Incidental Mutation 'IGL02082:Vmn1r113'
ID 283391
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r113
Ensembl Gene ENSMUSG00000091638
Gene Name vomeronasal 1 receptor 113
Synonyms Gm5748
Accession Numbers
Essential gene? Probably non essential (E-score: 0.060) question?
Stock # IGL02082
Quality Score
Status
Chromosome 7
Chromosomal Location 20521210-20522133 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 20521672 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Tyrosine at position 155 (H155Y)
Ref Sequence ENSEMBL: ENSMUSP00000133307 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000168794] [ENSMUST00000173723]
AlphaFold G3UWI8
Predicted Effect probably benign
Transcript: ENSMUST00000168794
AA Change: H155Y

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000126041
Gene: ENSMUSG00000091638
AA Change: H155Y

DomainStartEndE-ValueType
Pfam:TAS2R 8 288 4.2e-8 PFAM
Pfam:V1R 41 288 2.8e-8 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000173723
AA Change: H155Y

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000133307
Gene: ENSMUSG00000091638
AA Change: H155Y

DomainStartEndE-ValueType
Pfam:TAS2R 8 298 4e-16 PFAM
Pfam:7tm_1 31 290 9.3e-7 PFAM
Pfam:V1R 41 298 5e-17 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 23 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atp9b A C 18: 80,935,145 (GRCm39) probably benign Het
Brinp3 T C 1: 146,627,600 (GRCm39) C278R probably damaging Het
Cfap54 T C 10: 92,917,320 (GRCm39) S47G unknown Het
Clec16a T C 16: 10,432,432 (GRCm39) L484P probably damaging Het
Cnksr1 C A 4: 133,963,363 (GRCm39) G71C probably damaging Het
Dnah12 A T 14: 26,428,317 (GRCm39) N246I possibly damaging Het
Fbh1 T C 2: 11,768,938 (GRCm39) D285G probably benign Het
Focad C T 4: 88,148,815 (GRCm39) Q511* probably null Het
Gpr63 A G 4: 25,008,564 (GRCm39) probably benign Het
Iah1 C A 12: 21,367,405 (GRCm39) S37* probably null Het
Inpp4a T A 1: 37,405,708 (GRCm39) probably benign Het
Mcm2 A T 6: 88,865,218 (GRCm39) Y486* probably null Het
Mtmr10 A G 7: 63,983,238 (GRCm39) probably benign Het
Nbea A G 3: 55,875,588 (GRCm39) L1694S possibly damaging Het
Pafah1b1 A G 11: 74,590,159 (GRCm39) S4P probably benign Het
Rnase10 A T 14: 51,246,856 (GRCm39) E41V probably damaging Het
Slc17a6 G T 7: 51,318,777 (GRCm39) R473L probably benign Het
Spata31g1 A G 4: 42,970,198 (GRCm39) T2A probably benign Het
Tbc1d9b A G 11: 50,054,709 (GRCm39) D951G probably benign Het
Tk1 C A 11: 117,716,553 (GRCm39) probably null Het
Trim46 C A 3: 89,146,307 (GRCm39) A395S probably benign Het
Vmn1r222 A G 13: 23,416,499 (GRCm39) M238T probably damaging Het
Vmn2r72 A T 7: 85,387,374 (GRCm39) V730E probably benign Het
Other mutations in Vmn1r113
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01908:Vmn1r113 APN 7 20,521,943 (GRCm39) missense probably damaging 1.00
IGL02148:Vmn1r113 APN 7 20,521,747 (GRCm39) missense probably benign 0.14
IGL03169:Vmn1r113 APN 7 20,522,012 (GRCm39) missense probably benign 0.11
R0593:Vmn1r113 UTSW 7 20,521,388 (GRCm39) missense probably damaging 0.99
R0669:Vmn1r113 UTSW 7 20,521,345 (GRCm39) missense probably benign 0.00
R1212:Vmn1r113 UTSW 7 20,521,356 (GRCm39) missense probably benign 0.19
R1693:Vmn1r113 UTSW 7 20,521,532 (GRCm39) missense probably damaging 0.98
R2228:Vmn1r113 UTSW 7 20,521,832 (GRCm39) missense probably damaging 1.00
R3945:Vmn1r113 UTSW 7 20,521,637 (GRCm39) missense probably benign 0.00
R4209:Vmn1r113 UTSW 7 20,521,535 (GRCm39) missense probably benign 0.44
R5038:Vmn1r113 UTSW 7 20,521,419 (GRCm39) missense possibly damaging 0.70
R6306:Vmn1r113 UTSW 7 20,521,792 (GRCm39) missense probably damaging 1.00
R6623:Vmn1r113 UTSW 7 20,521,991 (GRCm39) missense probably benign 0.01
R6675:Vmn1r113 UTSW 7 20,521,903 (GRCm39) missense probably benign 0.02
R6677:Vmn1r113 UTSW 7 20,521,903 (GRCm39) missense probably benign 0.02
R6678:Vmn1r113 UTSW 7 20,521,903 (GRCm39) missense probably benign 0.02
R6968:Vmn1r113 UTSW 7 20,521,876 (GRCm39) missense probably damaging 1.00
R7054:Vmn1r113 UTSW 7 20,521,427 (GRCm39) missense probably benign 0.14
R7256:Vmn1r113 UTSW 7 20,521,370 (GRCm39) missense probably damaging 1.00
R8926:Vmn1r113 UTSW 7 20,521,874 (GRCm39) missense possibly damaging 0.82
R9131:Vmn1r113 UTSW 7 20,521,342 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16