Human (83 sources):
Abdominal pain,
Abnormal T-wave,
Arthralgia,
Ataxia,
Blurred vision,
Cerebral calcification,
Chondrocalcinosis,
Constipation,
Decreased urinary potassium,
Delayed puberty,
Diabetic ketoacidosis,
Diarrhea,
Enuresis,
Failure to thrive,
Fatigue,
Focal segmental glomerulosclerosis,
Generalized muscle weakness,
Glucose intolerance,
Gout,
Graves disease,
Growth delay,
Hashimoto thyroiditis,
Headache,
Hyperhidrosis,
Hypermagnesemia,
Hypocalcemia,
Hypocalciuria,
Hypokalemia,
Hypokalemic alkalosis,
Hypomagnesemia,
Hypotension,
Increased circulating renin level,
Insomnia,
Insulin resistance,
Iron deficiency anemia,
Low-to-normal blood pressure,
Maternal diabetes,
Metabolic alkalosis,
Mitochondrial encephalopathy,
Muscle spasm,
Muscle weakness,
Myalgia,
Nausea and vomiting,
Neoplasm of the pancreas,
Nocturia,
Palpitations,
Paralysis,
Parathyroid adenoma,
Paresthesia,
Pericardial effusion,
Polydipsia,
Polyuria,
Primary hyperaldosteronism,
Prolonged PR interval,
Prolonged QT interval,
Prominent U wave,
Proteinuria,
Raynaud phenomenon,
Recurrent fever,
Renal Fanconi syndrome,
Renal magnesium wasting,
Renal potassium wasting,
Renal tubular acidosis,
Respiratory distress,
Rhabdomyolysis,
ST segment depression,
Salt craving,
Scleroderma,
Seizure,
Syncope,
Tetany,
Tinnitus,
Tubulointerstitial nephritis,
Type I diabetes mellitus,
Type II diabetes mellitus,
Urinary incontinence,
Varicose veins,
Ventricular fibrillation,
Ventricular tachycardia,
Vertigo,
Vomiting,
obsolete Excessive daytime sleepiness,
obsolete Focal seizures, afebril
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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.