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
2-methylbutyric acid
amylose
cytarabine ocfosfate
dextrin
diosgenin
EC 2.4.1.1 (glycogen phosphorylase) inhibitor
endrin
glycogen
glycyrrhetic acid 3-O-glucuronide
lichenin
Maillard reaction product
mycocerosic acid
nateglinide
nitromethane
pneumocandin B0
poly(alpha-alkylene)
starch
Starch acetate
CL: Cell Ontology
astrocyte
atretic follicular cell of ovary
basophilic myelocyte
choroid epiplexus macrophage
choroid plexus macrophage
eosinophilic myelocyte
folliculostellate cell
glycinergic neuron
hepatic stellate cell
hepatoblast
L4 intratelencephalic projecting glutamatergic neuron
L4 intratelencephalic projecting glutamatergic neuron (Homo sapiens)
mature astrocyte
myelocyte
neural crest cell
neutrophilic myelocyte
outer wall Schlemm's canal endothelial cell
pancreatic stellate cell
retinal astrocyte
Schwann cell
serous acinar cell of salivary gland
skin fibroblast
starburst amacrine cell
stellate neuron
stellate pyramidal neuron
CMO: Clinical Measurement
acoustic startle response measurement
amount of time spent in voluntary immobility after start of conditioned stimulus in a two-way shuttle box
amplitude of the acoustic startle response
calculated acoustic startle response measurement
calculated left ventricular isovolumetric relaxation time
change in body weight to initial body weight ratio
duration of contractions above 10 mmHg of anorectal pressure
ejaculation duration
head and neck tumor measurement
left ventricular isovolumetric relaxation time
maximum tumor size decrease to pretreatment tumor size ratio
measurement of prepulse inhibition of the acoustic startle response
P wave duration
Q wave duration
QRS duration
R wave duration
ratio of change in renal sympathetic nerve activity
right ventricular isovolumetric relaxation time
S wave duration
time from start of drug therapy to immunocytoma regrowth
time to first grooming within an experimental apparatus
time to first grooming within an open field apparatus
time to first head dip within an elevated plus maze
time to first head dip within an experimental apparatus
time to first movement outside a discrete space in a two-way shuttle box after start of conditioned stimulus
time to first stretched attend posture movement in an elevated plus maze
time to first stretched attend posture movement in an experimental apparatus
urine amylase level
urine ketone body level
EFO: Experimental Factor Ontology
3 inflorescence detectable stage
A-kinase anchor protein 7 isoform alpha
A-kinase anchor protein 7 isoform beta (human)
A-kinase anchor protein 7 isoform gamma
Abdominal colic
acetyl-coenzyme A thioesterase
acetyl-coenzyme A thioesterase (human)
acoustic startle blink response measurement
adult onset asthma
age at onset
all-trans-retinol 13,14-reductase
all-trans-retinol 13,14-reductase (human)
Alzheimer disease 3
amount of glycogen [starch] synthase, muscle (human) in blood
astrocyte
ATOX1/GYS1 protein level ratio in blood
barcode offset
basophilic myelocyte
Benign familial neonatal seizures
benign infantile focal epilepsy with midline spikes and wave during sleep
benign partial epilepsy of infancy with complex partial seizures
benign partial epilepsy with secondarily generalized seizures in infancy
brain
Brodmann (1909) area 38
calcitonin isoform 1
calcitonin isoform h2 (human)
cap analysis gene expression
Cappable-Seq
cDNA read offset
cell barcode offset
ceramide transfer protein
ceramide transfer protein (human)
childhood eosinophilic esophagitis
childhood onset asthma
Chorea
choroid plexus macrophage
classic congenital lipoid adrenal hyperplasia due to STAR deficency
congenital hypothalamic hamartoma syndrome
congenital lipoid adrenal hyperplasia due to STAR deficency
congenital sucrase-isomaltase deficiency with minimal starch tolerance
congenital sucrase-isomaltase deficiency with starch and lactose intolerance
congenital sucrase-isomaltase deficiency with starch intolerance
congenital sucrase-isomaltase deficiency without starch intolerance
craniodigital syndrome-intellectual disability syndrome
dCas9-SAM
