- 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 |
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/6NTacUSA, wild-type C57BL/6NTacUSA |
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
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