- abnormal liver morphology / IMPC
- decreased circulating cholesterol level / IMPC
- abnormal retina vasculature morphology / IMPC
- increased mean corpuscular volume / IMPC
- abnormal retina blood vessel morphology / IMPC
- abnormal kidney morphology / IMPC
- prolonged QRS complex duration / IMPC
- preweaning lethality, incomplete penetrance / IMPC
STOCK Trmt1tm1a(EUCOMM)Hmgu/Ics
Status | Available to order |
EMMA ID | EM:10456 |
Citation information | RRID:IMSR_EM:10456 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 | STOCK Trmt1tm1a(EUCOMM)Hmgu/Ics |
Alternative name | HEPD0743_6_A06 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Trmt1tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Trmt1 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | ICS, Institut Clinique de la Souris |
Provider affiliation | ICS, Institut Clinique de la Souris |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0743_6_A06. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | ICS, Institut Clinique de la Souris, Illkirch-Graffenstaden, France |
Animals used for archiving | heterozygous males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Non-specific syndromic intellectual disability / Orphanet_528084
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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