Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Behavioral & Substance Use Disorder Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)

MAMMALIAN PHENOTYPE - ANNOTATIONS

The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.
Term:abnormal myoblast differentiation
go back to main search page
Accession:MP:0011808 term browser browse the term
Definition:anomaly in the process in which a relatively unspecialized cell acquires specialized features of a myoblast, a mononucleate cell type that, by fusion with other myoblasts, gives rise to the myotubes that eventually develop into striated muscle fibers
Synonyms:exact_synonym: abnormal myoblast cell differentiation


show annotations for term's descendants           Sort by:
abnormal myoblast differentiation term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Atp11a ATPase, class VI, type 11A IAGP MGI PMID:29799007 NCBI chr 8:12,807,016...12,918,728
Ensembl chr 8:12,807,014...12,918,728 		JBrowse link
G Cygb cytoglobin IAGP MGI PMID:24367119 NCBI chr11:116,536,421...116,544,887
Ensembl chr11:116,536,421...116,545,139 		JBrowse link
G Des desmin IAGP MGI PMID:25179606 NCBI chr 1:75,336,936...75,345,223
Ensembl chr 1:75,336,973...75,345,223 		JBrowse link
G Dll1 delta like canonical Notch ligand 1 IAGP MGI PMID:17194759 NCBI chr17:15,587,616...15,597,275
Ensembl chr17:15,587,616...15,597,134 		JBrowse link
G Dusp1 dual specificity phosphatase 1 IAGP MGI PMID:20371627 NCBI chr17:26,724,565...26,727,446
Ensembl chr17:26,724,564...26,781,102 		JBrowse link
G Kmt2a lysine (K)-specific methyltransferase 2A IAGP MGI PMID:23934123 NCBI chr 9:44,714,652...44,793,492
Ensembl chr 9:44,714,652...44,792,594 		JBrowse link
G Mapk14 mitogen-activated protein kinase 14 IAGP MGI PMID:17304211 NCBI chr17:28,910,316...28,967,379
Ensembl chr17:28,910,303...28,967,380 		JBrowse link
G Myf5 myogenic factor 5 IAGP MGI PMID:29799007 PMID:31685980 NCBI chr10:107,318,769...107,322,787
Ensembl chr10:107,318,769...107,321,995 		JBrowse link
G Mymk myomaker, myoblast fusion factor IAGP MGI PMID:23868259 NCBI chr 2:26,951,648...26,962,173
Ensembl chr 2:26,951,648...26,962,191 		JBrowse link
G Myog myogenin IAGP MGI PMID:7532173 NCBI chr 1:134,217,742...134,220,286
Ensembl chr 1:134,217,727...134,220,286 		JBrowse link
G Nf1 neurofibromin 1 IAGP MGI PMID:21478499 NCBI chr11:79,223,541...79,472,435
Ensembl chr11:79,230,519...79,472,438 		JBrowse link
G Pax7 paired box 7 IAGP MGI PMID:31685980 NCBI chr 4:139,464,357...139,560,841
Ensembl chr 4:139,464,373...139,560,839 		JBrowse link
G Prmt7 protein arginine N-methyltransferase 7 IAGP MGI PMID:26854227 NCBI chr 8:106,937,686...106,978,326
Ensembl chr 8:106,937,568...106,979,426 		JBrowse link
G Sox15 SRY (sex determining region Y)-box 15 IAGP MGI PMID:15367664 NCBI chr11:69,545,863...69,547,553
Ensembl chr11:69,546,140...69,547,553 		JBrowse link
G Syisl Synpo2 intron sense-overlapping lncRNA IAGP MGI PMID:30279181
G Synm synemin, intermediate filament protein IAGP MGI PMID:25179606 NCBI chr 7:67,379,909...67,409,490
Ensembl chr 7:67,379,908...67,409,490 		JBrowse link
G Tmem182 transmembrane protein 182 IAGP MGI PMID:34427057 NCBI chr 1:40,844,738...40,896,047
Ensembl chr 1:40,844,761...40,896,047 		JBrowse link
G Zfp422 zinc finger protein 422 IAGP MGI PMID:31685980 NCBI chr 6:116,600,977...116,605,960
Ensembl chr 6:116,600,977...116,605,960 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 17275
    cellular phenotype 5751
      abnormal cell physiology 5041
        abnormal cell differentiation 1104
          abnormal myoblast differentiation 18
Path 2
Term Annotations click to browse term
  mammalian phenotype 17275
    muscle phenotype 2012
      abnormal muscle morphology 1486
        abnormal muscle development 128
          abnormal myogenesis 81
            abnormal myoblast differentiation 18
paths to the root