Incidental Mutation 'R7672:Vmn1r202'
ID 592255
Institutional Source Beutler Lab
Gene Symbol Vmn1r202
Ensembl Gene ENSMUSG00000094379
Gene Name vomeronasal 1 receptor 202
Synonyms V1ri7
Accession Numbers
Essential gene? Probably non essential (E-score: 0.088) question?
Stock # R7672 (G1)
Quality Score 225.009
Status Not validated
Chromosome 13
Chromosomal Location 22685507-22686415 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 22685850 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 189 (V189A)
Ref Sequence ENSEMBL: ENSMUSP00000077711 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078642] [ENSMUST00000228020]
AlphaFold Q8R259
Predicted Effect probably benign
Transcript: ENSMUST00000078642
AA Change: V189A

PolyPhen 2 Score 0.452 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000077711
Gene: ENSMUSG00000094379
AA Change: V189A

DomainStartEndE-ValueType
Pfam:TAS2R 5 301 2.2e-11 PFAM
Pfam:V1R 35 300 5.6e-44 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000228020
AA Change: V189A

PolyPhen 2 Score 0.452 (Sensitivity: 0.89; Specificity: 0.90)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 78 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9130023H24Rik T C 7: 127,836,191 (GRCm39) H134R probably damaging Het
Adcy4 A G 14: 56,018,362 (GRCm39) M195T probably benign Het
Aktip T C 8: 91,856,285 (GRCm39) N64S possibly damaging Het
Aldoart1 C A 4: 72,770,747 (GRCm39) M20I probably benign Het
Alms1 T C 6: 85,592,333 (GRCm39) L395P probably damaging Het
Ankrd9 C A 12: 110,943,180 (GRCm39) V252F probably benign Het
Apof A T 10: 128,104,885 (GRCm39) H13L probably benign Het
Bahcc1 T C 11: 120,174,172 (GRCm39) F1644S possibly damaging Het
Baz2a A G 10: 127,959,726 (GRCm39) D1377G possibly damaging Het
Bbox1 T A 2: 110,135,794 (GRCm39) I62F probably damaging Het
BC028528 CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT 3: 95,795,448 (GRCm39) probably benign Het
BC028528 TCTGTGGTCACTGGT TCTGTGGTCACTGGTGCTGTGGTCACTGGT 3: 95,795,487 (GRCm39) probably benign Het
BC028528 GTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTG GTTCTGTGGTCACTGATTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTG 3: 95,795,455 (GRCm39) probably benign Het
Bcas3 C T 11: 85,286,213 (GRCm39) R124* probably null Het
Bpnt1 T C 1: 185,078,879 (GRCm39) V114A probably damaging Het
Ccnd1 C T 7: 144,487,793 (GRCm39) R228H possibly damaging Het
Cd244a T C 1: 171,404,853 (GRCm39) V235A probably benign Het
Cramp1 C T 17: 25,201,440 (GRCm39) E681K probably damaging Het
Crebbp C T 16: 3,902,574 (GRCm39) A2222T probably benign Het
Cyp1a2 T A 9: 57,589,620 (GRCm39) T65S probably benign Het
Cyp26b1 T G 6: 84,561,351 (GRCm39) K104Q probably benign Het
D430041D05Rik T C 2: 104,071,581 (GRCm39) I556V probably benign Het
Dnase1l2 A G 17: 24,661,219 (GRCm39) L102P probably damaging Het
Eef1ece2 C A 16: 20,457,417 (GRCm39) A483E probably damaging Het
Elac1 C T 18: 73,871,925 (GRCm39) G357S probably benign Het
Enam C A 5: 88,651,830 (GRCm39) T1113N possibly damaging Het
Eogt A T 6: 97,090,870 (GRCm39) I423N probably damaging Het
