Incidental Mutation 'R5178:Vmn1r87'
ID399471
Institutional Source Beutler Lab
Gene Symbol Vmn1r87
Ensembl Gene ENSMUSG00000070815
Gene Namevomeronasal 1 receptor 87
SynonymsV1rk1
MMRRC Submission 042758-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.051) question?
Stock #R5178 (G1)
Quality Score225
Status Not validated
Chromosome7
Chromosomal Location13130904-13140157 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to T at 13131865 bp
ZygosityHeterozygous
Amino Acid Change Alanine to Glutamic Acid at position 165 (A165E)
Ref Sequence ENSEMBL: ENSMUSP00000154184 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094827] [ENSMUST00000211249] [ENSMUST00000227443] [ENSMUST00000228800]
Predicted Effect possibly damaging
Transcript: ENSMUST00000094827
AA Change: A165E

PolyPhen 2 Score 0.792 (Sensitivity: 0.85; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000092422
Gene: ENSMUSG00000070815
AA Change: A165E

DomainStartEndE-ValueType
Pfam:TAS2R 1 285 1.2e-11 PFAM
Pfam:V1R 14 280 1.8e-36 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000211249
AA Change: A165E

PolyPhen 2 Score 0.792 (Sensitivity: 0.85; Specificity: 0.93)
Predicted Effect possibly damaging
Transcript: ENSMUST00000227443
AA Change: A165E

PolyPhen 2 Score 0.792 (Sensitivity: 0.85; Specificity: 0.93)
Predicted Effect possibly damaging
Transcript: ENSMUST00000228800
AA Change: A165E

PolyPhen 2 Score 0.792 (Sensitivity: 0.85; Specificity: 0.93)
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.3%
  • 20x: 95.3%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abt1 G T 13: 23,422,649 A94E possibly damaging Het
Carmil2 G T 8: 105,696,889 G1207V probably damaging Het
Cndp2 A T 18: 84,675,028 N202K probably benign Het
Cyp2c66 A G 19: 39,171,029 Y308C probably damaging Het
Dhx29 T G 13: 112,932,600 S155A possibly damaging Het
Dnah7b T G 1: 46,358,216 F3936V possibly damaging Het
Dsg1b G A 18: 20,397,503 G405E probably damaging Het
Exo5 A T 4: 120,921,537 probably null Het
Fam171b T C 2: 83,879,987 F668L probably damaging Het
Gemin5 A T 11: 58,146,518 S624T probably benign Het
Gm15922 T A 7: 3,739,397 K44* probably null Het
Gpc2 C A 5: 138,275,605 V444L possibly damaging Het
Hephl1 T A 9: 15,086,172 K399N probably damaging Het
Lair1 G A 7: 4,010,489 T82I possibly damaging Het
Lhx1 G T 11: 84,520,388 A155E possibly damaging Het
Maip1 G A 1: 57,415,690 D278N probably benign Het
Mcm4 T A 16: 15,635,303 D174V probably benign Het
Mcph1 T A 8: 18,607,326 D60E probably damaging Het
Mmp17 T A 5: 129,595,058 W132R probably damaging Het
Olfr1178 C T 2: 88,391,475 T76I possibly damaging Het
Olfr868 T A 9: 20,101,192 C144* probably null Het
Pds5a T C 5: 65,663,875 T169A probably damaging Het
Pfkm A G 15: 98,131,515 N697D probably benign Het
Ppwd1 A T 13: 104,220,435 S191T probably benign Het
Ranbp2 T A 10: 58,476,785 M1109K probably benign Het
Robo4 T C 9: 37,407,960 W535R probably damaging Het
Rsf1 A G 7: 97,661,872 D603G possibly damaging Het
Slc22a26 T C 19: 7,790,175 T289A possibly damaging Het
Sp2 A G 11: 96,955,838 F554L probably benign Het
Sp4 A G 12: 118,261,889 V580A possibly damaging Het
Tbc1d19 T A 5: 53,889,325 S413T possibly damaging Het
Tcrg-C4 A G 13: 19,344,762 probably benign Het
Tecta T C 9: 42,375,185 D725G probably damaging Het
Tmem200a T A 10: 25,994,379 Q4H probably benign Het
Tpx2 T A 2: 152,875,549 I122N probably benign Het
Ube4b T C 4: 149,342,992 M900V probably damaging Het
Vmn2r95 A G 17: 18,440,075 T250A probably benign Het
Wasf1 G A 10: 40,937,676 R518H unknown Het
Zfhx2 A T 14: 55,074,775 F154Y probably benign Het
Zfp729a A G 13: 67,637,645 probably null Het
Zfp976 A G 7: 42,612,501 probably null Het
Other mutations in Vmn1r87
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01400:Vmn1r87 APN 7 13132303 missense probably damaging 1.00
IGL01577:Vmn1r87 APN 7 13131848 missense probably benign 0.00
IGL02972:Vmn1r87 APN 7 13132329 nonsense probably null
IGL03246:Vmn1r87 APN 7 13132361 utr 5 prime probably benign
PIT4142001:Vmn1r87 UTSW 7 13132185 missense probably benign 0.00
R0153:Vmn1r87 UTSW 7 13132284 missense probably damaging 1.00
R0502:Vmn1r87 UTSW 7 13131656 missense probably damaging 1.00
R0658:Vmn1r87 UTSW 7 13131829 missense probably damaging 1.00
R1589:Vmn1r87 UTSW 7 13131776 missense possibly damaging 0.46
R1731:Vmn1r87 UTSW 7 13131776 missense possibly damaging 0.46
R2027:Vmn1r87 UTSW 7 13131896 missense probably damaging 0.99
R2044:Vmn1r87 UTSW 7 13131821 missense probably benign 0.02
R3124:Vmn1r87 UTSW 7 13131566 missense probably damaging 1.00
R4208:Vmn1r87 UTSW 7 13132258 missense probably benign 0.37
R4731:Vmn1r87 UTSW 7 13132327 missense possibly damaging 0.92
R4732:Vmn1r87 UTSW 7 13132327 missense possibly damaging 0.92
R4733:Vmn1r87 UTSW 7 13132327 missense possibly damaging 0.92
R5079:Vmn1r87 UTSW 7 13132326 missense probably benign 0.01
R5125:Vmn1r87 UTSW 7 13131865 missense possibly damaging 0.79
R6599:Vmn1r87 UTSW 7 13131959 nonsense probably null
R7067:Vmn1r87 UTSW 7 13131922 missense probably benign 0.02
R7560:Vmn1r87 UTSW 7 13131818 missense probably damaging 1.00
R7574:Vmn1r87 UTSW 7 13131686 missense probably benign 0.01
R7910:Vmn1r87 UTSW 7 13131905 missense probably damaging 1.00
R7991:Vmn1r87 UTSW 7 13131905 missense probably damaging 1.00
X0028:Vmn1r87 UTSW 7 13131983 missense possibly damaging 0.52
Predicted Primers PCR Primer
(F):5'- TCCAATACTGGGTTGCTCTTGG -3'
(R):5'- GTGGGCATGGCTTAAATCCAAG -3'

Sequencing Primer
(F):5'- TCTTGGGTTGGTAAAGTGAATAGAAG -3'
(R):5'- GCTTAAATCCAAGCTTGAGTCATGC -3'
Posted On2016-07-06