- decreased total retina thickness / IMPC
- decreased locomotor activity / IMPC
- increased total body fat amount / IMPC
- short tibia / IMPC
- decreased mean corpuscular volume / IMPC
- abnormal auditory brainstem response / IMPC
- decreased exploration in new environment / IMPC
- preweaning lethality, complete penetrance / IMPC
- abnormal motor capabilities/coordination/movement / IMPC
C57BL/6N-Atm1Brd Med25tm1a(KOMP)Wtsi/Ics
Status | Available to order |
EMMA ID | EM:09752 |
Citation information | RRID:IMSR_EM:09752 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 | C57BL/6N-Atm1Brd Med25tm1a(KOMP)Wtsi/Ics |
Alternative name | EPD0328_5_F06 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Med25tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Med25 |
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 KOMP ES clone EPD0328_5_F06. 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 |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive non-syndromic intellectual disability / Orphanet_88616
- Charcot-Marie-Tooth disease type 2B2 / Orphanet_101101
- Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome / Orphanet_464738
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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