ProfileGDS1065 / 204787_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 59% 71% 59% 77% 61% 75% 74% 76% 68% 76% 77% 60% 73% 64% 63% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 164.959
GSM24653Normal subject 2101.371
GSM24654Normal subject 379.859
GSM24655A3243G-MELAS subject 193.877
GSM24656A3243G-MELAS subject 273.161
GSM24657A3243G-MELAS subject 3207.975
GSM24658A3243G-MELAS subject 4121.474
GSM24659A3243G-PEO subject 1103.476
GSM24660A3243G-PEO subject 283.468
GSM24661A3243G-PEO subject 396.976
GSM24662A3243G-PEO subject 4123.777
GSM24663mtDNA "Common"-deletion subject 168.160
GSM24664mtDNA "Common"-deletion subject 2219.773
GSM24665mtDNA "Common"-deletion subject 311764
GSM24666mtDNA "Common"-deletion subject 4123.163