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

FGF10 Gene

protein-coding   GIFtS: 67
GCID: GC05M044340

fibroblast growth factor 10

 Explore 58 diseases affiliated with
FGF10 via our new
 Human Malady Compendium 
Biological research products
for FGF10
    

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

Aliases
Fibroblast Growth Factor 101 2
Keratinocyte Growth Factor 22 3
FGF-102 3
Produced By Fibroblasts Of Urinary Bladder Lamina Propria2

External Ids:    HGNC: 36661   Entrez Gene: 22552   Ensembl: ENSG000000701937   OMIM: 6021155   UniProtKB: O155203   

Export aliases for FGF10 gene to outside databases

Previous GC identifers: GC05M044614 GC05M045481 GC05M044305 GC05M044350


(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 FGF10:
The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess
broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including
embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein exhibits
mitogenic activity for keratinizing epidermal cells, but essentially no activity for fibroblasts, which is similar to
the biological activity of FGF7. Studies of the mouse homolog of suggested that this gene is required for embryonic
epidermal morphogenesis including brain development, lung morphogenesis, and initiation of lim bud formation. This
gene is also implicated to be a primary factor in the process of wound healing. (provided by RefSeq, Jul 2008)

UniProtKB/Swiss-Prot: FGF10_HUMAN, O15520
Function: Plays an important role in the regulation of embryonic development, cell proliferation and cell
differentiation. Required for normal branching morphogenesis. May play a role in wound healing

Gene Wiki entry for FGF10


(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_000005.9  NC_018916.1  NT_006576.16  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the FGF10 gene promoter:
         c-Fos   AP-1   ATF-2   STAT3   c-Jun   C/EBPalpha   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidFGF10 promoter sequence
   Search SABiosciences Chromatin IP Primers for FGF10

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat FGF10


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

Entrez Gene cytogenetic band: 5p13-p12   Ensembl cytogenetic band:  5p12   HGNC cytogenetic band: 5p13-p12

FGF10 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
FGF10 gene location

GeneLoc information about chromosome 5         GeneLoc Exon Structure

GeneLoc location for GC05M044340:  view genomic region     (about GC identifiers)

Start:
44,303,646 bp from pter      End:
44,389,808 bp from pter
Size:
86,163 bases      Orientation:
minus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: FGF10_HUMAN, O15520 (See protein sequence)
Recommended Name: Fibroblast growth factor 10 precursor  
Size: 208 amino acids; 23436 Da
Subunit: Interacts with FGFR1 and FGFR2. Interacts with FGFBP1
Subcellular location: Secreted (Potential)
1 PDB 3D structure from and Proteopedia for FGF10:
1NUN (3D)    
Secondary accessions: Q6FHT6 Q96P59

Explore the universe of human proteins at neXtProt for FGF10: NX_O15520

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_O15520

  • FGF10 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_004456.1  
    ENSEMBL proteins: 
     ENSP00000264664   ENSP00000426406  
    Reactome Protein details: O15520
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    Uscn Proteins for FGF10

    Gene Ontology (GO): 5/6 cellular component terms (GO ID links to tree view) (see all 6):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005576extracellular region TAS--
    GO:0005615extracellular space IDA16597614
    GO:0005634nucleus IDA16597614
    GO:0005886plasma membrane IDA16597614
    GO:0009986cell surface NAS11923311


    FGF10 for ontologies           About GeneDecksing



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

    FGF10 for domains           About GeneDecksing

    3 InterPro domains/families:
     IPR002348 IL1_HBGF
     IPR008996 Cytokine_IL1-like
     IPR002209 GF_heparin-bd

    Graphical View of Domain Structure for InterPro Entry O15520

    ProtoNet protein and cluster: O15520

    2 Blocks protein families:
    IPB002209 Heparin binding growth factor family signature
    IPB002348 IL1/HBGF family signature


    UniProtKB/Swiss-Prot: FGF10_HUMAN, O15520
    Similarity: Belongs to the heparin-binding growth factors 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: FGF10_HUMAN, O15520
    Function: Plays an important role in the regulation of embryonic development, cell proliferation and cell
    differentiation. Required for normal branching morphogenesis. May play a role in wound healing

         Genatlas biochemistry entry for FGF10:
    fibroblast growth factor 10,19kDa,essential regulator of lung and limb formation,involved in the mesenchymal cells for
    the initiation and growth of the mouse limb bud,triggering FGF8 expression in ectoderm and SHH expression in mesoderm

         Summary:  
    During embryonic development, FGF10 as signaling molecule is secreted from the following cells: Distal Mesodermal Progenitor Cells in Lung Mesoderm, Dorsal Pancreatic Mesenchymal Cells in Dorsal Pancreatic Mesenchyme (see all 7).

