Incidental Mutation 'IGL00844:Rnase11'
ID 13833
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rnase11
Ensembl Gene ENSMUSG00000059648
Gene Name ribonuclease, RNase A family, 11 (non-active)
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.083) question?
Stock # IGL00844
Quality Score
Status
Chromosome 14
Chromosomal Location 51286908-51287620 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 51287213 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Valine at position 114 (I114V)
Ref Sequence ENSEMBL: ENSMUSP00000075472 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000076106]
AlphaFold Q5GAM9
Predicted Effect possibly damaging
Transcript: ENSMUST00000076106
AA Change: I114V

PolyPhen 2 Score 0.455 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000075472
Gene: ENSMUSG00000059648
AA Change: I114V

DomainStartEndE-ValueType
low complexity region 5 15 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3425401B19Rik A T 14: 32,384,956 (GRCm39) C336* probably null Het
Adgrv1 T C 13: 81,688,238 (GRCm39) D994G probably damaging Het
Arhgap36 G T X: 48,586,631 (GRCm39) Q421H probably damaging Het
Arhgef17 A G 7: 100,578,656 (GRCm39) V764A probably benign Het
Atf7ip T C 6: 136,537,679 (GRCm39) V304A probably benign Het
Babam2 T A 5: 32,164,651 (GRCm39) F299L probably damaging Het
Ceacam11 T G 7: 17,707,595 (GRCm39) D126E possibly damaging Het
Dlg3 C A X: 99,850,199 (GRCm39) H197Q probably damaging Het
Dnmt3a T A 12: 3,955,622 (GRCm39) L590Q probably damaging Het
Fras1 A G 5: 96,682,712 (GRCm39) probably benign Het
Gabarapl1 T C 6: 129,515,598 (GRCm39) F79L probably benign Het
Gabbr2 A G 4: 46,875,711 (GRCm39) V137A probably damaging Het
Gphn T C 12: 78,711,342 (GRCm39) probably benign Het
Hnrnpr A G 4: 136,066,516 (GRCm39) I399M probably benign Het
Madd A C 2: 90,998,213 (GRCm39) S636A probably damaging Het
Pi15 T C 1: 17,691,764 (GRCm39) probably benign Het
Ppp3cb A T 14: 20,581,754 (GRCm39) M87K possibly damaging Het
Ptpro C A 6: 137,391,237 (GRCm39) H786N probably damaging Het
Sirt4 A G 5: 115,617,685 (GRCm39) probably null Het
Stab1 T C 14: 30,869,023 (GRCm39) D1534G probably damaging Het
Sulf2 A G 2: 165,936,412 (GRCm39) S185P possibly damaging Het
Svs6 A C 2: 164,159,507 (GRCm39) K90T possibly damaging Het
Tdrd6 A G 17: 43,928,087 (GRCm39) M2102T probably benign Het
Ttll5 T C 12: 85,890,600 (GRCm39) V77A probably damaging Het
Usp9x T G X: 12,994,685 (GRCm39) S959A probably benign Het
Vps50 C T 6: 3,532,177 (GRCm39) Q227* probably null Het
Zfp57 C A 17: 37,320,514 (GRCm39) Q120K possibly damaging Het
Zswim2 T C 2: 83,754,115 (GRCm39) N182D probably benign Het
Other mutations in Rnase11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01024:Rnase11 APN 14 51,287,321 (GRCm39) missense probably benign 0.05
R1638:Rnase11 UTSW 14 51,287,058 (GRCm39) missense possibly damaging 0.92
R1809:Rnase11 UTSW 14 51,287,184 (GRCm39) missense probably benign 0.00
R2844:Rnase11 UTSW 14 51,287,227 (GRCm39) missense probably damaging 0.99
R5478:Rnase11 UTSW 14 51,287,332 (GRCm39) missense probably damaging 0.99
R7607:Rnase11 UTSW 14 51,287,029 (GRCm39) missense probably damaging 0.99
R8077:Rnase11 UTSW 14 51,287,398 (GRCm39) missense probably damaging 0.99
R9743:Rnase11 UTSW 14 51,287,370 (GRCm39) missense probably benign 0.36
Z1176:Rnase11 UTSW 14 51,287,345 (GRCm39) missense possibly damaging 0.94
Posted On 2012-12-06