Incidental Mutation 'IGL02876:Vmn1r202'
ID 406221
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 # IGL02876
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: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl4fm2 A G 4: 144,282,343 (GRCm39) Y150H probably damaging Het
Abcb5 A G 12: 118,883,576 (GRCm39) V564A probably damaging Het
Adamts15 A T 9: 30,815,818 (GRCm39) N679K probably damaging Het
Angpt1 T G 15: 42,290,373 (GRCm39) D497A possibly damaging Het
Asap2 A G 12: 21,308,164 (GRCm39) K849R probably benign Het
Aspm T C 1: 139,401,391 (GRCm39) V1137A probably damaging Het
Atp12a A G 14: 56,610,746 (GRCm39) I297V probably benign Het
Atp2a2 A G 5: 122,604,071 (GRCm39) V454A probably benign Het
Carmil1 T A 13: 24,338,651 (GRCm39) probably benign Het
Csmd2 A T 4: 128,215,128 (GRCm39) K517* probably null Het
Csmd3 A T 15: 47,469,492 (GRCm39) probably benign Het
Cyp2d11 T A 15: 82,273,697 (GRCm39) Q427L possibly damaging Het
Eml5 C T 12: 98,825,100 (GRCm39) V706M probably damaging Het
Entpd8 A C 2: 24,975,072 (GRCm39) S428R probably benign Het
Gm10283 T C 8: 60,954,253 (GRCm39) probably benign Het
Gpatch3 T A 4: 133,307,995 (GRCm39) V363E probably damaging Het
Hoxb5 T A 11: 96,194,594 (GRCm39) M52K probably damaging Het
Ift52 T C 2: 162,878,627 (GRCm39) V307A probably benign Het
Igkv1-115 T C 6: 68,138,424 (GRCm39) noncoding transcript Het
Kdm5a T C 6: 120,367,605 (GRCm39) probably benign Het
Lama1 T A 17: 68,057,687 (GRCm39) probably null Het
Lrp6 G A 6: 134,433,077 (GRCm39) P1418L probably benign Het
Mill2 T C 7: 18,590,432 (GRCm39) F156L probably damaging Het
Mnat1 A G 12: 73,217,378 (GRCm39) R85G probably damaging Het
Myrip A T 9: 120,261,740 (GRCm39) D451V probably damaging Het
Or1e1f A T 11: 73,855,539 (GRCm39) Y35F possibly damaging Het
Pdzph1 C A 17: 59,281,064 (GRCm39) S406I probably benign Het
Ptprb A G 10: 116,184,116 (GRCm39) probably benign Het
Rxfp4 T A 3: 88,559,742 (GRCm39) R236S possibly damaging Het
Ryr2 T C 13: 11,722,679 (GRCm39) M2604V probably benign Het
Setd1a G A 7: 127,377,673 (GRCm39) probably benign Het
Spata33 A T 8: 123,948,719 (GRCm39) H88L probably damaging Het
Spcs3 A T 8: 54,979,486 (GRCm39) N98K probably damaging Het
Srgap3 A G 6: 112,748,414 (GRCm39) S413P probably damaging Het
Stap2 T C 17: 56,306,961 (GRCm39) R239G probably benign Het
Surf6 A G 2: 26,782,638 (GRCm39) Y230H probably damaging Het
Tasp1 C T 2: 139,676,283 (GRCm39) V382M probably benign Het
Tnc G T 4: 63,933,338 (GRCm39) A642E possibly damaging Het
Vmn2r110 T A 17: 20,794,558 (GRCm39) T704S probably damaging Het
Vtcn1 A T 3: 100,791,145 (GRCm39) D61V probably damaging Het
Zc3h12d G A 10: 7,738,364 (GRCm39) M223I probably damaging Het
Zfp592 T A 7: 80,687,875 (GRCm39) S934T probably benign 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
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 2016-08-02