Incidental Mutation 'R0591:Vmn1r184'
ID55976
Institutional Source Beutler Lab
Gene Symbol Vmn1r184
Ensembl Gene ENSMUSG00000046130
Gene Namevomeronasal 1 receptor, 184
Synonyms
MMRRC Submission 038781-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.067) question?
Stock #R0591 (G1)
Quality Score225
Status Validated
Chromosome7
Chromosomal Location26260334-26270619 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 26267075 bp
ZygosityHeterozygous
Amino Acid Change Aspartic acid to Valine at position 82 (D82V)
Ref Sequence ENSEMBL: ENSMUSP00000154576 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057123] [ENSMUST00000227230] [ENSMUST00000227232] [ENSMUST00000227534] [ENSMUST00000227790] [ENSMUST00000228145] [ENSMUST00000228369]
Predicted Effect probably damaging
Transcript: ENSMUST00000057123
AA Change: D82V

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000061885
Gene: ENSMUSG00000046130
AA Change: D82V

DomainStartEndE-ValueType
Pfam:TAS2R 8 308 1.7e-7 PFAM
Pfam:V1R 35 297 7.5e-31 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000227230
AA Change: D82V

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
Predicted Effect probably damaging
Transcript: ENSMUST00000227232
AA Change: D82V

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
Predicted Effect probably damaging
Transcript: ENSMUST00000227534
AA Change: D82V

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
Predicted Effect probably damaging
Transcript: ENSMUST00000227790
AA Change: D82V

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
Predicted Effect probably damaging
Transcript: ENSMUST00000228145
AA Change: D82V

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
Predicted Effect probably damaging
Transcript: ENSMUST00000228369
AA Change: D82V

