- 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 |
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 |
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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