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Strain: Wpk -/-

Symbol: Wpk -/-
Strain: Wpk
Full Name: Wpk homozygous rat
RGD ID: 15017094
Citation ID: RRID:RGD_15017094
Ontology ID: RS:0004764
Alleles: Tmem67wpk
Previously known as: Wpk -/- ; TMEM67−/−
Type: mutant
Source: Not Available
Origin: The wpk mutation was first recognized in 1994 in a colony of outbred Wistar rats at Utrecht University (Utrecht, The Netherlands). In 1996, a breeding pair of test-proven heterozygotes were transferred to the University of Rotterdam (Rotterdam, The Netherlands), and a new subcolony was initiated. This colony has been maintained by brother-sister matings for more than five generations. Individuals heterozygous for the mutant allele were identified in each generation by test-crossing phenotypically normal offspring from known heterozygotes. A single C to T substitution in exon 12 was identified as the mutated allele in the Wpk rat. This mutation converts a proline to a leucine in the protein products(P394L).
Genetic Status: Homozygous
Last Known Status: Unknown
Position
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.2525,536,458 - 25,589,378RGD_MAPPER_PIPELINEmRatBN7.2
Rnor_6.0525,666,138 - 25,721,056RGD_MAPPER_PIPELINERnor6.0
Rnor_5.0530,371,964 - 30,424,943RGD_MAPPER_PIPELINERnor5.0
RGSC_v3.4526,324,625 - 26,377,531RGD_MAPPER_PIPELINERGSC3.4





References

References - curated
# Reference Title Reference Citation
1. New rat model that phenotypically resembles autosomal recessive polycystic kidney disease. Nauta J, etal., J Am Soc Nephrol 2000 Dec;11(12):2272-84.
2. Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67 mutation. Shim JW, etal., Sci Rep. 2019 Jan 31;9(1):1069. doi: 10.1038/s41598-018-37620-5.

Region


Additional Information


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-11-12 Wpk -/-  Wpk homozygous rat  Wpk -/- (COPY)  Wpk homozygous rat  Symbol and/or name change 68913 APPROVED