Incidental Mutation 'R2338:Vmn2r65'
ID 246629
Institutional Source Beutler Lab
Gene Symbol Vmn2r65
Ensembl Gene ENSMUSG00000066372
Gene Name vomeronasal 2, receptor 65
Synonyms ENSMUSG00000070600
MMRRC Submission 040324-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.071) question?
Stock # R2338 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 84589377-84613217 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 84590051 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Isoleucine at position 622 (F622I)
Ref Sequence ENSEMBL: ENSMUSP00000036551 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000044583]
AlphaFold G3X931
Predicted Effect possibly damaging
Transcript: ENSMUST00000044583
AA Change: F622I

PolyPhen 2 Score 0.856 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000036551
Gene: ENSMUSG00000066372
AA Change: F622I

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
Pfam:ANF_receptor 73 435 5.6e-41 PFAM
Pfam:NCD3G 501 553 1.3e-21 PFAM
Pfam:7tm_3 584 821 2.3e-53 PFAM
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.5%
Validation Efficiency 98% (53/54)
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930474N05Rik A G 14: 35,817,109 (GRCm39) D53G probably benign Het
A1cf C T 19: 31,909,945 (GRCm39) P330S probably benign Het
Acta2 A G 19: 34,225,941 (GRCm39) probably benign Het
Actrt3 A G 3: 30,651,985 (GRCm39) *370R probably null Het
Aif1 G A 17: 35,391,127 (GRCm39) P44L probably benign Het
Btbd8 T C 5: 107,658,440 (GRCm39) L1158S probably damaging Het
Cadps2 C G 6: 23,838,977 (GRCm39) probably benign Het
Camsap3 C T 8: 3,656,808 (GRCm39) R1048C probably damaging Het
Cdkl2 C T 5: 92,181,538 (GRCm39) A148T possibly damaging Het
Dab2 T A 15: 6,464,733 (GRCm39) I395K possibly damaging Het
Dclk2 A G 3: 86,706,324 (GRCm39) F589S probably damaging Het
Ddx60 T C 8: 62,465,470 (GRCm39) S1376P possibly damaging Het
Eprs1 T C 1: 185,148,005 (GRCm39) F1256L probably damaging Het
Etaa1 A T 11: 17,895,605 (GRCm39) probably null Het
Fat2 T C 11: 55,202,727 (GRCm39) T116A possibly damaging Het
Fem1al C A 11: 29,773,718 (GRCm39) A580S probably benign Het
Fmnl3 T C 15: 99,268,108 (GRCm39) T26A probably benign Het
Foxp1 A G 6: 98,980,254 (GRCm39) V158A possibly damaging Het
G6pd2 T A 5: 61,967,351 (GRCm39) D375E probably benign Het
Gne C T 4: 44,042,196 (GRCm39) A460T probably damaging Het
Gprin1 T A 13: 54,886,238 (GRCm39) probably null Het
Hecw2 T C 1: 53,943,581 (GRCm39) M949V possibly damaging Het
Herc1 G A 9: 66,336,251 (GRCm39) V1599M possibly damaging Het
Hk2 A C 6: 82,708,096 (GRCm39) N628K probably damaging Het
Hmcn1 T C 1: 150,498,685 (GRCm39) T4065A possibly damaging Het
Ipo8 T A 6: 148,691,321 (GRCm39) Q683L probably benign Het
Krt81 A G 15: 101,361,217 (GRCm39) I121T probably benign Het
Lamb2 T C 9: 108,359,340 (GRCm39) L322P probably benign Het
Lilrb4a A G 10: 51,367,796 (GRCm39) M113V probably benign Het
Mnat1 G A 12: 73,265,917 (GRCm39) probably null Het
Mucl1 T A 15: 103,783,964 (GRCm39) T68S possibly damaging Het
Npnt G T 3: 132,597,170 (GRCm39) D461E probably damaging Het
Nrp1 A T 8: 129,224,385 (GRCm39) Q716L probably benign Het
Or11g25 A G 14: 50,723,097 (GRCm39) T61A possibly damaging Het
Or12k5 T G 2: 36,895,159 (GRCm39) S156R probably damaging Het
Or51b6b A T 7: 103,309,617 (GRCm39) I280N possibly damaging Het
