Incidental Mutation 'IGL01584:Vmn1r206'
ID 91461
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r206
Ensembl Gene ENSMUSG00000101578
Gene Name vomeronasal 1 receptor 206
Synonyms V1rh7
Accession Numbers
Essential gene? Probably non essential (E-score: 0.075) question?
Stock # IGL01584
Quality Score
Status
Chromosome 13
Chromosomal Location 22804267-22805205 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 22804964 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Arginine at position 81 (K81R)
Ref Sequence ENSEMBL: ENSMUSP00000154713 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000187140] [ENSMUST00000227244]
AlphaFold Q8R277
Predicted Effect probably damaging
Transcript: ENSMUST00000110445
AA Change: K81R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000106075
Gene: ENSMUSG00000071495
AA Change: K81R

DomainStartEndE-ValueType
low complexity region 3 21 N/A INTRINSIC
Pfam:V1R 32 297 6.7e-36 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000119308
Predicted Effect probably damaging
Transcript: ENSMUST00000187140
AA Change: K81R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000139772
Gene: ENSMUSG00000101578
AA Change: K81R

DomainStartEndE-ValueType
low complexity region 3 21 N/A INTRINSIC
Pfam:V1R 32 297 6.7e-36 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000227244
AA Change: K81R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca5 A G 11: 110,195,749 (GRCm39) V570A probably damaging Het
Abcb1a T C 5: 8,748,637 (GRCm39) S323P possibly damaging Het
Adcy8 C T 15: 64,687,170 (GRCm39) D445N probably damaging Het
Cdc14a A T 3: 116,186,474 (GRCm39) Y102* probably null Het
Cubn A G 2: 13,313,472 (GRCm39) probably benign Het
Dcaf7 T C 11: 105,944,653 (GRCm39) S279P probably benign Het
Dock10 T C 1: 80,511,567 (GRCm39) Q1514R probably damaging Het
Dtx2 G A 5: 136,055,420 (GRCm39) S369N possibly damaging Het
Dusp11 A G 6: 85,930,376 (GRCm39) F136S probably damaging Het
Fbxo32 T C 15: 58,047,632 (GRCm39) D227G probably damaging Het
Flg2 T A 3: 93,120,773 (GRCm39) V1215E unknown Het
Flg2 A T 3: 93,122,777 (GRCm39) D1649V unknown Het
Gabbr2 T C 4: 46,674,524 (GRCm39) K821R probably damaging Het
Gga2 T C 7: 121,590,761 (GRCm39) T516A probably benign Het
Gm15446 T A 5: 110,088,668 (GRCm39) *64K probably null Het
Gm5900 T C 7: 104,599,361 (GRCm39) noncoding transcript Het
Il17rb A G 14: 29,725,637 (GRCm39) F121S probably damaging Het
Ip6k3 C A 17: 27,370,034 (GRCm39) R128L probably benign Het
Kmt2d A T 15: 98,754,250 (GRCm39) probably benign Het
Lrrn4 A G 2: 132,719,996 (GRCm39) L268P probably damaging Het
Mthfd1l C A 10: 3,966,738 (GRCm39) S332R probably damaging Het
Or12d12 C T 17: 37,610,629 (GRCm39) R228H probably benign Het
Or5t17 G A 2: 86,832,495 (GRCm39) V61I probably benign Het
Pdzd2 T C 15: 12,592,569 (GRCm39) E25G probably damaging Het
Prima1 A T 12: 103,169,047 (GRCm39) probably null Het
Rbm26 A G 14: 105,368,968 (GRCm39) V737A probably damaging Het
Ryr2 C T 13: 11,616,644 (GRCm39) probably null Het
Sema5b G T 16: 35,465,793 (GRCm39) C114F probably damaging Het
Spata31f1e A C 4: 42,794,014 (GRCm39) S39R probably damaging Het
Speg T C 1: 75,407,581 (GRCm39) V3196A probably damaging Het
Svs3b T C 2: 164,097,943 (GRCm39) Y126C probably benign Het
Tmem171 T C 13: 98,828,683 (GRCm39) probably null Het
Tnrc6b T A 15: 80,763,883 (GRCm39) W462R probably benign Het
Trdmt1 T C 2: 13,524,739 (GRCm39) R239G probably benign Het
Usp5 A T 6: 124,796,350 (GRCm39) V583E probably damaging Het
Utrn A G 10: 12,602,111 (GRCm39) V639A probably benign Het
Vwa3a A G 7: 120,383,197 (GRCm39) I599M probably benign Het
Other mutations in Vmn1r206
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02016:Vmn1r206 APN 13 22,804,334 (GRCm39) missense probably damaging 0.99
IGL02754:Vmn1r206 APN 13 22,805,060 (GRCm39) nonsense probably null
R0317:Vmn1r206 UTSW 13 22,805,130 (GRCm39) missense possibly damaging 0.86
R0570:Vmn1r206 UTSW 13 22,804,583 (GRCm39) missense probably damaging 1.00
R1056:Vmn1r206 UTSW 13 22,804,784 (GRCm39) missense probably benign 0.10
R1497:Vmn1r206 UTSW 13 22,805,160 (GRCm39) missense probably benign 0.23
R2018:Vmn1r206 UTSW 13 22,804,358 (GRCm39) missense probably damaging 1.00
R2128:Vmn1r206 UTSW 13 22,804,782 (GRCm39) missense probably benign 0.09
R2129:Vmn1r206 UTSW 13 22,804,782 (GRCm39) missense probably benign 0.09
R5159:Vmn1r206 UTSW 13 22,804,775 (GRCm39) missense probably damaging 1.00
R7692:Vmn1r206 UTSW 13 22,804,827 (GRCm39) missense probably damaging 1.00
R7763:Vmn1r206 UTSW 13 22,804,839 (GRCm39) missense possibly damaging 0.74
R7910:Vmn1r206 UTSW 13 22,804,471 (GRCm39) nonsense probably null
R9580:Vmn1r206 UTSW 13 22,804,890 (GRCm39) missense probably damaging 1.00
X0026:Vmn1r206 UTSW 13 22,804,724 (GRCm39) missense possibly damaging 0.53
Posted On 2013-12-09