Incidental Mutation 'IGL03061:Vmn1r215'
ID 409435
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r215
Ensembl Gene ENSMUSG00000099917
Gene Name vomeronasal 1 receptor 215
Synonyms V1ri2
Accession Numbers
Essential gene? Probably non essential (E-score: 0.073) question?
Stock # IGL03061
Quality Score
Status
Chromosome 13
Chromosomal Location 23259962-23260864 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 23260088 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Phenylalanine at position 43 (V43F)
Ref Sequence ENSEMBL: ENSMUSP00000154763 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072972] [ENSMUST00000228092]
AlphaFold Q8R264
Predicted Effect probably damaging
Transcript: ENSMUST00000072972
AA Change: V43F

PolyPhen 2 Score 0.966 (Sensitivity: 0.77; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000072739
Gene: ENSMUSG00000099917
AA Change: V43F

DomainStartEndE-ValueType
Pfam:V1R 35 298 2.4e-37 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000228092
AA Change: V43F

PolyPhen 2 Score 0.966 (Sensitivity: 0.77; Specificity: 0.95)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsl1 T A 8: 46,961,374 (GRCm39) N106K probably damaging Het
Ak8 T C 2: 28,632,767 (GRCm39) probably benign Het
BC016579 C T 16: 45,449,849 (GRCm39) G190S probably damaging Het
C4bp A G 1: 130,564,454 (GRCm39) V410A probably damaging Het
Cacna2d3 T C 14: 28,780,388 (GRCm39) T658A probably damaging Het
Cadps2 T C 6: 23,287,659 (GRCm39) probably null Het
Car10 G T 11: 93,381,351 (GRCm39) V105F probably damaging Het
Car15 C T 16: 17,653,249 (GRCm39) C306Y possibly damaging Het
Casr C T 16: 36,316,250 (GRCm39) A530T probably benign Het
Col5a3 A G 9: 20,708,868 (GRCm39) probably null Het
Creld1 A G 6: 113,465,058 (GRCm39) E95G probably damaging Het
Dcstamp T A 15: 39,623,793 (GRCm39) D366E possibly damaging Het
Dnah11 T C 12: 117,866,856 (GRCm39) Y4095C probably damaging Het
Eps8l2 A G 7: 140,937,148 (GRCm39) probably benign Het
Gsn T C 2: 35,172,471 (GRCm39) probably benign Het
Ifi27l2a T C 12: 103,401,803 (GRCm39) V30A possibly damaging Het
Ifit1bl2 C T 19: 34,597,124 (GRCm39) R164Q probably benign Het
Impg2 T C 16: 56,088,779 (GRCm39) S1102P probably damaging Het
Kif24 G T 4: 41,394,323 (GRCm39) P984Q possibly damaging Het
Krtap29-1 T A 11: 99,869,455 (GRCm39) Q142L possibly damaging Het
Lpar6 C T 14: 73,476,510 (GRCm39) T157I probably benign Het
Lrrc32 A T 7: 98,148,629 (GRCm39) T470S probably benign Het
Lyl1 C T 8: 85,429,300 (GRCm39) P3L possibly damaging Het
Mroh9 A T 1: 162,854,071 (GRCm39) H776Q probably damaging Het
Myh7 T C 14: 55,228,661 (GRCm39) probably benign Het
Myh7b A G 2: 155,462,031 (GRCm39) N309S possibly damaging Het
Myo5b A T 18: 74,767,630 (GRCm39) T313S probably benign Het
Myo5b G A 18: 74,713,615 (GRCm39) probably benign Het
Npas4 C T 19: 5,036,365 (GRCm39) V600M probably damaging Het
Nrxn3 T A 12: 89,478,698 (GRCm39) Y557* probably null Het
Or2aj4 T C 16: 19,385,463 (GRCm39) T57A possibly damaging Het
Or52k2 A G 7: 102,253,946 (GRCm39) I128M probably damaging Het
Or8g53 T A 9: 39,683,458 (GRCm39) T213S probably benign Het
Pcdh15 A G 10: 74,152,843 (GRCm39) I383V probably damaging Het
Pdzrn3 C A 6: 101,128,816 (GRCm39) D617Y probably damaging Het
Prodh2 A T 7: 30,212,258 (GRCm39) K408* probably null Het
Ptprs T C 17: 56,725,830 (GRCm39) I1052V probably damaging Het
Rpl14 T C 9: 120,401,193 (GRCm39) V12A probably damaging Het
Sf3a1 C T 11: 4,125,493 (GRCm39) R428C probably damaging Het
