Incidental Mutation 'IGL01480:Vmn2r58'
ID 88569
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 # IGL01480
Quality Score
Status
Chromosome 7
Chromosomal Location 41486305-41522094 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 41514116 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 176 (I176F)
Ref Sequence ENSEMBL: ENSMUSP00000126966 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000171671]
AlphaFold K7N6V2
Predicted Effect probably benign
Transcript: ENSMUST00000171671
AA Change: I176F

PolyPhen 2 Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)
SMART Domains Protein: ENSMUSP00000126966
Gene: ENSMUSG00000090383
AA Change: I176F

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: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adck1 T A 12: 88,423,635 (GRCm39) C379* probably null Het
Ankrd10 A G 8: 11,685,592 (GRCm39) V9A probably benign Het
Ankrd13a A T 5: 114,938,879 (GRCm39) probably benign Het
Bbs1 T C 19: 4,944,421 (GRCm39) K403E probably damaging Het
Ccn3 A G 15: 54,615,687 (GRCm39) Y284C probably damaging Het
Cd200r2 A G 16: 44,729,629 (GRCm39) I95V probably null Het
Cyba T C 8: 123,151,684 (GRCm39) E171G probably benign Het
Dnah2 T A 11: 69,349,197 (GRCm39) M2480L possibly damaging Het
Fxyd7 A T 7: 30,746,799 (GRCm39) Y20* probably null Het
Il22ra1 T C 4: 135,472,112 (GRCm39) V216A probably benign Het
Mapk10 G A 5: 103,074,018 (GRCm39) probably benign Het
Mgat5b C A 11: 116,869,278 (GRCm39) T607K probably benign Het
Optn G A 2: 5,050,829 (GRCm39) S184L probably benign Het
Or10d5 G A 9: 39,861,284 (GRCm39) A261V probably benign Het
Or1j15 T A 2: 36,458,754 (GRCm39) L48H probably damaging Het
Or1p1c A T 11: 74,160,427 (GRCm39) I71L possibly damaging Het
Or7a42 T C 10: 78,791,978 (GRCm39) probably benign Het
Plxna1 A G 6: 89,321,078 (GRCm39) L462P possibly damaging Het
Prkca C T 11: 108,083,027 (GRCm39) V73M probably damaging Het
Prkca A G 11: 107,877,115 (GRCm39) F339L possibly damaging Het
Ptch2 T C 4: 116,971,279 (GRCm39) V1062A probably damaging Het
Serpina11 T A 12: 103,949,110 (GRCm39) K354* probably null Het
Sf1 T C 19: 6,422,052 (GRCm39) probably benign Het
Stam2 A G 2: 52,606,451 (GRCm39) S112P probably benign Het
Tlr5 G A 1: 182,801,064 (GRCm39) E123K probably benign Het
Tpp1 T C 7: 105,398,260 (GRCm39) E301G probably damaging 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
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
IGL03337:Vmn2r58 APN 7 41,513,810 (GRCm39) missense possibly damaging 0.93
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 2013-11-18