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 gene is located in a region on chromosome X, which i... See more...

Aliases for FGF13 Gene

Aliases for FGF13 Gene

  • Fibroblast Growth Factor 13 2 3 4 5
  • Fibroblast Growth Factor Homologous Factor 2 2 3 4
  • FHF2 2 3 4
  • FGF-13 3 4
  • FHF-2 3 4
  • FGF2 2 3
  • Long Intergenic Non-Protein Coding RNA 889 2
  • LINC00889 3
  • FLJ30672 2
  • FGF13 5

External Ids for FGF13 Gene

Previous HGNC Symbols for FGF13 Gene

  • LINC00889

Previous GeneCards Identifiers for FGF13 Gene

  • GC0XM132285
  • GC0XM134559
  • GC0XM135658
  • GC0XM136419
  • GC0XM137439
  • GC0XM137541
  • GC0XM137713
  • GC0XM126980
  • GC0XM138631

Summaries for FGF13 Gene

Entrez Gene Summary for FGF13 Gene

  • 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 gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked cognitive disability mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini. [provided by RefSeq, Nov 2008]

CIViC Summary for FGF13 Gene

GeneCards Summary for FGF13 Gene

FGF13 (Fibroblast Growth Factor 13) is a Protein Coding gene. Diseases associated with FGF13 include Borjeson-Forssman-Lehmann Syndrome and X-Linked Congenital Generalized Hypertrichosis. Among its related pathways are NF-KappaB Family Pathway and Activation of cAMP-Dependent PKA. Gene Ontology (GO) annotations related to this gene include microtubule binding and ion channel binding. An important paralog of this gene is FGF14.

UniProtKB/Swiss-Prot Summary for FGF13 Gene

  • Microtubule-binding protein which directly binds tubulin and is involved in both polymerization and stabilization of microtubules (By similarity). Through its action on microtubules, may participate in the refinement of axons by negatively regulating axonal and leading processes branching (By similarity). Plays a crucial role in neuron polarization and migration in the cerebral cortex and the hippocampus (By similarity). May regulate voltage-gated sodium channels transport and function (PubMed:15282281). May also play a role in MAPK signaling (By similarity). Required for the development of axonal initial segment-targeting inhibitory GABAergic synapses made by chandelier neurons (By similarity).

Gene Wiki entry for FGF13 Gene

Additional gene information for FGF13 Gene

No data available for Tocris Summary , PharmGKB "VIP" Summary , Rfam classification and piRNA Summary for FGF13 Gene

Genomics for FGF13 Gene

GeneHancer (GH) Regulatory Elements Pubs

Promoters and enhancers for FGF13 Gene
GeneHancer (GH) Identifier GH Type GH
Score
GH Sources Gene Association Score Total Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor
Binding Sites
Gene Targets
GH0XJ138710 Promoter/Enhancer 1.7 EPDnew Ensembl ENCODE CraniofacialAtlas 600 +512.2 512159 4.7 PATZ1 POLR2A ZNF341 ZNF561 SCRT2 CTCF ZBTB20 RAD21 ZNF316 OSR2 FGF13-AS1 FGF13 MIR504 RF00017-8764
GH0XJ139223 Promoter/Enhancer 0.8 EPDnew Ensembl ENCODE 600.7 +0.7 667 1.6 FGF13 lnc-MCF2-3
GH0XJ139169 Promoter 0.3 EPDnew 600.2 +53.6 53644 0.1 FGF13 piR-55036-120 piR-45932-119 lnc-MCF2-3
GH0XJ139200 Enhancer 0.8 Ensembl ENCODE 13.2 +22.1 22060 0.9 ZNF629 SCRT2 CTBP1 OSR2 BCL11A NR2C2 KLF4 WT1 ZNF644 DPF2 FGF13 lnc-MCF2-3 piR-55036-120
GH0XJ139343 Enhancer 0.3 Ensembl 31.2 -120.9 -120912 1.2 ZNF10 FGF13 SNURFL piR-50129-294 F9
- Elite GeneHancer and/or Elite GeneHancer-gene association Download GeneHancer data from 2017 publication | Request up-to-date GeneHancer data (full dataset)

