| Monarch Ortholog Phenotypes
|
Human (34 sources):
Abdominal pain,
Abnormal blistering of the skin,
Abnormality of metabolism/homeostasis,
Acute episodes of neuropathic symptoms,
Anxiety,
Arthralgia,
Atypical behavior,
Auditory hallucination,
Confusion,
Congenital hemolytic anemia,
Constipation,
Cutaneous photosensitivity,
Depression,
Diarrhea,
Hallucinations,
Hepatomegaly,
Hypermelanotic macule,
Hypertension,
Hypertrichosis,
Hyponatremia,
Insomnia,
Irritability,
Jaundice,
Myalgia,
Nausea and vomiting,
Paranoia,
Peripheral neuropathy,
Respiratory paralysis,
Seizure,
Splenomegaly,
Tachycardia,
Thin skin,
Visual hallucination,
Vomiting
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Mouse (12 sources):
abnormal lens fiber morphology,
absent forelimb buds,
decreased mean corpuscular volume,
embryonic growth retardation,
embryonic lethality during organogenesis, complete penetrance,
hydropic eye lens fibers,
increased circulating ferritin level,
increased erythroblast number,
increased red blood cell distribution width,
increased spleen red pulp amount,
[+]
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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.