Incidental Mutation 'R0455:Vmn2r107'
ID 39982
Institutional Source Beutler Lab
Gene Symbol Vmn2r107
Ensembl Gene ENSMUSG00000056910
Gene Name vomeronasal 2, receptor 107
Synonyms V2r6
MMRRC Submission 038655-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.117) question?
Stock # R0455 (G1)
Quality Score 194
Status Validated
Chromosome 17
Chromosomal Location 20565687-20596034 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 20595085 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000048706 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042090]
AlphaFold E9PZJ7
Predicted Effect probably benign
Transcript: ENSMUST00000042090
SMART Domains Protein: ENSMUSP00000048706
Gene: ENSMUSG00000056910

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:ANF_receptor 83 466 3.6e-40 PFAM
Pfam:NCD3G 509 562 5.1e-21 PFAM
Pfam:7tm_3 593 830 8e-51 PFAM
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.1%
  • 10x: 95.7%
  • 20x: 90.8%
Validation Efficiency 100% (56/56)
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921539E11Rik C T 4: 103,088,180 (GRCm39) G342D possibly damaging Het
Acvr2b C T 9: 119,261,675 (GRCm39) R399W probably damaging Het
Arb2a T A 13: 77,982,832 (GRCm39) probably benign Het
Atf6 A G 1: 170,662,492 (GRCm39) V256A probably benign Het
Atp2b4 A T 1: 133,656,454 (GRCm39) I732N probably damaging Het
C1qtnf9 A C 14: 61,009,820 (GRCm39) Q25H probably damaging Het
Ccdc6 T A 10: 69,978,401 (GRCm39) probably benign Het
Cds2 T C 2: 132,127,887 (GRCm39) probably null Het
Chdh A G 14: 29,756,603 (GRCm39) Y343C probably damaging Het
Col5a2 T C 1: 45,421,262 (GRCm39) probably benign Het
Cts3 G A 13: 61,716,024 (GRCm39) probably benign Het
Cyfip1 T A 7: 55,541,802 (GRCm39) D362E probably benign Het
Dsg1b T A 18: 20,529,082 (GRCm39) S273T probably benign Het
Dysf A T 6: 84,117,649 (GRCm39) H1274L probably benign Het
Eva1c T C 16: 90,672,986 (GRCm39) S187P probably benign Het
Fam13b G A 18: 34,578,581 (GRCm39) probably benign Het
Fbn2 C T 18: 58,168,408 (GRCm39) G2310S probably damaging Het
Fcna T C 2: 25,515,520 (GRCm39) Y183C probably damaging Het
Fnta T C 8: 26,491,056 (GRCm39) T263A probably benign Het
Gm94 T C 18: 43,914,309 (GRCm39) D83G possibly damaging Het
Gnal C T 18: 67,268,720 (GRCm39) probably benign Het
Grb7 T G 11: 98,343,014 (GRCm39) S244A probably benign Het
Grm3 T C 5: 9,562,477 (GRCm39) T458A probably benign Het
Hdac2 C T 10: 36,867,832 (GRCm39) R193C probably damaging Het
Hycc2 T C 1: 58,573,638 (GRCm39) probably benign Het
Ighmbp2 T C 19: 3,315,072 (GRCm39) R783G probably benign Het
Inpp5j G T 11: 3,453,122 (GRCm39) L43I possibly damaging Het
Itga11 A T 9: 62,604,243 (GRCm39) T44S probably damaging Het
Itsn1 C T 16: 91,665,036 (GRCm39) probably benign Het
Kdm6b G T 11: 69,297,822 (GRCm39) C233* probably null Het
Lamb3 T C 1: 193,025,700 (GRCm39) L1130P probably damaging Het
Lrch3 T C 16: 32,807,250 (GRCm39) F508L probably damaging Het
Lrrd1 T A 5: 3,916,425 (GRCm39) V814E probably benign Het
Megf10 C T 18: 57,386,054 (GRCm39) P356S probably benign Het
Myorg G A 4: 41,499,538 (GRCm39) R31* probably null Het
Naip1 A T 13: 100,559,727 (GRCm39) D1092E probably benign Het
Nus1 T A 10: 52,306,190 (GRCm39) V42E probably damaging Het
Or11g24 A G 14: 50,662,359 (GRCm39) I128V possibly damaging Het
Or2a51 A C 6: 43,179,006 (GRCm39) M143L probably benign Het
Padi3 T C 4: 140,523,024 (GRCm39) N306S probably damaging Het
Pex13 T C 11: 23,605,949 (GRCm39) S94G probably benign Het
Ppm1h G T 10: 122,638,229 (GRCm39) Q166H probably benign Het
Ptafr A T 4: 132,307,396 (GRCm39) Y262F probably benign Het
Rabgap1 T A 2: 37,377,132 (GRCm39) D321E probably damaging Het
Samsn1 C T 16: 75,742,113 (GRCm39) noncoding transcript Het
Scarb1 T C 5: 125,366,745 (GRCm39) N63D probably damaging Het
Serpinb7 T C 1: 107,379,340 (GRCm39) I249T possibly damaging Het
Srpra A G 9: 35,126,277 (GRCm39) K490R probably benign Het
Sycn A G 7: 28,240,398 (GRCm39) N22D probably benign Het
Tarbp1 C T 8: 127,167,612 (GRCm39) A1067T probably benign Het
Tex14 A G 11: 87,405,131 (GRCm39) D681G possibly damaging Het
Usp34 C T 11: 23,396,741 (GRCm39) probably benign Het
Vwde A T 6: 13,187,528 (GRCm39) M653K probably benign Het
Wrap73 T A 4: 154,233,200 (GRCm39) S125T possibly damaging Het
Other mutations in Vmn2r107
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01402:Vmn2r107 APN 17 20,596,009 (GRCm39) missense probably damaging 0.98
IGL01768:Vmn2r107 APN 17 20,565,868 (GRCm39) missense probably benign 0.32
IGL02086:Vmn2r107 APN 17 20,578,062 (GRCm39) missense probably benign 0.00
IGL02136:Vmn2r107 APN 17 20,595,168 (GRCm39) missense probably benign 0.02
IGL02266:Vmn2r107 APN 17 20,577,039 (GRCm39) missense probably damaging 1.00
IGL02285:Vmn2r107 APN 17 20,595,823 (GRCm39) missense probably damaging 1.00
IGL02724:Vmn2r107 APN 17 20,577,006 (GRCm39) missense possibly damaging 0.49
IGL02998:Vmn2r107 APN 17 20,578,017 (GRCm39) missense probably damaging 0.99
IGL03089:Vmn2r107 APN 17 20,595,974 (GRCm39) missense probably benign 0.05
IGL03284:Vmn2r107 APN 17 20,577,173 (GRCm39) missense probably benign 0.07
IGL03307:Vmn2r107 APN 17 20,577,038 (GRCm39) missense probably benign 0.09
IGL03399:Vmn2r107 APN 17 20,578,220 (GRCm39) splice site probably benign
3-1:Vmn2r107 UTSW 17 20,565,766 (GRCm39) missense probably benign
BB006:Vmn2r107 UTSW 17 20,565,706 (GRCm39) missense probably null 0.96
BB016:Vmn2r107 UTSW 17 20,565,706 (GRCm39) missense probably null 0.96
R0285:Vmn2r107 UTSW 17 20,565,873 (GRCm39) missense probably benign 0.00
R0497:Vmn2r107 UTSW 17 20,595,394 (GRCm39) missense probably damaging 1.00
R0506:Vmn2r107 UTSW 17 20,578,021 (GRCm39) missense probably benign
R0621:Vmn2r107 UTSW 17 20,595,252 (GRCm39) missense probably benign 0.01
R0667:Vmn2r107 UTSW 17 20,575,916 (GRCm39) missense possibly damaging 0.91
R1118:Vmn2r107 UTSW 17 20,576,860 (GRCm39) missense probably benign 0.03
R1204:Vmn2r107 UTSW 17 20,578,031 (GRCm39) missense probably benign
R1237:Vmn2r107 UTSW 17 20,576,947 (GRCm39) nonsense probably null
R1485:Vmn2r107 UTSW 17 20,595,109 (GRCm39) missense possibly damaging 0.95
R1783:Vmn2r107 UTSW 17 20,576,775 (GRCm39) missense possibly damaging 0.51
R1873:Vmn2r107 UTSW 17 20,565,840 (GRCm39) missense probably benign 0.10
R1974:Vmn2r107 UTSW 17 20,575,879 (GRCm39) splice site probably null
R2009:Vmn2r107 UTSW 17 20,595,729 (GRCm39) missense probably benign 0.01
R2029:Vmn2r107 UTSW 17 20,595,549 (GRCm39) missense probably benign 0.01
R2164:Vmn2r107 UTSW 17 20,595,904 (GRCm39) missense probably damaging 1.00
R2269:Vmn2r107 UTSW 17 20,595,817 (GRCm39) missense possibly damaging 0.58
R3087:Vmn2r107 UTSW 17 20,580,607 (GRCm39) missense probably benign 0.03
R3740:Vmn2r107 UTSW 17 20,595,151 (GRCm39) missense probably benign 0.00
R3961:Vmn2r107 UTSW 17 20,595,717 (GRCm39) missense probably damaging 1.00
R4031:Vmn2r107 UTSW 17 20,595,483 (GRCm39) missense probably benign 0.00
R4270:Vmn2r107 UTSW 17 20,576,041 (GRCm39) missense probably benign
R4963:Vmn2r107 UTSW 17 20,595,403 (GRCm39) missense probably damaging 1.00
R5121:Vmn2r107 UTSW 17 20,576,015 (GRCm39) missense probably benign 0.01
R5640:Vmn2r107 UTSW 17 20,595,426 (GRCm39) missense probably damaging 1.00
R6007:Vmn2r107 UTSW 17 20,595,316 (GRCm39) missense probably benign 0.19
R6238:Vmn2r107 UTSW 17 20,565,849 (GRCm39) missense probably benign 0.43
R6298:Vmn2r107 UTSW 17 20,576,044 (GRCm39) missense probably benign 0.00
R6467:Vmn2r107 UTSW 17 20,595,939 (GRCm39) missense probably damaging 0.99
R6726:Vmn2r107 UTSW 17 20,595,637 (GRCm39) missense probably damaging 0.96
R6782:Vmn2r107 UTSW 17 20,577,141 (GRCm39) missense probably damaging 1.00
R7299:Vmn2r107 UTSW 17 20,565,878 (GRCm39) missense probably benign 0.01
R7301:Vmn2r107 UTSW 17 20,565,878 (GRCm39) missense probably benign 0.01
R7375:Vmn2r107 UTSW 17 20,576,138 (GRCm39) missense probably benign
R7448:Vmn2r107 UTSW 17 20,595,994 (GRCm39) missense probably benign 0.00
R7495:Vmn2r107 UTSW 17 20,595,271 (GRCm39) missense possibly damaging 0.71
R7589:Vmn2r107 UTSW 17 20,595,634 (GRCm39) missense probably benign 0.05
R7594:Vmn2r107 UTSW 17 20,580,635 (GRCm39) missense probably benign 0.03
R7678:Vmn2r107 UTSW 17 20,576,901 (GRCm39) missense probably benign 0.01
R7929:Vmn2r107 UTSW 17 20,565,706 (GRCm39) missense probably null 0.96
R7974:Vmn2r107 UTSW 17 20,577,270 (GRCm39) missense probably benign 0.00
R8040:Vmn2r107 UTSW 17 20,595,808 (GRCm39) missense probably damaging 1.00
R8263:Vmn2r107 UTSW 17 20,580,614 (GRCm39) missense probably damaging 1.00
R8426:Vmn2r107 UTSW 17 20,577,239 (GRCm39) missense possibly damaging 0.91
R9175:Vmn2r107 UTSW 17 20,577,051 (GRCm39) missense possibly damaging 0.79
R9537:Vmn2r107 UTSW 17 20,595,149 (GRCm39) missense probably benign 0.00
R9642:Vmn2r107 UTSW 17 20,580,661 (GRCm39) missense probably damaging 1.00
R9711:Vmn2r107 UTSW 17 20,577,262 (GRCm39) missense probably damaging 1.00
X0022:Vmn2r107 UTSW 17 20,577,230 (GRCm39) missense possibly damaging 0.85
Predicted Primers
Posted On 2013-05-23