| Monarch Ortholog Phenotypes
|
|
Human (2 sources):
Abnormality of refraction,
Myopia
|
Mouse (22 sources):
abnormal DNA methylation,
abnormal active avoidance behavior,
abnormal discrimination learning,
abnormal excitatory postsynaptic potential,
abnormal imprinting,
abnormal long term spatial reference memory,
abnormal pituitary secretion,
abnormal spatial learning,
behavior/neurological phenotype,
cellular phenotype,
decreased circulating insulin-like growth factor I level,
decreased growth hormone level,
enhanced lipolysis,
impaired contextual conditioning behavior,
impaired social transmission of food preference,
impaired synaptic plasticity,
maternal imprinting,
nervous system phenotype,
no abnormal phenotype detected,
paternal imprinting,
reduced long term potentiation,
small pancreatic islets
[+]
|
View all ortholog results at Monarch
|
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.