Incidental Mutation 'IGL02554:Vmn2r69'
ID 298420
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r69
Ensembl Gene ENSMUSG00000091006
Gene Name vomeronasal 2, receptor 69
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.088) question?
Stock # IGL02554
Quality Score
Status
Chromosome 7
Chromosomal Location 85055584-85064884 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 85059014 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Proline to Serine at position 516 (P516S)
Ref Sequence ENSEMBL: ENSMUSP00000132726 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000171213]
AlphaFold G3XA45
Predicted Effect probably damaging
Transcript: ENSMUST00000171213
AA Change: P516S

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000132726
Gene: ENSMUSG00000091006
AA Change: P516S

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 77 465 1.3e-28 PFAM
Pfam:NCD3G 507 559 1.8e-20 PFAM
Pfam:7tm_3 592 827 3.2e-54 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207880
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9930111J21Rik1 T A 11: 48,838,830 (GRCm39) M586L probably damaging Het
Abcg3 T C 5: 105,117,318 (GRCm39) D204G possibly damaging Het
Acox3 C A 5: 35,765,710 (GRCm39) L588I probably damaging Het
Adamts9 G T 6: 92,857,828 (GRCm39) L849I probably benign Het
Alkbh3 T G 2: 93,826,692 (GRCm39) T170P probably damaging Het
Anks1b A T 10: 90,757,240 (GRCm39) H300L probably damaging Het
Arhgap29 T C 3: 121,786,173 (GRCm39) probably benign Het
Brd8dc A G 18: 34,726,068 (GRCm39) S112P probably benign Het
Cd86 C T 16: 36,438,847 (GRCm39) G181D probably benign Het
Cep68 A T 11: 20,190,096 (GRCm39) H305Q possibly damaging Het
Cimip4 A G 15: 78,262,736 (GRCm39) M245T possibly damaging Het
Clptm1l A T 13: 73,755,879 (GRCm39) D165V probably benign Het
Dctn1 T C 6: 83,159,704 (GRCm39) Y61H probably damaging Het
Dnah7a A T 1: 53,657,205 (GRCm39) M857K possibly damaging Het
Gpr158 A G 2: 21,831,407 (GRCm39) M836V probably benign Het
Gria1 G T 11: 57,180,314 (GRCm39) A755S possibly damaging Het
Helb G A 10: 119,925,617 (GRCm39) T920M probably damaging Het
Hr T C 14: 70,797,306 (GRCm39) probably benign Het
Igf2bp1 A G 11: 95,864,994 (GRCm39) S152P probably damaging Het
Iqsec1 T C 6: 90,646,327 (GRCm39) Y784C probably damaging Het
Ldah T A 12: 8,333,935 (GRCm39) C275* probably null Het
Lpin3 T C 2: 160,738,707 (GRCm39) S220P probably damaging Het
Med23 T C 10: 24,774,473 (GRCm39) probably null Het
Mllt1 T C 17: 57,206,806 (GRCm39) D346G probably benign Het
Myef2 A C 2: 124,942,345 (GRCm39) probably null Het
Myh2 A G 11: 67,079,991 (GRCm39) S1095G probably benign Het
Nav1 A G 1: 135,512,651 (GRCm39) silent Het
Or10a3m A G 7: 108,312,949 (GRCm39) M118V possibly damaging Het
Piwil2 G A 14: 70,628,935 (GRCm39) probably benign Het
Pkhd1l1 T A 15: 44,441,896 (GRCm39) F3612I probably damaging Het
Ror2 C T 13: 53,264,764 (GRCm39) S764N probably damaging Het
S100pbp A T 4: 129,075,644 (GRCm39) probably null Het
Scnn1b T C 7: 121,516,746 (GRCm39) I495T probably damaging Het
Sgo2b A C 8: 64,379,571 (GRCm39) V1087G probably damaging Het
Sil1 A T 18: 35,481,786 (GRCm39) V91E probably damaging Het
