Incidental Mutation 'IGL02086:Vmn2r9'
ID 285448
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r9
Ensembl Gene ENSMUSG00000091624
Gene Name vomeronasal 2, receptor 9
Synonyms EG435864
Accession Numbers
Essential gene? Probably non essential (E-score: 0.113) question?
Stock # IGL02086
Quality Score
Status
Chromosome 5
Chromosomal Location 108990813-109000376 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 108995433 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Cysteine at position 405 (Y405C)
Ref Sequence ENSEMBL: ENSMUSP00000129520 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000170419]
AlphaFold K7N6Z8
Predicted Effect probably damaging
Transcript: ENSMUST00000170419
AA Change: Y405C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000129520
Gene: ENSMUSG00000091624
AA Change: Y405C

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
Pfam:ANF_receptor 77 412 8.1e-29 PFAM
Pfam:NCD3G 507 561 2.3e-16 PFAM
Pfam:7tm_3 592 829 3.4e-54 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000176157
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930426L09Rik T C 2: 19,003,623 (GRCm39) probably benign Het
Abi3bp A G 16: 56,462,930 (GRCm39) probably benign Het
Asb4 T C 6: 5,398,386 (GRCm39) I117T probably benign Het
Birc6 T G 17: 74,946,822 (GRCm39) L2847R probably damaging Het
C2cd2 A G 16: 97,691,208 (GRCm39) probably benign Het
Ccdc77 C A 6: 120,316,119 (GRCm39) C186F possibly damaging Het
Cd300ld2 T A 11: 114,903,384 (GRCm39) probably benign Het
Cd55b A T 1: 130,345,919 (GRCm39) D166E probably benign Het
Cfap100 A G 6: 90,390,954 (GRCm39) F8L probably damaging Het
Col2a1 C T 15: 97,884,618 (GRCm39) probably null Het
Dbf4 A G 5: 8,453,189 (GRCm39) I270T probably benign Het
Dkk3 T C 7: 111,748,236 (GRCm39) S123G probably benign Het
Ep400 A G 5: 110,824,809 (GRCm39) probably benign Het
Fam184a A G 10: 53,575,351 (GRCm39) I30T probably damaging Het
Fam20a T C 11: 109,564,239 (GRCm39) I505V probably benign Het
Fbh1 T C 2: 11,768,938 (GRCm39) D285G probably benign Het
Fcho1 T C 8: 72,169,444 (GRCm39) E154G probably damaging Het
Klhdc1 A G 12: 69,329,958 (GRCm39) I362M probably benign Het
Knl1 A T 2: 118,931,255 (GRCm39) E1990D probably benign Het
Lancl2 A G 6: 57,711,024 (GRCm39) Y394C probably damaging Het
Lgi2 G A 5: 52,723,299 (GRCm39) S50F probably damaging Het
Map2k7 A G 8: 4,288,950 (GRCm39) E14G probably damaging Het
Mga A G 2: 119,754,517 (GRCm39) I1009V probably damaging Het
Nat9 C A 11: 115,074,234 (GRCm39) probably null Het
Nek2 G A 1: 191,563,401 (GRCm39) A422T probably benign Het
Nfkbiz A T 16: 55,636,034 (GRCm39) L509Q probably damaging Het
Or56b2 A T 7: 104,337,634 (GRCm39) R137S probably benign Het
Pgap1 T A 1: 54,587,147 (GRCm39) Q143L probably damaging Het
Pkd1l3 C T 8: 110,392,217 (GRCm39) T1937I probably damaging Het
Pou1f1 A G 16: 65,326,784 (GRCm39) E128G probably damaging Het
Ppfia3 T C 7: 44,989,996 (GRCm39) probably benign Het
Prkd1 T C 12: 50,434,046 (GRCm39) I566V probably benign Het
Psd2 A G 18: 36,138,959 (GRCm39) R528G probably damaging Het
Ptprg G T 14: 12,110,080 (GRCm38) E263* probably null Het
Radil T C 5: 142,529,576 (GRCm39) D40G probably benign Het
Ryr2 T A 13: 11,750,442 (GRCm39) Y1943F probably damaging Het
Slc30a4 C T 2: 122,543,947 (GRCm39) probably benign Het
Slc31a1 A T 4: 62,306,241 (GRCm39) T120S possibly damaging Het
Snrpe A G 1: 133,537,487 (GRCm39) probably benign Het
Stx3 G T 19: 11,796,046 (GRCm39) probably benign Het
Thoc2l A G 5: 104,666,867 (GRCm39) E463G possibly damaging Het
Ufsp1 T A 5: 137,293,178 (GRCm39) C43S probably damaging Het
Vac14 T A 8: 111,379,950 (GRCm39) M416K possibly damaging Het
Vmn1r81 A C 7: 11,993,792 (GRCm39) V272G possibly damaging Het
Vmn2r107 T A 17: 20,578,062 (GRCm39) I457K probably benign Het
Vmn2r72 A T 7: 85,387,374 (GRCm39) V730E probably benign Het
Zcchc17 T C 4: 130,210,440 (GRCm39) *242W probably null Het
Zfp503 T C 14: 22,037,354 (GRCm39) K83R possibly damaging Het
Other mutations in Vmn2r9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00920:Vmn2r9 APN 5 108,995,890 (GRCm39) missense possibly damaging 0.79
IGL00972:Vmn2r9 APN 5 108,996,903 (GRCm39) missense probably benign 0.02
IGL01102:Vmn2r9 APN 5 108,990,811 (GRCm39) splice site probably null
IGL01892:Vmn2r9 APN 5 108,995,700 (GRCm39) missense probably damaging 1.00
IGL02118:Vmn2r9 APN 5 108,991,502 (GRCm39) missense probably damaging 1.00
IGL02119:Vmn2r9 APN 5 108,991,502 (GRCm39) missense probably damaging 1.00
IGL02120:Vmn2r9 APN 5 108,991,502 (GRCm39) missense probably damaging 1.00
IGL02121:Vmn2r9 APN 5 108,991,502 (GRCm39) missense probably damaging 1.00
IGL02123:Vmn2r9 APN 5 108,991,502 (GRCm39) missense probably damaging 1.00
IGL02131:Vmn2r9 APN 5 108,991,502 (GRCm39) missense probably damaging 1.00
IGL02132:Vmn2r9 APN 5 108,991,502 (GRCm39) missense probably damaging 1.00
IGL02171:Vmn2r9 APN 5 108,991,502 (GRCm39) missense probably damaging 1.00
IGL02185:Vmn2r9 APN 5 108,991,502 (GRCm39) missense probably damaging 1.00
IGL02186:Vmn2r9 APN 5 108,991,502 (GRCm39) missense probably damaging 1.00
IGL02346:Vmn2r9 APN 5 108,990,850 (GRCm39) missense probably benign 0.07
IGL02508:Vmn2r9 APN 5 108,996,067 (GRCm39) missense possibly damaging 0.70
IGL02815:Vmn2r9 APN 5 108,990,856 (GRCm39) missense possibly damaging 0.69
IGL03077:Vmn2r9 APN 5 108,996,173 (GRCm39) splice site probably benign
IGL03269:Vmn2r9 APN 5 108,995,820 (GRCm39) missense probably damaging 1.00
IGL03293:Vmn2r9 APN 5 108,995,997 (GRCm39) missense probably damaging 1.00
R0112:Vmn2r9 UTSW 5 108,990,991 (GRCm39) missense probably damaging 1.00
R0328:Vmn2r9 UTSW 5 108,995,405 (GRCm39) missense probably benign 0.11
R0382:Vmn2r9 UTSW 5 108,995,463 (GRCm39) missense probably damaging 1.00
R0521:Vmn2r9 UTSW 5 108,996,154 (GRCm39) nonsense probably null
R0975:Vmn2r9 UTSW 5 108,991,169 (GRCm39) missense probably damaging 1.00
