U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from GEO Profiles

    • Showing Current items.

    FOXQ1 forkhead box Q1 [ Homo sapiens (human) ]

    Gene ID: 94234, updated on 27-Dec-2024

    Summary

    Official Symbol
    FOXQ1provided by HGNC
    Official Full Name
    forkhead box Q1provided by HGNC
    Primary source
    HGNC:HGNC:20951
    See related
    Ensembl:ENSG00000164379 MIM:612788; AllianceGenome:HGNC:20951
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    HFH1
    Summary
    FOXQ1 is a member of the FOX gene family, which is characterized by a conserved 110-amino acid DNA-binding motif called the forkhead or winged helix domain. FOX genes are involved in embryonic development, cell cycle regulation, tissue-specific gene expression, cell signaling, and tumorigenesis (Bieller et al., 2001 [PubMed 11747606]).[supplied by OMIM, May 2009]
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See FOXQ1 in Genome Data Viewer
    Location:
    6p25.3
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (1312098..1314758)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (1175612..1178272)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (1312333..1314993)

    Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene small nucleolar RNA U13 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:1226362-1226862 Neighboring gene uncharacterized LOC105374879 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr6:1286792-1287991 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr6:1312787-1313503 Neighboring gene long intergenic non-protein coding RNA 1394 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 FOXF2 divergent transcript Neighboring gene microRNA 6720 Neighboring gene forkhead box F2

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    Genome-wide association study of pancreatic cancer in Japanese population.
    EBI GWAS Catalog
    Large-scale genotyping identifies 41 new loci associated with breast cancer risk.
    EBI GWAS Catalog
    Linkage and association of successful aging to the 6q25 region in large Amish kindreds.
    EBI GWAS Catalog

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Gene Ontology Provided by GOA

    Process Evidence Code Pubs
    involved_in anatomical structure morphogenesis IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in cell differentiation IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in hair follicle morphogenesis IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in negative regulation of transcription by RNA polymerase II 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
     
    Component Evidence Code Pubs
    located_in chromatin ISA
    Inferred from Sequence Alignment
    more info
     
    located_in nucleus IEA
    Inferred from Electronic Annotation
    more info
     

    General protein information

    Preferred Names
    forkhead box protein Q1
    Names
    HFH-1
    HNF-3/forkhead-like protein 1
    hepatocyte nuclear factor 3 forkhead homolog 1
    winged helix/forkhead transcription factor

    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.

    mRNA and Protein(s)

    1. NM_033260.4NP_150285.3  forkhead box protein Q1

      See identical proteins and their annotated locations for NP_150285.3

      Status: VALIDATED

      Source sequence(s)
      AL499606, BC053850, BU566731
      Consensus CDS
      CCDS4471.1
      UniProtKB/Swiss-Prot
      Q9C009, Q9NS06
      Related
      ENSP00000296839.2, ENST00000296839.5
      Conserved Domains (1) summary
      cd00059
      Location:119197
      FH; Forkhead (FH), also known as a "winged helix". FH is named for the Drosophila fork head protein, a transcription factor which promotes terminal rather than segmental development. This family of transcription factor domains, which bind to B-DNA as ...

    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
      1312098..1314758
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060930.1 Alternate T2T-CHM13v2.0

      Range
      1175612..1178272
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)