OntologiesCurators at RGD make annotations to genes, QTLs and strains using standardized vocabularies/ontologies. Your search returned annotations to the terms below.ChEBI: ChEBI Ontology
C3 exoenzyme
RhoA inhibitor
EFO: Experimental Factor Ontology
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2 (human)
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3 (human)
GTP-binding protein RhoA
GTP-binding protein RhoA proteolytic cleavage product
level of BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2 (human) in cerebrospinal fluid
level of BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2 in blood serum
level of BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3 (human) in cerebrospinal fluid
level of BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3 in blood serum
level of GTP-binding protein RhoA in blood serum
level of transforming protein RhoA (human) in cerebrospinal fluid
methylthioribose-1-phosphate isomerase (human)
Rho guanine nucleotide exchange factor 25
Rho guanine nucleotide exchange factor 25 (human)
RHOA (human)
transforming protein RhoA (human)
transforming protein RhoA measurement
GO: Biological Process
cleavage furrow formation
negative regulation of axonogenesis
Rho-activating G protein-coupled receptor signaling pathway
ruffle assembly
GO: Molecular Function
GTPase activator activity
GTPase activity
guanyl-nucleotide exchange factor activity
OBA: Ontology of Biological Attributes
level of BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2 in blood serum
level of BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3 in blood serum
level of GTP-binding protein RhoA in blood serum
RDO: RGD Disease Ontology
ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES
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