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    FOXF2 forkhead box F2 [ Homo sapiens (human) ]

    Gene ID: 2295, updated on 12-Nov-2024

    Summary

    Official Symbol
    FOXF2provided by HGNC
    Official Full Name
    forkhead box F2provided by HGNC
    Primary source
    HGNC:HGNC:3810
    See related
    Ensembl:ENSG00000137273 MIM:603250; AllianceGenome:HGNC:3810
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    FKHL6; FREAC2; FREAC-2
    Summary
    FOXF2 encodes forkhead box F2, one of many human homologues of the Drosophila melanogaster transcription factor forkhead. FOXF2 is expressed in lung and placenta, and has been shown to transcriptionally activate several lung-specific genes. [provided by RefSeq, Jul 2008]
    Expression
    Biased expression in lung (RPKM 8.4), prostate (RPKM 6.0) and 13 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See FOXF2 in Genome Data Viewer
    Location:
    6p25.3
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (1389576..1395603)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (1252762..1258791)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (1389811..1395838)

    Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:1312787-1313503 Neighboring gene long intergenic non-protein coding RNA 1394 Neighboring gene forkhead box Q1 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr6:1348887-1349536 Neighboring gene Uncharacterized LOC132932482 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:1378296-1378809 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16819 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 16820 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:1384005-1384784 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:1384785-1385564 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:1390993-1391858 Neighboring gene FOXF2 divergent transcript Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:1400269-1400770 Neighboring gene ReSE screen-validated silencer GRCh37_chr6:1402119-1402268 Neighboring gene microRNA 6720 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:1407479-1408328 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:1410403-1411023 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:1416044-1417026 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:1433994-1434664 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:1437542-1438506 Neighboring gene uncharacterized LOC102723944 Neighboring gene uncharacterized LOC105374883 Neighboring gene uncharacterized LOC124901238 Neighboring gene RNA, 7SL, cytoplasmic 352, pseudogene

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    Genome-wide interaction study of smoking and bladder cancer risk.
    EBI GWAS Catalog

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Process Evidence Code Pubs
    involved_in animal organ morphogenesis IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in embryonic camera-type eye morphogenesis IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in embryonic digestive tract development IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in epithelial to mesenchymal transition NAS
    Non-traceable Author Statement
    more info
    PubMed 
    involved_in establishment of planar polarity of embryonic epithelium IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in extracellular matrix organization IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in genitalia development IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in negative regulation of DNA-templated transcription IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in positive regulation of DNA-templated transcription IDA
    Inferred from Direct Assay
    more info
    PubMed 
    acts_upstream_of_or_within positive regulation of transcription by RNA polymerase II IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in positive regulation of transcription by RNA polymerase II IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in regulation of proteasomal ubiquitin-dependent protein catabolic process IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in regulation of protein polyubiquitination IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in regulation of transcription by RNA polymerase II IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in roof of mouth development IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in chromatin ISA
    Inferred from Sequence Alignment
    more info
     
    located_in intracellular membrane-bounded organelle IDA
    Inferred from Direct Assay
    more info
     
    located_in nuclear body IDA
    Inferred from Direct Assay
    more info
     
    located_in nucleoplasm IDA
    Inferred from Direct Assay
    more info
     
    is_active_in nucleus IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in nucleus IC
    Inferred by Curator
    more info
    PubMed 
    located_in nucleus IDA
    Inferred from Direct Assay
    more info
    PubMed 
    part_of transcription regulator complex IDA
    Inferred from Direct Assay
    more info
    PubMed 

    General protein information

    Preferred Names
    forkhead box protein F2
    Names
    forkhead-like 6
    forkhead-related activator 2
    forkhead-related protein FKHL6
    forkhead-related transcription factor 2

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    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.

    Genomic

    1. NG_046984.1 RefSeqGene

      Range
      4743..10770
      Download
      GenBank, FASTA, Sequence Viewer (Graphics), LRG_1190

    mRNA and Protein(s)

    1. NM_001452.2NP_001443.1  forkhead box protein F2

      See identical proteins and their annotated locations for NP_001443.1

      Status: REVIEWED

      Source sequence(s)
      AL034346, CA448136, U13220
      Consensus CDS
      CCDS4472.1
      UniProtKB/Swiss-Prot
      Q12947, Q5TGJ1, Q9UQ85
      Related
      ENSP00000496415.1, ENST00000645481.2
      Conserved Domains (1) summary
      smart00339
      Location:100188
      FH; FORKHEAD

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000006.12 Reference GRCh38.p14 Primary Assembly

      Range
      1389576..1395603
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060930.1 Alternate T2T-CHM13v2.0

      Range
      1252762..1258791
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)