Incidental Mutation 'IGL03337:Vmn2r58'
ID 417059
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r58
Ensembl Gene ENSMUSG00000090383
Gene Name vomeronasal 2, receptor 58
Synonyms EG628422
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.377) question?
Stock # IGL03337
Quality Score
Status
Chromosome 7
Chromosomal Location 41486305-41522094 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 41513810 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 278 (I278F)
Ref Sequence ENSEMBL: ENSMUSP00000126966 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000171671]
AlphaFold K7N6V2
Predicted Effect possibly damaging
Transcript: ENSMUST00000171671
AA Change: I278F

PolyPhen 2 Score 0.928 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000126966
Gene: ENSMUSG00000090383
AA Change: I278F

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 77 471 8e-43 PFAM
Pfam:NCD3G 514 567 1.8e-23 PFAM
Pfam:7tm_3 597 835 2.9e-52 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 22 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca15 A G 7: 119,995,930 (GRCm39) I1356V probably benign Het
Akr1b8 T C 6: 34,331,209 (GRCm39) I15T probably benign Het
Arrdc3 G A 13: 81,038,766 (GRCm39) V23I probably benign Het
Bmp6 G A 13: 38,682,919 (GRCm39) V470I probably damaging Het
Cltc A T 11: 86,594,509 (GRCm39) I1476N possibly damaging Het
Dclk2 A C 3: 86,813,366 (GRCm39) I193M probably damaging Het
Dnah5 A G 15: 28,290,287 (GRCm39) M1226V probably benign Het
Firrm A G 1: 163,818,328 (GRCm39) S38P probably damaging Het
Gm6455 A G 5: 10,917,251 (GRCm39) noncoding transcript Het
Igkv4-62 A T 6: 69,376,946 (GRCm39) W68R probably damaging Het
Lbr C T 1: 181,659,788 (GRCm39) G136R possibly damaging Het
Ldhb C T 6: 142,439,882 (GRCm39) M219I probably benign Het
Lysmd2 A G 9: 75,542,945 (GRCm39) D184G probably damaging Het
Nrxn3 T A 12: 89,221,790 (GRCm39) M150K probably damaging Het
Pdss2 T C 10: 43,221,589 (GRCm39) V167A probably damaging Het
Scn7a A T 2: 66,506,304 (GRCm39) D1528E probably benign Het
Thsd7a C T 6: 12,405,173 (GRCm39) C757Y probably damaging Het
Tmem213 T C 6: 38,086,478 (GRCm39) probably null Het
Trip11 A G 12: 101,851,278 (GRCm39) S929P probably damaging Het
Utp20 T A 10: 88,590,428 (GRCm39) M2349L probably benign Het
Vmn2r61 A G 7: 41,916,509 (GRCm39) N374S possibly damaging Het
Vps8 A G 16: 21,381,918 (GRCm39) T1089A probably benign Het
Other mutations in Vmn2r58
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00089:Vmn2r58 APN 7 41,513,854 (GRCm39) missense possibly damaging 0.53
IGL00924:Vmn2r58 APN 7 41,486,891 (GRCm39) missense probably damaging 1.00
IGL01291:Vmn2r58 APN 7 41,513,935 (GRCm39) missense probably benign 0.02
IGL01480:Vmn2r58 APN 7 41,514,116 (GRCm39) missense probably benign 0.01
IGL01551:Vmn2r58 APN 7 41,514,703 (GRCm39) missense probably damaging 0.97
IGL01591:Vmn2r58 APN 7 41,514,753 (GRCm39) missense probably benign 0.03
IGL01940:Vmn2r58 APN 7 41,487,071 (GRCm39) missense probably benign 0.00
IGL01994:Vmn2r58 APN 7 41,486,394 (GRCm39) missense probably damaging 0.98
IGL02041:Vmn2r58 APN 7 41,514,703 (GRCm39) missense probably damaging 0.97
IGL02222:Vmn2r58 APN 7 41,513,449 (GRCm39) missense possibly damaging 0.81
IGL02317:Vmn2r58 APN 7 41,486,765 (GRCm39) missense possibly damaging 0.89
IGL02614:Vmn2r58 APN 7 41,486,553 (GRCm39) missense probably damaging 1.00
IGL02673:Vmn2r58 APN 7 41,514,082 (GRCm39) missense possibly damaging 0.90
IGL03323:Vmn2r58 APN 7 41,511,295 (GRCm39) missense probably benign 0.06
IGL03380:Vmn2r58 APN 7 41,513,874 (GRCm39) missense probably benign 0.00
ANU05:Vmn2r58 UTSW 7 41,513,935 (GRCm39) missense probably benign 0.02
R0138:Vmn2r58 UTSW 7 41,487,048 (GRCm39) missense probably damaging 1.00
R0141:Vmn2r58 UTSW 7 41,511,309 (GRCm39) missense probably benign 0.11
R0421:Vmn2r58 UTSW 7 41,514,628 (GRCm39) missense probably benign 0.02
