Incidental Mutation 'IGL03143:Vmn1r202'
ID 410752
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r202
Ensembl Gene ENSMUSG00000094379
Gene Name vomeronasal 1 receptor 202
Synonyms V1ri7
Accession Numbers
Essential gene? Probably non essential (E-score: 0.088) question?
Stock # IGL03143
Quality Score
Status
Chromosome 13
Chromosomal Location 22685507-22686415 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 22685640 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Isoleucine at position 259 (T259I)
Ref Sequence ENSEMBL: ENSMUSP00000154314 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078642] [ENSMUST00000228020]
AlphaFold Q8R259
Predicted Effect probably benign
Transcript: ENSMUST00000078642
AA Change: T259I

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000077711
Gene: ENSMUSG00000094379
AA Change: T259I

DomainStartEndE-ValueType
Pfam:TAS2R 5 301 2.2e-11 PFAM
Pfam:V1R 35 300 5.6e-44 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000228020
AA Change: T259I

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ackr2 T G 9: 121,738,333 (GRCm39) L236R probably damaging Het
Agbl1 C T 7: 76,069,793 (GRCm39) Q442* probably null Het
Ahrr G A 13: 74,405,614 (GRCm39) Q108* probably null Het
Ankrd23 T C 1: 36,570,726 (GRCm39) probably benign Het
Art5 A G 7: 101,747,104 (GRCm39) I225T probably damaging Het
Asxl3 T C 18: 22,656,031 (GRCm39) V1347A probably benign Het
Birc6 A G 17: 74,905,994 (GRCm39) M1326V possibly damaging Het
Bpifb6 A C 2: 153,744,655 (GRCm39) N32T probably damaging Het
Brip1 T A 11: 85,952,653 (GRCm39) T1043S possibly damaging Het
Cbx5 A T 15: 103,121,532 (GRCm39) V35E probably damaging Het
Ccdc175 T A 12: 72,182,832 (GRCm39) M396L probably benign Het
Ceacam3 G T 7: 16,892,045 (GRCm39) E263* probably null Het
Cyp4a12a A G 4: 115,159,200 (GRCm39) T157A probably benign Het
Dennd11 A T 6: 40,399,828 (GRCm39) probably benign Het
Derl3 T C 10: 75,730,324 (GRCm39) V129A possibly damaging Het
Dnajb1 T C 8: 84,335,103 (GRCm39) I48T probably damaging Het
Dop1b G A 16: 93,556,543 (GRCm39) E349K probably benign Het
Fkbp10 A T 11: 100,313,580 (GRCm39) I285F probably benign Het
Frrs1 A T 3: 116,692,836 (GRCm39) T37S probably damaging Het
Gata2 A G 6: 88,181,677 (GRCm39) Y377C probably damaging Het
Gm9789 T A 16: 88,954,883 (GRCm39) probably benign Het
Itpkb T A 1: 180,160,933 (GRCm39) V353D probably benign Het
Kcng4 T C 8: 120,352,509 (GRCm39) E467G probably damaging Het
Kdm3a A T 6: 71,573,845 (GRCm39) I906N probably damaging Het
Lama1 G A 17: 68,111,531 (GRCm39) G2261R probably damaging Het
Lamc1 A T 1: 153,208,020 (GRCm39) L89Q probably benign Het
Lef1 G T 3: 130,993,965 (GRCm39) E314* probably null Het
Lpin3 T C 2: 160,745,518 (GRCm39) probably benign Het
Mrtfb A G 16: 13,218,676 (GRCm39) N452D possibly damaging Het
Naaladl1 C T 19: 6,164,896 (GRCm39) T628I possibly damaging Het
Nell1 C T 7: 49,929,281 (GRCm39) Q259* probably null Het
Neu2 G T 1: 87,524,698 (GRCm39) E228* probably null Het
Or5b119 A T 19: 13,456,835 (GRCm39) H242Q probably damaging Het
Or5k15 A G 16: 58,709,824 (GRCm39) F253S probably damaging Het
Or8g21 T G 9: 38,906,732 (GRCm39) probably benign Het
Or8k20 T C 2: 86,106,580 (GRCm39) N84D probably benign Het
Osbpl6 T A 2: 76,378,716 (GRCm39) D124E probably damaging Het
Palm T C 10: 79,652,617 (GRCm39) probably benign Het
Parp8 C A 13: 117,047,497 (GRCm39) probably benign Het
Pax7 A G 4: 139,556,798 (GRCm39) probably benign Het
Pcnx3 G A 19: 5,735,423 (GRCm39) R468W probably damaging Het
Pds5b T A 5: 150,702,722 (GRCm39) V818D probably damaging Het
Piezo2 C T 18: 63,241,147 (GRCm39) V694I probably damaging Het
Plk1 A G 7: 121,760,877 (GRCm39) probably benign Het
