Compare GO annotations related to Deafness, autosomal recessive 36 using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0051015actin filament binding RGD:620652IPIRatRGD:632658|PMID:8799813
Molecular FunctionGO:0051015actin filament binding RGD:620652IDARatRGD:8799813
Molecular FunctionGO:0017124SH3 domain binding RGD:620652IPIRatRGD:12598619
Cellular ComponentGO:0015629actin cytoskeleton MGI:1861630IDAMouseMGI:MGI:1350756|PMID:10588661
Cellular ComponentGO:0015629actin cytoskeleton RGD:620652IDARatRGD:null
Cellular ComponentGO:0005903brush border RGD:620652IDARatRGD:9763424
Cellular ComponentGO:0005737cytoplasm RGD:620652IDARatRGD:null
Cellular ComponentGO:0031941filamentous actin RGD:620652IDARatRGD:8799813
Cellular ComponentGO:0005902microvillus RGD:620652IDARatRGD:null
Biological ProcessGO:0051017actin filament bundle formation MGI:1861630IDAMouseMGI:MGI:1350756|PMID:10588661
Biological ProcessGO:0007626locomotory behavior MGI:1861630IMPMouseMGI:MGI:3664354|PMID:16962269
Biological ProcessGO:0051494negative regulation of cytoskeleton organization and biogenesis MGI:1861630IDAMouseMGI:MGI:3688341|PMID:15190118
Biological ProcessGO:0030046parallel actin filament bundle formation MGI:1861630IDAMouseMGI:MGI:1350756|PMID:10588661