Incidental Mutation 'IGL00962:Vmn2r97'
ID 29323
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r97
Ensembl Gene ENSMUSG00000091491
Gene Name vomeronasal 2, receptor 97
Synonyms EG627367
Accession Numbers
Essential gene? Probably non essential (E-score: 0.071) question?
Stock # IGL00962
Quality Score
Status
Chromosome 17
Chromosomal Location 19134584-19168333 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 19149490 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 293 (T293A)
Ref Sequence ENSEMBL: ENSMUSP00000156141 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000168710] [ENSMUST00000232219]
AlphaFold K7N6Z2
Predicted Effect probably damaging
Transcript: ENSMUST00000168710
AA Change: T293A

PolyPhen 2 Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000129313
Gene: ENSMUSG00000091491
AA Change: T293A

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Pfam:ANF_receptor 82 442 2.9e-36 PFAM
Pfam:NCD3G 513 566 4.9e-21 PFAM
Pfam:7tm_3 599 834 1.7e-52 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000232219
AA Change: T293A

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000232325
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 21 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Afg3l2 C T 18: 67,564,723 (GRCm39) probably null Het
Atp8b1 C T 18: 64,664,515 (GRCm39) A1218T probably damaging Het
AY761185 T C 8: 21,434,611 (GRCm39) D39G possibly damaging Het
Fam167a G A 14: 63,699,904 (GRCm39) E155K probably damaging Het
Fat3 C T 9: 15,826,815 (GRCm39) G4379D probably benign Het
Fkbp10 A G 11: 100,312,643 (GRCm39) T300A probably benign Het
Gm6665 T C 18: 31,953,204 (GRCm39) K57R probably benign Het
Gnb4 T C 3: 32,647,318 (GRCm39) T86A probably benign Het
H2-Q2 A G 17: 35,561,825 (GRCm39) Y105C probably damaging Het
Ighv1-75 A G 12: 115,797,883 (GRCm39) probably benign Het
Ilvbl A G 10: 78,419,172 (GRCm39) T474A possibly damaging Het
Shld2 A T 14: 33,971,208 (GRCm39) V559E probably damaging Het
Slc45a3 T A 1: 131,905,265 (GRCm39) V96D probably damaging Het
Tmtc3 C T 10: 100,307,815 (GRCm39) G201R probably damaging Het
Tnfsf14 G A 17: 57,499,906 (GRCm39) Q83* probably null Het
Trpm2 A G 10: 77,779,750 (GRCm39) probably benign Het
Ubr5 A T 15: 37,986,178 (GRCm39) F2219I probably damaging Het
Utrn C T 10: 12,357,078 (GRCm39) V2747I possibly damaging Het
Vcan T C 13: 89,810,171 (GRCm39) N3207D probably damaging Het
Vmn1r35 A G 6: 66,656,361 (GRCm39) V103A possibly damaging Het
Wdr35 A G 12: 9,071,726 (GRCm39) probably benign Het
Other mutations in Vmn2r97
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00897:Vmn2r97 APN 17 19,167,921 (GRCm39) missense probably benign 0.37
IGL01704:Vmn2r97 APN 17 19,168,073 (GRCm39) missense probably damaging 0.99
IGL01888:Vmn2r97 APN 17 19,149,286 (GRCm39) nonsense probably null
IGL02429:Vmn2r97 APN 17 19,150,596 (GRCm39) missense possibly damaging 0.94
IGL02742:Vmn2r97 APN 17 19,149,432 (GRCm39) missense probably damaging 0.97
IGL02934:Vmn2r97 APN 17 19,149,947 (GRCm39) missense probably benign 0.00
IGL02978:Vmn2r97 APN 17 19,168,298 (GRCm39) missense probably benign 0.01
IGL03230:Vmn2r97 APN 17 19,149,668 (GRCm39) missense probably benign 0.10
IGL03241:Vmn2r97 APN 17 19,148,438 (GRCm39) missense probably benign 0.11
IGL03050:Vmn2r97 UTSW 17 19,167,900 (GRCm39) missense possibly damaging 0.84
PIT4469001:Vmn2r97 UTSW 17 19,149,878 (GRCm39) missense probably benign 0.00
R0482:Vmn2r97 UTSW 17 19,167,930 (GRCm39) missense probably damaging 1.00
R0514:Vmn2r97 UTSW 17 19,134,734 (GRCm39) missense probably benign 0.25
R0944:Vmn2r97 UTSW 17 19,167,665 (GRCm39) missense probably benign 0.13
R1061:Vmn2r97 UTSW 17 19,148,440 (GRCm39) nonsense probably null
R1546:Vmn2r97 UTSW 17 19,168,110 (GRCm39) missense probably damaging 1.00
R1725:Vmn2r97 UTSW 17 19,149,397 (GRCm39) missense probably benign 0.43
R1860:Vmn2r97 UTSW 17 19,167,648 (GRCm39) missense probably benign 0.01
R1938:Vmn2r97 UTSW 17 19,149,593 (GRCm39) missense probably benign 0.01
