ProfileGDS1065 / 221733_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 53% 63% 62% 66% 61% 61% 52% 66% 57% 58% 61% 56% 60% 61% 50% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 149.453
GSM24653Normal subject 272.163
GSM24654Normal subject 388.662
GSM24655A3243G-MELAS subject 159.466
GSM24656A3243G-MELAS subject 271.861
GSM24657A3243G-MELAS subject 3104.961
GSM24658A3243G-MELAS subject 443.352
GSM24659A3243G-PEO subject 167.666
GSM24660A3243G-PEO subject 253.657
GSM24661A3243G-PEO subject 343.458
GSM24662A3243G-PEO subject 458.761
GSM24663mtDNA "Common"-deletion subject 158.256
GSM24664mtDNA "Common"-deletion subject 2118.960
GSM24665mtDNA "Common"-deletion subject 3104.461
GSM24666mtDNA "Common"-deletion subject 467.150