Incidental Mutation 'IGL00938:Vmn1r185'
ID 27837
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r185
Ensembl Gene ENSMUSG00000091924
Gene Name vomeronasal 1 receptor 185
Synonyms V1re12
Accession Numbers
Essential gene? Probably non essential (E-score: 0.078) question?
Stock # IGL00938
Quality Score
Status
Chromosome 7
Chromosomal Location 26310544-26311503 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 26311116 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Valine at position 130 (I130V)
Ref Sequence ENSEMBL: ENSMUSP00000154688 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000171039] [ENSMUST00000226694] [ENSMUST00000227264] [ENSMUST00000227411] [ENSMUST00000227461] [ENSMUST00000227479] [ENSMUST00000228633] [ENSMUST00000228467] [ENSMUST00000228133] [ENSMUST00000228676] [ENSMUST00000227695] [ENSMUST00000228004] [ENSMUST00000228367]
AlphaFold Q8R299
Predicted Effect probably benign
Transcript: ENSMUST00000171039
AA Change: I130V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000128295
Gene: ENSMUSG00000091924
AA Change: I130V

DomainStartEndE-ValueType
Pfam:TAS2R 7 307 4.1e-8 PFAM
Pfam:V1R 38 297 1.5e-31 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000226694
AA Change: I130V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Predicted Effect probably benign
Transcript: ENSMUST00000227264
AA Change: I130V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Predicted Effect probably benign
Transcript: ENSMUST00000227411
AA Change: I130V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Predicted Effect probably benign
Transcript: ENSMUST00000227461
AA Change: I130V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Predicted Effect probably benign
Transcript: ENSMUST00000227479
AA Change: I130V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Predicted Effect probably benign
Transcript: ENSMUST00000228633
AA Change: I130V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Predicted Effect probably benign
Transcript: ENSMUST00000228467
AA Change: I130V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Predicted Effect probably benign
Transcript: ENSMUST00000228133
AA Change: I130V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Predicted Effect probably benign
Transcript: ENSMUST00000228676
AA Change: I130V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Predicted Effect probably benign
Transcript: ENSMUST00000227695
AA Change: I130V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Predicted Effect probably benign
Transcript: ENSMUST00000228004
AA Change: I130V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Predicted Effect probably benign
Transcript: ENSMUST00000228367
AA Change: I130V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 23 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamtsl1 A G 4: 86,260,515 (GRCm39) I909V possibly damaging Het
Alkal2 C A 12: 30,937,089 (GRCm39) H101N probably damaging Het
Camk2g C T 14: 20,787,398 (GRCm39) G500S probably damaging Het
Col4a1 G A 8: 11,286,456 (GRCm39) probably benign Het
Fry T A 5: 150,293,645 (GRCm39) V446E probably damaging Het
Gpc2 C A 5: 138,277,169 (GRCm39) R86L probably benign Het
Hnrnpm C A 17: 33,868,876 (GRCm39) R517L probably damaging Het
Krt16 A T 11: 100,139,543 (GRCm39) C58* probably null Het
Ltbp2 T C 12: 84,878,573 (GRCm39) R309G probably benign Het
Mapkapk5 T C 5: 121,675,166 (GRCm39) probably benign Het
Mpdz G A 4: 81,210,749 (GRCm39) A1665V probably damaging Het
Mpp7 T C 18: 7,353,297 (GRCm39) T470A probably benign Het
Mypn T A 10: 63,028,202 (GRCm39) D287V probably damaging Het
Nup160 T C 2: 90,563,171 (GRCm39) L1312P probably damaging Het
Or4a77 C T 2: 89,487,420 (GRCm39) V122M probably damaging Het
Or6k14 T C 1: 173,927,933 (GRCm39) M303T probably benign Het
Poln C A 5: 34,286,568 (GRCm39) C200F probably damaging Het
Pparg A G 6: 115,440,100 (GRCm39) I225V probably benign Het
Pspn T C 17: 57,306,629 (GRCm39) E100G probably benign Het
Slc12a8 G A 16: 33,361,267 (GRCm39) V50I probably damaging Het
Suz12 A G 11: 79,898,395 (GRCm39) probably benign Het
Ubiad1 A G 4: 148,520,814 (GRCm39) F270S probably benign Het
Vmn1r210 A T 13: 23,011,538 (GRCm39) C249* probably null Het
Other mutations in Vmn1r185
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00925:Vmn1r185 APN 7 26,310,615 (GRCm39) missense probably benign 0.00
IGL01413:Vmn1r185 APN 7 26,311,046 (GRCm39) missense probably damaging 0.99
R0207:Vmn1r185 UTSW 7 26,311,014 (GRCm39) missense possibly damaging 0.80
R1497:Vmn1r185 UTSW 7 26,311,219 (GRCm39) missense probably benign 0.01
R1505:Vmn1r185 UTSW 7 26,310,903 (GRCm39) missense probably damaging 0.99
R1966:Vmn1r185 UTSW 7 26,310,956 (GRCm39) missense probably benign 0.31
R2022:Vmn1r185 UTSW 7 26,310,935 (GRCm39) missense possibly damaging 0.86
R4010:Vmn1r185 UTSW 7 26,311,450 (GRCm39) missense possibly damaging 0.77
R4093:Vmn1r185 UTSW 7 26,311,208 (GRCm39) missense probably damaging 1.00
R4095:Vmn1r185 UTSW 7 26,311,208 (GRCm39) missense probably damaging 1.00
R4961:Vmn1r185 UTSW 7 26,310,716 (GRCm39) missense probably benign 0.43
R5049:Vmn1r185 UTSW 7 26,310,920 (GRCm39) missense possibly damaging 0.95
R6297:Vmn1r185 UTSW 7 26,311,046 (GRCm39) missense probably benign 0.10
R6903:Vmn1r185 UTSW 7 26,311,160 (GRCm39) missense probably damaging 1.00
R7046:Vmn1r185 UTSW 7 26,310,651 (GRCm39) missense probably damaging 1.00
R7429:Vmn1r185 UTSW 7 26,310,603 (GRCm39) missense probably benign 0.13
R8032:Vmn1r185 UTSW 7 26,310,558 (GRCm39) missense probably benign 0.15
R8919:Vmn1r185 UTSW 7 26,311,206 (GRCm39) missense probably damaging 1.00
R8922:Vmn1r185 UTSW 7 26,310,825 (GRCm39) missense probably damaging 0.98
R9200:Vmn1r185 UTSW 7 26,311,073 (GRCm39) missense possibly damaging 0.51
R9398:Vmn1r185 UTSW 7 26,311,056 (GRCm39) missense probably benign 0.05
R9629:Vmn1r185 UTSW 7 26,311,439 (GRCm39) missense probably damaging 1.00
R9726:Vmn1r185 UTSW 7 26,310,783 (GRCm39) missense probably damaging 1.00
X0063:Vmn1r185 UTSW 7 26,311,328 (GRCm39) missense probably damaging 1.00
Posted On 2013-04-17