About   Help   FAQ
Symbol
Name
ID
Tor1a
torsin family 1, member A (torsin A)
MGI:1353568
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Decreased fetal movement
Gastrostomy tube feeding in infancy
Depression
Disease(s) Associated with TOR1A
arthrogryposis multiplex congenita-5
torsion dystonia 1

Mouse Phenotypes
behavior/neurological phenotype
abnormal response to new environment
abnormal eating behavior
absent gastric milk in neonates
abnormal suckling behavior
increased freezing behavior
abnormal involuntary movement
abnormal reflex
limb grasping
dystonia
tremors
abnormal motor coordination/balance
impaired balance
impaired coordination
decreased grip strength
weakness
abnormal posture
abnormal limb posture
hunched posture
trunk curl
abnormal gait
decreased locomotor activity
hyperactivity
circling
increased stereotypic behavior
decreased vocalization
Availability Mouse Genotype
Tor1atm1Calak/Tor1atm1Calak
Tor1atm1Wtd/Tor1atm1Wtd
Tor1atm2.1Yql/Tor1atm2.1Yql
Tor1atm2Wtd/Tor1atm2Wtd
Tor1atm4.2Wtd/Tor1atm4.2Wtd
Tor1atm2Wtd/Tor1a+ *
Tor1atm2Wtd/Tor1atm4.2Wtd
Emx1tm1(cre)Yql/Emx1+
Tor1atm2Yql/Tor1atm2Yql  (conditional)
Tor1atm1Wtd/Tor1atm3.1Wtd
Emx1tm1(cre)Krj/Emx1+  (conditional)
En1tm2(cre)Wrst/En1+
Tor1atm1Wtd/Tor1atm3.1Wtd  (conditional)
En1tm2(cre)Wrst/En1+
Tor1atm2Wtd/Tor1atm3.1Wtd  (conditional)
Tor1atm1Wtd/Tor1atm3.1Wtd
Tg(Nes-cre)1Kln/0  (conditional)
Tor1atm1Wtd/Tor1atm3.1Wtd
Tg(dlx5a-cre)1Mekk/0  (conditional)
Tor1atm2Wtd/Tor1atm3.1Wtd
Tg(Nes-cre)1Kln/0  (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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/23/2024
MGI 6.23
The Jackson Laboratory