- increased startle reflex / IMPC
C57BL/6NTac-Cacnb4tm1a(EUCOMM)Hmgu/IcsOrl
Status | Available to order |
EMMA ID | EM:07656 |
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 |
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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