Incidental Mutation 'IGL01722:Vmn1r202'
ID 105130
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r202
Ensembl Gene ENSMUSG00000094379
Gene Name vomeronasal 1 receptor 202
Synonyms V1ri7
Accession Numbers
Essential gene? Probably non essential (E-score: 0.088) question?
Stock # IGL01722
Quality Score
Status
Chromosome 13
Chromosomal Location 22685507-22686415 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 22685890 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Glycine at position 176 (R176G)
Ref Sequence ENSEMBL: ENSMUSP00000154314 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078642] [ENSMUST00000228020]
AlphaFold Q8R259
Predicted Effect probably benign
Transcript: ENSMUST00000078642
AA Change: R176G

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000077711
Gene: ENSMUSG00000094379
AA Change: R176G

DomainStartEndE-ValueType
Pfam:TAS2R 5 301 2.2e-11 PFAM
Pfam:V1R 35 300 5.6e-44 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000228020
AA Change: R176G

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acvr1c T A 2: 58,173,561 (GRCm39) probably benign Het
Alb G A 5: 90,618,698 (GRCm39) probably null Het
Ankrd9 A G 12: 110,943,797 (GRCm39) V46A probably damaging Het
Apol11a A T 15: 77,401,307 (GRCm39) M265L probably benign Het
Ccdc158 T C 5: 92,810,598 (GRCm39) N97D possibly damaging Het
Cobl T G 11: 12,203,987 (GRCm39) H823P probably benign Het
Dnaja2 A T 8: 86,279,908 (GRCm39) H90Q probably benign Het
Dpagt1 T C 9: 44,238,899 (GRCm39) F73S possibly damaging Het
Dph3 C T 14: 31,807,417 (GRCm39) E20K possibly damaging Het
Fbxl13 G T 5: 21,695,412 (GRCm39) T660K possibly damaging Het
Gask1a G A 9: 121,794,149 (GRCm39) S101N possibly damaging Het
Glt6d1 T C 2: 25,684,431 (GRCm39) T192A probably benign Het
Mroh7 C T 4: 106,560,358 (GRCm39) V649I probably benign Het
Mta3 T C 17: 84,063,072 (GRCm39) Y4H possibly damaging Het
Myh14 A G 7: 44,292,956 (GRCm39) L369P probably damaging Het
Or2y1 G T 11: 49,385,793 (GRCm39) L144F probably damaging Het
Or4c52 T C 2: 89,845,351 (GRCm39) C26R probably benign Het
Paxx T C 2: 25,350,277 (GRCm39) D110G probably damaging Het
Pcyox1 T G 6: 86,365,735 (GRCm39) D493A probably damaging Het
Plk2 A G 13: 110,535,976 (GRCm39) E560G probably benign Het
Rnf6 A G 5: 146,147,036 (GRCm39) F661L probably benign Het
Sema4a T C 3: 88,345,491 (GRCm39) K531E probably benign Het
Svs5 T C 2: 164,079,446 (GRCm39) K154E possibly damaging Het
Tbx4 A T 11: 85,802,769 (GRCm39) Q242L probably damaging Het
Tgm3 A T 2: 129,886,488 (GRCm39) I570F probably damaging Het
Thrap3 A T 4: 126,059,322 (GRCm39) M908K possibly damaging Het
Trmo A G 4: 46,386,092 (GRCm39) probably null Het
Usp8 T A 2: 126,600,072 (GRCm39) L997Q probably damaging Het
Vps52 T A 17: 34,180,589 (GRCm39) Y308* probably null Het
Other mutations in Vmn1r202
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01472:Vmn1r202 APN 13 22,686,159 (GRCm39) missense possibly damaging 0.95
IGL01516:Vmn1r202 APN 13 22,685,632 (GRCm39) missense possibly damaging 0.57
IGL02641:Vmn1r202 APN 13 22,686,274 (GRCm39) missense probably benign 0.34
IGL02863:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL02876:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL02891:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL02943:Vmn1r202 APN 13 22,686,364 (GRCm39) missense probably benign 0.01
IGL03057:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL03114:Vmn1r202 APN 13 22,685,500 (GRCm39) utr 3 prime probably benign
IGL03114:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL03143:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL03159:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL03097:Vmn1r202 UTSW 13 22,685,640 (GRCm39) missense probably benign 0.00
R0611:Vmn1r202 UTSW 13 22,685,824 (GRCm39) missense probably damaging 1.00
R1350:Vmn1r202 UTSW 13 22,685,886 (GRCm39) missense probably benign 0.04
R1666:Vmn1r202 UTSW 13 22,685,540 (GRCm39) missense possibly damaging 0.94
R1668:Vmn1r202 UTSW 13 22,685,540 (GRCm39) missense possibly damaging 0.94
R1803:Vmn1r202 UTSW 13 22,686,313 (GRCm39) missense probably benign 0.00
R2035:Vmn1r202 UTSW 13 22,685,772 (GRCm39) missense probably damaging 0.98
R2112:Vmn1r202 UTSW 13 22,685,904 (GRCm39) missense possibly damaging 0.76
R2145:Vmn1r202 UTSW 13 22,685,953 (GRCm39) missense possibly damaging 0.79
R3026:Vmn1r202 UTSW 13 22,685,932 (GRCm39) missense probably benign 0.03
R3808:Vmn1r202 UTSW 13 22,686,070 (GRCm39) missense possibly damaging 0.83
R4714:Vmn1r202 UTSW 13 22,685,977 (GRCm39) missense probably damaging 1.00
R5016:Vmn1r202 UTSW 13 22,686,375 (GRCm39) missense probably damaging 1.00
R5124:Vmn1r202 UTSW 13 22,685,920 (GRCm39) missense probably benign 0.01
R6136:Vmn1r202 UTSW 13 22,685,632 (GRCm39) missense possibly damaging 0.90
R6365:Vmn1r202 UTSW 13 22,686,374 (GRCm39) missense probably benign 0.12
R6982:Vmn1r202 UTSW 13 22,685,917 (GRCm39) missense probably benign 0.02
R7293:Vmn1r202 UTSW 13 22,685,872 (GRCm39) missense probably benign 0.00
R7502:Vmn1r202 UTSW 13 22,686,188 (GRCm39) missense probably damaging 1.00
R7603:Vmn1r202 UTSW 13 22,685,790 (GRCm39) missense probably damaging 1.00
R7672:Vmn1r202 UTSW 13 22,685,850 (GRCm39) missense probably benign 0.45
R7822:Vmn1r202 UTSW 13 22,686,241 (GRCm39) missense probably damaging 1.00
R7954:Vmn1r202 UTSW 13 22,685,871 (GRCm39) missense probably benign 0.01
R8026:Vmn1r202 UTSW 13 22,686,314 (GRCm39) missense possibly damaging 0.65
R8419:Vmn1r202 UTSW 13 22,685,985 (GRCm39) missense probably damaging 1.00
R9079:Vmn1r202 UTSW 13 22,685,602 (GRCm39) missense probably benign 0.00
R9194:Vmn1r202 UTSW 13 22,686,316 (GRCm39) missense possibly damaging 0.48
Posted On 2014-01-21