Incidental Mutation 'R6368:Vmn2r111'
ID 512821
Institutional Source Beutler Lab
Gene Symbol Vmn2r111
Ensembl Gene ENSMUSG00000095093
Gene Name vomeronasal 2, receptor 111
Synonyms EG210876
MMRRC Submission 044518-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.080) question?
Stock # R6368 (G1)
Quality Score 225.009
Status Not validated
Chromosome 17
Chromosomal Location 22547941-22573273 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to A at 22571908 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Lysine to Asparagine at position 136 (K136N)
Ref Sequence ENSEMBL: ENSMUSP00000090148 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092491]
AlphaFold K7N674
Predicted Effect probably benign
Transcript: ENSMUST00000092491
AA Change: K136N

PolyPhen 2 Score 0.380 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000090148
Gene: ENSMUSG00000095093
AA Change: K136N

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 73 469 2.5e-29 PFAM
Pfam:NCD3G 512 565 1.1e-20 PFAM
Pfam:7tm_3 595 833 5.6e-54 PFAM
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.4%
  • 20x: 95.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930563M21Rik C A 9: 55,990,132 (GRCm38) E272D possibly damaging Het
Abi2 A G 1: 60,453,651 (GRCm38) T158A possibly damaging Het
Acacb T C 5: 114,216,823 (GRCm38) S1221P probably damaging Het
Agbl1 A G 7: 76,419,830 (GRCm38) D370G probably benign Het
Apeh A G 9: 108,087,243 (GRCm38) I487T probably damaging Het
Arid1b C A 17: 5,332,533 (GRCm38) N1297K possibly damaging Het
Ascc3 G A 10: 50,699,985 (GRCm38) G779S probably damaging Het
Atp7b A C 8: 22,020,755 (GRCm38) probably null Het
Bsn C T 9: 108,111,314 (GRCm38) probably benign Het
Caps2 C T 10: 112,194,968 (GRCm38) Q268* probably null Het
Cnfn C T 7: 25,367,961 (GRCm38) probably null Het
Cr2 A G 1: 195,168,472 (GRCm38) S229P probably damaging Het
Cubn T C 2: 13,430,995 (GRCm38) Y1050C probably damaging Het
Cubn T C 2: 13,476,123 (GRCm38) E307G probably damaging Het
Cyb5r3 A C 15: 83,160,124 (GRCm38) Y182D possibly damaging Het
Dclre1a A T 19: 56,546,791 (GRCm38) H120Q probably benign Het
Ddx6 T C 9: 44,635,776 (GRCm38) I457T probably damaging Het
E2f1 A T 2: 154,564,476 (GRCm38) H93Q possibly damaging Het
Fam186a T C 15: 99,943,317 (GRCm38) K1682R possibly damaging Het
Farsb A G 1: 78,466,965 (GRCm38) probably null Het
Flii A T 11: 60,721,136 (GRCm38) L347Q probably damaging Het
Galntl6 T G 8: 58,911,441 (GRCm38) T12P probably damaging Het
Gm11595 G A 11: 99,772,555 (GRCm38) R100C unknown Het
Gm21680 T C 5: 25,969,036 (GRCm38) N190S probably damaging Het
Ifit1bl2 T C 19: 34,619,125 (GRCm38) S364G probably benign Het
Kdm2a A G 19: 4,350,317 (GRCm38) I234T probably damaging Het
Kdm5b T C 1: 134,599,207 (GRCm38) C356R probably damaging Het
Kel A T 6: 41,688,851 (GRCm38) C174* probably null Het
Krt16 T A 11: 100,246,676 (GRCm38) D401V probably damaging Het
Ltb4r1 A C 14: 55,767,743 (GRCm38) I168L probably benign Het
Luzp1 T A 4: 136,541,780 (GRCm38) M438K probably benign Het
Mtf1 C T 4: 124,824,352 (GRCm38) T281M probably damaging Het
Myo9a T A 9: 59,924,948 (GRCm38) S2587T probably benign Het
Olfr1311 A T 2: 112,021,551 (GRCm38) I101N probably damaging Het
Olfr1377 T A 11: 50,984,786 (GRCm38) F28L probably benign Het
Olfr532 G T 7: 140,419,667 (GRCm38) Y35* probably null Het
Olfr860 T C 9: 19,846,409 (GRCm38) D70G probably damaging Het
Pcm1 T A 8: 41,293,544 (GRCm38) F1221Y probably benign Het
Pnldc1 A T 17: 12,905,864 (GRCm38) N90K probably damaging Het
Prickle2 A T 6: 92,420,237 (GRCm38) L169Q probably damaging Het
Ralgps2 A T 1: 156,884,574 (GRCm38) L147I probably damaging Het
Rfx3 A T 19: 27,768,609 (GRCm38) L674Q possibly damaging Het
Rpl3 C A 15: 80,082,544 (GRCm38) L14F probably damaging Het
Rrbp1 C T 2: 143,989,555 (GRCm38) G231R probably damaging Het
Sema3d C T 5: 12,571,013 (GRCm38) L529F probably damaging Het
Slain1 A T 14: 103,656,955 (GRCm38) T193S probably benign Het
Slc2a6 G T 2: 27,024,587 (GRCm38) Q256K possibly damaging Het
Slk A G 19: 47,620,183 (GRCm38) E525G possibly damaging Het
Spsb4 G T 9: 96,944,645 (GRCm38) Q252K probably benign Het
Taf1b A G 12: 24,558,257 (GRCm38) T552A possibly damaging Het
Tmprss15 T C 16: 79,006,057 (GRCm38) probably null Het
Tph2 T C 10: 115,179,326 (GRCm38) H177R probably damaging Het
