Incidental Mutation 'R2849:Vmn1r181'
ID 251951
Institutional Source Beutler Lab
Gene Symbol Vmn1r181
Ensembl Gene ENSMUSG00000097425
Gene Name vomeronasal 1 receptor 181
Synonyms V1rd20
MMRRC Submission 040442-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # R2849 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 23683386-23684473 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 23683943 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Isoleucine at position 136 (S136I)
Ref Sequence ENSEMBL: ENSMUSP00000154403 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000181796] [ENSMUST00000226843] [ENSMUST00000226978] [ENSMUST00000227637] [ENSMUST00000228399] [ENSMUST00000228842]
AlphaFold Q0P547
Predicted Effect possibly damaging
Transcript: ENSMUST00000077386
AA Change: S136I

PolyPhen 2 Score 0.878 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000076604
Gene: ENSMUSG00000057946
AA Change: S136I

DomainStartEndE-ValueType
Pfam:TAS2R 8 295 3.6e-12 PFAM
Pfam:7tm_1 30 282 4.6e-7 PFAM
Pfam:V1R 41 295 4.2e-14 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000181796
AA Change: S136I

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000137685
Gene: ENSMUSG00000097425
AA Change: S136I

DomainStartEndE-ValueType
Pfam:TAS2R 8 296 3.9e-9 PFAM
Pfam:V1R 41 295 2.7e-13 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000226843
AA Change: S136I

PolyPhen 2 Score 0.878 (Sensitivity: 0.82; Specificity: 0.94)
Predicted Effect possibly damaging
Transcript: ENSMUST00000226978
AA Change: S136I

PolyPhen 2 Score 0.878 (Sensitivity: 0.82; Specificity: 0.94)
Predicted Effect possibly damaging
Transcript: ENSMUST00000227637
AA Change: S136I

PolyPhen 2 Score 0.878 (Sensitivity: 0.82; Specificity: 0.94)
Predicted Effect possibly damaging
Transcript: ENSMUST00000228399
AA Change: S136I

PolyPhen 2 Score 0.878 (Sensitivity: 0.82; Specificity: 0.94)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000228531
Predicted Effect possibly damaging
Transcript: ENSMUST00000228842
AA Change: S136I

