- decreased bone mineral density / IMPC
- decreased body length / IMPC
- abnormal bone structure / IMPC
- decreased lean body mass / IMPC
- abnormal pelvic girdle bone morphology / IMPC
- decreased total body fat amount / IMPC
- decreased bone mineral content / IMPC
- decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number / IMPC
C57BL/6N-Atm1Brd Tniktm3a(EUCOMM)Wtsi/WtsiBiat
Status | Available to order |
EMMA ID | EM:05971 |
International strain name | C57BL/6N-Atm1Brd Tniktm3a(EUCOMM)Wtsi/WtsiBiat |
Alternative name | EPD0615_3_A04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Tniktm3a(EUCOMM)Wtsi, |
Gene/Transgene symbol | Tnik |
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 | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0615_3_A04. 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 | University of Veterinary Medicine, Vienna, Austria |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive non-syndromic intellectual disability / Orphanet_88616
IMPC phenotypes (allele matching)
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