Strain Data Sheet

RBRC-GD000108

Strain Information

Image
BRC No.RBRC-GD000108
TypeChemically-induced Mutation
SpeciesMus musculus
Strain nameTardbp<Rgsc02268>
Former Common nameM102268, RRM2Mut (F210I)
H-2 Haplotype
ES Cell line
Background strain
Appearance
Strain development
Strain descriptionMutant mouse strain established by RIKEN ENU-based gene-driven mutagenesis.Gene: Tardbp, Substitution: T→A
Colony maintenance
ReferencesEMBO J. 2018 Jun 1;37(11). 29764981

Health Report

Examination Date / Room / Rack

Gene

Gene info
Gene symbolGene nameChr.Allele symbolAllele nameCommon namesPromoter
TardbpTAR DNA binding protein4Tardbp<Rgsc02268>RIKEN Genomic Sciences Center (GSC), 2268

Ordering Information

Donor DNA
Research application
Specific Term and ConditionsThe RECIPIENT of for-profit institution must contact the DEPOSITOR separately.
The RECIPIENT of not for-profit institution must contact and discuss in good faith with the DEPOSITOR regarding inventorship, ownership, patent filing and licese fees and others, prior to filing a patent or make a contract with license fees with a third party for invention or products obtained from research results by using the BIOLOGICAL RESOURCES.
DepositorYoichi Gondo (RIKEN GSC)
Strain Statusan icon for Frozen spermFrozen sperm
Strain AvailabilityRecovered litters from cryopreserved sperm (2 to 4 months)
Additional Info.Necessary documents for ordering:
  1. Order form (Japanese / English)
  2. Category I MTA: MTA for distribution with RIKEN BRC (Japanese / English)

BRC mice in Publications

Fratta P, Sivakumar P, Humphrey J, Lo K, Ricketts T, Oliveira H, Brito-Armas JM, Kalmar B, Ule A, Yu Y, Birsa N, Bodo C, Collins T, Conicella AE, Mejia Maza A, Marrero-Gagliardi A, Stewart M, Mianne J, Corrochano S, Emmett W, Codner G, Groves M, Fukumura R, Gondo Y, Lythgoe M, Pauws E, Peskett E, Stanier P, Teboul L, Hallegger M, Calvo A, Chiò A, Isaacs AM, Fawzi NL, Wang E, Housman DE, Baralle F, Greensmith L, Buratti E, Plagnol V, Fisher EM, Acevedo-Arozena A.
Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis.
EMBO J 37(11) (2018) 29764981