| Monarch Ortholog Phenotypes
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Human (16 sources):
Abnormal dental morphology,
Abnormality of the face,
Adenomatous colonic polyposis,
Colon cancer,
Colorectal polyposis,
Hereditary nonpolyposis colorectal carcinoma,
Hypoplasia of the maxilla,
Microdontia,
Micrognathia,
Neoplasm of the rectum,
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Mouse (32 sources):
abnormal body wall morphology,
abnormal craniofacial morphology,
abnormal cranium morphology,
abnormal embryo size,
abnormal head size,
abnormal limb morphology,
abnormal neural plate morphology,
abnormal neurocranium morphology,
abnormal osteoblast physiology,
abnormal outer ear morphology,
abnormal pericardium morphology,
abnormal primitive streak morphology,
abnormal skeleton development,
abnormal skin coloration,
abnormal tail development,
abnormal tail morphology,
abnormal vibrissa morphology,
absent jugum limitans,
cardia bifida,
curly tail,
decreased cranium height,
embryonic growth arrest,
embryonic lethality during organogenesis, incomplete penetrance,
enhanced osteoblast differentiation,
increased osteoblast proliferation,
kinked tail,
no abnormal phenotype detected,
open neural tube,
premature intramembranous bone ossification,
premature metopic suture closure,
prenatal lethality, incomplete penetrance,
preweaning lethality, complete penetrance
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View all ortholog results at Monarch
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Gene expression phenotype annotations where the gene of interest has been
disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from
differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1,
FDR <= 0.05 and an absolute LogFC >= 2.