ProfileGDS1065 / 200044_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 65% 74% 72% 71% 75% 76% 77% 68% 67% 72% 63% 68% 73% 73% 78% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18265
GSM24653Normal subject 212174
GSM24654Normal subject 3145.372
GSM24655A3243G-MELAS subject 173.871
GSM24656A3243G-MELAS subject 2137.675
GSM24657A3243G-MELAS subject 3220.276
GSM24658A3243G-MELAS subject 4144.877
GSM24659A3243G-PEO subject 172.368
GSM24660A3243G-PEO subject 280.467
GSM24661A3243G-PEO subject 380.672
GSM24662A3243G-PEO subject 463.863
GSM24663mtDNA "Common"-deletion subject 197.268
GSM24664mtDNA "Common"-deletion subject 2210.773
GSM24665mtDNA "Common"-deletion subject 3187.173
GSM24666mtDNA "Common"-deletion subject 4276.778