dCas9-Suntag
dCas9-VP64
dCas9-VPR
developmental and epileptic encephalopathy, 9
distant metastasis free survival
DNA-directed RNA polymerase II subunit GRINL1A isoform 1
DNA-directed RNA polymerase II subunit GRINL1A isoform 2
DNA-directed RNA polymerase II subunit GRINL1A isoform 3
Early onset absence seizures
elongating embryo Ce
embryo stage
embryonic labial sensory complex
embryonic stage 12
embryonic stage 5
embryonic stage 7
embryonic stage 8
endrin
eosinophilic myelocyte
Epicanthus
Epicanthus inversus
epilepsy with generalized tonic-clonic seizures
EREG/GYS1 protein level ratio in blood
Exaggerated startle response
familial amyloid neuropathy
familial renal glucosuria
Generalized non-motor (absence) seizure
glycogen [starch] synthase, muscle
glycogen [starch] synthase, muscle (human)
GRO-seq
guanine nucleotide-binding protein G(s) subunit alpha isoform 3 (human)
guanine nucleotide-binding protein G(s) subunit alpha isoform 4 (human)
guanine nucleotide-binding protein G(s) subunit alpha isoform Gnas-1 (human)
guanine nucleotide-binding protein G(s) subunit alpha isoform Gnas-2 (human)
guanine nucleotide-binding protein G(s) subunit alpha isoform XLas-1 (human)
guanine nucleotide-binding protein G(s) subunit alpha isoform XLas-2 (human)
guanine nucleotide-binding protein G(s) subunit alpha isoform XLas-3 (human)
GYS1/ITGB1BP2 protein level ratio in blood
GYS1/MAP3K5 protein level ratio in blood
GYS1/PPP1R2 protein level ratio in blood
GYS1/STK11 protein level ratio in blood
GYS1/SUSD1 protein level ratio in blood
GYS1/TIA1 protein level ratio in blood
GYS1/USP8 protein level ratio in blood
GYS1/WASF1 protein level ratio in blood
HELLP syndrome
hepatic stellate cell
hereditary ATTR amyloidosis
hereditary hyperekplexia
human granulocytic anaplasmosis
hyperekplexia
hyperphenylalaninemia due to DNAJC12 deficiency
infantile-onset epilepsy
initial time point
kyphoscoliotic Ehlers-Danlos syndrome
level of glycogen [starch] synthase, muscle in blood
level of StAR-related lipid transfer protein 5 (human) in cerebrospinal fluid
level of StAR-related lipid transfer protein 5 in blood serum
level of StAR-related lipid transfer protein 7, mitochondrial (human) in cerebrospinal fluid
level of StAR-related lipid transfer protein 7, mitochondrial in blood serum
level of START domain-containing protein 10 (human) in cerebrospinal fluid
level of START domain-containing protein 10 in blood serum
lobar bronchus
lower respiratory tract
lymphocyte antigen 75 isoform 4 (human)
Mask-like facies
multifocal pattern dystrophy simulating fundus flavimaculatus
Multifocal seizures
mushroom body primordium
myelocyte
Myoclonic absence seizure
myofibrillar myopathy 1
nascent polypeptide-associated complex subunit alpha, muscle-specific form isoform 1
neocortex
neural crest cell
neuroendocrine secretory protein 55 isoform Nesp55 (human)
neurogenic scapuloperoneal syndrome, Kaeser type
neutrophilic myelocyte
non-classic congenital lipoid adrenal hyperplasia due to STAR deficency
nucleotide sequence offset
oral cavity
osteoarthritis, hand
P wave duration
pancreatic stellate cell
paronychia
PEAT
phosphatidylcholine transfer protein
phosphatidylcholine transfer protein (human)
platelet-type bleeding disorder 18
polyadenylate-binding protein 2 isoform 1 (human)
polyadenylate-binding protein 2 isoform 2 (human)
post dauer stage
potassium deficiency
primer
proliferating embryo Ce
Prolonged QT interval
protein O-linked glycosylation
pupa
pupal stage
QT interval
Rab GTPase-activating protein 1-like isoform 1
Rab GTPase-activating protein 1-like isoform 2 (human)
Rab GTPase-activating protein 1-like isoform 3 (human)
Rab GTPase-activating protein 1-like isoform 4 (human)
Rab GTPase-activating protein 1-like isoform 5 (human)
Rab GTPase-activating protein 1-like isoform 6 (human)
Rab GTPase-activating protein 1-like isoform 7 (human)
Rab GTPase-activating protein 1-like isoform 8
Rab GTPase-activating protein 1-like isoform 9
reflex epilepsy
sample barcode offset
Scapuloperoneal amyotrophy
Schwann cell
SD minus nitrogen
seed maturation stage
severe early-childhood-onset retinal dystrophy
