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Symbol
Name
ID
Nat2
N-acetyltransferase 2 (arylamine N-acetyltransferase)
MGI:109201
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Hyposmia
Blepharospasm
Eyelid apraxia
Retrocollis
Anorexia
Dysphagia
Photophobia
Spasticity
Abnormality of the nervous system
Astrocytosis
Gliosis
Cerebral cortical atrophy
Neuronal loss in basal ganglia
Cerebral atrophy
Neurofibrillary tangles
Granulovacuolar degeneration
Neuronal loss in central nervous system
Senile plaques
Bradykinesia
Parkinsonism
Chorea
Tremor
Postural tremor
Abnormal synaptic transmission
Aphasia
Delayed speech and language development
Dysarthria
Mutism
Depression
Emotional lability
Irritability
Anxiety
Panic attack
Psychosis
Hallucinations
Apathy
Reduced social reciprocity
Impulsivity
Agitation
Restless legs
Cognitive impairment
Memory impairment
Dementia
Frontal lobe dementia
Frontolimbic dementia
Short attention span
Micrographia
Insomnia
Hyperreflexia
Akinesia
Dyskinesia
Dystonia
Axial dystonia
Limb dystonia
Frontal release signs
Falls
Gait imbalance
Unsteady gait
Postural instability
Pseudobulbar signs
Seizure
Abnormal autonomic nervous system physiology
Disease(s) Associated with NAT1
pancreatic cancer
Disease(s) Associated with NAT2
Behcet's disease
pancreatic cancer
Parkinson's disease
progressive supranuclear palsy
systemic lupus erythematosus

Mouse Phenotypes
abnormal neural tube closure
Availability Mouse Genotype
Nat2tm1Esim/Nat2+

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory