Strain Report - Rat Genome Database

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Pathways

Strain: WF.BBDR-(D4Arb29-D4Rat44)/Wor

Symbol: WF.BBDR-(D4Arb29-D4Rat44)/Wor
Strain: WF.BBDR-(D4Arb29-D4Rat44)
Substrain: Wor
RGD ID: 1357172
Citation ID: RRID:RGD_1357172
Ontology ID: RS:0000986
Previously known as: N8 WF.iddm4; WF.BBDR/Wor-(D4Arb29-D4Rat44)/Wor; WF.BBDR-(D4Arb29-D4Rat44)/Wor
Type: congenic
Source: University of Massachusetts Medical School, Worcerster, MA
Origin: This congenic was generated by the marker-assisted protocol where a segment of BBDR/Wor is transferred to WF background and the animals were screened using microsatellite markers.
Last Known Status: Unknown
Position
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.2464,528,739 - 64,528,994RGD_MAPPER_PIPELINEmRatBN7.2
Rnor_6.0463,537,179 - 63,537,431RGD_MAPPER_PIPELINERnor6.0
Rnor_5.0463,250,011 - 183,837,621RGD_MAPPER_PIPELINERnor5.0
RGSC_v3.4463,276,741 - 121,645,621RGD_MAPPER_PIPELINERGSC3.4





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Mammalian Phenotype

References

References - curated
# Reference Title Reference Citation
1. The iddm4 locus segregates with diabetes susceptibility in congenic WF.iddm4 rats. Mordes JP, etal., Diabetes 2002 Nov;51(11):3254-62.
2. RGD Strain RSO annotation pipeline RGD Automated Pipelines

Region

Position Markers

Flank 1 / 1 (D4Arb29)
Rat AssemblyChrPosition (strand)Source
mRatBN7.2464,528,739 - 64,528,994 (+)MAPPER
Rnor_6.0463,537,179 - 63,537,431NCBI
Rnor_5.0463,250,011 - 63,250,263UniSTS
RGSC_v3.4463,276,741 - 63,276,994RGD
RGSC_v3.4463,276,742 - 63,276,994UniSTS
RGSC_v3.1463,552,871 - 63,553,124RGD
Celera459,571,279 - 59,571,505UniSTS
Cytogenetic Map4 RGD

Flank 2 / 1 (D4Rat44)
Rat AssemblyChrPosition (strand)Source
Rnor_5.04183,837,235 - 183,837,621NCBI
RGSC_v3.44121,645,236 - 121,645,621RGD
RGSC_v3.14121,889,717 - 121,890,102RGD
RH 3.4 Map4706.9RGD
RH 3.4 Map4706.9UniSTS
RH 2.0 Map4734.6RGD
SHRSP x BN Map452.12RGD

Additional Information

RGD Curation Notes
Note Type Note Reference
strain_characteristics These were studied for the susceptibility to diabetes as they have the Iddm4 region and are homozygous the ART2a allele. 1304485