Incidental Mutation 'IGL02086:Vmn1r81'
ID 285482
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r81
Ensembl Gene ENSMUSG00000115027
Gene Name vomeronasal 1 receptor 81
Synonyms V1rg9
Accession Numbers
Essential gene? Probably essential (E-score: 0.822) question?
Stock # IGL02086
Quality Score
Status
Chromosome 7
Chromosomal Location 11993686-11994606 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 11993792 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Glycine at position 272 (V272G)
Ref Sequence ENSEMBL: ENSMUSP00000153767 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000086232] [ENSMUST00000227080] [ENSMUST00000227973] [ENSMUST00000228482] [ENSMUST00000228764]
AlphaFold A0A2I3BPG7
Predicted Effect possibly damaging
Transcript: ENSMUST00000086232
AA Change: V272G

PolyPhen 2 Score 0.818 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000083409
Gene: ENSMUSG00000115027
AA Change: V272G

DomainStartEndE-ValueType
Pfam:TAS2R 3 301 5.4e-12 PFAM
Pfam:V1R 34 299 6.6e-31 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000227080
Predicted Effect possibly damaging
Transcript: ENSMUST00000227973
AA Change: V272G

PolyPhen 2 Score 0.818 (Sensitivity: 0.84; Specificity: 0.93)
Predicted Effect probably benign
Transcript: ENSMUST00000228482
Predicted Effect possibly damaging
Transcript: ENSMUST00000228764
AA Change: V272G

PolyPhen 2 Score 0.818 (Sensitivity: 0.84; Specificity: 0.93)
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
Vmn2r107 T A 17: 20,578,062 (GRCm39) I457K probably benign Het
Vmn2r72 A T 7: 85,387,374 (GRCm39) V730E probably benign Het
Vmn2r9 T C 5: 108,995,433 (GRCm39) Y405C probably damaging 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 Vmn1r81
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02026:Vmn1r81 APN 7 11,994,432 (GRCm39) missense probably damaging 1.00
IGL02751:Vmn1r81 APN 7 11,994,374 (GRCm39) missense probably damaging 1.00
IGL02879:Vmn1r81 APN 7 11,994,319 (GRCm39) missense probably benign 0.20
IGL03358:Vmn1r81 APN 7 11,994,232 (GRCm39) missense possibly damaging 0.57
PIT4305001:Vmn1r81 UTSW 7 11,994,590 (GRCm39) missense probably benign 0.01
R0359:Vmn1r81 UTSW 7 11,993,877 (GRCm39) missense probably damaging 1.00
R1615:Vmn1r81 UTSW 7 11,994,441 (GRCm39) missense probably damaging 1.00
R1938:Vmn1r81 UTSW 7 11,994,589 (GRCm39) missense possibly damaging 0.67
R2967:Vmn1r81 UTSW 7 11,993,964 (GRCm39) missense probably damaging 0.99
R2983:Vmn1r81 UTSW 7 11,994,596 (GRCm39) missense probably benign 0.02
R4549:Vmn1r81 UTSW 7 11,993,749 (GRCm39) missense probably damaging 0.99
R5099:Vmn1r81 UTSW 7 11,994,248 (GRCm39) missense possibly damaging 0.86
R5326:Vmn1r81 UTSW 7 11,994,034 (GRCm39) missense probably damaging 1.00
R5542:Vmn1r81 UTSW 7 11,994,034 (GRCm39) missense probably damaging 1.00
R6010:Vmn1r81 UTSW 7 11,994,349 (GRCm39) missense possibly damaging 0.88
R6630:Vmn1r81 UTSW 7 11,994,584 (GRCm39) nonsense probably null
R6724:Vmn1r81 UTSW 7 11,994,599 (GRCm39) missense probably damaging 1.00
R6754:Vmn1r81 UTSW 7 11,993,774 (GRCm39) missense probably damaging 0.98
R8198:Vmn1r81 UTSW 7 11,993,882 (GRCm39) missense possibly damaging 0.64
R9719:Vmn1r81 UTSW 7 11,994,449 (GRCm39) missense probably damaging 1.00
R9790:Vmn1r81 UTSW 7 11,994,113 (GRCm39) missense probably benign 0.15
R9791:Vmn1r81 UTSW 7 11,994,113 (GRCm39) missense probably benign 0.15
Posted On 2015-04-16