slc25a11 Phenotypes

Phenotypes

XB-GENEPAGE-979672

Gene Symbol: slc25a11 Gene Name: solute carrier family 25 (mitochondrial carrier; oxoglutarate carrier), member 11

Expression Phenotypes 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.
Computed annotations: slc25a11 assayed (3 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (43 sources): Adrenal pheochromocytoma, Aniridia, Arachnoid hemangiomatosis, Cerebral hemorrhage, Chest pain, Conductive hearing impairment, Congestive heart failure, Cranial nerve compression, Dysphonia, Elevated calcitonin, Elevated circulating catecholamine level, Elevated urinary dopamine, Elevated urinary epinephrine, Elevated urinary norepinephrine, Episodic abdominal pain, Episodic hyperhidrosis, Episodic paroxysmal anxiety, Extraadrenal pheochromocytoma, Fatigue, Flushing, Glomerular sclerosis, Hematuria, Hypercalcemia, Hypertension, Hypertension associated with pheochromocytoma, Hypertensive retinopathy, Nausea, Pallor, Palpitations, Panic attack, Paraganglioma, Paraganglioma of head and neck, Paroxysmal vertigo, Positive regitine blocking test, Proteinuria, Pulsatile tinnitus, Recurrent paroxysmal headache, Renal cell carcinoma, Retinal capillary hemangioma, Sinus tachycardia, Tremor, Vocal cord paralysis, Weight loss [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

These phenotypes are associated with this gene with a has phenotype relation via Monarch.

Human (43 sources): Adrenal pheochromocytoma, Aniridia, Arachnoid hemangiomatosis, Cerebral hemorrhage, Chest pain, Conductive hearing impairment, Congestive heart failure, Cranial nerve compression, Dysphonia, Elevated calcitonin, [+]