Incidental Mutation 'IGL02177:Vmn2r84'
ID 283136
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r84
Ensembl Gene ENSMUSG00000070601
Gene Name vomeronasal 2, receptor 84
Synonyms EG625068
Accession Numbers
Essential gene? Probably non essential (E-score: 0.070) question?
Stock # IGL02177
Quality Score
Status
Chromosome 10
Chromosomal Location 130221669-130230110 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 130227881 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Methionine at position 118 (I118M)
Ref Sequence ENSEMBL: ENSMUSP00000092079 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094502]
AlphaFold D3YWE3
Predicted Effect probably benign
Transcript: ENSMUST00000094502
AA Change: I118M

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
SMART Domains Protein: ENSMUSP00000092079
Gene: ENSMUSG00000070601
AA Change: I118M

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Pfam:ANF_receptor 77 448 1.3e-27 PFAM
Pfam:NCD3G 508 561 6.9e-21 PFAM
Pfam:7tm_3 594 830 4.6e-55 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Add3 T G 19: 53,205,323 (GRCm39) Y24* probably null Het
Catsperb A G 12: 101,507,721 (GRCm39) Y496C probably damaging Het
Ccdc183 C T 2: 25,502,095 (GRCm39) E260K probably benign Het
Ccdc81 A C 7: 89,524,988 (GRCm39) M531R possibly damaging Het
Cyp3a16 T A 5: 145,386,964 (GRCm39) N342I probably benign Het
Defb43 T C 14: 63,249,266 (GRCm39) V3A probably benign Het
Dpyd T A 3: 118,858,559 (GRCm39) I591N possibly damaging Het
Dpysl5 T G 5: 30,902,622 (GRCm39) V18G probably damaging Het
Erc2 A T 14: 27,620,580 (GRCm39) M69L probably benign Het
Fam184b G T 5: 45,690,157 (GRCm39) Y817* probably null Het
Fyb1 G T 15: 6,688,047 (GRCm39) probably null Het
Gpr33 G T 12: 52,070,863 (GRCm39) Q59K probably benign Het
Heatr3 T G 8: 88,883,351 (GRCm39) F278V probably benign Het
Hectd1 A T 12: 51,819,103 (GRCm39) D1292E probably damaging Het
Herc1 A T 9: 66,341,793 (GRCm39) M1861L probably benign Het
Hspg2 T A 4: 137,242,627 (GRCm39) L614Q probably damaging Het
Itpr3 A G 17: 27,318,588 (GRCm39) R915G possibly damaging Het
Jhy T C 9: 40,809,553 (GRCm39) D646G probably damaging Het
Lrig1 T A 6: 94,640,977 (GRCm39) N76I possibly damaging Het
Macc1 A G 12: 119,429,292 (GRCm39) D814G probably damaging Het
Mapk8ip1 T C 2: 92,217,092 (GRCm39) D401G probably damaging Het
Nedd4 T A 9: 72,654,439 (GRCm39) S865T probably damaging Het
Or9s27 G A 1: 92,516,479 (GRCm39) M142I possibly damaging Het
Pi4ka A T 16: 17,136,146 (GRCm39) D937E probably benign Het
Prkcd T A 14: 30,327,844 (GRCm39) I81F probably damaging Het
Ranbp9 A T 13: 43,573,193 (GRCm39) C280S probably damaging Het
Ror2 C T 13: 53,264,764 (GRCm39) S764N probably damaging Het
Scn1b T C 7: 30,816,655 (GRCm39) *219W probably null Het
Slain2 T C 5: 73,072,008 (GRCm39) V14A probably benign Het
Soat1 A T 1: 156,268,073 (GRCm39) probably benign Het
Tbc1d4 T A 14: 101,692,375 (GRCm39) M1030L possibly damaging Het
Tenm4 T C 7: 96,544,869 (GRCm39) V2295A probably benign Het
Tmem135 A G 7: 88,987,661 (GRCm39) Y46H probably damaging Het
Tnfsf18 A T 1: 161,331,354 (GRCm39) D168V probably damaging Het
Trdn T C 10: 33,015,169 (GRCm39) V41A probably damaging Het
Trpc5 G T X: 143,264,234 (GRCm39) L208I probably damaging Het
Vmn1r50 T C 6: 90,085,139 (GRCm39) Y295H probably benign Het
Vmn2r18 T G 5: 151,510,274 (GRCm39) H33P possibly damaging Het
Other mutations in Vmn2r84
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01461:Vmn2r84 APN 10 130,227,094 (GRCm39) missense possibly damaging 0.65
IGL01590:Vmn2r84 APN 10 130,221,964 (GRCm39) missense probably damaging 1.00
IGL01639:Vmn2r84 APN 10 130,225,141 (GRCm39) nonsense probably null
IGL01843:Vmn2r84 APN 10 130,222,148 (GRCm39) missense probably benign
IGL01911:Vmn2r84 APN 10 130,222,277 (GRCm39) missense probably damaging 0.99
IGL01937:Vmn2r84 APN 10 130,221,755 (GRCm39) missense probably damaging 1.00
IGL01977:Vmn2r84 APN 10 130,229,935 (GRCm39) missense probably benign 0.11
IGL02291:Vmn2r84 APN 10 130,226,617 (GRCm39) missense probably damaging 1.00
IGL02590:Vmn2r84 APN 10 130,227,356 (GRCm39) splice site probably benign
IGL02727:Vmn2r84 APN 10 130,229,995 (GRCm39) missense possibly damaging 0.95
IGL02900:Vmn2r84 APN 10 130,223,861 (GRCm39) splice site probably benign
IGL03383:Vmn2r84 APN 10 130,222,556 (GRCm39) missense probably damaging 1.00
PIT4378001:Vmn2r84 UTSW 10 130,221,784 (GRCm39) missense probably damaging 1.00
R0076:Vmn2r84 UTSW 10 130,230,062 (GRCm39) missense probably damaging 1.00
R0089:Vmn2r84 UTSW 10 130,222,588 (GRCm39) splice site probably benign
R0153:Vmn2r84 UTSW 10 130,227,877 (GRCm39) missense probably benign 0.06
R0611:Vmn2r84 UTSW 10 130,221,991 (GRCm39) missense probably damaging 1.00
R0883:Vmn2r84 UTSW 10 130,226,984 (GRCm39) missense probably damaging 0.99
R1237:Vmn2r84 UTSW 10 130,223,725 (GRCm39) splice site probably null
R1295:Vmn2r84 UTSW 10 130,225,008 (GRCm39) missense probably benign 0.12
R1401:Vmn2r84 UTSW 10 130,227,859 (GRCm39) missense possibly damaging 0.89
R1521:Vmn2r84 UTSW 10 130,225,137 (GRCm39) missense probably benign 0.10
R1590:Vmn2r84 UTSW 10 130,227,349 (GRCm39) critical splice acceptor site probably null
R1710:Vmn2r84 UTSW 10 130,226,968 (GRCm39) missense probably benign 0.02
R1891:Vmn2r84 UTSW 10 130,221,938 (GRCm39) missense possibly damaging 0.78
R1956:Vmn2r84 UTSW 10 130,226,677 (GRCm39) missense probably benign 0.01
R1957:Vmn2r84 UTSW 10 130,226,677 (GRCm39) missense probably benign 0.01
R1962:Vmn2r84 UTSW 10 130,226,591 (GRCm39) missense probably damaging 0.99
R1994:Vmn2r84 UTSW 10 130,221,878 (GRCm39) missense probably damaging 1.00
R2124:Vmn2r84 UTSW 10 130,227,100 (GRCm39) missense probably damaging 0.99
R2409:Vmn2r84 UTSW 10 130,227,940 (GRCm39) missense probably damaging 0.99
R2474:Vmn2r84 UTSW 10 130,222,392 (GRCm39) missense possibly damaging 0.50
R2851:Vmn2r84 UTSW 10 130,230,036 (GRCm39) missense probably benign 0.05
R3508:Vmn2r84 UTSW 10 130,226,777 (GRCm39) missense probably damaging 1.00
R3792:Vmn2r84 UTSW 10 130,221,669 (GRCm39) makesense probably null
R4051:Vmn2r84 UTSW 10 130,226,767 (GRCm39) missense probably damaging 1.00
