Incidental Mutation 'R0381:Vmn1r201'
ID 30981
Institutional Source Beutler Lab
Gene Symbol Vmn1r201
Ensembl Gene ENSMUSG00000094898
Gene Name vomeronasal 1 receptor 201
Synonyms V1ri4
MMRRC Submission 038587-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.139) question?
Stock # R0381 (G1)
Quality Score 225
Status Not validated
Chromosome 13
Chromosomal Location 22658788-22659690 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 22659193 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tryptophan to Arginine at position 136 (W136R)
Ref Sequence ENSEMBL: ENSMUSP00000154790 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000091730] [ENSMUST00000226330] [ENSMUST00000226965]
AlphaFold Q8R262
Predicted Effect probably damaging
Transcript: ENSMUST00000091730
AA Change: W136R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000089324
Gene: ENSMUSG00000094898
AA Change: W136R

DomainStartEndE-ValueType
Pfam:TAS2R 1 293 2.4e-9 PFAM
Pfam:V1R 35 299 1.1e-40 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000226330
AA Change: W136R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000226965
AA Change: W136R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.4%
  • 10x: 96.5%
  • 20x: 93.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc8 A G 7: 45,757,858 (GRCm39) V1297A possibly damaging Het
Agbl2 C T 2: 90,614,442 (GRCm39) H25Y probably damaging Het
Akap11 A T 14: 78,750,990 (GRCm39) W466R probably benign Het
Ccdc66 T A 14: 27,213,890 (GRCm39) Q471L probably damaging Het
Dennd1c G A 17: 57,380,822 (GRCm39) A210V probably damaging Het
F13b A G 1: 139,438,597 (GRCm39) K334E probably damaging Het
Fam186a A C 15: 99,840,055 (GRCm39) I2063R probably damaging Het
Fcrl5 T C 3: 87,353,767 (GRCm39) Y371H probably damaging Het
Fnbp1 C T 2: 30,923,041 (GRCm39) G549D probably benign Het
Fndc3a A G 14: 72,794,067 (GRCm39) Y869H probably benign Het
Gm7592 A G 1: 85,454,437 (GRCm39) noncoding transcript Het
Gucy2d C A 7: 98,108,209 (GRCm39) probably null Het
Hmcn1 C T 1: 150,479,562 (GRCm39) C4634Y probably damaging Het
Kctd5 A G 17: 24,278,194 (GRCm39) probably null Het
Kics2 T C 10: 121,581,280 (GRCm39) Y94H probably damaging Het
Mettl24 C A 10: 40,622,386 (GRCm39) H203N probably damaging Het
Mitf A G 6: 97,970,104 (GRCm39) E17G probably damaging Het
Mmut T A 17: 41,248,149 (GRCm39) W59R probably benign Het
Mrc1 G A 2: 14,312,720 (GRCm39) D881N probably benign Het
Mrm1 T C 11: 84,709,509 (GRCm39) T183A possibly damaging Het
Mylk G A 16: 34,605,344 (GRCm39) probably null Het
Nab2 G A 10: 127,500,936 (GRCm39) A19V probably damaging Het
Ntsr2 T A 12: 16,709,719 (GRCm39) Y333* probably null Het
Sephs1 A G 2: 4,904,371 (GRCm39) T250A probably benign Het
Sypl2 T C 3: 108,133,473 (GRCm39) E32G possibly damaging Het
Tasp1 T C 2: 139,793,403 (GRCm39) K258E probably damaging Het
Tcam1 G A 11: 106,174,904 (GRCm39) E120K probably benign Het
Tenm4 G T 7: 96,555,088 (GRCm39) V2561F probably damaging Het
Tmc1 T C 19: 20,776,409 (GRCm39) Y650C probably damaging Het
Trim34b T C 7: 103,979,062 (GRCm39) L103P probably damaging Het
Usp47 T C 7: 111,662,600 (GRCm39) probably null Het
Vmn2r104 A T 17: 20,268,264 (GRCm39) Y68* probably null Het
Wscd2 T A 5: 113,689,192 (GRCm39) L66Q probably damaging Het
Other mutations in Vmn1r201
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02792:Vmn1r201 APN 13 22,659,014 (GRCm39) missense probably damaging 0.97
IGL03137:Vmn1r201 APN 13 22,658,974 (GRCm39) missense probably benign 0.01
R0278:Vmn1r201 UTSW 13 22,659,194 (GRCm39) missense probably damaging 1.00
R0544:Vmn1r201 UTSW 13 22,659,316 (GRCm39) missense probably benign 0.04
R1411:Vmn1r201 UTSW 13 22,658,849 (GRCm39) missense probably benign 0.01
R1544:Vmn1r201 UTSW 13 22,658,968 (GRCm39) missense probably benign 0.20
R1850:Vmn1r201 UTSW 13 22,658,801 (GRCm39) missense probably benign 0.08
R1891:Vmn1r201 UTSW 13 22,659,425 (GRCm39) missense probably benign 0.01
R2071:Vmn1r201 UTSW 13 22,658,995 (GRCm39) missense probably benign 0.34
R4183:Vmn1r201 UTSW 13 22,659,022 (GRCm39) missense probably benign 0.01
R4924:Vmn1r201 UTSW 13 22,658,882 (GRCm39) missense probably benign 0.00
R4989:Vmn1r201 UTSW 13 22,659,622 (GRCm39) missense possibly damaging 0.95
R5028:Vmn1r201 UTSW 13 22,659,530 (GRCm39) nonsense probably null
R5318:Vmn1r201 UTSW 13 22,659,092 (GRCm39) missense probably damaging 1.00
R5369:Vmn1r201 UTSW 13 22,659,672 (GRCm39) missense probably benign 0.00
R5682:Vmn1r201 UTSW 13 22,659,355 (GRCm39) missense probably damaging 0.99
R5699:Vmn1r201 UTSW 13 22,659,409 (GRCm39) missense probably damaging 1.00
R6180:Vmn1r201 UTSW 13 22,659,499 (GRCm39) missense possibly damaging 0.94
R6273:Vmn1r201 UTSW 13 22,659,385 (GRCm39) missense probably damaging 1.00
R6295:Vmn1r201 UTSW 13 22,659,533 (GRCm39) missense probably benign 0.00
R6331:Vmn1r201 UTSW 13 22,659,521 (GRCm39) missense probably damaging 1.00
R7296:Vmn1r201 UTSW 13 22,659,509 (GRCm39) missense possibly damaging 0.69
R7758:Vmn1r201 UTSW 13 22,658,989 (GRCm39) missense not run
R7832:Vmn1r201 UTSW 13 22,659,538 (GRCm39) missense possibly damaging 0.76
R7887:Vmn1r201 UTSW 13 22,658,956 (GRCm39) missense probably damaging 0.99
R7976:Vmn1r201 UTSW 13 22,658,875 (GRCm39) missense probably benign 0.32
R8676:Vmn1r201 UTSW 13 22,659,422 (GRCm39) missense probably damaging 1.00
R9228:Vmn1r201 UTSW 13 22,659,670 (GRCm39) missense probably benign 0.21
R9570:Vmn1r201 UTSW 13 22,659,236 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGCAGTTTATCTGGCAAGGATGGC -3'
(R):5'- CACCGTGAAACCTGTGTAGAAGGAG -3'

Sequencing Primer
(F):5'- AGTCCCAGGACAACCATTTGG -3'
(R):5'- TGAGAACACTCCATGTAGCTCTG -3'
Posted On 2013-04-24