|Institutional Source||Beutler Lab|
|Gene Name||mutS homolog 2|
|Is this an essential gene?||Probably essential (E-score: 0.828)|
|Stock #||R6191 (G1)|
|Chromosomal Location||87672330-87723713 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||A to G at 87723472 bp|
|Amino Acid Change||Isoleucine to Valine at position 926 (I926V)|
|Ref Sequence||ENSEMBL: ENSMUSP00000024967 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000024967]|
|Predicted Effect||probably benign
AA Change: I926V
PolyPhen 2 Score 0.025 (Sensitivity: 0.95; Specificity: 0.81)
AA Change: I926V
|Meta Mutation Damage Score||0.0776|
|Coding Region Coverage||
|Validation Efficiency||99% (84/85)|
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This locus is frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). When cloned, it was discovered to be a human homolog of the E. coli mismatch repair gene mutS, consistent with the characteristic alterations in microsatellite sequences (RER+ phenotype) found in HNPCC. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]
PHENOTYPE: Mice homozygous for a number of different targeted mutations develop lymphomas. In addition, depending on the allele, mutants may show intestinal adenocarcinomas and reduced class switch recombination or adenocarcinomas and abnormal mismatch repair or squamous cell carcinomas and skin tumors. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Msh2||
(F):5'- TGCTTACGCTGGAGATGACC -3'
(R):5'- CCCAGCTACAGACGGTAATG -3'
(F):5'- GGTGGATCTTGACCATCTGTAAACC -3'
(R):5'- CCAGCTACAGACGGTAATGTTTTC -3'