OntologiesCurators at RGD make annotations to genes, QTLs and strains using standardized vocabularies/ontologies. Your search returned annotations to the terms below.EFO: Experimental Factor Ontology
level of protein N-lysine methyltransferase METTL21D in blood
level of protein-lysine methyltransferase METTL21C (human) in cerebrospinal fluid
level of protein-lysine methyltransferase METTL21C in blood serum
level of tRNA N(3)-cytidine methyltransferase METTL2B (human) in cerebrospinal fluid
level of tRNA N(3)-methylcytidine methyltransferase METTL2B in blood serum
methyltransferase-like 26
methyltransferase-like 26 (human)
METTL21C (human)
METTL24 (human)
METTL26 (human)
METTL2B (human)
probable methyltransferase-like protein 24
probable methyltransferase-like protein 24 (human)
protein N-lysine methyltransferase METTL21D
protein-lysine methyltransferase METTL21C
protein-lysine methyltransferase METTL21C (human)
tRNA N(3)-cytidine methyltransferase METTL2B
tRNA N(3)-cytidine methyltransferase METTL2B (human)
tRNA N(3)-cytidine methyltransferase METTL2B, initiator methionine removed form
GO: Molecular Function
histone methyltransferase activity
protein-lysine N-methyltransferase activity
OBA: Ontology of Biological Attributes
level of protein N-lysine methyltransferase METTL21D in blood
level of protein-lysine methyltransferase METTL21C in blood serum
level of tRNA N(3)-methylcytidine methyltransferase METTL2B in blood serum
RDO: RGD Disease Ontology
autosomal recessive intellectual developmental disorder 44
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