- decreased bone mineral density / IMPC
- decreased body length / IMPC
- increased circulating alanine transaminase level / IMPC
- increased circulating alkaline phosphatase level / IMPC
- increased circulating aspartate transaminase level / IMPC
- increased circulating magnesium level / IMPC
- decreased bone mineral content / IMPC
C57BL/6NTac-Hdac8tm1a(EUCOMM)Wtsi/WtsiBiat
Status | Available to order |
EMMA ID | EM:05717 |
Citation information | RRID:IMSR_EM:05717 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
International strain name | C57BL/6NTac-Hdac8tm1a(EUCOMM)Wtsi/WtsiBiat |
Alternative name | EPD0028_1_C04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Hdac8tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Hdac8 |
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 EPD0028_1_C04. 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
- Wilson-Turner syndrome / Orphanet_3459
- Cornelia de Lange syndrome / Orphanet_199
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- increased circulating aspartate transaminase level / IMPC
- increased circulating alkaline phosphatase level / IMPC
- increased circulating magnesium level / IMPC
- increased circulating alanine transaminase level / IMPC
- decreased bone mineral density / IMPC
- decreased bone mineral content / IMPC
- decreased body length / IMPC
MGI phenotypes (gene matching)
- decreased bone mineral density / MGI
- exencephaly / MGI
- intracranial hemorrhage / MGI
- genetic imprinting / MGI
- frontal bone foramen / MGI
- failure of intramembranous bone ossification / MGI
- decreased embryo weight / MGI
- decreased bone mineral content / MGI
- neonatal lethality, complete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
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