Strain Report - Rat Genome Database

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Strain: FHH.BN(D14Rat98-D14Hmgc4)/Mcwi

Symbol: FHH.BN(D14Rat98-D14Hmgc4)/Mcwi
Strain: FHH.BN(D14Rat98-D14Hmgc4)
Substrain: Mcwi
RGD ID: 8553187
Citation ID: RRID:RGD_8553187
Ontology ID: RS:0003765
Also known as: FHH.BN(D14Rat98-D14Hmgc4)/Mcwi
Type: congenic
Source: Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin
Origin: desired segments from BN were introgressed in FHH background
Last Known Status: Unknown
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.21413,015,311 - 19,848,266RGD_MAPPER_PIPELINEmRatBN7.2
Rnor_6.01414,673,206 - 21,555,302RGD_MAPPER_PIPELINERnor6.0
Rnor_5.01414,613,528 - 21,463,742RGD_MAPPER_PIPELINERnor5.0
RGSC_v3.41414,535,071 - 21,435,476RGD_MAPPER_PIPELINERGSC3.4

Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Mammalian Phenotype



Position Markers

Flank 1 / 1 (D14Rat98)
Rat AssemblyChrPosition (strand)Source
mRatBN7.21413,015,311 - 13,015,539 (+)MAPPER
Rnor_6.01414,673,206 - 14,673,433NCBI
Rnor_5.01414,613,528 - 14,613,755UniSTS
RGSC_v3.41414,535,071 - 14,535,299RGD
RGSC_v3.41414,535,072 - 14,535,299UniSTS
RGSC_v3.11414,535,071 - 14,535,299RGD
Celera1413,068,404 - 13,068,631UniSTS
FHH x ACI Map1414.9399UniSTS
FHH x ACI Map1414.9399RGD
Cytogenetic Map14p22UniSTS

Flank 2 / 1 (D14Hmgc4)
Rat AssemblyChrPosition (strand)Source
mRatBN7.21419,848,019 - 19,848,266 (+)MAPPER
Rnor_6.01421,555,056 - 21,555,302NCBI
Rnor_5.01421,463,496 - 21,463,742UniSTS
RGSC_v3.41421,383,835 - 21,384,058UniSTS
RGSC_v3.41421,435,229 - 21,435,476RGD
RGSC_v3.41421,383,834 - 21,384,058RGD
RGSC_v3.41421,435,230 - 21,435,476UniSTS
Celera1419,173,188 - 19,173,434UniSTS
Celera1419,122,967 - 19,123,184UniSTS
Cytogenetic Map14p22-p21UniSTS

Additional Information