Incidental Mutation 'R7798:Vmn2r65'
ID 600362
Institutional Source Beutler Lab
Gene Symbol Vmn2r65
Ensembl Gene ENSMUSG00000066372
Gene Name vomeronasal 2, receptor 65
Synonyms ENSMUSG00000070600
MMRRC Submission 045648-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.071) question?
Stock # R7798 (G1)
Quality Score 225.009
Status Not validated
Chromosome 7
Chromosomal Location 84589377-84613217 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 84596192 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Serine at position 164 (F164S)
Ref Sequence ENSEMBL: ENSMUSP00000036551 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000044583]
AlphaFold G3X931
Predicted Effect probably damaging
Transcript: ENSMUST00000044583
AA Change: F164S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000036551
Gene: ENSMUSG00000066372
AA Change: F164S

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
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 76 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700088E04Rik T A 15: 79,019,932 (GRCm39) N128I probably damaging Het
Abca13 A G 11: 9,241,664 (GRCm39) T1176A probably benign Het
Abca9 A G 11: 110,029,005 (GRCm39) V851A probably benign Het
Abcc6 C A 7: 45,626,277 (GRCm39) E1494* probably null Het
Adamts14 A T 10: 61,106,952 (GRCm39) V56E probably damaging Het
Adamts15 G A 9: 30,815,939 (GRCm39) T639M probably damaging Het
Albfm1 T C 5: 90,745,370 (GRCm39) S608P possibly damaging Het
Arhgap11a A C 2: 113,673,680 (GRCm39) V70G probably damaging Het
BC051665 A T 13: 60,932,249 (GRCm39) D113E probably benign Het
Best1 T C 19: 9,969,035 (GRCm39) Y227C probably damaging Het
Camk2b A G 11: 5,928,399 (GRCm39) S447P probably benign Het
Ccdc88a C A 11: 29,427,348 (GRCm39) Q1018K probably benign Het
Cdhr17 T C 5: 17,061,656 (GRCm39) F801L possibly damaging Het
Cfap74 T A 4: 155,507,079 (GRCm39) V180D Het
Clca3a1 T A 3: 144,463,723 (GRCm39) T185S probably damaging Het
Clca3b T C 3: 144,533,891 (GRCm39) S495G probably damaging Het
Cyb5r2 A T 7: 107,353,155 (GRCm39) Y96N possibly damaging Het
Cyp21a1 T C 17: 35,023,295 (GRCm39) K27E probably benign Het
Cyp2ab1 T C 16: 20,131,166 (GRCm39) E321G probably benign Het
Des T C 1: 75,339,003 (GRCm39) I228T probably damaging Het
Dis3l G T 9: 64,248,299 (GRCm39) P39T probably benign Het
Disp2 A C 2: 118,622,360 (GRCm39) I1031L probably benign Het
Ell3 TCTCCTC TCTC 2: 121,269,937 (GRCm39) probably benign Het
Etl4 G A 2: 20,786,757 (GRCm39) probably null Het
Fgf23 A T 6: 127,050,177 (GRCm39) D62V probably damaging Het
Galnt15 C T 14: 31,751,862 (GRCm39) T138I possibly damaging Het
Ggt6 A T 11: 72,326,367 (GRCm39) probably benign Het
Gpr180 T A 14: 118,391,098 (GRCm39) V209D probably damaging Het
Gzma A T 13: 113,232,858 (GRCm39) F78Y probably benign Het
Igkv8-30 A T 6: 70,094,355 (GRCm39) C19S probably benign Het
Il1r1 G A 1: 40,349,526 (GRCm39) V361I probably benign Het
Intu T C 3: 40,646,359 (GRCm39) V598A probably damaging Het
Itpr2 A G 6: 146,287,513 (GRCm39) F471L probably benign Het
