B6.Cg-Lgi1tm1.1Ics/Orl

Status

Available to order

EMMA IDEM:11505
International strain nameB6.Cg-Lgi1tm1.1Ics/Orl
Alternative nameLgi1 KO
Strain typeTargeted Mutant Strains : Knock-out
Allele/Transgene symbolLgi1tm1.1Ics
Gene/Transgene symbolLgi1

Information from provider

ProviderStephanie Baulac
Provider affiliationHopital PItié-Salpetriere, Institut du Cerveau et de la Moelle-ICM
Genetic informationKnockout of the Lgi1 gene.
Phenotypic informationHomozygous:
Homozygous mice do not survive after postnatal day 20. At postnatal day 10, first epileptic seizures occur. At postnatal day 14, mice are inactive.

Heterozygous:
Heterozygous mice have a lower threshold for audiogenic induced seizures.
Breeding historyThe substrain used for backcrossing is C57BL/6J.
References
  • Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice.;Chabrol Elodie, Navarro Vincent, Provenzano Giovanni, Cohen Ivan, Dinocourt Céline, Rivaud-Péchoux Sophie, Fricker Desdemona, Baulac Michel, Miles Richard, Leguern Eric, Baulac Stéphanie, ;2010;Brain : a journal of neurology;133;2749-62; 20659958
  • LGI1 acts presynaptically to regulate excitatory synaptic transmission during early postnatal development.;Boillot Morgane, Lee Chun-Yao, Allene Camille, Leguern Eric, Baulac Stéphanie, Rouach Nathalie, ;2016;Scientific reports;6;21769; 26878798
  • Epilepsy gene LGI1 regulates postnatal developmental remodeling of retinogeniculate synapses.;Zhou Yu-Dong, Zhang Dawei, Ozkaynak Ekim, Wang Xuan, Kasper Ekkehard M, Leguern Eric, Baulac Stéphanie, Anderson Matthew P, ;2012;The Journal of neuroscience : the official journal of the Society for Neuroscience;32;903-10; 22262888
Homozygous fertileno
Homozygous viableyes
Homozygous matings requiredno
Immunocompromisedno

Information from EMMA

Archiving centreInstitut de Transgenose, INTRAGENE, Orléans, France
Animals used for archivingheterozygous C57BL/6J

Disease and phenotype information

MGI allele-associated human disease models

Orphanet associated rare diseases, based on orthologous gene matching

MGI phenotypes (allele matching)
  • audiogenic seizures / MGI
  • abnormal cerebellum external granule cell layer morphology / MGI
  • decreased body weight / MGI
  • decreased body size / MGI
  • aphagia / MGI
  • postnatal growth retardation / MGI
  • seizures / MGI
  • gliosis / MGI
  • neurodegeneration / MGI
  • akinesia / MGI
  • abnormal hippocampal mossy fiber morphology / MGI
  • tonic-clonic seizures / MGI
  • abnormal cerebellar granule cell morphology / MGI
  • abnormal brain wave pattern / MGI
  • abnormal spike wave discharge / MGI
  • environmentally induced seizures / MGI
  • decreased total body fat amount / MGI
  • postnatal lethality, complete penetrance / MGI
MGI phenotypes (gene matching)
  • abnormal cerebellum external granule cell layer morphology / MGI
  • decreased body weight / MGI
  • decreased body size / MGI
  • aphagia / MGI
  • audiogenic seizures / MGI
  • postnatal growth retardation / MGI
  • seizures / MGI
  • premature death / MGI
  • gliosis / MGI
  • neurodegeneration / MGI
  • akinesia / MGI
  • abnormal hippocampal mossy fiber morphology / MGI
  • tonic seizures / MGI
  • abnormal glutamate-mediated receptor currents / MGI
  • increased susceptibility to pharmacologically induced seizures / MGI
  • nervous system phenotype / MGI
  • clonic seizures / MGI
  • tonic-clonic seizures / MGI
  • abnormal cerebellar granule cell morphology / MGI
  • abnormal miniature excitatory postsynaptic currents / MGI
  • abnormal brain wave pattern / MGI
  • abnormal spike wave discharge / MGI
  • environmentally induced seizures / MGI
  • decreased total body fat amount / MGI
  • postnatal lethality, complete penetrance / MGI

Literature references

  • Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice.;Chabrol Elodie, Navarro Vincent, Provenzano Giovanni, Cohen Ivan, Dinocourt Céline, Rivaud-Péchoux Sophie, Fricker Desdemona, Baulac Michel, Miles Richard, Leguern Eric, Baulac Stéphanie, ;2010;Brain : a journal of neurology;133;2749-62; 20659958
  • LGI1 acts presynaptically to regulate excitatory synaptic transmission during early postnatal development.;Boillot Morgane, Lee Chun-Yao, Allene Camille, Leguern Eric, Baulac Stéphanie, Rouach Nathalie, ;2016;Scientific reports;6;21769; 26878798
  • Epilepsy gene LGI1 regulates postnatal developmental remodeling of retinogeniculate synapses.;Zhou Yu-Dong, Zhang Dawei, Ozkaynak Ekim, Wang Xuan, Kasper Ekkehard M, Leguern Eric, Baulac Stéphanie, Anderson Matthew P, ;2012;The Journal of neuroscience : the official journal of the Society for Neuroscience;32;903-10; 22262888

Information on how we integrate external resources can be found here

Order

Availabilities

Requesting frozen sperm or embryos is generally advisable wherever possible, in order to minimise the shipment of live mice.

  • Frozen sperm. Delivered in 4 weeks (after paperwork in place). €1740*
  • Rederivation of mice from frozen stock, delivery time available upon request . €3880*

Due to the dynamic nature of our processes strain availability may change at short notice. The local repository manager will advise you in these circumstances.

* In addition users have to cover all the shipping costs (including the cost for returning dry-shippers, where applicable).

More details on pricing and delivery times

Practical information

Genotyping protocol

Example health report
(Current health report will be provided later)

Material Transfer Agreement (MTA)
For this strain no provider MTA is needed. Distribution is based on the EMMA conditions only.

EMMA conditions
Legally binding conditions for the transfer

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