    It affects the following cells: Apical Ectodermal Ridge Cells in Limb Ectoderm, Definitive Endoderm Cells in Definitive Endoderm (see all 10).

    FGF10 as growth factor is involved in stem cell differentiation protocols towards the derivation of the following cells: Nkx2-1 induced endoderm, Posterior foregut endoderm-like cells (see all 10).

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    Gene Ontology (GO): 5/6 molecular function terms (GO ID links to tree view) (see all 6):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005104fibroblast growth factor receptor binding IDA11923311
    GO:0005111type 2 fibroblast growth factor receptor binding IPI19224135
    GO:0005515protein binding ----
    GO:0008083growth factor activity IDA15690149
    GO:0008201heparin binding IDA11923311


    FGF10 for ontologies           About GeneDecksing


    2 GenomeRNAi human phenotypes for FGF10:
     Decreased G3BP1 protein expres  Increased circadian period len 

    Animal Models:
         Mouse knock-outs for FGF10: Fgf10tm1Ska Fgf10tm1Wss Fgf10tm1.1Sms
         15/23 MGI mutant phenotypes (inferred from 8 alleles(MGI details for Fgf10) (see all 23):
     adipose tissue  cardiovascular system  cellular  craniofacial  digestive/alimentary 
     embryogenesis  endocrine/exocrine gland  growth/size  hearing/vestibular/ear  hematopoietic system 
     homeostasis/metabolism  immune system  integument  limbs/digits/tail  mortality/aging 

    FGF10 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 - 5/30 super-pathways (see all 30About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Apoptotic Pathways in Synovial Fibroblasts
    8/14 pathways (see all 14)
    Apoptotic Pathways in Synovial Fibroblasts1.00
    ERK5 Signaling0.61
    p53 Mediated Apoptosis0.84
    eIF2 Pathway0.60
    Mitochondrial Apoptosis0.73
    Rac1 Pathway0.58
    Telomerase Components in Cell Signaling0.72
    Nuclear Receptor Activation by Vitamin-A0.57
    2Signaling by FGFR
    8/12 pathways (see all 12)
    Signaling by FGFR1.00
    DAP12 signaling0.83
    Downstream signaling of activated FGFR0.92
    Signaling by EGFR in Cancer0.83
    Signaling by FGFR in disease0.91
    DAP12 interactions0.76
    Signaling by ERBB20.89
    Signaling by PDGF0.72
    3PIP3 activates AKT signaling
    8/10 pathways (see all 10)
    PI-3K cascade1.00
    PI3K/AKT activation0.97
    PIP3 activates AKT signaling1.00
    GAB1 signalosome0.96
    PI3K/AKT Signaling in Cancer1.00
    Constitutive PI3K/AKT Signaling in Cancer0.88
    PI3K events in ERBB2 signaling1.00
    Signaling by SCF-KIT0.72
    4IRS-related events
    IRS-related events1.00
    Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R)0.90
    IRS-mediated signalling0.98
    IGF1R signaling cascade0.90
    Insulin receptor signalling cascade0.94
    PI3K Cascade0.84
    IRS-related events triggered by IGF1R0.93
    Signaling by Insulin receptor0.74
    5GPCR Pathway
    GPCR Pathway1.00
    Estrogen Pathway0.55
    Ras Pathway0.62
    Pancreatic Adenocarcinoma0.55
    Breast Cancer Regulation by Stathmin10.58
    Paxillin Interactions0.53
    NFAT in Immune Response0.58
    P2Y Receptor Signaling0.38

    Pathway sources
    See GeneCards unified pathways
    Show all pathways

    1 EMD Millipore Pathway for FGF10
        Development FGF-family signaling

    5/59 Downloadable PowerPoint Slides of QIAGEN Pathway Central Maps for FGF10 (see all 59)
        Nuclear Receptor Activation by Vitamin-A
    Paxillin Interactions
    Telomerase Components in Cell Signaling
    Mitochondrial Apoptosis
    Molecular Mechanisms of Cancer

    1 GeneGo (Thomson Reuters) Pathway for FGF10
        Development FGF-family signaling

    2 BioSystems Pathways for FGF10 
        Heart Development
    Regulation of Actin Cytoskeleton

    5/50        Reactome Pathways for FGF10 (see all 50)
        FGFR2 ligand binding and activation
    FGFR ligand binding and activation
    Signaling by EGFR in Cancer
    Signaling by FGFR2 mutants
    Downstream signal transduction


