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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 skeletal muscle fiber morphology
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Accession:MP:0003084 term browser browse the term
Definition:any structural anomaly of the skeletal muscle fibers, the large multinucleated cells that make up the skeletal muscles
Synonyms:exact_synonym: Abnormal muscle fiber morphology;   abnormal skeletal muscle fibre morphology
 xref: HP:0004303



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centrally nucleated skeletal muscle fibers term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Dmd dystrophin IMP RGD PMID:25005781 RGD:11040981 NCBI chr  X:47,272,324...49,504,219
Ensembl chr  X:47,272,331...49,504,207
JBrowse link
G Dmdem1Kykn dystrophin; CRISPR/Cas9 system induced mutant 1, Keitaro Yamanouchi IMP RGD PMID:25005781 RGD:11040981
decreased skeletal muscle fiber diameter term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Dmd dystrophin IMP RGD PMID:25310701 PMID:25005781 RGD:12880034, RGD:11040981 NCBI chr  X:47,272,324...49,504,219
Ensembl chr  X:47,272,331...49,504,207
JBrowse link
G Dmdem1Ang dystrophin; TALEN-induced mutant1, Ang IMP RGD PMID:25310701 RGD:12880034
G Dmdem1Kykn dystrophin; CRISPR/Cas9 system induced mutant 1, Keitaro Yamanouchi IMP RGD PMID:25005781 RGD:11040981
increased skeletal muscle fiber size term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Mstn myostatin IMP compared to wild type RGD PMID:25640143 RGD:151347429 NCBI chr 9:48,452,533...48,458,933
Ensembl chr 9:48,452,533...48,458,933
JBrowse link
G Mstnem1Mcwi myostatin; zinc finger nuclease induced mutant 1, Medical College of Wisconsin IMP compared to wild type RGD PMID:25640143 RGD:151347429

Term paths to the root
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Term Annotations click to browse term
  mammalian phenotype 5417
    muscle phenotype 199
      abnormal muscle morphology 98
        abnormal muscle fiber morphology 15
          abnormal skeletal muscle fiber morphology 8
            abnormal skeletal muscle fiber mitochondrial morphology + 0
            abnormal skeletal muscle fiber size + 8
            abnormal skeletal muscle fiber triad morphology 0
            centrally nucleated skeletal muscle fibers 3
            decreased skeletal muscle fiber number 0
            increased skeletal muscle fiber number 0
            skeletal muscle fiber degeneration 0
            skeletal muscle fiber necrosis 0
paths to the root