Incidental Mutation 'IGL03028:Vmn2r102'
ID 408260
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r102
Ensembl Gene ENSMUSG00000095961
Gene Name vomeronasal 2, receptor 102
Synonyms EG224572
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL03028
Quality Score
Status
Chromosome 17
Chromosomal Location 19880661-19915010 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 19914328 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Serine at position 631 (F631S)
Ref Sequence ENSEMBL: ENSMUSP00000126559 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000171741]
AlphaFold L7N279
Predicted Effect possibly damaging
Transcript: ENSMUST00000171741
AA Change: F631S

PolyPhen 2 Score 0.922 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000126559
Gene: ENSMUSG00000095961
AA Change: F631S

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:ANF_receptor 82 448 5.2e-38 PFAM
Pfam:NCD3G 509 562 1.1e-21 PFAM
Pfam:7tm_3 595 830 1.8e-53 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acat1 A C 9: 53,506,062 (GRCm39) V86G probably benign Het
Adgra3 A T 5: 50,174,194 (GRCm39) W115R probably benign Het
Ahr G A 12: 35,554,709 (GRCm39) A470V probably benign Het
Aoah A T 13: 21,000,752 (GRCm39) Q62L possibly damaging Het
Arhgef12 A T 9: 42,937,524 (GRCm39) D100E possibly damaging Het
Asic1 A G 15: 99,570,038 (GRCm39) N120D probably benign Het
Atp2b2 A G 6: 113,736,103 (GRCm39) L988P probably damaging Het
Atxn2 T A 5: 121,948,972 (GRCm39) H789Q probably damaging Het
Clk1 G T 1: 58,460,261 (GRCm39) S123* probably null Het
Col10a1 C T 10: 34,271,012 (GRCm39) A328V probably benign Het
Col26a1 G T 5: 136,771,972 (GRCm39) D415E possibly damaging Het
Ctla2a A G 13: 61,083,273 (GRCm39) probably benign Het
Cwf19l2 A G 9: 3,430,622 (GRCm39) E318G probably benign Het
Dnajc16 C T 4: 141,495,043 (GRCm39) W523* probably null Het
Ehhadh T C 16: 21,581,144 (GRCm39) E616G probably damaging Het
F5 A T 1: 164,020,569 (GRCm39) K1015* probably null Het
Fam78a A G 2: 31,972,894 (GRCm39) W9R possibly damaging Het
Frs2 A T 10: 116,909,838 (GRCm39) M508K possibly damaging Het
Gm3164 A T 14: 4,440,111 (GRCm38) M200L probably benign Het
Gm44511 T C 6: 128,757,358 (GRCm39) S179G probably damaging Het
Gpr25 G A 1: 136,188,550 (GRCm39) S21L probably benign Het
Hsdl2 A G 4: 59,594,471 (GRCm39) D34G probably damaging Het
Kcnt1 A G 2: 25,799,215 (GRCm39) probably null Het
Kl A G 5: 150,915,015 (GRCm39) Y914C probably damaging Het
Map3k3 T G 11: 106,001,577 (GRCm39) V45G probably damaging Het
Mppe1 A C 18: 67,360,755 (GRCm39) C261W probably damaging Het
Nin T C 12: 70,082,044 (GRCm39) T1640A probably benign Het
Or51a8 T A 7: 102,550,036 (GRCm39) I154N possibly damaging Het
Or51ac3 A G 7: 103,213,796 (GRCm39) probably null Het
Or5c1 C T 2: 37,221,968 (GRCm39) L70F probably damaging Het
Or5p59 T A 7: 107,703,380 (GRCm39) M288K probably damaging Het
Or7g26 A T 9: 19,230,664 (GRCm39) Y284F probably damaging Het
Oxr1 A G 15: 41,680,559 (GRCm39) N166D probably damaging Het
Pank4 T A 4: 155,054,442 (GRCm39) probably benign Het
Pgd A G 4: 149,246,084 (GRCm39) probably null Het
Pitrm1 C T 13: 6,624,429 (GRCm39) H831Y probably benign Het
Pkd1l2 G A 8: 117,792,484 (GRCm39) T436I probably benign Het
Rad51 A C 2: 118,946,795 (GRCm39) M1L possibly damaging Het
Recql5 G T 11: 115,785,257 (GRCm39) S746R possibly damaging Het