Shortened QT interval
signal-regulatory protein beta-1 isoform 1 (human)
signal-regulatory protein beta-1 isoform 2 (human)
single cell library construction
ST segment duration
STAR (human)
StAR-related lipid transfer protein 5
StAR-related lipid transfer protein 5 (human)
StAR-related lipid transfer protein 7, mitochondrial
StAR-related lipid transfer protein 7, mitochondrial (human)
STARD10 (human)
STARD5 (human)
STARD7 (human)
Stargardt disease
Stargardt disease 3
Stargardt disease 4
STARmap
STARR-Seq
START domain-containing protein 10
START domain-containing protein 10 (human)
Start-seq
starvation
steroidogenic acute regulatory protein, mitochondrial
steroidogenic acute regulatory protein, mitochondrial (human)
Stiff-Person syndrome
Syndactyly - telecanthus - anogenital and renal malformations
syndactyly-telecanthus-anogenital and renal malformations syndrome
T wave duration
torsin-1A-interacting protein 2 isoform TOR1AIP2 (human)
TP segment duration
TSS Sequencing
type 1 diabetes nephropathy
type 2 diabetes nephropathy
Typical absence seizure
UMI barcode offset
upper respiratory tract
ventral nerve cord primordium
GO: Biological Process
'de novo' UMP biosynthetic process
activation of meiosis
activation of meiosis I spindle assembly checkpoint
activation of meiosis involved in egg activation
activation of microtubule nucleation
activation of mitotic cell cycle spindle assembly checkpoint
activation of reciprocal meiotic recombination
aggregation involved in sorocarp development
amino acid catabolic process to alcohol via Ehrlich pathway
amino acid catabolic process to carboxylic acid via Ehrlich pathway
amino acid catabolic process via Ehrlich pathway
amyloplast organization
apical constriction involved in ventral furrow formation
apoptotic signaling pathway
aromatic amino acid family catabolic process to alcohol via Ehrlich pathway
aromatic amino acid family catabolic process to carboxylic acid via Ehrlich pathway
autophagosome assembly
behavioral response to starvation
bidirectional double-stranded viral DNA replication
blood coagulation, extrinsic pathway
branched-chain amino acid catabolic process to alcohol via Ehrlich pathway
branched-chain amino acid catabolic process to carboxylic acid via Ehrlich pathway
butyryl-CoA biosynthetic process from acetyl-CoA
C4 photosynthesis
cAMP/PKA signal transduction
carbon fixation by 3-hydroxypropionate cycle
cell development
cellular response to adenine starvation
cellular response to amino acid starvation
cellular response to biotin starvation
cellular response to boron-containing substance deprivation
cellular response to calcium ion starvation
cellular response to copper ion starvation
cellular response to glucose starvation
cellular response to inositol starvation
cellular response to iron ion starvation
cellular response to leucine starvation
cellular response to magnesium starvation
cellular response to nitrogen starvation
cellular response to phosphate starvation
cellular response to potassium ion starvation
cellular response to starvation
cellular response to sucrose starvation
cellular response to sulfate starvation
cellular response to sulfur starvation
cellular response to vitamin B1 starvation
cellular response to zinc ion starvation
chemical synaptic transmission
chromatin looping
chromosomal 5-methylcytosine DNA demethylation, oxidation pathway
dextrin transport
diterpene phytoalexin precursor biosynthetic process
DNA replication initiation
DNA-templated transcriptional start site selection
ERK1 and ERK2 cascade
ERK5 cascade
execution phase of apoptosis
execution phase of necroptosis
extrasynaptic signaling via GABA
extrinsic apoptotic signaling pathway
extrinsic apoptotic signaling pathway in absence of ligand
extrinsic apoptotic signaling pathway via death domain receptors
fibroblast growth factor receptor apoptotic signaling pathway
filamentous growth MAPK cascade
filamentous growth of a population of unicellular organisms in response to starvation
G protein-coupled opsin signaling pathway
G protein-coupled receptor signaling pathway
