Incidental Mutation 'IGL01328:Vmn2r86'
ID 74356
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r86
Ensembl Gene ENSMUSG00000092162
Gene Name vomeronasal 2, receptor 86
Synonyms EG625109
Accession Numbers
Essential gene? Probably non essential (E-score: 0.080) question?
Stock # IGL01328
Quality Score
Status
Chromosome 10
Chromosomal Location 130282068-130291763 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 130288365 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 379 (T379A)
Ref Sequence ENSEMBL: ENSMUSP00000126596 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000170257]
AlphaFold G5E8Y4
Predicted Effect possibly damaging
Transcript: ENSMUST00000170257
AA Change: T379A

PolyPhen 2 Score 0.779 (Sensitivity: 0.85; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000126596
Gene: ENSMUSG00000092162
AA Change: T379A

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
Pfam:ANF_receptor 77 425 1.1e-25 PFAM
Pfam:NCD3G 508 562 2.4e-19 PFAM
Pfam:7tm_3 595 829 6.4e-55 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts19 C T 18: 59,181,954 (GRCm39) S1131F possibly damaging Het
Alg14 G A 3: 121,155,232 (GRCm39) V151I probably benign Het
Ano5 G A 7: 51,206,019 (GRCm39) probably null Het
Arhgef28 A T 13: 98,106,831 (GRCm39) C698S probably damaging Het
Cacnb4 T C 2: 52,354,637 (GRCm39) H247R probably damaging Het
Clec12b A T 6: 129,356,517 (GRCm39) W216R probably damaging Het
Clnk C T 5: 38,941,871 (GRCm39) S35N possibly damaging Het
Cnot4 T A 6: 35,055,049 (GRCm39) N80I probably damaging Het
Cntn5 C T 9: 9,781,773 (GRCm39) M635I probably damaging Het
Dlg5 A G 14: 24,252,419 (GRCm39) V107A probably damaging Het
Dsc2 A T 18: 20,181,343 (GRCm39) F155I probably damaging Het
Dtwd1 A G 2: 126,006,739 (GRCm39) I254V probably damaging Het
Dzip3 A T 16: 48,792,621 (GRCm39) D221E probably damaging Het
F13b T A 1: 139,435,820 (GRCm39) probably benign Het
Fam131b G A 6: 42,295,206 (GRCm39) L324F probably damaging Het
Fam83a A T 15: 57,849,901 (GRCm39) R148S probably damaging Het
Farsb T C 1: 78,447,729 (GRCm39) I236V probably benign Het
Fat4 T A 3: 39,034,807 (GRCm39) F2820I probably damaging Het
Fat4 T A 3: 38,944,140 (GRCm39) V1011E probably damaging Het
Fgf7 A G 2: 125,930,164 (GRCm39) E99G probably damaging Het
Fign T C 2: 63,809,216 (GRCm39) T685A probably damaging Het
Fubp1 G A 3: 151,925,855 (GRCm39) G289E probably damaging Het
Gata6 G T 18: 11,064,530 (GRCm39) M477I probably damaging Het
Gm14496 A G 2: 181,637,673 (GRCm39) Y249C probably damaging Het
Hectd1 T C 12: 51,807,904 (GRCm39) D1768G probably damaging Het
Htatip2 T A 7: 49,420,697 (GRCm39) probably null Het
Irs2 C A 8: 11,054,792 (GRCm39) Q1213H probably damaging Het
Jak3 C T 8: 72,132,264 (GRCm39) R210C probably damaging Het
Klk1b27 T C 7: 43,705,303 (GRCm39) S157P probably damaging Het
Klri1 T C 6: 129,675,800 (GRCm39) S157G probably damaging Het
Mtmr2 G T 9: 13,713,223 (GRCm39) G395* probably null Het
Mx1 T A 16: 97,256,832 (GRCm39) I116F probably damaging Het
