- abnormal vitreous body morphology / IMPC
- abnormal retina blood vessel morphology / IMPC
- persistence of hyaloid vascular system / IMPC
- abnormal retina vasculature morphology / IMPC
- abnormal retina morphology / IMPC
- abnormal optic disk morphology / IMPC
- preweaning lethality, complete penetrance / IMPC
- decreased total body fat amount / IMPC
C57BL/6N-Nbastm1a(EUCOMM)Hmgu/Ieg
Status | Available to order |
EMMA ID | EM:07435 |
International strain name | C57BL/6N-Nbastm1a(EUCOMM)Hmgu/Ieg |
Alternative name | HEPD0716_4_B11 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Nbastm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Nbas |
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 | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0716_4_B11. 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 | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | heterozygous C57BL/6NTacUSA |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Fever-associated acute infantile liver failure syndrome / Orphanet_464724
- Short stature-optic atrophy-Pelger-Huët anomaly syndrome / Orphanet_391677
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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