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.7%
  • 3x: 99.2%
  • 10x: 97.7%
  • 20x: 95.3%
Validation Efficiency 100% (62/62)
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110002E22Rik G T 3: 138,068,943 E1298* probably null Het
Adam19 T C 11: 46,121,411 probably benign Het
Agt A T 8: 124,556,939 S480R possibly damaging Het
Anapc1 G T 2: 128,619,332 D1769E probably benign Het
Aox4 T C 1: 58,239,102 probably benign Het
Apol9b G A 15: 77,735,630 V209I possibly damaging Het
Appl2 A T 10: 83,624,645 I116K possibly damaging Het
B230118H07Rik A T 2: 101,576,117 D155E probably benign Het
BC051665 A G 13: 60,784,608 probably benign Het
Cactin G T 10: 81,324,003 E89* probably null Het
Carf G T 1: 60,125,914 probably benign Het
Ccdc167 A G 17: 29,705,261 probably benign Het
Ceacam3 G A 7: 17,151,883 probably null Het
Clca4b T A 3: 144,915,592 K574* probably null Het
Crabp1 T A 9: 54,765,603 I64N probably damaging Het
Dgkd T A 1: 87,915,104 I118N probably damaging Het
Dglucy T C 12: 100,859,518 probably benign Het
Dock10 C T 1: 80,541,219 probably benign Het
Ednrb A T 14: 103,823,274 probably null Het
Ercc6 T C 14: 32,558,016 probably benign Het
Gm5538 C A 3: 59,752,129 Y334* probably null Het
Golga3 A C 5: 110,188,743 Q416P probably damaging Het
Gpr12 A G 5: 146,583,635 V159A probably benign Het
Heatr5a A T 12: 51,910,101 probably benign Het
Helz2 A G 2: 181,232,116 I2195T probably damaging Het
Hikeshi A T 7: 89,920,087 N76K possibly damaging Het
Hsd11b1 T C 1: 193,229,676 probably benign Het
Inhba A T 13: 16,026,820 K322N probably damaging Het
Katnal1 A T 5: 148,892,516 F291L probably damaging Het
Kcnj9 T C 1: 172,323,098 E316G probably damaging Het
Lrsam1 A G 2: 32,933,923 probably benign Het
Mcf2l T G 8: 13,018,751 S1075A probably benign Het
Mios T C 6: 8,215,470 V222A possibly damaging Het
Mycbp2 A T 14: 103,196,391 probably benign Het
Nars A T 18: 64,500,567 I544N probably damaging Het
Olfr993 A G 2: 85,414,690 L63P possibly damaging Het
Pbrm1 A G 14: 31,046,430 probably benign Het
Plcb4 A G 2: 135,955,012 probably benign Het
Pnliprp1 A G 19: 58,734,706 D213G probably damaging Het
Psap A G 10: 60,300,855 N538D possibly damaging Het
Ptdss1 A G 13: 66,972,650 probably benign Het
Rap1b G A 10: 117,818,617 probably benign Het
Rhcg T A 7: 79,594,772 probably benign Het
Ryr1 G A 7: 29,104,795 T550I possibly damaging Het
Samm50 G A 15: 84,211,168 G452R probably benign Het
Scin A G 12: 40,080,930 probably null Het
Sesn3 T C 9: 14,308,558 L81S probably damaging Het
Skint6 A C 4: 112,858,169 probably benign Het
Slc30a4 A T 2: 122,685,240 L411H probably damaging Het
Slc44a5 C T 3: 154,234,145 probably benign Het
Slc4a3 C T 1: 75,549,021 A255V probably damaging Het
Slc9b1 A G 3: 135,382,832 N318S possibly damaging Het
Tcp11l2 A T 10: 84,604,594 H287L probably benign Het
Tex10 C T 4: 48,456,800 R637Q probably benign Het
Tnks2 T A 19: 36,872,562 Y605N probably damaging Het
Topbp1 T A 9: 103,349,838 N1490K probably benign Het
Ube4b T G 4: 149,357,577 probably benign Het
Usp4 G A 9: 108,348,029 probably benign Het
Vezf1 A T 11: 88,068,435 probably benign Het
Other mutations in Vmn1r184
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01396:Vmn1r184 APN 7 26267437 missense probably damaging 1.00
IGL01411:Vmn1r184 APN 7 26266895 missense probably benign 0.06
IGL02961:Vmn1r184 APN 7 26267650 missense probably benign 0.27
IGL03271:Vmn1r184 APN 7 26267609 missense probably benign
R0302:Vmn1r184 UTSW 7 26267543 missense probably damaging 1.00
R0384:Vmn1r184 UTSW 7 26267651 missense probably benign 0.41
R0620:Vmn1r184 UTSW 7 26267177 missense possibly damaging 0.46
R1644:Vmn1r184 UTSW 7 26267245 missense probably benign 0.00
R2304:Vmn1r184 UTSW 7 26267125 missense probably damaging 1.00
R2329:Vmn1r184 UTSW 7 26266962 missense probably damaging 1.00
R3522:Vmn1r184 UTSW 7 26267583 nonsense probably null
R5020:Vmn1r184 UTSW 7 26267530 missense possibly damaging 0.87
R5030:Vmn1r184 UTSW 7 26267456 missense probably benign 0.25
R5049:Vmn1r184 UTSW 7 26267368 missense possibly damaging 0.49
R5076:Vmn1r184 UTSW 7 26266921 missense probably benign 0.00
R5213:Vmn1r184 UTSW 7 26267711 missense probably damaging 0.99
R5554:Vmn1r184 UTSW 7 26266988 missense probably damaging 1.00
R6146:Vmn1r184 UTSW 7 26267392 missense probably benign 0.08
R6868:Vmn1r184 UTSW 7 26267302 missense probably benign 0.00
R6937:Vmn1r184 UTSW 7 26267325 missense probably benign 0.08
R6943:Vmn1r184 UTSW 7 26267138 missense possibly damaging 0.77
R7190:Vmn1r184 UTSW 7 26267680 missense probably damaging 1.00
R7239:Vmn1r184 UTSW 7 26267177 missense possibly damaging 0.79
R7472:Vmn1r184 UTSW 7 26267399 missense possibly damaging 0.82
Predicted Primers PCR Primer
(F):5'- GGCATCTTCTTTCACACCCAGCTATAA -3'
(R):5'- CAGGGAACATTACGAATGCTGCATAGA -3'

Sequencing Primer
(F):5'- AGCACAGAATAGCCTTCTGG -3'
(R):5'- TGTGCAAGATCCACATGAGG -3'
Posted On2013-07-11