GeneHancers around FGF13 on the GeneHancer Hub at the UCSC Golden Path

Cistromic (ChIP-Seq) regulation report from SPP (The Signaling Pathways Project) for FGF13

Top Transcription factor binding sites by QIAGEN in the FGF13 gene promoter:
  • CUTL1
  • FOXO4
  • GR
  • GR-alpha
  • GR-beta
  • Nkx2-5
  • Nkx3-1 v3
  • SRY

Genomic Locations for FGF13 Gene

Genomic Locations for FGF13 Gene
chrX:138,614,727-139,222,889
(GRCh38/hg38)
Size:
608,163 bases
Orientation:
Minus strand
chrX:137,713,734-138,304,939
(GRCh37/hg19)
Size:
591,206 bases
Orientation:
Minus strand

Genomic View for FGF13 Gene

Genes around FGF13 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
FGF13 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for FGF13 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for FGF13 Gene

Proteins for FGF13 Gene

  • Protein details for FGF13 Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    Q92913-FGF13_HUMAN
    Recommended name:
    Fibroblast growth factor 13
    Protein Accession:
    Q92913
    Secondary Accessions:
    • B1AK18
    • B7Z4M7
    • B7Z8N0
    • D3DWH4
    • O95830
    • Q9NZH9
    • Q9NZI0

    Protein attributes for FGF13 Gene

    Size:
    245 amino acids
    Molecular mass:
    27564 Da
    Quaternary structure:
    • Interacts with SCN8A; may regulate SCN8A activity. Interacts with SCN1A; may regulate SCN1A activity. Interacts with SCN5A; the interaction is direct and may regulate SNC5A density at membranes and function. May also interact with SCN2A and SCN11A. Interacts with MAPK8IP2; may regulate the MAPK8IP2 scaffolding activity.

    Three dimensional structures from OCA and Proteopedia for FGF13 Gene

    Alternative splice isoforms for FGF13 Gene

    UniProtKB/Swiss-Prot:

neXtProt entry for FGF13 Gene

Post-translational modifications for FGF13 Gene

No data available for DME Specific Peptides for FGF13 Gene

Domains & Families for FGF13 Gene

Gene Families for FGF13 Gene

Protein Domains for FGF13 Gene

InterPro:
Blocks:
  • Heparin binding growth factor family signature
  • IL1/HBGF family signature
ProtoNet:

Suggested Antigen Peptide Sequences for FGF13 Gene

GenScript: Design optimal peptide antigens:
  • cDNA FLJ76228, highly similar to Homo sapiens fibroblast growth factor 13 (FGF13), transcript variant 1A, mRNA (A8K1P5_HUMAN)
  • cDNA, FLJ79069, highly similar to Fibroblast growth factor 13 (B7Z4M7_HUMAN)
  • cDNA FLJ57068, highly similar to Fibroblast growth factor 13 (B7Z8N0_HUMAN)
  • Fibroblast growth factor 13, isoform CRA_b (D3DWH3_HUMAN)
  • Fibroblast growth factor homologous factor 2 (FGF13_HUMAN)

Graphical View of Domain Structure for InterPro Entry

Q92913

UniProtKB/Swiss-Prot:

FGF13_HUMAN :
  • Belongs to the heparin-binding growth factors family.
Family:
  • Belongs to the heparin-binding growth factors family.
genes like me logo Genes that share domains with FGF13: view

Function for FGF13 Gene

Molecular function for FGF13 Gene

UniProtKB/Swiss-Prot Function:
Microtubule-binding protein which directly binds tubulin and is involved in both polymerization and stabilization of microtubules (By similarity). Through its action on microtubules, may participate in the refinement of axons by negatively regulating axonal and leading processes branching (By similarity). Plays a crucial role in neuron polarization and migration in the cerebral cortex and the hippocampus (By similarity). May regulate voltage-gated sodium channels transport and function (PubMed:15282281). May also play a role in MAPK signaling (By similarity). Required for the development of axonal initial segment-targeting inhibitory GABAergic synapses made by chandelier neurons (By similarity).
GENATLAS Biochemistry:
fibroblast growth homologous factor 13,expressed principally in the nervous system and skeletal muscle with two alternatively spliced isoforms

