosis. (PubMed id 11890844)1, 4, 9 Giess R....Rieckmann P. (2002)
    4. Expression and characterization of recombinant human ciliary neurotrophic factor from Escherichia coli. (PubMed id 1883844)1, 2, 9 McDonald J.R.... Collins F. (1991)
    5. Cloning and expression of human ciliary neurotrophic factor. (PubMed id 1915374)1, 2, 9 Negro A.... Altruda F. (1991)
    6. Meta-analyses of the association between genetic polymorphisms of neurotrophic factors and schizophrenia. (PubMed id 15474906)1, 4, 9 Lin P.Y. and Tsai G. (2004)
    7. Neuropoietic cytokines in the hematopoietic fold. (PubMed id 1714745)1, 3, 9 Bazan J.F. (1991)
    8. Relation of weight maintenance and dietary restraint to peroxisome proliferator-activated receptor gamma2, glucocorticoid receptor, and ciliary neurotrophic factor polymorphisms. (PubMed id 16210701)1, 4, 9 Vogels N....Westerterp-Plantenga M.S. (2005)
    9. A null mutation in the CNTF gene is not associated with early onset of multiple sclerosis. (PubMed id 12470191)1, 4, 9 Hoffmann V. and Hardt C. (2002)
    10. Crystal structure of dimeric human ciliary neurotrophic factor determined by MAD phasing. (PubMed id 7796798)1, 2, 9 McDonald N.Q.... Hendrickson W.A. (1995)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Disorders
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      Query String
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    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: 1270 HGNC: 2169 AceView: CNTF Ensembl:ENSG00000242689 euGenes: HUgn1270
    ECgene: CNTF Kegg: 1270 H-InvDB: CNTF

    (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 CNTF Pharmacogenomics, SNPs, Pathways
    Wikipedia http://en.wikipedia.org/wiki/Ciliary_neurotrophic_factor

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

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



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