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Details
Link-It Detail - Jax Mouse Phenotype - maxillary shelf hypoplasia
Debug Stats
  • ### Total Build Time: 25 ms 24.204 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 333 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=2 ms Completed: 2 ms rowSize= 585 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 5.602 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 15.827 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
maxillary shelf hypoplasia MP:0009898
Definition (1)
underdevelopment, usually due to a deficiency in the number of cells, of the bony projection of the maxilla that normally fuses with palatine shelf to form secondary (hard) palate
Synonyms (1)
"hypoplastic palatal process of maxilla" EXACT
Parents (1)
img decreased maxillary shelf size MP:0009897
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:000538211img decreased maxillary shelf size MP:0009897
img mammalian phenotype MP:0000001img skeleton phenotype MP:000539012img decreased maxillary shelf size MP:0009897
img mammalian phenotype MP:0000001img digestive/alimentary phenotype MP:00053819img decreased maxillary shelf size MP:0009897
img mammalian phenotype MP:0000001img craniofacial phenotype MP:000538213img decreased maxillary shelf size MP:0009897
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanRSPO2340419R-spondin 2
img Jax MP, Pubmed Id: 15870292, MOUSE PHENOTYPE ID: MGI:1261813
img Jax MP, Pubmed Id: 17693063, MOUSE PHENOTYPE ID: MGI:102720
img Jax MP, Pubmed Id: 17693063, MOUSE PHENOTYPE ID: MGI:102720
img Jax MP, Pubmed Id: 9729491
img Jax MP, Pubmed Id: 9876178
img Jax MP, Pubmed Id: 17693063, MOUSE PHENOTYPE ID: MGI:102720
img Jax MP, Pubmed Id: 19233133, MOUSE PHENOTYPE ID: MGI:1922667
HumanMN14330meningioma (disrupted in balanced translocation) 1
img Jax MP, Pubmed Id: 17693063, MOUSE PHENOTYPE ID: MGI:102720
img Jax MP, Pubmed Id: 9876178
img Jax MP, Pubmed Id: 17693063, MOUSE PHENOTYPE ID: MGI:102720
img Jax MP, Pubmed Id: 17693063, MOUSE PHENOTYPE ID: MGI:102720
img Jax MP, Pubmed Id: 9729491
img Jax MP, Pubmed Id: 19233133, MOUSE PHENOTYPE ID: MGI:1922667
img Jax MP, Pubmed Id: 15870292, MOUSE PHENOTYPE ID: MGI:1261813
HumanEDNRB1910endothelin receptor type B
img Jax MP, Pubmed Id: 17693063, MOUSE PHENOTYPE ID: MGI:102720
img Jax MP, Pubmed Id: 19233133, MOUSE PHENOTYPE ID: MGI:1922667
img Jax MP, Pubmed Id: 15870292, MOUSE PHENOTYPE ID: MGI:1261813
img Jax MP, Pubmed Id: 9876178
img Jax MP, Pubmed Id: 17693063, MOUSE PHENOTYPE ID: MGI:102720
img Jax MP, Pubmed Id: 9729491
img Jax MP, Pubmed Id: 17693063, MOUSE PHENOTYPE ID: MGI:102720
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0009898maxillary shelf hypoplasia0self