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    Foxb1 forkhead box B1 [ Mus musculus (house mouse) ]

    Gene ID: 64290, updated on 2-Nov-2024

    Summary

    Official Symbol
    Foxb1provided by MGI
    Official Full Name
    forkhead box B1provided by MGI
    Primary source
    MGI:MGI:1927549
    See related
    Ensembl:ENSMUSG00000059246 AllianceGenome:MGI:1927549
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Mus musculus
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus
    Also known as
    C43; Mf3; Twh; Fkh5; Foxb1a; Foxb1b; Hfh-e5.1
    Summary
    Enables sequence-specific DNA binding activity. Involved in several processes, including mammary gland development; nervous system development; and visual learning. Located in nucleus. Is expressed in several structures, including central nervous system; embryo ectoderm; jaw; limb; and paraxial mesenchyme. Orthologous to human FOXB1 (forkhead box B1). [provided by Alliance of Genome Resources, Nov 2024]
    Expression
    Biased expression in whole brain E14.5 (RPKM 3.7), CNS E14 (RPKM 2.6) and 4 other tissues See more
    Orthologs
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    Genomic context

    See Foxb1 in Genome Data Viewer
    Location:
    9 D; 9 38.76 cM
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2024_02 current GRCm39 (GCF_000001635.27) 9 NC_000075.7 (69664992..69668222, complement)
    108.20200622 previous assembly GRCm38.p6 (GCF_000001635.26) 9 NC_000075.6 (69757710..69760940, complement)

    Chromosome 9 - NC_000075.7Genomic Context describing neighboring genes Neighboring gene predicted gene, 53538 Neighboring gene STARR-seq mESC enhancer starr_24521 Neighboring gene CapStarr-seq enhancer MGSCv37_chr9:69516656-69516839 Neighboring gene predicted gene, 31469 Neighboring gene CapStarr-seq enhancer MGSCv37_chr9:69605139-69605379 Neighboring gene RIKEN cDNA B230323A14 gene Neighboring gene predicted gene, 31530 Neighboring gene zinc finger, BED domain containing 4 pseudogene

    Genomic regions, transcripts, and products

    Expression

    • Project title: Mouse ENCODE transcriptome data Mouse ENCODE transcriptome data
    • Description: RNA profiling data sets generated by the Mouse ENCODE project.
    • BioProject: PRJNA66167
    • Publication: PMID 25409824
    • Analysis date: n/a

    Bibliography

    Variation

    Alleles

    Alleles of this type are documented at Mouse Genome Informatics  (MGI)
    • Endonuclease-mediated (1) 
    • Targeted (6)  1 citation

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Clone Names

    • MGC130499

    Gene Ontology Provided by MGI

    Process Evidence Code Pubs
    involved_in anatomical structure morphogenesis IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in axon target recognition IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in cell differentiation IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in cell migration in diencephalon IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in epithelial cell differentiation involved in mammary gland alveolus development IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in floor plate development IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in hypothalamus cell migration IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in inferior colliculus development IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in lactation IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in mammary gland lobule development IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in mammillary body development IEP
    Inferred from Expression Pattern
    more info
    PubMed 
    involved_in mammillary body development IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in mammillothalamic axonal tract development IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in midbrain development IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in negative regulation of neuron apoptotic process IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in regulation of DNA-templated transcription IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in regulation of transcription by RNA polymerase II IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in somitogenesis IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in spinal cord development IEP
    Inferred from Expression Pattern
    more info
    PubMed 
    involved_in telencephalon cell migration IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in thalamus development IEP
    Inferred from Expression Pattern
    more info
    PubMed 
    involved_in urogenital system development IEP
    Inferred from Expression Pattern
    more info
    PubMed 
    involved_in visual learning IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in nucleus IDA
    Inferred from Direct Assay
    more info
    PubMed 

    General protein information

    Preferred Names
    forkhead box protein B1
    Names
    forkhead box B1a
    forkhead box B1b
    mesoderm/mesenchyme forkhead 3
    transcription factor FKH-5

    NCBI Reference Sequences (RefSeq)

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    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    mRNA and Protein(s)

    1. NM_022378.3NP_071773.2  forkhead box protein B1

      See identical proteins and their annotated locations for NP_071773.2

      Status: VALIDATED

      Source sequence(s)
      AC158992
      Consensus CDS
      CCDS40677.1
      UniProtKB/Swiss-Prot
      O08753, Q2M2M4, Q64732
      Related
      ENSMUSP00000096197.3, ENSMUST00000071281.5
      Conserved Domains (1) summary
      smart00339
      Location:13101
      FH; FORKHEAD

    RefSeqs of Annotated Genomes: GCF_000001635.27-RS_2024_02

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCm39 C57BL/6J

    Genomic

    1. NC_000075.7 Reference GRCm39 C57BL/6J

      Range
      69664992..69668222 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)