B6Brd;B6Dnk;B6N-Tyrc-Brd-Kptntm1c(EUCOMM)Wtsi/WtsiCnbc
Status | Available to order |
EMMA ID | EM:14229 |
International strain name | B6Brd;B6Dnk;B6N-Tyrc-Brd-Kptntm1c(EUCOMM)Wtsi/WtsiCnbc |
Alternative name | EPD0183_4_C10 |
Strain type | Targeted Mutant Strains : Targeted Conditional |
Allele/Transgene symbol | Kptntm1c(EUCOMM)Wtsi |
Gene/Transgene symbol | Kptn |
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 line originates from EUCOMM ES clone EPD0183_4_C10, after breeding with a Flp recombinase deleter line to convert the original targeted allele tm1a (knock-out first allele) into a conditional allele tm1c. 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 | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Animals used for archiving | heterozygous C57BL/6Brd-Tyr |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Macrocephaly-developmental delay syndrome / Orphanet_397612
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- increased circulating calcium level / MGI
- increased body weight / MGI
- increased susceptibility to bacterial infection / MGI
- increased circulating serum albumin level / MGI
- increased circulating alkaline phosphatase level / MGI
- abnormal behavior / MGI
- hearing/vestibular/ear phenotype / MGI
- increased circulating total protein level / MGI
- increased total body fat amount / MGI
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