Strain: WAG-F8m1Ycb

Symbol: WAG-F8m1Ycb
Strain: WAG-F8m1
Substrain: Ycb
Ontology ID: RS:0003433
Alleles: F8m1Ycb
Type: mutant
Source: Comparative Medicine, Yale University, Connecticut
Origin: This mutant strain carrying a naturally occurring missense mutation displays inherited coagulopathy was arising in an inbred colony of WAG/RijYcb (RGD:2314861). Mutation in the nucleotide 578 of the rat F8 gene changes amino acid 193 in the rat protein(amino acid 176 in human)from Leucine to Proline.
Last Known Status: Unknown
Position
Rat AssemblyChrPosition (strand)SourceJBrowse
Rnor_6.018367,862 - 399,242RGD_MAPPER_PIPELINERnor6.0
Rnor_5.018413,447 - 444,491RGD_MAPPER_PIPELINERnor5.0
RGSC_v3.418121,134 - 162,008RGD_MAPPER_PIPELINERGSC3.4





Disease Annotations
Phenotype Annotations
Experimental Data Annotations
References - curated
RGD Disease Portals

Region


Additional Information

Nomenclature History
 
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RGD Object Information
RGD ID: 2314904
Created: 2009-12-08
Species: Rattus norvegicus
Last Modified: 2013-06-17
Status: ACTIVE