Phenotypes From GWAS Catalog for FGF13 Gene

Gene Ontology (GO) - Molecular Function for FGF13 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005515 protein binding IPI 15282281
GO:0008017 microtubule binding ISS --
GO:0008083 growth factor activity IEA --
GO:0017080 sodium channel regulator activity ISS 21817159
GO:0030295 protein kinase activator activity IGI 12244047
genes like me logo Genes that share ontologies with FGF13: view
genes like me logo Genes that share phenotypes with FGF13: view

Animal Models for FGF13 Gene

MGI Knock Outs for FGF13:

Animal Model Products

  • Taconic Biosciences Mouse Models for FGF13

CRISPR Products

Inhibitory RNA Products

  • Search GeneCopoeia for shRNA, lentivirus and/or AAV clone products for FGF13

Clone Products

No data available for Enzyme Numbers (IUBMB) , Human Phenotype Ontology , Transcription Factor Targets and HOMER Transcription for FGF13 Gene

Localization for FGF13 Gene

Subcellular locations from UniProtKB/Swiss-Prot for FGF13 Gene

Cell projection, filopodium. Cell projection, growth cone. Cell projection, dendrite. Nucleus. Cytoplasm. Note=Not secreted. {ECO:0000250}.
[Isoform 1]: Nucleus, nucleolus.
[Isoform 2]: Cytoplasm. Nucleus.

Subcellular locations from

COMPARTMENTS
Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for FGF13 gene
Compartment Confidence
plasma membrane 5
cytoskeleton 5
nucleus 5
cytosol 5
extracellular 4
mitochondrion 3
endoplasmic reticulum 2
endosome 2
lysosome 2
golgi apparatus 2
peroxisome 1

Subcellular locations from the

Human Protein Atlas (HPA)

Gene Ontology (GO) - Cellular Components for FGF13 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005576 extracellular region IEA --
GO:0005634 nucleus IDA,ISS 21817159
GO:0005730 nucleolus IEA --
GO:0005737 cytoplasm IPI,ISS 21817159
GO:0005829 cytosol IDA --
genes like me logo Genes that share ontologies with FGF13: view

Pathways & Interactions for FGF13 Gene

PathCards logo

SuperPathways for FGF13 Gene

SuperPathway Contained pathways
1 Apoptotic Pathways in Synovial Fibroblasts
.85
.85
.84
.84
.74
.72
.66
.65
.64
.62
.61
.60
.57
.57
2 GPCR Pathway
.73
.73
.62
.59
.58
.58
.55
.38
3 TGF-Beta Pathway
.60
.60
.57
.51
.43
.41
4 ERK Signaling
.61
.61
.58
.51
.49
5 Nanog in Mammalian ESC Pluripotency
.62
.62
.59
.48
genes like me logo Genes that share pathways with FGF13: view

Pathways by source for FGF13 Gene

2 BioSystems pathways for FGF13 Gene
59 Qiagen pathways for FGF13 Gene
  • 14-3-3 Induced Intracellular Signaling
  • Actin-Based Motility by Rho Family GTPases
  • Activation of cAMP-Dependent PKA
  • Activation of PKA through GPCR
  • Activation of PKC through GPCR

SIGNOR curated interactions for FGF13 Gene

Gene Ontology (GO) - Biological Process for FGF13 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000165 MAPK cascade IDA 12244047
GO:0001764 neuron migration ISS --
GO:0006814 sodium ion transport ISS 21817159
GO:0007026 negative regulation of microtubule depolymerization ISS --
GO:0007165 signal transduction IEA,TAS 8790420
genes like me logo Genes that share ontologies with FGF13: view

