| Monarch Ortholog Phenotypes
|
Human (41 sources):
Abdominal pain,
Abnormal urinary color,
Acute episodes of neuropathic symptoms,
Anorexia,
Anxiety,
Arrhythmia,
Arthralgia,
Behavioral abnormality,
Constipation,
Cranial nerve paralysis,
Depression,
Diaphragmatic paralysis,
Diarrhea,
Dysuria,
Elevated urinary delta-aminolevulinic acid,
Hallucinations,
Hepatocellular carcinoma,
Hyperhidrosis,
Hyperlipidemia,
Hypertension,
Hypertensive crisis,
Hyponatremia,
Insomnia,
Lethargy,
Muscle weakness,
Myalgia,
Nausea,
Nausea and vomiting,
Paralysis,
Paralytic ileus,
Paraparesis,
Paresthesia,
Psychotic episodes,
Renal insufficiency,
Respiratory paralysis,
Seizure,
Tachycardia,
Urinary incontinence,
Urinary retention,
Vomiting,
Weight loss
[+]
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Mouse (22 sources):
abnormal axon morphology,
abnormal embryo size,
abnormal locomotor activation,
abnormal motor capabilities/coordination/movement,
abnormal vitreous body morphology,
decreased body length,
decreased body size,
decreased hydroxymethylbilane synthase level,
decreased locomotor activity,
decreased myelin sheath amount,
delayed eyelid opening,
embryonic lethality prior to organogenesis,
increased erythrocyte protoporphyrin level,
increased startle reflex,
limb grasping,
no abnormal phenotype detected,
porphyria,
premature death,
prenatal lethality, complete penetrance,
preweaning lethality, complete penetrance,
short stride length,
skeletal muscle degeneration
[+]
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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.