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Details
Link-It Detail - Jax Mouse Phenotype - esophageal atresia
Debug Stats
  • ### Total Build Time: 43 ms 33.670 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 364 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 214 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 178 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=8 ms Completed: 8 ms rowSize= 584 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 1.581 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=20 ms Completed: 20 ms rowSize= 29.472 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.156 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
esophageal atresia MP:0003276
Definition (1)
congenital blockage or absence of the lumen of the esophagus
Synonyms (1)
"esophageal narrowing" EXACT
Parents (1)
img abnormal esophagus morphology MP:0000467
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img digestive/alimentary phenotype MP:00053815img abnormal esophagus morphology MP:0000467
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanRAB2557111RAB25, member RAS oncogene family
img Jax MP, Pubmed Id: 20197623, MOUSE PHENOTYPE ID: MGI:1858203
img Jax MP, Pubmed Id: 21653639, MOUSE PHENOTYPE ID: MGI:2682064
img Jax MP, Pubmed Id: 17260385, MOUSE PHENOTYPE ID: MGI:104327
img Jax MP, Pubmed Id: 9731531, MOUSE PHENOTYPE ID: MGI:95728
img Jax MP, Pubmed Id: 12194825, MOUSE PHENOTYPE ID: MGI:1919638
img Jax MP, Pubmed Id: 17522155, MOUSE PHENOTYPE ID: MGI:98364
HumanRIPK454101receptor-interacting serine-threonine kinase 4
img Jax MP, Pubmed Id: 21653639, MOUSE PHENOTYPE ID: MGI:2682064
img Jax MP, Pubmed Id: 9731531, MOUSE PHENOTYPE ID: MGI:95728
img Jax MP, Pubmed Id: 12194825, MOUSE PHENOTYPE ID: MGI:1919638
img Jax MP, Pubmed Id: 20197623, MOUSE PHENOTYPE ID: MGI:1858203
img Jax MP, Pubmed Id: 17522155, MOUSE PHENOTYPE ID: MGI:98364
img Jax MP, Pubmed Id: 17260385, MOUSE PHENOTYPE ID: MGI:104327
HumanIFT17226160intraflagellar transport 172 homolog (Chlamydomonas)
img Jax MP, Pubmed Id: 17522155, MOUSE PHENOTYPE ID: MGI:98364
img Jax MP, Pubmed Id: 12194825, MOUSE PHENOTYPE ID: MGI:1919638
img Jax MP, Pubmed Id: 20197623, MOUSE PHENOTYPE ID: MGI:1858203
img Jax MP, Pubmed Id: 17260385, MOUSE PHENOTYPE ID: MGI:104327
img Jax MP, Pubmed Id: 9731531, MOUSE PHENOTYPE ID: MGI:95728
img Jax MP, Pubmed Id: 21653639, MOUSE PHENOTYPE ID: MGI:2682064
HumanNOG9241noggin
img Jax MP, Pubmed Id: 21653639, MOUSE PHENOTYPE ID: MGI:2682064
img Jax MP, Pubmed Id: 17260385, MOUSE PHENOTYPE ID: MGI:104327
img Jax MP, Pubmed Id: 9731531, MOUSE PHENOTYPE ID: MGI:95728
img Jax MP, Pubmed Id: 20197623, MOUSE PHENOTYPE ID: MGI:1858203
img Jax MP, Pubmed Id: 12194825, MOUSE PHENOTYPE ID: MGI:1919638
img Jax MP, Pubmed Id: 17522155, MOUSE PHENOTYPE ID: MGI:98364
HumanSOX26657SRY (sex determining region Y)-box 2
img Jax MP, Pubmed Id: 20197623, MOUSE PHENOTYPE ID: MGI:1858203
img Jax MP, Pubmed Id: 17260385, MOUSE PHENOTYPE ID: MGI:104327
img Jax MP, Pubmed Id: 12194825, MOUSE PHENOTYPE ID: MGI:1919638
img Jax MP, Pubmed Id: 21653639, MOUSE PHENOTYPE ID: MGI:2682064
img Jax MP, Pubmed Id: 9731531, MOUSE PHENOTYPE ID: MGI:95728
img Jax MP, Pubmed Id: 17522155, MOUSE PHENOTYPE ID: MGI:98364
HumanGLI22736GLI family zinc finger 2
img Jax MP, Pubmed Id: 9731531, MOUSE PHENOTYPE ID: MGI:95728
img Jax MP, Pubmed Id: 17522155, MOUSE PHENOTYPE ID: MGI:98364
img Jax MP, Pubmed Id: 20197623, MOUSE PHENOTYPE ID: MGI:1858203
img Jax MP, Pubmed Id: 21653639, MOUSE PHENOTYPE ID: MGI:2682064
img Jax MP, Pubmed Id: 17260385, MOUSE PHENOTYPE ID: MGI:104327
img Jax MP, Pubmed Id: 12194825, MOUSE PHENOTYPE ID: MGI:1919638
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003276esophageal atresia0self