GCN2-mediated signaling
granzyme-mediated apoptotic signaling pathway
granzyme-mediated programmed cell death signaling pathway
growth factor signaling initiating cell movement involved in cerebral cortex radial glia guided migration
habituation
heterochromatin formation
hippo signaling
hormone-mediated apoptotic signaling pathway
immune complex clearance by erythrocytes
induction of conjugation upon carbon starvation
induction of conjugation upon nitrogen starvation
induction of conjugation upon nutrient starvation
inflammasome-mediated signaling pathway
initiation of appressorium formation
initiation of dorsal closure
insect visual primordium development
intrinsic apoptotic signaling pathway
JNK cascade
L-glutamate import involved in cellular response to nitrogen starvation
L-lysine import into vacuole involved in cellular response to nitrogen starvation
L-methionine catabolic process to 3-methylthiopropanoate
L-methionine catabolic process to 3-methylthiopropanol
lagging strand initiation
lobar bronchus development
long descending thin limb development
maltose metabolic process
maltose transport
mammary gland development
MAPK cascade
meiotic telophase I
meiotic telophase II
metanephric long descending thin limb development
mitotic G2 cell cycle arrest in response to glucose starvation
mitotic telophase
muscle atrophy
myotube differentiation
myotube differentiation involved in skeletal muscle regeneration
myxococcal fruiting body development
necroptotic signaling pathway
negative regulation of aggregation involved in sorocarp development
negative regulation of cellular response to amino acid starvation
negative regulation of cellular response to iron ion starvation
negative regulation of cellular response to nitrogen starvation
negative regulation of cellular response to phosphate starvation
negative regulation of gene expression via chromosomal CpG island methylation
negative regulation of glycogen (starch) synthase activity
negative regulation of macroautophagy
negative regulation of neurofibrillary tangle assembly
negative regulation of starch biosynthetic process
negative regulation of starch catabolic process
negative regulation of starch utilization system complex assembly
negative regulation of transcription initiation by RNA polymerase II
negative regulation of translational initiation in response to starvation
neurofibrillary tangle assembly
nitric oxide mediated signal transduction
oocyte maturation
p38MAPK cascade
pentose-phosphate shunt, non-oxidative branch
pheromone response MAPK cascade
phosphatidylinositol 3-kinase/protein kinase B signal transduction
phospholipase C-activating opsin-mediated signaling pathway
phospholipase C/protein kinase C signal transduction
PKR/eIFalpha signaling
positive regulation of aggregation involved in sorocarp development
positive regulation of cardiac epithelial to mesenchymal transition
positive regulation of cellular response to amino acid starvation
positive regulation of cellular response to phosphate starvation
positive regulation of filamentous growth of a population of unicellular organisms in response to starvation
positive regulation of G2/M transition of mitotic cell cycle involved in cellular response to nitrogen starvation
positive regulation of gene expression via chromosomal CpG island demethylation
positive regulation of glycogen (starch) synthase activity
positive regulation of L-glutamine biosynthetic process
positive regulation of macroautophagy
positive regulation of mitotic sister chromatid segregation
positive regulation of neurofibrillary tangle assembly
positive regulation of protein export from nucleus in response to glucose starvation
positive regulation of satellite cell activation involved in skeletal muscle regeneration
positive regulation of SCF-dependent proteasomal ubiquitin-dependent catabolic process
positive regulation of starch catabolic process
positive regulation of starch utilization system complex assembly
positive regulation of stress granule assembly
positive regulation of transcription initiation by RNA polymerase II
