- abnormal heart morphology / MGI
- abnormal heart development / MGI
- thin ventricular wall / MGI
- cranioschisis / MGI
- open neural tube / MGI
- anemia / MGI
- abnormal embryo development / MGI
- decreased embryo size / MGI
- pale yolk sac / MGI
- pericardial edema / MGI
- abnormal developmental patterning / MGI
- no abnormal phenotype detected / MGI
- small heart / MGI
- abnormal notochord morphology / MGI
- abnormal cardiovascular development / MGI
- no phenotypic analysis / MGI
- abnormal neural tube closure / MGI
- delayed somite formation / MGI
- embryonic growth retardation / MGI
- caudal body truncation / MGI
- failure of initiation of embryo turning / MGI
- failure of heart looping / MGI
- abnormal rostral-caudal axis patterning / MGI
- muscle phenotype / MGI
- increased trophoblast giant cell number / MGI
- myocardial trabeculae hypoplasia / MGI
- thin interventricular septum / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- embryonic lethality during organogenesis, incomplete penetrance / MGI
- abnormal muscle precursor cell morphology / MGI
- impaired skeletal muscle regeneration / MGI
129S5;B6N-Kdm6atm2a(EUCOMM)Wtsi/WtsiH
Status | Available to order |
EMMA ID | EM:07380 |
International strain name | 129S5;B6N-Kdm6atm2a(EUCOMM)Wtsi/WtsiH |
Alternative name | EPD0506_3_A01 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Kdm6atm2a(EUCOMM)Wtsi |
Gene/Transgene symbol | Kdm6a |
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 EPD0506_3_A01. 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 | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Kabuki syndrome / Orphanet_2322
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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