Incidental Mutation 'R2069:Vmn2r6'
ID 226917
Institutional Source Beutler Lab
Gene Symbol Vmn2r6
Ensembl Gene ENSMUSG00000090581
Gene Name vomeronasal 2, receptor 6
Synonyms EG620718, EG667069
MMRRC Submission 040074-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.184) question?
Stock # R2069 (G1)
Quality Score 225
Status Validated
Chromosome 3
Chromosomal Location 64537561-64565298 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 64556098 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Histidine to Glutamine at position 438 (H438Q)
Ref Sequence ENSEMBL: ENSMUSP00000135148 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000165012] [ENSMUST00000176481]
AlphaFold H3BK29
Predicted Effect possibly damaging
Transcript: ENSMUST00000165012
AA Change: H349Q

PolyPhen 2 Score 0.460 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000131831
Gene: ENSMUSG00000090581
AA Change: H349Q

DomainStartEndE-ValueType
Pfam:ANF_receptor 1 416 1.4e-72 PFAM
Pfam:Peripla_BP_6 58 244 1.2e-10 PFAM
Pfam:NCD3G 458 511 1.8e-17 PFAM
Pfam:7tm_3 542 779 3.9e-76 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000176481
AA Change: H438Q

PolyPhen 2 Score 0.889 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000135148
Gene: ENSMUSG00000090581
AA Change: H438Q

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
Pfam:ANF_receptor 88 505 9.8e-77 PFAM
Pfam:Peripla_BP_6 142 331 3.4e-10 PFAM
Pfam:NCD3G 547 600 5.4e-17 PFAM
Pfam:7tm_3 633 867 3.9e-47 PFAM
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.4%
Validation Efficiency 100% (104/104)
Allele List at MGI
Other mutations in this stock
Total: 104 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930519G04Rik T C 5: 114,874,280 (GRCm38) V86A probably benign Het
Abcc3 A T 11: 94,364,417 (GRCm38) I601N probably damaging Het
Abl2 T A 1: 156,620,827 (GRCm38) probably null Het
Adgrf4 C T 17: 42,666,898 (GRCm38) R518Q possibly damaging Het
Ahi1 C T 10: 20,959,996 (GRCm38) T76I probably damaging Het
Arhgap42 C T 9: 9,035,600 (GRCm38) G247D probably damaging Het
Arid2 C T 15: 96,362,590 (GRCm38) L407F probably damaging Het
Atp13a1 T C 8: 69,799,773 (GRCm38) F606L probably benign Het
Avl9 T A 6: 56,736,435 (GRCm38) probably benign Het
B3glct C T 5: 149,709,380 (GRCm38) A65V probably damaging Het
Bcorl1 T C X: 48,401,917 (GRCm38) probably benign Het
Bdp1 T C 13: 100,050,988 (GRCm38) T1624A probably benign Het
Bmp15 A G X: 6,316,021 (GRCm38) M263T probably benign Het
Brd8 T C 18: 34,614,479 (GRCm38) K110E probably damaging Het
Cachd1 A G 4: 100,990,844 (GRCm38) D1052G probably damaging Het
Capn9 G A 8: 124,605,711 (GRCm38) G430R possibly damaging Het
Ccdc113 G A 8: 95,557,296 (GRCm38) E333K probably benign Het
Ccnl2 A T 4: 155,812,481 (GRCm38) probably null Het
Ccr9 T C 9: 123,779,364 (GRCm38) F37S probably benign Het