Drugs & Compounds for FGF13 Gene

No Compound Related Data Available

Transcripts for FGF13 Gene

mRNA/cDNA for FGF13 Gene

6 REFSEQ mRNAs :
24 NCBI additional mRNA sequence :
8 Ensembl transcripts including schematic representations, and UCSC links to gene/alias where relevant :

CRISPR Products

Inhibitory RNA Products

  • Search GeneCopoeia for shRNA, lentivirus and/or AAV clone products for FGF13

Clone Products

Alternative Splicing Database (ASD) splice patterns (SP) for FGF13 Gene

No ASD Table

Relevant External Links for FGF13 Gene

GeneLoc Exon Structure for
FGF13

Expression for FGF13 Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and SAGE for FGF13 Gene

mRNA differential expression in normal tissues according to GTEx for FGF13 Gene

This gene is overexpressed in Brain - Hippocampus (x6.0), Brain - Amygdala (x4.7), Brain - Anterior cingulate cortex (BA24) (x4.5), and Brain - Nucleus accumbens (basal ganglia) (x4.2).

Protein differential expression in normal tissues from HIPED for FGF13 Gene

This gene is overexpressed in Plasma (49.8) and Fetal Brain (17.5).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB and MOPED for FGF13 Gene



Protein tissue co-expression partners for FGF13 Gene

Transcriptomic regulation report from SPP (The Signaling Pathways Project) for FGF13

SOURCE GeneReport for Unigene cluster for FGF13 Gene:

Hs.6540

mRNA Expression by UniProt/SwissProt for FGF13 Gene:

Q92913-FGF13_HUMAN
Tissue specificity: Ubiquitously expressed. Predominantly expressed in the nervous system.

Evidence on tissue expression from TISSUES for FGF13 Gene

  • Nervous system(4.9)
  • Eye(4.6)
  • Skin(4.6)
  • Kidney(4.5)
  • Lung(4.5)
  • Muscle(3.1)
  • Bone marrow(3.1)
  • Heart(3)
  • Intestine(2.8)
  • Blood(2.8)
  • Bone(2.7)
  • Lymph node(2.7)
  • Spleen(2.6)
  • Stomach(2.4)
  • Thyroid gland(2.4)
  • Liver(2.3)
  • Pancreas(2.1)
  • Adrenal gland(2)
genes like me logo Genes that share expression patterns with FGF13: view

No data available for Phenotype-based relationships between genes and organs from Gene ORGANizer for FGF13 Gene

Orthologs for FGF13 Gene

This gene was present in the common ancestor of chordates.

