MGI phenotypes (allele matching)
- no phenotypic analysis / MGI
B6;129P2-Pde4dtm1Dgen/H
| Status | Available to order |
| EMMA ID | EM:02363 |
| Citation information | RRID:IMSR_EM:02363 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 | B6;129P2-Pde4dtm1Dgen/H |
| Alternative name | DELTAGEN_T848 |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Pde4dtm1Dgen |
| Gene/Transgene symbol | Pde4d |
Information from provider
| Provider | Deltagen Inc. |
| Provider affiliation | Deltagen Inc. |
| Phenotypic information | No phenotype data was provided |
| References | None available |
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
- PDE4D haploinsufficiency syndrome / Orphanet_439822
- Acrodysostosis with multiple hormone resistance / Orphanet_280651
- Acrodysostosis / Orphanet_950
MGI phenotypes (gene matching)
- decreased body weight / MGI
- postnatal growth retardation / MGI
- reduced female fertility / MGI
- abnormal ovulation / MGI
- decreased litter size / MGI
- no phenotypic analysis / MGI
- immune system phenotype / MGI
- increased cardiac muscle contractility / MGI
- impaired neutrophil recruitment / MGI
- impaired neutrophil chemotaxis / MGI
- abnormal tumor necrosis factor level / MGI
- postnatal lethality, incomplete penetrance / MGI