Podxl2 T C 6: 88,826,178 (GRCm39) Q376R probably damaging Het
Pudp T C 18: 50,701,646 (GRCm39) D29G probably benign Het
Rrs1 C A 1: 9,616,026 (GRCm39) probably null Het
S1pr3 T C 13: 51,573,614 (GRCm39) I265T possibly damaging Het
Scgb1b2 A T 7: 30,991,038 (GRCm39) C23* probably null Het
Spag8 G T 4: 43,652,826 (GRCm39) R212S probably benign Het
Tacc2 A G 7: 130,335,299 (GRCm39) probably null Het
Trmt1l C T 1: 151,304,710 (GRCm39) probably benign Het
Trpa1 A T 1: 14,954,469 (GRCm39) L810Q probably damaging Het
Ugcg C T 4: 59,207,798 (GRCm39) P46S probably benign Het
Ugt3a1 T A 15: 9,292,059 (GRCm39) probably benign Het
Vmn2r23 T G 6: 123,681,384 (GRCm39) I97M possibly damaging Het
Vps13a C T 19: 16,697,817 (GRCm39) G766E probably damaging Het
Wnk1 T C 6: 119,946,495 (GRCm39) T553A probably benign Het
Xirp2 T A 2: 67,341,114 (GRCm39) D1118E probably damaging Het
Zfyve9 A C 4: 108,517,811 (GRCm39) D461E probably damaging Het
Other mutations in Vmn2r65
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00942:Vmn2r65 APN 7 84,592,761 (GRCm39) missense probably damaging 0.99
IGL01104:Vmn2r65 APN 7 84,589,996 (GRCm39) missense possibly damaging 0.93
IGL01154:Vmn2r65 APN 7 84,592,729 (GRCm39) missense probably benign 0.00
IGL01453:Vmn2r65 APN 7 84,589,708 (GRCm39) missense probably damaging 1.00
IGL01675:Vmn2r65 APN 7 84,596,587 (GRCm39) missense probably benign 0.00
IGL01748:Vmn2r65 APN 7 84,589,507 (GRCm39) missense probably damaging 1.00
IGL01997:Vmn2r65 APN 7 84,589,978 (GRCm39) missense probably damaging 1.00
IGL02527:Vmn2r65 APN 7 84,595,724 (GRCm39) missense possibly damaging 0.82
IGL02617:Vmn2r65 APN 7 84,589,549 (GRCm39) missense probably damaging 1.00
IGL02676:Vmn2r65 APN 7 84,589,381 (GRCm39) missense possibly damaging 0.86
IGL03084:Vmn2r65 APN 7 84,592,354 (GRCm39) missense probably damaging 1.00
A4554:Vmn2r65 UTSW 7 84,595,791 (GRCm39) missense probably damaging 0.96
PIT4651001:Vmn2r65 UTSW 7 84,595,461 (GRCm39) missense probably benign 0.12
R0322:Vmn2r65 UTSW 7 84,595,756 (GRCm39) missense probably benign 0.01
R0453:Vmn2r65 UTSW 7 84,595,442 (GRCm39) missense probably benign 0.03
R0862:Vmn2r65 UTSW 7 84,592,853 (GRCm39) missense probably benign 0.00
R1392:Vmn2r65 UTSW 7 84,596,624 (GRCm39) missense probably benign 0.14
R1392:Vmn2r65 UTSW 7 84,596,624 (GRCm39) missense probably benign 0.14
R1508:Vmn2r65 UTSW 7 84,589,886 (GRCm39) missense probably benign 0.00
R1687:Vmn2r65 UTSW 7 84,590,026 (GRCm39) missense probably benign 0.02
R1876:Vmn2r65 UTSW 7 84,595,505 (GRCm39) missense probably damaging 1.00
R2136:Vmn2r65 UTSW 7 84,592,781 (GRCm39) missense probably damaging 0.96
R2259:Vmn2r65 UTSW 7 84,590,119 (GRCm39) missense possibly damaging 0.86
R2880:Vmn2r65 UTSW 7 84,613,094 (GRCm39) missense probably damaging 1.00
R3410:Vmn2r65 UTSW 7 84,595,896 (GRCm39) missense probably benign 0.00
R3411:Vmn2r65 UTSW 7 84,595,896 (GRCm39) missense probably benign 0.00
R3770:Vmn2r65 UTSW 7 84,589,623 (GRCm39) missense probably damaging 1.00
R3800:Vmn2r65 UTSW 7 84,589,738 (GRCm39) missense possibly damaging 0.93
R3850:Vmn2r65 UTSW 7 84,595,859 (GRCm39) missense probably benign 0.00
R4105:Vmn2r65 UTSW 7 84,595,691 (GRCm39) missense probably benign 0.03
R4568:Vmn2r65 UTSW 7 84,596,677 (GRCm39) missense probably damaging 1.00
R4677:Vmn2r65 UTSW 7 84,613,082 (GRCm39) missense possibly damaging 0.55
