Incidental Mutation 'IGL02651:Vmn2r60'
ID 302127
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r60
Ensembl Gene ENSMUSG00000090619
Gene Name vomeronasal 2, receptor 60
Synonyms Casr-rs3, EG637898, Gprc2a-rs3
Accession Numbers
Essential gene? Probably non essential (E-score: 0.100) question?
Stock # IGL02651
Quality Score
Status
Chromosome 7
Chromosomal Location 41765895-41845200 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 41845010 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Serine at position 791 (F791S)
Ref Sequence ENSEMBL: ENSMUSP00000128493 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000166447]
AlphaFold A0A3B2WBC8
Predicted Effect probably damaging
Transcript: ENSMUST00000166447
AA Change: F791S

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000128493
Gene: ENSMUSG00000090619
AA Change: F791S

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 78 471 1.2e-44 PFAM
Pfam:NCD3G 514 567 5.1e-23 PFAM
Pfam:7tm_3 600 835 1.4e-51 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A1cf G A 19: 31,909,906 (GRCm39) G233S probably benign Het
Abcc1 T A 16: 14,283,990 (GRCm39) C1202S probably benign Het
Acaca C T 11: 84,136,030 (GRCm39) probably benign Het
Ap3b1 T A 13: 94,613,529 (GRCm39) F676Y probably damaging Het
Arhgef11 C A 3: 87,606,171 (GRCm39) Q309K probably damaging Het
Asgr1 T C 11: 69,947,956 (GRCm39) Y80H possibly damaging Het
Atp13a5 A T 16: 29,152,909 (GRCm39) probably benign Het
Atp2a3 C A 11: 72,866,165 (GRCm39) H262N probably benign Het
Atp8b2 A C 3: 89,861,896 (GRCm39) probably null Het
Btnl2 A G 17: 34,575,196 (GRCm39) M1V probably null Het
Cpsf3 T A 12: 21,343,298 (GRCm39) M121K probably damaging Het
Creb3l3 A G 10: 80,920,668 (GRCm39) I454T probably benign Het
Cyp2d12 A G 15: 82,440,941 (GRCm39) E153G probably damaging Het
Dnah5 A G 15: 28,350,768 (GRCm39) I2597V probably benign Het
Ercc5 C A 1: 44,196,104 (GRCm39) S32R probably damaging Het
Fchsd2 T A 7: 100,926,807 (GRCm39) N656K possibly damaging Het
Fga G A 3: 82,935,841 (GRCm39) E23K probably benign Het
Fn1 T C 1: 71,636,835 (GRCm39) T1925A possibly damaging Het
Fstl5 A T 3: 76,500,841 (GRCm39) E423D probably damaging Het
Glg1 C T 8: 111,887,359 (GRCm39) M465I possibly damaging Het
H2-M10.4 C A 17: 36,771,548 (GRCm39) R210L probably benign Het
Hbb-y T G 7: 103,501,957 (GRCm39) K105Q probably benign Het
Hspg2 A T 4: 137,284,756 (GRCm39) probably benign Het
Ipo11 T C 13: 107,012,114 (GRCm39) Y556C probably damaging Het
Itpr3 A G 17: 27,325,372 (GRCm39) M1322V probably damaging Het
Jhy A G 9: 40,828,631 (GRCm39) L425P probably damaging Het
Krt26 C T 11: 99,224,471 (GRCm39) R349Q probably benign Het
Ms4a6c A T 19: 11,455,669 (GRCm39) E159D possibly damaging Het
Msh6 A T 17: 88,296,943 (GRCm39) L1213F probably damaging Het
Npy1r A C 8: 67,157,675 (GRCm39) R328S possibly damaging Het
Or4a74 A T 2: 89,439,842 (GRCm39) N201K possibly damaging Het
Or5ak20 A C 2: 85,183,394 (GRCm39) L292R probably damaging Het
Pcdhb18 T G 18: 37,624,234 (GRCm39) Y521* probably null Het
Pkhd1l1 A T 15: 44,347,210 (GRCm39) Y192F probably damaging Het
Rdh12 T A 12: 79,268,826 (GRCm39) I301N probably damaging Het
Rptor T C 11: 119,783,438 (GRCm39) V1144A possibly damaging Het
Sap25 T C 5: 137,640,632 (GRCm39) F171L possibly damaging Het