Slc5a4b A G 10: 75,946,685 (GRCm39) I29T possibly damaging Het
Spink5 A T 18: 44,148,661 (GRCm39) N908I probably benign Het
Svopl A C 6: 37,993,978 (GRCm39) I351S probably damaging Het
Syngr3 A G 17: 24,905,302 (GRCm39) V198A probably benign Het
Tbck C A 3: 132,456,953 (GRCm39) Y622* probably null Het
Tkt T A 14: 30,280,737 (GRCm39) M56K probably damaging Het
Trip10 T C 17: 57,570,135 (GRCm39) V544A probably damaging Het
Txndc16 T C 14: 45,409,995 (GRCm39) E195G probably damaging Het
Vmn2r74 T C 7: 85,606,581 (GRCm39) N255S probably benign Het
Xpo4 T C 14: 57,827,545 (GRCm39) T884A probably benign Het
Zdhhc2 A G 8: 40,915,155 (GRCm39) N167S probably damaging Het
Other mutations in Vmn2r69
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01019:Vmn2r69 APN 7 85,055,739 (GRCm39) missense probably benign
IGL01457:Vmn2r69 APN 7 85,055,836 (GRCm39) missense possibly damaging 0.87
IGL01760:Vmn2r69 APN 7 85,056,072 (GRCm39) missense possibly damaging 0.90
IGL01834:Vmn2r69 APN 7 85,061,576 (GRCm39) missense probably damaging 1.00
IGL02001:Vmn2r69 APN 7 85,056,434 (GRCm39) missense probably benign 0.05
IGL02057:Vmn2r69 APN 7 85,060,990 (GRCm39) missense possibly damaging 0.93
IGL02289:Vmn2r69 APN 7 85,056,054 (GRCm39) missense probably damaging 1.00
IGL02472:Vmn2r69 APN 7 85,058,960 (GRCm39) missense probably benign 0.01
IGL02478:Vmn2r69 APN 7 85,055,889 (GRCm39) missense probably damaging 1.00
IGL02723:Vmn2r69 APN 7 85,059,416 (GRCm39) missense probably damaging 1.00
R0526:Vmn2r69 UTSW 7 85,060,711 (GRCm39) missense probably damaging 1.00
R0560:Vmn2r69 UTSW 7 85,058,922 (GRCm39) critical splice donor site probably null
R0909:Vmn2r69 UTSW 7 85,055,873 (GRCm39) missense probably benign 0.00
R0976:Vmn2r69 UTSW 7 85,056,108 (GRCm39) missense probably damaging 1.00
R1158:Vmn2r69 UTSW 7 85,059,058 (GRCm39) splice site probably benign
R1459:Vmn2r69 UTSW 7 85,055,908 (GRCm39) nonsense probably null
R1482:Vmn2r69 UTSW 7 85,056,082 (GRCm39) missense probably damaging 1.00
R1917:Vmn2r69 UTSW 7 85,060,891 (GRCm39) missense probably damaging 1.00
R2016:Vmn2r69 UTSW 7 85,056,493 (GRCm39) missense probably damaging 0.98
R2108:Vmn2r69 UTSW 7 85,059,404 (GRCm39) missense probably benign
R2571:Vmn2r69 UTSW 7 85,064,764 (GRCm39) missense probably benign
R2910:Vmn2r69 UTSW 7 85,055,918 (GRCm39) missense probably damaging 1.00
R2920:Vmn2r69 UTSW 7 85,060,973 (GRCm39) missense probably benign 0.08
R3708:Vmn2r69 UTSW 7 85,061,029 (GRCm39) missense probably damaging 0.98
R3710:Vmn2r69 UTSW 7 85,055,601 (GRCm39) missense probably benign
R4757:Vmn2r69 UTSW 7 85,061,575 (GRCm39) missense probably damaging 0.99
R4823:Vmn2r69 UTSW 7 85,060,508 (GRCm39) missense probably benign 0.21
R4870:Vmn2r69 UTSW 7 85,060,793 (GRCm39) missense possibly damaging 0.93
R4918:Vmn2r69 UTSW 7 85,055,967 (GRCm39) missense probably benign 0.06
R5022:Vmn2r69 UTSW 7 85,060,367 (GRCm39) missense possibly damaging 0.72
R5174:Vmn2r69 UTSW 7 85,064,739 (GRCm39) missense possibly damaging 0.92
R5200:Vmn2r69 UTSW 7 85,055,717 (GRCm39) missense probably damaging 1.00
R5278:Vmn2r69 UTSW 7 85,060,991 (GRCm39) missense probably benign 0.02
