MGI phenotypes (gene matching)
C3HeB/FeJ-AlbMhdabcl001/Ieg
| Status | Available to order |
| EMMA ID | EM:07469 |
| Citation information | RRID:IMSR_EM:07469 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-AlbMhdabcl001/Ieg |
| Alternative name | C3HeB/FeJ-AlbMhdAbcl001/ieg |
| Strain type | Induced Mutant Strains : Chemically-induced |
| Allele/Transgene symbol | AlbMhdabcl001 |
| Gene/Transgene symbol | Alb |
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 7 of Alb, c. 829T>C, p. C277R of the BCL001 (bone calcium low #001) mouse line. |
| Phenotypic information | Heterozygous mice show significantly decreased plasma values of inorganic total calcium and albumin and significantly increased activities of total alkaline phosphatase |
| Breeding history | >10 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
- Congenital analbuminemia / Orphanet_86816