- hypoglycemia / MGI
- adrenal gland hypoplasia / MGI
- increased anxiety-related response / MGI
- hyperactivity / MGI
- increased circulating adrenocorticotropin level / MGI
- abnormal glucose homeostasis / MGI
- decreased circulating corticosterone level / MGI
- decreased circulating aldosterone level / MGI
- increased susceptibility to pharmacologically induced seizures / MGI
- increased circulating chloride level / MGI
- abnormal gluconeogenesis / MGI
- increased spleen weight / MGI
- increased thymus weight / MGI
- lethargy / MGI
- decreased heart rate / MGI
- decreased percent body fat/body weight / MGI
- increased circulating potassium level / MGI
- decreased circulating adrenaline level / MGI
- abnormal adrenal gland zona fasciculata morphology / MGI
- adrenal cortical hyperplasia / MGI
- decreased brown fat lipid droplet number / MGI
- decreased total body fat amount / MGI
- postnatal lethality, incomplete penetrance / MGI
- abnormal adrenal gland capsule morphology / MGI
C57BL/6J-Mc2rem1H/H
| Status | Available to order |
| EMMA ID | EM:16097 |
| Citation information | RRID:IMSR_EM:16097 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 | C57BL/6J-Mc2rem1H/H |
| Alternative name | C57BL/6J-Mc2r |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Mc2rem1H |
| Gene/Transgene symbol | Mc2r |
Information from provider
| Provider | Mary Lyon Centre at MRC Harwell |
| Provider affiliation | Mary Lyon Centre at MRC Harwell |
| Genetic information | This strain carries a point mutation (F278C) introduced by electroporation of CRISPR/Cas9 reagents, sgRNAs protospacer sequence GCTCCGAAAGGCATATATAA and PAM sequence, and an ssODN donor sequence. |
| Phenotypic information | Homozygous:no data availableHeterozygous:no data available |
| Breeding history | Coisogenic on C57Bl/6J |
| References | None available |
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Familial glucocorticoid deficiency / Orphanet_361
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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