Incidental Mutation 'IGL01410:Vmn1r192'
ID 79953
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r192
Ensembl Gene ENSMUSG00000099787
Gene Name vomeronasal 1 receptor 192
Synonyms V1ri1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.065) question?
Stock # IGL01410
Quality Score
Status
Chromosome 13
Chromosomal Location 22371316-22372218 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 22372079 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Proline at position 47 (L47P)
Ref Sequence ENSEMBL: ENSMUSP00000072426 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072632]
AlphaFold Q8K4C9
Predicted Effect probably damaging
Transcript: ENSMUST00000072632
AA Change: L47P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000072426
Gene: ENSMUSG00000099787
AA Change: L47P

DomainStartEndE-ValueType
Pfam:TAS2R 1 293 2.6e-10 PFAM
Pfam:V1R 37 299 1.1e-35 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aox1 T A 1: 58,145,184 (GRCm39) probably null Het
Aspm C T 1: 139,410,182 (GRCm39) T1359I probably benign Het
Atp13a2 A G 4: 140,719,509 (GRCm39) D26G probably benign Het
Atrnl1 G A 19: 58,119,536 (GRCm39) A1343T probably damaging Het
Ccsap A C 8: 124,585,969 (GRCm39) S61A probably damaging Het
Cdh1 A T 8: 107,384,485 (GRCm39) M318L probably benign Het
Cfap69 G A 5: 5,696,979 (GRCm39) P106S probably damaging Het
Cfp G A X: 20,795,963 (GRCm39) T88I probably damaging Het
Chst1 A T 2: 92,444,475 (GRCm39) I316F probably damaging Het
Col7a1 A T 9: 108,793,686 (GRCm39) D1382V unknown Het
Cr2 T A 1: 194,845,542 (GRCm39) M514L possibly damaging Het
Cubn G A 2: 13,470,719 (GRCm39) H558Y probably benign Het
Cul9 A T 17: 46,839,572 (GRCm39) M802K probably damaging Het
Dennd2d A T 3: 106,398,542 (GRCm39) I169L probably damaging Het
Dnah11 T A 12: 118,010,991 (GRCm39) K162* probably null Het
Dnah3 T A 7: 119,566,943 (GRCm39) T2428S possibly damaging Het
Dock11 T A X: 35,301,296 (GRCm39) H1284Q probably damaging Het
Flrt2 T A 12: 95,745,966 (GRCm39) D101E probably damaging Het
Gabrr2 G A 4: 33,085,626 (GRCm39) V349M probably damaging Het
Gli2 C A 1: 118,764,621 (GRCm39) V1177L probably benign Het
Gm16506 A G 14: 43,961,630 (GRCm39) Y206H probably benign Het
Gm5612 C T 9: 18,338,869 (GRCm39) probably benign Het
Gvin3 C T 7: 106,202,258 (GRCm39) noncoding transcript Het
Heg1 C T 16: 33,545,936 (GRCm39) T460I possibly damaging Het
Lgals9 T G 11: 78,863,977 (GRCm39) D56A probably damaging Het
Lpgat1 A T 1: 191,508,544 (GRCm39) probably null Het
Megf6 T A 4: 154,337,020 (GRCm39) probably null Het
Megf8 G A 7: 25,059,296 (GRCm39) M2265I probably benign Het
Memo1 G A 17: 74,548,976 (GRCm39) R121* probably null Het
Morc1 T C 16: 48,432,677 (GRCm39) V715A probably benign Het
Mycbp2 A T 14: 103,466,928 (GRCm39) probably null Het
Ncapg2 T A 12: 116,388,270 (GRCm39) V318D possibly damaging Het
Ndst1 T C 18: 60,833,517 (GRCm39) Y498C probably damaging Het
Nod1 C T 6: 54,921,341 (GRCm39) A326T probably damaging Het
Or2ag15 A G 7: 106,340,706 (GRCm39) V145A probably benign Het
Or4c11 T A 2: 88,695,864 (GRCm39) M305K probably benign Het
Peg3 T C 7: 6,710,624 (GRCm39) S1533G probably benign Het
Pgc G T 17: 48,045,165 (GRCm39) G361V probably damaging Het
Phka1 C T X: 101,629,712 (GRCm39) R477H probably damaging Het
Plagl2 C T 2: 153,074,574 (GRCm39) R109Q probably damaging Het
