C3HeB/FeJ-Scg3m1Mhda/Ieg
| Status | Available to order |
| EMMA ID | EM:07466 |
| Citation information | RRID:IMSR_EM:07466 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 | C3HeB/FeJ-Scg3m1Mhda/Ieg |
| Alternative name | C3HeB/FeJ-Scg3N180KMhdA/ieg |
| Strain type | Induced Mutant Strains : Chemically-induced |
| Allele/Transgene symbol | Scg3m1Mhda |
| Gene/Transgene symbol | Scg3 |
Information from provider
| Provider | Sibylle Sabrautzki |
| Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
| Genetic information | Missense mutation in exon 5 of Scg3 c.540T->G, p.N180K. |
| Phenotypic information | Heterozygous mice with no overt phenotype, homozygous mice not analyzed. |
| Breeding history | More than 5 generations on pure C3HeB/FeJ background. |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | no |
| Immunocompromised | not known |
Information from EMMA
| Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
| Animals used for archiving | heterozygous C3H males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5 / Orphanet_353
IMPC phenotypes (gene matching)
MGI phenotypes (allele matching)
- no phenotypic analysis / MGI
MGI phenotypes (gene matching)
- no abnormal phenotype detected / MGI
- abnormal pancreas physiology / MGI
- decreased circulating insulin level / MGI
- no phenotypic analysis / MGI
- impaired glucose tolerance / MGI
- homeostasis/metabolism phenotype / MGI
- behavior/neurological phenotype / MGI
- reproductive system phenotype / MGI
- abnormal pituitary gland physiology / MGI
- increased susceptibility to diet-induced obesity / MGI
- mortality/aging / MGI
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