Entity Details

Primary name MYF5_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP13349
EntryNameMYF5_HUMAN
FullNameMyogenic factor 5
TaxID9606
Evidenceevidence at protein level
Length255
SequenceStatuscomplete
DateCreated1990-01-01
DateModified2021-06-02

Ontological Relatives

GenesMYF5

GO terms

Show/Hide Table
GOName
GO:0000785 chromatin
GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding
GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific
GO:0001228 DNA-binding transcription activator activity, RNA polymerase II-specific
GO:0001502 cartilage condensation
GO:0001503 ossification
GO:0001756 somitogenesis
GO:0001952 regulation of cell-matrix adhesion
GO:0005654 nucleoplasm
GO:0006357 regulation of transcription by RNA polymerase II
GO:0007517 muscle organ development
GO:0007519 skeletal muscle tissue development
GO:0030198 extracellular matrix organization
GO:0035914 skeletal muscle cell differentiation
GO:0042693 muscle cell fate commitment
GO:0043010 camera-type eye development
GO:0045663 positive regulation of myoblast differentiation
GO:0046983 protein dimerization activity
GO:0048704 embryonic skeletal system morphogenesis
GO:0048743 positive regulation of skeletal muscle fiber development
GO:0051149 positive regulation of muscle cell differentiation
GO:0060415 muscle tissue morphogenesis
GO:0090575 RNA polymerase II transcription regulator complex

Subcellular Location

Show/Hide Table
Subcellular Location
Nucleus

Domains

Show/Hide Table
DomainNameCategoryType
IPR002546 Myogenic muscle-specific protein, N-terminalDomainDomain
IPR011598 Myc-type, basic helix-loop-helix (bHLH) domainDomainDomain
IPR022032 Myogenic determination factor 5DomainDomain
IPR036638 Helix-loop-helix DNA-binding domain superfamilyFamilyHomologous superfamily
IPR039704 Myogenic factorFamilyFamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
618155 OMIMOphthalmoplegia, external, with rib and vertebral anomalies (EORVA)An autosomal recessive disorder characterized by congenital nonprogressive external ophthalmoplegia, ptosis, scoliosis, torticollis, and vertebral and rib anomalies. The disease is caused by variants affecting the gene represented in this entry.

Interactions

35 interactions

InteractorPartnerSourcesPublicationsLink
MYF5_HUMANZN417_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANPACRL_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANENKD1_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANAQP1_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANFIGLA_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANHEN2_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANZN575_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANPIN1_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANTEANC_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANSGF29_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANID1_HUMANBioGRID, HPRD, IntAct32296183 9242638 details
MYF5_HUMANSNPC5_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANZN587_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANCCD13_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANTLE5_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANF124B_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANCHIC2_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANSCX_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANMSGN1_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANZN835_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANRARG_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANID3_HUMANBioGRID, HPRD, IntAct32296183 9242638 details
MYF5_HUMANCN119_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANITB4_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANZN250_HUMANBioGRID, IntAct32296183 details
MYF5_HUMANMDFI_HUMANBioGRID, HPRD8797820 details
MYF5_HUMANID2_HUMANBioGRID, HPRD9242638 details
MYF5_HUMANTFE2_HUMANBioGRID, HPRD2385294 9242638 details
MYF5_HUMANANR11_HUMANBioGRID32296183 details
MYF5_HUMANMYF5_HUMANHPRD9242638 details
MYF5_HUMANCALM1_HUMANHPRD10757985 details
MYF5_HUMANCALM2_HUMANHPRD10757985 details
MYF5_HUMANCALM3_HUMANHPRD10757985 details
MYF5_HUMANCSK21_HUMANHPRD9461343 details
MYF5_HUMANCSK22_HUMANHPRD9461343 details