Incidental Mutation 'R6797:Vmn2r102'
ID 533075
Institutional Source Beutler Lab
Gene Symbol Vmn2r102
Ensembl Gene ENSMUSG00000095961
Gene Name vomeronasal 2, receptor 102
Synonyms EG224572
MMRRC Submission 044910-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6797 (G1)
Quality Score 225.009
Status Validated
Chromosome 17
Chromosomal Location 19880661-19915010 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to T at 19880694 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Stop codon at position 12 (Q12*)
Ref Sequence ENSEMBL: ENSMUSP00000126559 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000171741]
AlphaFold L7N279
Predicted Effect probably null
Transcript: ENSMUST00000171741
AA Change: Q12*
SMART Domains Protein: ENSMUSP00000126559
Gene: ENSMUSG00000095961
AA Change: Q12*

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
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.8%
  • 20x: 96.8%
Validation Efficiency 100% (42/42)
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akr1c18 T A 13: 4,195,276 (GRCm39) I61L probably benign Het
Angptl2 T C 2: 33,118,277 (GRCm39) V17A probably benign Het
Casp14 T C 10: 78,550,975 (GRCm39) D70G possibly damaging Het
Cckbr A G 7: 105,083,773 (GRCm39) M234V possibly damaging Het
Cd93 T C 2: 148,284,044 (GRCm39) N434S probably benign Het
Cenpe A T 3: 134,943,899 (GRCm39) Q938L possibly damaging Het
Col6a3 A C 1: 90,731,810 (GRCm39) V1481G probably damaging Het
Dnah5 G T 15: 28,233,384 (GRCm39) E248* probably null Het
Dnah5 G A 15: 28,451,609 (GRCm39) R4349Q probably damaging Het
F11 A G 8: 45,706,092 (GRCm39) Y98H probably benign Het
Fen1 A G 19: 10,178,067 (GRCm39) F126L probably benign Het
Gpr146 G A 5: 139,378,795 (GRCm39) G199D possibly damaging Het
Gramd1b A G 9: 40,219,702 (GRCm39) I324T probably benign Het
H2bc12 A T 13: 22,220,259 (GRCm39) N68I probably benign Het
Hivep1 C A 13: 42,310,557 (GRCm39) S932R probably benign Het
Hk3 A T 13: 55,158,644 (GRCm39) probably null Het
Hspbp1 T A 7: 4,663,781 (GRCm39) M355L possibly damaging Het
Jaml T C 9: 45,000,058 (GRCm39) C77R probably damaging Het
Kmt2e A G 5: 23,687,505 (GRCm39) N452D possibly damaging Het
Krt5 T C 15: 101,621,076 (GRCm39) Y57C unknown Het
Lipn A T 19: 34,058,160 (GRCm39) M294L probably benign Het
Magel2 A G 7: 62,029,907 (GRCm39) E937G unknown Het
Med13l G A 5: 118,897,329 (GRCm39) probably null Het
Mrgprb8 G A 7: 48,038,892 (GRCm39) V188I probably benign Het
Ocln T C 13: 100,676,223 (GRCm39) D90G probably damaging Het
Ofcc1 C T 13: 40,241,423 (GRCm39) R695Q possibly damaging Het
Or11h23 T A 14: 50,948,563 (GRCm39) Y259N probably damaging Het
Or52ab7 G A 7: 102,978,328 (GRCm39) V212I probably benign Het
Otogl G A 10: 107,612,978 (GRCm39) silent Het
Pak5 A T 2: 135,939,454 (GRCm39) H560Q probably damaging Het
Pigg T C 5: 108,480,694 (GRCm39) S493P probably damaging Het
Ppp6r3 A G 19: 3,564,719 (GRCm39) W185R probably damaging Het
Rnd2 C T 11: 101,359,825 (GRCm39) L57F probably damaging Het
Sacs T A 14: 61,450,522 (GRCm39) D4189E probably damaging Het
Serpinb9b A G 13: 33,213,467 (GRCm39) N8S possibly damaging Het
Slit3 A G 11: 35,524,779 (GRCm39) T730A possibly damaging Het
Srgap3 A T 6: 112,806,503 (GRCm39) F53I probably damaging Het
Stc2 T A 11: 31,315,351 (GRCm39) K163* probably null Het
Tasor2 T C 13: 3,626,769 (GRCm39) I1060M probably benign Het
Tlk1 T A 2: 70,568,770 (GRCm39) K411* probably null Het
Ttc27 G T 17: 75,036,883 (GRCm39) L185F probably benign Het
Vmn2r95 C T 17: 18,672,551 (GRCm39) probably benign Het
Vopp1 A G 6: 57,739,492 (GRCm39) Y19H possibly damaging Het
Wdr64 T A 1: 175,638,176 (GRCm39) probably null 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
IGL03028:Vmn2r102 APN 17 19,914,328 (GRCm39) missense possibly damaging 0.92
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
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
Predicted Primers PCR Primer
(F):5'- CCCAATGGCATTCTCAATCTCTTAG -3'
(R):5'- CCAAGTCATAAGAATTCTGAGTCTG -3'

Sequencing Primer
(F):5'- TGTACTGAGCACTGTTCT -3'
(R):5'- AATGTACTTACTGTATTCGATTGTCC -3'
Posted On 2018-08-29