Incidental Mutation 'IGL02261:Vmn1r167'
ID 286737
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r167
Ensembl Gene ENSMUSG00000090715
Gene Name vomeronasal 1 receptor 167
Synonyms Gm6279
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # IGL02261
Quality Score
Status
Chromosome 7
Chromosomal Location 23204067-23205014 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 23204261 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Valine at position 252 (M252V)
Ref Sequence ENSEMBL: ENSMUSP00000153774 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000164527] [ENSMUST00000227713]
AlphaFold G3UW71
Predicted Effect probably benign
Transcript: ENSMUST00000164527
AA Change: M252V

PolyPhen 2 Score 0.173 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000129193
Gene: ENSMUSG00000090715
AA Change: M252V

DomainStartEndE-ValueType
Pfam:TAS2R 19 307 1.5e-13 PFAM
Pfam:7tm_1 41 299 3.8e-6 PFAM
Pfam:V1R 52 306 2.1e-18 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000227713
AA Change: M252V

PolyPhen 2 Score 0.173 (Sensitivity: 0.92; Specificity: 0.87)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ambn G A 5: 88,604,807 (GRCm39) V27M probably damaging Het
Ank1 A G 8: 23,578,015 (GRCm39) N222D probably damaging Het
Bcas3 A T 11: 85,422,756 (GRCm39) T542S probably damaging Het
Btbd1 A T 7: 81,455,507 (GRCm39) I288N probably damaging Het
Ctps1 C T 4: 120,399,776 (GRCm39) V500I possibly damaging Het
Cul5 A C 9: 53,546,337 (GRCm39) V345G probably damaging Het
Dchs1 A G 7: 105,421,776 (GRCm39) Y215H probably damaging Het
Dmxl1 T A 18: 49,973,566 (GRCm39) M67K possibly damaging Het
Egln2 C T 7: 26,859,291 (GRCm39) E353K possibly damaging Het
Fbxw5 G T 2: 25,393,746 (GRCm39) A325S probably benign Het
Fhdc1 G A 3: 84,352,042 (GRCm39) A1061V possibly damaging Het
Gaa A G 11: 119,172,091 (GRCm39) *207W probably null Het
Herc2 A G 7: 55,856,492 (GRCm39) T3947A probably damaging Het
Ifit2 T A 19: 34,551,624 (GRCm39) I388N probably damaging Het
Ikzf4 T C 10: 128,472,591 (GRCm39) T209A possibly damaging Het
Il17re A T 6: 113,445,472 (GRCm39) probably benign Het
Insrr T A 3: 87,708,029 (GRCm39) L157Q probably damaging Het
Kcnq2 T G 2: 180,723,483 (GRCm39) Y631S probably damaging Het
Lrrfip1 A G 1: 91,039,890 (GRCm39) I198V probably benign Het
Mir7684 A T 15: 82,273,345 (GRCm39) probably benign Het
Mphosph9 C T 5: 124,398,150 (GRCm39) E1049K probably damaging Het
Mroh1 G A 15: 76,313,360 (GRCm39) R611Q probably benign Het
Mynn A T 3: 30,661,280 (GRCm39) I121F possibly damaging Het
Ndrg2 G A 14: 52,148,566 (GRCm39) R32C probably damaging Het
Or2ab1 T C 11: 58,488,630 (GRCm39) I138T probably benign Het
Or4p7 A G 2: 88,221,725 (GRCm39) I45V probably benign Het
Ppp1r9b A G 11: 94,892,936 (GRCm39) E260G probably damaging Het
Psd4 A G 2: 24,291,756 (GRCm39) S652G probably damaging Het
Psg25 C T 7: 18,255,268 (GRCm39) R416H probably benign Het
Pygm T A 19: 6,438,301 (GRCm39) N171K probably damaging Het
Rbm46 A T 3: 82,771,723 (GRCm39) D297E possibly damaging Het
Selenov T A 7: 27,990,004 (GRCm39) T167S probably benign Het
Serpina10 T C 12: 103,583,208 (GRCm39) Y358C probably damaging Het
Slc27a3 T C 3: 90,295,002 (GRCm39) R352G probably benign Het
Snx33 T C 9: 56,833,862 (GRCm39) D69G probably benign Het
St8sia2 G T 7: 73,616,594 (GRCm39) P127H probably damaging Het
Thbd T C 2: 148,248,401 (GRCm39) K489R probably benign Het
Ttn A T 2: 76,767,049 (GRCm39) C3039S probably damaging Het
Xdh A G 17: 74,220,960 (GRCm39) S590P possibly damaging Het
Zfp827 G A 8: 79,906,708 (GRCm39) V907I probably damaging Het
Other mutations in Vmn1r167
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02137:Vmn1r167 APN 7 23,204,864 (GRCm39) missense probably damaging 0.98
IGL02963:Vmn1r167 APN 7 23,204,975 (GRCm39) missense possibly damaging 0.60
R0054:Vmn1r167 UTSW 7 23,204,334 (GRCm39) missense possibly damaging 0.89
R0555:Vmn1r167 UTSW 7 23,204,512 (GRCm39) missense probably damaging 1.00
R0766:Vmn1r167 UTSW 7 23,204,548 (GRCm39) missense probably benign 0.01
R1312:Vmn1r167 UTSW 7 23,204,548 (GRCm39) missense probably benign 0.01
R1464:Vmn1r167 UTSW 7 23,204,681 (GRCm39) missense possibly damaging 0.62
R1464:Vmn1r167 UTSW 7 23,204,681 (GRCm39) missense possibly damaging 0.62
R1532:Vmn1r167 UTSW 7 23,204,204 (GRCm39) missense probably benign 0.01
R1937:Vmn1r167 UTSW 7 23,204,452 (GRCm39) missense probably benign 0.25
R2162:Vmn1r167 UTSW 7 23,204,224 (GRCm39) missense possibly damaging 0.91
R4639:Vmn1r167 UTSW 7 23,205,011 (GRCm39) missense probably benign 0.00
R4661:Vmn1r167 UTSW 7 23,204,117 (GRCm39) missense probably damaging 1.00
R4845:Vmn1r167 UTSW 7 23,204,158 (GRCm39) missense probably benign 0.01
R4868:Vmn1r167 UTSW 7 23,204,161 (GRCm39) missense probably benign
R4993:Vmn1r167 UTSW 7 23,204,653 (GRCm39) missense probably damaging 1.00
R5693:Vmn1r167 UTSW 7 23,204,646 (GRCm39) nonsense probably null
R6622:Vmn1r167 UTSW 7 23,205,014 (GRCm39) start codon destroyed probably null
R7800:Vmn1r167 UTSW 7 23,204,069 (GRCm39) makesense probably null
R8297:Vmn1r167 UTSW 7 23,204,215 (GRCm39) missense probably damaging 1.00
R8365:Vmn1r167 UTSW 7 23,204,200 (GRCm39) missense probably benign 0.03
R8411:Vmn1r167 UTSW 7 23,204,981 (GRCm39) missense possibly damaging 0.86
R9667:Vmn1r167 UTSW 7 23,204,990 (GRCm39) missense probably benign 0.06
Posted On 2015-04-16