Incidental Mutation 'IGL03144:Vmn2r125'
ID 410812
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r125
Ensembl Gene ENSMUSG00000096042
Gene Name vomeronasal 2, receptor 125
Synonyms Gm20782
Accession Numbers
Essential gene? Probably non essential (E-score: 0.078) question?
Stock # IGL03144
Quality Score
Status
Chromosome 4
Chromosomal Location 156696567-156708037 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 156702314 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Phenylalanine at position 33 (L33F)
Ref Sequence ENSEMBL: ENSMUSP00000094556 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000096794]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000096794
AA Change: L33F

PolyPhen 2 Score 0.763 (Sensitivity: 0.85; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000094556
Gene: ENSMUSG00000096042
AA Change: L33F

DomainStartEndE-ValueType
Pfam:ANF_receptor 9 355 7e-32 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca3 C A 17: 24,600,938 (GRCm39) Q451K probably benign Het
Acly A T 11: 100,405,909 (GRCm39) D294E possibly damaging Het
Arid3a C T 10: 79,782,316 (GRCm39) probably benign Het
Ascc3 T C 10: 50,643,539 (GRCm39) V1830A probably benign Het
Atp6v1b1 T C 6: 83,735,333 (GRCm39) V467A probably benign Het
Ccdc171 A T 4: 83,736,327 (GRCm39) I1233L probably damaging Het
Ccdc74a C A 16: 17,466,730 (GRCm39) Q146K possibly damaging Het
Cdh26 A G 2: 178,109,967 (GRCm39) D420G probably damaging Het
Ceacam20 T C 7: 19,705,444 (GRCm39) V145A possibly damaging Het
Cmya5 C A 13: 93,227,376 (GRCm39) A2571S probably damaging Het
Cog2 T C 8: 125,267,763 (GRCm39) S360P probably damaging Het
Col26a1 G T 5: 136,794,202 (GRCm39) T132N probably damaging Het
Col6a2 T A 10: 76,450,259 (GRCm39) H224L probably benign Het
Cpm C T 10: 117,519,319 (GRCm39) S409L probably benign Het
Dock4 G T 12: 40,742,906 (GRCm39) probably benign Het
Dpy19l2 T A 9: 24,557,603 (GRCm39) N391Y possibly damaging Het
Exosc9 G A 3: 36,608,284 (GRCm39) G126D probably damaging Het
Eya3 T C 4: 132,420,453 (GRCm39) S256P probably benign Het
Fat3 T C 9: 16,286,541 (GRCm39) D994G probably damaging Het
Fat4 A G 3: 39,011,008 (GRCm39) Q2036R possibly damaging Het
Fryl T C 5: 73,258,798 (GRCm39) Q662R probably null Het
Gm13271 A G 4: 88,673,636 (GRCm39) R178G probably benign Het
Gpr165 T A X: 95,760,560 (GRCm39) L279Q probably damaging Het
Htr1b A G 9: 81,513,998 (GRCm39) L203P probably damaging Het
Kcnb2 T C 1: 15,780,112 (GRCm39) L328P probably damaging Het
Klhl26 C T 8: 70,905,214 (GRCm39) R198H probably damaging Het
Nhsl2 A G X: 101,123,115 (GRCm39) R973G possibly damaging Het
Nmi A T 2: 51,842,546 (GRCm39) F182Y probably damaging Het
Nop2 T A 6: 125,114,475 (GRCm39) probably null Het
Nrn1 C A 13: 36,914,080 (GRCm39) probably null Het
Ooep G T 9: 78,285,289 (GRCm39) A109E possibly damaging Het
Or1j21 A G 2: 36,684,093 (GRCm39) T282A probably benign Het
Pan3 T C 5: 147,387,591 (GRCm39) probably benign Het
Pcdhb6 A G 18: 37,467,459 (GRCm39) N127D probably damaging Het
Rabgap1 G A 2: 37,430,544 (GRCm39) R695H probably damaging Het
Rxrg G A 1: 167,426,327 (GRCm39) G3R possibly damaging Het
Slc17a3 T C 13: 24,030,423 (GRCm39) M178T probably benign Het
Slc39a8 A G 3: 135,589,971 (GRCm39) E287G probably benign Het
Slc44a5 G T 3: 153,949,177 (GRCm39) D217Y possibly damaging Het
Slc4a10 G T 2: 62,080,810 (GRCm39) V346L probably benign Het
Slc9a4 T C 1: 40,651,362 (GRCm39) Y547H probably damaging Het
St6galnac3 A C 3: 152,911,164 (GRCm39) Y266D probably damaging Het
Stard6 A T 18: 70,609,182 (GRCm39) Y3F possibly damaging Het
Stk25 C A 1: 93,556,858 (GRCm39) L53F probably damaging Het
Tep1 A T 14: 51,081,474 (GRCm39) probably benign Het
Tmem151a T A 19: 5,135,400 (GRCm39) M1L probably benign Het
Trim10 T C 17: 37,187,740 (GRCm39) S319P probably damaging Het
Trmt44 G T 5: 35,721,766 (GRCm39) P466T probably benign Het
Unc79 T C 12: 103,008,401 (GRCm39) I256T probably 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 4 156,703,521 (GRCm39) missense probably benign
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 4 156,703,195 (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
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
R0785:Vmn2r125 UTSW 4 156,703,396 (GRCm39) missense probably benign
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
Posted On 2016-08-02