Cdh7 A T 1: 110,138,159 (GRCm38) D721V probably damaging Het
Ceacam10 A T 7: 24,778,372 (GRCm38) N104I probably damaging Het
Cenpk T A 13: 104,236,176 (GRCm38) probably benign Het
Cfi A G 3: 129,858,804 (GRCm38) probably null Het
Chd1 T C 17: 15,742,294 (GRCm38) F771S probably damaging Het
Chil4 G A 3: 106,219,455 (GRCm38) L4F probably benign Het
Cilp G A 9: 65,278,090 (GRCm38) R489Q possibly damaging Het
Cntnap5b G A 1: 100,358,725 (GRCm38) G402R probably benign Het
Coq8b A G 7: 27,257,377 (GRCm38) E485G probably damaging Het
Cse1l A G 2: 166,941,492 (GRCm38) S733G probably benign Het
Dnah5 G A 15: 28,312,388 (GRCm38) probably null Het
Dnmt3l T C 10: 78,052,732 (GRCm38) V156A probably damaging Het
Duox1 A T 2: 122,333,062 (GRCm38) T792S probably benign Het
Duox2 T C 2: 122,287,108 (GRCm38) D915G probably benign Het
Efcab5 A T 11: 77,172,321 (GRCm38) M115K probably benign Het
Eif2s1 G A 12: 78,877,185 (GRCm38) D139N probably benign Het
Erg A G 16: 95,361,078 (GRCm38) F390L probably damaging Het
Fam193b A T 13: 55,542,998 (GRCm38) S650R probably damaging Het
Fbp2 T A 13: 62,854,061 (GRCm38) K113N possibly damaging Het
Fnbp4 T G 2: 90,758,372 (GRCm38) S496A probably damaging Het
Gab3 C A X: 75,000,095 (GRCm38) R475L probably damaging Het
Gm7534 T G 4: 134,201,941 (GRCm38) N351T possibly damaging Het
Gsap T C 5: 21,226,839 (GRCm38) probably benign Het
Gucy1a2 C T 9: 3,582,697 (GRCm38) L160F probably damaging Het
Hivep1 C T 13: 42,183,786 (GRCm38) A2447V possibly damaging Het
Hrasls5 T C 19: 7,612,638 (GRCm38) S10P possibly damaging Het
Insc G T 7: 114,804,593 (GRCm38) probably null Het
Jph2 A G 2: 163,339,685 (GRCm38) S520P possibly damaging Het
Kidins220 T A 12: 24,987,006 (GRCm38) probably benign Het
Krtap29-1 A G 11: 99,978,612 (GRCm38) S148P probably damaging Het
Ltbp2 A C 12: 84,793,733 (GRCm38) C1000G probably damaging Het
Map2k3 T C 11: 60,950,027 (GRCm38) F294S probably damaging Het
Map4k2 C A 19: 6,342,738 (GRCm38) probably benign Het
Mboat2 T C 12: 24,951,443 (GRCm38) V281A probably benign Het
Mdga2 G A 12: 66,568,917 (GRCm38) R570* probably null Het
Mlxipl A G 5: 135,107,005 (GRCm38) D28G probably damaging Het
Morc2b T C 17: 33,136,760 (GRCm38) I679M probably benign Het
Myh4 T C 11: 67,246,366 (GRCm38) probably benign Het
Nfib A C 4: 82,498,615 (GRCm38) L61R probably damaging Het
Noc2l C A 4: 156,241,450 (GRCm38) Y227* probably null Het
Nrde2 A G 12: 100,142,232 (GRCm38) S367P probably damaging Het
Nup93 C A 8: 94,243,739 (GRCm38) P89T probably damaging Het
Obsl1 G A 1: 75,486,756 (GRCm38) T1764M probably benign Het
Olfr1240 C T 2: 89,439,583 (GRCm38) R232H probably benign Het
Olfr1283 A G 2: 111,369,095 (GRCm38) I154M probably benign Het
Olfr6 A T 7: 106,956,287 (GRCm38) Y216* probably null Het
Olfr714 A T 7: 107,074,619 (GRCm38) K264* probably null Het
