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
(2R,6R)-6-[(3R,10S,12S,13R,17R)-3-(2-Carboxyacetyl)oxy-12-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methyl-3-methylideneheptanoic acid
2-[[4-(2-butoxy-5-chloroanilino)-6-(1-pyrrolidinyl)-1,3,5-triazin-2-yl]amino]ethanol
Anhydrocochlioquinone A
CBL0137
chlorambucil
cob(III)alamin
cyanocob(III)alamin
hydroxocobalamin
N-[[(2R,3S,4R)-1-acetyl-4-(hydroxymethyl)-3-(4-phenylphenyl)-2-azetidinyl]methyl]-2-methoxy-N-methylacetamide
N-[[(2S,3R,4R)-1-acetyl-4-(hydroxymethyl)-3-(4-phenylphenyl)-2-azetidinyl]methyl]-2-methoxy-N-methylacetamide
N-[[(2S,3S,4S)-1-acetyl-4-(hydroxymethyl)-3-(4-phenylphenyl)-2-azetidinyl]methyl]-2-methoxy-N-methylacetamide
EFO: Experimental Factor Ontology
CA9/CBLIF protein level ratio in blood
calcineurin subunit B type 2
calcineurin subunit B type 2 (human)
CBL (human)
CBL-related disorder
CBLC (human)
CBLIF (human)
CBLN1 (human)
CBLN2 (human)
CBLN4 (human)
CBLN4/RET protein level ratio in blood
cerebellin-1
cerebellin-1 (human)
cerebellin-1 proteolytic cleavage product
cerebellin-2
cerebellin-2 (human)
cerebellin-4
cerebellin-4 (human)
cerebellin-4, signal peptide removed form
cobalamin binding intrinsic factor
cobalamin binding intrinsic factor (human)
cobalamin metabolic process
cobalamin trafficking protein CblD
cobalamin trafficking protein CblD (human)
cyanocobalamin reductase / alkylcobalamin dealkylase
cyanocobalamin reductase / alkylcobalamin dealkylase (human)
E3 ubiquitin-protein ligase CBL
E3 ubiquitin-protein ligase CBL (human)
E3 ubiquitin-protein ligase CBL measurement
E3 ubiquitin-protein ligase CBL-C
E3 ubiquitin-protein ligase CBL-C (human)
homocystinuria without methylmalonic aciduria
homocystinuria-megaloblastic anemia cblD type
Imerslund-Grasbeck syndrome type 2
isolated methylmalonic aciduria cblD type
level of cobalamin trafficking protein CblD (human) in cerebrospinal fluid
level of cobalamin trafficking protein CblD in blood serum
level of E3 ubiquitin-protein ligase CBL (human) in cerebrospinal fluid
level of E3 ubiquitin-protein ligase CBL in blood serum
level of E3 ubiquitin-protein ligase CBL-C (human) in cerebrospinal fluid
level of E3 ubiquitin-protein ligase CBL-C in blood serum
methylcobalamin deficiency type cblDv1
methylcobalamin deficiency type cblE
methylcobalamin deficiency type cblG
methylmalonic acidemia
Methylmalonic acidemia with homocystinuria
Methylmalonic acidemia with homocystinuria type cblF
Methylmalonic acidemia with homocystinuria, type cblC
Methylmalonic acidemia with homocystinuria, type cblD
methylmalonic acidemia with homocystinuria, type cblJ
methylmalonic acidemia with homocystinuria, type cblX
methylmalonic aciduria (cobalamin deficiency) cblA type
methylmalonic aciduria and homocystinuria
methylmalonic aciduria and homocystinuria type cblC
methylmalonic aciduria and homocystinuria type cblD
methylmalonic aciduria and homocystinuria type cblE
methylmalonic aciduria and homocystinuria type cblF
methylmalonic aciduria and homocystinuria type cblG
methylmalonic aciduria and/or homocystinuria, cblD type
methylmalonic aciduria cblb type
methylmalonic aciduria, cblA type
methylmalonic aciduria, cblB type
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
SH3 domain-containing kinase-binding protein 1
SH3 domain-containing kinase-binding protein 1 (human)
ubiquitin-associated and SH3 domain-containing protein A
ubiquitin-associated and SH3 domain-containing protein A (human)
ubiquitin-associated and SH3 domain-containing protein B
ubiquitin-associated and SH3 domain-containing protein B (human)
vitamin B12-responsive methylmalonic acidemia
Vitamin B12-responsive methylmalonic acidemia type cblA
Vitamin B12-responsive methylmalonic acidemia type cblB
vitamin B12-responsive methylmalonic acidemia, type cblDv2
GO: Biological Process
cobalamin metabolic process
GO: Cellular Component
RNA N6-methyladenosine methyltransferase complex
GO: Molecular Function
ABC-type vitamin B12 transporter activity
cargo receptor activity
cargo receptor ligand activity
peptidase activity
protein tyrosine kinase activity
ubiquitin protein ligase activity
ubiquitin-protein transferase activity
HP: Human Phenotype
Methylmalonic aciduria
MP: Mammalian Phenotype
methylmalonic aciduria
OBA: Ontology of Biological Attributes
CA9/CBLIF protein level ratio in blood
CBLN4/RET protein level ratio in blood
level of cobalamin trafficking protein CblD in blood serum
level of E3 ubiquitin-protein ligase CBL in blood serum
level of E3 ubiquitin-protein ligase CBL-C in blood serum
PW: Pathway Ontology
altered cobalamin metabolic pathway
cobalamin metabolic pathway
RDO: RGD Disease Ontology
Homocystinuria-megaloblastic anemia cblD type
homocystinuria-megaloblastic anemia cblE type
homocystinuria-megaloblastic anemia cblG type
infantile onset multisystem autoimmune disease 3
juvenile myelomonocytic leukemia
methylmalonic acidemia and homocysteinemia cblX type
methylmalonic acidemia cblA type
methylmalonic acidemia cblB type
methylmalonic acidemia cblD type
methylmalonic aciduria and homocystinuria type cblC
methylmalonic aciduria and homocystinuria type cblD
methylmalonic aciduria and homocystinuria type cblE
methylmalonic aciduria and homocystinuria type cblF
methylmalonic aciduria and homocystinuria type cblG
Methylmalonic Aciduria and Homocystinuria, cblJ Type
Methylmalonic Aciduria and Homocystinuria, cblL Type
Noonan Syndrome-Like Disorder with or without Juvenile Myelomonocytic Leukemia
RS: Rat Strains
KDP-Tg(CAG-Cblb)1Nyo
KDP-Tg(H2Kd-Cblb)1Nyo
KDP-Tg(H2Kd-Cblb)2Nyo
KDP-Tg(INS-Cblb)1Nyo
PVG.KDP-Cblb/Nyo
TM.KDP-Cblb(D9Rat13-D9Rat4)(D12Rat5-D12Rat45)(D18Mit9-D18Rat44)/Nyo
TM.KDP-Cblb/Nyo
UBERON: Cross-Species Anatomy
cerebellum lobe
dentate nucleus
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