Compare GO annotations related to Ceroid-lipofuscinosis, neuronal-5, variant late infantile using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0005515protein binding O75503IPIHumanPMID:12134079
Cellular ComponentGO:0005783endoplasmic reticulum O75503IDAHumanPMID:12134079
Cellular ComponentGO:0005794Golgi apparatus O75503IDAHumanPMID:12134079
Cellular ComponentGO:0016021integral to membrane O75503IDAHumanPMID:12134079
Cellular ComponentGO:0005765lysosomal membrane O75503IDAHumanPMID:12134079
Cellular ComponentGO:0005764lysosome MGI:2442253IDAMouseMGI:MGI:3046133|PMID:15207259
Cellular ComponentGO:0048471perinuclear region of cytoplasm O75503IDAHumanPMID:10992246
Cellular ComponentGO:0005775vacuolar lumen MGI:2442253IDAMouseMGI:MGI:3046133|PMID:15207259
Biological ProcessGO:0007420brain development O75503IEPHumanPMID:10992246
Biological ProcessGO:0007042lysosomal lumen acidification O75503IMPHumanPMID:11722572
Biological ProcessGO:0007040lysosome organization and biogenesis MGI:2442253IMPMouseMGI:MGI:3512689|PMID:15459177
Biological ProcessGO:0022008neurogenesis O75503IEPHumanPMID:10992246
Biological ProcessGO:0007601visual perception MGI:2442253IMPMouseMGI:MGI:3512689|PMID:15459177