Olfr749 T A 14: 50,736,576 (GRCm38) E195D possibly damaging Het
Olfr824 A G 10: 130,126,205 (GRCm38) I284T possibly damaging Het
Oxct1 G T 15: 4,092,525 (GRCm38) A319S probably null Het
P2ry10 A G X: 107,103,253 (GRCm38) S265G probably benign Het
Peak1 A T 9: 56,258,759 (GRCm38) N628K probably damaging Het
Pkdrej T A 15: 85,821,231 (GRCm38) Q168L probably benign Het
Plec A G 15: 76,188,926 (GRCm38) M604T probably benign Het
Pmfbp1 A T 8: 109,532,103 (GRCm38) N680I possibly damaging Het
Pnmal2 T C 7: 16,945,789 (GRCm38) W233R probably damaging Het
Pxn A G 5: 115,545,667 (GRCm38) N186S probably benign Het
Rsad1 A C 11: 94,549,125 (GRCm38) probably benign Het
Runx2 A G 17: 44,735,342 (GRCm38) I112T probably benign Het
S1pr2 A T 9: 20,967,494 (GRCm38) L346Q probably damaging Het
Skint6 A G 4: 113,238,132 (GRCm38) I110T probably damaging Het
Slc36a4 T A 9: 15,726,980 (GRCm38) F234Y probably damaging Het
Slitrk2 T A X: 66,654,629 (GRCm38) V242D probably damaging Het
Sp100 A G 1: 85,681,142 (GRCm38) probably null Het
Spryd3 A C 15: 102,118,181 (GRCm38) L352V probably benign Het
Ssc4d A C 5: 135,970,317 (GRCm38) W11G possibly damaging Het
Stx17 T A 4: 48,158,870 (GRCm38) D83E probably damaging Het
Tlk2 A T 11: 105,240,440 (GRCm38) Q204L probably benign Het
Tnfrsf21 A T 17: 43,037,938 (GRCm38) H147L possibly damaging Het
Tnrc18 A T 5: 142,766,087 (GRCm38) D1154E unknown Het
Trap1 A G 16: 4,068,336 (GRCm38) S86P probably benign Het
Trim32 T A 4: 65,614,776 (GRCm38) C523* probably null Het
Ttc38 G T 15: 85,838,788 (GRCm38) D146Y probably damaging Het
Ttc9 T A 12: 81,631,796 (GRCm38) L131Q probably damaging Het
Ttn C T 2: 76,813,339 (GRCm38) G11436R probably damaging Het
Ttn T C 2: 76,726,848 (GRCm38) probably benign Het
Ubash3b G A 9: 41,043,573 (GRCm38) P92S possibly damaging Het
Ube4a T C 9: 44,948,099 (GRCm38) N367S probably damaging Het
Ubr4 T A 4: 139,479,540 (GRCm38) H4899Q possibly damaging Het
Ufl1 C T 4: 25,269,036 (GRCm38) G265D possibly damaging Het
Vmn2r27 T A 6: 124,224,483 (GRCm38) I172F probably damaging Het
Vmn2r61 A G 7: 42,300,001 (GRCm38) D615G probably benign Het
Wdr24 T A 17: 25,826,282 (GRCm38) D330E probably damaging Het
Zbbx A T 3: 75,078,412 (GRCm38) N444K probably benign Het
Zc3h7b A T 15: 81,792,328 (GRCm38) Q757L probably damaging Het
Other mutations in Vmn2r6
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01547:Vmn2r6 APN 3 64,538,104 (GRCm38) missense probably damaging 1.00
IGL01968:Vmn2r6 APN 3 64,556,345 (GRCm38) missense possibly damaging 0.94
IGL02009:Vmn2r6 APN 3 64,537,902 (GRCm38) missense possibly damaging 0.61
IGL02039:Vmn2r6 APN 3 64,556,189 (GRCm38) missense probably damaging 1.00
IGL02652:Vmn2r6 APN 3 64,556,328 (GRCm38) missense probably benign 0.24
IGL02737:Vmn2r6 APN 3 64,556,490 (GRCm38) missense possibly damaging 0.55
