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Term Information

Accession
GO:0060797
Name
transforming growth factor beta receptor signaling pathway involved in primary germ layer cell fate commitment
Ontology
biological_process
Synonyms
transforming growth factor beta receptor signalling pathway involved in primary germ layer cell fate commitment
Alternate IDs
None
Definition
The series of molecular signals initiated by an extracellular ligand binding to a transforming growth factor beta receptor on the surface of a target cell, which contributes to an unspecified cell adopting a mesoderm fate. Source: GOC:dph, GOC:tb, GOC:sdb_2009
Comment
None
History
See term history for GO:0060797 at QuickGO
Subset
None
Feedback
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Parents of transforming growth factor beta receptor signaling pathway involved in primary germ layer cell fate commitment (GO:0060797)
subject[Reorder by subject] relation[Reorder by relation] object[Reorder by object]
transforming growth factor beta receptor signaling pathway involved in primary germ layer cell fate commitment [is_a relation] is_a  transforming growth factor beta receptor signaling pathway (GO:0007179)
transforming growth factor beta receptor signaling pathway involved in primary germ layer cell fate commitment [BFO:0000050 relation] BFO:0000050  cell fate commitment involved in formation of primary germ layer (GO:0060795)
Children of transforming growth factor beta receptor signaling pathway involved in primary germ layer cell fate commitment (GO:0060797)
subject[Reorder by subject] relation[Reorder by relation] object[Reorder by object]
transforming growth factor beta receptor signaling pathway involved in mesodermal cell fate specification (GO:0060798) [is_a relation] is_a  transforming growth factor beta receptor signaling pathway involved in primary germ layer cell fate commitment
transforming growth factor beta receptor signaling pathway involved in endodermal cell fate specification (GO:0060799) [is_a relation] is_a  transforming growth factor beta receptor signaling pathway involved in primary germ layer cell fate commitment
None.