Compare GO annotations related to Persistent Mullerian duct syndrome, type II using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0005125cytokine activity P14174IDAHumanPMID:12782713
Molecular FunctionGO:0042562hormone binding Q16671IPIHumanPMID:14750901
Molecular FunctionGO:0005515protein binding P14174IPIHumanPMID:12782713
Molecular FunctionGO:0005515protein binding P14174IPIHumanPMID:12681488
Molecular FunctionGO:0004872receptor activity Q16671IMPHumanPMID:7493017
Molecular FunctionGO:0005026transforming growth factor beta receptor activity, type II RGD:70964IDARatRGD:null
Molecular FunctionGO:0004675transmembrane receptor protein serine/threonine kinase activity RGD:70964IDARatRGD:70669|PMID:8119126
Cellular ComponentGO:0005576extracellular region P14174IDAHumanPMID:12782713
Cellular ComponentGO:0005887integral to plasma membrane RGD:70964IDARatRGD:null
Biological ProcessGO:0008283cell proliferation P14174IDAHumanPMID:12782713
Biological ProcessGO:0007166cell surface receptor linked signal transduction P14174IDAHumanPMID:12782713
Biological ProcessGO:0043066negative regulation of apoptosis P14174IDAHumanPMID:12782713
Biological ProcessGO:0001516prostaglandin biosynthetic process P14174IDAHumanPMID:12782713
Biological ProcessGO:0007548sex differentiation MGI:105062IMPMouseMGI:MGI:83469|PMID:8895659
Biological ProcessGO:0007165signal transduction Q16671IMPHumanPMID:7493017
Biological ProcessGO:0007179transforming growth factor beta receptor signaling pathway RGD:70964IDARatRGD:null