positive regulation of translational initiation in response to starvation
pre-B cell receptor expression
prepulse inhibition
prepupal development
programmed necrotic cell death in response to starvation
protein localization to chloroplast starch grain
protein O-linked glycosylation
protein O-linked glycosylation via arabinose
protein O-linked glycosylation via fucose
protein O-linked glycosylation via galactose
protein O-linked glycosylation via glucose
protein O-linked glycosylation via mannose
protein O-linked glycosylation via N-acetyl-galactosamine
protein O-linked glycosylation via xylose
RAM/MOR signaling
regulation of aggregation involved in sorocarp development
regulation of cellular response to amino acid starvation
regulation of cellular response to glucose starvation
regulation of cellular response to iron ion starvation
regulation of cellular response to phosphate starvation
regulation of filamentous growth of a population of unicellular organisms in response to starvation
regulation of glycogen (starch) synthase activity
regulation of induction of conjugation upon nitrogen starvation
regulation of initiation of mating projection growth
regulation of macroautophagy
regulation of neurofibrillary tangle assembly
regulation of satellite cell activation involved in skeletal muscle regeneration
regulation of starch biosynthetic process
regulation of starch catabolic process
regulation of starch metabolic process
regulation of starch utilization system complex assembly
regulation of transcription initiation by RNA polymerase II
regulation of transcription, start site selection
regulation of transcriptional start site selection at RNA polymerase II promoter
regulation of translational initiation in response to starvation
regulatory ncRNA-mediated gene silencing
response to amino acid starvation
response to carbon starvation
response to copper ion starvation
response to iron ion starvation
response to manganese ion starvation
response to metal ion starvation
response to molybdenum starvation
response to nitrate starvation
response to starvation
response to zinc ion starvation
satellite cell activation involved in skeletal muscle regeneration
signal transduction involved in positive regulation of conjugation with cellular fusion
skeletal muscle atrophy
skeletal muscle fiber differentiation
SMAD protein signal transduction
smooth muscle atrophy
starch biosynthetic process
starch catabolic process
starch granule initiation
starch metabolic process
starch utilization system complex assembly
startle response
stress-activated MAPK cascade
stress-induced homeostatically regulated protein degradation pathway
striated muscle atrophy
stringent response
synapse pruning
synaptic transmission, cholinergic
synaptic transmission, dopaminergic
synaptic transmission, GABAergic
synaptic transmission, glutamatergic
synaptic transmission, glycinergic
synaptic transmission, noradrenergic
synaptic transmission, serotonergic
telophase
transcription pausing by RNA polymerase II
transcriptional start site selection at RNA polymerase II promoter
transcriptional start site selection at RNA polymerase III promoter
transducin-mediated opsin signaling pathway
translation reinitiation
translational attenuation
transposition
traversing start control point of mitotic cell cycle
ventral furrow formation
very long-chain fatty acid beta-oxidation
viral budding
viral budding from endoplasmic reticulum membrane
viral budding from Golgi membrane
viral budding from nuclear membrane
viral budding from plasma membrane
viral latency
viral translational shunt
viral translational termination-reinitiation
GO: Cellular Component
alkanesulfonate monooxygenase complex
amyloplast
amyloplast starch grain
chloroplast starch grain
eNoSc complex
eukaryotic 48S preinitiation complex
ferritin complex
mitochondrial translation initiation complex
neurofibrillary tangle
new growing cell tip
nucleolar peripheral inclusion body
PKM2 protein kinase complex
preprophase band
serine palmitoyltransferase complex
SsuD-SsuE complex
starch grain
starch utilization system complex
stromule
taurine dioxygenase complex
