Incidental Mutation 'R1906:Vmn2r82'
ID 214389
Institutional Source Beutler Lab
Gene Symbol Vmn2r82
Ensembl Gene ENSMUSG00000091468
Gene Name vomeronasal 2, receptor 82
Synonyms EG624845
MMRRC Submission 039925-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # R1906 (G1)
Quality Score 225
Status Not validated
Chromosome 10
Chromosomal Location 79192425-79232600 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 79232344 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Serine at position 781 (N781S)
Ref Sequence ENSEMBL: ENSMUSP00000130114 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000170596]
AlphaFold G3UWA2
Predicted Effect probably damaging
Transcript: ENSMUST00000170596
AA Change: N781S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000130114
Gene: ENSMUSG00000091468
AA Change: N781S

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 79 474 6e-35 PFAM
Pfam:NCD3G 517 570 9.3e-22 PFAM
Pfam:7tm_3 603 838 6.5e-49 PFAM
Coding Region Coverage
  • 1x: 97.3%
  • 3x: 96.7%
  • 10x: 94.9%
  • 20x: 91.5%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aass G A 6: 23,072,984 (GRCm39) T923I probably benign Het
Abhd13 T A 8: 10,038,170 (GRCm39) C256S probably benign Het
Adamts5 C T 16: 85,665,573 (GRCm39) W576* probably null Het
Adnp A T 2: 168,024,287 (GRCm39) S1003T probably benign Het
AI987944 C T 7: 41,024,550 (GRCm39) R146Q probably benign Het
Apol6 G T 15: 76,935,060 (GRCm39) V110F probably damaging Het
Arhgap27 A G 11: 103,223,751 (GRCm39) F651L probably damaging Het
Atm T C 9: 53,417,868 (GRCm39) D813G probably damaging Het
Casd1 T A 6: 4,641,979 (GRCm39) I752N probably damaging Het
Cdr2 A G 7: 120,581,224 (GRCm39) Y18H probably damaging Het
Cntn4 T C 6: 106,330,607 (GRCm39) F75S probably benign Het
Col20a1 G A 2: 180,640,490 (GRCm39) R549H probably benign Het
Col28a1 A T 6: 7,999,644 (GRCm39) N1024K probably benign Het
Dnah10 T A 5: 124,878,048 (GRCm39) V2654D probably damaging Het
Dnph1 A T 17: 46,807,787 (GRCm39) I18F probably damaging Het
Dsn1 G A 2: 156,838,163 (GRCm39) R334W probably damaging Het
Egf T A 3: 129,518,873 (GRCm39) K325N probably benign Het
Eps15 T G 4: 109,181,398 (GRCm39) S311A possibly damaging Het
Fmo3 G T 1: 162,794,475 (GRCm39) D198E probably damaging Het
Folh1 C G 7: 86,391,374 (GRCm39) probably null Het
Foxn1 A G 11: 78,262,636 (GRCm39) probably null Het
Gm10604 T G 4: 11,979,989 (GRCm39) D105A unknown Het
Gpx8 A G 13: 113,182,110 (GRCm39) C108R probably damaging Het
Herc2 A T 7: 55,764,612 (GRCm39) I1013L probably benign Het
Hyal4 T G 6: 24,756,110 (GRCm39) N109K probably damaging Het
Il22ra1 T G 4: 135,478,544 (GRCm39) C538W probably damaging Het
Ints13 A T 6: 146,453,868 (GRCm39) probably null Het
Krt75 T A 15: 101,481,801 (GRCm39) T156S possibly damaging Het
Lama2 A C 10: 26,932,523 (GRCm39) probably null Het
Lifr G T 15: 7,217,612 (GRCm39) V847L probably damaging Het
Lmf1 T A 17: 25,831,309 (GRCm39) I185N probably damaging Het
Mast1 G A 8: 85,642,895 (GRCm39) R967C probably damaging Het
Ms4a15 T C 19: 10,960,644 (GRCm39) I94V probably benign Het
Mycbpap A T 11: 94,396,447 (GRCm39) M131K probably benign Het
Ncor1 A T 11: 62,240,211 (GRCm39) M920K possibly damaging Het
Neb A G 2: 52,198,538 (GRCm39) Y437H probably damaging Het
Npy5r A T 8: 67,134,125 (GRCm39) W223R probably damaging Het
Or10ak11 G A 4: 118,687,467 (GRCm39) H56Y probably damaging Het
Or10x4 C A 1: 174,218,730 (GRCm39) L32M probably damaging Het
Or4c114 A G 2: 88,905,414 (GRCm39) V7A possibly damaging Het
