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Details
Link-It Detail - Jax Mouse Phenotype - palatine bone hypoplasia
Debug Stats
  • ### Total Build Time: 10 ms 13.782 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 376 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 425 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 588 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.916 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=4 ms Completed: 4 ms rowSize= 8.195 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
palatine bone hypoplasia MP:0004475
Definition (1)
underdevelopment or reduced size, usually due to a reduced number of cells, in either of either of two irregularly L-shaped bones located posterior to the maxilla that in part forms the back of the hard palate, part of the nasal cavity and part of the floor of the orbits
Parents (1)
img abnormal palatine bone morphology MP:0005249
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053828img abnormal palatine bone morphology MP:0005249
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053909img abnormal palatine bone morphology MP:0005249
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanGSC145258goosecoid homeobox
img Jax MP, Pubmed Id: 9449665, MOUSE PHENOTYPE ID: MGI:1101357
img Jax MP, Pubmed Id: 7555718, MOUSE PHENOTYPE ID: MGI:95841
img Jax MP, Pubmed Id: 16938878, MOUSE PHENOTYPE ID: MGI:892003
HumanTCOF16949Treacher Collins-Franceschetti syndrome 1
img Jax MP, Pubmed Id: 16938878, MOUSE PHENOTYPE ID: MGI:892003
img Jax MP, Pubmed Id: 9449665, MOUSE PHENOTYPE ID: MGI:1101357
img Jax MP, Pubmed Id: 7555718, MOUSE PHENOTYPE ID: MGI:95841
HumanECE11889endothelin converting enzyme 1
img Jax MP, Pubmed Id: 16938878, MOUSE PHENOTYPE ID: MGI:892003
img Jax MP, Pubmed Id: 9449665, MOUSE PHENOTYPE ID: MGI:1101357
img Jax MP, Pubmed Id: 7555718, MOUSE PHENOTYPE ID: MGI:95841
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004475palatine bone hypoplasia0self