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Symbol
Name
ID

Tor1a
torsin family 1, member A (torsin A)
MGI:1353568

Phenotype annotations related to mortality/aging

!	Indicates phenotype varies with strain background.
	Darker colors indicate more annotations

Human Phenotypes	Death in infancy
Disease(s) Associated with TOR1A	Death in infancy
arthrogryposis multiplex congenita-5

Mouse Phenotypes		increased susceptibility to induced morbidity/mortality	premature death	neonatal lethality, complete penetrance	postnatal lethality, complete penetrance	postnatal lethality, incomplete penetrance	preweaning lethality, complete penetrance	preweaning lethality, incomplete penetrance
Availability	Mouse Genotype	increased susceptibility to induced morbidity/mortality	premature death	neonatal lethality, complete penetrance	postnatal lethality, complete penetrance	postnatal lethality, incomplete penetrance	preweaning lethality, complete penetrance	preweaning lethality, incomplete penetrance
	Tor1a^em1(IMPC)H/Tor1a^em1(IMPC)H
	Tor1a^tm1Calak/Tor1a^tm1Calak
	Tor1a^tm1Wtd/Tor1a^tm1Wtd
	Tor1a^tm2.1Yql/Tor1a^tm2.1Yql
	Tor1a^tm2Wtd/Tor1a^tm2Wtd			!	!
	Tor1a^tm4.2Wtd/Tor1a^tm4.2Wtd
	Tor1a^tm2Wtd/Tor1a^tm4.2Wtd
	Tor1a^tm1Wtd/Tor1a^tm3.1Wtd 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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