PolyPhen 2 Score 0.878 (Sensitivity: 0.82; Specificity: 0.94)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000228607
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca17 G C 17: 24,508,481 (GRCm39) T1018R probably damaging Het
Abca8a T C 11: 109,932,931 (GRCm39) D1231G probably damaging Het
Adcy7 A G 8: 89,054,021 (GRCm39) I1017V probably benign Het
Agpat2 A G 2: 26,487,251 (GRCm39) I109T probably damaging Het
Aldh9a1 G A 1: 167,180,197 (GRCm39) R97H probably damaging Het
Als2 G A 1: 59,245,697 (GRCm39) T593M probably damaging Het
Ap3d1 G C 10: 80,577,742 (GRCm39) H28Q possibly damaging Het
Atxn1 A T 13: 45,720,175 (GRCm39) D573E probably damaging Het
Begain T A 12: 108,999,044 (GRCm39) M576L probably benign Het
Bod1l T C 5: 41,995,419 (GRCm39) N109S probably damaging Het
Boll A G 1: 55,385,532 (GRCm39) M131T possibly damaging Het
Celf2 T C 2: 6,608,936 (GRCm39) R282G probably damaging Het
Cers2 T C 3: 95,229,770 (GRCm39) F330L probably benign Het
Chst13 T C 6: 90,286,140 (GRCm39) D274G probably benign Het
Cimap1a A G 7: 140,429,182 (GRCm39) T156A probably benign Het
Cstdc5 T A 16: 36,187,814 (GRCm39) Q17L probably damaging Het
Dclk2 A G 3: 86,700,530 (GRCm39) V649A probably damaging Het
Deaf1 T C 7: 140,894,367 (GRCm39) *54W probably null Het
Fbf1 C T 11: 116,048,514 (GRCm39) probably null Het
Fbxo32 C T 15: 58,071,368 (GRCm39) S71N probably benign Het
Fbxo42 T A 4: 140,927,821 (GRCm39) N700K probably damaging Het
Fis1 T C 5: 136,991,971 (GRCm39) I55T possibly damaging Het
Fyco1 A T 9: 123,663,891 (GRCm39) L121* probably null Het
Gm2381 G A 7: 42,469,831 (GRCm39) P98S probably damaging Het
Grm7 G T 6: 110,623,309 (GRCm39) V161F probably damaging Het
Gtf2ird1 G A 5: 134,387,861 (GRCm39) T946I probably damaging Het
Hmcn1 G T 1: 150,439,350 (GRCm39) Y5494* probably null Het
Josd2 A G 7: 44,118,397 (GRCm39) probably null Het
Lfng T A 5: 140,597,622 (GRCm39) D149E probably damaging Het
Lrp1 C T 10: 127,378,165 (GRCm39) A4052T probably damaging Het
Lrrtm3 T C 10: 63,924,810 (GRCm39) N119S probably damaging Het
Lypd6 C T 2: 50,055,664 (GRCm39) P38L probably damaging Het
Msl3l2 T C 10: 55,991,538 (GRCm39) C88R probably benign Het
Nsd1 A G 13: 55,361,505 (GRCm39) T158A probably damaging Het
Nudt22 A T 19: 6,970,852 (GRCm39) S239R probably benign Het
Or4g7 T C 2: 111,309,699 (GRCm39) M190T probably benign Het
Or52r1c A T 7: 102,735,319 (GRCm39) D193V probably damaging Het
Osbpl8 T A 10: 111,105,297 (GRCm39) S251T probably benign Het
Otop3 T C 11: 115,235,384 (GRCm39) F339L probably damaging Het
Pcdhga10 T A 18: 37,881,253 (GRCm39) V338E possibly damaging Het
Pcnx2 A G 8: 126,487,666 (GRCm39) F1779S probably damaging Het
Plxna4 T C 6: 32,162,467 (GRCm39) K1349E probably damaging Het
Poteg A T 8: 27,971,704 (GRCm39) N406I probably benign Het
Ppp4r4 T C 12: 103,573,192 (GRCm39) V697A probably benign Het
Ptpra C A 2: 130,386,919 (GRCm39) H603Q probably benign Het
Rnf10 T C 5: 115,387,171 (GRCm39) D439G probably benign Het
Rnf43 T A 11: 87,623,093 (GRCm39) N731K probably benign Het
Slc2a4 T A 11: 69,836,997 (GRCm39) N116Y probably damaging Het
Slc6a15 C A 10: 103,240,552 (GRCm39) H392N probably benign Het
Slco6d1 C T 1: 98,394,441 (GRCm39) T375I probably benign Het
Smpd4 A G 16: 17,460,076 (GRCm39) D436G probably damaging Het
Spata22 G A 11: 73,244,571 (GRCm39) W311* probably null Het
Syt3 G A 7: 44,042,866 (GRCm39) V383I probably benign Het
Tle6 T A 10: 81,430,235 (GRCm39) I306F probably damaging Het
Tox3 G A 8: 90,975,018 (GRCm39) Q538* probably null Het
Trim24 T A 6: 37,933,388 (GRCm39) S656T probably damaging Het
Trnau1ap C A 4: 132,049,045 (GRCm39) V119F possibly damaging Het
Vmn1r82 T C 7: 12,039,333 (GRCm39) V202A probably damaging Het
Zfp607b G A 7: 27,401,819 (GRCm39) V92I probably benign Het
Zfp964 G C 8: 70,116,504 (GRCm39) C368S unknown Het
Zw10 A G 9: 48,968,941 (GRCm39) probably null Het
Other mutations in Vmn1r181
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01443:Vmn1r181 APN 7 23,684,006 (GRCm39) missense possibly damaging 0.91
IGL02055:Vmn1r181 APN 7 23,683,978 (GRCm39) missense probably damaging 1.00
IGL02444:Vmn1r181 APN 7 23,683,948 (GRCm39) missense probably damaging 1.00
IGL03012:Vmn1r181 APN 7 23,684,027 (GRCm39) missense probably damaging 0.98
IGL03026:Vmn1r181 APN 7 23,684,000 (GRCm39) missense possibly damaging 0.94
R0255:Vmn1r181 UTSW 7 23,683,759 (GRCm39) missense probably benign 0.02
R1481:Vmn1r181 UTSW 7 23,684,137 (GRCm39) missense probably damaging 1.00
R2847:Vmn1r181 UTSW 7 23,683,943 (GRCm39) missense possibly damaging 0.88
R2848:Vmn1r181 UTSW 7 23,683,943 (GRCm39) missense possibly damaging 0.88
R3441:Vmn1r181 UTSW 7 23,684,308 (GRCm39) missense probably benign 0.05
R3757:Vmn1r181 UTSW 7 23,683,909 (GRCm39) missense possibly damaging 0.90
R3945:Vmn1r181 UTSW 7 23,683,577 (GRCm39) missense probably damaging 0.98
R3983:Vmn1r181 UTSW 7 23,684,234 (GRCm39) missense probably benign 0.23
R4780:Vmn1r181 UTSW 7 23,684,008 (GRCm39) missense possibly damaging 0.64
R4999:Vmn1r181 UTSW 7 23,683,790 (GRCm39) missense probably damaging 0.99
R5463:Vmn1r181 UTSW 7 23,683,787 (GRCm39) missense probably benign 0.02
R5672:Vmn1r181 UTSW 7 23,683,741 (GRCm39) missense probably damaging 1.00
R6229:Vmn1r181 UTSW 7 23,683,580 (GRCm39) missense probably damaging 1.00
R6315:Vmn1r181 UTSW 7 23,684,183 (GRCm39) missense probably benign 0.23
R6316:Vmn1r181 UTSW 7 23,684,183 (GRCm39) missense probably benign 0.23
R6317:Vmn1r181 UTSW 7 23,684,183 (GRCm39) missense probably benign 0.23
R6324:Vmn1r181 UTSW 7 23,684,183 (GRCm39) missense probably benign 0.23
R6326:Vmn1r181 UTSW 7 23,684,183 (GRCm39) missense probably benign 0.23
R6988:Vmn1r181 UTSW 7 23,684,272 (GRCm39) missense probably damaging 1.00
R7446:Vmn1r181 UTSW 7 23,684,356 (GRCm39) missense probably benign 0.01
R7972:Vmn1r181 UTSW 7 23,683,871 (GRCm39) missense probably benign 0.30
R8465:Vmn1r181 UTSW 7 23,684,309 (GRCm39) missense possibly damaging 0.65
R9096:Vmn1r181 UTSW 7 23,684,444 (GRCm39) missense probably benign 0.00
R9097:Vmn1r181 UTSW 7 23,684,444 (GRCm39) missense probably benign 0.00
X0067:Vmn1r181 UTSW 7 23,684,326 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- ACATAGCTGTGGCCAATGC -3'
(R):5'- GTGGCATCATGGGCAAATC -3'

Sequencing Primer
(F):5'- CATGGCTTTTGCTCCAAGAAG -3'
(R):5'- CATCATGGGCAAATCGCAAG -3'
Posted On 2014-12-04