IMPC phenotypes (gene matching)
C3H;C-HephSla/H
| Status | Available to order |
| EMMA ID | EM:01692 |
| Citation information | RRID:IMSR_EM:01692 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;C-HephSla/H |
| Alternative name | Heph |
| Strain type | Induced Mutant Strains : Chemically-induced |
| Allele/Transgene symbol | HephSla |
| Gene/Transgene symbol | Heph |
Information from provider
| Provider | Jo Peters |
| Provider affiliation | Institute of Hearing Research, MRC (Medical Research Council) |
| Genetic information | Dominant sex linked anaemia allele of hephaestin (Heph). |
| Phenotypic information | Haematopoietic effects, anaemia. |
| References | None available |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
MGI phenotypes (allele matching)
- anemia / MGI
MGI phenotypes (gene matching)
- decreased hematocrit / MGI
- macrocytosis / MGI
- abnormal coat/ hair morphology / MGI
- anemia / MGI
- abnormal iron level / MGI
- abnormal definitive hematopoiesis / MGI
- no abnormal phenotype detected / MGI
- abnormal erythrocyte morphology / MGI
- decreased mean corpuscular volume / MGI
- anisopoikilocytosis / MGI
- microcytosis / MGI
- decreased hemoglobin content / MGI
- decreased erythrocyte cell number / MGI
- abnormal placental transport / MGI
- polychromatophilia / MGI
- hematopoietic system phenotype / MGI
- decreased mean corpuscular hemoglobin / MGI
- decreased mean corpuscular hemoglobin concentration / MGI
- hypochromic anemia / MGI
- increased intestinal iron level / MGI