Compare GO annotations related to Craniofrontonasal dysplasia using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0046875ephrin receptor binding MGI:102708IPIMouseMGI:MGI:3037383|PMID:14988728
Molecular FunctionGO:0005515protein binding MGI:102708IPIMouseMGI:MGI:3037383|PMID:14988728
Molecular FunctionGO:0005515protein binding P98172IPIHumanPMID:9883737
Molecular FunctionGO:0005515protein binding RGD:2540IDARatRGD:null
Molecular FunctionGO:0005515protein binding RGD:2540IPIRatRGD:null
Molecular FunctionGO:0005515protein binding RGD:2540IPIRatRGD:10558890
Cellular ComponentGO:0045121lipid raft MGI:102708IDAMouseMGI:MGI:1334095|PMID:10197531
Cellular ComponentGO:0045202synapse RGD:2540IDARatRGD:null
Biological ProcessGO:0007411axon guidance MGI:102708IMPMouseMGI:MGI:2153438|PMID:11731465
Biological ProcessGO:0009880embryonic pattern specification MGI:102708IMPMouseMGI:MGI:3037600|PMID:15037550
Biological ProcessGO:0007399nervous system development RGD:2540IMPRatRGD:727396|PMID:12139920
Biological ProcessGO:0001755neural crest cell migration MGI:102708IMPMouseMGI:MGI:3037600|PMID:15037550
Biological ProcessGO:0042102positive regulation of T cell proliferation MGI:102708IDAMouseMGI:MGI:3522541|PMID:15502157