TRAPPI protein complex
vacuole-isolation membrane contact site
GO: Molecular Function
1,4-alpha-glucan branching enzyme activity
1,4-alpha-oligoglucan phosphorylase activity
alkanesulfonate monooxygenase activity
alpha-1,4-glucan glucosyltransferase (ADP-glucose donor) activity
alpha-1,4-glucan glucosyltransferase (NDP-glucose donor) activity
alpha-1,4-glucan glucosyltransferase (UDP-glucose donor) activity
alpha-amylase activity
alpha-glucan, water dikinase activity
cis-regulatory region sequence-specific DNA binding
core promoter sequence-specific DNA binding
dextrin transmembrane transporter activity
GC-box binding
general transcription initiation factor binding
glycogen binding
lipid transfer activity
maltose transmembrane transporter activity
maltose transporting porin activity
mitochondrial RNA polymerase general transcription initiation factor activity
oligo-1,6-glucosidase activity
protein serine/threonine kinase activity
RNA polymerase I cis-regulatory region sequence-specific DNA binding
RNA polymerase I core promoter sequence-specific DNA binding
RNA polymerase I general transcription initiation factor activity
RNA polymerase II cis-regulatory region sequence-specific DNA binding
RNA polymerase II cis-regulatory region sequence-specific DNA binding, bending
RNA polymerase II general transcription initiation factor activity
RNA polymerase III cis-regulatory region sequence-specific DNA binding
RNA polymerase III general transcription initiation factor activity
RNA polymerase III type 1 promoter sequence-specific DNA binding
RNA polymerase III type 2 promoter sequence-specific DNA binding
RNA polymerase III type 3 promoter sequence-specific DNA binding
starch binding
T/G mismatch-specific endonuclease activity
translation initiation factor activity
HP: Human Phenotype
Abdominal colic
Abnormal circulating amylase concentration
Abnormal diminished volition
Abnormal nasal cavity morphology
Abnormal QT interval
Abnormally increased volition
Acanthocytosis
Acral lentiginous melanoma
Acute respiratory distress syndrome
Asymmetric bilateral cleft lip
Bilateral tonic-clonic seizure with generalized onset
Breath-holding spell
Chorea
Complete bilateral cleft lip
Complete cleft of the upper lip
Complete unilateral cleft lip
Decreased number of sternal ossification centers
Delayed menarche
Delayed onset bleeding
Early onset absence seizures
Epicanthus
Epicanthus inversus
Exaggerated startle response
Fragmented sleep
Frontalis muscle overactivity
Generalized non-motor (absence) seizure
Hyperamylasemia
Hypnic jerks
Hypoamylasemia
Incomplete bilateral cleft lip
Incomplete unilateral cleft lip
Infantile spasms
Infra-orbital fold
Insomnia
Mask-like facies
Metabolic ketoacidosis
Multifocal seizures
Myoclonic absence seizure
New medication added in recent weeks
Nodular melanoma
Ocular cystine crystal deposition
Oculogyric crisis
Paronychia
Pericentral retinitis pigmentosa
Peripheral cystoid retinal degeneration
Posttraumatic stress symptom
Prolonged QT interval
Prolonged reptilase time
Pyoderma gangrenosum
Renal cell carcinoma
Retinopathy of prematurity stage 4b
Rubeosis iridis
Shortened QT interval
Skeletal muscle hyperechogenicity
Small yellow foveal lesion with surrounding gray zone
Somatosensory-induced seizure
Starch intolerance
Staring gaze
Starry sky appearance on hepatic sonography
Startle-induced seizure
Triggered by excitement
Typical absence seizure
MI: Molecular Interactions
feature range status
genetic over-suppression
genomic coordinates
primer extension assay
primer specific pcr
quantitative pcr
translocation
translocation start
MMO: Measurement Methods
blood carbohydrates and carbohydrate derivative analysis
Morris water maze method
novel cage apparatus method
novel cage apparatus test utilizing automatic movement detection system
puzzle box apparatus method
MP: Mammalian Phenotype
abnormal autophagosome formation
abnormal bulbourethral gland development
abnormal circulating amylase level
abnormal circulating ketone body level
abnormal corpora amylacea number
abnormal folliculo-stellate cell morphology
