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    HEY1 hes related family bHLH transcription factor with YRPW motif 1 [ Homo sapiens (human) ]

    Gene ID: 23462, updated on 9-Dec-2024

    Summary

    Official Symbol
    HEY1provided by HGNC
    Official Full Name
    hes related family bHLH transcription factor with YRPW motif 1provided by HGNC
    Primary source
    HGNC:HGNC:4880
    See related
    Ensembl:ENSG00000164683 MIM:602953; AllianceGenome:HGNC:4880
    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
    CHF2; OAF1; HERP2; HESR1; HRT-1; NERP2; hHRT1; BHLHb31
    Summary
    This gene encodes a nuclear protein belonging to the hairy and enhancer of split-related (HESR) family of basic helix-loop-helix (bHLH)-type transcriptional repressors. Expression of this gene is induced by the Notch and c-Jun signal transduction pathways. Two similar and redundant genes in mouse are required for embryonic cardiovascular development, and are also implicated in neurogenesis and somitogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]
    Expression
    Biased expression in brain (RPKM 32.0), lung (RPKM 10.8) and 9 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See HEY1 in Genome Data Viewer
    Location:
    8q21.13
    Exon count:
    6
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (79764010..79767767, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (80195346..80199104, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (80676245..80680002, complement)

    Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124901965 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr8:80635352-80636551 Neighboring gene uncharacterized LOC107986893 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27548 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27549 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27550 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19311 Neighboring gene uncharacterized LOC101927040 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19313 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19312 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:80695841-80696641 Neighboring gene long intergenic non-protein coding RNA 1607 Neighboring gene U7 small nuclear RNA Neighboring gene RNA, U7 small nuclear 85 pseudogene Neighboring gene Sharpr-MPRA regulatory region 4298 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27551 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19315 Neighboring gene uncharacterized LOC124901966 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19316 Neighboring gene TPD52-MRPS28 readthrough Neighboring gene mitochondrial ribosomal protein S28

    Genomic regions, transcripts, and products

    Expression

    • Project title: 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?

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Clone Names

    • MGC1274

    Gene Ontology Provided by GOA

    Process Evidence Code Pubs
    involved_in Notch signaling pathway IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in Notch signaling pathway IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in Notch signaling pathway ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in angiogenesis IEP
    Inferred from Expression Pattern
    more info
    PubMed 
    involved_in anterior/posterior pattern specification IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in aortic valve morphogenesis ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in arterial endothelial cell differentiation ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in atrioventricular valve formation ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in cardiac conduction system development NAS
    Non-traceable Author Statement
    more info
    PubMed 
    involved_in cardiac epithelial to mesenchymal transition ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in cardiac septum morphogenesis ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in cardiac ventricle morphogenesis ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in circulatory system development IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in dorsal aorta morphogenesis ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in endocardial cushion morphogenesis ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in heart trabecula formation ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in labyrinthine layer blood vessel development ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in negative regulation of DNA-templated transcription IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in negative regulation of Notch signaling pathway IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in negative regulation of biomineral tissue development ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in negative regulation of neuron differentiation IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in negative regulation of smooth muscle cell differentiation IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in negative regulation of transcription by RNA polymerase II IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in negative regulation of transcription by RNA polymerase II IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in negative regulation of transcription by RNA polymerase II ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in positive regulation of transcription by RNA polymerase II ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in pulmonary valve morphogenesis ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in regulation of neurogenesis IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in regulation of transcription by RNA polymerase II IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in regulation of vasculogenesis ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in umbilical cord morphogenesis ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in ventricular septum morphogenesis ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    Component Evidence Code Pubs
    located_in chromatin ISA
    Inferred from Sequence Alignment
    more info
     
    located_in cytoplasm ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    located_in nucleoplasm TAS
    Traceable Author Statement
    more info
     
    is_active_in nucleus IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in nucleus ISS
    Inferred from Sequence or Structural Similarity
    more info
     

    General protein information

    Preferred Names
    hairy/enhancer-of-split related with YRPW motif protein 1
    Names
    HES-related repressor protein 1
    HES-related repressor protein 2
    basic helix-loop-helix protein OAF1
    cardiovascular helix-loop-helix factor 2
    class B basic helix-loop-helix protein 31
    hairy and enhancer of split-related protein 1
    hairy-related transcription factor 1
    hairy/enhancer-of-split related with YRPW motif 1

    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_001040708.2NP_001035798.1  hairy/enhancer-of-split related with YRPW motif protein 1 isoform b

      See identical proteins and their annotated locations for NP_001035798.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2), also known as HESR1-12nt, uses an alternate in-frame splice site in the central coding region, compared to variant 1, resulting in a longer protein (isoform b).
      Source sequence(s)
      AF232239, BC001873, BP283540
      Consensus CDS
      CCDS43749.1
      UniProtKB/TrEMBL
      B3KQB8, Q96PR6
      Related
      ENSP00000338272.5, ENST00000337919.9
      Conserved Domains (2) summary
      smart00511
      Location:124170
      ORANGE; Orange domain
      cl00081
      Location:41126
      bHLH_SF; basic Helix Loop Helix (bHLH) domain superfamily
    2. NM_001282851.2NP_001269780.1  hairy/enhancer-of-split related with YRPW motif protein 1 isoform c

      See identical proteins and their annotated locations for NP_001269780.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) uses an alternate 5' structure which results in the use of a downstream start codon compared to variant 1. The encoded isoform (c) is shorter and has a distinct N-terminus compared to isoform 1.
      Source sequence(s)
      AF151522, AK293646, R61374
      UniProtKB/TrEMBL
      B4DEI9
      Related
      ENST00000435063.4
      Conserved Domains (1) summary
      smart00511
      Location:3076
      ORANGE; Orange domain
    3. NM_012258.4NP_036390.3  hairy/enhancer-of-split related with YRPW motif protein 1 isoform a

      See identical proteins and their annotated locations for NP_036390.3

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) encodes the predominant isoform (a).
      Source sequence(s)
      AF232239, BC001873, DA561783
      Consensus CDS
      CCDS6225.1
      UniProtKB/Swiss-Prot
      B2R883, Q5TZS3, Q8NAM2, Q9NYP4, Q9Y5J3
      UniProtKB/TrEMBL
      B3KQB8, Q96PR6
      Related
      ENSP00000346761.3, ENST00000354724.8
      Conserved Domains (2) summary
      smart00511
      Location:120166
      ORANGE; Orange domain
      cl00081
      Location:41122
      bHLH_SF; basic Helix Loop Helix (bHLH) domain superfamily

    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_000008.11 Reference GRCh38.p14 Primary Assembly

      Range
      79764010..79767767 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060932.1 Alternate T2T-CHM13v2.0

      Range
      80195346..80199104 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)