    4         Kegg Pathways  (Kegg details for FGF10):
        MAPK signaling pathway
    Regulation of actin cytoskeleton
    Pathways in cancer
    Melanoma


    FGF10 for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for FGF10

    STRING Interaction Network Preview (showing 5 interactants - click image to see 24)

    5/25 Interacting proteins for FGF10 (O155202, 3 ENSP000002646644) via UniProtKB, MINT, STRING, and/or I2D (see all 25)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    FGFR2P218022, 3, ENSP000004102944MINT-24798 I2D: score=4 STRING: ENSP00000410294
    POMCP011893, ENSP000002647084I2D: score=1 STRING: ENSP00000264708
    FGFBP1Q145123I2D: score=1 
    FGF1ENSP000003385484STRING: ENSP00000338548
    FGF18ENSP000002746254STRING: ENSP00000274625
    About this table

    Gene Ontology (GO): 5/125 biological process terms (GO ID links to tree view) (see all 125):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000187activation of MAPK activity IDA14975937
    GO:0001525angiogenesis IEA--
    GO:0001656metanephros development IEP18437684
    GO:0001759organ induction IEA--
    GO:0001823mesonephros development IEP18437684


    FGF10 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

    FGF10 for compounds           About GeneDecksing

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

    Browse Tocris compounds for FGF10
    8 Novoseek chemical compound relationships for FGF10 gene    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    bromodeoxyuridine 44.3 6 11286634 (1), 10503993 (1), 15690149 (1), 15137055 (1) (see all 5)
    heparan sulfate 40.6 11 19755711 (2), 14707131 (1)
    dextran sulfate sodium 33.5 2 10381813 (1)
    tyrosine 26.2 6 11286634 (2), 17449030 (1), 19863897 (1), 16501574 (1)
    heparin 26.2 3 12818887 (1), 9582367 (1), 9740653 (1)
    retinoic acid 19.9 5 16622850 (1), 18977204 (1), 10862743 (1), 20301097 (1)
    vegf 8.2 8 14706196 (3), 14996996 (2), 18437684 (1), 20503389 (1)
    testosterone 0 6 18068633 (2), 15843416 (1), 10503993 (1), 15094393 (1) (see all 5)

    Search CenterWatch for drugs/clinical trials and news about FGF10 

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
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    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for FGF10 gene: 
    NM_004465.1  

    Unigene Cluster for FGF10:

    Fibroblast growth factor 10
    Hs.664499  [show with all ESTs]
    Unigene Representative Sequence: AK315314
    2 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000264664(uc003jog.1) ENST00000513107

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    Additional cDNA sequence: 

    AB002097.1 AF411527.1 AF508782.1 AK315314.1 BC069561.1 BC105021.1 BC105023.1 BC143772.1 
    CR541665.1 CR541688.1 GQ351295.1 U67918.1 

    3 DOTS entries:

    DT.91752709  DT.120862189  DT.120862177 

    16 AceView cDNA sequences:

    AB002097 NM_004465 BX471703 BX280011 U67918 CA394078 BC069561 BX955123 
    AL603565 AF411527 CR541688 BX484361 CR541665 AF508782 BP380072 BF983177 

    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

    FGF10 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: AACAAGAAGG

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

    About this image

    FGF10 expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    10/27 LifeMap In Vivo Development Anatomical Compartments/Cells (see all 27
    Tissue Anatomical Compartment CellCategory (developmental path)
    AdiposeVascular AdiposeStromal Vascular Preadipocyte Progenitor CellsAdipose
    HeartHeart TubeHeart Tube CellsMyocardium
    LungLung MesodermDistal Mesodermal Progenitor CellsLung
    HeartCardiac CrescentCardiac Crescent CellsMyocardium
    HeartPrimitive Heart TubePrimitive Heart Tube CellsMyocardium
    LungTracheaAirway Smooth Muscle CellsLung, Smooth Muscle
    AdiposeBody Subcutaneous White AdiposeSubcutaneous White PreadipocytesAdipose
    AdiposeCranial Subcutaneous White AdiposeSubcutaneous White PreadipocytesAdipose
    AdiposeFacial Subcutaneous White AdiposeSubcutaneous White PreadipocytesAdipose
    AdiposeSubcutaneous White AdiposeSubcutaneous White PreadipocytesAdipose
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization

    See FGF10 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for FGF10

    SOURCE GeneReport for Unigene cluster: Hs.664499
        SABiosciences Expression via Pathway-Focused PCR Arrays including FGF10 (see all 6): 
              Growth Factors in human mouse rat
              Wound Healing in human mouse rat
              Mesenchymal Stem Cell in human mouse rat
              Common Cytokines in human mouse rat
              Inflammatory Response & Autoimmunity 384HT in human mouse rat

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    In Situ
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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 animals.

