ProfileGDS1065 / 200627_at
TitleMitochondrial encephalomyopathies associated with mitochondrial DNA mutations
OrganismHomo sapiens


wild type A3243G large deletion normal MELAS PEO GSM24652 GSM24653 GSM24654 GSM24655 GSM24656 GSM24657 GSM24658 GSM24659 GSM24660 GSM24661 GSM24662 GSM24663 GSM24664 GSM24665 GSM24666 96% 96% 97% 96% 97% 96% 95% 94% 97% 95% 95% 96% 97% 96% 97% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11234.796
GSM24653Normal subject 21288.696
GSM24654Normal subject 3181097
GSM24655A3243G-MELAS subject 1728.296
GSM24656A3243G-MELAS subject 21274.597
GSM24657A3243G-MELAS subject 31999.696
GSM24658A3243G-MELAS subject 4915.795
GSM24659A3243G-PEO subject 1481.294
GSM24660A3243G-PEO subject 2127397
GSM24661A3243G-PEO subject 3667.195
GSM24662A3243G-PEO subject 4834.695
GSM24663mtDNA "Common"-deletion subject 11058.796
GSM24664mtDNA "Common"-deletion subject 22349.897
GSM24665mtDNA "Common"-deletion subject 32202.196
GSM24666mtDNA "Common"-deletion subject 42841.697