Compare GO annotations related to Molybdenum cofactor deficiency, type B using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0042802identical protein binding MGI:1336894IPIMouseMGI:MGI:3609918|PMID:11591653
Molecular FunctionGO:0005515protein binding RGD:69194IPIRatRGD:1601270|PMID:12812758
Molecular FunctionGO:0032947protein complex scaffold RGD:69194IDARatRGD:1599854|PMID:10844024
Molecular FunctionGO:0042803protein homodimerization activity RGD:69194IDARatRGD:1300220|PMID:14976213
Molecular FunctionGO:0005102receptor binding RGD:69194IPIRatRGD:1300220|PMID:14976213
Cellular ComponentGO:0005622intracellular MGI:109602IDAMouseMGI:MGI:3706198|PMID:17145751
Biological ProcessGO:0007529establishment of synaptic specificity at neuromuscular junction MGI:109602IMPMouseMGI:MGI:1346942|PMID:10531433
Biological ProcessGO:0051260protein homooligomerization RGD:69194IDARatRGD:1300220|PMID:14976213
Biological ProcessGO:0007416synaptogenesis RGD:69194IEPRatRGD:1599855|PMID:9130666