Incidental Mutation 'R3149:Vmn1r86'
ID 264349
Institutional Source Beutler Lab
Gene Symbol Vmn1r86
Ensembl Gene ENSMUSG00000070816
Gene Name vomeronasal 1 receptor 86
Synonyms Gm10301
MMRRC Submission 040601-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.050) question?
Stock # R3149 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 12835924-12836874 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 12836358 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 123 (K123*)
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: K173*
SMART Domains Protein: ENSMUSP00000092423
Gene: ENSMUSG00000070816
AA Change: K173*

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: K173*
Predicted Effect probably null
Transcript: ENSMUST00000227220
AA Change: K173*
Predicted Effect probably null
Transcript: ENSMUST00000227700
AA Change: K123*
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 95.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsbg3 G A 17: 57,183,348 (GRCm39) A30T probably benign Het
Atox1 A G 11: 55,341,379 (GRCm39) L52P possibly damaging Het
Cel T C 2: 28,446,143 (GRCm39) D576G probably benign Het
Csf2ra C A 19: 61,215,758 (GRCm39) A16S possibly damaging Het
Cyp4f18 T C 8: 72,747,044 (GRCm39) D317G possibly damaging Het
Dus1l T C 11: 120,683,930 (GRCm39) T173A possibly damaging Het
Dzip1 T C 14: 119,148,780 (GRCm39) T300A probably benign Het
Ggta1 A T 2: 35,292,635 (GRCm39) I224N probably damaging Het
Gm5150 A G 3: 16,060,479 (GRCm39) L3P probably damaging Het
Gm5592 A G 7: 40,937,804 (GRCm39) E362G probably benign Het
Gm7137 T C 10: 77,623,839 (GRCm39) probably benign Het
Gpatch2l A G 12: 86,291,089 (GRCm39) T91A possibly damaging Het
Hoxa13 G T 6: 52,237,284 (GRCm39) probably benign Het
Ift46 A G 9: 44,695,045 (GRCm39) D65G probably damaging Het
Kirrel1 C T 3: 86,996,458 (GRCm39) M380I probably null Het
Mapk11 T C 15: 89,029,653 (GRCm39) probably null Het
Mettl25 T C 10: 105,662,214 (GRCm39) D252G probably benign Het
Mrc2 G A 11: 105,239,257 (GRCm39) probably null Het
Or10ab4 C T 7: 107,654,989 (GRCm39) R267C probably benign Het
Pecam1 A G 11: 106,575,107 (GRCm39) V601A possibly damaging Het
Prkx A T X: 76,814,881 (GRCm39) F260I probably damaging Het
Rassf9 A T 10: 102,380,687 (GRCm39) D21V possibly damaging Het
Rmnd5a T A 6: 71,406,085 (GRCm39) I68L probably benign Het
Rock2 T C 12: 17,015,092 (GRCm39) S762P probably damaging Het
Septin4 T C 11: 87,458,070 (GRCm39) V148A possibly damaging Het
Srgap2 T C 1: 131,220,327 (GRCm39) T216A probably benign Het
Tasor2 G A 13: 3,624,359 (GRCm39) P1182S probably damaging Het
Vmn2r68 A C 7: 84,886,875 (GRCm39) V13G probably benign Het
Vps13d G C 4: 144,853,147 (GRCm39) N2322K possibly damaging Het
Xpo5 A G 17: 46,553,173 (GRCm39) probably null Het
Zswim9 T C 7: 13,011,196 (GRCm39) T51A possibly damaging 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
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
Predicted Primers PCR Primer
(F):5'- AACAGGATGCTGTGAGTGGC -3'
(R):5'- TAAGCACGTTCCAAGTCATCAC -3'

Sequencing Primer
(F):5'- CTTTGCGCTCAGGAGATGGC -3'
(R):5'- TCCCAGTAACTCTAAGTGGGC -3'
Posted On 2015-02-05