Oip5 A C 2: 119,442,314 (GRCm39) M200R possibly damaging Het
Or10ag56 T A 2: 87,139,925 (GRCm39) L284Q possibly damaging Het
Or10g3 T C 14: 52,609,967 (GRCm39) D181G probably damaging Het
Or4b1d T C 2: 89,969,418 (GRCm39) K22E probably benign Het
Or4k39 A G 2: 111,239,564 (GRCm39) Y268C probably damaging Het
Pamr1 T A 2: 102,472,482 (GRCm39) S594T probably benign Het
Phf13 C T 4: 152,080,285 (GRCm39) E13K probably benign Het
Plekha6 A T 1: 133,200,074 (GRCm39) probably null Het
Rad17 A C 13: 100,754,311 (GRCm39) N636K probably benign Het
Rad21 T A 15: 51,836,520 (GRCm39) D217V probably damaging Het
Slc7a10 A G 7: 34,885,917 (GRCm39) D4G possibly damaging Het
Stc1 A G 14: 69,275,726 (GRCm39) D173G probably benign Het
Supt16 C T 14: 52,414,489 (GRCm39) E438K probably benign Het
Tex15 C T 8: 34,061,424 (GRCm39) Q559* probably null Het
Trim44 T A 2: 102,230,365 (GRCm39) E222V probably benign Het
Ubr5 T C 15: 37,981,767 (GRCm39) E2343G possibly damaging Het
Vmn2r93 A G 17: 18,545,819 (GRCm39) T564A probably benign Het
Vsir C A 10: 60,203,539 (GRCm39) probably benign Het
Vwc2l T A 1: 70,768,163 (GRCm39) probably null Het
Xrn2 T C 2: 146,871,850 (GRCm39) V396A possibly damaging Het
Zbbx T A 3: 75,000,382 (GRCm39) K208* probably null Het
Zfhx4 C A 3: 5,309,344 (GRCm39) L857M probably damaging Het
Zfp180 A G 7: 23,800,904 (GRCm39) D53G probably benign Het
Other mutations in Vmn2r86
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01295:Vmn2r86 APN 10 130,288,895 (GRCm39) missense probably damaging 0.99
IGL01377:Vmn2r86 APN 10 130,288,855 (GRCm39) missense probably damaging 0.99
IGL01548:Vmn2r86 APN 10 130,282,151 (GRCm39) missense probably benign 0.22
IGL01804:Vmn2r86 APN 10 130,288,858 (GRCm39) missense probably damaging 0.99
IGL01921:Vmn2r86 APN 10 130,291,610 (GRCm39) missense probably benign 0.00
IGL02406:Vmn2r86 APN 10 130,284,508 (GRCm39) missense possibly damaging 0.81
IGL02625:Vmn2r86 APN 10 130,288,781 (GRCm39) missense probably damaging 1.00
IGL02960:Vmn2r86 APN 10 130,289,636 (GRCm39) missense possibly damaging 0.74
IGL03104:Vmn2r86 APN 10 130,282,501 (GRCm39) missense probably damaging 1.00
R0408:Vmn2r86 UTSW 10 130,282,723 (GRCm39) missense probably damaging 1.00
R0437:Vmn2r86 UTSW 10 130,282,412 (GRCm39) missense probably damaging 1.00
R0577:Vmn2r86 UTSW 10 130,288,444 (GRCm39) missense probably benign 0.04
R0726:Vmn2r86 UTSW 10 130,282,265 (GRCm39) missense probably damaging 1.00
R0811:Vmn2r86 UTSW 10 130,289,497 (GRCm39) missense probably benign 0.00
R0812:Vmn2r86 UTSW 10 130,289,497 (GRCm39) missense probably benign 0.00
R1055:Vmn2r86 UTSW 10 130,282,226 (GRCm39) missense probably damaging 1.00
R1066:Vmn2r86 UTSW 10 130,282,145 (GRCm39) missense probably benign 0.01
R1199:Vmn2r86 UTSW 10 130,284,443 (GRCm39) splice site probably benign
R1332:Vmn2r86 UTSW 10 130,282,739 (GRCm39) missense probably damaging 1.00
R1568:Vmn2r86 UTSW 10 130,289,010 (GRCm39) missense probably benign 0.09
