IMPC phenotypes (allele matching)
C57BL/6NTac-Tktem1(IMPC)H/H
| Status | Available to order |
| EMMA ID | EM:13352 |
| International strain name | C57BL/6NTac-Tktem1(IMPC)H/H |
| Alternative name | |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Tktem1(IMPC)H |
| Gene/Transgene symbol | Tkt |
Information from provider
| Provider | MRC, Medical Research Council |
| Provider affiliation | Mary Lyon Centre at MRC Harwell |
| Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project page at the IMPC portal. |
| Phenotypic information | Potential phenotyping data in the IMPC portal |
| 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
- Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome / Orphanet_93358
- Transketolase deficiency / Orphanet_488618
MGI phenotypes (gene matching)
- decreased body weight / MGI
- microphthalmia / MGI
- postnatal growth retardation / MGI
- decreased white adipose tissue amount / MGI
- reduced fertility / MGI
- decreased brain weight / MGI
- abnormal sexual interaction / MGI
- decreased heart weight / MGI
- decreased liver weight / MGI
- decreased kidney weight / MGI
- decreased testis weight / MGI
- embryonic lethality before implantation, complete penetrance / MGI