Senp5 A G 16: 31,808,897 (GRCm39) L92P probably benign Het
Sfmbt1 T C 14: 30,537,494 (GRCm39) S736P probably damaging Het
Tacr1 T C 6: 82,469,622 (GRCm39) S169P probably damaging Het
Tbc1d21 A T 9: 58,270,384 (GRCm39) Y130* probably null Het
Tle2 G A 10: 81,422,723 (GRCm39) G428D probably damaging Het
Tmem117 T A 15: 94,992,442 (GRCm39) N367K probably damaging Het
Tmem210 A G 2: 25,179,101 (GRCm39) T130A possibly damaging Het
Ttn T G 2: 76,680,368 (GRCm39) probably benign Het
Ttyh1 T C 7: 4,127,678 (GRCm39) L122P probably damaging Het
Vps13d A T 4: 144,891,129 (GRCm39) N575K probably benign Het
Vps8 T C 16: 21,336,086 (GRCm39) V746A probably damaging Het
Wdfy3 A T 5: 102,044,341 (GRCm39) M1888K probably benign Het
Zfp595 T C 13: 67,469,017 (GRCm39) D3G probably benign Het
Other mutations in Vmn2r60
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01622:Vmn2r60 APN 7 41,785,910 (GRCm39) missense probably benign 0.09
IGL01623:Vmn2r60 APN 7 41,785,910 (GRCm39) missense probably benign 0.09
IGL02363:Vmn2r60 APN 7 41,844,578 (GRCm39) missense probably benign 0.02
IGL02485:Vmn2r60 APN 7 41,844,890 (GRCm39) missense possibly damaging 0.54
IGL02660:Vmn2r60 APN 7 41,791,720 (GRCm39) nonsense probably null
IGL03135:Vmn2r60 APN 7 41,786,018 (GRCm39) missense probably benign 0.13
IGL03307:Vmn2r60 APN 7 41,765,971 (GRCm39) missense probably benign 0.14
R0310:Vmn2r60 UTSW 7 41,844,564 (GRCm39) missense possibly damaging 0.54
R0314:Vmn2r60 UTSW 7 41,784,985 (GRCm39) splice site probably benign
R0328:Vmn2r60 UTSW 7 41,791,744 (GRCm39) splice site probably benign
R0464:Vmn2r60 UTSW 7 41,785,255 (GRCm39) missense probably damaging 0.99
R0755:Vmn2r60 UTSW 7 41,844,869 (GRCm39) missense probably damaging 1.00
R1119:Vmn2r60 UTSW 7 41,844,365 (GRCm39) missense possibly damaging 0.68
R1162:Vmn2r60 UTSW 7 41,845,195 (GRCm39) missense probably benign 0.29
R1241:Vmn2r60 UTSW 7 41,786,476 (GRCm39) missense probably benign 0.01
R1404:Vmn2r60 UTSW 7 41,786,211 (GRCm39) missense probably damaging 0.99
R1404:Vmn2r60 UTSW 7 41,786,211 (GRCm39) missense probably damaging 0.99
R1488:Vmn2r60 UTSW 7 41,786,137 (GRCm39) missense probably benign 0.17
R1623:Vmn2r60 UTSW 7 41,785,279 (GRCm39) nonsense probably null
R1628:Vmn2r60 UTSW 7 41,785,830 (GRCm39) nonsense probably null
R1883:Vmn2r60 UTSW 7 41,786,094 (GRCm39) missense probably damaging 0.99
R1884:Vmn2r60 UTSW 7 41,786,094 (GRCm39) missense probably damaging 0.99
R2182:Vmn2r60 UTSW 7 41,844,931 (GRCm39) missense probably benign 0.06
R2275:Vmn2r60 UTSW 7 41,786,251 (GRCm39) nonsense probably null
R2847:Vmn2r60 UTSW 7 41,785,857 (GRCm39) missense probably benign 0.07
R2885:Vmn2r60 UTSW 7 41,790,403 (GRCm39) missense possibly damaging 0.91
R2894:Vmn2r60 UTSW 7 41,785,220 (GRCm39) missense probably benign
R2921:Vmn2r60 UTSW 7 41,790,459 (GRCm39) missense probably damaging 0.98
R2922:Vmn2r60 UTSW 7 41,790,459 (GRCm39) missense probably damaging 0.98
R3772:Vmn2r60 UTSW 7 41,765,980 (GRCm39) missense probably benign 0.35
R3820:Vmn2r60 UTSW 7 41,785,125 (GRCm39) missense probably damaging 0.98
R3822:Vmn2r60 UTSW 7 41,785,125 (GRCm39) missense probably damaging 0.98
R3872:Vmn2r60 UTSW 7 41,785,878 (GRCm39) missense probably benign 0.19
R4222:Vmn2r60 UTSW 7 41,765,952 (GRCm39) missense probably benign 0.08
