Incidental Mutation 'IGL02673:Vmn2r58'
ID 303003
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 # IGL02673
Quality Score
Status
Chromosome 7
Chromosomal Location 41486305-41522094 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 41514082 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Phenylalanine at position 187 (Y187F)
Ref Sequence ENSEMBL: ENSMUSP00000126966 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000171671]
AlphaFold K7N6V2
Predicted Effect possibly damaging
Transcript: ENSMUST00000171671
AA Change: Y187F

PolyPhen 2 Score 0.896 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000126966
Gene: ENSMUSG00000090383
AA Change: Y187F

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: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9930012K11Rik T A 14: 70,395,056 (GRCm39) T33S probably benign Het
Abca4 T C 3: 121,897,150 (GRCm39) Y610H probably damaging Het
Agl A T 3: 116,575,248 (GRCm39) C630S probably benign Het
Alkbh6 G T 7: 30,013,536 (GRCm39) G202C probably damaging Het
Ascc3 A T 10: 50,536,769 (GRCm39) M701L probably benign Het
Bpgm T A 6: 34,464,769 (GRCm39) L162Q probably damaging Het
Ccdc150 A G 1: 54,368,149 (GRCm39) T592A probably benign Het
Chpf2 G A 5: 24,796,302 (GRCm39) R416Q probably benign Het
Col14a1 G A 15: 55,282,178 (GRCm39) G813E unknown Het
Col18a1 C T 10: 76,894,997 (GRCm39) G983D probably damaging Het
Col5a1 C T 2: 27,864,727 (GRCm39) A737V unknown Het
Cyp2a22 T G 7: 26,637,525 (GRCm39) K157Q probably benign Het
Dhx57 A G 17: 80,574,974 (GRCm39) V668A probably damaging Het
Eps8l1 T A 7: 4,481,731 (GRCm39) V743E probably damaging Het
Fnbp4 C T 2: 90,593,816 (GRCm39) T557M probably benign Het
Fzd5 C T 1: 64,774,265 (GRCm39) E499K possibly damaging Het
Gm57858 A C 3: 36,100,848 (GRCm39) probably benign Het
Il1r2 A G 1: 40,154,323 (GRCm39) Y230C probably damaging Het
Insrr A C 3: 87,720,368 (GRCm39) E1002A possibly damaging Het
Kdm4a C T 4: 118,025,769 (GRCm39) D146N probably benign Het
Kidins220 G A 12: 25,044,991 (GRCm39) V262M probably damaging Het
Kif26b C T 1: 178,649,170 (GRCm39) P430L probably damaging Het
Mamdc4 T C 2: 25,460,066 (GRCm39) S62G probably benign Het
Mcu C A 10: 59,303,466 (GRCm39) V124F probably damaging Het
Mlf1 A G 3: 67,301,280 (GRCm39) M98V probably benign Het
Mogs T C 6: 83,095,199 (GRCm39) V672A probably damaging Het
Ntrk3 T C 7: 77,900,512 (GRCm39) D609G probably damaging Het
Or1n1 C T 2: 36,750,188 (GRCm39) M57I probably benign Het
Pdlim5 T A 3: 142,058,548 (GRCm39) E65D probably damaging Het
Peg3 T C 7: 6,713,413 (GRCm39) N603S probably damaging Het
Pkd1 A G 17: 24,790,257 (GRCm39) Y980C probably benign Het
Rack1 A G 11: 48,691,357 (GRCm39) T23A probably benign Het
Rad50 A T 11: 53,579,067 (GRCm39) I497K probably benign Het
Sin3a C A 9: 57,014,725 (GRCm39) Q649K probably damaging Het
Sirt6 A G 10: 81,461,671 (GRCm39) F46L probably damaging Het
Slc40a1 A T 1: 45,957,576 (GRCm39) I136N possibly damaging Het
Sspo G A 6: 48,452,794 (GRCm39) R2834H probably damaging Het
Sspo G T 6: 48,475,709 (GRCm39) probably null Het
Sycp2 T A 2: 178,036,004 (GRCm39) T228S possibly damaging Het
Uhrf2 T A 19: 30,070,207 (GRCm39) N785K probably damaging Het
Vmn2r80 A G 10: 79,005,318 (GRCm39) I318M probably benign Het
Vps13c T C 9: 67,785,380 (GRCm39) L249P probably damaging Het
Zw10 T A 9: 48,988,893 (GRCm39) probably null 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
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 2015-04-16