- increased circulating HDL cholesterol level / IMPC
- increased total retina thickness / IMPC
- persistence of hyaloid vascular system / IMPC
- enlarged thyroid gland / IMPC
- abnormal retina blood vessel morphology / IMPC
- increased circulating bilirubin level / IMPC
- increased circulating calcium level / IMPC
- abnormal lens morphology / IMPC
- abnormal retina morphology / IMPC
- cataract / IMPC
- improved glucose tolerance / IMPC
- abnormal retina vasculature morphology / IMPC
- decreased body weight / IMPC
- increased circulating cholesterol level / IMPC
C57BL/6N-Hnf4atm1a(EUCOMM)Hmgu/Ieg
Status | Available to order |
EMMA ID | EM:08243 |
Citation information | RRID:IMSR_EM:08243 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/6N-Hnf4atm1a(EUCOMM)Hmgu/Ieg |
Alternative name | HEPD0635_7_A08 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Hnf4atm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Hnf4a |
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 HEPD0635_7_A08. 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/6NTac (USA) males, wild-type C57BL/6NTac (USA) females |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- HNF1B-related autosomal dominant tubulointerstitial kidney disease / Orphanet_93111
- MODY / Orphanet_552
- Hyperinsulinism due to HNF4A deficiency / Orphanet_263455
- Atypical Fanconi syndrome-neonatal hyperinsulinism syndrome / Orphanet_544628
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal embryo development / MGI
- abnormal ectoderm development / MGI
- absent mesoderm / MGI
- abnormal gastrulation / MGI
- decreased embryo size / MGI
- abnormal embryonic tissue morphology / MGI
- abnormal extraembryonic tissue morphology / MGI
- abnormal lipid homeostasis / MGI
- no abnormal phenotype detected / MGI
- abnormal primitive streak formation / MGI
- increased circulating ketone body level / MGI
- hepatic steatosis / MGI
- decreased circulating triglyceride level / MGI
- decreased circulating free fatty acid level / MGI
- absent allantois / MGI
- increased ectoderm apoptosis / MGI
- embryonic growth retardation / MGI
- hypokalemia / MGI
- decreased circulating iron level / MGI
- absent amnion / MGI
- decreased circulating cholesterol level / MGI
- impaired glucose tolerance / MGI
- increased circulating bilirubin level / MGI
- absent chorion / MGI
- embryonic lethality, complete penetrance / MGI
- preweaning lethality, complete penetrance / MGI
- delayed gastrulation / MGI
- small visceral yolk sac / MGI
- increased embryonic tissue cell apoptosis / MGI
Information on how we integrate external resources can be found here
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