- 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
C3H.C-Casp3m1H/H
| Status | Available to order |
| EMMA ID | EM:04615 |
| Citation information | RRID: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 name | C3H.C-Casp3m1H/H |
| Alternative name | Casp3-I216F |
| Strain type | Induced Mutant Strains : Chemically-induced |
| Allele/Transgene symbol | Casp3m1H |
| Gene/Transgene symbol | Casp3 |
Information from provider
| Provider | Shoumo Bhattacharya |
| Provider affiliation | Dept of Cardiovascular Medicine, University of Oxford |
| Additional owner | The 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 information | The 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 information | Reduced apoptosis in homozygotes. Phenocopies Caspase 3 null alleles. |
| Breeding history | Backcrossed to C3H for 10+ generations. |
| References | None available |
| Homozygous fertile | no |
| Homozygous viable | no |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
| Animals used for archiving | heterozygous C3H/HeH males |
| Breeding at archiving centre | None. Mice were archived at the time of arrival at the archiving centre. |
Disease and phenotype information
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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