MGI phenotypes (allele matching)
- no phenotypic analysis / MGI
B6;129P2-Pde4dtm1Dgen/H
| Status | Available to order |
| EMMA ID | EM:02363 |
| 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