Incidental Mutation 'IGL03393:Vmn1r10'
ID421141
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r10
Ensembl Gene ENSMUSG00000115181
Gene Namevomeronasal 1 receptor 10
SynonymsV1rc1
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.288) question?
Stock #IGL03393
Quality Score
Status
Chromosome6
Chromosomal Location57109454-57115035 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) T to A at 57114057 bp
ZygosityHeterozygous
Amino Acid Change Tyrosine to Stop codon at position 211 (Y211*)
Ref Sequence ENSEMBL: ENSMUSP00000154213 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000176073] [ENSMUST00000228270]
Predicted Effect probably null
Transcript: ENSMUST00000176073
AA Change: Y211*
SMART Domains Protein: ENSMUSP00000134901
Gene: ENSMUSG00000115181
AA Change: Y211*

DomainStartEndE-ValueType
Pfam:V1R 28 293 4.1e-55 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000228270
AA Change: Y211*
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700113H08Rik A G 10: 87,074,038 probably benign Het
Adamts5 G T 16: 85,868,195 S627Y probably damaging Het
Allc G A 12: 28,560,011 R196C probably damaging Het
Ccdc65 A C 15: 98,720,687 E241A probably benign Het
Dclk3 T C 9: 111,488,673 probably benign Het
Fzd4 T C 7: 89,407,297 V184A probably benign Het
Gfap T A 11: 102,893,257 probably null Het
Gpr149 A G 3: 62,603,945 V211A probably benign Het
Gprc6a A G 10: 51,615,259 I623T probably damaging Het
Gucy2c T C 6: 136,719,667 T687A probably benign Het
Kcnc4 T G 3: 107,447,927 M402L possibly damaging Het
Ktn1 T C 14: 47,690,934 L584S probably damaging Het
Mrgprb2 C T 7: 48,552,902 S25N probably benign Het
Muc5b T A 7: 141,864,138 V3607E probably benign Het
Olfr48 C A 2: 89,844,569 V135L probably benign Het
Olfr803 T C 10: 129,691,278 I254M probably damaging Het
Otx2 A G 14: 48,661,324 I75T probably damaging Het
Pabpc4l T C 3: 46,446,537 D224G probably damaging Het
Peg3 A T 7: 6,707,649 C1525S probably damaging Het
Polq A T 16: 37,044,794 L669F probably damaging Het
Prss40 A C 1: 34,558,101 V122G probably damaging Het
Rims2 A G 15: 39,462,613 probably null Het
Rrp12 A T 19: 41,871,793 M997K possibly damaging Het
Sbno2 G A 10: 80,066,901 R414W probably damaging Het
Scn1a T C 2: 66,318,018 D41G probably benign Het
Serpinb1c A T 13: 32,882,061 D300E probably damaging Het
Timeless G A 10: 128,252,055 D1165N probably damaging Het
Tnpo1 T G 13: 98,888,473 K66N probably damaging Het
Trappc11 A T 8: 47,510,877 N629K possibly damaging Het
Ubr4 T A 4: 139,452,678 L255M probably damaging Het
Vmn2r76 T G 7: 86,229,826 N422T probably benign Het
Xylt1 C A 7: 117,593,713 N415K probably damaging Het
Zfp786 A T 6: 47,821,524 V160E possibly damaging Het
Other mutations in Vmn1r10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01062:Vmn1r10 APN 6 57113836 missense possibly damaging 0.70
IGL03255:Vmn1r10 APN 6 57113926 missense probably benign 0.05
R0310:Vmn1r10 UTSW 6 57113501 missense probably damaging 0.97
R2271:Vmn1r10 UTSW 6 57114103 missense probably damaging 1.00
R2411:Vmn1r10 UTSW 6 57114139 missense probably benign 0.14
R3700:Vmn1r10 UTSW 6 57114302 missense probably benign 0.05
R3731:Vmn1r10 UTSW 6 57113734 missense probably damaging 0.99
R4805:Vmn1r10 UTSW 6 57113617 missense possibly damaging 0.94
R4922:Vmn1r10 UTSW 6 57113826 missense probably damaging 0.99
R5697:Vmn1r10 UTSW 6 57113489 missense probably damaging 1.00
R5936:Vmn1r10 UTSW 6 57114317 missense probably benign 0.01
R6119:Vmn1r10 UTSW 6 57114233 missense probably benign 0.01
R7107:Vmn1r10 UTSW 6 57113630 missense possibly damaging 0.90
R7531:Vmn1r10 UTSW 6 57113939 missense possibly damaging 0.90
R7635:Vmn1r10 UTSW 6 57114041 missense probably benign 0.00
R7860:Vmn1r10 UTSW 6 57113701 missense probably benign 0.19
R7943:Vmn1r10 UTSW 6 57113701 missense probably benign 0.19
Posted On2016-08-02