C3H.C-Casp3m1H/H

Status

Available to order

EMMA IDEM:04615
Citation informationRRID:IMSR_EM:04615 

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 nameC3H.C-Casp3m1H/H
Alternative nameCasp3-I216F
Strain typeInduced Mutant Strains : Chemically-induced
Allele/Transgene symbolCasp3m1H
Gene/Transgene symbolCasp3

Information from provider

ProviderShoumo Bhattacharya
Provider affiliationDept of Cardiovascular Medicine, University of Oxford
Additional ownerThe original mutation was identified from the MRC-Harwell's paired DNA-sperm library of ENU-mutagenised males. Harwell Science and Innovation Campus Oxfordshire OX11 0RD UK
Genetic informationThe original mutation was identified from the MRC-Harwell's paired DNA-sperm library of ENU-mutagenised males. The molecular lesion is an Isoleucine to Phenylalanine change at amino acid 216 which introduces an MboII restriction site. It has been backcrossed to C3H for 10+ generations. Last SNP genotyping determined only 2 Mb region remaining BALB/c background.
Phenotypic informationReduced apoptosis in homozygotes. Phenocopies Caspase 3 null alleles.
Breeding historyBackcrossed to C3H for 10+ generations.
ReferencesNone available
Homozygous fertileno
Homozygous viableno
Homozygous matings requiredno
Immunocompromisedno

Information from EMMA

Archiving centreMary Lyon Centre at MRC Harwell, Oxford, United Kingdom
Animals used for archivingheterozygous C3H/HeH males
Breeding at archiving centreNone. Mice were archived at the time of arrival at the archiving centre.

Disease and phenotype information

MGI phenotypes (gene matching)
  • cochlear degeneration / MGI
  • abnormal organ of Corti morphology / MGI
  • delayed bone ossification / MGI
  • decreased bone mineral density / MGI
  • cleft palate / MGI
  • abnormal bone marrow development / MGI
  • decreased thymocyte number / MGI
  • abnormal forebrain morphology / MGI
  • abnormal olfactory bulb morphology / MGI
  • abnormal diencephalon morphology / MGI
  • abnormal cerebellum development / MGI
  • abnormal cerebellum external granule cell layer morphology / MGI
  • abnormal cerebellar granule layer morphology / MGI
  • abnormal cerebellar molecular layer / MGI
  • cranioschisis / MGI
  • abnormal ovarian follicle morphology / MGI
  • decreased body size / MGI
  • abnormal eye development / MGI
  • microphthalmia / MGI
  • cataract / MGI
  • abnormal retina morphology / MGI
  • abnormal gait / MGI
  • abnormal osteoclast physiology / MGI
  • abnormal blood vessel morphology / MGI
  • abnormal apoptosis / MGI
  • decreased inflammatory response / MGI
  • hydroencephaly / MGI
  • deafness / MGI
  • premature death / MGI
  • abnormal eye morphology / MGI
  • abnormal ear morphology / MGI
  • abnormal skeleton development / MGI
  • abnormal brain morphology / MGI
  • abnormal cochlear hair cell morphology / MGI
  • abnormal olfactory bulb development / MGI
  • cochlear ganglion degeneration / MGI
  • abnormal bone remodeling / MGI
  • no phenotypic analysis / MGI
  • decreased neuron apoptosis / MGI
  • increased cardiomyocyte apoptosis / MGI
  • abnormal lens epithelium morphology / MGI
  • abnormal keratinocyte physiology / MGI
  • nervous system phenotype / MGI
  • abnormal retinal inner nuclear layer morphology / MGI
  • abnormal sagittal suture morphology / MGI
  • abnormal optic stalk morphology / MGI
  • cochlear hair cell degeneration / MGI
  • cochlear inner hair cell degeneration / MGI
  • cochlear outer hair cell degeneration / MGI
  • abnormal outer hair cell stereociliary bundle morphology / MGI
  • fused outer hair cell stereocilia / MGI
  • absent distortion product otoacoustic emissions / MGI
  • abnormal retinal pigment epithelium morphology / MGI
  • abnormal brainstem morphology / MGI
  • renal/urinary system phenotype / MGI
  • hearing/vestibular/ear phenotype / MGI
  • cellular phenotype / MGI
  • immune system phenotype / MGI
  • respiratory system phenotype / MGI
  • reproductive system phenotype / MGI
  • vision/eye phenotype / MGI
  • abnormal lens development / MGI
  • decreased apoptosis / MGI
  • abnormal olfactory sensory neuron morphology / MGI
  • absent pinna reflex / MGI
  • absent startle reflex / MGI
  • abnormal bone ossification / MGI
  • increased cellular sensitivity to ultraviolet irradiation / MGI
  • abnormal granulosa cell morphology / MGI
  • decreased physiological sensitivity to xenobiotic / MGI
  • increased sensitivity to induced cell death / MGI
  • decreased sensitivity to induced cell death / MGI
  • decreased trabecular bone thickness / MGI
  • decreased keratinocyte apoptosis / MGI
  • postnatal lethality, complete penetrance / MGI
  • perinatal lethality, incomplete penetrance / MGI
  • prenatal lethality, incomplete penetrance / MGI
  • abnormal auditory brainstem response waveform shape / MGI
  • increased or absent threshold for auditory brainstem response / MGI
  • encephalomeningocele / MGI
  • decreased fibroblast apoptosis / MGI
  • cranial bossing / MGI

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*
  • Tissue - Types of tissue, service fee and delivery time available upon request

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)
MTA will be issued after an order has been submitted.

EMMA conditions
Legally binding conditions for the transfer

Right strain for your research?

The information provided on this page is, to the best of EMMA’s knowledge, based on data supplied by the original provider. End users are responsible for reviewing these details and for validating the strain and its suitability for their experimental use.​
Not found what you were looking for? Search here for other strains available from EMMA.


Search
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).