- kyphosis / MGI
- abnormal long bone hypertrophic chondrocyte zone / MGI
- diluted coat color / MGI
- hindlimb paralysis / MGI
- abnormal ovarian folliculogenesis / MGI
- absent corpus luteum / MGI
- small testis / MGI
- abnormal body weight / MGI
- decreased body weight / MGI
- decreased body size / MGI
- abnormal lens morphology / MGI
- cataract / MGI
- hypoactivity / MGI
- abnormal coat appearance / MGI
- infertility / MGI
- male infertility / MGI
- female infertility / MGI
- abnormal coat/hair pigmentation / MGI
- abnormal glucose homeostasis / MGI
- premature death / MGI
- abnormal postnatal growth/weight/body size / MGI
- abnormal skeleton development / MGI
- disproportionate dwarf / MGI
- oligozoospermia / MGI
- short tibia / MGI
- short femur / MGI
- priapism / MGI
- abnormal long bone epiphyseal plate proliferative zone / MGI
- abnormal reproductive system development / MGI
- decreased bone mass / MGI
- small vertebrae / MGI
- increased osteoclast cell number / MGI
- skeleton phenotype / MGI
- decreased thyroxine level / MGI
- decreased long bone epiphyseal plate size / MGI
- decreased spleen red pulp amount / MGI
- nervous / MGI
- nuclear cataracts / MGI
- decreased glutathione level / MGI
- glutathionuria / MGI
- decreased circulating cysteine level / MGI
- increased circulating glutathione level / MGI
C57BL/6NTac-Ggt1tm1a(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:04434 |
International strain name | C57BL/6NTac-Ggt1tm1a(EUCOMM)Wtsi/H |
Alternative name | EPD0183_3_C02 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Ggt1tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Ggt1 |
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 | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0183_3_C02. 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 | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Animals used for archiving | heterozygous C57BL/6NTac |
Breeding at archiving centre | Chimeras were mated to C57BL/6NTac and maintained on this background thereafter. |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Gamma-glutamyl transpeptidase deficiency / Orphanet_33573
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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