MGI phenotypes (allele matching)
- decreased circulating alkaline phosphatase level / MGI
C3HeB/FeJ-AlplMhdabap26/Ieg
| Status | Available to order |
| EMMA ID | EM:05249 |
| International strain name | C3HeB/FeJ-AlplMhdabap26/Ieg |
| Alternative name | BAP026 |
| Strain type | Induced Mutant Strains : Chemically-induced |
| Allele/Transgene symbol | AlplMhdabap26, |
| Gene/Transgene symbol | Alpl |
Information from provider
| Provider | Sibylle Wagner |
| Provider affiliation | Institute of Experimental Genetics, GSF Research Centre |
| Genetic information | c.997+2 T to C, splice site mutation. |
| Phenotypic information | Low total alkaline phosphatase activity. |
| Breeding history | Pure C3HeB/FeJ, inbred more than 10 generations. |
| 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 |
Disease and phenotype information
MGI allele-associated human disease models
Orphanet associated rare diseases, based on orthologous gene matching
- Infantile hypophosphatasia / Orphanet_247651
- Odontohypophosphatasia / Orphanet_247685
- Adult hypophosphatasia / Orphanet_247676
- Childhood-onset hypophosphatasia / Orphanet_247667
- Perinatal lethal hypophosphatasia / Orphanet_247623
- Prenatal benign hypophosphatasia / Orphanet_247638