IGL02808:Vmn2r6 APN 3 64,556,496 (GRCm38) missense probably damaging 1.00
IGL03066:Vmn2r6 APN 3 64,565,153 (GRCm38) missense probably damaging 0.99
IGL03331:Vmn2r6 APN 3 64,538,007 (GRCm38) missense probably damaging 1.00
BB010:Vmn2r6 UTSW 3 64,559,803 (GRCm38) missense probably benign 0.02
BB020:Vmn2r6 UTSW 3 64,559,803 (GRCm38) missense probably benign 0.02
R0010:Vmn2r6 UTSW 3 64,559,545 (GRCm38) nonsense probably null
R0206:Vmn2r6 UTSW 3 64,539,912 (GRCm38) missense probably benign
R0206:Vmn2r6 UTSW 3 64,539,912 (GRCm38) missense probably benign
R0208:Vmn2r6 UTSW 3 64,539,912 (GRCm38) missense probably benign
R0427:Vmn2r6 UTSW 3 64,559,587 (GRCm38) missense probably damaging 1.00
R0466:Vmn2r6 UTSW 3 64,556,302 (GRCm38) missense probably damaging 1.00
R1018:Vmn2r6 UTSW 3 64,556,840 (GRCm38) missense probably benign 0.00
R1104:Vmn2r6 UTSW 3 64,538,066 (GRCm38) missense possibly damaging 0.93
R1186:Vmn2r6 UTSW 3 64,565,067 (GRCm38) missense probably benign 0.01
R1245:Vmn2r6 UTSW 3 64,556,790 (GRCm38) missense possibly damaging 0.53
R1295:Vmn2r6 UTSW 3 64,538,273 (GRCm38) missense probably damaging 1.00
R1473:Vmn2r6 UTSW 3 64,538,158 (GRCm38) nonsense probably null
R1498:Vmn2r6 UTSW 3 64,556,469 (GRCm38) missense probably damaging 1.00
R1925:Vmn2r6 UTSW 3 64,556,277 (GRCm38) missense possibly damaging 0.87
R2044:Vmn2r6 UTSW 3 64,537,841 (GRCm38) missense probably damaging 0.96
R2253:Vmn2r6 UTSW 3 64,559,718 (GRCm38) missense probably damaging 1.00
R2261:Vmn2r6 UTSW 3 64,556,669 (GRCm38) missense probably benign 0.24
R2262:Vmn2r6 UTSW 3 64,556,669 (GRCm38) missense probably benign 0.24
R2350:Vmn2r6 UTSW 3 64,556,352 (GRCm38) missense probably benign 0.01
R2680:Vmn2r6 UTSW 3 64,538,286 (GRCm38) missense possibly damaging 0.91
R2846:Vmn2r6 UTSW 3 64,556,790 (GRCm38) missense possibly damaging 0.53
R2860:Vmn2r6 UTSW 3 64,547,339 (GRCm38) missense probably benign 0.00
R2861:Vmn2r6 UTSW 3 64,547,339 (GRCm38) missense probably benign 0.00
R3766:Vmn2r6 UTSW 3 64,556,508 (GRCm38) missense probably benign 0.19
R3870:Vmn2r6 UTSW 3 64,556,621 (GRCm38) missense probably damaging 0.96
R4018:Vmn2r6 UTSW 3 64,556,472 (GRCm38) missense probably benign 0.05
R4024:Vmn2r6 UTSW 3 64,538,250 (GRCm38) missense possibly damaging 0.73
R4026:Vmn2r6 UTSW 3 64,538,250 (GRCm38) missense possibly damaging 0.73
R4227:Vmn2r6 UTSW 3 64,537,948 (GRCm38) missense probably damaging 0.99
R4526:Vmn2r6 UTSW 3 64,537,724 (GRCm38) missense probably benign 0.32
R4570:Vmn2r6 UTSW 3 64,559,647 (GRCm38) missense probably benign 0.31
R4894:Vmn2r6 UTSW 3 64,547,408 (GRCm38) missense probably benign
R4934:Vmn2r6 UTSW 3 64,556,345 (GRCm38) missense probably damaging 0.99
R5057:Vmn2r6 UTSW 3 64,537,786 (GRCm38) missense probably damaging 1.00
R5059:Vmn2r6 UTSW 3 64,537,623 (GRCm38) missense possibly damaging 0.89
R5148:Vmn2r6 UTSW 3 64,556,594 (GRCm38) missense probably damaging 0.99
