Incidental Mutation 'IGL01577:Vmn1r87'
ID 91306
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r87
Ensembl Gene ENSMUSG00000070815
Gene Name vomeronasal 1 receptor 87
Synonyms V1rk1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.050) question?
Stock # IGL01577
Quality Score
Status
Chromosome 7
Chromosomal Location 12865398-12866285 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 12865775 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Phenylalanine at position 171 (V171F)
Ref Sequence ENSEMBL: ENSMUSP00000154184 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094827] [ENSMUST00000211249] [ENSMUST00000227443] [ENSMUST00000228800]
AlphaFold Q8R255
Predicted Effect probably benign
Transcript: ENSMUST00000094827
AA Change: V171F

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000092422
Gene: ENSMUSG00000070815
AA Change: V171F

DomainStartEndE-ValueType
Pfam:TAS2R 1 285 1.2e-11 PFAM
Pfam:V1R 14 280 1.8e-36 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000211249
AA Change: V171F

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
Predicted Effect probably benign
Transcript: ENSMUST00000227443
AA Change: V171F

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
Predicted Effect probably benign
Transcript: ENSMUST00000228800
AA Change: V171F

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actr8 A G 14: 29,709,232 (GRCm39) T279A probably benign Het
Adamts9 T G 6: 92,835,128 (GRCm39) probably benign Het
Apba3 G A 10: 81,108,053 (GRCm39) G403D probably damaging Het
Atp13a4 C T 16: 29,260,102 (GRCm39) V235I possibly damaging Het
Brca2 T A 5: 150,465,085 (GRCm39) C1616* probably null Het
Ccdc7a T A 8: 129,715,244 (GRCm39) E280V probably damaging Het
Cdc42bpb A G 12: 111,268,477 (GRCm39) I1241T possibly damaging Het
Cplx4 G T 18: 66,103,015 (GRCm39) A35E probably damaging Het
Cyp2j8 T G 4: 96,367,308 (GRCm39) D270A probably damaging Het
Cyp7a1 T C 4: 6,273,618 (GRCm39) D96G probably damaging Het
Ddx11 G A 17: 66,446,398 (GRCm39) R429H possibly damaging Het
Depdc5 C A 5: 33,113,241 (GRCm39) T419N possibly damaging Het
Diaph3 A C 14: 87,143,467 (GRCm39) I737R probably damaging Het
Elf2 C T 3: 51,163,773 (GRCm39) probably benign Het
Epha6 T A 16: 59,777,289 (GRCm39) I673L possibly damaging Het
Ephx1 A G 1: 180,829,545 (GRCm39) M1T probably null Het
Fndc3a A T 14: 72,827,298 (GRCm39) M84K probably damaging Het
Gad2 T C 2: 22,571,292 (GRCm39) probably benign Het
Gba2 G A 4: 43,573,753 (GRCm39) Q180* probably null Het
Gga2 A G 7: 121,589,006 (GRCm39) Y574H probably damaging Het
Gm7168 A T 17: 14,169,649 (GRCm39) R339W probably damaging Het
Hdac10 T C 15: 89,010,416 (GRCm39) E302G possibly damaging Het
Ighv1-72 A G 12: 115,721,893 (GRCm39) V21A possibly damaging Het
Kif15 A G 9: 122,825,399 (GRCm39) E774G probably benign Het
Lig3 A G 11: 82,674,303 (GRCm39) N43S probably benign Het
Nmnat1 T A 4: 149,554,135 (GRCm39) D135V possibly damaging Het
