Incidental Mutation 'IGL00492:Vmn1r86'
ID 6313
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r86
Ensembl Gene ENSMUSG00000070816
Gene Name vomeronasal 1 receptor 86
Synonyms Gm10301
Accession Numbers
Essential gene? Probably non essential (E-score: 0.050) question?
Stock # IGL00492
Quality Score
Status
Chromosome 7
Chromosomal Location 12835924-12836874 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 12836468 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Tyrosine at position 86 (C86Y)
Ref Sequence ENSEMBL: ENSMUSP00000154464 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094828] [ENSMUST00000226604] [ENSMUST00000227220] [ENSMUST00000227700]
AlphaFold L7N213
Predicted Effect probably benign
Transcript: ENSMUST00000094828
AA Change: C136Y

PolyPhen 2 Score 0.046 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000092423
Gene: ENSMUSG00000070816
AA Change: C136Y

DomainStartEndE-ValueType
Pfam:TAS2R 1 306 1.1e-14 PFAM
Pfam:V1R 35 301 4e-31 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000210729
Predicted Effect probably benign
Transcript: ENSMUST00000226604
AA Change: C136Y

PolyPhen 2 Score 0.046 (Sensitivity: 0.94; Specificity: 0.83)
Predicted Effect probably benign
Transcript: ENSMUST00000227220
AA Change: C136Y

PolyPhen 2 Score 0.046 (Sensitivity: 0.94; Specificity: 0.83)
Predicted Effect possibly damaging
Transcript: ENSMUST00000227700
AA Change: C86Y

PolyPhen 2 Score 0.906 (Sensitivity: 0.82; Specificity: 0.94)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap29 G T 3: 121,796,961 (GRCm39) E108* probably null Het
Braf A T 6: 39,637,933 (GRCm39) probably null Het
Calr3 G A 8: 73,185,240 (GRCm39) Q112* probably null Het
Dis3 A G 14: 99,320,110 (GRCm39) I649T probably damaging Het
Dop1b T C 16: 93,577,670 (GRCm39) V65A probably benign Het
Dpp4 A G 2: 62,209,646 (GRCm39) Y126H probably damaging Het
Dtwd2 A T 18: 49,856,776 (GRCm39) Y170* probably null Het
Efcab7 A G 4: 99,719,700 (GRCm39) T61A probably benign Het
Fbxl3 G T 14: 103,332,730 (GRCm39) L83M probably damaging Het
Fbxo17 A C 7: 28,434,766 (GRCm39) S184R probably damaging Het
Fcf1 T C 12: 85,029,106 (GRCm39) probably null Het
Hcrtr2 T C 9: 76,153,723 (GRCm39) Y223C probably damaging Het
Kcnn1 A G 8: 71,300,706 (GRCm39) F432S probably benign Het
Kmt2a C T 9: 44,719,231 (GRCm39) probably benign Het
Lce1j T C 3: 92,696,713 (GRCm39) T22A unknown Het
Lrfn5 T A 12: 61,890,912 (GRCm39) S734T probably benign Het
Lyst T A 13: 13,852,760 (GRCm39) S2253R possibly damaging Het
Msantd5f1 C T 4: 73,605,570 (GRCm39) T327I probably damaging Het
Myrfl G A 10: 116,632,011 (GRCm39) L645F possibly damaging Het
Nudt9 A G 5: 104,209,628 (GRCm39) probably benign Het
Ostn T A 16: 27,140,132 (GRCm39) M15K possibly damaging Het
Psg20 T C 7: 18,408,536 (GRCm39) T395A possibly damaging Het
Rpf1 G A 3: 146,218,002 (GRCm39) H171Y probably benign Het
Shprh A G 10: 11,063,902 (GRCm39) E1325G probably damaging Het
Slc22a8 G T 19: 8,571,499 (GRCm39) V77L probably benign Het
Tbck A C 3: 132,428,501 (GRCm39) K285N probably benign Het
Zdhhc20 A G 14: 58,111,381 (GRCm39) I73T probably damaging Het
Zfp512b T C 2: 181,228,862 (GRCm39) D701G probably damaging Het
Zfp735 T A 11: 73,602,192 (GRCm39) Y379N possibly damaging Het
Znfx1 G T 2: 166,878,843 (GRCm39) H980Q probably damaging Het
Other mutations in Vmn1r86
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01124:Vmn1r86 APN 7 12,836,856 (GRCm39) missense probably benign 0.04
IGL01291:Vmn1r86 APN 7 12,836,433 (GRCm39) missense probably benign 0.14
IGL02347:Vmn1r86 APN 7 12,836,574 (GRCm39) missense probably damaging 0.99
IGL02457:Vmn1r86 APN 7 12,836,707 (GRCm39) missense probably benign
IGL02983:Vmn1r86 APN 7 12,836,741 (GRCm39) missense probably damaging 1.00
ANU05:Vmn1r86 UTSW 7 12,836,433 (GRCm39) missense probably benign 0.14
R0304:Vmn1r86 UTSW 7 12,836,707 (GRCm39) missense probably benign
R0525:Vmn1r86 UTSW 7 12,836,088 (GRCm39) missense probably benign 0.13
R1958:Vmn1r86 UTSW 7 12,836,621 (GRCm39) missense possibly damaging 0.94
R2227:Vmn1r86 UTSW 7 12,836,847 (GRCm39) missense probably benign 0.00
R3149:Vmn1r86 UTSW 7 12,836,358 (GRCm39) nonsense probably null
R3896:Vmn1r86 UTSW 7 12,836,093 (GRCm39) missense probably benign 0.18
R4735:Vmn1r86 UTSW 7 12,836,221 (GRCm39) missense probably damaging 1.00
R5219:Vmn1r86 UTSW 7 12,836,382 (GRCm39) missense probably damaging 1.00
R6003:Vmn1r86 UTSW 7 12,836,125 (GRCm39) nonsense probably null
R6457:Vmn1r86 UTSW 7 12,836,279 (GRCm39) missense possibly damaging 0.70
R7442:Vmn1r86 UTSW 7 12,835,983 (GRCm39) missense possibly damaging 0.70
R7622:Vmn1r86 UTSW 7 12,836,685 (GRCm39) missense probably benign 0.07
R8436:Vmn1r86 UTSW 7 12,836,771 (GRCm39) missense probably benign 0.25
R9141:Vmn1r86 UTSW 7 12,836,789 (GRCm39) nonsense probably null
R9374:Vmn1r86 UTSW 7 12,836,781 (GRCm39) missense possibly damaging 0.86
R9398:Vmn1r86 UTSW 7 12,836,261 (GRCm39) missense probably damaging 0.98
R9551:Vmn1r86 UTSW 7 12,836,781 (GRCm39) missense possibly damaging 0.86
R9552:Vmn1r86 UTSW 7 12,836,781 (GRCm39) missense possibly damaging 0.86
R9606:Vmn1r86 UTSW 7 12,836,741 (GRCm39) missense probably damaging 1.00
Posted On 2012-04-20