Incidental Mutation 'IGL02682:Vmn2r18'
ID 303400
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r18
Ensembl Gene ENSMUSG00000091794
Gene Name vomeronasal 2, receptor 18
Synonyms EG632671
Accession Numbers
Essential gene? Probably non essential (E-score: 0.082) question?
Stock # IGL02682
Quality Score
Status
Chromosome 5
Chromosomal Location 151485126-151529232 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 151508102 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Asparagine at position 341 (H341N)
Ref Sequence ENSEMBL: ENSMUSP00000127506 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000165928]
AlphaFold A0A3B2WB67
Predicted Effect probably damaging
Transcript: ENSMUST00000165928
AA Change: H341N

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000127506
Gene: ENSMUSG00000091794
AA Change: H341N

DomainStartEndE-ValueType
Pfam:ANF_receptor 1 403 5.7e-39 PFAM
Pfam:NCD3G 446 499 5.5e-20 PFAM
Pfam:7tm_3 531 767 5e-53 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acvr1 A G 2: 58,367,823 (GRCm39) S113P probably benign Het
Arhgdib A T 6: 136,901,166 (GRCm39) W188R probably damaging Het
Bcr T A 10: 75,001,878 (GRCm39) N927K possibly damaging Het
Cd209c A G 8: 3,990,324 (GRCm39) Y165H probably damaging Het
Cnnm2 A G 19: 46,750,515 (GRCm39) K102E probably benign Het
Col12a1 T C 9: 79,606,623 (GRCm39) E600G probably damaging Het
Ddx4 A T 13: 112,758,720 (GRCm39) H280Q probably benign Het
Eya4 T C 10: 22,992,498 (GRCm39) Y462C probably damaging Het
Fibcd1 T A 2: 31,728,576 (GRCm39) I94F probably damaging Het
Gm4846 C A 1: 166,322,195 (GRCm39) G124V probably damaging Het
Gm5624 A G 14: 44,797,469 (GRCm39) I108T possibly damaging Het
Gpr179 A T 11: 97,242,691 (GRCm39) M51K probably benign Het
Hck A G 2: 152,976,054 (GRCm39) I198V probably damaging Het
Kcnd2 T A 6: 21,216,924 (GRCm39) C209* probably null Het
Klhl1 T A 14: 96,438,778 (GRCm39) I507F possibly damaging Het
Knl1 A T 2: 118,908,450 (GRCm39) K1693N possibly damaging Het
Mcam T C 9: 44,051,714 (GRCm39) V490A possibly damaging Het
Mrgprx1 A T 7: 47,671,740 (GRCm39) D2E probably damaging Het
Mtg1 T C 7: 139,724,642 (GRCm39) probably benign Het
Myof C A 19: 37,909,929 (GRCm39) R1512L probably benign Het
Nrp2 C T 1: 62,810,996 (GRCm39) T679I probably benign Het
Nwd2 C A 5: 63,962,020 (GRCm39) L535I probably benign Het
Nwd2 T A 5: 63,962,021 (GRCm39) L535H probably damaging Het
Or4f14b T A 2: 111,775,285 (GRCm39) N172I probably damaging Het
Or52j3 A T 7: 102,836,221 (GRCm39) I138F probably damaging Het
Or5b94 T C 19: 12,652,033 (GRCm39) S155P probably damaging Het
Phkb A G 8: 86,602,275 (GRCm39) *41W probably null Het
Prl5a1 T A 13: 28,329,403 (GRCm39) N27K probably benign Het
Rims1 T C 1: 22,358,708 (GRCm39) T1292A probably damaging Het
Rnf38 G A 4: 44,133,745 (GRCm39) A376V probably damaging Het
Slc34a2 T C 5: 53,216,580 (GRCm39) V117A possibly damaging Het
Slfn8 A T 11: 82,894,517 (GRCm39) F707L probably damaging Het
Snx16 G A 3: 10,503,235 (GRCm39) P4L probably damaging Het
Snx6 T C 12: 54,801,130 (GRCm39) D289G probably damaging Het
St8sia3 G T 18: 64,402,750 (GRCm39) V130F probably damaging Het
U2surp A G 9: 95,363,704 (GRCm39) probably null Het
Ubqln3 A G 7: 103,791,272 (GRCm39) F273L probably benign Het
Vmn2r101 A T 17: 19,832,507 (GRCm39) R834S possibly damaging Het
Vrk3 A G 7: 44,403,244 (GRCm39) I2V probably benign Het
Zglp1 A G 9: 20,977,534 (GRCm39) S94P probably benign Het
Other mutations in Vmn2r18
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01098:Vmn2r18 APN 5 151,496,296 (GRCm39) missense probably damaging 0.99
IGL01564:Vmn2r18 APN 5 151,508,633 (GRCm39) missense possibly damaging 0.69
IGL01602:Vmn2r18 APN 5 151,510,106 (GRCm39) missense possibly damaging 0.64
IGL01605:Vmn2r18 APN 5 151,510,106 (GRCm39) missense possibly damaging 0.64
IGL01619:Vmn2r18 APN 5 151,510,229 (GRCm39) missense probably benign 0.25
IGL02177:Vmn2r18 APN 5 151,510,274 (GRCm39) missense possibly damaging 0.76
IGL02751:Vmn2r18 APN 5 151,508,072 (GRCm39) missense probably benign 0.09
IGL02977:Vmn2r18 APN 5 151,510,149 (GRCm39) missense probably damaging 1.00
R0089:Vmn2r18 UTSW 5 151,508,269 (GRCm39) missense probably benign 0.00
R0282:Vmn2r18 UTSW 5 151,508,668 (GRCm39) missense probably benign 0.02
R0529:Vmn2r18 UTSW 5 151,485,988 (GRCm39) missense probably damaging 0.99
R0812:Vmn2r18 UTSW 5 151,496,395 (GRCm39) splice site probably benign
R1467:Vmn2r18 UTSW 5 151,510,301 (GRCm39) missense possibly damaging 0.48
R1467:Vmn2r18 UTSW 5 151,510,301 (GRCm39) missense possibly damaging 0.48
R1506:Vmn2r18 UTSW 5 151,499,099 (GRCm39) splice site probably null
R1562:Vmn2r18 UTSW 5 151,510,301 (GRCm39) missense probably benign 0.12
R1637:Vmn2r18 UTSW 5 151,508,222 (GRCm39) missense probably damaging 1.00
R1651:Vmn2r18 UTSW 5 151,485,464 (GRCm39) missense probably damaging 1.00
R1883:Vmn2r18 UTSW 5 151,499,190 (GRCm39) missense probably benign 0.37
R1884:Vmn2r18 UTSW 5 151,499,190 (GRCm39) missense probably benign 0.37
R1914:Vmn2r18 UTSW 5 151,499,286 (GRCm39) missense probably benign 0.02
R2051:Vmn2r18 UTSW 5 151,486,016 (GRCm39) missense possibly damaging 0.90
R2056:Vmn2r18 UTSW 5 151,508,160 (GRCm39) missense probably damaging 0.98
R2252:Vmn2r18 UTSW 5 151,508,441 (GRCm39) missense possibly damaging 0.59
R2265:Vmn2r18 UTSW 5 151,510,127 (GRCm39) missense probably damaging 1.00
R2266:Vmn2r18 UTSW 5 151,510,127 (GRCm39) missense probably damaging 1.00
R2267:Vmn2r18 UTSW 5 151,510,127 (GRCm39) missense probably damaging 1.00
R2843:Vmn2r18 UTSW 5 151,485,749 (GRCm39) missense probably damaging 1.00
R3023:Vmn2r18 UTSW 5 151,485,148 (GRCm39) missense probably benign 0.13
R3694:Vmn2r18 UTSW 5 151,508,033 (GRCm39) missense probably benign 0.00
R3763:Vmn2r18 UTSW 5 151,508,644 (GRCm39) missense probably damaging 1.00
R3816:Vmn2r18 UTSW 5 151,485,148 (GRCm39) missense probably benign 0.13
R4007:Vmn2r18 UTSW 5 151,508,711 (GRCm39) missense probably damaging 0.99
R4152:Vmn2r18 UTSW 5 151,485,730 (GRCm39) missense probably damaging 1.00
R4308:Vmn2r18 UTSW 5 151,508,268 (GRCm39) nonsense probably null
R4362:Vmn2r18 UTSW 5 151,496,368 (GRCm39) missense probably damaging 1.00
R4618:Vmn2r18 UTSW 5 151,508,424 (GRCm39) missense possibly damaging 0.64
R4716:Vmn2r18 UTSW 5 151,485,602 (GRCm39) missense possibly damaging 0.87
R4817:Vmn2r18 UTSW 5 151,508,897 (GRCm39) splice site probably null
R5111:Vmn2r18 UTSW 5 151,485,913 (GRCm39) missense possibly damaging 0.85
R5692:Vmn2r18 UTSW 5 151,485,724 (GRCm39) missense possibly damaging 0.65
R6115:Vmn2r18 UTSW 5 151,508,462 (GRCm39) missense possibly damaging 0.81
R6244:Vmn2r18 UTSW 5 151,508,116 (GRCm39) missense probably damaging 1.00
R6595:Vmn2r18 UTSW 5 151,485,889 (GRCm39) missense probably damaging 1.00
R6997:Vmn2r18 UTSW 5 151,485,338 (GRCm39) missense possibly damaging 0.95
R7227:Vmn2r18 UTSW 5 151,496,264 (GRCm39) missense probably damaging 1.00
R7349:Vmn2r18 UTSW 5 151,485,682 (GRCm39) nonsense probably null
R7506:Vmn2r18 UTSW 5 151,508,485 (GRCm39) missense possibly damaging 0.51
R7590:Vmn2r18 UTSW 5 151,485,194 (GRCm39) missense probably damaging 1.00
R7721:Vmn2r18 UTSW 5 151,510,158 (GRCm39) missense possibly damaging 0.53
R7877:Vmn2r18 UTSW 5 151,508,437 (GRCm39) missense probably damaging 1.00
R7882:Vmn2r18 UTSW 5 151,485,329 (GRCm39) missense probably damaging 1.00
R7984:Vmn2r18 UTSW 5 151,485,526 (GRCm39) missense probably damaging 1.00
R8295:Vmn2r18 UTSW 5 151,508,621 (GRCm39) missense probably damaging 0.97
R8353:Vmn2r18 UTSW 5 151,485,373 (GRCm39) missense probably damaging 1.00
R8453:Vmn2r18 UTSW 5 151,485,373 (GRCm39) missense probably damaging 1.00
R8670:Vmn2r18 UTSW 5 151,485,854 (GRCm39) missense probably damaging 1.00
R8725:Vmn2r18 UTSW 5 151,508,462 (GRCm39) missense probably damaging 0.99
R8727:Vmn2r18 UTSW 5 151,508,462 (GRCm39) missense probably damaging 0.99
R8895:Vmn2r18 UTSW 5 151,485,140 (GRCm39) missense possibly damaging 0.46
R9286:Vmn2r18 UTSW 5 151,499,175 (GRCm39) missense probably benign 0.00
R9339:Vmn2r18 UTSW 5 151,485,132 (GRCm39) missense probably damaging 0.99
Z1176:Vmn2r18 UTSW 5 151,508,498 (GRCm39) missense probably damaging 0.99
Z1187:Vmn2r18 UTSW 5 151,508,497 (GRCm39) missense probably benign 0.00
Posted On 2015-04-16