- decreased circulating HDL cholesterol level / IMPC
- decreased circulating phosphate level / IMPC
- decreased leukocyte cell number / IMPC
- hypoactivity / IMPC
- decreased startle reflex / IMPC
- male infertility / IMPC
- female infertility / IMPC
- decreased circulating alkaline phosphatase level / IMPC
- thrombocytopenia / IMPC
- abnormal behavior / IMPC
- decreased circulating cholesterol level / IMPC
- decreased circulating serum albumin level / IMPC
- decreased prepulse inhibition / IMPC
- decreased grip strength / IMPC
- decreased red blood cell distribution width / IMPC
- decreased respiratory quotient / IMPC
- decreased food intake / IMPC
C57BL/6N-Gatmtm1b(KOMP)Wtsi/Ieg
Status | Available to order |
EMMA ID | EM:09101 |
International strain name | C57BL/6N-Gatmtm1b(KOMP)Wtsi/Ieg |
Alternative name | EPD0218_5_E08 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Gatmtm1b(KOMP)Wtsi, |
Gene/Transgene symbol | Gatm |
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 KOMP ES clone EPD0218_5_E08. For further details on the construction of this clone see the page at the IMPC portal. The critical exon(s) were flanked by loxP sites, and subsequent cre expression excised this critical sequence resulting in a knockout reporter allele (Gt(ROSA)26Sor |
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, heterozygous C57BL/6NTac |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Primary Fanconi renotubular syndrome / Orphanet_3337
- L-Arginine:glycine amidinotransferase deficiency / Orphanet_35704
IMPC phenotypes (allele matching)
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