| Monarch Ortholog Phenotypes
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Human (1 source):
Meningioma
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Mouse (26 sources):
abnormal frontal bone morphology,
abnormal interparietal bone morphology,
abnormal pterygoid process morphology,
abnormal sphenoid bone morphology,
abnormal suckling behavior,
abnormal supraoccipital bone morphology,
absent alisphenoid bone,
absent temporal bone squamous part,
absent vomer bone,
alisphenoid bone hypoplasia,
basisphenoid bone hypoplasia,
large cranial foramen ovale,
large foramen rotundum,
maxillary shelf hypoplasia,
neonatal lethality, incomplete penetrance,
palatal shelves fail to meet at midline,
palate bone hypoplasia,
palatine bone horizontal plate hypoplasia,
perinatal lethality, complete penetrance,
presphenoid bone hypoplasia,
pterygoid bone hypoplasia,
temporal bone hypoplasia,
thin frontal bone,
thin interparietal bone,
thin parietal bone,
vomer bone hypoplasia
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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.