ProfileGDS1065 / 210988_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 68% 68% 75% 68% 69% 62% 59% 62% 70% 67% 66% 67% 70% 73% 68% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 194.968
GSM24653Normal subject 290.768
GSM24654Normal subject 3172.375
GSM24655A3243G-MELAS subject 164.368
GSM24656A3243G-MELAS subject 210269
GSM24657A3243G-MELAS subject 3107.862
GSM24658A3243G-MELAS subject 458.959
GSM24659A3243G-PEO subject 157.462
GSM24660A3243G-PEO subject 291.570
GSM24661A3243G-PEO subject 362.967
GSM24662A3243G-PEO subject 472.666
GSM24663mtDNA "Common"-deletion subject 193.667
GSM24664mtDNA "Common"-deletion subject 2183.470
GSM24665mtDNA "Common"-deletion subject 3177.973
GSM24666mtDNA "Common"-deletion subject 4152.368