- 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 |
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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