Incidental Mutation 'IGL01619:Vmn2r121'
ID 92492
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r121
Ensembl Gene ENSMUSG00000072049
Gene Name vomeronasal 2, receptor 121
Synonyms EG625699
Accession Numbers
Essential gene? Probably non essential (E-score: 0.076) question?
Stock # IGL01619
Quality Score
Status
Chromosome X
Chromosomal Location 123037036-123045607 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 123041997 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Leucine at position 387 (M387L)
Ref Sequence ENSEMBL: ENSMUSP00000092067 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094491]
AlphaFold A2BE32
Predicted Effect probably benign
Transcript: ENSMUST00000094491
AA Change: M387L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000092067
Gene: ENSMUSG00000072049
AA Change: M387L

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
Pfam:ANF_receptor 75 448 3.2e-26 PFAM
Pfam:NCD3G 506 560 2.1e-19 PFAM
Pfam:7tm_3 593 828 3.8e-56 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ankrd46 T C 15: 36,486,113 (GRCm39) T47A possibly damaging Het
Asxl3 T G 18: 22,656,385 (GRCm39) V1465G probably damaging Het
Celsr3 A T 9: 108,711,756 (GRCm39) D1657V probably damaging Het
Celsr3 A G 9: 108,714,603 (GRCm39) H1995R probably benign Het
Cimip2b G A 4: 43,427,814 (GRCm39) T170I possibly damaging Het
Cntn6 G A 6: 104,705,335 (GRCm39) probably benign Het
Def6 C T 17: 28,426,838 (GRCm39) L8F probably damaging Het
Dnah9 T A 11: 65,722,441 (GRCm39) K1940* probably null Het
Dock10 A G 1: 80,612,015 (GRCm39) probably benign Het
Fam72a A G 1: 131,461,650 (GRCm39) I112V probably benign Het
Fgl1 A T 8: 41,650,008 (GRCm39) W258R probably damaging Het
Ints6l G T X: 55,542,104 (GRCm39) probably benign Het
Lifr A T 15: 7,220,643 (GRCm39) N1091I probably damaging Het
Mga T C 2: 119,762,309 (GRCm39) I1100T possibly damaging Het
Mrpl40 T A 16: 18,691,294 (GRCm39) M139L probably benign Het
Myom1 T C 17: 71,351,471 (GRCm39) probably benign Het
Or2m12 T A 16: 19,104,909 (GRCm39) T195S probably damaging Het
Pcdhb5 T C 18: 37,455,992 (GRCm39) F791L probably damaging Het
Prss29 T C 17: 25,540,113 (GRCm39) probably null Het
Ranbp2 A G 10: 58,299,900 (GRCm39) probably null Het
Serpinb9e A G 13: 33,439,108 (GRCm39) K178R probably damaging Het
Shtn1 A G 19: 59,016,601 (GRCm39) S233P probably damaging Het
Smpd1 G A 7: 105,204,549 (GRCm39) V143M possibly damaging Het
Terb1 G A 8: 105,199,646 (GRCm39) H433Y probably benign Het
Traf6 C T 2: 101,520,443 (GRCm39) Q164* probably null Het
Trip12 C A 1: 84,792,631 (GRCm39) R4L probably damaging Het
Ttn G A 2: 76,693,879 (GRCm39) P208S possibly damaging Het
Ube2c T C 2: 164,613,232 (GRCm39) I50T probably damaging Het
Uggt1 T C 1: 36,200,775 (GRCm39) D1174G probably damaging Het
Vmn2r18 T A 5: 151,510,229 (GRCm39) N48I probably benign Het
Zc3h15 T C 2: 83,490,517 (GRCm39) L217P probably damaging Het
Zyg11a T A 4: 108,062,414 (GRCm39) E129V probably damaging Het
Other mutations in Vmn2r121
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00990:Vmn2r121 APN X 123,043,413 (GRCm39) missense probably benign 0.00
IGL00990:Vmn2r121 APN X 123,037,480 (GRCm39) missense possibly damaging 0.95
IGL00990:Vmn2r121 APN X 123,037,499 (GRCm39) missense probably benign 0.04
IGL01125:Vmn2r121 APN X 123,042,504 (GRCm39) missense probably damaging 0.99
IGL01450:Vmn2r121 APN X 123,040,888 (GRCm39) missense possibly damaging 0.57
IGL01797:Vmn2r121 APN X 123,041,048 (GRCm39) splice site probably benign
IGL02227:Vmn2r121 APN X 123,042,378 (GRCm39) missense probably benign 0.44
IGL02971:Vmn2r121 APN X 123,037,591 (GRCm39) missense probably damaging 1.00
IGL03058:Vmn2r121 APN X 123,042,618 (GRCm39) missense probably benign 0.00
IGL03142:Vmn2r121 APN X 123,042,635 (GRCm39) missense possibly damaging 0.94
IGL03183:Vmn2r121 APN X 123,042,023 (GRCm39) missense probably benign 0.03
E0370:Vmn2r121 UTSW X 123,037,617 (GRCm39) missense probably benign 0.01
R0196:Vmn2r121 UTSW X 123,041,879 (GRCm39) missense probably benign 0.03
R1381:Vmn2r121 UTSW X 123,037,837 (GRCm39) missense probably damaging 1.00
R1399:Vmn2r121 UTSW X 123,039,545 (GRCm39) missense possibly damaging 0.94
R1423:Vmn2r121 UTSW X 123,039,602 (GRCm39) missense possibly damaging 0.52
R1687:Vmn2r121 UTSW X 123,042,488 (GRCm39) missense probably benign 0.39
R2121:Vmn2r121 UTSW X 123,043,439 (GRCm39) splice site probably null
R2124:Vmn2r121 UTSW X 123,043,439 (GRCm39) splice site probably null
R3151:Vmn2r121 UTSW X 123,040,849 (GRCm39) missense probably benign 0.20
R4460:Vmn2r121 UTSW X 123,038,281 (GRCm39) missense probably benign 0.01
R4735:Vmn2r121 UTSW X 123,038,335 (GRCm39) missense probably benign
R5332:Vmn2r121 UTSW X 123,043,272 (GRCm39) missense probably benign
R6102:Vmn2r121 UTSW X 123,043,272 (GRCm39) missense probably benign
X0023:Vmn2r121 UTSW X 123,045,354 (GRCm39) missense possibly damaging 0.64
Posted On 2013-12-09