Incidental Mutation 'IGL03169:Vmn1r113'
ID 411745
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r113
Ensembl Gene ENSMUSG00000091638
Gene Name vomeronasal 1 receptor 113
Synonyms Gm5748
Accession Numbers
Essential gene? Probably non essential (E-score: 0.060) question?
Stock # IGL03169
Quality Score
Status
Chromosome 7
Chromosomal Location 20521210-20522133 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 20522012 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Leucine at position 268 (H268L)
Ref Sequence ENSEMBL: ENSMUSP00000133307 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000168794] [ENSMUST00000173723]
AlphaFold G3UWI8
Predicted Effect probably benign
Transcript: ENSMUST00000168794
AA Change: H258L

PolyPhen 2 Score 0.062 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000126041
Gene: ENSMUSG00000091638
AA Change: H258L

DomainStartEndE-ValueType
Pfam:TAS2R 8 288 4.2e-8 PFAM
Pfam:V1R 41 288 2.8e-8 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000173723
AA Change: H268L

PolyPhen 2 Score 0.106 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000133307
Gene: ENSMUSG00000091638
AA Change: H268L

DomainStartEndE-ValueType
Pfam:TAS2R 8 298 4e-16 PFAM
Pfam:7tm_1 31 290 9.3e-7 PFAM
Pfam:V1R 41 298 5e-17 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrl1 A T 8: 84,658,624 (GRCm39) I548F probably damaging Het
Adgrv1 T A 13: 81,652,019 (GRCm39) Q2995L probably damaging Het
Capn9 T C 8: 125,332,616 (GRCm39) I485T probably damaging Het
Ccdc17 T A 4: 116,454,957 (GRCm39) I197N probably damaging Het
Chl1 T A 6: 103,642,928 (GRCm39) L222Q probably damaging Het
Ctla4 T C 1: 60,953,764 (GRCm39) probably benign Het
Cyp2d12 T C 15: 82,443,492 (GRCm39) S485P probably benign Het
Ddx50 A T 10: 62,457,166 (GRCm39) probably null Het
Dlgap4 C A 2: 156,552,938 (GRCm39) probably null Het
Dpysl4 G A 7: 138,679,826 (GRCm39) probably null Het
Erbin T C 13: 103,977,740 (GRCm39) M606V possibly damaging Het
Fat4 T G 3: 39,011,547 (GRCm39) S2216A probably benign Het
Frem2 T C 3: 53,429,713 (GRCm39) N2779S probably benign Het
Fut1 T C 7: 45,268,457 (GRCm39) V82A probably benign Het
Gnb1l C T 16: 18,359,205 (GRCm39) A2V probably damaging Het
Hdac1 C T 4: 129,412,624 (GRCm39) E327K probably null Het
Hdlbp A G 1: 93,344,309 (GRCm39) V819A possibly damaging Het
Ift122 T C 6: 115,882,922 (GRCm39) probably benign Het
Iqgap2 T C 13: 95,867,785 (GRCm39) probably null Het
Kntc1 T C 5: 123,913,884 (GRCm39) V613A possibly damaging Het
Lamb1 T C 12: 31,373,645 (GRCm39) V1458A probably damaging Het
Lef1 A G 3: 130,988,312 (GRCm39) K265R probably damaging Het
Lrp2 T C 2: 69,353,538 (GRCm39) D574G probably damaging Het
Mterf2 C T 10: 84,956,324 (GRCm39) R100H probably benign Het
Nr1d2 C T 14: 18,216,703 (GRCm38) R155Q probably damaging Het
Obscn T C 11: 58,964,122 (GRCm39) T3304A probably damaging Het
Or2j3 G T 17: 38,615,992 (GRCm39) S120Y probably damaging Het
Or4a78 A G 2: 89,497,831 (GRCm39) I133T possibly damaging Het
Os9 G A 10: 126,934,463 (GRCm39) T391M probably benign Het
Parp6 C A 9: 59,557,300 (GRCm39) Y131* probably null Het
Plxdc1 T C 11: 97,823,146 (GRCm39) E358G possibly damaging Het
Ppef2 C T 5: 92,383,759 (GRCm39) W450* probably null Het
Ptprc A T 1: 138,041,357 (GRCm39) S167R probably benign Het
Rad54l2 T C 9: 106,596,263 (GRCm39) D225G probably benign Het
Rgs7 T C 1: 175,098,401 (GRCm39) I53V possibly damaging Het
Rpa1 T C 11: 75,192,183 (GRCm39) D607G probably damaging Het
Shisa5 T A 9: 108,885,560 (GRCm39) H213Q probably damaging Het
Syncrip A G 9: 88,338,496 (GRCm39) probably benign Het
Taf4b T G 18: 14,954,592 (GRCm39) V556G probably damaging Het
Tgif1 A C 17: 71,151,836 (GRCm39) S258R possibly damaging Het
Tmem106a T C 11: 101,481,284 (GRCm39) probably benign Het
Vmn1r40 A T 6: 89,692,005 (GRCm39) Q274L probably damaging Het
Wdr70 A C 15: 7,913,821 (GRCm39) I609M possibly damaging Het
Wdr91 G A 6: 34,882,426 (GRCm39) S241L possibly damaging Het
Zfyve9 T C 4: 108,553,022 (GRCm39) Y713C probably damaging Het
Other mutations in Vmn1r113
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01908:Vmn1r113 APN 7 20,521,943 (GRCm39) missense probably damaging 1.00
IGL02082:Vmn1r113 APN 7 20,521,672 (GRCm39) missense probably benign
IGL02148:Vmn1r113 APN 7 20,521,747 (GRCm39) missense probably benign 0.14
R0593:Vmn1r113 UTSW 7 20,521,388 (GRCm39) missense probably damaging 0.99
R0669:Vmn1r113 UTSW 7 20,521,345 (GRCm39) missense probably benign 0.00
R1212:Vmn1r113 UTSW 7 20,521,356 (GRCm39) missense probably benign 0.19
R1693:Vmn1r113 UTSW 7 20,521,532 (GRCm39) missense probably damaging 0.98
R2228:Vmn1r113 UTSW 7 20,521,832 (GRCm39) missense probably damaging 1.00
R3945:Vmn1r113 UTSW 7 20,521,637 (GRCm39) missense probably benign 0.00
R4209:Vmn1r113 UTSW 7 20,521,535 (GRCm39) missense probably benign 0.44
R5038:Vmn1r113 UTSW 7 20,521,419 (GRCm39) missense possibly damaging 0.70
R6306:Vmn1r113 UTSW 7 20,521,792 (GRCm39) missense probably damaging 1.00
R6623:Vmn1r113 UTSW 7 20,521,991 (GRCm39) missense probably benign 0.01
R6675:Vmn1r113 UTSW 7 20,521,903 (GRCm39) missense probably benign 0.02
R6677:Vmn1r113 UTSW 7 20,521,903 (GRCm39) missense probably benign 0.02
R6678:Vmn1r113 UTSW 7 20,521,903 (GRCm39) missense probably benign 0.02
R6968:Vmn1r113 UTSW 7 20,521,876 (GRCm39) missense probably damaging 1.00
R7054:Vmn1r113 UTSW 7 20,521,427 (GRCm39) missense probably benign 0.14
R7256:Vmn1r113 UTSW 7 20,521,370 (GRCm39) missense probably damaging 1.00
R8926:Vmn1r113 UTSW 7 20,521,874 (GRCm39) missense possibly damaging 0.82
R9131:Vmn1r113 UTSW 7 20,521,342 (GRCm39) missense probably damaging 1.00
Posted On 2016-08-02