- decreased hematocrit / IMPC
- abnormal head morphology / IMPC
- abnormal cranium morphology / IMPC
- decreased body length / IMPC
- persistence of hyaloid vascular system / IMPC
- abnormal lens morphology / IMPC
- cataract / IMPC
- abnormal cornea morphology / IMPC
- abnormal iris morphology / IMPC
- abnormal retina morphology / IMPC
- decreased anxiety-related response / IMPC
- hyperactivity / IMPC
- decreased locomotor activity / IMPC
- increased hematocrit / IMPC
- abnormal vitreous body morphology / IMPC
- decreased vertical activity / IMPC
- abnormal retina vasculature morphology / IMPC
- decreased hemoglobin content / IMPC
- decreased erythrocyte cell number / IMPC
- iris synechia / IMPC
- abnormal auditory brainstem response / IMPC
- abnormal behavior / IMPC
- increased spleen weight / IMPC
- decreased blood urea nitrogen level / IMPC
- abnormal optic disk morphology / IMPC
- increased grip strength / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- decreased thigmotaxis / IMPC
C57BL/6NCrl-Mettl5em1(IMPC)Hmgu/Ieg
Status | Available to order |
EMMA ID | EM:13474 |
Citation information | RRID:IMSR_EM:13474 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/6NCrl-Mettl5em1(IMPC)Hmgu/Ieg |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Mettl5em1(IMPC)Hmgu |
Gene/Transgene symbol | Mettl5 |
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 CRISPR zygote microinjection. For further details see the project page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References |
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Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | heterozygous C57BL/6N males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive primary microcephaly / Orphanet_2512
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- abnormal cornea morphology / IMPC
- abnormal head morphology / IMPC
- persistence of hyaloid vascular system / IMPC
- abnormal iris morphology / IMPC
- cataract / IMPC
- abnormal auditory brainstem response / IMPC
- decreased hemoglobin content / IMPC
- decreased thigmotaxis / IMPC
- decreased erythrocyte cell number / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- abnormal cranium morphology / IMPC
- abnormal vitreous body morphology / IMPC
- iris synechia / IMPC
- hyperactivity / IMPC
- decreased vertical activity / IMPC
- abnormal optic disk morphology / IMPC
- abnormal lens morphology / IMPC
- decreased locomotor activity / IMPC
- abnormal retina morphology / IMPC
- decreased body length / IMPC
- abnormal behavior / IMPC
- increased grip strength / IMPC
- abnormal retina vasculature morphology / IMPC
- increased spleen weight / IMPC
- decreased anxiety-related response / IMPC
- increased hematocrit / IMPC
- decreased blood urea nitrogen level / IMPC
- decreased hematocrit / IMPC
Literature references
- The rRNA m6A methyltransferase METTL5 is involved in pluripotency and developmental programs.;Ignatova Valentina V, Stolz Paul, Kaiser Steffen, Gustafsson Tobias H, Lastres Palma Rico, Sanz-Moreno Adrián, Cho Yi-Li, Amarie Oana V, Aguilar-Pimentel Antonio, Klein-Rodewald Tanja, Calzada-Wack Julia, Becker Lore, Marschall Susan, Kraiger Markus, Garrett Lillian, Seisenberger Claudia, Hölter Sabine M, Borland Kayla, Van De Logt Erik, Jansen Pascal W T C, Baltissen Marijke P, Valenta Magdalena, Vermeulen Michiel, Wurst Wolfgang, Gailus-Durner Valerie, Fuchs Helmut, Hrabe de Angelis Martin, Rando Oliver J, Kellner Stefanie M, Bultmann Sebastian, Schneider Robert, ;2020;Genes & development;34;715-729; 32217665
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