Prr36 T A 8: 4,266,230 (GRCm39) I107F probably benign Het
Ptpdc1 T A 13: 48,740,080 (GRCm39) R450S probably damaging Het
Ptprb A T 10: 116,138,179 (GRCm39) D361V possibly damaging Het
Rbm44 A G 1: 91,096,551 (GRCm39) D970G probably benign Het
Scrn2 T G 11: 96,921,396 (GRCm39) V52G probably benign Het
Sdk1 C T 5: 142,197,875 (GRCm39) T2176I probably benign Het
Serpina1d T A 12: 103,729,993 (GRCm39) E396D probably benign Het
Slc38a5 A C X: 8,146,070 (GRCm39) Q465P probably benign Het
Slc38a5 G T X: 8,146,071 (GRCm39) Q465H probably benign Het
Smarca1 T C X: 46,981,255 (GRCm39) T48A possibly damaging Het
Trak2 A T 1: 58,962,766 (GRCm39) I132N probably damaging Het
Trank1 A G 9: 111,194,117 (GRCm39) T714A probably benign Het
Trank1 T C 9: 111,194,327 (GRCm39) S784P probably benign Het
Trp53i13 G A 11: 77,399,083 (GRCm39) probably benign Het
Trrap A C 5: 144,767,831 (GRCm39) D2596A probably benign Het
Ttyh1 A T 7: 4,127,656 (GRCm39) T19S probably damaging Het
Tyk2 C T 9: 21,020,660 (GRCm39) V947M probably damaging Het
Ugt2b34 G A 5: 87,040,689 (GRCm39) A411V possibly damaging Het
Virma T A 4: 11,518,929 (GRCm39) Y725* probably null Het
Vmn2r74 T C 7: 85,610,500 (GRCm39) D64G possibly damaging Het
Other mutations in Vmn1r192
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01869:Vmn1r192 APN 13 22,371,750 (GRCm39) missense probably damaging 1.00
R0975:Vmn1r192 UTSW 13 22,371,633 (GRCm39) missense probably damaging 1.00
R1751:Vmn1r192 UTSW 13 22,371,441 (GRCm39) missense probably benign 0.08
R1767:Vmn1r192 UTSW 13 22,371,441 (GRCm39) missense probably benign 0.08
R1880:Vmn1r192 UTSW 13 22,371,764 (GRCm39) missense probably benign 0.12
R1881:Vmn1r192 UTSW 13 22,371,764 (GRCm39) missense probably benign 0.12
R2113:Vmn1r192 UTSW 13 22,371,800 (GRCm39) missense possibly damaging 0.67
R4290:Vmn1r192 UTSW 13 22,371,465 (GRCm39) missense probably damaging 1.00
R4292:Vmn1r192 UTSW 13 22,371,465 (GRCm39) missense probably damaging 1.00
R4294:Vmn1r192 UTSW 13 22,371,465 (GRCm39) missense probably damaging 1.00
R4295:Vmn1r192 UTSW 13 22,371,465 (GRCm39) missense probably damaging 1.00
R4921:Vmn1r192 UTSW 13 22,371,650 (GRCm39) missense probably damaging 1.00
R5377:Vmn1r192 UTSW 13 22,371,801 (GRCm39) missense probably benign 0.01
R5569:Vmn1r192 UTSW 13 22,371,384 (GRCm39) missense possibly damaging 0.91
R6181:Vmn1r192 UTSW 13 22,371,452 (GRCm39) missense probably damaging 1.00
R6455:Vmn1r192 UTSW 13 22,372,000 (GRCm39) missense probably benign 0.08
R6860:Vmn1r192 UTSW 13 22,372,122 (GRCm39) missense probably benign
R7246:Vmn1r192 UTSW 13 22,371,944 (GRCm39) missense probably damaging 1.00
R7762:Vmn1r192 UTSW 13 22,371,845 (GRCm39) missense probably damaging 0.97
R8066:Vmn1r192 UTSW 13 22,371,565 (GRCm39) nonsense probably null
R8378:Vmn1r192 UTSW 13 22,372,029 (GRCm39) nonsense probably null
R9075:Vmn1r192 UTSW 13 22,371,333 (GRCm39) missense probably benign
R9206:Vmn1r192 UTSW 13 22,371,401 (GRCm39) missense probably damaging 1.00
R9208:Vmn1r192 UTSW 13 22,371,401 (GRCm39) missense probably damaging 1.00
R9313:Vmn1r192 UTSW 13 22,372,191 (GRCm39) missense probably benign 0.38
R9367:Vmn1r192 UTSW 13 22,371,800 (GRCm39) missense possibly damaging 0.67
R9694:Vmn1r192 UTSW 13 22,372,119 (GRCm39) missense probably benign
R9760:Vmn1r192 UTSW 13 22,372,010 (GRCm39) missense probably damaging 1.00
Posted On 2013-11-05