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Details
Link-It Detail - Jax Mouse Phenotype - basisphenoid bone hypoplasia
Debug Stats
  • ### Total Build Time: 59 ms 14.145 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 384 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 524 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 187 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=16 ms Completed: 16 ms rowSize= 578 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=23 ms Completed: 23 ms rowSize= 5.562 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 5.630 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.166 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
basisphenoid bone hypoplasia MP:0004461
Definition (1)
underdevelopment or reduced size, usually due to reduced cell number, in part of the base of the cranium between the basioccipital and the presphenoid, which usually ossifies separately in the embryo or in the young, and becomes a part of the sphenoid in the adult; in many animals it persists as a separate bone between the basioccipital bone and the presphenoidal bone
Synonyms (1)
"hypoplastic basisphenoid bone" EXACT
Parents (1)
img small basisphenoid bone MP:0004462
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053829img small basisphenoid bone MP:0004462
img mammalian phenotype MP:0000001img skeleton phenotype MP:000539010img small basisphenoid bone MP:0004462
img mammalian phenotype MP:0000001img craniofacial phenotype MP:000538210img small basisphenoid bone MP:0004462
img mammalian phenotype MP:0000001img skeleton phenotype MP:000539011img small basisphenoid bone MP:0004462
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanMN14330meningioma (disrupted in balanced translocation) 1
img Jax MP, Pubmed Id: 15870292, MOUSE PHENOTYPE ID: MGI:1261813
img Jax MP, Pubmed Id: 10886375, MOUSE PHENOTYPE ID: MGI:108015
img Jax MP, Pubmed Id: 15870292, MOUSE PHENOTYPE ID: MGI:1261813
HumanNKX3-2579
img Jax MP, Pubmed Id: 15870292, MOUSE PHENOTYPE ID: MGI:1261813
img Jax MP, Pubmed Id: 10886375, MOUSE PHENOTYPE ID: MGI:108015
img Jax MP, Pubmed Id: 15870292, MOUSE PHENOTYPE ID: MGI:1261813
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004461basisphenoid bone hypoplasia0self