Compare GO annotations related to Hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia using OMIM genes and OrthoDisease orthologs

A table of the annotations represented in this image is provided below.
CategoryIDTermDB ObjectEvidenceOrganismReference
Molecular FunctionGO:0003677DNA binding RGD:620434IDARatRGD:1600302|PMID:15888455
Molecular FunctionGO:0003677DNA binding RGD:620434IMPRatRGD:727430|PMID:12237116
Molecular FunctionGO:0005515protein binding MGI:97492IPIMouseMGI:MGI:3693390|PMID:12441357
Molecular FunctionGO:0043565sequence-specific DNA binding RGD:620434IDARatRGD:628521|PMID:11145590
Molecular FunctionGO:0016563transcription activator activity MGI:97492IDAMouseMGI:MGI:3693390|PMID:12441357
Molecular FunctionGO:0016563transcription activator activity RGD:620434IDARatRGD:727430|PMID:12237116
Cellular ComponentGO:0005654nucleoplasm RGD:620434IDARatRGD:null
Cellular ComponentGO:0005634nucleus RGD:620434IDARatRGD:628521|PMID:11145590
Biological ProcessGO:0030154cell differentiation MGI:97492IMPMouseMGI:MGI:1203285|PMID:9590297
Biological ProcessGO:0001656metanephros development MGI:97492IGIMouseMGI:MGI:2445273|PMID:12435636
Biological ProcessGO:0045944positive regulation of transcription from RNA polymerase II promoter RGD:620434IDARatRGD:9214635
Biological ProcessGO:0006355regulation of transcription, DNA-dependent RGD:620434IMPRatRGD:628521|PMID:11145590
Biological ProcessGO:0030878thyroid gland development MGI:97492IMPMouseMGI:MGI:1203285|PMID:9590297