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Symbol
Name
ID

Gba1
glucosylceramidase beta 1
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

Depression

Low frustration tolerance

Apathy

Reduced social reciprocity

Personality changes

Abnormal temper tantrums

Impulsivity

Agitation

Restless legs

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

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
	Gba1^tm1.1Clk/Gba1^tm1.1Clk
	Gba1^tm1Nsb/Gba1^tm1Nsb
	Gba1^tm2Rlp/Gba1^tm2Rlp
	Gba1^tm1Karl/Gba1^tm1Karl Tg(Nes-cre)1Kln/? (conditional)
	Gba1^tm2Karl/Gba1^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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