Symbol Name ID |
Stx1a
syntaxin 1A (brain) MGI:109355 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Abdominal pain |
Depression |
Apathy |
Personality changes |
Disease(s) Associated with STX1A | ||||
Creutzfeldt-Jakob disease | ||||
Hirschsprung's disease |
Mouse Phenotypes | behavior/neurological phenotype |
impaired contextual conditioning behavior |
abnormal cued conditioning behavior |
abnormal latent inhibition of conditioning behavior |
abnormal spatial working memory |
abnormal depression-related behavior |
decreased anxiety-related response |
abnormal response to novel object |
increased startle reflex |
decreased grip strength |
increased locomotor activity |
abnormal social investigation |
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Availability | Mouse Genotype | ||||||||||||
Stx1atm1b(EUCOMM)Hmgu/Stx1atm1b(EUCOMM)Hmgu | |||||||||||||
Stx1atm1Gwz/Stx1atm1Gwz | * | ||||||||||||
Stx1atm1Tfuj/Stx1atm1Tfuj | |||||||||||||
Stx1atm1Migar/Stx1a+ | |||||||||||||
Stx1atm1Tfuj/Stx1a+ |
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 04/16/2024 MGI 6.23 |
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