Rhbdl3 C T 11: 80,214,287 (GRCm39) Q133* probably null Het
Rpp40 A T 13: 36,088,494 (GRCm39) L59Q probably damaging Het
Rtca C A 3: 116,286,741 (GRCm39) probably benign Het
Rtkn C T 6: 83,124,853 (GRCm39) Q108* probably null Het
Shoc1 A C 4: 59,094,274 (GRCm39) I150S possibly damaging Het
Sirt6 C T 10: 81,463,375 (GRCm39) probably benign Het
Slc9a4 G A 1: 40,649,537 (GRCm39) V517M probably benign Het
Smarca2 G T 19: 26,655,712 (GRCm39) probably benign Het
Snx33 A T 9: 56,833,735 (GRCm39) D111E probably benign Het
Tgfb1 T C 7: 25,403,621 (GRCm39) I311T probably damaging Het
Tgfb2 C T 1: 186,362,806 (GRCm39) probably null Het
Tmem232 T C 17: 65,563,384 (GRCm39) T670A probably benign Het
Tnfsf4 T C 1: 161,223,213 (GRCm39) F21L possibly damaging Het
Ubr5 T C 15: 38,047,837 (GRCm39) T47A probably benign Het
Unc79 T C 12: 103,139,785 (GRCm39) V2515A possibly damaging Het
Utp6 T C 11: 79,844,450 (GRCm39) K192E probably damaging Het
Zfp516 A C 18: 82,974,038 (GRCm39) I79L possibly damaging Het
Other mutations in Vmn2r102
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00944:Vmn2r102 APN 17 19,899,154 (GRCm39) missense probably damaging 1.00
IGL00974:Vmn2r102 APN 17 19,897,771 (GRCm39) missense possibly damaging 0.93
IGL00978:Vmn2r102 APN 17 19,899,185 (GRCm39) splice site probably null
IGL01589:Vmn2r102 APN 17 19,899,066 (GRCm39) missense probably benign
IGL01738:Vmn2r102 APN 17 19,898,020 (GRCm39) missense probably damaging 1.00
IGL01994:Vmn2r102 APN 17 19,880,731 (GRCm39) missense probably benign 0.00
IGL02066:Vmn2r102 APN 17 19,914,191 (GRCm39) missense probably benign 0.01
IGL02525:Vmn2r102 APN 17 19,901,447 (GRCm39) missense probably benign
IGL02589:Vmn2r102 APN 17 19,901,480 (GRCm39) missense probably damaging 1.00
IGL02814:Vmn2r102 APN 17 19,898,170 (GRCm39) missense probably damaging 1.00
IGL03162:Vmn2r102 APN 17 19,914,286 (GRCm39) missense probably damaging 1.00
PIT4431001:Vmn2r102 UTSW 17 19,896,958 (GRCm39) missense possibly damaging 0.68
R0042:Vmn2r102 UTSW 17 19,880,851 (GRCm39) missense probably damaging 0.98
R0131:Vmn2r102 UTSW 17 19,899,025 (GRCm39) missense probably benign 0.42
R0131:Vmn2r102 UTSW 17 19,899,025 (GRCm39) missense probably benign 0.42
R0132:Vmn2r102 UTSW 17 19,899,025 (GRCm39) missense probably benign 0.42
R0268:Vmn2r102 UTSW 17 19,898,112 (GRCm39) missense probably benign 0.00
R0441:Vmn2r102 UTSW 17 19,914,630 (GRCm39) missense probably damaging 1.00
R0583:Vmn2r102 UTSW 17 19,897,043 (GRCm39) missense probably benign 0.01
R0600:Vmn2r102 UTSW 17 19,898,277 (GRCm39) missense probably benign 0.00
R0606:Vmn2r102 UTSW 17 19,899,106 (GRCm39) missense possibly damaging 0.93
R0674:Vmn2r102 UTSW 17 19,898,129 (GRCm39) missense probably benign 0.00
R0709:Vmn2r102 UTSW 17 19,897,881 (GRCm39) missense probably benign 0.01
R0879:Vmn2r102 UTSW 17 19,914,454 (GRCm39) missense probably damaging 1.00
R1349:Vmn2r102 UTSW 17 19,880,887 (GRCm39) splice site probably benign
R1473:Vmn2r102 UTSW 17 19,914,843 (GRCm39) missense probably benign 0.00
R1630:Vmn2r102 UTSW 17 19,899,032 (GRCm39) missense possibly damaging 0.60
R1727:Vmn2r102 UTSW 17 19,897,770 (GRCm39) missense probably damaging 0.99
R1759:Vmn2r102 UTSW 17 19,914,755 (GRCm39) missense probably damaging 1.00
R1809:Vmn2r102 UTSW 17 19,897,881 (GRCm39) missense probably benign 0.01
R2013:Vmn2r102 UTSW 17 19,897,006 (GRCm39) missense probably benign 0.03
