- persistence of hyaloid vascular system / IMPC
- abnormal retina morphology / IMPC
- decreased exploration in new environment / IMPC
- increased startle reflex / IMPC
- abnormal lens morphology / IMPC
- increased circulating alanine transaminase level / IMPC
- preweaning lethality, complete penetrance / IMPC
- abnormal retina vasculature morphology / IMPC
C57BL/6N-Lama1tm2a(EUCOMM)Hmgu/Ieg
Status | Available to order |
EMMA ID | EM:08512 |
International strain name | C57BL/6N-Lama1tm2a(EUCOMM)Hmgu/Ieg |
Alternative name | HEPD0596_1_A03 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Lama1tm2a(EUCOMM)Hmgu |
Gene/Transgene symbol | Lama1 |
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 HEPD0596_1_A03. 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 |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome / Orphanet_370022
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- persistence of hyaloid vascular system / MGI
- abnormal retina morphology / MGI
- abnormal gastrulation / MGI
- decreased embryo size / MGI
- no abnormal phenotype detected / MGI
- absent blastocoele / MGI
- abnormal vitreous body morphology / MGI
- abnormal retinal vasculature morphology / MGI
- abnormal ocular fundus morphology / MGI
- vitreal fibroplasia / MGI
- abnormal Reichert's membrane morphology / MGI
- embryonic growth retardation / MGI
- abnormal ectoplacental cone morphology / MGI
- abnormal Muller cell morphology / MGI
- abnormal eye electrophysiology / MGI
- thin retinal ganglion layer / MGI
- thin retinal inner nuclear layer / MGI
- abnormal retinal blood vessel morphology / MGI
- abnormal retinal blood vessel pattern / MGI
- abnormal retina inner limiting membrane morphology / MGI
- embryonic lethality between implantation and somite formation, complete penetrance / MGI
- absent Reichert's membrane / MGI
- abnormal visceral endoderm morphology / MGI
- abnormal parietal endoderm morphology / MGI
- retinal spots / MGI
- increased embryonic tissue cell apoptosis / MGI
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