Incidental Mutation 'R6003:Vmn1r86'
ID 478460
Institutional Source Beutler Lab
Gene Symbol Vmn1r86
Ensembl Gene ENSMUSG00000070816
Gene Name vomeronasal 1 receptor 86
Synonyms Gm10301
MMRRC Submission 043252-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.050) question?
Stock # R6003 (G1)
Quality Score 225.009
Status Not validated
Chromosome 7
Chromosomal Location 12835924-12836874 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to T at 12836125 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tryptophan to Stop codon at position 200 (W200*)
Ref Sequence ENSEMBL: ENSMUSP00000154464 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094828] [ENSMUST00000226604] [ENSMUST00000227220] [ENSMUST00000227700]
AlphaFold L7N213
Predicted Effect probably null
Transcript: ENSMUST00000094828
AA Change: W250*
SMART Domains Protein: ENSMUSP00000092423
Gene: ENSMUSG00000070816
AA Change: W250*

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 null
Transcript: ENSMUST00000226604
AA Change: W250*
Predicted Effect probably null
Transcript: ENSMUST00000227220
AA Change: W250*
Predicted Effect probably null
Transcript: ENSMUST00000227700
AA Change: W200*
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.4%
  • 10x: 97.2%
  • 20x: 90.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A4galt T C 15: 83,112,312 (GRCm39) E157G probably benign Het
Abcb11 T C 2: 69,073,811 (GRCm39) K1238R probably benign Het
Ankar T A 1: 72,738,046 (GRCm39) E45D probably damaging Het
Antxrl G T 14: 33,797,592 (GRCm39) K522N possibly damaging Het
Ap1m1 A G 8: 73,003,011 (GRCm39) Y93C probably damaging Het
As3mt C T 19: 46,696,567 (GRCm39) T35M possibly damaging Het
Aspg T C 12: 112,079,476 (GRCm39) S85P probably damaging Het
Cachd1 T C 4: 100,809,216 (GRCm39) S234P possibly damaging Het
Ccdc3 T C 2: 5,146,218 (GRCm39) probably null Het
Cnpy1 T C 5: 28,450,759 (GRCm39) T16A probably benign Het
Cope T C 8: 70,757,285 (GRCm39) L43P probably benign Het
E2f8 T C 7: 48,520,525 (GRCm39) M599V probably benign Het
Eif3a A T 19: 60,755,319 (GRCm39) D954E unknown Het
Gfpt1 T A 6: 87,065,230 (GRCm39) probably null Het
Ggps1 T G 13: 14,228,587 (GRCm39) S145R probably benign Het
Gon4l A G 3: 88,803,400 (GRCm39) D1337G probably damaging Het
Gtf2a1l G T 17: 89,001,531 (GRCm39) G82V probably damaging Het
Gucy1b1 C A 3: 81,965,584 (GRCm39) L87F probably damaging Het
Hoxc9 T C 15: 102,890,311 (GRCm39) V76A probably benign Het
Ints2 T C 11: 86,129,294 (GRCm39) E460G probably damaging Het
Kdm4b C T 17: 56,703,916 (GRCm39) R756W probably damaging Het
Lax1 T A 1: 133,611,834 (GRCm39) I34F probably benign Het
Marveld3 A T 8: 110,680,960 (GRCm39) C312S probably damaging Het
Ncoa2 T C 1: 13,237,254 (GRCm39) D824G possibly damaging Het
Nrxn2 C A 19: 6,548,358 (GRCm39) A17D possibly damaging Het
Nup133 A T 8: 124,665,031 (GRCm39) I220N probably damaging Het
Nup205 T C 6: 35,189,751 (GRCm39) V984A probably benign Het
Nup54 A T 5: 92,570,853 (GRCm39) D318E probably damaging Het
Obp2a A T 2: 25,591,151 (GRCm39) K94N probably damaging Het
Or2ak5 A T 11: 58,611,196 (GRCm39) I226N probably benign Het
Or5b3 T C 19: 13,388,403 (GRCm39) S157P probably benign Het
Pappa2 T C 1: 158,763,820 (GRCm39) I564V probably benign Het
Parpbp A G 10: 87,969,020 (GRCm39) V142A possibly damaging Het
Rdh16f2 A T 10: 127,712,201 (GRCm39) R219S probably benign Het
Rfx6 C T 10: 51,584,683 (GRCm39) R228C probably damaging Het
Rpap2 A G 5: 107,749,767 (GRCm39) probably null Het
Rskr T G 11: 78,183,846 (GRCm39) probably null Het
Slc15a2 T C 16: 36,574,910 (GRCm39) I531V probably benign Het
Srebf1 T C 11: 60,097,930 (GRCm39) E58G possibly damaging Het
Tmem214 C A 5: 31,028,068 (GRCm39) T96K possibly damaging Het
Usp19 T C 9: 108,373,579 (GRCm39) Y691H probably damaging Het
Vmn2r8 A T 5: 108,945,248 (GRCm39) S786R probably damaging Het
Vps52 T A 17: 34,175,068 (GRCm39) M1K probably null Het
Zzef1 T A 11: 72,714,891 (GRCm39) probably null Het
Other mutations in Vmn1r86
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00492:Vmn1r86 APN 7 12,836,468 (GRCm39) missense possibly damaging 0.91
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
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
Predicted Primers PCR Primer
(F):5'- AAAGTGTGGGTTTCAGTTCAGC -3'
(R):5'- CATGATCTCATCTATGTGGCTGTC -3'

Sequencing Primer
(F):5'- TCAGTTCAGCCATGGAGTGAAC -3'
(R):5'- CTGTCATGATGTGGGCCAGC -3'
Posted On 2017-06-26