- increased brown adipose tissue amount / MGI
- decreased bone mineral density / MGI
- kyphoscoliosis / MGI
- kyphosis / MGI
- muscle spasm / MGI
- tremors / MGI
- weakness / MGI
- decreased body weight / MGI
- decreased body size / MGI
- abnormal maternal nurturing / MGI
- ataxia / MGI
- hypoactivity / MGI
- abnormal gait / MGI
- decreased exploration in new environment / MGI
- abnormal spatial learning / MGI
- abnormal contextual conditioning behavior / MGI
- reduced long term potentiation / MGI
- reduced long term depression / MGI
- hunched posture / MGI
- limb grasping / MGI
- impaired righting response / MGI
- impaired limb coordination / MGI
- impaired balance / MGI
- reduced fertility / MGI
- reduced female fertility / MGI
- male infertility / MGI
- premature death / MGI
- abnormal fertility/fecundity / MGI
- abnormal nervous system electrophysiology / MGI
- abnormal sexual interaction / MGI
- albuminuria / MGI
- abnormal excitatory postsynaptic currents / MGI
- nervous system phenotype / MGI
- abnormal proximal convoluted tubule morphology / MGI
- increased susceptibility to injury / MGI
- glomerulosclerosis / MGI
- narrow eye opening / MGI
- abnormal podocyte morphology / MGI
- behavior/neurological phenotype / MGI
- podocyte foot process effacement / MGI
- decreased bone mineral content / MGI
- abnormal renal glomerulus basement membrane morphology / MGI
- renal cast / MGI
- increased renal glomerulus basement membrane thickness / MGI
- abnormal glomerular filtration barrier function / MGI
- abnormal electroretinogram waveform feature / MGI
C57BL/6NTac-Grm1em2(IMPC)H/H
Status | Available to order |
EMMA ID | EM:12463 |
Citation information | RRID:IMSR_EM:12463 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/6NTac-Grm1em2(IMPC)H/H |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Grm1em2(IMPC)H |
Gene/Transgene symbol | Grm1 |
Information from provider
Provider | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
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 | None available |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency / Orphanet_324262
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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