Ttll1 A G 15: 83,489,617 (GRCm38) S332P probably damaging Het
Twf2 T G 9: 106,212,833 (GRCm38) N128K probably benign Het
Vegfc T A 8: 54,181,230 (GRCm38) C315S probably damaging Het
Wnk2 T C 13: 49,061,338 (GRCm38) E496G probably damaging Het
Zfp148 C A 16: 33,497,198 (GRCm38) Q705K probably damaging Het
Zw10 C T 9: 49,073,235 (GRCm38) A539V probably damaging Het
Other mutations in Vmn2r111
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00932:Vmn2r111 APN 17 22,548,753 (GRCm38) missense probably benign 0.00
IGL01306:Vmn2r111 APN 17 22,568,984 (GRCm38) missense probably damaging 0.99
IGL01309:Vmn2r111 APN 17 22,569,016 (GRCm38) missense possibly damaging 0.51
IGL01457:Vmn2r111 APN 17 22,571,985 (GRCm38) nonsense probably null
IGL01465:Vmn2r111 APN 17 22,548,737 (GRCm38) missense probably benign 0.00
IGL01505:Vmn2r111 APN 17 22,548,572 (GRCm38) missense probably benign 0.00
IGL01571:Vmn2r111 APN 17 22,571,392 (GRCm38) missense probably damaging 0.99
IGL01715:Vmn2r111 APN 17 22,569,073 (GRCm38) splice site probably benign
IGL01962:Vmn2r111 APN 17 22,548,284 (GRCm38) missense possibly damaging 0.90
IGL02190:Vmn2r111 APN 17 22,570,773 (GRCm38) missense probably benign 0.00
IGL02496:Vmn2r111 APN 17 22,568,856 (GRCm38) missense probably benign
IGL02519:Vmn2r111 APN 17 22,548,339 (GRCm38) missense possibly damaging 0.80
IGL02616:Vmn2r111 APN 17 22,571,050 (GRCm38) missense possibly damaging 0.67
IGL02641:Vmn2r111 APN 17 22,573,224 (GRCm38) missense possibly damaging 0.82
IGL02690:Vmn2r111 APN 17 22,559,042 (GRCm38) critical splice donor site probably null
IGL02698:Vmn2r111 APN 17 22,571,245 (GRCm38) missense probably damaging 1.00
IGL03017:Vmn2r111 APN 17 22,570,858 (GRCm38) missense probably damaging 1.00
R0046:Vmn2r111 UTSW 17 22,548,009 (GRCm38) missense probably benign
R0064:Vmn2r111 UTSW 17 22,572,072 (GRCm38) missense probably benign 0.00
R0519:Vmn2r111 UTSW 17 22,573,121 (GRCm38) missense probably benign 0.02
R1439:Vmn2r111 UTSW 17 22,571,116 (GRCm38) missense probably benign 0.00
R1467:Vmn2r111 UTSW 17 22,571,047 (GRCm38) missense probably damaging 0.99
R1467:Vmn2r111 UTSW 17 22,571,047 (GRCm38) missense probably damaging 0.99
R1636:Vmn2r111 UTSW 17 22,571,399 (GRCm38) missense probably damaging 1.00
R1647:Vmn2r111 UTSW 17 22,569,061 (GRCm38) missense probably benign 0.03
R1648:Vmn2r111 UTSW 17 22,569,061 (GRCm38) missense probably benign 0.03
R1697:Vmn2r111 UTSW 17 22,548,060 (GRCm38) missense probably benign 0.26
R1996:Vmn2r111 UTSW 17 22,548,081 (GRCm38) missense probably benign 0.21
R2040:Vmn2r111 UTSW 17 22,548,414 (GRCm38) missense probably damaging 1.00
R2075:Vmn2r111 UTSW 17 22,559,062 (GRCm38) missense probably damaging 1.00
R2134:Vmn2r111 UTSW 17 22,573,104 (GRCm38) missense possibly damaging 0.68
R2357:Vmn2r111 UTSW 17 22,559,170 (GRCm38) splice site probably benign
R3700:Vmn2r111 UTSW 17 22,571,161 (GRCm38) nonsense probably null
R3782:Vmn2r111 UTSW 17 22,571,320 (GRCm38) missense possibly damaging 0.89
R4085:Vmn2r111 UTSW 17 22,559,115 (GRCm38) missense probably benign 0.00
R4323:Vmn2r111 UTSW 17 22,573,178 (GRCm38) missense probably benign 0.02
R4900:Vmn2r111 UTSW 17 22,548,656 (GRCm38) missense possibly damaging 0.94
R5072:Vmn2r111 UTSW 17 22,548,041 (GRCm38) missense probably damaging 0.99
R5123:Vmn2r111 UTSW 17 22,571,143 (GRCm38) missense possibly damaging 0.82
R5181:Vmn2r111 UTSW 17 22,571,020 (GRCm38) missense possibly damaging 0.56
R5357:Vmn2r111 UTSW 17 22,548,102 (GRCm38) nonsense probably null
R5398:Vmn2r111 UTSW 17 22,573,271 (GRCm38) start codon destroyed probably null 0.88
R5434:Vmn2r111 UTSW 17 22,548,489 (GRCm38) missense probably damaging 0.99
R5462:Vmn2r111 UTSW 17 22,548,257 (GRCm38) missense probably damaging 1.00
R6149:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6149:Vmn2r111 UTSW 17 22,548,815 (GRCm38) missense probably benign 0.00
R6207:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6281:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6282:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6283:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6307:Vmn2r111 UTSW 17 22,573,089 (GRCm38) missense probably benign 0.00
