NBRP Rat No: 0756 |
Strain name: F344.GRY-Cacna1agryScn1am1Kyo/Okym |
Commmon Name: RGD: F344-Cacna1agryScn1am1Kyo/Okym |
Rat Genome Database |
Principal Investigator: |
Iori Ohmori Okayama University Tsushima 3-chome 1-1, Kita-ku, Okayama 700-8530 Japan |
Tel: Fax: |
Email: iori@md.okayama-u.ac.jp |
Preservation Status: |
Embryo Sperm Living Animals |
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Coat Color |
アルビノ |
Inbred Generations |
F23 |
Usage Restrictions |
In publishing the research results to be obtained by use of the BIOLOGICAL RESOURCE, an acknowledgment to the DEPOSITOR is requested. |
Genetic Status |
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Comercial Availability |
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Research Category |
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Gene Affected |
Cacna1a-M251K ヘテロ Scn1a-N1417H ホモ |
Origin |
GRY/Idr (GRY/Idr has the M251K mutation in the Cacna1a gene) was backcrossed to F344/NSlc, and then crossed to HISS rat (HISS rat has the N1417H mutation in the Scn1a gene) to generate Scn1a/Cacna1a double mutant rats. |
Strain characteristics |
Homo double mutant rats are smaller in size than each single mutant rat. This strain has cerebellar ataxia and walks with its hind limbs wobbling in a wide position. This strain is complicated by epileptic seizures, with absence and myoclonic seizures and seizures similar to partial seizures. In addition, the cramp threshold for hyperthermia is low. |
Breeding Conditions |
Homo double mutant rats, both males and females, are unable to reproduce by natural mating.
Cacna1a hetero mutant rats and Scn1a homo mutant rats must be crossed to create homo double mutant rats. |
Genotyping |
Primers: Forward 5'-TCTCTGTCTCCCCAGGTTTAC-3', Reverse 5'-GTGGCTAACACACAGCTTTGC-3'
PCR analysis: 94℃ 3 min, 40 cycles of 94℃ 30 sec/ 64℃ 1 min/ 72℃ 1 min, and 72℃ 7 min
Digestion of PCR products by PsiI (37℃, 2 hrs). |
References |
Scn1a and Cacna1a mutations mutually alter their original phenotypes in rats.
Ohmori I, Kobayashi K, Ouchida M.
Neurochemistry International, 2020. |
Additional strain information |
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