OntologiesCurators at RGD make annotations to genes, QTLs and strains using standardized vocabularies/ontologies. Your search returned annotations to the terms below.CL: Cell Ontology
basophil mast progenitor cell
basophil progenitor cell
common myeloid progenitor, CD34-positive
granulocyte monocyte progenitor cell
neutrophilic metamyelocyte
neutrophilic myeloblast
neutrophilic myelocyte
neutrophilic promyelocyte
preadipocyte
EFO: Experimental Factor Ontology
acute myeloid leukemia, biallelic CEBPA gene mutation
acute myeloid leukemia, CEBPA gene mutation
acute myeloid leukemia, monoallelic CEBPA gene mutation
basophil mast progenitor cell
basophil progenitor cell
BLaER1
CCAAT/enhancer-binding protein alpha
CCAAT/enhancer-binding protein alpha (human)
CCAAT/enhancer-binding protein beta
CCAAT/enhancer-binding protein beta (human)
CCAAT/enhancer-binding protein epsilon
CCAAT/enhancer-binding protein epsilon (human)
CCAAT/enhancer-binding protein gamma
CCAAT/enhancer-binding protein gamma (human)
DNA damage-inducible transcript 3 protein
ficolin-2
ficolin-2 (human)
granulocyte monocyte progenitor cell
MEND syndrome
neutrophilic metamyelocyte
neutrophilic myeloblast
neutrophilic myelocyte
neutrophilic promyelocyte
nuclear factor NF-kappa-B p105 subunit
nuclear factor NF-kappa-B p105 subunit (human)
Pelger-Huet-like anomaly and episodic fever with abdominal pain
preadipocyte
proliferation-associated protein 2G4
proliferation-associated protein 2G4 (human)
resistin
resistin (human)
X-linked chondrodysplasia punctata 2
GO: Cellular Component
C/EBP complex
CFTR-NHERF-ezrin complex
CHOP-ATF3 complex
CHOP-ATF4 complex
CHOP-C/EBP complex
super elongation complex
GO: Molecular Function
steroid Delta-isomerase activity
MP: Mammalian Phenotype
abnormal granulocyte monocyte progenitor cell morphology
abnormal granulocyte monocyte progenitor cell number
absent granulocyte monocyte progenitor cells
decreased granulocyte monocyte progenitor cell number
increased granulocyte monocyte progenitor cell number
PW: Pathway Ontology
X-linked dominant chondrodysplasia punctata 2 pathway
RDO: RGD Disease Ontology
MEND syndrome
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