Compare GO annotations related to Otofaciocervical syndrome using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0005515protein binding MGI:109344IPIMouseMGI:MGI:3722498|PMID:11734542
Molecular FunctionGO:0004725protein tyrosine phosphatase activity MGI:109344IDAMouseMGI:MGI:2680856|PMID:14628052
Biological ProcessGO:0048856anatomical structure development MGI:109344IGIMouseMGI:MGI:3624596|PMID:16530750
Biological ProcessGO:0045165cell fate commitment MGI:109344IMPMouseMGI:MGI:3577160|PMID:15817220
Biological ProcessGO:0045165cell fate commitment MGI:109344IMPMouseMGI:MGI:3588889|PMID:16018995
Biological ProcessGO:0042472inner ear morphogenesis MGI:109344IMPMouseMGI:MGI:3577160|PMID:15817220
Biological ProcessGO:0001656metanephros development MGI:109344IMPMouseMGI:MGI:3588889|PMID:16018995
Biological ProcessGO:0043066negative regulation of apoptosis MGI:109344IMPMouseMGI:MGI:3577160|PMID:15817220
Biological ProcessGO:0009887organ morphogenesis MGI:109344IMPMouseMGI:MGI:2389277|PMID:12070080
Biological ProcessGO:0007389pattern specification process MGI:109344IGIMouseMGI:MGI:3624596|PMID:16530750
Biological ProcessGO:0006470protein amino acid dephosphorylation MGI:109344IDAMouseMGI:MGI:2680856|PMID:14628052
Biological ProcessGO:0045664regulation of neuron differentiation MGI:109344IMPMouseMGI:MGI:3512702|PMID:15496442
Biological ProcessGO:0001657ureteric bud development MGI:109344IGIMouseMGI:MGI:3588889|PMID:16018995