Incidental Mutation 'IGL02527:Vmn2r65'
ID 297152
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r65
Ensembl Gene ENSMUSG00000066372
Gene Name vomeronasal 2, receptor 65
Synonyms ENSMUSG00000070600
Accession Numbers
Essential gene? Probably non essential (E-score: 0.071) question?
Stock # IGL02527
Quality Score
Status
Chromosome 7
Chromosomal Location 84589377-84613217 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 84595724 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Methionine at position 320 (K320M)
Ref Sequence ENSEMBL: ENSMUSP00000036551 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000044583]
AlphaFold G3X931
Predicted Effect possibly damaging
Transcript: ENSMUST00000044583
AA Change: K320M

PolyPhen 2 Score 0.817 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000036551
Gene: ENSMUSG00000066372
AA Change: K320M

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
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2m T C 6: 121,638,392 (GRCm39) V868A probably damaging Het
Adam25 T A 8: 41,206,785 (GRCm39) I17K possibly damaging Het
Arap2 A T 5: 62,906,650 (GRCm39) M123K probably benign Het
Asic3 A G 5: 24,621,275 (GRCm39) M332V probably benign Het
Atp2a3 C A 11: 72,866,165 (GRCm39) H262N probably benign Het
Cand1 A T 10: 119,042,712 (GRCm39) M1126K probably damaging Het
Capn3 A G 2: 120,334,966 (GRCm39) T818A probably damaging Het
Cda G A 4: 138,070,832 (GRCm39) Q104* probably null Het
Cfhr4 T C 1: 139,680,783 (GRCm39) N245S probably damaging Het
Cpeb1 T C 7: 81,009,635 (GRCm39) D234G probably damaging Het
Cpq A G 15: 33,302,509 (GRCm39) Y220C probably damaging Het
Diaph3 T C 14: 87,047,795 (GRCm39) K1026R possibly damaging Het
Dpep1 T C 8: 123,925,487 (GRCm39) F47L probably damaging Het
Dppa4 G T 16: 48,109,456 (GRCm39) R66L possibly damaging Het
Elac1 C A 18: 73,880,304 (GRCm39) E31* probably null Het
Fggy A G 4: 95,585,306 (GRCm39) K62E probably damaging Het
Ficd T A 5: 113,875,027 (GRCm39) M32K probably benign Het
Foxd4 A G 19: 24,877,178 (GRCm39) S341P probably benign Het
Gnb4 G T 3: 32,644,015 (GRCm39) T181K probably benign Het
Grin2b T A 6: 135,900,389 (GRCm39) Y164F probably damaging Het
Hmmr A G 11: 40,598,932 (GRCm39) L564P probably damaging Het
Hsd17b4 G A 18: 50,293,231 (GRCm39) V257I probably benign Het
Itga10 C A 3: 96,562,940 (GRCm39) probably benign Het
Kcnk18 T C 19: 59,223,707 (GRCm39) V284A probably damaging Het
Klf11 T A 12: 24,705,322 (GRCm39) S259T probably benign Het
Kmt2d C T 15: 98,739,628 (GRCm39) probably benign Het
Manea A G 4: 26,336,619 (GRCm39) probably null Het
Mybl1 T C 1: 9,760,373 (GRCm39) H75R probably damaging Het
Neb G A 2: 52,153,959 (GRCm39) T2384M probably damaging Het
Neb A G 2: 52,039,225 (GRCm39) I6938T probably benign Het
Ntrk3 T C 7: 78,101,697 (GRCm39) D412G probably benign Het
Olah T C 2: 3,343,979 (GRCm39) E211G probably damaging Het
Or10ag2 T C 2: 87,249,181 (GRCm39) L261S probably damaging Het
Paxbp1 A T 16: 90,834,161 (GRCm39) N208K possibly damaging Het
Prrc1 T A 18: 57,522,419 (GRCm39) M417K probably benign Het
Ptprq G A 10: 107,522,424 (GRCm39) T543M probably benign Het
Rasal1 T C 5: 120,804,469 (GRCm39) V447A probably damaging Het
Rbl1 T C 2: 157,035,968 (GRCm39) E287G probably benign Het
Rusf1 T A 7: 127,875,403 (GRCm39) T317S possibly damaging Het
Tec A G 5: 72,936,758 (GRCm39) probably null Het
Tex26 A G 5: 149,380,407 (GRCm39) D61G probably damaging Het
Tgfb1i1 G A 7: 127,851,734 (GRCm39) probably benign Het
Tmem132c T C 5: 127,436,675 (GRCm39) Y55H possibly damaging Het
Tmem63a T A 1: 180,780,539 (GRCm39) probably null Het
Umod C T 7: 119,068,690 (GRCm39) G452D probably damaging Het
Vcan G A 13: 89,838,776 (GRCm39) T2256I possibly damaging Het
Vmn1r31 A T 6: 58,449,778 (GRCm39) I29K probably benign Het
Vmn2r117 A G 17: 23,696,199 (GRCm39) Y403H possibly damaging Het
Vmn2r124 A T 17: 18,286,764 (GRCm39) probably null 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
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
R2338:Vmn2r65 UTSW 7 84,590,051 (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
Posted On 2015-04-16