Or6c6c T G 10: 129,541,365 (GRCm39) V206G probably benign Het
Polg T C 7: 79,110,070 (GRCm39) K353E probably damaging Het
Proz C G 8: 13,123,686 (GRCm39) probably null Het
Pus7 T C 5: 23,983,209 (GRCm39) D86G probably damaging Het
Rhpn1 T C 15: 75,583,673 (GRCm39) V386A probably benign Het
Rigi T C 4: 40,206,054 (GRCm39) K846R probably benign Het
Sptbn4 A G 7: 27,090,856 (GRCm39) probably null Het
Srp68 A T 11: 116,141,587 (GRCm39) I424N probably damaging Het
Stard9 A G 2: 120,526,908 (GRCm39) E1055G probably benign Het
Taf4b A G 18: 14,955,159 (GRCm39) I571V probably benign Het
Tas2r107 T C 6: 131,636,951 (GRCm39) M33V probably benign Het
Thap12 T C 7: 98,365,947 (GRCm39) L705P probably damaging Het
Tom1 T C 8: 75,778,218 (GRCm39) V100A probably damaging Het
Tox3 A G 8: 90,975,057 (GRCm39) probably benign Het
Vwa5b1 A T 4: 138,327,547 (GRCm39) V343E possibly damaging Het
Zbbx A G 3: 74,979,047 (GRCm39) Y467H probably damaging Het
Zbtb46 G A 2: 181,065,632 (GRCm39) R173W probably damaging Het
Zfp112 A G 7: 23,821,720 (GRCm39) D20G probably benign Het
Zfp777 A C 6: 48,018,995 (GRCm39) M313R probably damaging Het
Other mutations in Vmn2r82
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01800:Vmn2r82 APN 10 79,192,581 (GRCm39) missense probably benign 0.03
IGL01860:Vmn2r82 APN 10 79,214,691 (GRCm39) missense probably benign 0.18
IGL01927:Vmn2r82 APN 10 79,213,906 (GRCm39) missense probably damaging 1.00
IGL01929:Vmn2r82 APN 10 79,214,545 (GRCm39) missense probably damaging 1.00
IGL02028:Vmn2r82 APN 10 79,215,057 (GRCm39) missense probably benign
IGL02112:Vmn2r82 APN 10 79,231,833 (GRCm39) missense probably benign 0.19
IGL02632:Vmn2r82 APN 10 79,192,542 (GRCm39) missense probably benign 0.45
IGL02665:Vmn2r82 APN 10 79,215,205 (GRCm39) missense probably damaging 0.99
IGL02716:Vmn2r82 APN 10 79,213,678 (GRCm39) missense probably benign 0.20
IGL03030:Vmn2r82 APN 10 79,217,149 (GRCm39) missense possibly damaging 0.85
IGL03190:Vmn2r82 APN 10 79,192,643 (GRCm39) splice site probably null
IGL03349:Vmn2r82 APN 10 79,213,703 (GRCm39) missense probably benign 0.25
IGL03048:Vmn2r82 UTSW 10 79,232,460 (GRCm39) missense probably damaging 0.98
R0080:Vmn2r82 UTSW 10 79,232,339 (GRCm39) missense probably benign 0.00
R0193:Vmn2r82 UTSW 10 79,217,129 (GRCm39) missense probably damaging 1.00
R0217:Vmn2r82 UTSW 10 79,214,634 (GRCm39) missense possibly damaging 0.46
R0285:Vmn2r82 UTSW 10 79,232,391 (GRCm39) missense probably damaging 1.00
R1193:Vmn2r82 UTSW 10 79,213,739 (GRCm39) nonsense probably null
R1385:Vmn2r82 UTSW 10 79,232,325 (GRCm39) nonsense probably null
R1386:Vmn2r82 UTSW 10 79,214,545 (GRCm39) missense probably damaging 1.00
R1442:Vmn2r82 UTSW 10 79,215,201 (GRCm39) missense probably benign 0.03
R1467:Vmn2r82 UTSW 10 79,232,133 (GRCm39) missense probably benign 0.00
R1467:Vmn2r82 UTSW 10 79,232,133 (GRCm39) missense probably benign 0.00
R1518:Vmn2r82 UTSW 10 79,214,702 (GRCm39) missense probably damaging 1.00
R1538:Vmn2r82 UTSW 10 79,192,578 (GRCm39) missense possibly damaging 0.92
R1607:Vmn2r82 UTSW 10 79,215,253 (GRCm39) missense possibly damaging 0.67
R1812:Vmn2r82 UTSW 10 79,215,046 (GRCm39) missense probably benign 0.33
R1954:Vmn2r82 UTSW 10 79,231,890 (GRCm39) missense probably damaging 1.00
R1972:Vmn2r82 UTSW 10 79,214,680 (GRCm39) missense probably damaging 1.00
R2093:Vmn2r82 UTSW 10 79,231,813 (GRCm39) missense probably benign 0.30
R2156:Vmn2r82 UTSW 10 79,214,722 (GRCm39) missense probably damaging 1.00
R2202:Vmn2r82 UTSW 10 79,192,519 (GRCm39) missense probably benign
