Incidental Mutation 'R5166:Vmn1r226'
ID 397328
Institutional Source Beutler Lab
Gene Symbol Vmn1r226
Ensembl Gene ENSMUSG00000042848
Gene Name vomeronasal 1 receptor 226
Synonyms V1re2
Accession Numbers
Essential gene? Probably non essential (E-score: 0.050) question?
Stock # R5166 (G1)
Quality Score 225
Status Not validated
Chromosome 17
Chromosomal Location 20907770-20908666 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 20908125 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Valine at position 119 (E119V)
Ref Sequence ENSEMBL: ENSMUSP00000058266 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000061756]
AlphaFold Q8R2A8
Predicted Effect probably benign
Transcript: ENSMUST00000061756
AA Change: E119V

PolyPhen 2 Score 0.434 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000058266
Gene: ENSMUSG00000042848
AA Change: E119V

DomainStartEndE-ValueType
Pfam:TAS2R 1 286 5.2e-12 PFAM
Pfam:7tm_1 22 285 9.1e-7 PFAM
Pfam:V1R 33 292 8.7e-26 PFAM
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acad12 T C 5: 121,738,083 (GRCm39) T435A probably benign Het
Adcy3 T A 12: 4,184,438 (GRCm39) I38N probably damaging Het
Aff1 A G 5: 103,902,523 (GRCm39) probably benign Het
Asxl1 A G 2: 153,243,041 (GRCm39) E1197G probably damaging Het
Brinp3 T A 1: 146,777,105 (GRCm39) N517K probably damaging Het
Carmil1 C T 13: 24,338,966 (GRCm39) probably null Het
Ccdc185 G A 1: 182,576,564 (GRCm39) Q42* probably null Het
Cdc23 C A 18: 34,784,742 (GRCm39) V7L unknown Het
Cdh10 A G 15: 19,013,446 (GRCm39) E682G probably damaging Het
Col6a3 C A 1: 90,738,330 (GRCm39) R456L probably damaging Het
Egf C T 3: 129,529,489 (GRCm39) R307H probably benign Het
Flt4 T C 11: 49,524,084 (GRCm39) probably null Het
Fstl5 A C 3: 76,536,267 (GRCm39) K26Q possibly damaging Het
Gk5 G T 9: 96,056,821 (GRCm39) A413S probably damaging Het
Glcci1 T A 6: 8,537,854 (GRCm39) S157R probably benign Het
Gzmc G A 14: 56,471,433 (GRCm39) A36V probably damaging Het
Hexb T C 13: 97,318,512 (GRCm39) N283S probably benign Het
Hydin A G 8: 111,249,774 (GRCm39) E2239G possibly damaging Het
Igkv10-95 A T 6: 68,657,544 (GRCm39) Y20F probably benign Het
Il17re A G 6: 113,439,923 (GRCm39) T181A probably benign Het
Kcnh6 G A 11: 105,911,145 (GRCm39) A514T possibly damaging Het
Kcnk10 G A 12: 98,401,254 (GRCm39) R460W probably damaging Het
Krtap5-2 A T 7: 141,728,721 (GRCm39) S320T unknown Het
Larp1b G T 3: 40,918,487 (GRCm39) E24* probably null Het
Mettl22 A G 16: 8,296,115 (GRCm39) T135A probably benign Het
Mlh1 A G 9: 111,070,581 (GRCm39) V378A probably benign Het
Mmrn1 A T 6: 60,953,474 (GRCm39) H585L probably benign Het
Myh14 A G 7: 44,278,279 (GRCm39) F1024L probably damaging Het
Nbea A T 3: 55,926,874 (GRCm39) H776Q probably damaging Het
Nod2 A G 8: 89,390,875 (GRCm39) D372G possibly damaging Het
Nptn C T 9: 58,526,263 (GRCm39) R137* probably null Het
Or9k2 T C 10: 129,998,430 (GRCm39) Y255C possibly damaging Het
Pm20d2 C T 4: 33,181,803 (GRCm39) V267I probably benign Het
Rassf10 A G 7: 112,553,627 (GRCm39) D76G probably benign Het