R4223:Vmn2r60 UTSW 7 41,765,952 (GRCm39) missense probably benign 0.08
R4224:Vmn2r60 UTSW 7 41,765,952 (GRCm39) missense probably benign 0.08
R4526:Vmn2r60 UTSW 7 41,844,667 (GRCm39) missense probably damaging 0.96
R4547:Vmn2r60 UTSW 7 41,785,087 (GRCm39) missense probably null 0.54
R4840:Vmn2r60 UTSW 7 41,785,285 (GRCm39) missense probably damaging 1.00
R5173:Vmn2r60 UTSW 7 41,844,935 (GRCm39) missense probably damaging 0.97
R5231:Vmn2r60 UTSW 7 41,786,448 (GRCm39) missense possibly damaging 0.93
R5480:Vmn2r60 UTSW 7 41,785,154 (GRCm39) missense probably damaging 0.98
R5521:Vmn2r60 UTSW 7 41,845,049 (GRCm39) missense probably damaging 0.99
R5834:Vmn2r60 UTSW 7 41,765,932 (GRCm39) missense probably benign 0.17
R6038:Vmn2r60 UTSW 7 41,844,386 (GRCm39) missense probably benign 0.04
R6038:Vmn2r60 UTSW 7 41,844,386 (GRCm39) missense probably benign 0.04
R6112:Vmn2r60 UTSW 7 41,844,847 (GRCm39) missense probably damaging 1.00
R6149:Vmn2r60 UTSW 7 41,786,400 (GRCm39) missense probably damaging 1.00
R6170:Vmn2r60 UTSW 7 41,785,045 (GRCm39) missense possibly damaging 0.94
R6383:Vmn2r60 UTSW 7 41,765,895 (GRCm39) start codon destroyed probably null 0.04
R6811:Vmn2r60 UTSW 7 41,844,310 (GRCm39) missense probably damaging 1.00
R6876:Vmn2r60 UTSW 7 41,785,087 (GRCm39) missense probably null 0.54
R6997:Vmn2r60 UTSW 7 41,791,716 (GRCm39) missense probably benign 0.00
R7040:Vmn2r60 UTSW 7 41,791,666 (GRCm39) missense probably benign 0.00
R7116:Vmn2r60 UTSW 7 41,786,487 (GRCm39) missense probably benign 0.00
R7128:Vmn2r60 UTSW 7 41,844,536 (GRCm39) missense probably damaging 0.96
R7232:Vmn2r60 UTSW 7 41,786,166 (GRCm39) missense possibly damaging 0.83
R7296:Vmn2r60 UTSW 7 41,785,826 (GRCm39) missense probably benign 0.01
R7376:Vmn2r60 UTSW 7 41,844,631 (GRCm39) missense probably damaging 1.00
R7526:Vmn2r60 UTSW 7 41,845,158 (GRCm39) frame shift probably null
R7527:Vmn2r60 UTSW 7 41,845,158 (GRCm39) frame shift probably null
R7528:Vmn2r60 UTSW 7 41,845,158 (GRCm39) frame shift probably null
R7764:Vmn2r60 UTSW 7 41,844,535 (GRCm39) missense probably damaging 0.99
R7843:Vmn2r60 UTSW 7 41,844,511 (GRCm39) missense probably benign 0.00
R8080:Vmn2r60 UTSW 7 41,790,521 (GRCm39) missense probably benign 0.30
R8290:Vmn2r60 UTSW 7 41,791,690 (GRCm39) missense probably damaging 1.00
R8342:Vmn2r60 UTSW 7 41,790,494 (GRCm39) missense possibly damaging 0.63
R8362:Vmn2r60 UTSW 7 41,844,954 (GRCm39) missense probably damaging 1.00
R8418:Vmn2r60 UTSW 7 41,844,850 (GRCm39) missense probably damaging 0.97
R8848:Vmn2r60 UTSW 7 41,786,169 (GRCm39) missense probably damaging 1.00
R8860:Vmn2r60 UTSW 7 41,791,654 (GRCm39) missense probably damaging 0.99
R8882:Vmn2r60 UTSW 7 41,790,518 (GRCm39) missense probably benign 0.00
R8913:Vmn2r60 UTSW 7 41,785,778 (GRCm39) missense probably benign 0.27
R9190:Vmn2r60 UTSW 7 41,844,935 (GRCm39) missense probably damaging 0.99
R9229:Vmn2r60 UTSW 7 41,791,723 (GRCm39) missense possibly damaging 0.95
R9295:Vmn2r60 UTSW 7 41,785,955 (GRCm39) missense probably benign 0.01
R9335:Vmn2r60 UTSW 7 41,844,332 (GRCm39) missense probably damaging 1.00
R9796:Vmn2r60 UTSW 7 41,785,172 (GRCm39) missense probably benign
RF024:Vmn2r60 UTSW 7 41,790,363 (GRCm39) missense probably benign 0.01
X0023:Vmn2r60 UTSW 7 41,790,538 (GRCm39) missense probably benign 0.01
Posted On 2015-04-16