abnormal hair follicle peg morphology
abnormal mammary gland growth during lactation
abnormal mandibular canal morphology
abnormal myotube differentiation
abnormal oral cavity morphology
abnormal pancreatic amylase secretion
abnormal prepulse inhibition
abnormal starburst amacrine cell morphology
abnormal startle reflex
abnormal stellate reticulum morphology
abnormal theca cell layer morphology
abnormal tympanic cavity morphology
absent startle reflex
decreased circulating amylase level
decreased circulating ketone body level
decreased corpora amylacea number
decreased pancreatic amylase secretion
decreased prepulse inhibition
decreased startle reflex
decreased susceptibility to induced muscular atrophy
hyperekplexia
increased circulating amylase level
increased circulating ketone body level
increased corpora amylacea number
increased pancreatic amylase secretion
increased prepulse inhibition
increased startle reflex
increased susceptibility to induced muscular atrophy
ketoaciduria
maximal tonic hindlimb extension seizures
mesangiolysis
NBO: Neuro Behavioral Ontology
acoustic startle reflex
complex partial status epilepticus
hyperekplexia
startle reflex
sucking reflex
OBA: Ontology of Biological Attributes
amount of glycogen [starch] synthase, muscle (human) in blood
ATOX1/GYS1 protein level ratio in blood
EREG/GYS1 protein level ratio in blood
GYS1/ITGB1BP2 protein level ratio in blood
GYS1/MAP3K5 protein level ratio in blood
GYS1/PPP1R2 protein level ratio in blood
GYS1/STK11 protein level ratio in blood
GYS1/SUSD1 protein level ratio in blood
GYS1/TIA1 protein level ratio in blood
GYS1/USP8 protein level ratio in blood
GYS1/WASF1 protein level ratio in blood
level of glycogen [starch] synthase, muscle in blood
level of StAR-related lipid transfer protein 5 in blood serum
level of StAR-related lipid transfer protein 7, mitochondrial in blood serum
level of START domain-containing protein 10 in blood serum
startle reflex amount
startle reflex quality
startle reflex rate
startle response amount
PW: Pathway Ontology
biphenyl degradation pathway
C18-steroid hormone biosynthetic pathway
C19-steroid hormone biosynthetic pathway
C21-steroid hormone biosynthetic pathway
DNA replication initiation pathway
fatty acid biosynthetic pathway
ketone bodies degradation pathway
ketone bodies metabolic pathway
mitotic telophase pathway
ribosome biogenesis pathway
starch and cellulose biosynthetic pathway
starch and cellulose metabolic pathway
starch and sucrose metabolic pathway
starch biosynthetic pathway
RDO: RGD Disease Ontology
Alzheimer's disease
attention deficit hyperactivity disorder
bone lymphoma
chondromalacia patellae
developmental and epileptic encephalopathy 68
distal myopathy with anterior tibial onset
Dravet syndrome
Duchenne muscular dystrophy
early onset absence epilepsy
ehrlichiosis
epilepsy with generalized tonic-clonic seizures
familial adult myoclonic epilepsy 2
familial cold autoinflammatory syndrome 4
human granulocytic anaplasmosis
Hutchinson's Melanotic Freckle
hyperekplexia
hypomyelinating leukodystrophy 20
hypomyelinating leukodystrophy 9
immunodeficiency 57
Ketosis
kidney osteogenic sarcoma
Lipoid Congenital Adrenal Hyperplasia
malignant astrocytoma
morphine withdrawal syndrome
NEURODEGENERATION WITH DEVELOPMENTAL DELAY, EARLY RESPIRATORY FAILURE, MYOCLONIC SEIZURES, AND BRAIN ABNORMALITIES
neurogenic scapuloperoneal syndrome Kaeser type
Nodding Syndrome
organ system cancer
paronychia
Potassium Deficiency
Severe Acute Malnutrition
Sleep-Wake Transition Disorders
soft tissue sarcoma
SPOAN syndrome
Stargardt disease
Stargardt Disease 1
Stargardt Disease 3
Stargardt Disease 4
Stargardt Macular Degeneration Absent or Hypoplastic Corpus Callosum Mental Retardation and Dysmorphic Features
Starvation
Stiff-Person syndrome
syndactyly-telecanthus-anogenital and renal malformations syndrome
SO: Sequence Ontology
5_prime_UTR_premature_start_codon_gain_variant
5_prime_UTR_premature_start_codon_loss_variant
5_prime_UTR_premature_start_codon_variant
AACCCT_box
AUG_initiated_uORF
CAAT_signal
CAGE_tag
CDS
clone_insert_start
