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Symbol
Name
ID 		Gstm1
glutathione S-transferase, mu 1
MGI:95860
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Cerebellar hemorrhage
Cerebral hemorrhage
Microcephaly
Hyposmia
Aganglionic megacolon
Anorexia
Pituitary adenoma
Spasticity
Cerebellar calcifications
Abnormality of the nervous system
Abnormal nervous system morphology
Glioblastoma multiforme
Abnormal cranial nerve morphology
Hydrocephalus
Ventriculomegaly
Cerebellar cyst
Spina bifida
Spinal cord compression
Spinal cord tumor
Benign neoplasm of the central nervous system
Medulloblastoma
Cerebellar medulloblastoma
Neuroblastoma
Ataxia
Cerebellar ataxia associated with quadrupedal gait
Dysmetria
Progressive cerebellar ataxia
Bradykinesia
Chorea
Tremor
Intention tremor
Abnormal pyramidal sign
Hemiplegia/hemiparesis
Cranial nerve paralysis
EEG abnormality
Increased intracranial pressure
Abnormal nonverbal communicative behavior
Abnormality of speech or vocalization
Delayed speech and language development
Dysarthria
Dysgraphia
Depression
Irritability
Disturbed sensory perception
Delusion
Anxiety
Panic attack
Psychosis
Schizophrenia
Hallucinations
Atypical behavior
Apathy
Lethargy
Negativism
Lack of spontaneous play
Reduced social reciprocity
Impaired ability to form peer relationships
Autism
Polydipsia
Polyphagia
Addictive alcohol use
Attention deficit hyperactivity disorder
Impulsivity
Inflexible adherence to routines
Agitation
Restless legs
Motor stereotypy
Restrictive behavior
Cognitive impairment
Memory impairment
Dementia
Frontal lobe dementia
Social and occupational deterioration
Short attention span
Intellectual disability
Insomnia
Hyperreflexia
Dyskinesia
Dystonia
Gait disturbance
Gait imbalance
Postural instability
Abnormal brain FDG positron emission tomography
Headache
Migraine
Developmental regression
Global developmental delay
Seizure
Paresthesia
Abnormal autonomic nervous system physiology
Disease(s) Associated with GSTM1
autistic disorder
cystic fibrosis
Fanconi anemia
graft-versus-host disease
Hirschsprung's disease
Lynch syndrome
medulloblastoma
multiple myeloma
Parkinson's disease
polycythemia vera
porphyria cutanea tarda
schizophrenia
systemic lupus erythematosus
type 1 diabetes mellitus

Mouse Phenotypes
increased neuron apoptosis
decreased prepulse inhibition
Availability Mouse Genotype
Gstm1tm1Gcw/Gstm1tm1Gcw
Gstm6tm1b(EUCOMM)Hmgu/Gstm6tm1b(EUCOMM)Hmgu
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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Funding Information
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Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory