Incidental Mutation 'IGL01803:Vmn2r83'
ID 155565
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r83
Ensembl Gene ENSMUSG00000091381
Gene Name vomeronasal 2, receptor 83
Synonyms EG625029
Accession Numbers
Essential gene? Probably non essential (E-score: 0.141) question?
Stock # IGL01803
Quality Score
Status
Chromosome 10
Chromosomal Location 79304792-79327988 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 79304894 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Asparagine at position 35 (H35N)
Ref Sequence ENSEMBL: ENSMUSP00000131426 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000167976]
AlphaFold E9Q0G7
Predicted Effect probably benign
Transcript: ENSMUST00000167976
AA Change: H35N

PolyPhen 2 Score 0.012 (Sensitivity: 0.96; Specificity: 0.78)
SMART Domains Protein: ENSMUSP00000131426
Gene: ENSMUSG00000091381
AA Change: H35N

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
Pfam:ANF_receptor 79 473 1.5e-33 PFAM
Pfam:NCD3G 516 569 6.2e-22 PFAM
Pfam:7tm_3 602 837 8.1e-52 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts19 T A 18: 59,085,541 (GRCm39) L532Q probably damaging Het
Bod1l A T 5: 41,974,732 (GRCm39) V2194D probably damaging Het
Cenpf G A 1: 189,386,968 (GRCm39) Q1771* probably null Het
Cfap100 C A 6: 90,392,717 (GRCm39) R131L probably benign Het
Coch A T 12: 51,650,082 (GRCm39) Q357L probably benign Het
Col14a1 A G 15: 55,282,210 (GRCm39) T824A unknown Het
Dnah9 T C 11: 66,009,655 (GRCm39) Y744C probably damaging Het
Dusp13b A G 14: 21,783,907 (GRCm39) V201A probably damaging Het
Egf T A 3: 129,530,415 (GRCm39) H249L probably benign Het
Elmod1 G A 9: 53,838,764 (GRCm39) P132L probably benign Het
Eps8l2 T C 7: 140,938,143 (GRCm39) V459A probably benign Het
Fbn1 T C 2: 125,192,207 (GRCm39) D1434G probably damaging Het
Fbn1 G A 2: 125,143,645 (GRCm39) T2828I probably benign Het
Gbp9 C T 5: 105,242,039 (GRCm39) D173N probably damaging Het
Gbp9 T C 5: 105,232,884 (GRCm39) D256G probably damaging Het
Gpsm1 G A 2: 26,236,921 (GRCm39) A580T probably damaging Het
Hnrnpf T C 6: 117,884,094 (GRCm39) probably benign Het
Krt33a T C 11: 99,902,843 (GRCm39) E327G probably benign Het
M1ap T A 6: 82,982,565 (GRCm39) I283K probably benign Het
Mars2 A G 1: 55,277,155 (GRCm39) S253G probably damaging Het
Myh6 A T 14: 55,182,000 (GRCm39) M1767K probably damaging Het
Myo3a T A 2: 22,245,926 (GRCm39) D16E probably damaging Het
Pitrm1 T A 13: 6,629,471 (GRCm39) Y978N probably benign Het
Plekha6 G T 1: 133,200,152 (GRCm39) E66* probably null Het
Polk C T 13: 96,641,030 (GRCm39) V176M probably damaging Het
Pom121 G T 5: 135,410,463 (GRCm39) probably benign Het
Rnf213 T A 11: 119,332,133 (GRCm39) D2447E probably damaging Het
Sall3 T C 18: 81,013,047 (GRCm39) M1130V possibly damaging Het
Scn3a A G 2: 65,352,127 (GRCm39) probably benign Het
Sel1l A T 12: 91,797,504 (GRCm39) M241K probably benign Het
Septin4 G A 11: 87,459,075 (GRCm39) S483N probably benign Het
Ssh2 T G 11: 77,316,156 (GRCm39) L259R probably damaging Het
Tnr G T 1: 159,695,813 (GRCm39) G579W probably damaging Het
Vmn1r85 G T 7: 12,818,496 (GRCm39) A216D probably damaging Het
Zar1l T A 5: 150,441,569 (GRCm39) Y19F probably benign Het
Other mutations in Vmn2r83
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00226:Vmn2r83 APN 10 79,314,805 (GRCm39) missense probably damaging 1.00
IGL01096:Vmn2r83 APN 10 79,313,662 (GRCm39) missense probably damaging 1.00
IGL01542:Vmn2r83 APN 10 79,314,846 (GRCm39) missense probably benign 0.30
IGL02110:Vmn2r83 APN 10 79,327,534 (GRCm39) missense possibly damaging 0.82
IGL02347:Vmn2r83 APN 10 79,316,067 (GRCm39) missense possibly damaging 0.75
IGL02417:Vmn2r83 APN 10 79,314,881 (GRCm39) missense probably benign 0.00
IGL02544:Vmn2r83 APN 10 79,317,293 (GRCm39) splice site probably benign
IGL02683:Vmn2r83 APN 10 79,327,115 (GRCm39) missense probably benign
IGL02976:Vmn2r83 APN 10 79,304,832 (GRCm39) missense probably benign 0.00
PIT4378001:Vmn2r83 UTSW 10 79,304,849 (GRCm39) missense probably benign 0.00
PIT4468001:Vmn2r83 UTSW 10 79,313,884 (GRCm39) missense probably damaging 1.00
R0092:Vmn2r83 UTSW 10 79,327,798 (GRCm39) missense probably damaging 1.00
R1391:Vmn2r83 UTSW 10 79,314,931 (GRCm39) missense probably damaging 0.96
R1539:Vmn2r83 UTSW 10 79,327,759 (GRCm39) missense probably damaging 1.00
R1575:Vmn2r83 UTSW 10 79,314,956 (GRCm39) missense probably damaging 0.98
R2033:Vmn2r83 UTSW 10 79,327,653 (GRCm39) missense probably benign 0.03
R3916:Vmn2r83 UTSW 10 79,314,744 (GRCm39) missense probably benign 0.01
R3967:Vmn2r83 UTSW 10 79,327,154 (GRCm39) missense probably benign 0.00
R4840:Vmn2r83 UTSW 10 79,313,682 (GRCm39) missense possibly damaging 0.73
R5063:Vmn2r83 UTSW 10 79,314,921 (GRCm39) missense probably benign 0.04
R5630:Vmn2r83 UTSW 10 79,327,785 (GRCm39) missense possibly damaging 0.94
R5707:Vmn2r83 UTSW 10 79,327,183 (GRCm39) missense possibly damaging 0.53
R5980:Vmn2r83 UTSW 10 79,314,626 (GRCm39) missense probably benign 0.04
R6294:Vmn2r83 UTSW 10 79,313,688 (GRCm39) missense probably damaging 0.99
R6302:Vmn2r83 UTSW 10 79,304,837 (GRCm39) missense possibly damaging 0.95
R6769:Vmn2r83 UTSW 10 79,313,856 (GRCm39) missense probably damaging 1.00
R6986:Vmn2r83 UTSW 10 79,316,093 (GRCm39) missense probably benign
R7221:Vmn2r83 UTSW 10 79,316,001 (GRCm39) missense probably benign 0.02
R7376:Vmn2r83 UTSW 10 79,314,790 (GRCm39) missense probably benign 0.00
R7431:Vmn2r83 UTSW 10 79,327,306 (GRCm39) missense probably damaging 0.99
R7501:Vmn2r83 UTSW 10 79,327,771 (GRCm39) missense probably damaging 0.98
R7526:Vmn2r83 UTSW 10 79,327,392 (GRCm39) missense probably damaging 1.00
R7663:Vmn2r83 UTSW 10 79,314,956 (GRCm39) missense probably damaging 0.98
R7881:Vmn2r83 UTSW 10 79,314,261 (GRCm39) missense probably benign 0.01
R7939:Vmn2r83 UTSW 10 79,314,651 (GRCm39) missense probably damaging 1.00
R8314:Vmn2r83 UTSW 10 79,317,313 (GRCm39) missense possibly damaging 0.76
R8364:Vmn2r83 UTSW 10 79,316,037 (GRCm39) missense probably benign 0.12
R8802:Vmn2r83 UTSW 10 79,314,261 (GRCm39) missense probably benign 0.01
R8947:Vmn2r83 UTSW 10 79,304,873 (GRCm39) missense probably benign 0.00
R8969:Vmn2r83 UTSW 10 79,313,853 (GRCm39) missense probably benign 0.15
R8983:Vmn2r83 UTSW 10 79,327,360 (GRCm39) missense probably damaging 1.00
R9018:Vmn2r83 UTSW 10 79,316,020 (GRCm39) missense probably damaging 1.00
R9082:Vmn2r83 UTSW 10 79,304,894 (GRCm39) missense probably benign 0.00
R9390:Vmn2r83 UTSW 10 79,317,322 (GRCm39) nonsense probably null
X0026:Vmn2r83 UTSW 10 79,314,486 (GRCm39) missense probably benign
X0026:Vmn2r83 UTSW 10 79,304,849 (GRCm39) missense probably benign 0.00
Z1176:Vmn2r83 UTSW 10 79,314,756 (GRCm39) missense possibly damaging 0.74
Posted On 2014-02-04