    Orthologs for FGF10 gene from 5/15 species (see all 15)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves FGF101 fibroblast growth factor 10 84.39(n)
    88.29(a)
      395432  NM_204696.1  NP_990027.1 
    lizard
    (Anolis carolinensis)
    Reptilia --
    --
    68(a)
    1 ↔ 1
    2(5625236-5711595)
    African clawed frog
    (Xenopus laevis)
    Amphibia fgf10-A2 fibroblast growth factor-10 79.35(n)    AB073747.1 
    zebrafish
    (Danio rerio)
    Actinopterygii fgf102 fibroblast growth factor 10 77.77(n)   359830  AF544025.1 
    worm
    (Caenorhabditis elegans)
    Secernentea let-7566
    Protein let-756
    10(a)
    1 → many
    III(6407076-6409965)


    ENSEMBL Gene Tree for FGF10 (if available)
    TreeFam Gene Tree for FGF10 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for FGF10 gene
    FGF122  FGF52  FGF202  FGF162  FGF42  FGF92  FGF62  FGF32  
    FGF72  FGF112  FGF132  FGF222  FGF142  
    18/19 SIMAP similar genes for FGF10 using alignment to 5 protein entries:     FGF10_HUMAN (see all proteins) (see all similar genes):
    KGFLP2    FGF22    KGFLP1    PRED3    FGF16    FGF7
    FGF9    FGF20    FGF12    FGF11    FGF3    FGF13
    FGF5    FGF2    FGF6    FGF14    FGF4    fgf gene

    FGF10 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

    10/1441 NCBI SNPs in FGF10 are shown (see all 1441    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 5 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1048938841,2
    C,pathogenic44258105(-) AAACAC/G/TGAAGG 3 R G * mis1 stg10--------
    rs1048938861,2
    Cpathogenic44258215(-) GAGGAG/TAGAGG 2 R I mis10--------
    rs1048938891,2
    Cpathogenic44263503(-) GAAGGA/GGAAAC 2 E G mis10--------
    rs1048938871,2
    Cpathogenic44263507(-) ACAAGA/TAGGGG 2 K * stg10--------
    rs1048938851,2
    Cpathogenic44341387(-) GAACTG/TCCCGT 2 C F mis10--------
    rs1048938881,2
    Cpathogenic44341464(-) TGGAGA/CAAGCT 2 R S mis10--------
    rs1117639651,2
    C,F,--44258050(+) TTGCCT/ATCCTC 1 -- ds50013Minor allele frequency- A:0.00CSA EU 1328
    rs1477155091,2
    C,F,--44258062(+) ATGAGC/G/TGTACC 3 H P R mis12NA EU 5873
    rs172346391,2
    C,F,H,--44258091(-) AACACC/TTCTGC 2 T syn1 ese38Minor allele frequency- T:0.04NS NA WA 5628
    rs172282551,2
    C,F,--44258332(-) GGACTG/AGAGTT 1 -- int12Minor allele frequency- A:0.01NS NA 286

    HapMap Linkage Disequilibrium report for FGF10 (44303646 - 44389808 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 4 variations for FGF10
         4 Indels: 93012 93010 80895 93011
    Human Gene Mutation Database (HGMD): FGF10

    SABiosciences Cancer Mutation PCR Assays
    QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing FGF10
    DNA2.0 Custom Variant and Variant Library Synthesis for FGF10

    (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

    FGF10 for disorders           About GeneDecksing

    OMIM gene information: 602115   
    OMIM disorders: 180920  149730  
    UniProtKB/Swiss-Prot: FGF10_HUMAN, O15520
  • Defects in FGF10 are the cause of autosomal dominant aplasia of lacrimal and salivary glands (ALSG)
  • [MIM:180920]. ALSG has variable expressivity, and affected individuals may have aplasia or hypoplasia of the lacrimal,
    parotid, submandibular and sublingual glands and absence of the lacrimal puncta. The disorder is characterized by
    irritable eyes, recurrent eye infections, epiphora (constant tearing) and xerostomia (dryness of the mouth), which
    increases the risk of dental erosion, dental caries, periodontal disease and oral infections
  • Defects in FGF10 are a cause of lacrimo-auriculo-dento-digital syndrome (LADDS) [MIM:149730]; also known as
  • Levy-Hollister syndrome. LADDS is a form of ectodermal dysplasia, a heterogeneous group of disorders due to abnormal
    development of two or more ectodermal structures. LADDS is an autosomal dominant syndrome characterized by
    aplastic/hypoplastic lacrimal and salivary glands and ducts, cup-shaped ears, hearing loss, hypodontia and enamel
    hypoplasia, and distal limb segments anomalies. In addition to these cardinal features, facial dysmorphism,
    malformations of the kidney and respiratory system and abnormal genitalia have been reported. Craniosynostosis and
    severe syndactyly are not observed

