MYF5 myogenic factor 5 [hom*o sapiens (human)] - Gene (2024)

Gene ID: 4617, updated on 12-Sep-2024

Summary

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Official Symbol
MYF5provided by HGNC
Official Full Name
myogenic factor 5provided by HGNC
Primary source
HGNC:HGNC:7565
See related
Ensembl:ENSG00000111049 MIM:159990; AllianceGenome:HGNC:7565
Gene type
protein coding
RefSeq status
VALIDATED
Organism
hom*o sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; hom*o
Also known as
EORVA; bHLHc2
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to contribute to E-box binding activity. Predicted to be involved in several processes, including muscle cell fate commitment; positive regulation of cell differentiation; and skeletal muscle cell differentiation. Predicted to act upstream of or within several processes, including animal organ development; regulation of cell-matrix adhesion; and somitogenesis. Located in nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]
Expression
Low expression observed in reference dataset See more
Orthologs
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Genomic context

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Location:
12q21.31
Exon count:
3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (80716912..80719671)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (80695622..80698381)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (81110691..81113450)

Chromosome 12 - NC_000012.12MYF5 myogenic factor 5 [hom*o sapiens (human)] - Gene (1)Neighboring gene protein tyrosine phosphatase receptor type QNeighboring gene uncharacterized LOC105369867Neighboring gene akirin 1 pseudogene 1Neighboring gene Sharpr-MPRA regulatory region 7448Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr12:81026458-81027020Neighboring gene Sharpr-MPRA regulatory region 15034Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr12:81077757-81078395Neighboring gene ATAC-STARR-seq lymphoblastoid active region 6688Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:81101213-81102122Neighboring gene myogenic factor 6Neighboring gene MED14-independent group 3 enhancer GRCh37_chr12:81171500-81172699Neighboring gene long intergenic non-protein coding RNA 1490Neighboring gene lin-7 hom*olog A, crumbs cell polarity complex componentNeighboring gene microRNA 617

Genomic regions, transcripts, and products

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Go to reference sequence details

Go to nucleotide: Graphics FASTA GenBank

Expression

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  • 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

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Related articles in PubMed

  1. Recessive MYF5 Mutations Cause External Ophthalmoplegia, Rib, and Vertebral Anomalies. Di Gioia SA, et al. Am J Hum Genet, 2018 Jul 5. PMID 29887215, Free PMC Article
  2. Efficient in vitro myogenic reprogramming of human primary mesenchymal stem cells and endothelial cells by Myf5. Dimicoli-Salazar S, et al. Biol Cell, 2011 Nov. PMID 21810080
  3. Critical activities of Rac1 and Cdc42Hs in skeletal myogenesis: antagonistic effects of JNK and p38 pathways. Meriane M, et al. Mol Biol Cell, 2000 Aug. PMID 10930450, Free PMC Article
  4. Altered binding of MYF-5 to FOXE1 promoter in non-syndromic and CHARGE-associated cleft palate. Venza M, et al. J Oral Pathol Med, 2009 Jan. PMID 19192046
  5. Assignment of the human myogenic factors 5 and 6 (MYF5, MYF6) gene cluster to 12q21 by in situ hybridization and physical mapping of the locus between D12S350 and D12S106. Cupelli L, et al. Cytogenet Cell Genet, 1996. PMID 8978788

See all (29) citations in PubMed

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

  1. Identification of a Novel Frameshift Variant in MYF5 Leading to External Ophthalmoplegia with Rib and Vertebral Anomalies.

    Title: Identification of a Novel Frameshift Variant in MYF5 Leading to External Ophthalmoplegia with Rib and Vertebral Anomalies.

  2. SNAIL silencing allows the re-expression of MYF5 and canonical MYOD binding, promoting alveolar rhabdomyosarcoma cell myogenic differentiation.

    Title: SNAIL is a key regulator of alveolar rhabdomyosarcoma tumor growth and differentiation through repression of MYF5 and MYOD function.

  3. The direct role of MYF5 in rib, spine, and extraocular muscle formation in humans.

    Title: Recessive MYF5 Mutations Cause External Ophthalmoplegia, Rib, and Vertebral Anomalies.

  4. Analysis of human rhabdomyosarcoma revealed that MYF5 and MYOD are mutually-exclusively expressed and each is required for sustained tumor growth.

    Title: Myogenic regulatory transcription factors regulate growth in rhabdomyosarcoma.

  5. Pitx2c expression is reactivated, while expression of Myf5 is downregulated in human systolic heart failure as determined by qRT-PCR and Western blot analyses.

    Title: Pitx2c is reactivated in the failing myocardium and stimulates myf5 expression in cultured cardiomyocytes.

  6. results are the first demonstration of a myogenic conversion of human mesenchymal and endothelial cells by Myf5

    Title: Efficient in vitro myogenic reprogramming of human primary mesenchymal stem cells and endothelial cells by Myf5.

