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Details
Link-It Detail - Jax Mouse Phenotype - abnormal synchondrosis
Debug Stats
  • ### Total Build Time: 41 ms 31.573 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 372 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 211 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=7 ms Completed: 7 ms rowSize= 585 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 1.570 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 27.550 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.160 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal synchondrosis MP:0004053
Definition (1)
anomalous or persistent cartilaginous fusion of two bones
Parents (1)
img abnormal cartilage development MP:0000164
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053906img abnormal cartilage development MP:0000164
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanPTH1R5745parathyroid hormone 1 receptor
img Jax MP
img Jax MP, Pubmed Id: 18652813, MOUSE PHENOTYPE ID: MGI:97603
img Jax MP, Pubmed Id: 11181569, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 16278811, MOUSE PHENOTYPE ID: MGI:2176261
img Jax MP, Pubmed Id: 23026747, MOUSE PHENOTYPE ID: MGI:1890596
img Jax MP, Pubmed Id: 10587515, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 10587515, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 18652813, MOUSE PHENOTYPE ID: MGI:2447280
img Jax MP, Pubmed Id: 8662561, MOUSE PHENOTYPE ID: MGI:97801
HumanPKD15310polycystic kidney disease 1 (autosomal dominant)
img Jax MP, Pubmed Id: 8662561, MOUSE PHENOTYPE ID: MGI:97801
img Jax MP, Pubmed Id: 10587515, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 11181569, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 18652813, MOUSE PHENOTYPE ID: MGI:2447280
img Jax MP, Pubmed Id: 23026747, MOUSE PHENOTYPE ID: MGI:1890596
img Jax MP, Pubmed Id: 10587515, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 16278811, MOUSE PHENOTYPE ID: MGI:2176261
img Jax MP
img Jax MP, Pubmed Id: 18652813, MOUSE PHENOTYPE ID: MGI:97603
HumanFGFR32261fibroblast growth factor receptor 3
img Jax MP, Pubmed Id: 18652813, MOUSE PHENOTYPE ID: MGI:2447280
img Jax MP, Pubmed Id: 8662561, MOUSE PHENOTYPE ID: MGI:97801
img Jax MP, Pubmed Id: 10587515, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 10587515, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 23026747, MOUSE PHENOTYPE ID: MGI:1890596
img Jax MP, Pubmed Id: 18652813, MOUSE PHENOTYPE ID: MGI:97603
img Jax MP
img Jax MP, Pubmed Id: 16278811, MOUSE PHENOTYPE ID: MGI:2176261
img Jax MP, Pubmed Id: 11181569, MOUSE PHENOTYPE ID: MGI:95524
HumanEVC2121Ellis van Creveld syndrome
img Jax MP, Pubmed Id: 23026747, MOUSE PHENOTYPE ID: MGI:1890596
img Jax MP, Pubmed Id: 10587515, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 8662561, MOUSE PHENOTYPE ID: MGI:97801
img Jax MP, Pubmed Id: 16278811, MOUSE PHENOTYPE ID: MGI:2176261
img Jax MP
img Jax MP, Pubmed Id: 18652813, MOUSE PHENOTYPE ID: MGI:97603
img Jax MP, Pubmed Id: 10587515, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 11181569, MOUSE PHENOTYPE ID: MGI:95524
img Jax MP, Pubmed Id: 18652813, MOUSE PHENOTYPE ID: MGI:2447280
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004053abnormal synchondrosis0self