C3HeB/FeJ-Hgdaku-Yah/Orl
| Status | Available to order |
| EMMA ID | EM:04500 |
| Citation information | RRID:IMSR_EM:04500 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-Hgdaku-Yah/Orl |
| Alternative name | C3Fe Hgd |
| Strain type | Induced Mutant Strains : Chemically-induced |
| Allele/Transgene symbol | Hgdaku-Yah |
| Gene/Transgene symbol | Hgd |
Information from provider
| Provider | Yann Herault |
| Provider affiliation | MOPRHEM group, CNRS IME |
| Genetic information | ENU-induced mutation of the Hgd gene, selected during the PhenHoMut Screen on the urine color (oxidation). Point mutation detected in the open reading frame located in exon10: TGG -->TGA inducing a stop codon W(233)X. |
| Phenotypic information | Urine and bedding color is brownish. |
| References | None available |
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | CNRS-TAAM – Typing and Archiving of Animal Models, Orléans, France |
| Animals used for archiving | heterozygous C3Fe males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Alkaptonuria / Orphanet_56
MGI phenotypes (gene matching)
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