R6323:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6325:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6367:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6369:Vmn2r111 UTSW 17 22,548,602 (GRCm38) missense probably damaging 1.00
R6489:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6490:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6546:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6547:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6557:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6654:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6655:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6657:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6659:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6660:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6664:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6798:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6799:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6801:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6893:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6895:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6897:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6922:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6923:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6944:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R6945:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R7017:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R7018:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R7024:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R7031:Vmn2r111 UTSW 17 22,571,245 (GRCm38) missense probably damaging 1.00
R7039:Vmn2r111 UTSW 17 22,548,184 (GRCm38) missense probably damaging 1.00
R7053:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R7054:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R7055:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R7056:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R7145:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R7146:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R7246:Vmn2r111 UTSW 17 22,548,714 (GRCm38) missense probably damaging 1.00
R7259:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R7260:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R7327:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R7401:Vmn2r111 UTSW 17 22,571,086 (GRCm38) missense possibly damaging 0.93
R7514:Vmn2r111 UTSW 17 22,548,399 (GRCm38) missense probably benign 0.05
R7651:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R7781:Vmn2r111 UTSW 17 22,570,733 (GRCm38) missense probably benign 0.17
R7816:Vmn2r111 UTSW 17 22,573,102 (GRCm38) missense probably damaging 0.97
R7821:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R7838:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R8078:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R8080:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R8117:Vmn2r111 UTSW 17 22,571,488 (GRCm38) missense probably benign 0.12
R8171:Vmn2r111 UTSW 17 22,573,092 (GRCm38) missense probably benign 0.10
R8195:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R8197:Vmn2r111 UTSW 17 22,559,051 (GRCm38) missense possibly damaging 0.50
R8411:Vmn2r111 UTSW 17 22,548,581 (GRCm38) missense probably benign 0.03
R8539:Vmn2r111 UTSW 17 22,571,293 (GRCm38) missense probably benign 0.23
R8540:Vmn2r111 UTSW 17 22,559,043 (GRCm38) missense probably damaging 1.00
R8540:Vmn2r111 UTSW 17 22,559,042 (GRCm38) critical splice donor site probably null
R8557:Vmn2r111 UTSW 17 22,571,929 (GRCm38) nonsense probably null
R8720:Vmn2r111 UTSW 17 22,573,213 (GRCm38) missense possibly damaging 0.88
R8729:Vmn2r111 UTSW 17 22,548,258 (GRCm38) missense probably damaging 1.00
R8843:Vmn2r111 UTSW 17 22,548,030 (GRCm38) missense probably benign 0.00
R9184:Vmn2r111 UTSW 17 22,571,841 (GRCm38) missense probably benign
R9374:Vmn2r111 UTSW 17 22,568,878 (GRCm38) missense probably benign 0.17
R9452:Vmn2r111 UTSW 17 22,559,151 (GRCm38) missense probably damaging 1.00
X0026:Vmn2r111 UTSW 17 22,548,695 (GRCm38) missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- CCTATGCCTAGCAAGGTCATGC -3'
(R):5'- TTACAGAACTCAGACTGAAAATCGC -3'

Sequencing Primer
(F):5'- TCATGCTGGCACAAGAGATAC -3'
(R):5'- CAAATATGCTCTGGCTTTGGC -3'
Posted On 2018-04-27