R2086:Vmn2r102 UTSW 17 19,896,949 (GRCm39) missense probably damaging 1.00
R2241:Vmn2r102 UTSW 17 19,897,003 (GRCm39) missense probably benign 0.00
R2378:Vmn2r102 UTSW 17 19,914,930 (GRCm39) missense probably damaging 1.00
R3814:Vmn2r102 UTSW 17 19,899,093 (GRCm39) missense probably damaging 0.98
R3827:Vmn2r102 UTSW 17 19,914,787 (GRCm39) missense probably damaging 1.00
R4159:Vmn2r102 UTSW 17 19,898,088 (GRCm39) missense probably damaging 1.00
R4505:Vmn2r102 UTSW 17 19,880,845 (GRCm39) missense probably benign 0.00
R4515:Vmn2r102 UTSW 17 19,901,475 (GRCm39) missense probably damaging 1.00
R4517:Vmn2r102 UTSW 17 19,901,475 (GRCm39) missense probably damaging 1.00
R4534:Vmn2r102 UTSW 17 19,914,975 (GRCm39) missense probably benign
R4535:Vmn2r102 UTSW 17 19,914,975 (GRCm39) missense probably benign
R4662:Vmn2r102 UTSW 17 19,901,424 (GRCm39) missense probably damaging 1.00
R4708:Vmn2r102 UTSW 17 19,914,576 (GRCm39) missense probably benign 0.00
R4734:Vmn2r102 UTSW 17 19,897,795 (GRCm39) missense probably damaging 1.00
R4834:Vmn2r102 UTSW 17 19,898,203 (GRCm39) missense probably damaging 0.99
R4927:Vmn2r102 UTSW 17 19,880,661 (GRCm39) start codon destroyed probably benign 0.00
R5077:Vmn2r102 UTSW 17 19,897,834 (GRCm39) missense probably benign 0.20
R5181:Vmn2r102 UTSW 17 19,897,003 (GRCm39) missense probably benign 0.00
R5277:Vmn2r102 UTSW 17 19,914,393 (GRCm39) missense possibly damaging 0.49
R5418:Vmn2r102 UTSW 17 19,914,415 (GRCm39) missense probably damaging 1.00
R5810:Vmn2r102 UTSW 17 19,897,804 (GRCm39) missense probably benign 0.20
R5864:Vmn2r102 UTSW 17 19,914,943 (GRCm39) missense possibly damaging 0.55
R6168:Vmn2r102 UTSW 17 19,914,402 (GRCm39) missense possibly damaging 0.83
R6266:Vmn2r102 UTSW 17 19,899,007 (GRCm39) missense probably benign
R6432:Vmn2r102 UTSW 17 19,901,483 (GRCm39) missense possibly damaging 0.61
R6487:Vmn2r102 UTSW 17 19,898,169 (GRCm39) missense probably damaging 1.00
R6597:Vmn2r102 UTSW 17 19,914,450 (GRCm39) missense probably damaging 0.99
R6797:Vmn2r102 UTSW 17 19,880,694 (GRCm39) nonsense probably null
R7009:Vmn2r102 UTSW 17 19,914,456 (GRCm39) missense probably damaging 0.99
R7098:Vmn2r102 UTSW 17 19,914,670 (GRCm39) missense probably damaging 1.00
R7134:Vmn2r102 UTSW 17 19,897,749 (GRCm39) missense probably benign 0.01
R7463:Vmn2r102 UTSW 17 19,896,886 (GRCm39) missense probably damaging 1.00
R7511:Vmn2r102 UTSW 17 19,901,405 (GRCm39) missense probably damaging 1.00
R7512:Vmn2r102 UTSW 17 19,914,363 (GRCm39) missense probably damaging 1.00
R7556:Vmn2r102 UTSW 17 19,898,093 (GRCm39) missense probably benign
R8126:Vmn2r102 UTSW 17 19,880,712 (GRCm39) missense probably benign 0.02
R8385:Vmn2r102 UTSW 17 19,914,088 (GRCm39) missense possibly damaging 0.89
R8410:Vmn2r102 UTSW 17 19,898,196 (GRCm39) missense possibly damaging 0.85
R9045:Vmn2r102 UTSW 17 19,880,841 (GRCm39) missense probably benign 0.00
R9267:Vmn2r102 UTSW 17 19,896,928 (GRCm39) missense probably damaging 1.00
R9325:Vmn2r102 UTSW 17 19,897,558 (GRCm39) missense probably damaging 1.00
R9363:Vmn2r102 UTSW 17 19,897,614 (GRCm39) missense probably benign 0.04
R9524:Vmn2r102 UTSW 17 19,897,564 (GRCm39) missense possibly damaging 0.74
R9747:Vmn2r102 UTSW 17 19,898,129 (GRCm39) missense probably benign 0.00
Z1176:Vmn2r102 UTSW 17 19,914,305 (GRCm39) nonsense probably null
Posted On 2016-08-02