Compare GO annotations related to Night blindness, congenital stationary, X-linked, type 2 using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0015270dihydropyridine-sensitive calcium channel activity O60840IDAHumanPMID:15897456
Cellular ComponentGO:0043025cell soma RGD:621535IDARatRGD:11526344
Cellular ComponentGO:0016021integral to membrane O60840IDAHumanPMID:15897456
Cellular ComponentGO:0000299integral to membrane of membrane fraction RGD:621535IDARatRGD:11526344
Cellular ComponentGO:0016020membrane RGD:621535IDARatRGD:11526344
Cellular ComponentGO:0043204perikaryon RGD:621535IDARatRGD:1582593|PMID:16736476
Cellular ComponentGO:0005891voltage-gated calcium channel complex O60840IDAHumanPMID:15897456
Biological ProcessGO:0050908detection of light stimulus during visual perception O60840IMPHumanPMID:7571473
Biological ProcessGO:0007276gamete generation WBGene00001187IMPWormWB:WBPaper00006395|PMID:14551910
Biological ProcessGO:0040035hermaphrodite genitalia development WBGene00001187IMPWormWB:WBPaper00006395|PMID:14551910
Biological ProcessGO:0018991oviposition WBGene00001187IMPWormWB:WBPaper00005654|PMID:12529635
Biological ProcessGO:0043051regulation of pharyngeal pumping WBGene00001187IMPWormWB:WBPaper00024250|PMID:15238517
Biological ProcessGO:0007601visual perception RGD:621535IEPRatRGD:632484|PMID:11526344