R4768:Vmn2r65 UTSW 7 84,596,602 (GRCm39) missense probably damaging 1.00
R4778:Vmn2r65 UTSW 7 84,592,801 (GRCm39) missense possibly damaging 0.47
R5057:Vmn2r65 UTSW 7 84,589,819 (GRCm39) missense probably damaging 1.00
R5279:Vmn2r65 UTSW 7 84,589,849 (GRCm39) missense probably damaging 1.00
R5280:Vmn2r65 UTSW 7 84,595,542 (GRCm39) missense probably damaging 0.99
R5394:Vmn2r65 UTSW 7 84,595,862 (GRCm39) missense probably benign 0.04
R5487:Vmn2r65 UTSW 7 84,595,529 (GRCm39) missense possibly damaging 0.76
R5580:Vmn2r65 UTSW 7 84,596,802 (GRCm39) missense probably damaging 0.99
R5638:Vmn2r65 UTSW 7 84,590,047 (GRCm39) missense probably damaging 1.00
R5673:Vmn2r65 UTSW 7 84,596,615 (GRCm39) missense probably benign 0.23
R5688:Vmn2r65 UTSW 7 84,589,900 (GRCm39) missense probably benign 0.00
R5935:Vmn2r65 UTSW 7 84,592,869 (GRCm39) missense probably benign 0.00
R6354:Vmn2r65 UTSW 7 84,589,574 (GRCm39) missense probably benign 0.35
R6372:Vmn2r65 UTSW 7 84,589,861 (GRCm39) missense probably damaging 1.00
R6924:Vmn2r65 UTSW 7 84,613,198 (GRCm39) missense probably benign 0.20
R7021:Vmn2r65 UTSW 7 84,596,587 (GRCm39) missense probably benign 0.00
R7195:Vmn2r65 UTSW 7 84,592,347 (GRCm39) critical splice donor site probably null
R7422:Vmn2r65 UTSW 7 84,595,569 (GRCm39) missense probably damaging 0.99
R7654:Vmn2r65 UTSW 7 84,590,261 (GRCm39) missense probably damaging 1.00
R7686:Vmn2r65 UTSW 7 84,589,744 (GRCm39) missense probably damaging 0.99
R7691:Vmn2r65 UTSW 7 84,592,851 (GRCm39) missense probably benign 0.30
R7798:Vmn2r65 UTSW 7 84,596,192 (GRCm39) missense probably damaging 1.00
R7798:Vmn2r65 UTSW 7 84,595,530 (GRCm39) missense probably benign 0.00
R8103:Vmn2r65 UTSW 7 84,595,919 (GRCm39) missense probably damaging 1.00
R8272:Vmn2r65 UTSW 7 84,596,817 (GRCm39) missense probably benign 0.02
R8303:Vmn2r65 UTSW 7 84,589,391 (GRCm39) nonsense probably null
R8354:Vmn2r65 UTSW 7 84,589,402 (GRCm39) missense possibly damaging 0.73
R8454:Vmn2r65 UTSW 7 84,589,402 (GRCm39) missense possibly damaging 0.73
R8489:Vmn2r65 UTSW 7 84,589,964 (GRCm39) missense possibly damaging 0.85
R8554:Vmn2r65 UTSW 7 84,595,960 (GRCm39) missense probably benign 0.00
R8680:Vmn2r65 UTSW 7 84,589,388 (GRCm39) missense probably benign 0.00
R8731:Vmn2r65 UTSW 7 84,589,447 (GRCm39) nonsense probably null
R8839:Vmn2r65 UTSW 7 84,595,489 (GRCm39) nonsense probably null
R8847:Vmn2r65 UTSW 7 84,590,212 (GRCm39) missense probably damaging 1.00
R8916:Vmn2r65 UTSW 7 84,595,665 (GRCm39) missense probably benign 0.21
R9254:Vmn2r65 UTSW 7 84,596,650 (GRCm39) missense probably damaging 0.99
R9379:Vmn2r65 UTSW 7 84,596,650 (GRCm39) missense probably damaging 0.99
R9392:Vmn2r65 UTSW 7 84,589,718 (GRCm39) missense possibly damaging 0.95
R9563:Vmn2r65 UTSW 7 84,589,880 (GRCm39) nonsense probably null
R9686:Vmn2r65 UTSW 7 84,590,084 (GRCm39) missense probably benign 0.45
X0067:Vmn2r65 UTSW 7 84,590,113 (GRCm39) missense probably benign 0.04
Z1088:Vmn2r65 UTSW 7 84,592,473 (GRCm39) critical splice acceptor site probably null
Z1177:Vmn2r65 UTSW 7 84,590,234 (GRCm39) missense probably damaging 0.97
Predicted Primers PCR Primer
(F):5'- TCATGGTGCAGATGGGAATG -3'
(R):5'- AAAGTTGTGACCTTCCTGGCTTATG -3'

Sequencing Primer
(F):5'- AGTTAGGTGCCCTTGTTACTAAC -3'
(R):5'- TGAAGACCCCTTAGGAATGACTCTG -3'
Posted On 2014-10-30