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Details
Link-It Detail - Jax Mouse Phenotype - abnormal perichondrium morphology
Debug Stats
  • ### Total Build Time: 16 ms 21.826 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 394 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 252 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 181 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 583 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.568 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 17.558 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.171 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal perichondrium morphology MP:0006322
Definition (1)
any structural anomaly of the fibrous connective tissue that surrounds all non-joint end cartilage
Synonyms (1)
"perichondrium dysplasia" EXACT
Parents (1)
img abnormal skeleton morphology MP:0005508
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053904img abnormal skeleton morphology MP:0005508
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanSMPD355512sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
img Jax MP, Pubmed Id: 18652813, MOUSE PHENOTYPE ID: MGI:2447280
img Jax MP, Pubmed Id: 15037550, MOUSE PHENOTYPE ID: MGI:102708
img Jax MP, Pubmed Id: 17166921, MOUSE PHENOTYPE ID: MGI:2450928
img Jax MP, Pubmed Id: 11771668, MOUSE PHENOTYPE ID: MGI:4940991
img Jax MP, Pubmed Id: 19906844, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 8456819, MOUSE PHENOTYPE ID: MGI:1927578
img Jax MP, Pubmed Id: 19906844, MOUSE PHENOTYPE ID: MGI:95729
HumanGLI32737GLI family zinc finger 3
img Jax MP, Pubmed Id: 19906844, MOUSE PHENOTYPE ID: MGI:95729
img Jax MP, Pubmed Id: 18652813, MOUSE PHENOTYPE ID: MGI:2447280
img Jax MP, Pubmed Id: 19906844, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 17166921, MOUSE PHENOTYPE ID: MGI:2450928
img Jax MP, Pubmed Id: 15037550, MOUSE PHENOTYPE ID: MGI:102708
img Jax MP, Pubmed Id: 8456819, MOUSE PHENOTYPE ID: MGI:1927578
img Jax MP, Pubmed Id: 11771668, MOUSE PHENOTYPE ID: MGI:4940991
HumanEFNB11947ephrin-B1
img Jax MP, Pubmed Id: 15037550, MOUSE PHENOTYPE ID: MGI:102708
img Jax MP, Pubmed Id: 11771668, MOUSE PHENOTYPE ID: MGI:4940991
img Jax MP, Pubmed Id: 19906844, MOUSE PHENOTYPE ID: MGI:95729
img Jax MP, Pubmed Id: 8456819, MOUSE PHENOTYPE ID: MGI:1927578
img Jax MP, Pubmed Id: 18652813, MOUSE PHENOTYPE ID: MGI:2447280
img Jax MP, Pubmed Id: 17166921, MOUSE PHENOTYPE ID: MGI:2450928
img Jax MP, Pubmed Id: 19906844, MOUSE PHENOTYPE ID: MGI:104735
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006322abnormal perichondrium morphology0self