Incidental Mutation 'R3414:Vmn1r2'
ID 266721
Institutional Source Beutler Lab
Gene Symbol Vmn1r2
Ensembl Gene ENSMUSG00000115072
Gene Name vomeronasal 1 receptor 2
Synonyms Gm11776
MMRRC Submission 040632-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.841) question?
Stock # R3414 (G1)
Quality Score 175
Status Not validated
Chromosome 4
Chromosomal Location 3172083-3173003 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 3172696 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Lysine at position 205 (M205K)
Ref Sequence ENSEMBL: ENSMUSP00000154142 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000105160] [ENSMUST00000226198]
AlphaFold A2AMT6
Predicted Effect probably damaging
Transcript: ENSMUST00000105160
AA Change: M205K

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000100791
Gene: ENSMUSG00000115072
AA Change: M205K

DomainStartEndE-ValueType
Pfam:TAS2R 7 302 2.7e-8 PFAM
Pfam:V1R 30 298 6.3e-33 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000226198
AA Change: M205K

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.1%
Validation Efficiency 98% (42/43)
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3425401B19Rik T A 14: 32,383,559 (GRCm39) Q802L probably benign Het
Atp8b4 C A 2: 126,217,677 (GRCm39) W613L probably damaging Het
AW554918 C A 18: 25,533,129 (GRCm39) T261K possibly damaging Het
Cttnbp2 A G 6: 18,389,204 (GRCm39) V1178A probably benign Het
Ddx18 T C 1: 121,489,878 (GRCm39) N177S probably benign Het
Dhx29 A G 13: 113,083,807 (GRCm39) K621E probably damaging Het
Eef2 G T 10: 81,013,692 (GRCm39) R66L probably damaging Het
Ergic2 A G 6: 148,108,179 (GRCm39) probably benign Het
Fcna G C 2: 25,517,505 (GRCm39) P49A probably damaging Het
Hace1 T A 10: 45,524,771 (GRCm39) D234E possibly damaging Het
Ifi202b A G 1: 173,791,479 (GRCm39) S400P probably benign Het
Ighv1-23 C T 12: 114,728,087 (GRCm39) V112I probably benign Het
Il4i1 T C 7: 44,486,082 (GRCm39) L22P probably damaging Het
Il7 G T 3: 7,641,093 (GRCm39) Q67K probably benign Het
Inpp5d C A 1: 87,595,779 (GRCm39) T175N possibly damaging Het
Klk1b26 A G 7: 43,666,297 (GRCm39) I247V probably benign Het
Klrc1 A G 6: 129,654,726 (GRCm39) probably null Het
Lama1 T C 17: 68,044,598 (GRCm39) C166R probably damaging Het
Mrps5 A G 2: 127,438,832 (GRCm39) D219G probably benign Het
Mtus1 T C 8: 41,501,100 (GRCm39) T806A probably damaging Het
Naip2 G A 13: 100,325,771 (GRCm39) R46* probably null Het
Nos2 A T 11: 78,848,414 (GRCm39) Y1107F probably benign Het
Nsd3 T C 8: 26,190,047 (GRCm39) I135T probably damaging Het
Or13c7b C T 4: 43,821,258 (GRCm39) M34I probably benign Het
Or2d4 G T 7: 106,543,383 (GRCm39) S275* probably null Het
Or6c65 A G 10: 129,604,301 (GRCm39) H312R probably benign Het
Pla2g4f T C 2: 120,133,587 (GRCm39) S579G probably benign Het
Ppip5k1 A T 2: 121,158,142 (GRCm39) S252R probably damaging Het
Proc T A 18: 32,256,738 (GRCm39) T310S probably benign Het
Psg21 A T 7: 18,386,305 (GRCm39) L227Q probably damaging Het
Rusc2 T G 4: 43,415,935 (GRCm39) S414A probably damaging Het
Sec24a T A 11: 51,620,285 (GRCm39) N456Y probably damaging Het
Slc1a7 A G 4: 107,868,191 (GRCm39) E497G probably benign Het
Spag8 T A 4: 43,651,606 (GRCm39) S423C probably damaging Het
Spata13 A G 14: 60,944,172 (GRCm39) T522A probably benign Het
Top1mt T C 15: 75,529,025 (GRCm39) N573S probably benign Het
Trim69 T C 2: 122,009,125 (GRCm39) V395A probably benign Het
Ttn A T 2: 76,641,587 (GRCm39) L5176Q possibly damaging Het
Tusc1 C A 4: 93,223,173 (GRCm39) R162L probably damaging Het
Unc13b T A 4: 43,234,658 (GRCm39) probably benign Het
Utp25 A C 1: 192,810,810 (GRCm39) S64R possibly damaging Het
Zfhx4 A G 3: 5,468,883 (GRCm39) K3014E probably damaging Het
Other mutations in Vmn1r2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00328:Vmn1r2 APN 4 3,172,807 (GRCm39) missense probably damaging 0.98
PIT4151001:Vmn1r2 UTSW 4 3,172,623 (GRCm39) missense probably benign 0.00
PIT4354001:Vmn1r2 UTSW 4 3,172,162 (GRCm39) missense probably benign 0.23
R1836:Vmn1r2 UTSW 4 3,172,836 (GRCm39) missense probably damaging 1.00
R1855:Vmn1r2 UTSW 4 3,172,588 (GRCm39) missense probably damaging 1.00
R2319:Vmn1r2 UTSW 4 3,172,083 (GRCm39) start codon destroyed probably null 0.02
R3824:Vmn1r2 UTSW 4 3,172,413 (GRCm39) missense probably damaging 1.00
R5654:Vmn1r2 UTSW 4 3,172,261 (GRCm39) missense probably benign 0.17
R7084:Vmn1r2 UTSW 4 3,172,134 (GRCm39) missense probably benign 0.44
R7661:Vmn1r2 UTSW 4 3,172,149 (GRCm39) missense probably benign 0.00
R9134:Vmn1r2 UTSW 4 3,172,884 (GRCm39) missense probably damaging 1.00
R9324:Vmn1r2 UTSW 4 3,172,678 (GRCm39) missense probably damaging 0.99
R9614:Vmn1r2 UTSW 4 3,172,587 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GCTCAGTCAGTTGCCTTGTG -3'
(R):5'- CCCCATATCACTGGATAGTTTAAGTAG -3'

Sequencing Primer
(F):5'- TCTAAACATCTTGACTCCACTAAGAG -3'
(R):5'- GGTTCTAATGATAGCCACAATGG -3'
Posted On 2015-02-18