coq9 Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (143)

Interactants (240)

XB-GENEPAGE-948679

Gene Symbol: coq9 Gene Name: coenzyme Q9

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: coq9 assayed (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (20 sources): Bradycardia, Cerebellar atrophy, Cerebral atrophy, Dystonia, Encephalopathy, Feeding difficulties, Generalized hypotonia, Global developmental delay, Hyperalaninemia, Hyperreflexia, Hypotonia, Increased circulating lactate concentration, Intrauterine growth retardation, Lactic acidosis, Left ventricular hypertrophy, Respiratory insufficiency, Secondary microcephaly, Seizure, Spasticity, Weak cry [+]
Mouse (16 sources): abnormal dendrite morphology, abnormal enzyme/coenzyme level, abnormal mitochondrial ATP synthesis coupled electron transport, abnormal mitochondrial physiology, brain vacuoles, cardiac fibrosis, decreased body size, decreased circulating alanine transaminase level, decreased locomotor activity, decreased vertical activity, hindlimb paralysis, increased neuron apoptosis, oxidative stress, premature death, premature hair loss, spongiform encephalopathy [+]
View all ortholog results at Monarch