R5643:Vmn2r69 UTSW 7 85,056,404 (GRCm39) missense probably damaging 0.98
R5996:Vmn2r69 UTSW 7 85,061,117 (GRCm39) splice site probably null
R6083:Vmn2r69 UTSW 7 85,055,711 (GRCm39) missense probably damaging 1.00
R6140:Vmn2r69 UTSW 7 85,060,657 (GRCm39) missense probably damaging 0.99
R6306:Vmn2r69 UTSW 7 85,064,799 (GRCm39) missense probably benign 0.04
R6330:Vmn2r69 UTSW 7 85,060,835 (GRCm39) missense probably benign
R6380:Vmn2r69 UTSW 7 85,061,067 (GRCm39) missense probably benign
R6466:Vmn2r69 UTSW 7 85,056,378 (GRCm39) missense probably benign 0.01
R6542:Vmn2r69 UTSW 7 85,060,413 (GRCm39) nonsense probably null
R6583:Vmn2r69 UTSW 7 85,059,017 (GRCm39) missense probably benign
R6623:Vmn2r69 UTSW 7 85,056,309 (GRCm39) missense possibly damaging 0.84
R6709:Vmn2r69 UTSW 7 85,061,069 (GRCm39) missense probably benign 0.03
R6732:Vmn2r69 UTSW 7 85,060,351 (GRCm39) missense probably benign 0.00
R6741:Vmn2r69 UTSW 7 85,061,724 (GRCm39) missense probably benign 0.01
R7070:Vmn2r69 UTSW 7 85,060,688 (GRCm39) missense probably damaging 0.98
R7234:Vmn2r69 UTSW 7 85,056,315 (GRCm39) missense probably benign 0.22
R7323:Vmn2r69 UTSW 7 85,060,972 (GRCm39) missense possibly damaging 0.95
R7427:Vmn2r69 UTSW 7 85,060,467 (GRCm39) missense probably benign 0.28
R7428:Vmn2r69 UTSW 7 85,060,467 (GRCm39) missense probably benign 0.28
R7453:Vmn2r69 UTSW 7 85,060,768 (GRCm39) frame shift probably null
R7532:Vmn2r69 UTSW 7 85,059,622 (GRCm39) missense probably benign 0.36
R7556:Vmn2r69 UTSW 7 85,060,768 (GRCm39) frame shift probably null
R7562:Vmn2r69 UTSW 7 85,056,420 (GRCm39) missense probably benign
R7592:Vmn2r69 UTSW 7 85,060,768 (GRCm39) frame shift probably null
R7708:Vmn2r69 UTSW 7 85,061,755 (GRCm39) missense possibly damaging 0.87
R7803:Vmn2r69 UTSW 7 85,056,324 (GRCm39) missense probably benign 0.00
R7960:Vmn2r69 UTSW 7 85,055,973 (GRCm39) missense probably benign
R7966:Vmn2r69 UTSW 7 85,060,762 (GRCm39) missense possibly damaging 0.81
R8071:Vmn2r69 UTSW 7 85,055,713 (GRCm39) nonsense probably null
R8237:Vmn2r69 UTSW 7 85,060,340 (GRCm39) missense probably benign 0.02
R8347:Vmn2r69 UTSW 7 85,064,838 (GRCm39) missense probably benign 0.00
R8737:Vmn2r69 UTSW 7 85,055,783 (GRCm39) missense probably damaging 1.00
R8795:Vmn2r69 UTSW 7 85,064,883 (GRCm39) start codon destroyed probably null 0.94
R8831:Vmn2r69 UTSW 7 85,059,018 (GRCm39) nonsense probably null
R8856:Vmn2r69 UTSW 7 85,061,663 (GRCm39) missense probably benign 0.00
R8998:Vmn2r69 UTSW 7 85,060,307 (GRCm39) missense probably benign 0.33
R8999:Vmn2r69 UTSW 7 85,060,307 (GRCm39) missense probably benign 0.33
R9161:Vmn2r69 UTSW 7 85,056,177 (GRCm39) missense possibly damaging 0.88
R9228:Vmn2r69 UTSW 7 85,064,697 (GRCm39) missense probably benign 0.01
R9494:Vmn2r69 UTSW 7 85,060,768 (GRCm39) missense probably damaging 1.00
R9494:Vmn2r69 UTSW 7 85,056,084 (GRCm39) missense probably benign 0.08
R9541:Vmn2r69 UTSW 7 85,056,209 (GRCm39) missense probably benign
R9620:Vmn2r69 UTSW 7 85,061,504 (GRCm39) missense probably benign 0.10
Z1176:Vmn2r69 UTSW 7 85,055,696 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16