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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 limb muscle morphology
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Accession:MP:0021206 term browser browse the term
Definition:any structural anomaly in the muscles that are part of a limb



show annotations for term's descendants           Sort by:
abnormal soleus morphology term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Bckdk branched chain ketoacid dehydrogenase kinase IAGP DNA:missense mutation:cds:G369E (rat) RGD PMID:27472223 RGD:39131293 NCBI chr 1:182,515,335...182,520,007
Ensembl chr 1:182,515,327...182,536,633
JBrowse link
decreased gastrocnemius weight term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ngly1 N-glycanase 1 IMP RGD PMID:32259258 RGD:39457703 NCBI chr15:9,153,738...9,210,228
Ensembl chr15:9,153,738...9,204,630
JBrowse link
G Ngly1em1Ta N-glycanase 1; CRISPR/Cas9 induced mutant 1, Ta IMP RGD PMID:32259258 RGD:39457703
decreased tibialis anterior weight term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Dmd dystrophin IMP RGD PMID:25310701 RGD:12880034 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 Ngly1 N-glycanase 1 IMP RGD PMID:32259258 RGD:39457703 NCBI chr15:9,153,738...9,210,228
Ensembl chr15:9,153,738...9,204,630
JBrowse link
G Ngly1em1Ta N-glycanase 1; CRISPR/Cas9 induced mutant 1, Ta IMP RGD PMID:32259258 RGD:39457703
increased tibialis anterior weight 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

Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 5402
    limbs/digits/tail phenotype 76
      abnormal limb morphology 67
        abnormal limb muscle morphology 11
          abnormal autopod muscle morphology 0
          abnormal extensor digitorum longus morphology + 0
          abnormal gastrocnemius morphology + 3
          abnormal quadriceps morphology + 0
          abnormal soleus morphology + 3
          abnormal tibialis anterior morphology + 8
Path 2
Term Annotations click to browse term
  mammalian phenotype 5402
    muscle phenotype 199
      abnormal muscle morphology 98
        abnormal skeletal muscle morphology 24
          abnormal hypaxial muscle morphology 11
            abnormal limb muscle morphology 11
              abnormal autopod muscle morphology 0
              abnormal extensor digitorum longus morphology + 0
              abnormal gastrocnemius morphology + 3
              abnormal quadriceps morphology + 0
              abnormal soleus morphology + 3
              abnormal tibialis anterior morphology + 8
paths to the root