Epc2 T C 2: 49,435,831 (GRCm39) S612P possibly damaging Het
Fam107b T C 2: 3,773,959 (GRCm39) V24A probably damaging Het
Fhip2a A G 19: 57,373,750 (GRCm39) H670R possibly damaging Het
Foxj3 C T 4: 119,477,429 (GRCm39) P413L unknown Het
Frg1 T C 8: 41,870,040 (GRCm39) probably benign Het
Fsip2 T A 2: 82,820,455 (GRCm39) V5396D possibly damaging Het
Hdlbp T C 1: 93,364,821 (GRCm39) T149A possibly damaging Het
Heatr1 A T 13: 12,453,545 (GRCm39) Q2140L probably damaging Het
Iqcd T C 5: 120,744,881 (GRCm39) L403P probably damaging Het
Kifbp A G 10: 62,413,852 (GRCm39) I102T probably benign Het
Kpna2 T G 11: 106,879,789 (GRCm39) N505T probably benign Het
Lipo3 T A 19: 33,757,785 (GRCm39) E228V probably benign Het
Map4k3 C T 17: 80,922,500 (GRCm39) V474I possibly damaging Het
Mrpl11 T C 19: 5,012,424 (GRCm39) S2P probably damaging Het
Mug2 A G 6: 122,017,678 (GRCm39) I472V probably benign Het
Myom1 G A 17: 71,391,235 (GRCm39) V915M possibly damaging Het
Nedd9 A T 13: 41,492,198 (GRCm39) I104N possibly damaging Het
Nphp3 A G 9: 103,909,159 (GRCm39) M790V probably benign Het
Nr3c2 C T 8: 77,635,838 (GRCm39) P313L probably damaging Het
Obsl1 A G 1: 75,469,365 (GRCm39) V1192A probably benign Het
Or10j2 C T 1: 173,098,440 (GRCm39) R233W probably benign Het
Or52e7 A G 7: 104,684,750 (GRCm39) H115R probably damaging Het
Or5t16 T C 2: 86,818,663 (GRCm39) I286V possibly damaging Het
Prr5l T G 2: 101,565,083 (GRCm39) E151A probably damaging Het
Psmb8 G T 17: 34,417,404 (GRCm39) R11L probably benign Het
Ptprg T A 14: 12,211,668 (GRCm38) H983Q probably benign Het
Ptprj T C 2: 90,290,940 (GRCm39) N600D possibly damaging Het
Rasgrp1 T C 2: 117,118,424 (GRCm39) I522V probably damaging Het
Rc3h1 A G 1: 160,778,454 (GRCm39) S460G probably damaging Het
Rhot2 A G 17: 26,062,079 (GRCm39) probably null Het
Sall1 T C 8: 89,757,927 (GRCm39) T726A probably damaging Het
Samd9l G A 6: 3,373,646 (GRCm39) T1205I probably benign Het
Sh2b3 C T 5: 121,956,822 (GRCm39) probably null Het
Slc22a18 G T 7: 143,044,557 (GRCm39) C170F probably damaging Het
Slc24a1 G A 9: 64,855,209 (GRCm39) T566I unknown Het
Slc4a5 T A 6: 83,237,517 (GRCm39) C167S probably damaging Het
Slc8b1 T G 5: 120,671,100 (GRCm39) V579G probably damaging Het
Snrnp200 T C 2: 127,063,822 (GRCm39) V667A probably damaging Het
Sp8 C A 12: 118,813,070 (GRCm39) S308R possibly damaging Het
Srsf9 T A 5: 115,468,619 (GRCm39) V85E probably damaging Het
Syne1 T C 10: 5,168,527 (GRCm39) I5285V probably benign Het
Tmem245 T C 4: 56,947,069 (GRCm39) I115V probably benign Het
Triqk A G 4: 12,980,502 (GRCm39) D82G probably benign Het
Trmt11 A T 10: 30,463,520 (GRCm39) S198R probably damaging Het
Ube4b C T 4: 149,471,661 (GRCm39) R75Q probably benign Het
Ugt3a1 C T 15: 9,310,779 (GRCm39) Q354* probably null Het
Vmn2r26 A G 6: 124,016,606 (GRCm39) I357V probably benign Het
Wdr6 T C 9: 108,450,947 (GRCm39) K914R probably benign Het
Zfat T C 15: 68,130,535 (GRCm39) M1V probably null Het
Zfp207 A G 11: 80,280,116 (GRCm39) M171V probably benign Het
Zfp568 C T 7: 29,697,212 (GRCm39) T44I probably damaging Het
