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URL: https://rgd.mcw.edu/rgdweb/report/strain/main.html?id=13782371
Proper Citation: RRID:RGD_13782371
Description: Rattus norvegicus with name SD-Cacna1f csnb from RGD.
Species: Rattus norvegicus
Notes: A naturally-occurring mutation in Cacna1f was identified in a male Sprague Dawley rat with the phenotype of congenital stationary night blindness.Sequence analysis revealed a point mutation of C to T at position 2941, which changes codon 981 from arginine (CGA) to a stop codon (TGA). This R981Stop point mutation was predicted to lead to a version of protein shortened by a total of 999 amino acids, and missing the C-terminal and, in particular, part of the third and all of the fourth ion transport domains.
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Source: Integrated Animals
Source Database: Rat Genome Database (RGD)
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