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Details
Link-It Detail - Jax Mouse Phenotype - otocephaly
Debug Stats
  • ### Total Build Time: 19 ms 6.688 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 348 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 299 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=10 ms Completed: 10 ms rowSize= 574 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.563 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=4 ms Completed: 4 ms rowSize= 2.632 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
otocephaly MP:0009578
Definition (1)
a structural anomaly of the head consisting of absence or malformation of the lower jaw and the ears united or closely approaching below the face
Parents (1)
img abnormal head shape MP:0011495
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053826img abnormal head shape MP:0011495
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanOTX25015orthodenticle homeobox 2
img Jax MP, Pubmed Id: 9895322, MOUSE PHENOTYPE ID: MGI:97451
img Jax MP, Pubmed Id: 4019727
img Jax MP, Pubmed Id: 10529425
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0009578otocephaly0self