R1216:Vmn2r9 UTSW 5 108,995,440 (GRCm39) missense probably damaging 1.00
R1458:Vmn2r9 UTSW 5 108,996,850 (GRCm39) missense probably benign 0.44
R1469:Vmn2r9 UTSW 5 108,991,694 (GRCm39) missense probably benign
R1469:Vmn2r9 UTSW 5 108,991,694 (GRCm39) missense probably benign
R1704:Vmn2r9 UTSW 5 108,994,266 (GRCm39) missense probably damaging 1.00
R1967:Vmn2r9 UTSW 5 108,995,388 (GRCm39) missense probably benign 0.03
R1991:Vmn2r9 UTSW 5 108,994,305 (GRCm39) missense probably damaging 0.99
R2410:Vmn2r9 UTSW 5 108,996,123 (GRCm39) missense probably damaging 1.00
R3419:Vmn2r9 UTSW 5 108,994,299 (GRCm39) missense probably damaging 0.96
R3852:Vmn2r9 UTSW 5 108,995,997 (GRCm39) missense probably damaging 1.00
R3873:Vmn2r9 UTSW 5 108,995,701 (GRCm39) missense probably benign 0.14
R3905:Vmn2r9 UTSW 5 108,995,785 (GRCm39) missense probably benign 0.37
R3908:Vmn2r9 UTSW 5 108,995,785 (GRCm39) missense probably benign 0.37
R3921:Vmn2r9 UTSW 5 108,996,921 (GRCm39) missense probably benign
R4156:Vmn2r9 UTSW 5 108,995,743 (GRCm39) missense possibly damaging 0.64
R4477:Vmn2r9 UTSW 5 108,994,143 (GRCm39) missense probably benign
R4478:Vmn2r9 UTSW 5 108,994,143 (GRCm39) missense probably benign
R4544:Vmn2r9 UTSW 5 108,995,551 (GRCm39) missense probably benign 0.00
R4546:Vmn2r9 UTSW 5 108,995,551 (GRCm39) missense probably benign 0.00
R4627:Vmn2r9 UTSW 5 108,995,463 (GRCm39) missense probably damaging 1.00
R5215:Vmn2r9 UTSW 5 108,994,351 (GRCm39) missense probably benign 0.03
R5361:Vmn2r9 UTSW 5 108,995,929 (GRCm39) missense probably damaging 1.00
R5587:Vmn2r9 UTSW 5 108,995,427 (GRCm39) missense probably damaging 1.00
R6054:Vmn2r9 UTSW 5 108,996,126 (GRCm39) missense probably damaging 0.99
R6106:Vmn2r9 UTSW 5 108,992,902 (GRCm39) missense probably benign
R6125:Vmn2r9 UTSW 5 108,990,836 (GRCm39) missense probably benign 0.01
R6137:Vmn2r9 UTSW 5 108,996,882 (GRCm39) missense probably benign 0.00
R6920:Vmn2r9 UTSW 5 108,996,912 (GRCm39) missense possibly damaging 0.72
R7579:Vmn2r9 UTSW 5 108,992,948 (GRCm39) missense probably damaging 1.00
R8683:Vmn2r9 UTSW 5 108,996,873 (GRCm39) missense probably benign
R8964:Vmn2r9 UTSW 5 108,996,031 (GRCm39) missense probably benign 0.05
R9022:Vmn2r9 UTSW 5 108,992,923 (GRCm39) missense possibly damaging 0.90
R9118:Vmn2r9 UTSW 5 108,990,937 (GRCm39) missense probably damaging 0.99
R9125:Vmn2r9 UTSW 5 108,996,047 (GRCm39) missense
R9240:Vmn2r9 UTSW 5 108,996,099 (GRCm39) missense possibly damaging 0.78
R9327:Vmn2r9 UTSW 5 108,996,841 (GRCm39) missense probably damaging 0.96
R9412:Vmn2r9 UTSW 5 108,991,484 (GRCm39) missense probably damaging 1.00
R9499:Vmn2r9 UTSW 5 108,995,584 (GRCm39) missense probably damaging 1.00
R9757:Vmn2r9 UTSW 5 108,995,908 (GRCm39) missense possibly damaging 0.87
R9790:Vmn2r9 UTSW 5 108,995,409 (GRCm39) missense probably damaging 0.99
R9791:Vmn2r9 UTSW 5 108,995,409 (GRCm39) missense probably damaging 0.99
Posted On 2015-04-16