Gene: Slc7a9em2Mcwi (solute carrier family 7 (glycoprotein-associated amino acid transporter light chain, bo,+ system), member 9; zinc finger nuclease induced mutant 2, Medical College of Wisconsin)  Rattus norvegicus

Symbol: Slc7a9em2Mcwi
Name: solute carrier family 7 (glycoprotein-associated amino acid transporter light chain, bo,+ system), member 9; zinc finger nuclease induced mutant 2, Medical College of Wisconsin
Description: This allele was made by ZFN mutagenesis. The resulting mutation is a 10-bp frameshift deletion in exon 6 (del 746-755)
Type: allele  of Slc7a9  
Also known as: Slc7a9em2Mcwi
Latest Assembly: RGSC Genome Assembly v3.4
Position:
MapChrPositionStrandSource
 1  RGD
Model
This feature is not available in GBrowse. This may be because it does not have a position on the current reference assembly, or because it maps to either the mitochondrial (MT) chromosome or an unknown (Un) chromosome.
Browse the genome for the Rat reference assembly: v3.4


References - curated

Genomics

Related Rat Strains

Sequence

Nucleotide Sequences

Additional Information

 
More on Slc7a9em2Mcwi
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 5687701
Created: 2012-02-09
Species: Rattus norvegicus
Last Modified: 2012-02-09
Status: ACTIVE