R5155:Vmn2r6 UTSW 3 64,538,514 (GRCm38) missense probably benign 0.44
R5179:Vmn2r6 UTSW 3 64,537,990 (GRCm38) missense probably benign 0.00
R5256:Vmn2r6 UTSW 3 64,556,842 (GRCm38) missense probably benign 0.33
R5861:Vmn2r6 UTSW 3 64,556,033 (GRCm38) missense probably benign 0.00
R5950:Vmn2r6 UTSW 3 64,565,231 (GRCm38) missense probably benign 0.05
R6081:Vmn2r6 UTSW 3 64,556,532 (GRCm38) missense probably benign 0.25
R6173:Vmn2r6 UTSW 3 64,559,755 (GRCm38) missense probably damaging 1.00
R6190:Vmn2r6 UTSW 3 64,538,003 (GRCm38) missense probably benign 0.04
R6240:Vmn2r6 UTSW 3 64,556,805 (GRCm38) missense probably damaging 1.00
R6433:Vmn2r6 UTSW 3 64,547,380 (GRCm38) nonsense probably null
R6645:Vmn2r6 UTSW 3 64,556,876 (GRCm38) missense probably damaging 1.00
R6791:Vmn2r6 UTSW 3 64,538,159 (GRCm38) missense probably damaging 1.00
R7265:Vmn2r6 UTSW 3 64,556,774 (GRCm38) missense probably benign 0.00
R7503:Vmn2r6 UTSW 3 64,539,951 (GRCm38) nonsense probably null
R7562:Vmn2r6 UTSW 3 64,556,520 (GRCm38) missense probably benign 0.00
R7584:Vmn2r6 UTSW 3 64,565,262 (GRCm38) missense probably benign 0.07
R7611:Vmn2r6 UTSW 3 64,565,142 (GRCm38) missense probably damaging 0.98
R7759:Vmn2r6 UTSW 3 64,556,570 (GRCm38) missense probably damaging 1.00
R7834:Vmn2r6 UTSW 3 64,538,022 (GRCm38) missense probably damaging 1.00
R7933:Vmn2r6 UTSW 3 64,559,803 (GRCm38) missense probably benign 0.02
R7982:Vmn2r6 UTSW 3 64,559,820 (GRCm38) missense probably damaging 1.00
R8024:Vmn2r6 UTSW 3 64,559,824 (GRCm38) missense probably benign 0.40
R8074:Vmn2r6 UTSW 3 64,547,643 (GRCm38) intron probably benign
R8169:Vmn2r6 UTSW 3 64,539,889 (GRCm38) missense probably benign 0.01
R8337:Vmn2r6 UTSW 3 64,556,105 (GRCm38) nonsense probably null
R8736:Vmn2r6 UTSW 3 64,559,800 (GRCm38) missense probably damaging 1.00
R8962:Vmn2r6 UTSW 3 64,556,155 (GRCm38) missense probably damaging 1.00
R9139:Vmn2r6 UTSW 3 64,556,856 (GRCm38) missense probably benign 0.12
R9206:Vmn2r6 UTSW 3 64,559,611 (GRCm38) missense probably damaging 0.97
R9295:Vmn2r6 UTSW 3 64,556,063 (GRCm38) missense probably benign 0.00
R9332:Vmn2r6 UTSW 3 64,547,250 (GRCm38) missense probably benign 0.01
R9616:Vmn2r6 UTSW 3 64,538,303 (GRCm38) missense probably damaging 1.00
R9663:Vmn2r6 UTSW 3 64,556,128 (GRCm38) missense possibly damaging 0.90
R9685:Vmn2r6 UTSW 3 64,556,660 (GRCm38) missense probably benign 0.19
X0020:Vmn2r6 UTSW 3 64,538,450 (GRCm38) missense probably benign
X0066:Vmn2r6 UTSW 3 64,547,378 (GRCm38) missense probably damaging 1.00
Z1176:Vmn2r6 UTSW 3 64,556,325 (GRCm38) missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- TGGAAGCAAATTAGCAGTTTCAGAG -3'
(R):5'- TCTGGCAAACTGCTTTTAACTG -3'

Sequencing Primer
(F):5'- GCAAATTAGCAGTTTCAGAGGTATG -3'
(R):5'- GCACTGTGCCATACAATGTG -3'
Posted On 2014-09-17