R1866:Vmn2r86 UTSW 10 130,282,255 (GRCm39) missense probably damaging 1.00
R1897:Vmn2r86 UTSW 10 130,288,314 (GRCm39) missense probably damaging 1.00
R2017:Vmn2r86 UTSW 10 130,282,582 (GRCm39) missense probably benign 0.39
R3162:Vmn2r86 UTSW 10 130,291,673 (GRCm39) missense probably damaging 0.99
R3162:Vmn2r86 UTSW 10 130,291,673 (GRCm39) missense probably damaging 0.99
R3858:Vmn2r86 UTSW 10 130,291,594 (GRCm39) missense probably benign
R4049:Vmn2r86 UTSW 10 130,282,966 (GRCm39) missense probably damaging 0.98
R4378:Vmn2r86 UTSW 10 130,288,469 (GRCm39) missense possibly damaging 0.67
R4411:Vmn2r86 UTSW 10 130,288,469 (GRCm39) missense possibly damaging 0.67
R4413:Vmn2r86 UTSW 10 130,288,469 (GRCm39) missense possibly damaging 0.67
R4422:Vmn2r86 UTSW 10 130,288,845 (GRCm39) missense possibly damaging 0.87
R4738:Vmn2r86 UTSW 10 130,282,939 (GRCm39) missense probably damaging 0.99
R4767:Vmn2r86 UTSW 10 130,291,606 (GRCm39) missense probably benign 0.00
R4872:Vmn2r86 UTSW 10 130,289,460 (GRCm39) missense probably damaging 0.98
R4880:Vmn2r86 UTSW 10 130,289,484 (GRCm39) missense probably benign 0.33
R5092:Vmn2r86 UTSW 10 130,282,456 (GRCm39) missense probably damaging 1.00
R5421:Vmn2r86 UTSW 10 130,282,805 (GRCm39) missense probably benign 0.41
R6007:Vmn2r86 UTSW 10 130,289,535 (GRCm39) missense probably damaging 1.00
R6330:Vmn2r86 UTSW 10 130,282,396 (GRCm39) missense probably benign 0.05
R6355:Vmn2r86 UTSW 10 130,291,763 (GRCm39) start codon destroyed probably damaging 0.98
R6397:Vmn2r86 UTSW 10 130,282,131 (GRCm39) nonsense probably null
R6419:Vmn2r86 UTSW 10 130,282,795 (GRCm39) missense probably damaging 1.00
R6933:Vmn2r86 UTSW 10 130,282,126 (GRCm39) missense probably damaging 1.00
R6937:Vmn2r86 UTSW 10 130,284,523 (GRCm39) missense probably damaging 1.00
R6959:Vmn2r86 UTSW 10 130,282,400 (GRCm39) missense probably damaging 1.00
R7010:Vmn2r86 UTSW 10 130,291,726 (GRCm39) missense probably benign
R7549:Vmn2r86 UTSW 10 130,282,697 (GRCm39) missense probably damaging 1.00
R8179:Vmn2r86 UTSW 10 130,288,953 (GRCm39) missense probably benign 0.00
R8257:Vmn2r86 UTSW 10 130,288,279 (GRCm39) missense possibly damaging 0.87
R8286:Vmn2r86 UTSW 10 130,285,855 (GRCm39) missense probably benign 0.03
R8479:Vmn2r86 UTSW 10 130,282,735 (GRCm39) missense probably damaging 1.00
R8805:Vmn2r86 UTSW 10 130,282,396 (GRCm39) missense probably benign 0.05
R8960:Vmn2r86 UTSW 10 130,289,672 (GRCm39) missense probably benign 0.27
R9021:Vmn2r86 UTSW 10 130,282,934 (GRCm39) missense probably damaging 1.00
R9120:Vmn2r86 UTSW 10 130,289,677 (GRCm39) missense probably benign 0.00
R9137:Vmn2r86 UTSW 10 130,282,409 (GRCm39) missense probably damaging 1.00
R9311:Vmn2r86 UTSW 10 130,288,440 (GRCm39) missense probably damaging 1.00
R9312:Vmn2r86 UTSW 10 130,288,406 (GRCm39) missense probably benign 0.02
R9433:Vmn2r86 UTSW 10 130,282,567 (GRCm39) missense possibly damaging 0.88
R9696:Vmn2r86 UTSW 10 130,285,702 (GRCm39) missense possibly damaging 0.49
Posted On 2013-10-07