Incidental Mutation 'IGL02891:Vmn1r202'
ID 363174
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 # IGL02891
Quality Score
Status
Chromosome 13
Chromosomal Location 22685507-22686415 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 22685640 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Isoleucine at position 259 (T259I)
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: T259I

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000077711
Gene: ENSMUSG00000094379
AA Change: T259I

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: T259I

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca17 A G 17: 24,500,340 (GRCm39) S1284P probably damaging Het
Adgrf1 T C 17: 43,622,052 (GRCm39) V763A probably damaging Het
Adhfe1 T A 1: 9,628,396 (GRCm39) M256K probably benign Het
Afg2a T A 3: 37,480,341 (GRCm39) V130D probably damaging Het
Chit1 A G 1: 134,073,048 (GRCm39) S125G probably benign Het
Clu T A 14: 66,213,433 (GRCm39) F273Y probably damaging Het
Dgki T C 6: 36,890,676 (GRCm39) D869G probably benign Het
Elapor1 C T 3: 108,371,708 (GRCm39) R672Q probably benign Het
Emx1 T C 6: 85,181,067 (GRCm39) probably benign Het
Ercc2 T G 7: 19,127,211 (GRCm39) F316C probably damaging Het
Fam81a A G 9: 70,017,558 (GRCm39) L129P probably damaging Het
Fat4 T A 3: 39,005,422 (GRCm39) N1940K probably damaging Het
Fbxl13 G A 5: 21,727,098 (GRCm39) probably benign Het
Ift70b C T 2: 75,767,404 (GRCm39) V450M possibly damaging Het
Kcnt2 T A 1: 140,502,544 (GRCm39) D879E probably damaging Het
Kti12 T G 4: 108,705,730 (GRCm39) S215A probably benign Het
Lama1 G A 17: 68,111,531 (GRCm39) G2261R probably damaging Het
Ntn5 G T 7: 45,335,648 (GRCm39) L26F probably damaging Het
Nwd2 A G 5: 63,882,570 (GRCm39) N74S possibly damaging Het
Or12d17 T A 17: 37,777,835 (GRCm39) V246E probably damaging Het
Or2d3c A G 7: 106,526,288 (GRCm39) V126A probably damaging Het
Phactr4 T C 4: 132,114,334 (GRCm39) D20G probably damaging Het
Ptpn23 G A 9: 110,217,088 (GRCm39) Q923* probably null Het
Rfx6 T A 10: 51,599,942 (GRCm39) S333T possibly damaging Het
Skint10 T A 4: 112,586,023 (GRCm39) I198F probably benign Het
Taf3 G A 2: 9,926,038 (GRCm39) P647L probably damaging Het
Tbcb T C 7: 29,932,859 (GRCm39) probably benign Het
Tmem63c T C 12: 87,118,042 (GRCm39) F216L probably benign Het
Uba5 A G 9: 103,931,392 (GRCm39) probably benign Het
Usp34 C A 11: 23,437,166 (GRCm39) Q217K probably benign Het
Vmn2r99 G A 17: 19,598,952 (GRCm39) W212* probably null Het
Zfp687 G T 3: 94,919,257 (GRCm39) P172T probably damaging 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
IGL01722:Vmn1r202 APN 13 22,685,890 (GRCm39) missense probably benign 0.00
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
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 2015-12-18