Rbbp5 A G 1: 132,418,303 (GRCm39) T41A possibly damaging Het
Rttn T C 18: 89,031,218 (GRCm39) V643A possibly damaging Het
Sbno2 C A 10: 79,902,762 (GRCm39) E421* probably null Het
Slc17a3 T C 13: 24,026,525 (GRCm39) probably null Het
Slc1a6 T A 10: 78,632,103 (GRCm39) probably null Het
Slco2b1 A G 7: 99,338,220 (GRCm39) S106P possibly damaging Het
Spef1 T C 2: 131,016,511 (GRCm39) N28S probably damaging Het
Srebf2 C A 15: 82,069,603 (GRCm39) T675N probably damaging Het
Srp68 C A 11: 116,156,300 (GRCm39) E147D probably damaging Het
Tbcd T A 11: 121,500,216 (GRCm39) L1114H possibly damaging Het
Tex15 T C 8: 34,066,420 (GRCm39) V1950A probably benign Het
Tnfsf9 T A 17: 57,413,263 (GRCm39) F148Y possibly damaging Het
Traf6 A G 2: 101,520,402 (GRCm39) D150G probably benign Het
Ttn A G 2: 76,693,717 (GRCm39) Y262H possibly damaging Het
Unc93b1 A G 19: 3,994,027 (GRCm39) Y386C probably damaging Het
Wrn A T 8: 33,842,100 (GRCm39) probably null Het
Zfp398 A G 6: 47,842,838 (GRCm39) I165V probably benign Het
Zfp850 A T 7: 27,689,781 (GRCm39) C142* probably null Het
Other mutations in Vmn1r226
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01081:Vmn1r226 APN 17 20,908,166 (GRCm39) missense probably damaging 1.00
IGL02103:Vmn1r226 APN 17 20,907,926 (GRCm39) missense probably damaging 0.98
IGL03394:Vmn1r226 APN 17 20,908,446 (GRCm39) missense probably benign 0.00
R0243:Vmn1r226 UTSW 17 20,907,839 (GRCm39) missense probably benign 0.00
R0605:Vmn1r226 UTSW 17 20,908,133 (GRCm39) missense probably benign 0.12
R1463:Vmn1r226 UTSW 17 20,907,994 (GRCm39) missense probably benign 0.00
R1571:Vmn1r226 UTSW 17 20,908,538 (GRCm39) missense probably damaging 0.97
R1677:Vmn1r226 UTSW 17 20,908,335 (GRCm39) missense probably damaging 1.00
R1917:Vmn1r226 UTSW 17 20,907,842 (GRCm39) missense probably damaging 0.99
R1918:Vmn1r226 UTSW 17 20,907,842 (GRCm39) missense probably damaging 0.99
R1919:Vmn1r226 UTSW 17 20,907,842 (GRCm39) missense probably damaging 0.99
R1980:Vmn1r226 UTSW 17 20,908,308 (GRCm39) missense possibly damaging 0.81
R2291:Vmn1r226 UTSW 17 20,908,475 (GRCm39) missense probably damaging 1.00
R2377:Vmn1r226 UTSW 17 20,907,992 (GRCm39) missense probably benign 0.05
R3878:Vmn1r226 UTSW 17 20,908,260 (GRCm39) missense possibly damaging 0.79
R6510:Vmn1r226 UTSW 17 20,908,115 (GRCm39) missense probably benign 0.37
R6599:Vmn1r226 UTSW 17 20,908,551 (GRCm39) missense probably benign 0.01
R7304:Vmn1r226 UTSW 17 20,908,011 (GRCm39) missense probably damaging 1.00
R8836:Vmn1r226 UTSW 17 20,908,133 (GRCm39) missense probably benign 0.00
R8955:Vmn1r226 UTSW 17 20,908,287 (GRCm39) missense possibly damaging 0.79
R9387:Vmn1r226 UTSW 17 20,907,831 (GRCm39) missense probably damaging 1.00
X0066:Vmn1r226 UTSW 17 20,908,512 (GRCm39) missense probably damaging 0.99
Z1177:Vmn1r226 UTSW 17 20,908,479 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- GGACTCCCTGAAGTAGTGAAAGC -3'
(R):5'- CACTGGAACTTACAATGAGCAG -3'

Sequencing Primer
(F):5'- CTCCCTGAAGTAGTGAAAGCTTTTG -3'
(R):5'- GACTTCAGGAAATACACAAAATGCTG -3'
Posted On 2016-07-06