Other mutations in Vmn1r202
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01472:Vmn1r202 APN 13 22,686,159 (GRCm39) missense possibly damaging 0.95
IGL01516:Vmn1r202 APN 13 22,685,632 (GRCm39) missense possibly damaging 0.57
IGL01722:Vmn1r202 APN 13 22,685,890 (GRCm39) missense probably benign 0.00
IGL02641:Vmn1r202 APN 13 22,686,274 (GRCm39) missense probably benign 0.34
IGL02863:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL02876:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL02891:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL02943:Vmn1r202 APN 13 22,686,364 (GRCm39) missense probably benign 0.01
IGL03057:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL03114:Vmn1r202 APN 13 22,685,500 (GRCm39) utr 3 prime probably benign
IGL03114:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL03143:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL03159:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL03097:Vmn1r202 UTSW 13 22,685,640 (GRCm39) missense probably benign 0.00
R0611:Vmn1r202 UTSW 13 22,685,824 (GRCm39) missense probably damaging 1.00
R1350:Vmn1r202 UTSW 13 22,685,886 (GRCm39) missense probably benign 0.04
R1666:Vmn1r202 UTSW 13 22,685,540 (GRCm39) missense possibly damaging 0.94
R1668:Vmn1r202 UTSW 13 22,685,540 (GRCm39) missense possibly damaging 0.94
R1803:Vmn1r202 UTSW 13 22,686,313 (GRCm39) missense probably benign 0.00
R2035:Vmn1r202 UTSW 13 22,685,772 (GRCm39) missense probably damaging 0.98
R2112:Vmn1r202 UTSW 13 22,685,904 (GRCm39) missense possibly damaging 0.76
R2145:Vmn1r202 UTSW 13 22,685,953 (GRCm39) missense possibly damaging 0.79
R3026:Vmn1r202 UTSW 13 22,685,932 (GRCm39) missense probably benign 0.03
R3808:Vmn1r202 UTSW 13 22,686,070 (GRCm39) missense possibly damaging 0.83
R4714:Vmn1r202 UTSW 13 22,685,977 (GRCm39) missense probably damaging 1.00
R5016:Vmn1r202 UTSW 13 22,686,375 (GRCm39) missense probably damaging 1.00
R5124:Vmn1r202 UTSW 13 22,685,920 (GRCm39) missense probably benign 0.01
R6136:Vmn1r202 UTSW 13 22,685,632 (GRCm39) missense possibly damaging 0.90
R6365:Vmn1r202 UTSW 13 22,686,374 (GRCm39) missense probably benign 0.12
R6982:Vmn1r202 UTSW 13 22,685,917 (GRCm39) missense probably benign 0.02
R7293:Vmn1r202 UTSW 13 22,685,872 (GRCm39) missense probably benign 0.00
R7502:Vmn1r202 UTSW 13 22,686,188 (GRCm39) missense probably damaging 1.00
R7603:Vmn1r202 UTSW 13 22,685,790 (GRCm39) missense probably damaging 1.00
R7822:Vmn1r202 UTSW 13 22,686,241 (GRCm39) missense probably damaging 1.00
R7954:Vmn1r202 UTSW 13 22,685,871 (GRCm39) missense probably benign 0.01
R8026:Vmn1r202 UTSW 13 22,686,314 (GRCm39) missense possibly damaging 0.65
R8419:Vmn1r202 UTSW 13 22,685,985 (GRCm39) missense probably damaging 1.00
R9079:Vmn1r202 UTSW 13 22,685,602 (GRCm39) missense probably benign 0.00
R9194:Vmn1r202 UTSW 13 22,686,316 (GRCm39) missense possibly damaging 0.48
Predicted Primers PCR Primer
(F):5'- ACTGTGGAACCTGTGTATAAGGAG -3'
(R):5'- CTCAGACACCATGGCATGTTC -3'

Sequencing Primer
(F):5'- TGTATAAGGAGAAAATGAAATCTGCC -3'
(R):5'- GCATGTTCTTGCCTTTCTCC -3'
Posted On 2019-11-12