Kntc1 T A 5: 123,924,357 (GRCm39) V1081E probably benign Het
Kntc1 T A 5: 123,957,180 (GRCm39) V2163E possibly damaging Het
Macf1 T C 4: 123,271,893 (GRCm39) K6552E probably damaging Het
Marf1 T C 16: 13,956,315 (GRCm39) H842R probably benign Het
Mgat4b A G 11: 50,116,497 (GRCm39) T10A possibly damaging Het
Muc21 C G 17: 35,932,146 (GRCm39) G680A unknown Het
Muc5ac T C 7: 141,347,778 (GRCm39) probably null Het
Nrk CGCAGCAGCAGCAGCAGCAGC CGCAGCAGCAGCAGCAGC X: 137,883,426 (GRCm39) probably benign Het
Nsun4 T G 4: 115,908,371 (GRCm39) S730R possibly damaging Het
Or12e1 A T 2: 87,022,636 (GRCm39) I202L probably benign Het
Or12k7 A T 2: 36,959,186 (GRCm39) S290C probably damaging Het
Or1n1 T C 2: 36,750,348 (GRCm39) E4G probably benign Het
Or4f6 A G 2: 111,838,617 (GRCm39) F305L probably benign Het
Or4k15 A T 14: 50,364,895 (GRCm39) Y287F probably damaging Het
Padi3 C T 4: 140,513,750 (GRCm39) E653K probably benign Het
Pde4a A G 9: 21,109,959 (GRCm39) E280G possibly damaging Het
Phactr3 G A 2: 177,925,703 (GRCm39) R326H probably benign Het
Prob1 G A 18: 35,786,397 (GRCm39) P619L possibly damaging Het
Ptk2 G A 15: 73,167,224 (GRCm39) R368W probably damaging Het
Rgs6 A G 12: 83,116,293 (GRCm39) T240A probably benign Het
Rpa1 A T 11: 75,203,635 (GRCm39) Y356N probably damaging Het
Rxrb T A 17: 34,252,579 (GRCm39) D165E probably damaging Het
Sco1 A G 11: 66,944,628 (GRCm39) T84A possibly damaging Het
Sepsecs T C 5: 52,804,531 (GRCm39) I380V probably benign Het
Sfmbt1 T A 14: 30,538,759 (GRCm39) W793R probably damaging Het
Slco3a1 A G 7: 73,968,344 (GRCm39) S459P probably benign Het
Smg1 A T 7: 117,771,162 (GRCm39) S1503R possibly damaging Het
Sox2 G A 3: 34,704,791 (GRCm39) R76H probably damaging Het
Spty2d1 G A 7: 46,645,804 (GRCm39) S613F probably damaging Het
Stab2 A T 10: 86,793,776 (GRCm39) Y440N probably damaging Het
Syn3 A G 10: 85,916,117 (GRCm39) Y290H probably damaging Het
Tex15 C T 8: 34,071,875 (GRCm39) S2474F possibly damaging Het
Tgtp1 A G 11: 48,878,159 (GRCm39) F182S probably benign Het
Tmcc1 A T 6: 116,020,539 (GRCm39) S304R Het
Tmem130 T G 5: 144,680,580 (GRCm39) K275Q probably damaging Het
Tmem9 C A 1: 135,961,927 (GRCm39) T174K probably damaging Het
Ttyh3 C T 5: 140,620,538 (GRCm39) R233Q probably damaging Het
Tut7 A T 13: 59,963,389 (GRCm39) M323K possibly damaging Het
Twnk T C 19: 44,996,107 (GRCm39) M180T probably benign Het
Ube4a A G 9: 44,844,629 (GRCm39) V874A probably damaging Het
Ugt2a3 T C 5: 87,475,582 (GRCm39) N350S probably damaging Het
Vegfa C T 17: 46,342,761 (GRCm39) G19D probably damaging Het
Vmn2r2 C A 3: 64,041,518 (GRCm39) C399F possibly 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
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 84,595,530 (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'- ACAGACTTTGTGTTTGTGCATC -3'
(R):5'- CATTTTCTGGCACATACATGACATC -3'

Sequencing Primer
(F):5'- GCATCTCTCCTCTCAACTTAAAGAG -3'
(R):5'- TGGCACATACATGACATCATTATTAG -3'
Posted On 2019-11-26