Incidental Mutation 'R0785:Vmn2r125'
ID 76812
Institutional Source Beutler Lab
Gene Symbol Vmn2r125
Ensembl Gene ENSMUSG00000096042
Gene Name vomeronasal 2, receptor 125
Synonyms Gm20782
MMRRC Submission 038965-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.078) question?
Stock # R0785 (G1)
Quality Score 109
Status Not validated
Chromosome 4
Chromosomal Location 156696567-156708037 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 156703396 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Aspartic acid at position 258 (A258D)
Ref Sequence ENSEMBL: ENSMUSP00000094556 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000096794]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000096794
AA Change: A258D

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000094556
Gene: ENSMUSG00000096042
AA Change: A258D

DomainStartEndE-ValueType
Pfam:ANF_receptor 9 355 7e-32 PFAM
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.2%
  • 10x: 95.1%
  • 20x: 87.1%
Validation Efficiency 100% (36/36)
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca14 G A 7: 119,893,380 (GRCm39) G1277R probably damaging Het
Adam10 A G 9: 70,675,170 (GRCm39) E593G possibly damaging Het
Adh6a T C 3: 138,034,829 (GRCm39) probably benign Het
Akap6 T A 12: 52,933,405 (GRCm39) I299N probably benign Het
Bltp1 T C 3: 37,013,483 (GRCm39) probably benign Het
Bod1l A T 5: 41,977,359 (GRCm39) N1318K probably benign Het
Ccdc121rt2 A G 5: 112,598,434 (GRCm39) D327G probably benign Het
Eif2b2 C A 12: 85,268,335 (GRCm39) T170K probably damaging Het
Ermard T A 17: 15,242,239 (GRCm39) H138Q probably damaging Het
Ern2 A T 7: 121,770,884 (GRCm39) probably null Het
Fkbp11 T C 15: 98,624,430 (GRCm39) K108R probably damaging Het
Golgb1 A G 16: 36,719,152 (GRCm39) K353E possibly damaging Het
Hipk1 G T 3: 103,661,641 (GRCm39) probably null Het
Itga4 A G 2: 79,119,649 (GRCm39) D485G possibly damaging Het
Krt1c C A 15: 101,726,356 (GRCm39) G61C unknown Het
Med12l T A 3: 59,168,253 (GRCm39) L1561Q probably damaging Het
Mtmr14 T C 6: 113,254,908 (GRCm39) probably null Het
Myorg A G 4: 41,497,539 (GRCm39) V697A probably benign Het
Naip1 A G 13: 100,559,584 (GRCm39) M1140T probably benign Het
Naip1 C T 13: 100,559,593 (GRCm39) R1137Q probably benign Het
Nav2 T A 7: 49,070,081 (GRCm39) H251Q probably benign Het
Nphp4 A G 4: 152,646,566 (GRCm39) D1366G possibly damaging Het
Or2b7 A G 13: 21,739,958 (GRCm39) V78A probably benign Het
Or6c75 A G 10: 129,336,750 (GRCm39) probably null Het
Pde6c A C 19: 38,121,628 (GRCm39) M79L probably benign Het
Pld5 C T 1: 175,803,018 (GRCm39) probably benign Het
Polr1g G C 7: 19,091,210 (GRCm39) S299C probably benign Het
Rps6kc1 A G 1: 190,541,142 (GRCm39) V387A probably damaging Het
Tas2r136 T C 6: 132,754,890 (GRCm39) D79G probably benign Het
Tmem243 A T 5: 9,168,488 (GRCm39) K90I probably damaging Het
Topbp1 A G 9: 103,192,289 (GRCm39) H260R probably damaging Het
Trappc1 A G 11: 69,215,636 (GRCm39) probably benign Het
Zfp300 T C X: 20,949,164 (GRCm39) Y200C possibly damaging Het
Other mutations in Vmn2r125
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00990:Vmn2r125 APN 4 156,703,194 (GRCm39) missense probably benign
IGL00990:Vmn2r125 APN 4 156,703,333 (GRCm39) missense probably benign 0.06
IGL00990:Vmn2r125 APN 4 156,703,332 (GRCm39) missense probably benign 0.16
IGL00990:Vmn2r125 APN 4 156,703,521 (GRCm39) missense probably benign
IGL00990:Vmn2r125 APN 4 156,703,678 (GRCm39) missense probably benign 0.00
IGL00990:Vmn2r125 APN 4 156,703,261 (GRCm39) missense probably benign 0.01
IGL00990:Vmn2r125 APN 4 156,703,195 (GRCm39) missense probably benign 0.35
IGL01018:Vmn2r125 APN 4 156,703,333 (GRCm39) missense probably benign 0.06
IGL01018:Vmn2r125 APN 4 156,703,332 (GRCm39) missense probably benign 0.16
IGL01018:Vmn2r125 APN 4 156,703,521 (GRCm39) missense probably benign
IGL01018:Vmn2r125 APN 4 156,703,195 (GRCm39) missense probably benign 0.35
IGL01018:Vmn2r125 APN 4 156,703,194 (GRCm39) missense probably benign
IGL01018:Vmn2r125 APN 4 156,703,140 (GRCm39) missense probably damaging 1.00
IGL01018:Vmn2r125 APN 4 156,702,907 (GRCm39) splice site probably benign
IGL02644:Vmn2r125 APN 4 156,703,294 (GRCm39) missense probably benign 0.01
IGL03144:Vmn2r125 APN 4 156,702,314 (GRCm39) missense possibly damaging 0.76
BB013:Vmn2r125 UTSW 4 156,702,988 (GRCm39) missense probably damaging 1.00
FR4342:Vmn2r125 UTSW 4 156,703,260 (GRCm39) missense probably benign 0.01
R0408:Vmn2r125 UTSW 4 156,703,153 (GRCm39) missense probably damaging 0.99
R1185:Vmn2r125 UTSW 4 156,703,396 (GRCm39) missense probably benign
R1185:Vmn2r125 UTSW 4 156,703,396 (GRCm39) missense probably benign
R1530:Vmn2r125 UTSW 4 156,703,447 (GRCm39) missense probably damaging 1.00
R1698:Vmn2r125 UTSW 4 156,703,333 (GRCm39) missense probably benign 0.06
R1780:Vmn2r125 UTSW 4 156,703,668 (GRCm39) missense probably damaging 1.00
R1977:Vmn2r125 UTSW 4 156,707,162 (GRCm39) splice site probably null
R2917:Vmn2r125 UTSW 4 156,703,564 (GRCm39) missense probably benign 0.01
R3428:Vmn2r125 UTSW 4 156,702,436 (GRCm39) missense probably benign 0.34
R3712:Vmn2r125 UTSW 4 156,702,419 (GRCm39) nonsense probably null
R4274:Vmn2r125 UTSW 4 156,702,382 (GRCm39) missense probably benign 0.00
R4575:Vmn2r125 UTSW 4 156,702,272 (GRCm39) missense probably null 0.30
R4707:Vmn2r125 UTSW 4 156,702,276 (GRCm39) missense probably damaging 1.00
R5229:Vmn2r125 UTSW 4 156,703,333 (GRCm39) missense probably benign 0.06
R5504:Vmn2r125 UTSW 4 156,703,456 (GRCm39) missense possibly damaging 0.81
R5587:Vmn2r125 UTSW 4 156,702,433 (GRCm39) missense probably damaging 1.00
R5987:Vmn2r125 UTSW 4 156,702,292 (GRCm39) missense probably damaging 1.00
R6037:Vmn2r125 UTSW 4 156,703,396 (GRCm39) missense probably benign
R6183:Vmn2r125 UTSW 4 156,702,364 (GRCm39) missense probably damaging 0.97
R6456:Vmn2r125 UTSW 4 156,703,357 (GRCm39) missense probably benign 0.41
R7342:Vmn2r125 UTSW 4 156,703,138 (GRCm39) missense probably damaging 1.00
R7926:Vmn2r125 UTSW 4 156,702,988 (GRCm39) missense probably damaging 1.00
R8113:Vmn2r125 UTSW 4 156,703,642 (GRCm39) missense probably damaging 1.00
R8191:Vmn2r125 UTSW 4 156,703,709 (GRCm39) missense probably damaging 1.00
R8272:Vmn2r125 UTSW 4 156,702,373 (GRCm39) missense probably damaging 1.00
R8962:Vmn2r125 UTSW 4 156,703,186 (GRCm39) missense possibly damaging 0.50
R9187:Vmn2r125 UTSW 4 156,703,554 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GGACCATTTAATCCTAACCTACGCGAC -3'
(R):5'- TGTGGGCCGCAACATAAACAGC -3'

Sequencing Primer
(F):5'- CTCAGATGATGATCAGGGTATTCAG -3'
(R):5'- ATCACTCATCGCCATATCATAGTTG -3'
Posted On 2013-10-16