Polb T C 8: 23,130,367 (GRCm39) probably benign Het
Rad54b A G 4: 11,599,755 (GRCm39) T320A probably damaging Het
Reg3b G A 6: 78,349,183 (GRCm39) W103* probably null Het
Slc17a3 T G 13: 24,039,962 (GRCm39) probably null Het
Snrnp200 C T 2: 127,071,962 (GRCm39) probably benign Het
Stox2 T A 8: 47,646,839 (GRCm39) H207L possibly damaging Het
Tbx15 A C 3: 99,259,514 (GRCm39) M462L possibly damaging Het
Tcirg1 G A 19: 3,948,811 (GRCm39) T458I probably damaging Het
Tnfrsf25 A G 4: 152,201,384 (GRCm39) probably benign Het
Trank1 A G 9: 111,195,155 (GRCm39) K1060E probably damaging Het
Ttc16 T C 2: 32,664,457 (GRCm39) D3G possibly damaging Het
Vmn1r199 A C 13: 22,567,299 (GRCm39) N155H probably damaging Het
Other mutations in Vmn1r202
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01472:Vmn1r202 APN 13 22,686,159 (GRCm39) missense possibly damaging 0.95
IGL01516:Vmn1r202 APN 13 22,685,632 (GRCm39) missense possibly damaging 0.57
IGL01722:Vmn1r202 APN 13 22,685,890 (GRCm39) missense probably benign 0.00
IGL02641:Vmn1r202 APN 13 22,686,274 (GRCm39) missense probably benign 0.34
IGL02863:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL02876:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL02891:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL02943:Vmn1r202 APN 13 22,686,364 (GRCm39) missense probably benign 0.01
IGL03057:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL03114:Vmn1r202 APN 13 22,685,500 (GRCm39) utr 3 prime probably benign
IGL03114:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL03159:Vmn1r202 APN 13 22,685,640 (GRCm39) missense probably benign 0.00
IGL03097:Vmn1r202 UTSW 13 22,685,640 (GRCm39) missense probably benign 0.00
R0611:Vmn1r202 UTSW 13 22,685,824 (GRCm39) missense probably damaging 1.00
R1350:Vmn1r202 UTSW 13 22,685,886 (GRCm39) missense probably benign 0.04
R1666:Vmn1r202 UTSW 13 22,685,540 (GRCm39) missense possibly damaging 0.94
R1668:Vmn1r202 UTSW 13 22,685,540 (GRCm39) missense possibly damaging 0.94
R1803:Vmn1r202 UTSW 13 22,686,313 (GRCm39) missense probably benign 0.00
R2035:Vmn1r202 UTSW 13 22,685,772 (GRCm39) missense probably damaging 0.98
R2112:Vmn1r202 UTSW 13 22,685,904 (GRCm39) missense possibly damaging 0.76
R2145:Vmn1r202 UTSW 13 22,685,953 (GRCm39) missense possibly damaging 0.79
R3026:Vmn1r202 UTSW 13 22,685,932 (GRCm39) missense probably benign 0.03
R3808:Vmn1r202 UTSW 13 22,686,070 (GRCm39) missense possibly damaging 0.83
R4714:Vmn1r202 UTSW 13 22,685,977 (GRCm39) missense probably damaging 1.00
R5016:Vmn1r202 UTSW 13 22,686,375 (GRCm39) missense probably damaging 1.00
R5124:Vmn1r202 UTSW 13 22,685,920 (GRCm39) missense probably benign 0.01
R6136:Vmn1r202 UTSW 13 22,685,632 (GRCm39) missense possibly damaging 0.90
R6365:Vmn1r202 UTSW 13 22,686,374 (GRCm39) missense probably benign 0.12
R6982:Vmn1r202 UTSW 13 22,685,917 (GRCm39) missense probably benign 0.02
R7293:Vmn1r202 UTSW 13 22,685,872 (GRCm39) missense probably benign 0.00
R7502:Vmn1r202 UTSW 13 22,686,188 (GRCm39) missense probably damaging 1.00
R7603:Vmn1r202 UTSW 13 22,685,790 (GRCm39) missense probably damaging 1.00
R7672:Vmn1r202 UTSW 13 22,685,850 (GRCm39) missense probably benign 0.45
R7822:Vmn1r202 UTSW 13 22,686,241 (GRCm39) missense probably damaging 1.00
R7954:Vmn1r202 UTSW 13 22,685,871 (GRCm39) missense probably benign 0.01
R8026:Vmn1r202 UTSW 13 22,686,314 (GRCm39) missense possibly damaging 0.65
R8419:Vmn1r202 UTSW 13 22,685,985 (GRCm39) missense probably damaging 1.00
R9079:Vmn1r202 UTSW 13 22,685,602 (GRCm39) missense probably benign 0.00
R9194:Vmn1r202 UTSW 13 22,686,316 (GRCm39) missense possibly damaging 0.48
Posted On 2016-08-02