Symbol Name ID |
Tor1a
torsin family 1, member A (torsin A) MGI:1353568 |
Darker colors indicate more annotations |
Human Phenotypes | Optic disc pallor |
Strabismus |
Ptosis |
Disease(s) Associated with TOR1A | |||
arthrogryposis multiplex congenita-5 |
Mouse Phenotypes | narrow eye opening |
delayed eyelid opening |
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Availability | Mouse Genotype | ||
Tor1atm4.2Wtd/Tor1atm4.2Wtd | |||
Tor1atm2Wtd/Tor1atm4.2Wtd | |||
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 08/02/2024 MGI 6.24 |
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