B6Brd;B6N-Tyrc-Brd Sytl1tm1a(KOMP)Wtsi/Wtsi

Status

Available to order

EMMA IDEM:12069
International strain nameB6Brd;B6N-Tyrc-Brd Sytl1tm1a(KOMP)Wtsi/Wtsi
Alternative nameEPD0084_1_C03
Strain typeTargeted Mutant Strains
Allele/Transgene symbolSytl1tm1a(KOMP)Wtsi
Gene/Transgene symbolSytl1
DisclaimerPlease note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
  1. We can not guarantee a null mutation for Knock-out first alleles (tm1a alleles, see http://www.mousephenotype.org/about-ikmc/targeting-strategies) as the critical exon has not been deleted.
  2. That the structure of the targeted mutation in the ES cells obtained from EUCOMM/KOMP to generate EUCOMM/KOMP mice is not verified by INFRAFRONTIER/EMMA. It is recommended that the recipient confirms the mutation structure.
  3. No check for determining the copy number of the targeting construct in ES cells obtained from EUCOMM/KOMP is done by INFRAFRONTIER/EMMA.
  4. The level of quality control before mice are released is to confirm the individual mouse genotype by short range PCR.

Information from provider

Provider Wellcome Trust Sanger Institute
Provider affiliationWellcome Trust Sanger Institute
Genetic informationThis mouse line originates from KOMP ES clone EPD0084_1_C03. For further details on the construction of this clone see the page at the IMPC portal.
Phenotypic informationPotential phenotyping data in the IMPC portal
References
  • Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes.;White Jacqueline K, Gerdin Anna-Karin, Karp Natasha A, Ryder Ed, Buljan Marija, Bussell James N, Salisbury Jennifer, Clare Simon, Ingham Neil J, Podrini Christine, Houghton Richard, Estabel Jeanne, Bottomley Joanna R, Melvin David G, Sunter David, Adams Niels C, null null, Tannahill David, Logan Darren W, Macarthur Daniel G, Flint Jonathan, Mahajan Vinit B, Tsang Stephen H, Smyth Ian, Watt Fiona M, Skarnes William C, Dougan Gordon, Adams David J, Ramirez-Solis Ramiro, Bradley Allan, Steel Karen P, ;2013;Cell;154;452-64; 23870131

Information from EMMA

Archiving centreWellcome Trust Sanger Institute, Hinxton, United Kingdom
Animals used for archivinghomozygous C57BL/6Brd-Tyr;C57BL/6N

Disease and phenotype information

IMPC phenotypes (allele matching)
  • increased leukocyte cell number / IMPC
  • abnormal coat/hair pigmentation / IMPC
  • increased hematocrit / IMPC
  • abnormal response to tactile stimuli / IMPC
  • increased blood uric acid level / IMPC
IMPC phenotypes (gene matching)
  • abnormal coat/hair pigmentation / IMPC
  • increased leukocyte cell number / IMPC
  • increased hematocrit / IMPC
  • increased blood uric acid level / IMPC
  • abnormal response to tactile stimuli / IMPC
MGI phenotypes (allele matching)
  • increased mean platelet volume / MGI
  • vertebral transformation / MGI
  • abnormal locomotor coordination / MGI
  • epididymal inflammation / MGI
  • caudal vertebral transformation / MGI
  • increased regulatory T cell number / MGI
  • decreased T cell number / MGI
  • CNS inflammation / MGI
  • decreased CD4-positive, alpha beta T cell number / MGI
  • decreased mature B cell number / MGI
  • decreased IgG2b level / MGI
  • decreased circulating amylase level / MGI
  • increased hematocrit / MGI
  • decreased hemoglobin content / MGI
MGI phenotypes (gene matching)
  • increased mean platelet volume / MGI
  • increased hematocrit / MGI
  • abnormal pancreas secretion / MGI
  • decreased hemoglobin content / MGI
  • vertebral transformation / MGI
  • decreased insulin secretion / MGI
  • abnormal locomotor coordination / MGI
  • epididymal inflammation / MGI
  • caudal vertebral transformation / MGI
  • increased regulatory T cell number / MGI
  • decreased T cell number / MGI
  • homeostasis/metabolism phenotype / MGI
  • CNS inflammation / MGI
  • decreased CD4-positive, alpha beta T cell number / MGI
  • decreased mature B cell number / MGI
  • decreased IgG2b level / MGI
  • decreased circulating amylase level / MGI
  • pancreatic acinar cell zymogen granule accumulation / MGI

Literature references

  • Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes.;White Jacqueline K, Gerdin Anna-Karin, Karp Natasha A, Ryder Ed, Buljan Marija, Bussell James N, Salisbury Jennifer, Clare Simon, Ingham Neil J, Podrini Christine, Houghton Richard, Estabel Jeanne, Bottomley Joanna R, Melvin David G, Sunter David, Adams Niels C, null null, Tannahill David, Logan Darren W, Macarthur Daniel G, Flint Jonathan, Mahajan Vinit B, Tsang Stephen H, Smyth Ian, Watt Fiona M, Skarnes William C, Dougan Gordon, Adams David J, Ramirez-Solis Ramiro, Bradley Allan, Steel Karen P, ;2013;Cell;154;452-64; 23870131

Information on how we integrate external resources can be found here

Register interest

Availabilities

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

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

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

Material Transfer Agreement (MTA)
Distribution of this strain is subject to a provider MTA. Both signing of the MTA and submission of the online EMMA Mutant Request Form are required before material can be shipped.

EMMA conditions
Legally binding conditions for the transfer

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