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    GRHL2 grainyhead like transcription factor 2 [ Homo sapiens (human) ]

    Gene ID: 79977, updated on 3-Nov-2024

    Summary

    Official Symbol
    GRHL2provided by HGNC
    Official Full Name
    grainyhead like transcription factor 2provided by HGNC
    Primary source
    HGNC:HGNC:2799
    See related
    Ensembl:ENSG00000083307 MIM:608576; AllianceGenome:HGNC:2799
    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
    BOM; ECTDS; PPCD4; DFNA28; TFCP2L3
    Summary
    The protein encoded by this gene is a transcription factor that can act as a homodimer or as a heterodimer with either GRHL1 or GRHL3. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal dominant type 28 (DFNA28).[provided by RefSeq, Mar 2009]
    Expression
    Broad expression in skin (RPKM 14.0), prostate (RPKM 13.5) and 14 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See GRHL2 in Genome Data Viewer
    Location:
    8q22.3
    Exon count:
    17
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (101492439..101681200)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (102618002..102807085)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (102504667..102681954)

    Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107986897 Neighboring gene long intergenic non-protein coding RNA 2845 Neighboring gene RNA, 7SL, cytoplasmic 563, pseudogene Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr8:102472256-102472756 Neighboring gene Sharpr-MPRA regulatory region 9085 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:102504685-102505213 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:102513194-102514170 Neighboring gene GRHL2 divergent transcript Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27730 Neighboring gene SAP domain containing ribonucleoprotein pseudogene Neighboring gene probable ribosome biogenesis protein RLP24 Neighboring gene Sharpr-MPRA regulatory region 9664 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr8:102655529-102656728 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:102659137-102659637 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:102668311-102669171 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27732 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27733 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr8:102762302-102763501 Neighboring gene neurocalcin delta Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27734 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27735 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:102799260-102799806 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:102799807-102800353 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27736 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19433 Neighboring gene small nucleolar RNA U13 Neighboring gene PDCL3 pseudogene 2

    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

    Associated conditions

    Description Tests
    Autosomal dominant nonsyndromic hearing loss 28
    MedGen: C1837640 OMIM: 608641 GeneReviews: Genetic Hearing Loss Overview
    not available
    Corneal dystrophy, posterior polymorphous, 4
    MedGen: C4747961 OMIM: 618031 GeneReviews: Not available
    not available
    Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome
    MedGen: C4014987 OMIM: 616029 GeneReviews: Not available
    not available

    EBI GWAS Catalog

    Description
    A genome-wide association study (GWAS) for bronchopulmonary dysplasia.
    EBI GWAS Catalog
    Genetics of rheumatoid arthritis contributes to biology and drug discovery.
    EBI GWAS Catalog

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Clone Names

    • FLJ11172, FLJ13782, MGC149294, MGC149295

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables DNA-binding transcription activator activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables DNA-binding transcription activator activity, RNA polymerase II-specific IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables DNA-binding transcription activator activity, RNA polymerase II-specific IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables DNA-binding transcription activator activity, RNA polymerase II-specific IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    enables DNA-binding transcription factor activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables DNA-binding transcription factor activity ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    enables DNA-binding transcription factor activity, RNA polymerase II-specific ISA
    Inferred from Sequence Alignment
    more info
     
    enables DNA-binding transcription factor binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables chromatin DNA binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables identical protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables intronic transcription regulatory region sequence-specific DNA binding ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables sequence-specific DNA binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in anterior neural tube closure IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in bicellular tight junction assembly IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in brain development IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in camera-type eye development IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in cardiac ventricle morphogenesis IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in cell adhesion IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in cell junction assembly IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in embryonic cranial skeleton morphogenesis IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in embryonic digit morphogenesis IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in epithelial cell morphogenesis IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in epithelial cell morphogenesis ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in epithelial cell morphogenesis involved in placental branching IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in epithelium migration ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in face development IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in keratinocyte differentiation IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in lung epithelial cell differentiation ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in lung lobe morphogenesis IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in multicellular organism growth IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in neural tube closure ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in neural tube development IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in 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 positive regulation of transcription by RNA polymerase II ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in regulation of transcription by RNA polymerase II IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in regulation of transcription by RNA polymerase II IDA
    Inferred from Direct Assay
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in cell-cell junction IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in chromatin ISA
    Inferred from Sequence Alignment
    more info
     
    located_in membrane IEA
    Inferred from Electronic Annotation
    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 IDA
    Inferred from Direct Assay
    more info
    PubMed 

    General protein information

    Preferred Names
    grainyhead-like protein 2 homolog
    Names
    brother of mammalian grainyhead
    brother-of-MGR
    grainyhead-like 2
    transcription factor CP2-like 3

    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_011971.3 RefSeqGene

      Range
      5002..182289
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001330593.2NP_001317522.1  grainyhead-like protein 2 homolog isoform 2

      Status: REVIEWED

      Source sequence(s)
      AK296817, AP000426, AP001207, BC069633, BX117477, DN916458
      Consensus CDS
      CCDS83312.1
      UniProtKB/TrEMBL
      A8K9Y8
      Related
      ENSP00000379260.1, ENST00000395927.1
      Conserved Domains (1) summary
      pfam04516
      Location:213422
      CP2; CP2 transcription factor
    2. NM_024915.4NP_079191.2  grainyhead-like protein 2 homolog isoform 1

      See identical proteins and their annotated locations for NP_079191.2

      Status: REVIEWED

      Source sequence(s)
      AP000426, AP001207, BC069638
      Consensus CDS
      CCDS34931.1
      UniProtKB/Swiss-Prot
      A1L303, Q6ISB3, Q6NT03, Q9H8B8
      UniProtKB/TrEMBL
      A8K9Y8
      Related
      ENSP00000495564.1, ENST00000646743.1
      Conserved Domains (1) summary
      pfam04516
      Location:229438
      CP2; CP2 transcription factor

    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
      101492439..101681200
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_011517307.4XP_011515609.1  grainyhead-like protein 2 homolog isoform X2

      UniProtKB/TrEMBL
      A8K9Y8
      Conserved Domains (1) summary
      pfam04516
      Location:229438
      CP2; CP2 transcription factor
    2. XM_011517306.4XP_011515608.1  grainyhead-like protein 2 homolog isoform X1

      See identical proteins and their annotated locations for XP_011515608.1

      UniProtKB/TrEMBL
      A8K9Y8
      Conserved Domains (1) summary
      pfam04516
      Location:213422
      CP2; CP2 transcription factor

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060932.1 Alternate T2T-CHM13v2.0

      Range
      102618002..102807085
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054361285.1XP_054217260.1  grainyhead-like protein 2 homolog isoform X1

    2. XM_054361286.1XP_054217261.1  grainyhead-like protein 2 homolog isoform X2