Orthologs for FGF13 Gene

Organism Taxonomy Gene Similarity Type Details
Chimpanzee
(Pan troglodytes)
Mammalia FGF13 30 31
  • 100 (n)
OneToOne
Mouse
(Mus musculus)
Mammalia Fgf13 30 17 31
  • 95.51 (n)
OneToOne
Cow
(Bos Taurus)
Mammalia FGF13 30 31
  • 95.51 (n)
OneToOne
Rat
(Rattus norvegicus)
Mammalia Fgf13 30
  • 94.9 (n)
Oppossum
(Monodelphis domestica)
Mammalia FGF13 31
  • 94 (a)
OneToOne
Dog
(Canis familiaris)
Mammalia LOC492174 30
  • 93.61 (n)
FGF13 31
  • 78 (a)
OneToOne
Platypus
(Ornithorhynchus anatinus)
Mammalia FGF13 31
  • 76 (a)
OneToOne
Chicken
(Gallus gallus)
Aves FGF13 30 31
  • 83.61 (n)
OneToOne
Lizard
(Anolis carolinensis)
Reptilia FGF13 31
  • 97 (a)
OneToOne
Tropical Clawed Frog
(Silurana tropicalis)
Amphibia fgf13 30
  • 79.96 (n)
Str.13293 30
Zebrafish
(Danio rerio)
Actinopterygii fgf13a 30 31
  • 80.33 (n)
OneToOne
Species where no ortholog for FGF13 was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Eremothecium gossypii)
  • Actinobacteria (Mycobacterium tuberculosis)
  • African clawed frog (Xenopus laevis)
  • African malaria mosquito (Anopheles gambiae)
  • Alicante grape (Vitis vinifera)
  • Alpha proteobacteria (Wolbachia pipientis)
  • Amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • Baker's yeast (Saccharomyces cerevisiae)
  • Barley (Hordeum vulgare)
  • Beta proteobacteria (Neisseria meningitidis)
  • Bread mold (Neurospora crassa)
  • Chromalveolata (Phytophthora infestans)
  • Common water flea (Daphnia pulex)
  • Corn (Zea mays)
  • E. coli (Escherichia coli)
  • Filamentous fungi (Aspergillus nidulans)
  • Firmicute Bacteria (Streptococcus pneumoniae)
  • Fission Yeast (Schizosaccharomyces pombe)
  • Fruit Fly (Drosophila melanogaster)
  • Green Algae (Chlamydomonas reinhardtii)
  • Honey Bee (Apis mellifera)
  • K. Lactis Yeast (Kluyveromyces lactis)
  • Loblloly Pine (Pinus taeda)
  • Malaria Parasite (Plasmodium falciparum)
  • Medicago Trunc (Medicago Truncatula)
  • Moss (Physcomitrella patens)
  • Orangutan (Pongo pygmaeus)
  • Pig (Sus scrofa)
  • Rainbow Trout (Oncorhynchus mykiss)
  • Rice (Oryza sativa)
  • Rice Blast Fungus (Magnaporthe grisea)
  • Schistosome Parasite (Schistosoma mansoni)
  • Sea Anemone (Nematostella vectensis)
  • Sea Vase (Ciona intestinalis)
  • Sea Squirt (Ciona savignyi)
  • Sea Urchin (Strongylocentrotus purpuratus)
  • Sorghum (Sorghum bicolor)
  • Soybean (Glycine max)
  • Stem Rust Fungus (Puccinia graminis)
  • Sugarcane (Saccharum officinarum)
  • Thale Cress (Arabidopsis thaliana)
  • Tomato (Lycopersicon esculentum)
  • Toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • Wheat (Triticum aestivum)
  • Worm (Caenorhabditis elegans)

Evolution for FGF13 Gene

ENSEMBL:
Gene Tree for FGF13 (if available)
TreeFam:
Gene Tree for FGF13 (if available)
Aminode:
Evolutionary constrained regions (ECRs) for FGF13: view image

Paralogs for FGF13 Gene

(17) SIMAP similar genes for FGF13 Gene using alignment to 7 proteins:

  • FGF13_HUMAN
  • A8K1P5_HUMAN
  • B1AJW0_HUMAN
  • B1AK17_HUMAN
  • B1B1H9_HUMAN
  • D3DWH3_HUMAN
  • Q9Y643_HUMAN
genes like me logo Genes that share paralogs with FGF13: view

Variants for FGF13 Gene

Sequence variations, with clinical significance, from ClinVar and Humsavar, with links to dbSNP for FGF13 Gene

SNP ID Clinical significance and condition Chr 0X pos Variation AA Info Type
710910 Benign: not provided 138,632,895(-) G/A SYNONYMOUS_VARIANT
741299 Likely Benign: not provided 138,632,900(-) A/G MISSENSE_VARIANT
758760 Likely Benign: not provided 138,710,845(-) G/T SYNONYMOUS_VARIANT,INTRON_VARIANT
rs17510270 - p.Lys197Gln