Or1s2 A G 19: 13,758,162 (GRCm39) Y62C probably damaging Het
Or52n2 A G 7: 104,542,730 (GRCm39) F35S probably benign Het
Pak6 A C 2: 118,524,129 (GRCm39) K428T probably benign Het
Pou2f3 G A 9: 43,058,178 (GRCm39) Q56* probably null Het
Prep T C 10: 44,948,144 (GRCm39) probably benign Het
Psd4 C T 2: 24,293,234 (GRCm39) P700S probably damaging Het
Rad18 A T 6: 112,642,302 (GRCm39) probably benign Het
Rbbp5 A G 1: 132,420,393 (GRCm39) K209E possibly damaging Het
Smurf1 G A 5: 144,829,998 (GRCm39) T335I probably damaging Het
Tbcd G A 11: 121,387,838 (GRCm39) R72Q probably damaging Het
Tsga10 T C 1: 37,874,538 (GRCm39) T116A possibly damaging Het
Unc80 A G 1: 66,569,127 (GRCm39) probably null Het
Ythdc2 A T 18: 44,991,349 (GRCm39) M786L probably benign Het
Zmym6 C A 4: 126,999,223 (GRCm39) T469K probably damaging Het
Other mutations in Vmn1r87
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01400:Vmn1r87 APN 7 12,866,230 (GRCm39) missense probably damaging 1.00
IGL02972:Vmn1r87 APN 7 12,866,256 (GRCm39) nonsense probably null
IGL03246:Vmn1r87 APN 7 12,866,288 (GRCm39) utr 5 prime probably benign
PIT4142001:Vmn1r87 UTSW 7 12,866,112 (GRCm39) missense probably benign 0.00
R0153:Vmn1r87 UTSW 7 12,866,211 (GRCm39) missense probably damaging 1.00
R0502:Vmn1r87 UTSW 7 12,865,583 (GRCm39) missense probably damaging 1.00
R0658:Vmn1r87 UTSW 7 12,865,756 (GRCm39) missense probably damaging 1.00
R1589:Vmn1r87 UTSW 7 12,865,703 (GRCm39) missense possibly damaging 0.46
R1731:Vmn1r87 UTSW 7 12,865,703 (GRCm39) missense possibly damaging 0.46
R2027:Vmn1r87 UTSW 7 12,865,823 (GRCm39) missense probably damaging 0.99
R2044:Vmn1r87 UTSW 7 12,865,748 (GRCm39) missense probably benign 0.02
R3124:Vmn1r87 UTSW 7 12,865,493 (GRCm39) missense probably damaging 1.00
R4208:Vmn1r87 UTSW 7 12,866,185 (GRCm39) missense probably benign 0.37
R4731:Vmn1r87 UTSW 7 12,866,254 (GRCm39) missense possibly damaging 0.92
R4732:Vmn1r87 UTSW 7 12,866,254 (GRCm39) missense possibly damaging 0.92
R4733:Vmn1r87 UTSW 7 12,866,254 (GRCm39) missense possibly damaging 0.92
R5079:Vmn1r87 UTSW 7 12,866,253 (GRCm39) missense probably benign 0.01
R5125:Vmn1r87 UTSW 7 12,865,792 (GRCm39) missense possibly damaging 0.79
R5178:Vmn1r87 UTSW 7 12,865,792 (GRCm39) missense possibly damaging 0.79
R6599:Vmn1r87 UTSW 7 12,865,886 (GRCm39) nonsense probably null
R7067:Vmn1r87 UTSW 7 12,865,849 (GRCm39) missense probably benign 0.02
R7560:Vmn1r87 UTSW 7 12,865,745 (GRCm39) missense probably damaging 1.00
R7574:Vmn1r87 UTSW 7 12,865,613 (GRCm39) missense probably benign 0.01
R7910:Vmn1r87 UTSW 7 12,865,832 (GRCm39) missense probably damaging 1.00
R8040:Vmn1r87 UTSW 7 12,866,086 (GRCm39) missense possibly damaging 0.87
R8220:Vmn1r87 UTSW 7 12,865,427 (GRCm39) missense possibly damaging 0.72
R9690:Vmn1r87 UTSW 7 12,866,263 (GRCm39) missense probably benign 0.01
X0028:Vmn1r87 UTSW 7 12,865,910 (GRCm39) missense possibly damaging 0.52
Posted On 2013-12-09