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Details
Link-It Detail - Jax Mouse Phenotype - abnormal esophageal epithelium morphology
Debug Stats
  • ### Total Build Time: 23 ms 14.527 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 410 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 246 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 193 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=4 ms Completed: 4 ms rowSize= 584 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.052 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.581 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 9.172 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.179 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal esophageal epithelium morphology MP:0000468
Definition (1)
any structural anomaly of the epithelial layer that lines the luminal space of the esophagus
Synonyms (1)
"esophageal epithelium abnormalities" BROAD
Parents (1)
img abnormal esophagus morphology MP:0000467
Children (2)
img abnormal esophageal squamous epithelium morphology MP:0000469
img esophageal epithelium hyperplasia MP:0000466
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img digestive/alimentary phenotype MP:00053815img abnormal esophagus morphology MP:0000467
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanRAB2557111RAB25, member RAS oncogene family
INFERRED
HumanKEAP19817kelch-like ECH-associated protein 1
Click here to display 18 evidence detail records.
HumanKLF49314Kruppel-like factor 4 (gut)
Click here to display 18 evidence detail records.
HumanTP638626tumor protein p63
Click here to display 18 evidence detail records.
HumanFZD48322frizzled family receptor 4
INFERRED
HumanTERF17013telomeric repeat binding factor (NIMA-interacting) 1
Click here to display 18 evidence detail records.
HumanSOX26657SRY (sex determining region Y)-box 2
INFERRED
HumanSLC9A36550solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3
INFERRED
HumanSLC4A26522solute carrier family 4 (anion exchanger), member 2
Click here to display 18 evidence detail records.
HumanRARA5914retinoic acid receptor, alpha
Click here to display 18 evidence detail records.
HumanKRT53852keratin 5
Click here to display 18 evidence detail records.
HumanKRT43851keratin 4
Click here to display 18 evidence detail records.
HumanITGB43691integrin, beta 4
Click here to display 18 evidence detail records.
HumanEGFR1956epidermal growth factor receptor
Click here to display 18 evidence detail records.
HumanBRCA1672breast cancer 1, early onset
Click here to display 18 evidence detail records.
HumanATP2A2488ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000468abnormal esophageal epithelium morphology0self