129S5;B6N-Chd7tm2a(EUCOMM)Wtsi/WtsiCnbc
Status | Available to order |
EMMA ID | EM:04817 |
International strain name | 129S5;B6N-Chd7tm2a(EUCOMM)Wtsi/WtsiCnbc |
Alternative name | EPD0019_1_D07 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Chd7tm2a(EUCOMM)Wtsi, |
Gene/Transgene symbol | Chd7 |
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 EPD0019_1_D07. 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 |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Omenn syndrome / Orphanet_39041
- Normosmic congenital hypogonadotropic hypogonadism / Orphanet_432
- Kallmann syndrome / Orphanet_478
- CHARGE syndrome / Orphanet_138
IMPC phenotypes (allele matching)
MGI phenotypes (allele matching)
- circling / MGI
- head bobbing / MGI
- hyperactivity / MGI
- decreased lumbar vertebrae number / MGI
- abnormal behavior / MGI
- thin atrioventricular cushion / MGI
- embryonic growth arrest / MGI
- thin myocardium / MGI
- increased cardiomyocyte apoptosis / MGI
- cardiovascular system phenotype / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- decreased fetal cardiomyocyte proliferation / MGI
- abnormal epigenetic regulation of gene expression / MGI
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