Incidental Mutation 'IGL01921:Vmn2r86'
ID 180087
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 # IGL01921
Quality Score
Status
Chromosome 10
Chromosomal Location 130282068-130291763 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 130291610 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 52 (T52A)
Ref Sequence ENSEMBL: ENSMUSP00000126596 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000170257]
AlphaFold G5E8Y4
Predicted Effect probably benign
Transcript: ENSMUST00000170257
AA Change: T52A

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000126596
Gene: ENSMUSG00000092162
AA Change: T52A

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: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam34l C A 8: 44,078,548 (GRCm39) V559L probably damaging Het
Agtpbp1 T C 13: 59,660,297 (GRCm39) T310A possibly damaging Het
Ccdc102a T C 8: 95,640,019 (GRCm39) T92A probably damaging Het
Ciao1 C T 2: 127,084,755 (GRCm39) V328I probably benign Het
Col12a1 T A 9: 79,557,299 (GRCm39) Q1943L possibly damaging Het
Diaph1 T C 18: 37,989,261 (GRCm39) D898G possibly damaging Het
Dio3 A T 12: 110,245,789 (GRCm39) T42S possibly damaging Het
Dnah8 T A 17: 30,955,115 (GRCm39) I2048N probably benign Het
Egr2 T A 10: 67,376,208 (GRCm39) probably null Het
Epc2 T A 2: 49,422,209 (GRCm39) Y368N probably damaging Het
Furin A G 7: 80,045,702 (GRCm39) probably benign Het
Gga1 T C 15: 78,777,995 (GRCm39) M620T possibly damaging Het
Gm21976 T A 13: 98,441,829 (GRCm39) Y45* probably null Het
Gpn1 T C 5: 31,656,612 (GRCm39) V105A probably damaging Het
Hoxb8 A T 11: 96,175,181 (GRCm39) N206I probably damaging Het
Kif15 T A 9: 122,808,569 (GRCm39) L67Q probably damaging Het
Krt40 T A 11: 99,433,989 (GRCm39) probably benign Het
Mat1a T C 14: 40,836,292 (GRCm39) probably benign Het
Mkrn1 T C 6: 39,382,847 (GRCm39) D99G possibly damaging Het
Plxnb2 T C 15: 89,048,474 (GRCm39) Y645C possibly damaging Het
Ppp1r13b A G 12: 111,799,671 (GRCm39) V702A probably benign Het
Ppp4r4 G T 12: 103,542,569 (GRCm39) M1I probably null Het
Prss21 T A 17: 24,091,414 (GRCm39) M217K possibly damaging Het
R3hcc1l A G 19: 42,552,220 (GRCm39) S406G possibly damaging Het
Rfesd T C 13: 76,156,385 (GRCm39) E7G probably benign Het
Ripk4 T C 16: 97,544,565 (GRCm39) E694G possibly damaging Het
Rlf T C 4: 121,003,943 (GRCm39) D1679G probably damaging Het
Ryr2 C T 13: 11,569,436 (GRCm39) C4956Y possibly damaging Het
Scart1 G T 7: 139,808,632 (GRCm39) E848* probably null Het
Uri1 T A 7: 37,681,072 (GRCm39) K111* probably null Het
Usf1 A G 1: 171,244,424 (GRCm39) E108G possibly damaging Het
Vmn1r71 C A 7: 10,482,199 (GRCm39) R163L probably benign Het
Vmn2r129 C T 4: 156,690,549 (GRCm39) noncoding transcript Het
Washc5 A T 15: 59,213,958 (GRCm39) probably null Het
Zfp583 T C 7: 6,328,569 (GRCm39) T7A possibly damaging Het
Zim1 T G 7: 6,685,184 (GRCm39) probably benign Het
Other mutations in Vmn2r86
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01295:Vmn2r86 APN 10 130,288,895 (GRCm39) missense probably damaging 0.99
IGL01328:Vmn2r86 APN 10 130,288,365 (GRCm39) missense possibly damaging 0.78
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
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 2014-05-07