Sgsm2 G T 11: 74,741,962 (GRCm39) N1009K probably damaging Het
Slc28a2 A T 2: 122,284,980 (GRCm39) I323F probably damaging Het
Snx19 T A 9: 30,344,928 (GRCm39) F676I probably damaging Het
Stxbp2 A T 8: 3,691,971 (GRCm39) I538F probably benign Het
Tg A C 15: 66,543,254 (GRCm39) D56A probably damaging Het
Tln1 G T 4: 43,545,694 (GRCm39) A928E probably damaging Het
Tmem94 T C 11: 115,683,247 (GRCm39) S677P possibly damaging Het
Ttc41 C A 10: 86,572,721 (GRCm39) H698N possibly damaging Het
Vcan T C 13: 89,851,394 (GRCm39) T1189A probably benign Het
Vmn2r28 A T 7: 5,487,015 (GRCm39) N549K probably damaging Het
Zfp598 T C 17: 24,898,566 (GRCm39) V455A probably benign Het
Other mutations in Vmn1r215
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00923:Vmn1r215 APN 13 23,260,419 (GRCm39) missense probably damaging 0.98
IGL02515:Vmn1r215 APN 13 23,259,990 (GRCm39) missense probably benign 0.21
PIT4651001:Vmn1r215 UTSW 13 23,260,530 (GRCm39) missense probably damaging 0.97
R0196:Vmn1r215 UTSW 13 23,260,254 (GRCm39) missense probably damaging 1.00
R0816:Vmn1r215 UTSW 13 23,260,124 (GRCm39) missense probably benign 0.00
R0817:Vmn1r215 UTSW 13 23,260,124 (GRCm39) missense probably benign 0.00
R0820:Vmn1r215 UTSW 13 23,260,124 (GRCm39) missense probably benign 0.00
R1104:Vmn1r215 UTSW 13 23,260,758 (GRCm39) missense possibly damaging 0.50
R1733:Vmn1r215 UTSW 13 23,260,848 (GRCm39) missense probably benign 0.43
R1912:Vmn1r215 UTSW 13 23,260,673 (GRCm39) missense possibly damaging 0.94
R2010:Vmn1r215 UTSW 13 23,260,378 (GRCm39) missense probably damaging 1.00
R2510:Vmn1r215 UTSW 13 23,260,343 (GRCm39) missense probably benign 0.00
R2511:Vmn1r215 UTSW 13 23,260,343 (GRCm39) missense probably benign 0.00
R2877:Vmn1r215 UTSW 13 23,260,731 (GRCm39) missense probably benign 0.01
R3429:Vmn1r215 UTSW 13 23,260,378 (GRCm39) missense probably damaging 1.00
R3854:Vmn1r215 UTSW 13 23,260,058 (GRCm39) missense probably benign
R4124:Vmn1r215 UTSW 13 23,260,163 (GRCm39) missense probably benign 0.42
R4235:Vmn1r215 UTSW 13 23,260,101 (GRCm39) missense probably benign 0.31
R4979:Vmn1r215 UTSW 13 23,260,064 (GRCm39) missense probably benign 0.04
R4991:Vmn1r215 UTSW 13 23,260,697 (GRCm39) missense probably damaging 1.00
R5011:Vmn1r215 UTSW 13 23,260,721 (GRCm39) missense probably damaging 1.00
R5026:Vmn1r215 UTSW 13 23,260,449 (GRCm39) missense probably benign 0.30
R5070:Vmn1r215 UTSW 13 23,260,666 (GRCm39) missense probably benign 0.03
R5589:Vmn1r215 UTSW 13 23,260,190 (GRCm39) missense probably damaging 1.00
R5589:Vmn1r215 UTSW 13 23,260,189 (GRCm39) missense probably damaging 1.00
R5651:Vmn1r215 UTSW 13 23,259,981 (GRCm39) missense possibly damaging 0.93
R5928:Vmn1r215 UTSW 13 23,260,487 (GRCm39) missense possibly damaging 0.50
R6176:Vmn1r215 UTSW 13 23,260,528 (GRCm39) missense probably damaging 1.00
R6228:Vmn1r215 UTSW 13 23,260,633 (GRCm39) missense probably benign 0.19
R7270:Vmn1r215 UTSW 13 23,260,089 (GRCm39) missense possibly damaging 0.77
R7313:Vmn1r215 UTSW 13 23,260,484 (GRCm39) missense probably benign 0.01
R7820:Vmn1r215 UTSW 13 23,260,715 (GRCm39) missense probably damaging 1.00
R8492:Vmn1r215 UTSW 13 23,260,056 (GRCm39) missense possibly damaging 0.79
R8515:Vmn1r215 UTSW 13 23,260,037 (GRCm39) missense probably benign 0.00
R8835:Vmn1r215 UTSW 13 23,260,409 (GRCm39) missense possibly damaging 0.68
R9428:Vmn1r215 UTSW 13 23,260,749 (GRCm39) missense probably benign 0.03
Posted On 2016-08-02