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Details
Link-It Detail - Jax Mouse Phenotype - impaired osteoblast differentiation
Debug Stats
  • ### Total Build Time: 95 ms 18.343 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 398 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 404 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 196 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=10 ms Completed: 10 ms rowSize= 590 bytes
  • CONCEPT_CHILDREN gt=9 ms Completed: 9 ms rowSize= 592 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=40 ms Completed: 40 ms rowSize= 4.258 KB
  • CONCEPT_RELATIONSHIPS gt=6 ms Completed: 6 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=22 ms Completed: 22 ms rowSize= 10.639 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.173 KB
  • CONCEPT_ANCILLARY gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
impaired osteoblast differentiation MP:0011711
Definition (1)
reduced ability or inability to produce skeletogenic cells that secrete osteoid, are capable of producing mineralized (hydroxyapatite) matrix, are located adjacent to or within osteoid tissue, and arise from the transformation of a preosteoblast cell
Synonyms (1)
"decreased osteoblast differentiation" RELATED
Parents (1)
img abnormal osteoblast differentiation MP:0008395
Children (1)
img arrested osteoblast differentiation MP:0011712
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cellular phenotype MP:00053846img abnormal osteoblast differentiation MP:0008395
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053907img abnormal osteoblast differentiation MP:0008395
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053906img abnormal osteoblast differentiation MP:0008395
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanEVC2132884Ellis van Creveld syndrome 2
img Jax MP, Pubmed Id: 22615579, MOUSE PHENOTYPE ID: MGI:2136853
img Jax MP, Pubmed Id: 23026747, MOUSE PHENOTYPE ID: MGI:1915775
img Jax MP, Pubmed Id: 21809421, MOUSE PHENOTYPE ID: MGI:4818260
img Jax MP, Pubmed Id: 23026747, MOUSE PHENOTYPE ID: MGI:1890596
HumanFAM20C56975family with sequence similarity 20, member C
img Jax MP, Pubmed Id: 21809421, MOUSE PHENOTYPE ID: MGI:4818260
img Jax MP, Pubmed Id: 22615579, MOUSE PHENOTYPE ID: MGI:2136853
img Jax MP, Pubmed Id: 23026747, MOUSE PHENOTYPE ID: MGI:1890596
img Jax MP, Pubmed Id: 23026747, MOUSE PHENOTYPE ID: MGI:1915775
HumanEVC2121Ellis van Creveld syndrome
img Jax MP, Pubmed Id: 22615579, MOUSE PHENOTYPE ID: MGI:2136853
img Jax MP, Pubmed Id: 23026747, MOUSE PHENOTYPE ID: MGI:1915775
img Jax MP, Pubmed Id: 23026747, MOUSE PHENOTYPE ID: MGI:1890596
img Jax MP, Pubmed Id: 21809421, MOUSE PHENOTYPE ID: MGI:4818260
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011711impaired osteoblast differentiation0self