Incidental Mutation 'R6263:Vmn1r82'
ID506822
Institutional Source Beutler Lab
Gene Symbol Vmn1r82
Ensembl Gene ENSMUSG00000058132
Gene Namevomeronasal 1 receptor 82
SynonymsV1rg12
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.058) question?
Stock #R6263 (G1)
Quality Score225.009
Status Validated
Chromosome7
Chromosomal Location12300430-12308582 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to T at 12305534 bp
ZygosityHeterozygous
Amino Acid Change Valine to Phenylalanine at position 127 (V127F)
Ref Sequence ENSEMBL: ENSMUSP00000154524 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072801] [ENSMUST00000191002] [ENSMUST00000227672]
Predicted Effect probably damaging
Transcript: ENSMUST00000072801
AA Change: V244F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000072580
Gene: ENSMUSG00000058132
AA Change: V244F

DomainStartEndE-ValueType
Pfam:V1R 35 295 1.3e-28 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000191002
AA Change: V245F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000140782
Gene: ENSMUSG00000058132
AA Change: V245F

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
Pfam:V1R 36 296 8.4e-27 PFAM
Pfam:7tm_1 39 290 2e-5 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000227672
AA Change: V127F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.4%
  • 20x: 95.7%
Validation Efficiency 97% (66/68)
Allele List at MGI
Other mutations in this stock
Total: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931423N10Rik T A 2: 23,266,733 probably benign Het
4932438A13Rik T A 3: 36,931,111 N863K probably benign Het
Ahnak A G 19: 9,018,277 I5642V probably benign Het
Atp5a1 A G 18: 77,779,230 probably null Het
Bsn A T 9: 108,113,254 F1766L probably damaging Het
Ccdc141 T C 2: 77,108,463 Q266R probably damaging Het
Cdh10 T A 15: 18,964,068 D105E possibly damaging Het
Clca3a1 T A 3: 144,749,778 D418V probably damaging Het
Cnnm2 C A 19: 46,856,905 T612K probably benign Het
Col3a1 T C 1: 45,321,575 V55A unknown Het
Cpd A C 11: 76,846,271 D232E probably benign Het
Csde1 A G 3: 103,040,017 H95R probably benign Het
Ctcfl T A 2: 173,095,337 H596L probably benign Het
Cwc22 T C 2: 77,896,171 R855G possibly damaging Het
Cwc25 A G 11: 97,753,227 Y227H probably damaging Het
Cyp2c38 G A 19: 39,392,215 P409S probably damaging Het
Ddx5 A G 11: 106,788,313 S2P possibly damaging Het
Dnah2 C A 11: 69,457,412 G2570W probably damaging Het
Dnajc10 T A 2: 80,343,948 V528E probably damaging Het
Fmo1 A G 1: 162,850,060 probably null Het
Gm11639 G A 11: 104,919,486 D3150N unknown Het
Gpatch1 C A 7: 35,303,423 D221Y probably damaging Het
Ino80 T C 2: 119,383,414 Y1225C probably damaging Het
Itga7 T A 10: 128,944,086 D501E probably benign Het
Lgr4 T C 2: 110,011,898 S743P possibly damaging Het
Lilra5 A T 7: 4,238,361 Y99F probably damaging Het
Lmna A G 3: 88,502,958 V49A probably damaging Het
Lrrc72 G A 12: 36,208,604 R267* probably null Het
Mapkbp1 T C 2: 120,023,291 S1199P probably damaging Het
Mmp25 G A 17: 23,630,794 A541V possibly damaging Het
Myh10 A T 11: 68,810,232 N1756Y probably damaging Het
Nfe2 A G 15: 103,250,951 I31T probably damaging Het
Nfe2l1 A T 11: 96,817,744 F732I probably benign Het
Olfr1238 C G 2: 89,406,730 M116I possibly damaging Het
Olfr1255 T A 2: 89,816,760 C145S probably damaging Het
Olfr603 C A 7: 103,383,196 V269F possibly damaging Het
Pax6 T C 2: 105,692,854 probably null Het
Phb A G 11: 95,678,115 E192G probably damaging Het
Plekhn1 A T 4: 156,225,193 probably null Het
Plxnb2 A T 15: 89,161,986 V942E probably damaging Het
Rsrc2 G A 5: 123,739,688 probably benign Het
Sept8 G A 11: 53,548,383 C460Y probably benign Het
Slc13a2 CGTTATCTGT CGT 11: 78,403,480 probably benign Het
Slc16a7 A G 10: 125,294,639 I59T probably benign Het
Slc35d1 A T 4: 103,208,168 I172N possibly damaging Het
Smg5 A T 3: 88,341,901 N40Y possibly damaging Het
Smurf1 A G 5: 144,881,731 V633A probably damaging Het
Snx9 T C 17: 5,887,049 V22A probably damaging Het
Sox6 A T 7: 115,477,060 M741K probably damaging Het
Spata31d1d T C 13: 59,725,983 Q1246R probably benign Het
Sval1 A G 6: 41,951,726 E24G probably damaging Het
Tas2r124 A G 6: 132,754,904 I59V probably benign Het
Tmem151b T A 17: 45,547,066 T85S probably benign Het
Tpr T A 1: 150,442,245 probably null Het
Trpm6 A C 19: 18,854,108 T1446P possibly damaging Het
Tsc22d4 A T 5: 137,768,179 K502N possibly damaging Het
Tssk3 C T 4: 129,489,258 S207N probably benign Het
Ttbk1 G T 17: 46,467,262 P618Q probably damaging Het
Ttll6 A T 11: 96,156,545 M657L probably benign Het
Ubash3a T A 17: 31,215,095 I138N probably benign Het
Ush2a A G 1: 188,358,642 Y490C probably damaging Het
Vmn2r32 A T 7: 7,476,692 S161T possibly damaging Het
Wdr49 T C 3: 75,481,517 I58M possibly damaging Het
Wiz A T 17: 32,360,443 probably null Het
Wrap53 A T 11: 69,562,793 Y324* probably null Het
Zfp747 A C 7: 127,375,966 probably benign Het
Zfp827 A G 8: 79,179,073 Y33C probably damaging Het
Other mutations in Vmn1r82
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01509:Vmn1r82 APN 7 12305169 missense probably damaging 0.99
IGL01955:Vmn1r82 APN 7 12305723 unclassified probably null
IGL02267:Vmn1r82 APN 7 12305346 missense probably damaging 1.00
R0336:Vmn1r82 UTSW 7 12305321 missense probably benign 0.26
R2373:Vmn1r82 UTSW 7 12305055 missense probably damaging 0.99
R2849:Vmn1r82 UTSW 7 12305406 missense probably damaging 1.00
R4621:Vmn1r82 UTSW 7 12305336 missense possibly damaging 0.71
R5628:Vmn1r82 UTSW 7 12305278 missense probably damaging 1.00
R6180:Vmn1r82 UTSW 7 12305085 missense probably damaging 0.97
R6877:Vmn1r82 UTSW 7 12305363 missense possibly damaging 0.79
Predicted Primers PCR Primer
(F):5'- TCAGCATCTGTTTCTGGCAC -3'
(R):5'- ATTAACGTTTCCACCAACAGTG -3'

Sequencing Primer
(F):5'- AGCATCTGTTTCTGGCACTATTG -3'
(R):5'- CCAACAGTGAAGATAGAGCCTAG -3'
Posted On2018-03-15