Incidental Mutation 'R6036:Vmn1r70'
ID 479204
Institutional Source Beutler Lab
Gene Symbol Vmn1r70
Ensembl Gene ENSMUSG00000045340
Gene Name vomeronasal 1 receptor 70
Synonyms V1rl1
MMRRC Submission 043257-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.068) question?
Stock # R6036 (G1)
Quality Score 225.009
Status Not validated
Chromosome 7
Chromosomal Location 10631532-10636530 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 10633903 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Glutamine to Arginine at position 87 (Q87R)
Ref Sequence ENSEMBL: ENSMUSP00000154793 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055847] [ENSMUST00000226255] [ENSMUST00000228090]
AlphaFold Q8R254
Predicted Effect probably damaging
Transcript: ENSMUST00000055847
AA Change: Q106R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000054445
Gene: ENSMUSG00000045340
AA Change: Q106R

DomainStartEndE-ValueType
Pfam:TAS2R 1 292 2.6e-9 PFAM
Pfam:V1R 33 295 3.1e-31 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000226182
Predicted Effect probably damaging
Transcript: ENSMUST00000226255
AA Change: Q106R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000228090
AA Change: Q87R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 99.0%
  • 10x: 92.6%
  • 20x: 72.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abi3 T C 11: 95,832,858 probably benign Het
Ago1 C T 4: 126,443,228 R228H probably damaging Het
Alpk3 G A 7: 81,093,257 V941M probably benign Het
Ano4 A G 10: 88,982,265 W588R possibly damaging Het
Atp6v1a A G 16: 44,098,831 Y464H probably benign Het
Barx2 A T 9: 31,913,008 D28E probably damaging Het
Cabp5 A T 7: 13,401,335 M67L probably damaging Het
Col10a1 A G 10: 34,395,282 T417A probably benign Het
Dnah2 C T 11: 69,458,920 R2399Q probably benign Het
Eif4enif1 T C 11: 3,239,420 S227P probably damaging Het
Erv3 G A 2: 131,856,005 H145Y possibly damaging Het
Exoc5 T C 14: 49,014,322 T591A possibly damaging Het
F5 A T 1: 164,184,996 E493V probably damaging Het
Gm8444 G T 15: 81,843,593 probably benign Het
Gria4 T A 9: 4,537,646 I221L probably benign Het
Hc T C 2: 35,039,684 T249A probably benign Het
Herc2 A G 7: 56,068,053 T48A probably benign Het
Hist1h2bl A T 13: 21,715,978 S56T probably damaging Het
Hp A G 8: 109,576,774 probably null Het
Ifna15 T G 4: 88,558,073 D58A possibly damaging Het
Kcnj1 A T 9: 32,397,125 M262L probably benign Het
Krt83 A C 15: 101,487,531 I320S possibly damaging Het
Megf10 A G 18: 57,242,727 N242D probably damaging Het
Nup155 A G 15: 8,128,411 T451A probably benign Het
Olfr1277 C T 2: 111,269,612 G252R probably damaging Het
Olfr1288 T C 2: 111,478,988 L68P probably damaging Het
Olfr559 T A 7: 102,724,485 I2F probably benign Het
Olfr701 A T 7: 106,818,460 I126F probably damaging Het
Olfr930 A G 9: 38,930,920 I250V probably damaging Het
Pdzd8 G A 19: 59,305,209 P403S probably damaging Het
Piezo2 G A 18: 63,114,948 Q494* probably null Het
Plag1 T C 4: 3,904,618 E191G possibly damaging Het
Pou4f2 A T 8: 78,435,474 S167T probably damaging Het
Scd4 G A 19: 44,344,792 D319N probably damaging Het
Senp2 A T 16: 22,028,558 R279* probably null Het
Sh3rf3 G A 10: 58,813,984 G137D probably benign Het
Simc1 C T 13: 54,524,621 P261S probably benign Het
Slc26a1 T A 5: 108,673,570 D151V probably damaging Het
Snx29 A G 16: 11,738,437 probably null Het
Stard9 C T 2: 120,700,075 A2271V probably benign Het
Stat6 A G 10: 127,655,444 N485D possibly damaging Het
Tpcn2 T C 7: 145,268,869 T280A possibly damaging Het
Ttc23 A G 7: 67,711,366 I378V possibly damaging Het
Ttc29 A G 8: 78,325,576 D362G probably benign Het
Ttll7 A G 3: 146,940,162 I592V probably benign Het
Ugt3a1 A T 15: 9,306,086 H107L probably benign Het
Wdfy4 G T 14: 33,146,990 S360R probably damaging Het
Zfp780b A G 7: 27,963,568 Y521H probably damaging Het
Other mutations in Vmn1r70
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03092:Vmn1r70 APN 7 10634259 missense probably benign 0.23
IGL03250:Vmn1r70 APN 7 10634281 missense probably damaging 1.00
R0375:Vmn1r70 UTSW 7 10634060 missense probably damaging 1.00
R0482:Vmn1r70 UTSW 7 10634277 missense probably damaging 1.00
R0497:Vmn1r70 UTSW 7 10634026 missense probably benign 0.19
R1964:Vmn1r70 UTSW 7 10633810 missense possibly damaging 0.88
R2067:Vmn1r70 UTSW 7 10634337 missense possibly damaging 0.61
R3807:Vmn1r70 UTSW 7 10633788 missense probably benign 0.01
R4573:Vmn1r70 UTSW 7 10633629 splice site probably null
R5070:Vmn1r70 UTSW 7 10634398 missense probably benign 0.04
R5442:Vmn1r70 UTSW 7 10633950 missense possibly damaging 0.69
R5558:Vmn1r70 UTSW 7 10634475 missense probably benign 0.01
R6036:Vmn1r70 UTSW 7 10633903 missense probably damaging 1.00
R6189:Vmn1r70 UTSW 7 10633671 missense probably benign 0.04
R6976:Vmn1r70 UTSW 7 10634044 missense probably benign 0.02
R7571:Vmn1r70 UTSW 7 10633944 missense probably benign 0.00
R9236:Vmn1r70 UTSW 7 10634089 missense probably damaging 1.00
R9568:Vmn1r70 UTSW 7 10634365 missense probably benign 0.03
X0020:Vmn1r70 UTSW 7 10633590 missense probably benign
Predicted Primers
Posted On 2017-06-26