B6.129P2-Plod1Gt(RST531)Byg/Oulu

Status

Available to order

EMMA IDEM:08328
Citation informationRRID:IMSR_EM:08328 

Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information.

International strain nameB6.129P2-Plod1Gt(RST531)Byg/Oulu
Alternative namePlod1Gt(RST531)Byg
Strain typeGene-trap
Allele/Transgene symbolPlod1Gt(RST531)Byg
Gene/Transgene symbolPlod1

Information from provider

ProviderRaija Soininen
Provider affiliationBiocenter Oulu, University of Oulu
Genetic informationGene-trap insertion into intron 11 of the Plod1 gene.
Phenotypic informationHomozygous:
Homozygotes were not analyzed.

Heterozygous:
Heterozygotes were used for expression analyses (X-gal staining), other analyses were not performed.
Breeding historyBackcrossed, N=10
References
  • Tissue-specific changes in the hydroxylysine content and cross-links of collagens and alterations in fibril morphology in lysyl hydroxylase 1 knock-out mice.;Takaluoma Kati, Hyry Marjo, Lantto Juha, Sormunen Raija, Bank Ruud A, Kivirikko Kari I, Myllyharju Johanna, Soininen Raija, ;2007;The Journal of biological chemistry;282;6588-96; 17197443
Homozygous fertilenot known
Homozygous viablenot known
Homozygous matings requiredno
Immunocompromisedno

Information from EMMA

Archiving centreUniversity of Oulu, Oulu, Finland
Animals used for archivingheterozygous 129P2/OlaHsd x C57BL/6 males, wild-type C57BL/6JOlaHsd females
Stage of embryosMorula

Disease and phenotype information

Orphanet associated rare diseases, based on orthologous gene matching

    • Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency / Orphanet_1900
IMPC phenotypes (gene matching)
  • decreased grip strength / IMPC
  • hyperplasia / IMPC
  • fibro-osseous lesion / IMPC
  • decreased prepulse inhibition / IMPC
MGI phenotypes (allele matching)
  • no phenotypic analysis / MGI
MGI phenotypes (gene matching)
  • paralysis / MGI
  • hemorrhage / MGI
  • abnormal motor capabilities/coordination/movement / MGI
  • premature death / MGI
  • no phenotypic analysis / MGI
  • aortic dissection / MGI
  • hypotonia / MGI
  • abnormal cutaneous collagen fibril morphology / MGI
  • abnormal aorta smooth muscle morphology / MGI
  • abnormal aorta wall morphology / MGI

Literature references

  • Tissue-specific changes in the hydroxylysine content and cross-links of collagens and alterations in fibril morphology in lysyl hydroxylase 1 knock-out mice.;Takaluoma Kati, Hyry Marjo, Lantto Juha, Sormunen Raija, Bank Ruud A, Kivirikko Kari I, Myllyharju Johanna, Soininen Raija, ;2007;The Journal of biological chemistry;282;6588-96; 17197443

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Order

Availabilities

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

  • Frozen embryos. Delivered in 4 weeks (after paperwork in place). €1740*
  • 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)
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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