Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4617
Gene name Gene Name - the full gene name approved by the HGNC.
Myogenic factor 5
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MYF5
Synonyms (NCBI Gene) Gene synonyms aliases
EORVA, bHLHc2
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q21.31
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs1555216163 AGTTCTCACC>- Pathogenic Frameshift variant, coding sequence variant
rs1565864693 C>T Pathogenic Missense variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019252 hsa-miR-148b-3p Microarray 17612493
MIRT439121 hsa-miR-10b-5p 3'LIFE 25074381
MIRT439121 hsa-miR-10b-5p 3'LIFE 25074381
MIRT1168077 hsa-miR-1248 CLIP-seq
MIRT1168078 hsa-miR-127-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin ISA
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific ISA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific TAS 2311584
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
159990 7565 ENSG00000111049
Protein
UniProt ID P13349
Protein name Myogenic factor 5 (Myf-5) (Class C basic helix-loop-helix protein 2) (bHLHc2)
Protein function Transcriptional activator that promotes transcription of muscle-specific target genes and plays a role in muscle differentiation (PubMed:29887215). Together with MYOG and MYOD1, co-occupies muscle-specific gene promoter core region during myogen
PDB 7Z5I , 7Z5K
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01586 Basic 13 83 Myogenic Basic domain Family
PF00010 HLH 84 135 Helix-loop-helix DNA-binding domain Domain
PF12232 Myf5 143 214 Myogenic determination factor 5 Family
Sequence
Sequence length 255
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Signaling pathways regulating pluripotency of stem cells   Myogenesis
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
OPHTHALMOPLEGIA, WITH RIB AND VERTEBRAL ANOMALIES ophthalmoplegia, external, with rib and vertebral anomalies rs1565864693, rs1555216163 N/A
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Diabetic Nephropathies Inhibit 27825100
Leiomyosarcoma Associate 28884746
Myasthenic Syndromes Congenital Associate 27286495
Neoplasms Associate 1764365
Pancreatic Neoplasms Associate 35146962
Pulmonary Disease Chronic Obstructive Associate 22556020, 24666540, 34831227
Rhabdoid Tumor Associate 14662021
Rhabdomyosarcoma Associate 1764365, 19299559
Rhabdomyosarcoma Alveolar Associate 23999248
Sarcoma Alveolar Soft Part Associate 19146682