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Symbol
Name
ID
Tor1a
torsin family 1, member A (torsin A)
MGI:1353568
Phenotype annotations related to growth/size/body
Darker colors indicate more annotations
Human Phenotypes
Torticollis
Short neck
Inguinal hernia
Umbilical hernia
Growth delay
Intrauterine growth retardation
Disease(s) Associated with TOR1A
arthrogryposis multiplex congenita-5
torsion dystonia 1

Mouse Phenotypes
decreased body weight
weight loss
decreased body size
postnatal growth retardation
Availability Mouse Genotype
Tor1atm1Calak/Tor1atm1Calak
Tor1atm4.2Wtd/Tor1atm4.2Wtd
Tor1atm2Wtd/Tor1atm4.2Wtd
En1tm2(cre)Wrst/En1+
Tor1atm1Wtd/Tor1atm3.1Wtd  (conditional)
Tor1atm1Wtd/Tor1atm3.1Wtd
Tg(Nes-cre)1Kln/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)
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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory