Incidental Mutation 'IGL02485:Vmn2r60'
ID 295393
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r60
Ensembl Gene ENSMUSG00000090619
Gene Name vomeronasal 2, receptor 60
Synonyms Casr-rs3, EG637898, Gprc2a-rs3
Accession Numbers
Essential gene? Probably non essential (E-score: 0.100) question?
Stock # IGL02485
Quality Score
Status
Chromosome 7
Chromosomal Location 41765895-41845200 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 41844890 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Asparagine at position 751 (T751N)
Ref Sequence ENSEMBL: ENSMUSP00000128493 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000166447]
AlphaFold A0A3B2WBC8
Predicted Effect possibly damaging
Transcript: ENSMUST00000166447
AA Change: T751N

PolyPhen 2 Score 0.543 (Sensitivity: 0.88; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000128493
Gene: ENSMUSG00000090619
AA Change: T751N

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 78 471 1.2e-44 PFAM
Pfam:NCD3G 514 567 5.1e-23 PFAM
Pfam:7tm_3 600 835 1.4e-51 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 25 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agl A G 3: 116,572,729 (GRCm39) S841P probably benign Het
Cd59b A C 2: 103,911,449 (GRCm39) probably benign Het
Dop1b T C 16: 93,567,710 (GRCm39) L1379P probably damaging Het
Ercc2 G A 7: 19,127,970 (GRCm39) A433T possibly damaging Het
Gm17175 T C 14: 51,807,068 (GRCm39) probably benign Het
Gm5150 A T 3: 16,044,916 (GRCm39) I103N probably damaging Het
Igf1 A G 10: 87,700,608 (GRCm39) M11V probably benign Het
Incenp T C 19: 9,870,732 (GRCm39) N299S unknown Het
Maneal A T 4: 124,750,563 (GRCm39) S398T probably damaging Het
Map1a A G 2: 121,129,769 (GRCm39) N195S probably damaging Het
Mars2 T C 1: 55,276,750 (GRCm39) F118L possibly damaging Het
Mast4 A G 13: 102,872,004 (GRCm39) S2263P probably benign Het
Mrgprb1 C A 7: 48,097,465 (GRCm39) R149L possibly damaging Het
Myo1d T C 11: 80,557,407 (GRCm39) D511G probably damaging Het
Ntan1 T C 16: 13,652,540 (GRCm39) probably benign Het
Nxf2 A G X: 133,857,216 (GRCm39) F158L probably damaging Het
Odr4 A G 1: 150,239,240 (GRCm39) probably null Het
Or10g3b T A 14: 52,587,501 (GRCm39) M1L possibly damaging Het
Potefam1 A T 2: 111,058,670 (GRCm39) V94E probably damaging Het
Trpm1 C T 7: 63,918,862 (GRCm39) A734V possibly damaging Het
Upf2 G A 2: 6,032,102 (GRCm39) E883K unknown Het
Ush1c T C 7: 45,878,674 (GRCm39) I83V probably damaging Het
Zfp146 A G 7: 29,862,015 (GRCm39) I9T probably benign Het
Zfp592 G A 7: 80,687,718 (GRCm39) probably benign Het
Zswim8 C T 14: 20,761,955 (GRCm39) L243F probably damaging Het
Other mutations in Vmn2r60
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01622:Vmn2r60 APN 7 41,785,910 (GRCm39) missense probably benign 0.09
IGL01623:Vmn2r60 APN 7 41,785,910 (GRCm39) missense probably benign 0.09
IGL02363:Vmn2r60 APN 7 41,844,578 (GRCm39) missense probably benign 0.02
IGL02651:Vmn2r60 APN 7 41,845,010 (GRCm39) missense probably damaging 0.99
IGL02660:Vmn2r60 APN 7 41,791,720 (GRCm39) nonsense probably null
IGL03135:Vmn2r60 APN 7 41,786,018 (GRCm39) missense probably benign 0.13
IGL03307:Vmn2r60 APN 7 41,765,971 (GRCm39) missense probably benign 0.14
R0310:Vmn2r60 UTSW 7 41,844,564 (GRCm39) missense possibly damaging 0.54
R0314:Vmn2r60 UTSW 7 41,784,985 (GRCm39) splice site probably benign
R0328:Vmn2r60 UTSW 7 41,791,744 (GRCm39) splice site probably benign
R0464:Vmn2r60 UTSW 7 41,785,255 (GRCm39) missense probably damaging 0.99
R0755:Vmn2r60 UTSW 7 41,844,869 (GRCm39) missense probably damaging 1.00
R1119:Vmn2r60 UTSW 7 41,844,365 (GRCm39) missense possibly damaging 0.68
R1162:Vmn2r60 UTSW 7 41,845,195 (GRCm39) missense probably benign 0.29
R1241:Vmn2r60 UTSW 7 41,786,476 (GRCm39) missense probably benign 0.01
R1404:Vmn2r60 UTSW 7 41,786,211 (GRCm39) missense probably damaging 0.99
R1404:Vmn2r60 UTSW 7 41,786,211 (GRCm39) missense probably damaging 0.99
R1488:Vmn2r60 UTSW 7 41,786,137 (GRCm39) missense probably benign 0.17
R1623:Vmn2r60 UTSW 7 41,785,279 (GRCm39) nonsense probably null
R1628:Vmn2r60 UTSW 7 41,785,830 (GRCm39) nonsense probably null
R1883:Vmn2r60 UTSW 7 41,786,094 (GRCm39) missense probably damaging 0.99
R1884:Vmn2r60 UTSW 7 41,786,094 (GRCm39) missense probably damaging 0.99
R2182:Vmn2r60 UTSW 7 41,844,931 (GRCm39) missense probably benign 0.06
R2275:Vmn2r60 UTSW 7 41,786,251 (GRCm39) nonsense probably null
R2847:Vmn2r60 UTSW 7 41,785,857 (GRCm39) missense probably benign 0.07
R2885:Vmn2r60 UTSW 7 41,790,403 (GRCm39) missense possibly damaging 0.91
R2894:Vmn2r60 UTSW 7 41,785,220 (GRCm39) missense probably benign
R2921:Vmn2r60 UTSW 7 41,790,459 (GRCm39) missense probably damaging 0.98
R2922:Vmn2r60 UTSW 7 41,790,459 (GRCm39) missense probably damaging 0.98
R3772:Vmn2r60 UTSW 7 41,765,980 (GRCm39) missense probably benign 0.35
R3820:Vmn2r60 UTSW 7 41,785,125 (GRCm39) missense probably damaging 0.98
R3822:Vmn2r60 UTSW 7 41,785,125 (GRCm39) missense probably damaging 0.98
R3872:Vmn2r60 UTSW 7 41,785,878 (GRCm39) missense probably benign 0.19
R4222:Vmn2r60 UTSW 7 41,765,952 (GRCm39) missense probably benign 0.08
R4223:Vmn2r60 UTSW 7 41,765,952 (GRCm39) missense probably benign 0.08
R4224:Vmn2r60 UTSW 7 41,765,952 (GRCm39) missense probably benign 0.08
R4526:Vmn2r60 UTSW 7 41,844,667 (GRCm39) missense probably damaging 0.96
R4547:Vmn2r60 UTSW 7 41,785,087 (GRCm39) missense probably null 0.54
R4840:Vmn2r60 UTSW 7 41,785,285 (GRCm39) missense probably damaging 1.00
R5173:Vmn2r60 UTSW 7 41,844,935 (GRCm39) missense probably damaging 0.97
R5231:Vmn2r60 UTSW 7 41,786,448 (GRCm39) missense possibly damaging 0.93