R2442:Vmn2r82 UTSW 10 79,221,210 (GRCm39) missense probably damaging 1.00
R2444:Vmn2r82 UTSW 10 79,213,702 (GRCm39) missense possibly damaging 0.65
R2857:Vmn2r82 UTSW 10 79,217,090 (GRCm39) missense probably damaging 0.98
R2858:Vmn2r82 UTSW 10 79,217,090 (GRCm39) missense probably damaging 0.98
R2884:Vmn2r82 UTSW 10 79,232,082 (GRCm39) missense probably benign 0.00
R2886:Vmn2r82 UTSW 10 79,232,082 (GRCm39) missense probably benign 0.00
R4369:Vmn2r82 UTSW 10 79,231,914 (GRCm39) missense probably benign 0.01
R4445:Vmn2r82 UTSW 10 79,214,874 (GRCm39) missense possibly damaging 0.87
R4589:Vmn2r82 UTSW 10 79,192,548 (GRCm39) missense probably damaging 1.00
R4703:Vmn2r82 UTSW 10 79,214,641 (GRCm39) missense probably damaging 1.00
R4908:Vmn2r82 UTSW 10 79,214,589 (GRCm39) missense probably benign 0.00
R4937:Vmn2r82 UTSW 10 79,215,010 (GRCm39) missense probably benign 0.01
R5199:Vmn2r82 UTSW 10 79,231,921 (GRCm39) missense probably damaging 1.00
R5391:Vmn2r82 UTSW 10 79,192,491 (GRCm39) missense probably null 0.01
R5601:Vmn2r82 UTSW 10 79,232,025 (GRCm39) missense probably damaging 1.00
R5635:Vmn2r82 UTSW 10 79,214,652 (GRCm39) missense probably benign 0.33
R6065:Vmn2r82 UTSW 10 79,221,210 (GRCm39) missense probably damaging 1.00
R6074:Vmn2r82 UTSW 10 79,232,377 (GRCm39) missense probably damaging 1.00
R6340:Vmn2r82 UTSW 10 79,231,727 (GRCm39) missense probably benign 0.00
R6474:Vmn2r82 UTSW 10 79,214,871 (GRCm39) missense possibly damaging 0.55
R6995:Vmn2r82 UTSW 10 79,232,377 (GRCm39) missense probably damaging 1.00
R7111:Vmn2r82 UTSW 10 79,214,605 (GRCm39) missense probably benign 0.22
R7212:Vmn2r82 UTSW 10 79,215,268 (GRCm39) missense probably benign 0.00
R7335:Vmn2r82 UTSW 10 79,214,722 (GRCm39) missense probably damaging 1.00
R7353:Vmn2r82 UTSW 10 79,232,452 (GRCm39) missense probably benign 0.11
R7354:Vmn2r82 UTSW 10 79,192,464 (GRCm39) missense probably benign 0.00
R7362:Vmn2r82 UTSW 10 79,232,451 (GRCm39) missense probably benign 0.00
R7378:Vmn2r82 UTSW 10 79,232,276 (GRCm39) nonsense probably null
R7430:Vmn2r82 UTSW 10 79,217,087 (GRCm39) missense probably damaging 1.00
R7509:Vmn2r82 UTSW 10 79,231,842 (GRCm39) missense possibly damaging 0.82
R7874:Vmn2r82 UTSW 10 79,232,345 (GRCm39) missense probably damaging 1.00
R7943:Vmn2r82 UTSW 10 79,232,079 (GRCm39) missense possibly damaging 0.74
R8158:Vmn2r82 UTSW 10 79,213,636 (GRCm39) missense probably benign 0.12
R8324:Vmn2r82 UTSW 10 79,214,727 (GRCm39) nonsense probably null
R8340:Vmn2r82 UTSW 10 79,217,036 (GRCm39) missense probably benign 0.00
R8787:Vmn2r82 UTSW 10 79,213,894 (GRCm39) missense probably damaging 1.00
R8929:Vmn2r82 UTSW 10 79,232,541 (GRCm39) missense probably benign 0.00
R9018:Vmn2r82 UTSW 10 79,232,539 (GRCm39) missense probably damaging 1.00
R9399:Vmn2r82 UTSW 10 79,214,768 (GRCm39) nonsense probably null
R9517:Vmn2r82 UTSW 10 79,213,641 (GRCm39) nonsense probably null
R9587:Vmn2r82 UTSW 10 79,214,936 (GRCm39) missense possibly damaging 0.70
R9602:Vmn2r82 UTSW 10 79,214,880 (GRCm39) missense probably benign 0.07
Z1088:Vmn2r82 UTSW 10 79,192,456 (GRCm39) missense probably damaging 1.00
Z1177:Vmn2r82 UTSW 10 79,232,369 (GRCm39) missense probably damaging 1.00
Z1177:Vmn2r82 UTSW 10 79,192,429 (GRCm39) missense probably benign 0.03
Predicted Primers PCR Primer
(F):5'- GTTGCTGACATCACAGGTCC -3'
(R):5'- TGTAGCACTTAGGAGCAAAGAC -3'

Sequencing Primer
(F):5'- GCTGACATCACAGGTCCCTAAATTTG -3'
(R):5'- GACTATGATAAGAATGCTTGCACTGG -3'
Posted On 2014-07-14