Compare GO annotations related to Congenital bilateral absence of vas deferens using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0030165PDZ domain binding P13569IDAHumanPMID:11707463
Molecular FunctionGO:0005515protein binding P13569IPIHumanPMID:15247260
Molecular FunctionGO:0005515protein binding P13569IPIHumanPMID:11707463
Cellular ComponentGO:0016324apical plasma membrane P13569IDAHumanPMID:15247260
Cellular ComponentGO:0016324apical plasma membrane RGD:2332IDARatRGD:724710|PMID:11083465
Cellular ComponentGO:0030659cytoplasmic vesicle membrane RGD:2332IDARatRGD:724710|PMID:11083465
Biological ProcessGO:0030324lung development RGD:2332IMPRatRGD:1599597|PMID:15694001
Biological ProcessGO:0042493response to drug RGD:2332IEPRatRGD:1599592|PMID:16916328
Biological ProcessGO:0043627response to estrogen stimulus RGD:2332IEPRatRGD:1599595|PMID:16051669
Biological ProcessGO:0043434response to peptide hormone stimulus RGD:2332IEPRatRGD:1599594|PMID:16614390
Biological ProcessGO:0030321transepithelial chloride transport RGD:2332IMPRatRGD:1599591|PMID:17122162
Biological ProcessGO:0042311vasodilation RGD:2332IMPRatRGD:1599593|PMID:16859673