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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	abnormal food intake	aphagia	absent gastric milk in neonates	akinesia	abnormal gait	paralysis	seizures
	Gba^tm1.1Clk/Gba^tm1.1Clk
	Gba^tm1Nsb/Gba^tm1Nsb
	Gba^tm2Rlp/Gba^tm2Rlp
	Gba^tm1Karl/Gba^tm1Karl Tg(Nes-cre)1Kln/? (conditional)
	Gba^tm2Karl/Gba^tm2Karl 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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