- megacephaly / MGI
- abnormal social investigation / MGI
- increased brain weight / MGI
- abnormal barrel cortex morphology / MGI
- enhanced conditioned place preference behavior / MGI
- hyperactivity / MGI
- social withdrawal / MGI
- decreased exploration in new environment / MGI
- behavioral despair / MGI
- abnormal response to novel object / MGI
- abnormal heart valve morphology / MGI
- dilated cardiomyopathy / MGI
- cardiac fibrosis / MGI
- heart valve hyperplasia / MGI
- decreased cardiac muscle contractility / MGI
- abnormal serotonin level / MGI
- heart right ventricle hypertrophy / MGI
- abnormal pulmonary artery morphology / MGI
- abnormal sleep pattern / MGI
- abnormal brain morphology / MGI
- abnormal thermal nociception / MGI
- abnormal heart ventricle morphology / MGI
- increased right ventricle systolic pressure / MGI
- hypoactivity / MGI
- abnormal body temperature homeostasis / MGI
B6.129-Slc6a4tm1Kpl/Cnrm
Status | Available to order |
EMMA ID | EM:05002 |
International strain name | B6.129-Slc6a4tm1Kpl/Cnrm |
Alternative name | SERT-KO |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Slc6a4tm1Kpl |
Gene/Transgene symbol | Slc6a4 |
Information from provider
Provider | Klaus-Peter Lesch |
Provider affiliation | Mollecular Psychiatry, University of Wurzburg |
Additional owner | Dr Cornelius Gross, EMBL Mouse Biology Unit, Monterotondo/Rome, Italy |
Genetic information | A neomycin selection cassette replaced a DNA segment containing exon 2 of the Slc6a4 (serotonin transporter, Sert) gene. |
Phenotypic information | Behavior/Neurological: homozygotes display behavioral despair, decreased exploration in new environment, enhanced conditioned place preference, abnormal response to novel object, abnormal serotonin concentration, abnormal thermal nociception, abnormal sleep pattern. |
Breeding history | The line was backcrossed in C57BL/6J for 10 generations and it is currently maintained by siblings breedings. |
References |
|
Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Disease and phenotype information
MGI allele-associated human disease models
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- heart right ventricle hypertrophy / MGI
- abnormal heart valve morphology / MGI
- megacephaly / MGI
- abnormal pulmonary artery morphology / MGI
- abnormal social investigation / MGI
- social withdrawal / MGI
- abnormal anxiety-related response / MGI
- hyperactivity / MGI
- hypoactivity / MGI
- abnormal response to new environment / MGI
- decreased exploration in new environment / MGI
- abnormal sleep pattern / MGI
- abnormal body temperature homeostasis / MGI
- abnormal fear/anxiety-related behavior / MGI
- abnormal brain morphology / MGI
- no abnormal phenotype detected / MGI
- increased brain weight / MGI
- behavioral despair / MGI
- abnormal thermal nociception / MGI
- dilated cardiomyopathy / MGI
- abnormal active avoidance behavior / MGI
- cardiac fibrosis / MGI
- abnormal response to novel object / MGI
- abnormal serotonergic neuron morphology / MGI
- heart valve hyperplasia / MGI
- abnormal barrel cortex morphology / MGI
- abnormal neuron physiology / MGI
- decreased cardiac muscle contractility / MGI
- abnormal heart ventricle morphology / MGI
- growth/size/body region phenotype / MGI
- abnormal action potential / MGI
- decreased physiological sensitivity to xenobiotic / MGI
- enhanced conditioned place preference behavior / MGI
- impaired behavioral response to xenobiotic / MGI
- decreased serotonin level / MGI
- increased right ventricle systolic pressure / MGI
- mortality/aging / MGI
- postnatal lethality, incomplete penetrance / MGI
Literature references
- Altered brain serotonin homeostasis and locomotor insensitivity to 3, 4-methylenedioxymethamphetamine ("Ecstasy") in serotonin transporter-deficient mice.;Bengel D, Murphy D L, Andrews A M, Wichems C H, Feltner D, Heils A, Mössner R, Westphal H, Lesch K P, ;1998;Molecular pharmacology;53;649-55; 9547354
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