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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 cartilage development
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Accession:MP:0000164 term browser browse the term
Definition:anomaly in the formation of the nonvascular, resilient, flexible connective tissue found primarily in joints, walls of the thorax, and tubular structures, but which also comprises most of the skeleton in early fetal life
Synonyms:exact_synonym: abnormal cartilage formation;   abnormal chondrogenesis;   dyschondrogenesis



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abnormal long bone hypertrophic chondrocyte zone term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Prkg2 protein kinase cGMP-dependent 2 IAGP DNA:deletion:cds (rat) RGD PMID:15466490 RGD:150429792 NCBI chr14:10,559,882...10,668,479
Ensembl chr14:10,559,882...10,666,888
JBrowse link
decreased width of hypertrophic chondrocyte zone term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Nppc natriuretic peptide C IMP compared to wild type RGD PMID:29566041 RGD:127284867 NCBI chr 9:87,320,051...87,324,251
Ensembl chr 9:87,320,051...87,324,251
JBrowse link
G Nppcem3Kyo natriuretic peptide C; ZFN induced mutant 3, Kyo IMP compared to wild type RGD PMID:29566041 RGD:127284867
G Nppcem4Kyo natriuretic peptide C; ZFN induced mutant 4, Kyo IMP compared to wild type RGD PMID:29566041 RGD:127284867

Term paths to the root
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Term Annotations click to browse term
  mammalian phenotype 5369
    skeleton phenotype 431
      abnormal skeleton morphology 336
        abnormal skeleton development 13
          abnormal cartilage development 7
            abnormal cranial cartilage development + 0
            abnormal intervertebral disk development 0
            abnormal long bone epiphyseal plate proliferative zone 0
            abnormal long bone hypertrophic chondrocyte zone + 7
            abnormal synchondrosis + 0
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