Additional dbSNP identifiers (rs#s) for FGF13 Gene

Structural Variations from Database of Genomic Variants (DGV) for FGF13 Gene

Variant ID Type Subtype PubMed ID
dgv2485e212 CNV loss 25503493
dgv2486e212 CNV loss 25503493
dgv2487e212 CNV loss 25503493
esv1007548 CNV deletion 20482838
esv2385287 CNV deletion 18987734
esv2477107 CNV deletion 19546169
esv2623043 CNV deletion 19546169
esv2667866 CNV deletion 23128226
esv2675863 CNV deletion 23128226
esv2740505 CNV deletion 23290073
esv2740507 CNV deletion 23290073
esv2740508 CNV deletion 23290073
esv2740509 CNV deletion 23290073
esv2740510 CNV deletion 23290073
esv2871 CNV loss 18987735
esv3302950 CNV tandem duplication 20981092
esv3345728 CNV insertion 20981092
esv3559384 CNV deletion 23714750
esv3559385 CNV deletion 23714750
esv3559386 CNV deletion 23714750
esv3559387 CNV deletion 23714750
esv3559389 CNV deletion 23714750
esv3574774 CNV loss 25503493
esv3574776 CNV loss 25503493
esv3574777 CNV loss 25503493
esv3574780 CNV loss 25503493
esv3574794 CNV loss 25503493
esv3577423 CNV gain 25503493
esv3577424 CNV gain 25503493
esv3577425 CNV gain 25503493
esv8695 CNV loss 19470904
nsv1140070 CNV duplication 24896259
nsv1141083 CNV deletion 24896259
nsv1141084 CNV deletion 24896259
nsv1147814 CNV deletion 26484159
nsv1151407 CNV duplication 26484159
nsv510563 OTHER sequence alteration 20534489
nsv523403 CNV gain 19592680
nsv524567 CNV gain 19592680
nsv525867 CNV gain 19592680
nsv525867 CNV gain 19592680
nsv7115 CNV insertion 18451855
nsv957795 CNV deletion 24416366

Variation tolerance for FGF13 Gene

Residual Variation Intolerance Score: 46.3% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 0.03; 0.61% of all genes are more intolerant (likely to be disease-causing)

Additional Variant Information for FGF13 Gene

Human Gene Mutation Database (HGMD)
FGF13
SNPedia medical, phenotypic, and genealogical associations of SNPs for
FGF13

SNP Genotyping and Copy Number Assay Products

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for FGF13 Gene

Disorders for FGF13 Gene

MalaCards: The human disease database

(15) MalaCards diseases for FGF13 Gene - From: DISEASES and GeneCards

Disorder Aliases PubMed IDs
borjeson-forssman-lehmann syndrome
  • bfls
x-linked congenital generalized hypertrichosis
  • hypertrichosis, congenital generalized
wildervanck syndrome
  • cervicooculoacoustic syndrome
genetic epilepsy with febrile seizures plus
  • generalized epilepsy with febrile seizures plus
crouzon syndrome
  • craniofacial dysostosis, type i; cfd1
- elite association - COSMIC cancer census association via MalaCards
Search FGF13 in MalaCards View complete list of genes associated with diseases

Additional Disease Information for FGF13

Genetic Association Database
(GAD)
Human Genome Epidemiology Navigator
(HuGE)
ATLAS of Genetics and Cytogenetics in Oncology and Haematology
Open Targets Platform
genes like me logo Genes that share disorders with FGF13: view

No data available for UniProtKB/Swiss-Prot and Genatlas for FGF13 Gene

Publications for FGF13 Gene

  1. Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patient. (PMID: 10071193) Gecz J … Mulley JC (Human genetics 1999) 3 4 23
  2. Fibroblast growth factor (FGF) homologous factors: new members of the FGF family implicated in nervous system development. (PMID: 8790420) Smallwood PM … Nathans J (Proceedings of the National Academy of Sciences of the United States of America 1996) 2 3 4
  3. Fibroblast growth factor homologous factor 13 regulates Na+ channels and conduction velocity in murine hearts. (PMID: 21817159) Wang C … Pitt GS (Circulation research 2011) 3 4
  4. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PMID: 15489334) Gerhard DS … MGC Project Team (Genome research 2004) 3 4
  5. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PMID: 14702039) Ota T … Sugano S (Nature genetics 2004) 3 4

Products for FGF13 Gene

  • Signalway ELISA kits for FGF13
  • Signalway Proteins for FGF13

Sources for FGF13 Gene