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XB-GENEPAGE-6457661
timmdc1 translocase of inner mitochondrial membrane domain containing 1
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.
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Computed annotations: timmdc1 assayed (2 sources) |
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (59 sources): Abnormal mitochondria in muscle tissue, Acute necrotizing encephalopathy, Ataxia, Babinski sign, Blindness, Cerebellar atrophy, Cerebral edema, Coma, Decreased activity of mitochondrial complex I, Decreased activity of mitochondrial respiratory chain, [+] |
Mouse (7 sources): abnormal chorion morphology, abnormal coat appearance, abnormal trophoblast layer morphology, increased CD4-positive, alpha beta T cell number, increased circulating alkaline phosphatase level, lethality throughout fetal growth and development, complete penetrance, preweaning lethality, complete penetrance |
View all ortholog results at Monarch |