- 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 |
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 0 |
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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