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Details
Link-It Detail - Jax Mouse Phenotype - impaired ossification of basisphenoid bone
Debug Stats
  • ### Total Build Time: 78 ms 16.214 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 412 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 309 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=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=9 ms Completed: 9 ms rowSize= 1.046 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=41 ms Completed: 41 ms rowSize= 6.964 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 5.977 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.180 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
impaired ossification of basisphenoid bone MP:0000105
Definition (1)
anomaly in the formation of the bone at the base of the sphenoid bone; arises from an ossification center independent of the remainder of the sphenoid bone
Synonyms (1)
"defective ossification of basisphenoid" EXACT
Parents (2)
img abnormal intramembranous bone ossification MP:0008273
img abnormal basisphenoid bone morphology MP:0000106
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053906img abnormal intramembranous bone ossification MP:0008273
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053828img abnormal basisphenoid bone morphology MP:0000106
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053909img abnormal basisphenoid bone morphology MP:0000106
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053829img abnormal basisphenoid bone morphology MP:0000106
img mammalian phenotype MP:0000001img skeleton phenotype MP:000539010img abnormal basisphenoid bone morphology MP:0000106
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanPDGFRA5156platelet-derived growth factor receptor, alpha polypeptide
img Jax MP, Pubmed Id: 9753320, MOUSE PHENOTYPE ID: MGI:1306796
img Jax MP, Pubmed Id: 9226440, MOUSE PHENOTYPE ID: MGI:97530
img Jax MP, Pubmed Id: 9226440, MOUSE PHENOTYPE ID: MGI:97530
HumanAPAF1317apoptotic peptidase activating factor 1
img Jax MP, Pubmed Id: 9753320, MOUSE PHENOTYPE ID: MGI:1306796
img Jax MP, Pubmed Id: 9226440, MOUSE PHENOTYPE ID: MGI:97530
img Jax MP, Pubmed Id: 9226440, MOUSE PHENOTYPE ID: MGI:97530
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000105impaired ossification of basisphenoid bone0self