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Mitochondria Phenome Knowledgebase

Please enter a Gene. Or Disease (Phenotypic Feature). MitoPhenome is a publicly available internet tool by Stanford University. Its aim is to aid clinicians and researchers in understanding how genetic variation among individuals contributes to clinical disease phenotypes and traits. MitoPhenome’s focus is on disorders associated with genes involved in the function and biogenesis of mitochondria. JPG, 62KB] from PubMed. Full-text articles and classified based on the hierarchical MeSH ontology.

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Mitochondria Phenome Knowledgebase | mitophenome.org Reviews
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Please enter a Gene. Or Disease (Phenotypic Feature). MitoPhenome is a publicly available internet tool by Stanford University. Its aim is to aid clinicians and researchers in understanding how genetic variation among individuals contributes to clinical disease phenotypes and traits. MitoPhenome’s focus is on disorders associated with genes involved in the function and biogenesis of mitochondria. JPG, 62KB] from PubMed. Full-text articles and classified based on the hierarchical MeSH ontology.
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Mitochondria Phenome Knowledgebase | mitophenome.org Reviews

https://mitophenome.org

Please enter a Gene. Or Disease (Phenotypic Feature). MitoPhenome is a publicly available internet tool by Stanford University. Its aim is to aid clinicians and researchers in understanding how genetic variation among individuals contributes to clinical disease phenotypes and traits. MitoPhenome’s focus is on disorders associated with genes involved in the function and biogenesis of mitochondria. JPG, 62KB] from PubMed. Full-text articles and classified based on the hierarchical MeSH ontology.

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mitophenome.org mitophenome.org
1

Mitochondria Phenome Knowledgebase

http://www.mitophenome.org/genes/list

LKR/SDH; LKRSDH; LORSDH. Alpha-aminoadipic semialdehyde synthase, mitochondrial precursor (LKR/SDH). GABA-AT; GABAT; NPD009. 4-aminobutyrate aminotransferase, mitochondrial precursor. Deficiency of GABA transaminase [ 137150. Susceptibility for autism [ 209850. ABC7; ASAT; Atm1p; EST140535. ATP-binding cassette, sub-family B, member 7, mitochondrial precursor. Sideroblastic anemia and spinocerebellar ataxia (ASAT) [ 301310. ABC42; ALD; ALDP; AMN. Adrenoleukodystrophy (ALD) [ 300100. ACAD1; MCAD; MCADH.

2

Mitochondria Phenome Knowledgebase

http://www.mitophenome.org/phenotypes/list

C04557.450.550.400. C04557.450.590.450. C04557.450.590.455. C04557.450.590.550.660. C04557.450.795.620. C04557.470.565.165. C04557.470.565.625. C04557.580.625.650. C04557.580.625.650.200. C04557.580.625.650. C04557.580.625.650.240.325. C04557.580.625.650. C04557.580.625.650.510. C04557.580.625.650. C04557.580.625.650.595. C04557.580.625.650. C04557.580.625.650.700. C04557.580.625.650. C04557.580.625.650.700.725. C04557.580.625.650. C04588.274.476.411.307. C04588.274.476.767. C04588.274.623.160.

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Please enter a Gene. Or Disease (Phenotypic Feature). MitoPhenome is a publicly available internet tool by Stanford University. Its aim is to aid clinicians and researchers in understanding how genetic variation among individuals contributes to clinical disease phenotypes and traits. MitoPhenome’s focus is on disorders associated with genes involved in the function and biogenesis of mitochondria. JPG, 62KB] from PubMed. Full-text articles and classified based on the hierarchical MeSH ontology.

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