  7. DUX4c induces the MYF5 protein and myoblast proliferation, and has a role in facioscapulohumeral muscular dystrophy

    Title: DUX4c is up-regulated in FSHD. It induces the MYF5 protein and human myoblast proliferation.

  8. Observational study of gene-disease association. (HuGE Navigator)

    Title: High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men.

  9. A novel hom*ozygous polymorphism that prevented the binding of MYF-5 to FOXE1 promoter and affected the FOXE1 expression was found in 45% nonsyndromic cleft palate.

    Title: Altered binding of MYF-5 to FOXE1 promoter in non-syndromic and CHARGE-associated cleft palate.

  10. The myogenic basic helix-loop-helix family of transcription factors, MyoD, Myf5, myogenin, and MRF4, can each activate the muscle differentiation program.

    Title: The myogenic basic helix-loop-helix family of transcription factors shows similar requirements for SWI/SNF chromatin remodeling enzymes during muscle differentiation in culture.

Pathways from PubChem

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Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Markers

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables DNA-binding transcription activator activity, RNA polymerase II-specific IEA

Inferred from Electronic Annotation
more info

enables DNA-binding transcription factor activity, RNA polymerase II-specific IBA

Inferred from Biological aspect of Ancestor
more info

enables DNA-binding transcription factor activity, RNA polymerase II-specific ISA

Inferred from Sequence Alignment
more info

contributes_to E-box binding ISS

Inferred from Sequence or Structural Similarity
more info

enables RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA

Inferred from Biological aspect of Ancestor
more info

enables protein binding IPI

Inferred from Physical Interaction
more info

PubMed
enables protein dimerization activity IEA

Inferred from Electronic Annotation
more info

Process Evidence Code Pubs
involved_in camera-type eye development IEA

Inferred from Electronic Annotation
more info

involved_in cartilage condensation IEA

Inferred from Electronic Annotation
more info

involved_in embryonic skeletal system morphogenesis IEA

Inferred from Electronic Annotation
more info

involved_in extracellular matrix organization IEA

Inferred from Electronic Annotation
more info

involved_in muscle cell fate commitment ISS

Inferred from Sequence or Structural Similarity
more info

involved_in muscle organ development TAS

Traceable Author Statement
more info

PubMed
involved_in muscle tissue morphogenesis IEA

Inferred from Electronic Annotation
more info

involved_in ossification IEA

Inferred from Electronic Annotation
more info

involved_in positive regulation of myoblast differentiation IBA

Inferred from Biological aspect of Ancestor
more info

involved_in positive regulation of skeletal muscle fiber development IBA

Inferred from Biological aspect of Ancestor
more info

involved_in positive regulation of transcription by RNA polymerase II IEA

Inferred from Electronic Annotation
more info

involved_in regulation of cell-matrix adhesion 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 skeletal muscle cell differentiation IBA

Inferred from Biological aspect of Ancestor
more info

involved_in skeletal muscle tissue development TAS

Traceable Author Statement
more info

PubMed
involved_in somitogenesis IEA

Inferred from Electronic Annotation
more info

Component Evidence Code Pubs
part_of RNA polymerase II transcription regulator complex ISS

Inferred from Sequence or Structural Similarity
more info

PubMed
part_of chromatin ISA

Inferred from Sequence Alignment
more info

located_in nucleoplasm IDA

Inferred from Direct Assay
more info

located_in nucleoplasm TAS

Traceable Author Statement
more info

General protein information

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Preferred Names
myogenic factor 5
Names
class C basic helix-loop-helix protein 2
myf-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_005593.3NP_005584.2 myogenic factor 5

    See identical proteins and their annotated locations for NP_005584.2

    Status: VALIDATED

    Source sequence(s)
    AC025568, BC069373, BP231293, BX089431, X14894
    Consensus CDS
    CCDS9020.1
    UniProtKB/Swiss-Prot
    P13349, Q6ISR9
    UniProtKB/TrEMBL
    Q5U0P5
    Related
    ENSP00000228644.3, ENST00000228644.4
    Conserved Domains (3) summary
    smart00520
    Location:188
    BASIC; Basic domain in HLH proteins of MYOD family
    pfam00010
    Location:84135
    HLH; Helix-loop-helix DNA-binding domain
    pfam12232
    Location:143214
    Myf5; Myogenic determination factor 5

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_000012.12Reference GRCh38.p14 Primary Assembly

    Range
    80716912..80719671
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1Alternate T2T-CHM13v2.0

    Range
    80695622..80698381
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

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Nucleotide Protein
Heading Accession and Version
Protein Accession Links
GenPept Link UniProtKB Link
P13349.2 GenPept UniProtKB/Swiss-Prot:P13349

Additional links

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Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Molecular Biology Databases

MYF5 myogenic factor 5 [hom*o sapiens (human)] - Gene (2024)
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