Compare GO annotations related to Alport syndrome, autosomal recessive using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0005178integrin binding Q01955IDAHumanPMID:12682293
Molecular FunctionGO:0005515protein binding Q01955IPIHumanPMID:10212244
Molecular FunctionGO:0005515protein binding Q01955IPIHumanPMID:12682293
Cellular ComponentGO:0005604basement membrane MGI:104688IDAMouseMGI:MGI:2157737|PMID:11732842
Cellular ComponentGO:0005587collagen type IV MGI:104688IDAMouseMGI:MGI:2183884|PMID:12101409
Cellular ComponentGO:0005587collagen type IV Q01955IDAHumanPMID:10766752
Biological ProcessGO:0006919caspase activation Q01955IDAHumanPMID:10766752
Biological ProcessGO:0008283cell proliferation Q01955IDAHumanPMID:10766752
Biological ProcessGO:0007166cell surface receptor linked signal transduction MGI:104688IDAMouseMGI:MGI:3706464|PMID:12842087
Biological ProcessGO:0006917induction of apoptosis Q01955IDAHumanPMID:10766752
Biological ProcessGO:0016525negative regulation of angiogenesis MGI:104688IDAMouseMGI:MGI:3706481|PMID:16877525
Biological ProcessGO:0016525negative regulation of angiogenesis Q01955IDAHumanPMID:10766752
Biological ProcessGO:0016525negative regulation of angiogenesis Q01955IDAHumanPMID:12682293