ProfileGDS1065 / 204911_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 51% 44% 52% 59% 48% 50% 43% 45% 58% 47% 58% 56% 48% 54% 49% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 146.551
GSM24653Normal subject 232.944
GSM24654Normal subject 357.852
GSM24655A3243G-MELAS subject 144.959
GSM24656A3243G-MELAS subject 244.248
GSM24657A3243G-MELAS subject 364.750
GSM24658A3243G-MELAS subject 428.943
GSM24659A3243G-PEO subject 131.745
GSM24660A3243G-PEO subject 257.458
GSM24661A3243G-PEO subject 327.647
GSM24662A3243G-PEO subject 452.458
GSM24663mtDNA "Common"-deletion subject 158.256
GSM24664mtDNA "Common"-deletion subject 272.148
GSM24665mtDNA "Common"-deletion subject 376.654
GSM24666mtDNA "Common"-deletion subject 46349