| Monarch Ortholog Phenotypes
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Human (35 sources):
Abnormal blistering of the skin,
Abnormal urinary color,
Abnormality of the orbital region,
Abnormality of vision,
Anxiety,
Ataxia,
Calcium oxalate nephrolithiasis,
Cutaneous photosensitivity,
EEG abnormality,
Emotional lability,
Episodic ataxia,
Gingivitis,
Global developmental delay,
Glossitis,
Hallucinations,
Hydroxyprolinuria,
Hyperglycinuria,
Hyperreflexia,
Hypopigmented skin patches,
Hypotonia,
Infectious encephalitis,
Intellectual disability,
Irregular hyperpigmentation,
Malabsorption,
Migraine,
Neutral hyperaminoaciduria,
Nystagmus,
Photophobia,
Prolinuria,
Psychosis,
Seizure,
Short stature,
Skin rash,
Spasticity,
Strabismus
[+]
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|
Mouse (8 sources):
abnormal coat appearance,
abnormal intestine physiology,
abnormal renal transport,
decreased body size,
decreased lean body mass,
digestive/alimentary phenotype,
hearing/vestibular/ear phenotype,
homeostasis/metabolism phenotype
|
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.