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XB-GENEPAGE-12531593
cdh1 cadherin 1, type 1
Anatomical Phenotypes
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abnormal cell migration in neural crest (3 sources), abnormal cell adhesion (1 source), abnormally increased mobility of non-neural ectoderm (1 source), abnormal trachea morphology (1 source), abnormal tracheoesophageal septum (1 source), decreased cell adhesion in mesodermal cell (1 source), decreased size of the branchial arch skeleton (1 source) |
Expression Phenotypes
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Manual annotations: cdh1 assayed (15 sources) |
Computed annotations: cdh1 assayed (12 sources) |
Diseases
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esophageal atresia (1AP source), esophageal atresia/tracheoesophageal fistula (1AP source) |
Experiments (Reagents)
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Xla Wt + cdh1 MO (4 sources), Xla Wt + cdh1 MO (1 source), Xla Wt + KD-Pak1 + fn1 MO + cdh3 MO (1 source), Xtr Wt + deltaLL-Cdh1-GFP (1 source) |
Monarch Ortholog Phenotypes
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Human (35 sources): Abnormal eyelid morphology, Abnormal hair quantity, Abnormality of metabolism/homeostasis, Abnormality of the orbital region, Abnormality of vision, Anal atresia, Atrophic gastritis, Breast carcinoma, Carious teeth, Choanal atresia, [+] |
Mouse (39 sources): abnormal cell adhesion, abnormal embryo development, abnormal embryonic tissue morphology, abnormal enterocyte physiology, abnormal extraembryonic tissue morphology, abnormal mammary gland growth during lactation, abnormal mammary gland growth during pregnancy, abnormal milk composition, abnormal pancreatic islet morphology, abnormal placental labyrinth vasculature morphology, [+] |
View all ortholog results at Monarch |