Compare GO annotations related to Leigh syndrome, French-Canadian type using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0048487beta-tubulin binding P42704IDAHumanPMID:12762840
Molecular FunctionGO:0005515protein binding MGI:1919666IPIMouseMGI:MGI:3689757|PMID:17050673
Molecular FunctionGO:0005515protein binding P42704IPIHumanPMID:17353931
Molecular FunctionGO:0005515protein binding P42704IPIHumanPMID:17050673
Molecular FunctionGO:0003697single-stranded DNA binding MGI:1919666IDAMouseMGI:MGI:2664354|PMID:12071956
Cellular ComponentGO:0000794condensed nuclear chromosome P42704IDAHumanPMID:12762840
Cellular ComponentGO:0005737cytoplasm MGI:1919666IDAMouseMGI:MGI:2664354|PMID:12071956
Cellular ComponentGO:0005856cytoskeleton P42704IDAHumanPMID:12762840
Cellular ComponentGO:0005739mitochondrion MGI:1919666IDAMouseMGI:MGI:2682130|PMID:14651853
Cellular ComponentGO:0005739mitochondrion P42704IDAHumanPMID:12832482
Cellular ComponentGO:0005634nucleus MGI:1919666IDAMouseMGI:MGI:2664354|PMID:12071956
Cellular ComponentGO:0005634nucleus P42704IDAHumanPMID:12832482
Cellular ComponentGO:0048471perinuclear region of cytoplasm P42704IDAHumanPMID:12762840