R5480:Vmn2r60 UTSW 7 41,785,154 (GRCm39) missense probably damaging 0.98
R5521:Vmn2r60 UTSW 7 41,845,049 (GRCm39) missense probably damaging 0.99
R5834:Vmn2r60 UTSW 7 41,765,932 (GRCm39) missense probably benign 0.17
R6038:Vmn2r60 UTSW 7 41,844,386 (GRCm39) missense probably benign 0.04
R6038:Vmn2r60 UTSW 7 41,844,386 (GRCm39) missense probably benign 0.04
R6112:Vmn2r60 UTSW 7 41,844,847 (GRCm39) missense probably damaging 1.00
R6149:Vmn2r60 UTSW 7 41,786,400 (GRCm39) missense probably damaging 1.00
R6170:Vmn2r60 UTSW 7 41,785,045 (GRCm39) missense possibly damaging 0.94
R6383:Vmn2r60 UTSW 7 41,765,895 (GRCm39) start codon destroyed probably null 0.04
R6811:Vmn2r60 UTSW 7 41,844,310 (GRCm39) missense probably damaging 1.00
R6876:Vmn2r60 UTSW 7 41,785,087 (GRCm39) missense probably null 0.54
R6997:Vmn2r60 UTSW 7 41,791,716 (GRCm39) missense probably benign 0.00
R7040:Vmn2r60 UTSW 7 41,791,666 (GRCm39) missense probably benign 0.00
R7116:Vmn2r60 UTSW 7 41,786,487 (GRCm39) missense probably benign 0.00
R7128:Vmn2r60 UTSW 7 41,844,536 (GRCm39) missense probably damaging 0.96
R7232:Vmn2r60 UTSW 7 41,786,166 (GRCm39) missense possibly damaging 0.83
R7296:Vmn2r60 UTSW 7 41,785,826 (GRCm39) missense probably benign 0.01
R7376:Vmn2r60 UTSW 7 41,844,631 (GRCm39) missense probably damaging 1.00
R7526:Vmn2r60 UTSW 7 41,845,158 (GRCm39) frame shift probably null
R7527:Vmn2r60 UTSW 7 41,845,158 (GRCm39) frame shift probably null
R7528:Vmn2r60 UTSW 7 41,845,158 (GRCm39) frame shift probably null
R7764:Vmn2r60 UTSW 7 41,844,535 (GRCm39) missense probably damaging 0.99
R7843:Vmn2r60 UTSW 7 41,844,511 (GRCm39) missense probably benign 0.00
R8080:Vmn2r60 UTSW 7 41,790,521 (GRCm39) missense probably benign 0.30
R8290:Vmn2r60 UTSW 7 41,791,690 (GRCm39) missense probably damaging 1.00
R8342:Vmn2r60 UTSW 7 41,790,494 (GRCm39) missense possibly damaging 0.63
R8362:Vmn2r60 UTSW 7 41,844,954 (GRCm39) missense probably damaging 1.00
R8418:Vmn2r60 UTSW 7 41,844,850 (GRCm39) missense probably damaging 0.97
R8848:Vmn2r60 UTSW 7 41,786,169 (GRCm39) missense probably damaging 1.00
R8860:Vmn2r60 UTSW 7 41,791,654 (GRCm39) missense probably damaging 0.99
R8882:Vmn2r60 UTSW 7 41,790,518 (GRCm39) missense probably benign 0.00
R8913:Vmn2r60 UTSW 7 41,785,778 (GRCm39) missense probably benign 0.27
R9190:Vmn2r60 UTSW 7 41,844,935 (GRCm39) missense probably damaging 0.99
R9229:Vmn2r60 UTSW 7 41,791,723 (GRCm39) missense possibly damaging 0.95
R9295:Vmn2r60 UTSW 7 41,785,955 (GRCm39) missense probably benign 0.01
R9335:Vmn2r60 UTSW 7 41,844,332 (GRCm39) missense probably damaging 1.00
R9796:Vmn2r60 UTSW 7 41,785,172 (GRCm39) missense probably benign
RF024:Vmn2r60 UTSW 7 41,790,363 (GRCm39) missense probably benign 0.01
X0023:Vmn2r60 UTSW 7 41,790,538 (GRCm39) missense probably benign 0.01
Posted On 2015-04-16