Incidental Mutation 'R5401:Qng1'
ID 430010
Institutional Source Beutler Lab
Gene Symbol Qng1
Ensembl Gene ENSMUSG00000021550
Gene Name Q-nucleotide N-glycosylase 1
Synonyms 2210016F16Rik
MMRRC Submission 042972-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.139) question?
Stock # R5401 (G1)
Quality Score 225
Status Validated
Chromosome 13
Chromosomal Location 58527860-58533039 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 58530405 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Serine at position 202 (A202S)
Ref Sequence ENSEMBL: ENSMUSP00000022032 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022032]
AlphaFold G3X8U3
Predicted Effect probably benign
Transcript: ENSMUST00000022032
AA Change: A202S

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000022032
Gene: ENSMUSG00000021550
AA Change: A202S

DomainStartEndE-ValueType
low complexity region 31 41 N/A INTRINSIC
Pfam:Q_salvage 53 338 9.7e-122 PFAM
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.7%
  • 10x: 97.3%
  • 20x: 95.4%
Validation Efficiency 97% (66/68)
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700001J11Rik A G 9: 39,962,338 (GRCm39) noncoding transcript Het
1700025H01Rik G T 16: 30,018,801 (GRCm39) noncoding transcript Het
9330159F19Rik T C 10: 29,101,136 (GRCm39) V503A probably benign Het
Acacb A G 5: 114,347,914 (GRCm39) N995S possibly damaging Het
Anapc4 A G 5: 53,020,991 (GRCm39) K630R probably benign Het
Ankrd13a A C 5: 114,930,234 (GRCm39) Q206H probably damaging Het
Ano10 A T 9: 122,090,356 (GRCm39) L319Q probably damaging Het
Camkk2 T A 5: 122,884,398 (GRCm39) D341V probably damaging Het
Ccdc88a A G 11: 29,413,279 (GRCm39) I606V probably benign Het
Cdv3 G T 9: 103,242,316 (GRCm39) probably benign Het
Cep97 A G 16: 55,745,315 (GRCm39) V155A probably benign Het
Cmya5 T C 13: 93,228,476 (GRCm39) E2204G probably damaging Het
Cracr2b A G 7: 141,046,136 (GRCm39) *395W probably null Het
Defa27 A G 8: 21,805,710 (GRCm39) E50G possibly damaging Het
Dnah7a A G 1: 53,670,812 (GRCm39) I480T probably benign Het
Ep400 C A 5: 110,831,037 (GRCm39) D2210Y unknown Het
Fam170a T A 18: 50,413,618 (GRCm39) S28T probably benign Het
Fancc C A 13: 63,550,767 (GRCm39) K18N probably damaging Het
Flt4 AC ACC 11: 49,541,861 (GRCm39) probably null Het
Fndc8 T G 11: 82,788,676 (GRCm39) S169A possibly damaging Het
Get3 A T 8: 85,745,173 (GRCm39) I298N possibly damaging Het
Herc1 T C 9: 66,409,338 (GRCm39) Y4688H probably damaging Het
Ighv11-2 A T 12: 114,011,959 (GRCm39) D85E possibly damaging Het
Kat14 T C 2: 144,231,180 (GRCm39) F196L possibly damaging Het
Kctd19 C T 8: 106,109,617 (GRCm39) V942I probably benign Het
Llgl1 A G 11: 60,597,297 (GRCm39) S249G probably benign Het
Map1a T C 2: 121,130,153 (GRCm39) V323A probably damaging Het
Or4m1 C A 14: 50,557,566 (GRCm39) C242F probably damaging Het
Phf21a C A 2: 92,182,097 (GRCm39) T342K possibly damaging Het
