B6Brd;B6N-Tyrc-Brd Ltbp1tm1a(EUCOMM)Wtsi/WtsiH

Status

Available to order

EMMA IDEM:05861
International strain nameB6Brd;B6N-Tyrc-Brd Ltbp1tm1a(EUCOMM)Wtsi/WtsiH
Alternative nameEPD0127_1_A03
Strain typeTargeted Mutant Strains
Allele/Transgene symbolLtbp1tm1a(EUCOMM)Wtsi
Gene/Transgene symbolLtbp1
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 EUCOMM ES clone EPD0127_1_A03. For further details on the construction of this clone see the page at the IMPC portal.
Phenotypic informationPotential phenotyping data in the IMPC portal
ReferencesNone available

Information from EMMA

Archiving centreMary Lyon Centre at MRC Harwell, Oxford, United Kingdom
Animals used for archivingheterozygous C57BL/6NTac
Breeding at archiving centreReceived as frozen sperm. Due to the possible presence of C57BL/6Brd-Tyrc-Brd, albino pups might be produced by intercrossing.

Disease and phenotype information

Orphanet associated rare diseases, based on orthologous gene matching

IMPC phenotypes (allele matching)
  • abnormal cranium morphology / IMPC
  • abnormal snout morphology / IMPC
  • abnormal radius morphology / IMPC
  • decreased body length / IMPC
  • decreased body weight / IMPC
  • abnormal coat/hair pigmentation / IMPC
  • abnormal tooth morphology / IMPC
  • vertebral fusion / IMPC
  • abnormal ulna morphology / IMPC
  • increased circulating bilirubin level / IMPC
  • abnormal incisor morphology / IMPC
  • increased hemoglobin content / IMPC
  • decreased total body fat amount / IMPC
  • decreased bone mineral content / IMPC
  • lipid deposition / IMPC
IMPC phenotypes (gene matching)
  • decreased body weight / IMPC
  • decreased body length / IMPC
  • lipid deposition / IMPC
  • abnormal snout morphology / IMPC
  • increased hemoglobin content / IMPC
  • abnormal coat/hair pigmentation / IMPC
  • decreased total body fat amount / IMPC
  • abnormal ulna morphology / IMPC
  • vertebral fusion / IMPC
  • abnormal radius morphology / IMPC
  • increased circulating bilirubin level / IMPC
  • abnormal tooth morphology / IMPC
  • abnormal cranium morphology / IMPC
  • abnormal incisor morphology / IMPC
  • decreased bone mineral content / IMPC
MGI phenotypes (allele matching)
  • increased leukocyte cell number / MGI
  • decreased circulating LDL cholesterol level / MGI
  • decreased circulating HDL cholesterol level / MGI
  • abnormal cranium morphology / MGI
  • abnormal snout morphology / MGI
  • abnormal radius morphology / MGI
  • decreased body length / MGI
  • decreased body weight / MGI
  • abnormal tooth morphology / MGI
  • decreased circulating alanine transaminase level / MGI
  • decreased circulating iron level / MGI
  • abnormal ulna morphology / MGI
  • decreased circulating cholesterol level / MGI
  • abnormal incisor morphology / MGI
  • decreased circulating serum albumin level / MGI
  • increased mean corpuscular hemoglobin / MGI
  • increased hemoglobin content / MGI
  • increased blood urea nitrogen level / MGI
  • decreased circulating total protein level / MGI
  • decreased circulating aspartate transaminase level / MGI
  • decreased total body fat amount / MGI
  • decreased bone mineral content / MGI
MGI phenotypes (gene matching)
  • short mandible / MGI
  • short maxilla / MGI
  • decreased circulating LDL cholesterol level / MGI
  • decreased circulating HDL cholesterol level / MGI
  • increased leukocyte cell number / MGI
  • double outlet right ventricle / MGI
  • abnormal cranium morphology / MGI
  • abnormal snout morphology / MGI
  • short snout / MGI
  • abnormal jaw morphology / MGI
  • abnormal radius morphology / MGI
  • decreased body length / MGI
  • decreased body weight / MGI
  • cyanosis / MGI
  • abnormal tooth morphology / MGI
  • persistent truncus arteriosis / MGI
  • dilated renal tubules / MGI
  • decreased circulating alanine transaminase level / MGI
  • liver fibrosis / MGI
  • abnormal coronary artery morphology / MGI
  • decreased circulating iron level / MGI
  • interrupted aortic arch / MGI
  • right aortic arch / MGI
  • small basioccipital bone / MGI
  • small basisphenoid bone / MGI
  • abnormal ulna morphology / MGI
  • decreased circulating cholesterol level / MGI
  • abnormal incisor morphology / MGI
  • decreased circulating serum albumin level / MGI
  • increased mean corpuscular hemoglobin / MGI
  • increased hemoglobin content / MGI
  • increased blood urea nitrogen level / MGI
  • decreased circulating total protein level / MGI
  • abnormal vascular smooth muscle morphology / MGI
  • decreased circulating aspartate transaminase level / MGI
  • abnormal fourth pharyngeal arch artery morphology / MGI
  • polycystic kidney / MGI
  • decreased total body fat amount / MGI
  • decreased bone mineral content / MGI
  • common atrium / MGI
  • perimembraneous ventricular septal defect / MGI
  • abnormal truncus arteriosus septation / MGI
  • vascular ring / MGI
  • abnormal ascending aorta and coronary artery attachment / MGI
  • integument phenotype / MGI
  • neonatal lethality, complete penetrance / MGI
  • lethality throughout fetal growth and development, incomplete penetrance / MGI
  • renal glomerulus cysts / MGI
  • abnormal cardiac neural crest cell morphology / MGI
  • abnormal lower incisor morphology / MGI

Information on how we integrate external resources can be found here

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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

Genotyping protocol

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

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MTA will be issued after an order has been submitted.

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