R1944:Vmn2r97 UTSW 17 19,160,500 (GRCm39) missense probably benign 0.00
R2027:Vmn2r97 UTSW 17 19,149,944 (GRCm39) missense unknown
R2106:Vmn2r97 UTSW 17 19,168,100 (GRCm39) missense probably damaging 1.00
R2151:Vmn2r97 UTSW 17 19,167,584 (GRCm39) nonsense probably null
R2153:Vmn2r97 UTSW 17 19,167,584 (GRCm39) nonsense probably null
R2154:Vmn2r97 UTSW 17 19,167,584 (GRCm39) nonsense probably null
R2516:Vmn2r97 UTSW 17 19,167,814 (GRCm39) missense probably benign
R3739:Vmn2r97 UTSW 17 19,148,413 (GRCm39) missense probably damaging 1.00
R3744:Vmn2r97 UTSW 17 19,149,890 (GRCm39) missense probably benign
R3885:Vmn2r97 UTSW 17 19,148,596 (GRCm39) missense possibly damaging 0.90
R3899:Vmn2r97 UTSW 17 19,167,873 (GRCm39) missense probably damaging 0.96
R4115:Vmn2r97 UTSW 17 19,148,332 (GRCm39) missense probably benign 0.01
R4247:Vmn2r97 UTSW 17 19,167,542 (GRCm39) missense possibly damaging 0.83
R4287:Vmn2r97 UTSW 17 19,168,337 (GRCm39) intron probably benign
R4439:Vmn2r97 UTSW 17 19,150,616 (GRCm39) missense probably benign 0.00
R4523:Vmn2r97 UTSW 17 19,149,333 (GRCm39) missense probably benign 0.03
R4783:Vmn2r97 UTSW 17 19,149,550 (GRCm39) missense probably benign
R4948:Vmn2r97 UTSW 17 19,167,561 (GRCm39) missense possibly damaging 0.95
R4981:Vmn2r97 UTSW 17 19,160,436 (GRCm39) nonsense probably null
R5029:Vmn2r97 UTSW 17 19,168,173 (GRCm39) missense probably damaging 1.00
R5200:Vmn2r97 UTSW 17 19,148,615 (GRCm39) missense probably damaging 1.00
R5541:Vmn2r97 UTSW 17 19,148,617 (GRCm39) nonsense probably null
R5637:Vmn2r97 UTSW 17 19,167,628 (GRCm39) nonsense probably null
R5765:Vmn2r97 UTSW 17 19,167,442 (GRCm39) nonsense probably null
R5885:Vmn2r97 UTSW 17 19,168,035 (GRCm39) missense possibly damaging 0.50
R6272:Vmn2r97 UTSW 17 19,167,861 (GRCm39) missense possibly damaging 0.70
R6553:Vmn2r97 UTSW 17 19,150,566 (GRCm39) nonsense probably null
R6818:Vmn2r97 UTSW 17 19,168,193 (GRCm39) missense possibly damaging 0.95
R6880:Vmn2r97 UTSW 17 19,134,770 (GRCm39) missense probably benign 0.00
R7012:Vmn2r97 UTSW 17 19,167,756 (GRCm39) missense probably damaging 0.99
R7023:Vmn2r97 UTSW 17 19,134,663 (GRCm39) missense probably damaging 1.00
R7044:Vmn2r97 UTSW 17 19,134,629 (GRCm39) missense probably benign 0.05
R7191:Vmn2r97 UTSW 17 19,150,548 (GRCm39) missense probably damaging 1.00
R7503:Vmn2r97 UTSW 17 19,148,470 (GRCm39) missense probably benign
R7862:Vmn2r97 UTSW 17 19,167,416 (GRCm39) missense probably damaging 1.00
R7876:Vmn2r97 UTSW 17 19,149,326 (GRCm39) missense probably damaging 0.97
R7890:Vmn2r97 UTSW 17 19,149,802 (GRCm39) missense probably benign 0.00
R7936:Vmn2r97 UTSW 17 19,150,662 (GRCm39) missense probably damaging 1.00
R7978:Vmn2r97 UTSW 17 19,167,854 (GRCm39) missense probably damaging 1.00
R8405:Vmn2r97 UTSW 17 19,134,802 (GRCm39) critical splice donor site probably null
R8755:Vmn2r97 UTSW 17 19,168,104 (GRCm39) missense probably damaging 1.00
R8790:Vmn2r97 UTSW 17 19,160,472 (GRCm39) missense probably damaging 1.00
R8850:Vmn2r97 UTSW 17 19,149,607 (GRCm39) missense probably benign 0.00
R9060:Vmn2r97 UTSW 17 19,134,585 (GRCm39) start codon destroyed probably null 0.94
R9079:Vmn2r97 UTSW 17 19,149,640 (GRCm39) missense probably benign
R9252:Vmn2r97 UTSW 17 19,167,849 (GRCm39) missense probably benign 0.00
R9278:Vmn2r97 UTSW 17 19,134,762 (GRCm39) missense probably benign 0.00
R9342:Vmn2r97 UTSW 17 19,149,368 (GRCm39) missense probably benign
R9422:Vmn2r97 UTSW 17 19,149,333 (GRCm39) missense probably benign 0.03
R9496:Vmn2r97 UTSW 17 19,149,227 (GRCm39) missense probably damaging 1.00
R9571:Vmn2r97 UTSW 17 19,149,919 (GRCm39) missense probably benign
R9601:Vmn2r97 UTSW 17 19,134,770 (GRCm39) missense probably benign
R9672:Vmn2r97 UTSW 17 19,149,442 (GRCm39) missense probably benign 0.00
R9773:Vmn2r97 UTSW 17 19,168,221 (GRCm39) missense probably benign 0.01
R9795:Vmn2r97 UTSW 17 19,167,561 (GRCm39) missense probably damaging 1.00
Posted On 2013-04-17