Compare GO annotations related to Neuropathy, distal hereditary motor, type II 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 Q9UJY1IPIHumanPMID:14594798
Molecular FunctionGO:0005515protein binding MGI:2135756IPIMouseMGI:MGI:3609918|PMID:11591653
Cellular ComponentGO:0005622intracellular Q9UJY1IDAHumanPMID:11256614