R0604:Vmn2r58 UTSW 7 41,510,000 (GRCm39) missense possibly damaging 0.78
R0854:Vmn2r58 UTSW 7 41,486,562 (GRCm39) missense probably damaging 1.00
R1413:Vmn2r58 UTSW 7 41,513,387 (GRCm39) missense probably benign 0.01
R1441:Vmn2r58 UTSW 7 41,486,864 (GRCm39) missense probably damaging 1.00
R1678:Vmn2r58 UTSW 7 41,513,480 (GRCm39) missense probably benign 0.40
R1691:Vmn2r58 UTSW 7 41,486,913 (GRCm39) missense possibly damaging 0.95
R1699:Vmn2r58 UTSW 7 41,509,951 (GRCm39) missense probably benign
R1865:Vmn2r58 UTSW 7 41,486,682 (GRCm39) missense possibly damaging 0.95
R2008:Vmn2r58 UTSW 7 41,509,924 (GRCm39) missense probably damaging 1.00
R2036:Vmn2r58 UTSW 7 41,513,417 (GRCm39) missense probably benign
R2202:Vmn2r58 UTSW 7 41,513,594 (GRCm39) missense probably benign 0.07
R3787:Vmn2r58 UTSW 7 41,513,498 (GRCm39) missense probably benign 0.01
R3883:Vmn2r58 UTSW 7 41,513,914 (GRCm39) nonsense probably null
R3944:Vmn2r58 UTSW 7 41,513,885 (GRCm39) missense probably benign 0.03
R3949:Vmn2r58 UTSW 7 41,513,348 (GRCm39) missense probably benign 0.08
R4232:Vmn2r58 UTSW 7 41,487,011 (GRCm39) missense possibly damaging 0.91
R4409:Vmn2r58 UTSW 7 41,522,051 (GRCm39) missense possibly damaging 0.69
R4411:Vmn2r58 UTSW 7 41,511,360 (GRCm39) missense possibly damaging 0.85
R4413:Vmn2r58 UTSW 7 41,511,360 (GRCm39) missense possibly damaging 0.85
R4600:Vmn2r58 UTSW 7 41,522,046 (GRCm39) missense probably benign 0.03
R4610:Vmn2r58 UTSW 7 41,487,117 (GRCm39) missense probably benign
R4646:Vmn2r58 UTSW 7 41,509,935 (GRCm39) missense probably damaging 0.96
R4793:Vmn2r58 UTSW 7 41,514,495 (GRCm39) missense probably damaging 0.99
R4870:Vmn2r58 UTSW 7 41,486,639 (GRCm39) missense possibly damaging 0.76
R4981:Vmn2r58 UTSW 7 41,486,885 (GRCm39) missense probably damaging 1.00
R4993:Vmn2r58 UTSW 7 41,487,176 (GRCm39) missense probably benign 0.00
R5024:Vmn2r58 UTSW 7 41,513,746 (GRCm39) missense probably damaging 0.99
R5064:Vmn2r58 UTSW 7 41,486,534 (GRCm39) missense probably damaging 0.99
R5330:Vmn2r58 UTSW 7 41,513,384 (GRCm39) nonsense probably null
R5526:Vmn2r58 UTSW 7 41,522,069 (GRCm39) missense probably benign 0.01
R5980:Vmn2r58 UTSW 7 41,514,480 (GRCm39) missense possibly damaging 0.81
R6163:Vmn2r58 UTSW 7 41,486,825 (GRCm39) missense probably benign 0.31
R6365:Vmn2r58 UTSW 7 41,513,607 (GRCm39) missense probably benign 0.42
R6567:Vmn2r58 UTSW 7 41,514,673 (GRCm39) missense probably benign 0.34
R6594:Vmn2r58 UTSW 7 41,486,535 (GRCm39) missense possibly damaging 0.69
R6980:Vmn2r58 UTSW 7 41,513,662 (GRCm39) missense possibly damaging 0.64
R7373:Vmn2r58 UTSW 7 41,487,212 (GRCm39) missense probably damaging 1.00
R7458:Vmn2r58 UTSW 7 41,487,123 (GRCm39) missense probably benign 0.06
R7630:Vmn2r58 UTSW 7 41,513,611 (GRCm39) missense probably damaging 0.99
R7807:Vmn2r58 UTSW 7 41,521,910 (GRCm39) missense probably benign 0.05
R8114:Vmn2r58 UTSW 7 41,511,392 (GRCm39) missense probably damaging 1.00
R8232:Vmn2r58 UTSW 7 41,514,076 (GRCm39) missense probably damaging 0.97
R8313:Vmn2r58 UTSW 7 41,521,952 (GRCm39) missense probably benign 0.01
R8412:Vmn2r58 UTSW 7 41,513,722 (GRCm39) missense probably benign 0.01
R8530:Vmn2r58 UTSW 7 41,513,576 (GRCm39) missense probably damaging 1.00
R8851:Vmn2r58 UTSW 7 41,487,219 (GRCm39) missense probably benign
R8881:Vmn2r58 UTSW 7 41,486,609 (GRCm39) missense probably benign 0.05
R8936:Vmn2r58 UTSW 7 41,513,981 (GRCm39) missense
R9045:Vmn2r58 UTSW 7 41,487,087 (GRCm39) missense probably benign 0.00
R9166:Vmn2r58 UTSW 7 41,513,431 (GRCm39) missense probably damaging 1.00
R9706:Vmn2r58 UTSW 7 41,510,000 (GRCm39) missense probably damaging 0.99
RF006:Vmn2r58 UTSW 7 41,486,383 (GRCm39) frame shift probably null
RF027:Vmn2r58 UTSW 7 41,486,383 (GRCm39) frame shift probably null
Z1176:Vmn2r58 UTSW 7 41,513,789 (GRCm39) missense probably benign 0.01
Posted On 2016-08-02