Symbol Name ID |
Tor1a
torsin family 1, member A (torsin A) MGI:1353568 |
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 |
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Availability | Mouse Genotype | ||||
Tor1atm1Calak/Tor1atm1Calak | |||||
Tor1atm4.2Wtd/Tor1atm4.2Wtd | |||||
Tor1atm2Wtd/Tor1atm4.2Wtd | |||||
En1tm2(cre)Wrst/En1+ Tor1atm1Wtd/Tor1atm3.1Wtd (conditional) |
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Tor1atm1Wtd/Tor1atm3.1Wtd Tg(Nes-cre)1Kln/0 (conditional) |
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Tor1atm2Wtd/Tor1atm3.1Wtd Tg(Nes-cre)1Kln/0 (conditional) |
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 |
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