- increased startle reflex / IMPC
C57BL/6NTac-Cacnb4tm1a(EUCOMM)Hmgu/IcsOrl
Status | Available to order |
EMMA ID | EM:07656 |
Citation information | RRID:IMSR_EM:07656 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-Cacnb4tm1a(EUCOMM)Hmgu/IcsOrl |
Alternative name | HEPD0507_8_G08 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Cacnb4tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Cacnb4 |
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 | ICS, Institut Clinique de la Souris |
Provider affiliation | ICS, Institut Clinique de la Souris |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0507_8_G08. 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 | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NTac males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Juvenile myoclonic epilepsy / Orphanet_307
- Episodic ataxia type 5 / Orphanet_211067
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- increased startle reflex / IMPC
MGI phenotypes (gene matching)
- abnormal head movements / MGI
- pituitary gland hyperplasia / MGI
- small spleen / MGI
- enlarged lymph nodes / MGI
- small thymus / MGI
- abnormal motor neuron morphology / MGI
- convulsive seizures / MGI
- abnormal neuromuscular synapse morphology / MGI
- absent corpus luteum / MGI
- decreased body size / MGI
- abnormal locomotor behavior / MGI
- ataxia / MGI
- circling / MGI
- hypoactivity / MGI
- impaired coordination / MGI
- abnormal gait / MGI
- abnormal posture / MGI
- impaired righting response / MGI
- impaired limb coordination / MGI
- postnatal growth retardation / MGI
- abnormal thymus involution / MGI
- reduced fertility / MGI
- male infertility / MGI
- seizures / MGI
- abnormal fear/anxiety-related behavior / MGI
- abnormal motor capabilities/coordination/movement / MGI
- premature death / MGI
- abnormal CNS synaptic transmission / MGI
- abnormal lymph node morphology / MGI
- abnormal Peyer's patch germinal center morphology / MGI
- tonic seizures / MGI
- abnormal locomotor activation / MGI
- nervous system phenotype / MGI
- clonic seizures / MGI
- increased length of allograft survival / MGI
- abnormal behavior / MGI
- abnormal brain wave pattern / MGI
- decreased lymphocyte cell number / MGI
- diarrhea / MGI
- decreased double-positive T cell number / MGI
- cachexia / MGI
- lethargy / MGI
- hearing/vestibular/ear phenotype / MGI
- behavior/neurological phenotype / MGI
- vision/eye phenotype / MGI
- abnormal nerve conduction / MGI
- abnormal CD4-positive, alpha-beta T cell physiology / MGI
- abnormal eye electrophysiology / MGI
- decreased Peyer's patch number / MGI
- small Peyer's patches / MGI
- increased IgG1 level / MGI
- decreased interferon-gamma secretion / MGI
- abnormal interleukin secretion / MGI
- decreased interleukin-2 secretion / MGI
- decreased nerve conduction velocity / MGI
- impaired behavioral response to xenobiotic / MGI
- absent thymus corticomedullary boundary / MGI
- facial muscle spasm / MGI
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