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Symbol
Name
ID
Gba
glucosidase, beta, acid
MGI:95665
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Decreased fetal movement
Fetal akinesia sequence
Abdominal pain
Anorexia
Feeding difficulties
Feeding difficulties in infancy
Bone pain
Apathy
Low frustration tolerance
Impaired social interactions
Abnormal temper tantrums
Delusions
Hallucinations
Visual hallucinations
Anxiety
Panic attack
Depression
Impulsivity
Personality changes
Agitation
Schizophrenia
Short attention span
Sleep disturbance
Insomnia
Restless legs
Monotonic speech
Weak voice
Fatigue
Arthralgia
Disease(s) Associated with GBA1
Gaucher's disease
Gaucher's disease perinatal lethal
Gaucher's disease type I
Gaucher's disease type II
Gaucher's disease type III
Gaucher's disease type IIIC
late onset Parkinson's disease
Lewy body dementia
Parkinson's disease

Mouse Phenotypes
abnormal food intake
aphagia
absent gastric milk in neonates
akinesia
abnormal gait
paralysis
seizures
Availability Mouse Genotype
Gbatm1.1Clk/Gbatm1.1Clk
Gbatm1Nsb/Gbatm1Nsb
Gbatm2Rlp/Gbatm2Rlp
Gbatm1Karl/Gbatm1Karl
Tg(Nes-cre)1Kln/?  (conditional)
Gbatm2Karl/Gbatm2Karl
Tg(KRT14-cre)8Brn/?  (conditional)

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
01/24/2023
MGI 6.22
The Jackson Laboratory