B.Cg-Pgk1a/WsH
| Status | Available to order |
| EMMA ID | EM:02605 |
| Citation information | RRID:IMSR_EM:02605 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 | B.Cg-Pgk1a/WsH |
| Alternative name | Pgk1a/Ws |
| Strain type | Spontaneous |
| Allele/Transgene symbol | Pgk1a |
| Gene/Transgene symbol | Pgk1 |
Information from provider
| Provider | John West |
| Provider affiliation | Genes and Development Group, University of Edinburgh |
| Genetic information | Electrophoretic variant of phosphoglycerate kinase 1a. |
| Breeding history | Partial congenic (N9) on C57BL/6Ola. |
| References |
|
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | no |
| Immunocompromised | not known |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Glycogen storage disease due to phosphoglycerate kinase 1 deficiency / Orphanet_713
Literature references
- Electrophoretic variation for x-chromosome-linked phosphoglycerate kinase (pgk-1) in the mouse.;Nielsen J T, Chapman V M, ;1977;Genetics;87;319-25; 17248765