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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 dermomyotome development
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Accession:MP:0004206 term browser browse the term
Definition:any structural anomaly of the portion of the embryonic somite that remains after migration of the sclerotomic tissue
Synonyms:exact_synonym: abnormal dermamyotome development



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abnormal dermomyotome development term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Aph1a aph1 homolog A, gamma secretase subunit IAGP MGI PMID:15665098 NCBI chr 3:95,801,233...95,805,904
Ensembl chr 3:95,801,281...95,805,600
JBrowse link
G Disp1 dispatched RND transporter family member 1 IAGP MGI PMID:12421714 NCBI chr 1:182,867,828...183,010,257
Ensembl chr 1:182,867,830...183,003,086
JBrowse link
G Dll3 delta like canonical Notch ligand 3 IEA MGI NCBI chr 7:27,992,980...28,001,210
Ensembl chr 7:27,992,978...28,001,663
JBrowse link
G Dmrt2 doublesex and mab-3 related transcription factor 2 IAGP MGI PMID:16387292 NCBI chr19:25,649,758...25,656,355
Ensembl chr19:25,649,775...25,656,355
JBrowse link
G Foxc2 forkhead box C2 IAGP MGI PMID:10364424 NCBI chr 8:121,842,910...121,845,634
Ensembl chr 8:121,842,910...121,845,634
JBrowse link
G Meox1 mesenchyme homeobox 1 IAGP MGI PMID:12925591 NCBI chr11:101,768,336...101,785,309
Ensembl chr11:101,768,336...101,785,200
JBrowse link
G Meox2 mesenchyme homeobox 2 IAGP MGI PMID:12925591 NCBI chr12:37,158,539...37,229,533
Ensembl chr12:37,158,539...37,229,533
JBrowse link
G Mesp2 mesoderm posterior 2 IAGP MGI PMID:9242490 NCBI chr 7:79,460,475...79,463,179
Ensembl chr 7:79,460,475...79,463,187
JBrowse link
G Pax1 paired box 1 IAGP MGI PMID:10364424 NCBI chr 2:147,203,850...147,216,972
Ensembl chr 2:147,203,845...147,235,215
JBrowse link
G Pax3 paired box 3 IAGP MGI PMID:8631247 PMID:14665670 PMID:16951257 PMID:21512107 NCBI chr 1:78,077,904...78,173,773
Ensembl chr 1:78,077,904...78,173,771
JBrowse link
G Prdm1 PR domain containing 1, with ZNF domain IAGP MGI PMID:15750184 NCBI chr10:44,313,170...44,404,579
Ensembl chr10:44,313,173...44,404,497
JBrowse link
G Rtel1 regulator of telomere elongation helicase 1 IAGP MGI PMID:15210109 NCBI chr 2:180,961,504...180,998,409
Ensembl chr 2:180,961,532...180,998,409
JBrowse link
G Wdr19 WD repeat domain 19 IAGP MGI PMID:22228095 NCBI chr 5:65,357,039...65,417,758
Ensembl chr 5:65,357,039...65,417,758
JBrowse link
G Wnt1 wingless-type MMTV integration site family, member 1 IAGP MGI PMID:9811581 NCBI chr15:98,687,738...98,691,711
Ensembl chr15:98,687,738...98,691,718
JBrowse link
G Wnt3a wingless-type MMTV integration site family, member 3A IAGP MGI PMID:9811581 NCBI chr11:59,138,859...59,181,579
Ensembl chr11:59,138,859...59,181,578
JBrowse link

Term paths to the root
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Term Annotations click to browse term
  mammalian phenotype 16734
    muscle phenotype 1953
      abnormal muscle morphology 1444
        abnormal muscle development 126
          abnormal myogenesis 79
            abnormal myotome development 24
              abnormal dermomyotome development 15
paths to the root