R4061:Vmn2r84 UTSW 10 130,221,898 (GRCm39) missense probably damaging 1.00
R4091:Vmn2r84 UTSW 10 130,227,238 (GRCm39) missense probably damaging 1.00
R4190:Vmn2r84 UTSW 10 130,227,163 (GRCm39) nonsense probably null
R4520:Vmn2r84 UTSW 10 130,222,391 (GRCm39) missense probably damaging 1.00
R4584:Vmn2r84 UTSW 10 130,226,582 (GRCm39) missense probably benign 0.00
R4588:Vmn2r84 UTSW 10 130,221,809 (GRCm39) missense probably damaging 0.98
R4655:Vmn2r84 UTSW 10 130,229,973 (GRCm39) nonsense probably null
R4860:Vmn2r84 UTSW 10 130,221,712 (GRCm39) missense probably damaging 0.99
R4860:Vmn2r84 UTSW 10 130,221,712 (GRCm39) missense probably damaging 0.99
R5022:Vmn2r84 UTSW 10 130,222,417 (GRCm39) missense probably damaging 1.00
R5146:Vmn2r84 UTSW 10 130,221,971 (GRCm39) missense probably damaging 1.00
R5237:Vmn2r84 UTSW 10 130,221,863 (GRCm39) missense probably damaging 0.99
R5695:Vmn2r84 UTSW 10 130,225,064 (GRCm39) missense probably benign 0.12
R5793:Vmn2r84 UTSW 10 130,221,754 (GRCm39) missense probably damaging 0.99
R6210:Vmn2r84 UTSW 10 130,222,114 (GRCm39) missense probably damaging 1.00
R6286:Vmn2r84 UTSW 10 130,226,737 (GRCm39) missense possibly damaging 0.65
R6580:Vmn2r84 UTSW 10 130,225,110 (GRCm39) missense possibly damaging 0.93
R6607:Vmn2r84 UTSW 10 130,226,731 (GRCm39) missense possibly damaging 0.87
R6818:Vmn2r84 UTSW 10 130,222,147 (GRCm39) missense probably benign 0.09
R6956:Vmn2r84 UTSW 10 130,225,136 (GRCm39) missense probably damaging 0.98
R6994:Vmn2r84 UTSW 10 130,226,876 (GRCm39) missense possibly damaging 0.90
R7075:Vmn2r84 UTSW 10 130,226,941 (GRCm39) missense probably damaging 0.99
R7225:Vmn2r84 UTSW 10 130,222,552 (GRCm39) missense probably damaging 0.99
R7252:Vmn2r84 UTSW 10 130,222,279 (GRCm39) missense probably damaging 1.00
R7263:Vmn2r84 UTSW 10 130,225,077 (GRCm39) missense probably damaging 1.00
R7297:Vmn2r84 UTSW 10 130,227,119 (GRCm39) missense probably benign 0.19
R7439:Vmn2r84 UTSW 10 130,227,982 (GRCm39) missense possibly damaging 0.90
R7441:Vmn2r84 UTSW 10 130,227,982 (GRCm39) missense possibly damaging 0.90
R7857:Vmn2r84 UTSW 10 130,226,738 (GRCm39) missense probably benign 0.00
R8263:Vmn2r84 UTSW 10 130,227,037 (GRCm39) missense probably damaging 1.00
R8555:Vmn2r84 UTSW 10 130,230,100 (GRCm39) missense probably benign 0.28
R8766:Vmn2r84 UTSW 10 130,222,241 (GRCm39) missense probably damaging 0.98
R8821:Vmn2r84 UTSW 10 130,226,968 (GRCm39) missense probably benign 0.02
R8831:Vmn2r84 UTSW 10 130,226,968 (GRCm39) missense probably benign 0.02
R8970:Vmn2r84 UTSW 10 130,222,244 (GRCm39) missense probably damaging 0.98
R9164:Vmn2r84 UTSW 10 130,221,669 (GRCm39) makesense probably null
R9190:Vmn2r84 UTSW 10 130,226,843 (GRCm39) missense probably benign 0.03
R9261:Vmn2r84 UTSW 10 130,229,976 (GRCm39) missense probably benign 0.00
R9310:Vmn2r84 UTSW 10 130,227,993 (GRCm39) missense possibly damaging 0.81
R9434:Vmn2r84 UTSW 10 130,221,745 (GRCm39) missense possibly damaging 0.65
R9613:Vmn2r84 UTSW 10 130,226,591 (GRCm39) missense probably damaging 0.99
Z1177:Vmn2r84 UTSW 10 130,227,771 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16