ProfileGDS1065 / 204965_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 35% 47% 20% 38% 25% 40% 10% 37% 45% 14% 36% 41% 35% 26% 31% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 122.335
GSM24653Normal subject 238.447
GSM24654Normal subject 31020
GSM24655A3243G-MELAS subject 120.338
GSM24656A3243G-MELAS subject 214.425
GSM24657A3243G-MELAS subject 341.640
GSM24658A3243G-MELAS subject 43.510
GSM24659A3243G-PEO subject 121.937
GSM24660A3243G-PEO subject 233.345
GSM24661A3243G-PEO subject 34.414
GSM24662A3243G-PEO subject 421.236
GSM24663mtDNA "Common"-deletion subject 13041
GSM24664mtDNA "Common"-deletion subject 241.535
GSM24665mtDNA "Common"-deletion subject 319.526
GSM24666mtDNA "Common"-deletion subject 426.531