Compare GO annotations related to Hypercholanemia, familial using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0016410N-acyltransferase activity MGI:106642IDAMouseMGI:MGI:893269|PMID:9215542
Molecular FunctionGO:0005515protein binding MGI:1341872IPIMouseMGI:MGI:1350677|PMID:10601346
Molecular FunctionGO:0005515protein binding Q9UDY2IPIHumanPMID:17353931
Molecular FunctionGO:0008022protein C-terminus binding RGD:619807IPIRatRGD:1582683|PMID:15980428
Cellular ComponentGO:0005777peroxisome RGD:2190IDARatRGD:1599435|PMID:17256745
Cellular ComponentGO:0005777peroxisome RGD:2190IDARatRGD:14561759
Cellular ComponentGO:0005886plasma membrane MGI:1341872IDAMouseMGI:MGI:2181897|PMID:12060405
Cellular ComponentGO:0005923tight junction RGD:619807IDARatRGD:631940|PMID:10559001
Biological ProcessGO:0008206bile acid metabolic process MGI:106642IDAMouseMGI:MGI:893269|PMID:9215542
Biological ProcessGO:0010033response to organic substance RGD:619807IEPRatRGD:1600164|PMID:15634758