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
(3R,6aS,8S,10aS)-N-(3-chlorophenyl)-3-hydroxy-8-[2-oxo-2-[[(1S)-1-phenylethyl]amino]ethyl]-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocine-1-carboxamide
1,2-dichloroethane
2,3-dihydro-3S-hydroxy-6,7-dimethoxy-2,2-dimethyl-4H-1-benzopyran-4-one
Anachelin
Bancroftinone
benzestrol
dutasteride
dutomycin
dUTP
dUTP(3-)
dUTP(4-)
Emericellene C
ethyl-dUTP
LSM-24670
Lys-Glu-Phe
N-[(3R,4R,5S,6R)-5-[(2S,3S,4R,5R,6R)-5-[(2S,3R,4R,5S,6R)-3-Acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2R,3S,4S,5S,6R)-3-[(2S,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2S,3S,4S,5S,6R)-3-[(2S,3R,4R,5S,6R)-3-acetamido-4-hydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3-hydroxyoxan-2-yl]oxy-2,4-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide
N-[(3R,4R,5S,6R)-5-[(2S,3S,4R,5R,6R)-5-[(2S,3R,4R,5S,6R)-3-Acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2S,3S,4S,5S,6R)-3-[(2S,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4-[(2R,3S,4S,5S,6R)-3-[(2S,3R,4R,5S,6R)-3-acetamido-4-hydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-hydroxyoxan-2-yl]oxy-2,4-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide
quinolin-2-ol
CL: Cell Ontology
basal cell of epithelium of bronchus
enteroendocrine cell
intestinal crypt stem cell of small intestine
myeloid leukocyte
CMO: Clinical Measurement
TUNEL-positive cell number to total cell number ratio
EFO: Experimental Factor Ontology
ABeta amyloidosis, dutch type
autosomal dominant ichthyosis vulgaris
autosomal recessive spinocerebellar ataxia 7
bullous dystrophy, macular type
cerebral amyloid angiopathy
cerebral amyloid angiopathy, APP-related
deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial
deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial (human)
DUT (human)
European ancestry
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
hyperimmunoglobulinemia D with periodic fever
myeloid leukocyte
Nathalie syndrome
roundabout homolog 1
roundabout homolog 1 (human)
Trismus - pseudocamptodactyly
trismus-pseudocamptodactyly syndrome
GO: Biological Process
dUTP biosynthetic process
dUTP catabolic process
dUTP metabolic process
GO: Molecular Function
dCTP deaminase activity
dUTP diphosphatase activity
dUTP pyrophosphatase inhibitor activity
uracil DNA N-glycosylase activity
HP: Human Phenotype
Lymph-node Dutcher bodies
Occupational exposure history
Occupational silver exposure
MI: Molecular Interactions
uracil interference assay
RDO: RGD Disease Ontology
Alpha-Thalassemia 2
APP-related cerebral amyloid angiopathy
Bone Marrow Failure and Diabetes Mellitus Syndrome
cerebral amyloid angiopathy
CST3-related cerebral amyloid angiopathy
distal arthrogryposis type 7
hyperimmunoglobulinemia D periodic fever syndrome
tick-borne relapsing fever
UBERON: Cross-Species Anatomy
sweat gland of eyelid
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