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Details
Link-It Detail - Jax Mouse Phenotype - presphenoid bone hypoplasia
Debug Stats
  • ### Total Build Time: 23 ms 22.862 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 414 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 186 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=5 ms Completed: 5 ms rowSize= 591 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.923 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 17.086 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
presphenoid bone hypoplasia MP:0004450
Definition (1)
underdevelopment or reduced size, usually due to a reduced number of cells, of the anterior part of the body of the sphenoid bone in front of the basisphenoid; it is usually a separate bone in the young or fetus, but becomes a part of the sphenoid in the adult
Synonyms (1)
"hypoplastic presphenoid bone" EXACT
Parents (1)
img abnormal presphenoid bone morphology MP:0004448
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053829img abnormal presphenoid bone morphology MP:0004448
img mammalian phenotype MP:0000001img skeleton phenotype MP:000539010img abnormal presphenoid bone morphology MP:0004448
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanGSC145258goosecoid homeobox
img Jax MP, Pubmed Id: 12810603, MOUSE PHENOTYPE ID: MGI:1313268
img Jax MP, Pubmed Id: 19776033, MOUSE PHENOTYPE ID: MGI:3584243
img Jax MP, Pubmed Id: 15870292, MOUSE PHENOTYPE ID: MGI:1261813
img Jax MP, Pubmed Id: 15870292, MOUSE PHENOTYPE ID: MGI:1261813
img Jax MP, Pubmed Id: 9533949, MOUSE PHENOTYPE ID: MGI:95841
HumanMKS154903Meckel syndrome, type 1
img Jax MP, Pubmed Id: 19776033, MOUSE PHENOTYPE ID: MGI:3584243
img Jax MP, Pubmed Id: 15870292, MOUSE PHENOTYPE ID: MGI:1261813
img Jax MP, Pubmed Id: 15870292, MOUSE PHENOTYPE ID: MGI:1261813
img Jax MP, Pubmed Id: 9533949, MOUSE PHENOTYPE ID: MGI:95841
img Jax MP, Pubmed Id: 12810603, MOUSE PHENOTYPE ID: MGI:1313268
HumanCHRD8646chordin
img Jax MP, Pubmed Id: 9533949, MOUSE PHENOTYPE ID: MGI:95841
img Jax MP, Pubmed Id: 19776033, MOUSE PHENOTYPE ID: MGI:3584243
img Jax MP, Pubmed Id: 15870292, MOUSE PHENOTYPE ID: MGI:1261813
img Jax MP, Pubmed Id: 15870292, MOUSE PHENOTYPE ID: MGI:1261813
img Jax MP, Pubmed Id: 12810603, MOUSE PHENOTYPE ID: MGI:1313268
HumanMN14330meningioma (disrupted in balanced translocation) 1
img Jax MP, Pubmed Id: 19776033, MOUSE PHENOTYPE ID: MGI:3584243
img Jax MP, Pubmed Id: 12810603, MOUSE PHENOTYPE ID: MGI:1313268
img Jax MP, Pubmed Id: 9533949, MOUSE PHENOTYPE ID: MGI:95841
img Jax MP, Pubmed Id: 15870292, MOUSE PHENOTYPE ID: MGI:1261813
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:0004450presphenoid bone hypoplasia0self