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Details
Link-It Detail - Jax Mouse Phenotype - decreased maxillary shelf size
Debug Stats
  • ### Total Build Time: 20 ms 28.052 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 276 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 189 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= 590 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 583 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 5.621 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 19.140 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
decreased maxillary shelf size MP:0009897
Definition (1)
reduced size of the bony projection of the maxilla that normally fuses with palatine shelf to form secondary (hard) palate
Synonyms (1)
"decreased palatine process size" EXACT
Parents (1)
img abnormal maxillary shelf morphology MP:0004538
Children (1)
img maxillary shelf hypoplasia MP:0009898
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:000538210img abnormal maxillary shelf morphology MP:0004538
img mammalian phenotype MP:0000001img skeleton phenotype MP:000539011img abnormal maxillary shelf morphology MP:0004538
img mammalian phenotype MP:0000001img digestive/alimentary phenotype MP:00053818img abnormal maxillary shelf morphology MP:0004538
img mammalian phenotype MP:0000001img craniofacial phenotype MP:000538212img abnormal maxillary shelf morphology MP:0004538
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanRSPO2340419R-spondin 2
INFERRED
HumanCDON50937cell adhesion associated, oncogene regulated
img Jax MP, Pubmed Id: 21183473, MOUSE PHENOTYPE ID: MGI:1926387
img Jax MP, Pubmed Id: 21183473, MOUSE PHENOTYPE ID: MGI:1926387
img Jax MP, Pubmed Id: 10471511, MOUSE PHENOTYPE ID: MGI:109344
img Jax MP, Pubmed Id: 21183473, MOUSE PHENOTYPE ID: MGI:1926387
img Jax MP, Pubmed Id: 21183473, MOUSE PHENOTYPE ID: MGI:1926387
img Jax MP, Pubmed Id: 10433909, MOUSE PHENOTYPE ID: MGI:101926
img Jax MP, Pubmed Id: 21183473, MOUSE PHENOTYPE ID: MGI:1926387
HumanMN14330meningioma (disrupted in balanced translocation) 1
INFERRED
HumanEYA12138eyes absent homolog 1 (Drosophila)
img Jax MP, Pubmed Id: 21183473, MOUSE PHENOTYPE ID: MGI:1926387
img Jax MP, Pubmed Id: 21183473, MOUSE PHENOTYPE ID: MGI:1926387
img Jax MP, Pubmed Id: 10471511, MOUSE PHENOTYPE ID: MGI:109344
img Jax MP, Pubmed Id: 21183473, MOUSE PHENOTYPE ID: MGI:1926387
img Jax MP, Pubmed Id: 10433909, MOUSE PHENOTYPE ID: MGI:101926
img Jax MP, Pubmed Id: 21183473, MOUSE PHENOTYPE ID: MGI:1926387
img Jax MP, Pubmed Id: 21183473, MOUSE PHENOTYPE ID: MGI:1926387
HumanEDNRB1910endothelin receptor type B
INFERRED
HumanDLX51749distal-less homeobox 5
img Jax MP, Pubmed Id: 21183473, MOUSE PHENOTYPE ID: MGI:1926387
img Jax MP, Pubmed Id: 21183473, MOUSE PHENOTYPE ID: MGI:1926387
img Jax MP, Pubmed Id: 21183473, MOUSE PHENOTYPE ID: MGI:1926387
img Jax MP, Pubmed Id: 10433909, MOUSE PHENOTYPE ID: MGI:101926
img Jax MP, Pubmed Id: 21183473, MOUSE PHENOTYPE ID: MGI:1926387
img Jax MP, Pubmed Id: 10471511, MOUSE PHENOTYPE ID: MGI:109344
img Jax MP, Pubmed Id: 21183473, MOUSE PHENOTYPE ID: MGI:1926387
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0009897decreased maxillary shelf size0self