IMPC phenotypes (gene matching)
C3H;C-HephSla/H
| Status | Available to order |
| EMMA ID | EM:01692 |
| 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