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Symbol
Name
ID
Agtr2
angiotensin II receptor, type 2
MGI:87966
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Drooling
Microcephaly
Postnatal microcephaly
Spasticity
EEG abnormality
Hypsarrhythmia
Poor fine motor coordination
Language impairment
Absent speech
Poor speech
Hyperreflexia
Hyperactivity
Stereotypy
Behavioral abnormality
Aggressive behavior
Poor eye contact
Autistic behavior
Autism
Anxiety
Psychosis
Restlessness
Agitation
Short attention span
Intellectual disability
Intellectual disability, mild
Intellectual disability, moderate
Delayed speech and language development
Global developmental delay
Motor delay
Delayed gross motor development
Seizures
Absence seizures
Febrile seizures
Generalized myoclonic seizures
Disease(s) Associated with AGTR2
non-syndromic X-linked intellectual disability

Mouse Phenotypes
abnormal habenula morphology
abnormal thalamus morphology
abnormal amygdala morphology
abnormal hippocampus CA1 region morphology
abnormal hippocampus CA2 region morphology
abnormal hippocampus CA3 region morphology
abnormal piriform cortex morphology
abnormal baroreceptor physiology
Availability Mouse Genotype
Agtr2tm1Tin/Y

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/11/2018
MGI 6.12
The Jackson Laboratory