Piezo2 T A 18: 63,217,811 (GRCm39) D1122V possibly damaging Het
Pklr A G 3: 89,049,173 (GRCm39) Y173C probably damaging Het
Plcz1 G T 6: 139,938,778 (GRCm39) probably null Het
Polr3a T C 14: 24,505,009 (GRCm39) I1084V possibly damaging Het
Prom1 A T 5: 44,158,147 (GRCm39) Y845N probably damaging Het
Ret A T 6: 118,158,936 (GRCm39) S159T probably benign Het
Rfx1 C A 8: 84,793,005 (GRCm39) probably null Het
Scp2 A T 4: 108,001,976 (GRCm39) probably null Het
Sh3bp5 C A 14: 31,099,452 (GRCm39) R265L probably benign Het
Slc22a30 G A 19: 8,321,757 (GRCm39) Q436* probably null Het
Smad5 T C 13: 56,875,282 (GRCm39) F157L probably benign Het
Smarcc2 C A 10: 128,301,373 (GRCm39) D210E probably damaging Het
Sptlc3 T C 2: 139,478,643 (GRCm39) L534P possibly damaging Het
Srrm1 A G 4: 135,051,380 (GRCm39) probably benign Het
Srsf11 C T 3: 157,728,981 (GRCm39) probably benign Het
Sugct T A 13: 17,032,455 (GRCm39) Q432H probably damaging Het
Tex9 A T 9: 72,394,060 (GRCm39) probably null Het
Tsc1 C A 2: 28,576,920 (GRCm39) S1073* probably null Het
Vmn1r72 T C 7: 11,403,843 (GRCm39) S202G probably damaging Het
Vmn2r55 A G 7: 12,385,871 (GRCm39) V703A probably benign Het
Vmn2r67 A T 7: 84,785,765 (GRCm39) Y747N probably damaging Het
Zcchc4 A G 5: 52,964,419 (GRCm39) I292V probably benign Het
Zfp998 T C 13: 66,579,722 (GRCm39) R254G probably benign Het
Zswim2 C T 2: 83,755,589 (GRCm39) G104E possibly damaging Het
Other mutations in Qng1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01160:Qng1 APN 13 58,529,790 (GRCm39) missense probably damaging 1.00
IGL02302:Qng1 APN 13 58,529,749 (GRCm39) missense probably damaging 1.00
PIT1430001:Qng1 UTSW 13 58,532,827 (GRCm39) nonsense probably null
R0055:Qng1 UTSW 13 58,531,980 (GRCm39) missense probably damaging 1.00
R0055:Qng1 UTSW 13 58,531,980 (GRCm39) missense probably damaging 1.00
R2874:Qng1 UTSW 13 58,530,384 (GRCm39) missense probably damaging 1.00
R3954:Qng1 UTSW 13 58,532,203 (GRCm39) missense probably damaging 0.97
R3956:Qng1 UTSW 13 58,532,203 (GRCm39) missense probably damaging 0.97
R4012:Qng1 UTSW 13 58,529,800 (GRCm39) nonsense probably null
R4212:Qng1 UTSW 13 58,529,805 (GRCm39) missense probably damaging 1.00
R4469:Qng1 UTSW 13 58,530,239 (GRCm39) missense probably damaging 1.00
R4712:Qng1 UTSW 13 58,529,617 (GRCm39) missense probably benign 0.06
R6876:Qng1 UTSW 13 58,532,910 (GRCm39) missense probably damaging 1.00
R6957:Qng1 UTSW 13 58,529,775 (GRCm39) missense probably damaging 1.00
R7285:Qng1 UTSW 13 58,532,199 (GRCm39) missense probably damaging 1.00
R7599:Qng1 UTSW 13 58,529,649 (GRCm39) missense probably damaging 0.99
R8553:Qng1 UTSW 13 58,532,694 (GRCm39) missense probably damaging 0.96
R8939:Qng1 UTSW 13 58,532,875 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GCAAACCTTTGAGGAGCTTC -3'
(R):5'- GCACTGAGGTTTAACTTGCATG -3'

Sequencing Primer
(F):5'- GCAAACCTTTGAGGAGCTTCTTTAG -3'
(R):5'- TATCACATCACCTGGGACTGAGTG -3'
Posted On 2016-09-06