Compare GO annotations related to 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0005515protein binding Q99714IPIHumanPMID:9338779
Cellular ComponentGO:0005783endoplasmic reticulum MGI:1333871IDAMouseMGI:MGI:3583039|PMID:15962010
Cellular ComponentGO:0005743mitochondrial inner membrane MGI:1333871IDAMouseMGI:MGI:3590069|PMID:12865426
Cellular ComponentGO:0005739mitochondrion MGI:1333871IDAMouseMGI:MGI:2682130|PMID:14651853
Cellular ComponentGO:0005739mitochondrion RGD:69231IDARatRGD:68798|PMID:11165016
Biological ProcessGO:0007276gamete generation WBGene00000181IMPWormWB:WBPaper00006395|PMID:14551910
Biological ProcessGO:0040007growth WBGene00000181IMPWormWB:WBPaper00006395|PMID:14551910
Biological ProcessGO:0040035hermaphrodite genitalia development WBGene00000181IMPWormWB:WBPaper00006395|PMID:14551910
Biological ProcessGO:0002119larval development (sensu Nematoda) WBGene00000181IMPWormWB:WBPaper00006395|PMID:14551910
Biological ProcessGO:0007626locomotory behavior WBGene00000181IMPWormWB:WBPaper00006395|PMID:14551910
Biological ProcessGO:0040017positive regulation of locomotion WBGene00000181IMPWormWB:WBPaper00006395|PMID:14551910