ProfileGDS1065 / 219785_s_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 61% 66% 54% 69% 61% 72% 56% 62% 64% 79% 75% 67% 64% 59% 70% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 171.261
GSM24653Normal subject 281.166
GSM24654Normal subject 362.154
GSM24655A3243G-MELAS subject 16669
GSM24656A3243G-MELAS subject 273.561
GSM24657A3243G-MELAS subject 3182.972
GSM24658A3243G-MELAS subject 450.456
GSM24659A3243G-PEO subject 15862
GSM24660A3243G-PEO subject 27264
GSM24661A3243G-PEO subject 3117.779
GSM24662A3243G-PEO subject 4113.775
GSM24663mtDNA "Common"-deletion subject 194.567
GSM24664mtDNA "Common"-deletion subject 2142.564
GSM24665mtDNA "Common"-deletion subject 394.359
GSM24666mtDNA "Common"-deletion subject 4176.370