- decreased bone mineral density / IMPC
- abnormal forelimb morphology / IMPC
- abnormal gait / IMPC
- abnormal response to new environment / IMPC
- increased startle reflex / IMPC
- limb grasping / IMPC
- increased mean corpuscular volume / IMPC
- abnormal bone mineralization / IMPC
- abnormal locomotor activation / IMPC
- increased lean body mass / IMPC
- decreased lean body mass / IMPC
- corneal vascularization / IMPC
- decreased circulating amylase level / IMPC
- increased circulating iron level / IMPC
- increased total body fat amount / IMPC
- increased bone mineral content / IMPC
- preweaning lethality, complete penetrance / IMPC
C3H.C-Trpc3Mwk/H
| Status | Available to order |
| EMMA ID | EM:00431 |
| Citation information | RRID:IMSR_EM:00431 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 | C3H.C-Trpc3Mwk/H |
| Alternative name | BHV7 |
| Strain type | Induced Mutant Strains : Chemically-induced |
| Allele/Transgene symbol | Trpc3Mwk |
| Gene/Transgene symbol | Trpc3 |
Information from provider
| Provider | Pat Nolan |
| Provider affiliation | MRC Mammalian Genetics Unit |
| Genetic information | ENU-induced point mutation in exon 7: an A-to-G nucleotide change at position 1903. This causes a threonine-to-alanine amino acid change at residue 635 in the highly conserved S4/S5 linker region. |
| Phenotypic information | Mice heterozygous for this mutation are usually small and exhibit a staggering phenotype. These ataxic mice have limited movement in their back legs. Homozygotes have not been tested. |
| 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
- Spinocerebellar ataxia type 41 / Orphanet_458798
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- decreased circulating amylase level / IMPC
- decreased lean body mass / IMPC
- increased circulating iron level / IMPC
- abnormal gait / IMPC
- abnormal locomotor activation / IMPC
- increased lean body mass / IMPC
- abnormal bone mineralization / IMPC
- corneal vascularization / IMPC
- increased bone mineral content / IMPC
- increased total body fat amount / IMPC
- decreased bone mineral density / IMPC
- limb grasping / IMPC
- increased startle reflex / IMPC
- preweaning lethality, complete penetrance / IMPC
- abnormal response to new environment / IMPC
- increased mean corpuscular volume / IMPC
- abnormal forelimb morphology / IMPC
MGI phenotypes (gene matching)
- abnormal Purkinje cell morphology / MGI
- decreased Purkinje cell number / MGI
- decreased body size / MGI
- abnormal gait / MGI
- impaired limb coordination / MGI
- impaired balance / MGI
- premature death / MGI
- abnormal nervous system electrophysiology / MGI
- abnormal excitatory postsynaptic currents / MGI
- nervous system phenotype / MGI
- abnormal eye physiology / MGI
- immune system phenotype / MGI
- hematopoietic system phenotype / MGI
- abnormal Purkinje cell dendrite morphology / MGI
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