    20/58 diseases for FGF10 (see all 58):    About MalaCards
    gilles de la tourette syndrome    aplasia of lacrimal and salivary glands    mesenteric vascular occlusion    attention deficit hyperactivity disorder
    cleft lip/palate    cleft lip    graft versus host disease    clear cell acanthoma
    congenital diaphragmatic hernia    pfeiffer syndrome    bronchopulmonary dysplasia    dental caries
    craniosynostosis    intestinal atresia    tourette syndrome    ladd syndrome
    ectodermal dysplasia    acrocephalosyndactylia    muscle hypertrophy    acanthoma

    7 diseases from the University of Copenhagen DISEASES database for FGF10:
    LADD syndrome     Intestinal atresia     Cleft palate     Esophageal atresia
    Synostosis     Congenital diaphragmatic hernia     Mesenteric vascular occlusion

    10/22 Novoseek disease relationships for FGF10 gene (see all 22)    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    aplasia 60.8 13 19376597 (2), 16476029 (1), 15972105 (1), 17213838 (1) (see all 5)
    apert syndrome 60.6 2 19581825 (1), 14613973 (1)
    pfeiffer syndrome 54.8 1 14613973 (1)
    craniosynostosis 48.6 1 15282208 (1)
    hypoplasia 45.6 1 19376597 (1)
    atresia 39.3 1 15234214 (1)
    mucositis 31.9 5 11511852 (1), 15995938 (1), 15623608 (1)
    hypospadias 17.7 4 17264867 (3), 15843416 (1)
    bronchopulmonary dysplasia 16.9 5 17071719 (4)
    colitis ulcerative 11.2 1 12786629 (1)

    Human Genome Epidemiology (HuGE) Navigator: FGF10 (9 documents)

    Export disorders for FGF10 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 FGF10 gene, integrated from 9 sources (see all 211):
    (articles sorted by number of sources associating them with FGF10)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Structure and expression of human fibroblast growth factor-10. (PubMed id 9287324)1, 2, 3, 9 Emoto H....Itoh N. (1997)
    2. Structural basis by which alternative splicing confers specificity in fibroblast growth factor receptors. (PubMed id 12591959)1, 2, 9 Yeh B.K.... Mohammadi M. (2003)
    3. The fibroblast growth factor binding protein is a novel interaction partner of FGF-7, FGF-10 and FGF-22 and regulates FGF activity: implications for epithelial repair. (PubMed id 15806171)1, 2, 9 Beer H.-D....Werner S. (2005)
    4. Mutations in different components of FGF signaling in LADD syndrome. (PubMed id 16501574)1, 2, 9 Rohmann E.... Wollnik B. (2006)
    5. Receptor specificity of the fibroblast growth factor family. The complete mammalian FGF family. (PubMed id 16597617)1, 2 Zhang X....Ornitz D.M. (2006)
    6. LADD syndrome is caused by FGF10 mutations. (PubMed id 16630169)1, 2 Milunsky J.M.... Everman D.B. (2006)
    7. Mutations in the gene encoding fibroblast growth factor 10 are associated with aplasia of lacrimal and salivary glands. (PubMed id 15654336)1, 2 Entesarian M.... Dahl N. (2005)
    8. 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)
    9. FGF-10 is a chemotactic factor for distal epithelial buds during lung development. (PubMed id 9740653)1, 9 Park W.Y....Cardoso W.V. (1998)
    10. FGF-10 and specific structural elements of dermatan sulfate size and sulfation promote maximal keratinocyte migration and cellular proliferation. (PubMed id 19152659)1, 9 Radek K.A....Gallo R.L. (2009)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Disorders
    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: 2255 HGNC: 3666 AceView: FGF10 Ensembl:ENSG00000070193 euGenes: HUgn2255
    ECgene: FGF10 Kegg: 2255 H-InvDB: FGF10

    (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 FGF10 Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for FGF10 Genetics and Cytogenetics in Oncology and Haematology
    NIEHS-SNPshttp://egp.gs.washington.edu/data/fgf10/

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for FGF10 gene:
    Search GeneIP for patents involving FGF10

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



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     Regulatory tfbs in FGF10 promoter
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