About Help FAQ

Symbol
Name
ID

Psap
prosaposin
MGI:97783

Phenotype annotations related to behavior/neurological

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Feeding difficulties	Bone pain	Depression	Low frustration tolerance	Apathy	Personality changes	Impulsivity	Agitation	Weak voice	Chronic fatigue
Disease(s) Associated with PSAP	Feeding difficulties	Bone pain	Depression	Low frustration tolerance	Apathy	Personality changes	Impulsivity	Agitation	Weak voice	Chronic fatigue
atypical Gaucher's disease due to saposin c deficiency
combined saposin deficiency
late onset Parkinson's disease

Mouse Phenotypes

behavior/neurological phenotype

abnormal behavior

abnormal habituation

polydipsia

abnormal food intake

decreased anxiety-related response

abnormal motor capabilities/coordination/movement

abnormal involuntary movement

limb grasping

tremors

abnormal motor coordination/balance

ataxia

impaired balance

impaired coordination

impaired limb coordination

abnormal head movements

head shaking

straub tail

abnormal locomotor behavior

abnormal gait

short stride length

increased vertical activity

decreased locomotor activity

hyperactivity

hindlimb paralysis

paraparesis

seizures

tonic seizures

Availability

Mouse Genotype

Psap^m1Btlr/Psap^m1Btlr

Psap^tm1Ggb/Psap^tm1Ggb

Psap^tm1Juma/Psap^tm1Juma

Psap^tm1Suz/Psap^tm1Suz

Psap^tm2.1Juma/Psap^tm2.1Juma

Psap^tm2Ggb/Psap^tm2Ggb

*

Psap^tm2Suz/Psap^tm2Suz

Psap^tm3.1Ggb/Psap^tm3.1Ggb

Psap^tm4.1Ggb/Psap^tm4.1Ggb

Psap^tm1Suz/Psap^tm2.1Juma

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23