ProfileGDS1065 / 221832_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 64% 61% 49% 66% 59% 68% 61% 69% 59% 58% 76% 61% 62% 56% 52% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 181.664
GSM24653Normal subject 266.961
GSM24654Normal subject 350.249
GSM24655A3243G-MELAS subject 159.166
GSM24656A3243G-MELAS subject 266.859
GSM24657A3243G-MELAS subject 3143.168
GSM24658A3243G-MELAS subject 463.961
GSM24659A3243G-PEO subject 176.169
GSM24660A3243G-PEO subject 258.159
GSM24661A3243G-PEO subject 343.758
GSM24662A3243G-PEO subject 4117.276
GSM24663mtDNA "Common"-deletion subject 17261
GSM24664mtDNA "Common"-deletion subject 2127.162
GSM24665mtDNA "Common"-deletion subject 383.656
GSM24666mtDNA "Common"-deletion subject 472.852