coding_start
CTG_start_codon
disruptive_inframe_deletion
encodes_alternate_transcription_start_sites
encodes_overlapping_peptides_different_start
encodes_overlapping_polypeptides_different_start_and_stop
eukaryotic_promoter
five_prime_cis_splice_site
five_prime_coding_exon_noncoding_region
five_prime_UTR_premature_start_codon_location_variant
four_bp_start_codon
GC_rich_promoter_region
gene_with_non_canonical_start_codon
gene_with_start_codon_CUG
H2AK5_acetylation_site
H2AK9_acetylation_site
H2AZK11_acetylation_site
H2AZK13_acetylation_site
H2AZK15_acetylation_site
H2AZK4_acetylation_site
H2AZK7_acetylation_site
H2BK120_acetylation_site
H2BK12_acetylation_site
H2BK15_acetylation_site
H2BK20_acetylation_site
H2BK5_acetylation_site
H2BK5_monomethylation_site
H3K14_acetylation_site
H3K18_acetylation_site
H3K20_trimethylation_site
H3K23_acetylation_site
H3K23_dimethylation_site
H3K27_acetylation_site
H3K27_dimethylation_site
H3K27_methylation_site
H3K27_monomethylation_site
H3K27_trimethylation_site
H3K36_acetylation_site
H3K36_dimethylation_site
H3K36_methylation_site
H3K36_monomethylation_site
H3K36_trimethylation_site
H3K4_acetylation_site
H3K4_dimethylation_site
H3K4_methylation_site
H3K4_monomethylation_site
H3K4_trimethylation
H3K56_acetylation_site
H3K79_dimethylation_site
H3K79_methylation_site
H3K79_monomethylation_site
H3K79_trimethylation_site
H3K9_acetylation_site
H3K9_dimethylation_site
H3K9_methylation_site
H3K9_monomethylation_site
H3K9_trimethylation_site
H3R2_dimethylation_site
H3R2_monomethylation_site
H4K12_acetylation_site
H4K16_acetylation_site
H4K20_monomethylation_site
H4K4_trimethylation_site
H4K5_acetylation_site
H4K8_acetylation_site
H4K91_acetylation_site
H4R3_dimethylation_site
initiator_codon_variant
INR_motif
leucoplast_sequence
lincRNA
major_TSS
minor_TSS
minus_10_signal
minus_12_signal
minus_24_signal
minus_35_signal
miRNA_antiguide
non_canonical_start_codon
origin_of_replication
proximal_promoter_element
reading_frame
replication_start_site
splice_donor_5th_base_variant
splice_site_variant
start_codon
start_lost
start_retained_variant
STREP_motif
TATA_box
transcription_start_cluster
TSS
U2_snRNA
upstream_AUG_codon
viral_promoter
UBERON: Cross-Species Anatomy
alveolar gland
anterior fontanel
avian uterine tube isthmus
brain
Brodmann (1909) area 38
cardiac stomach
cranial temporal line
echinoderm pyloric cecum
embryo stage
extensor carpi radialis longus muscle
hair peg
infraorbital
lesser omentum
lobar bronchus
long descending thin limb
lower respiratory tract
madreporite
metanephric long descending thin limb
nasal artery
nasal tentacle
neocortex
oral cavity
pedicellaria
planum temporale
prepupa
primary ossification center
prime adult stage
primitive knot
pupa
pupal stage
pyloric stomach
right lung accessory lobe lobar bronchus
start of life cycle
start of neonate stage
stellate reticulum
stellate vein of kidney
thyroid primordium
tube foot
upper respiratory tract
water vascular system
VT: Vertebrate Trait Ontology
blood amylase amount
blood glycerol amount
blood ketone body amount
carbohydrate absorption trait
cranial suture closure initiation trait
ear emergence initiation trait
ear unfolding initiation trait
endochondral ossification initiation trait
intramembranous ossification initiation trait
kidney development initiation trait
menarche initiation trait
ossification initiation trait
prepulse inhibition trait
skeletal myogenesis initiation trait
somite differentiation initiation trait
somite formation initiation trait
startle reflex trait
urine ketone body amount
XCO: Experimental Condition
carbohydrate
carbon tetrachloride
controlled ethanol content drinking water
controlled ethanol content drinking water with no other optional drink source
controlled ethanol content drinking water with water as an optional drink source
controlled serum-free condition
inulin
serial subtraction exercise
soy-free diet
tritiated inulin
PathwaysPathways with diagrams.ribosome biogenesis pathway fatty acid biosynthetic pathway ketone bodies metabolic pathway |
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