MGI phenotypes (allele matching)
C3H;102-CrygeNo3/H
| Status | Available to order |
| EMMA ID | EM:01297 |
| Citation information | RRID:IMSR_EM:01297 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;102-CrygeNo3/H |
| Alternative name | No3-F,No3 |
| Strain type | Induced Mutant Strains : Chemically-induced |
| Allele/Transgene symbol | CrygeNo3 |
| Gene/Transgene symbol | Cryge |
Information from provider
| Provider | Mary Lyon |
| Provider affiliation | MRC Mammalian Genetics Unit |
| Phenotypic information | Heterozygotes have small nuclear opacity. Homozygotes have more severe opacity. |
| References | None available |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
MGI phenotypes (gene matching)
- microphthalmia / MGI
- abnormal lens morphology / MGI
- cataract / MGI
- small lens / MGI
- small pupils / MGI
- abnormal iris morphology / MGI
- abnormal lens fiber morphology / MGI
- abnormal lens capsule morphology / MGI
- abnormal lens development / MGI
- ruptured lens capsule / MGI
- nuclear cataracts / MGI
- total cataracts / MGI
- vacuolated lens / MGI
- immature cataract / MGI