Incidental Mutation 'IGL01808:Vmn1r203'
ID 155726
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r203
Ensembl Gene ENSMUSG00000069289
Gene Name vomeronasal 1 receptor 203
Synonyms V1rh11
Accession Numbers
Essential gene? Probably non essential (E-score: 0.080) question?
Stock # IGL01808
Quality Score
Status
Chromosome 13
Chromosomal Location 22708221-22709156 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 22708717 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 166 (I166T)
Ref Sequence ENSEMBL: ENSMUSP00000154399 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000091729] [ENSMUST00000227520] [ENSMUST00000228889]
AlphaFold Q8R273
Predicted Effect probably benign
Transcript: ENSMUST00000091729
AA Change: I166T

PolyPhen 2 Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
SMART Domains Protein: ENSMUSP00000089322
Gene: ENSMUSG00000069289
AA Change: I166T

DomainStartEndE-ValueType
transmembrane domain 19 41 N/A INTRINSIC
Pfam:V1R 43 304 5.8e-35 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000137651
Predicted Effect probably benign
Transcript: ENSMUST00000227520
AA Change: I166T

PolyPhen 2 Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
Predicted Effect probably benign
Transcript: ENSMUST00000228889
AA Change: I166T

PolyPhen 2 Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 24 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ager A T 17: 34,818,431 (GRCm39) Q266L probably damaging Het
Amz1 A G 5: 140,727,034 (GRCm39) probably benign Het
Ebf2 C T 14: 67,651,932 (GRCm39) A488V probably benign Het
Gm5885 A T 6: 133,508,181 (GRCm39) noncoding transcript Het
Gnas T C 2: 174,140,490 (GRCm39) S220P probably damaging Het
Gpr171 G A 3: 59,005,572 (GRCm39) P68S probably damaging Het
H2ax T C 9: 44,246,246 (GRCm39) I63T possibly damaging Het
H2-M9 A T 17: 36,952,711 (GRCm39) probably null Het
Igsf9 T C 1: 172,312,370 (GRCm39) V27A probably benign Het
Kcnh6 G T 11: 105,914,753 (GRCm39) probably benign Het
Mapkbp1 A G 2: 119,853,650 (GRCm39) probably null Het
Mllt6 C A 11: 97,563,310 (GRCm39) H298N possibly damaging Het
Mtmr3 A G 11: 4,447,404 (GRCm39) I352T probably damaging Het
Mtrr T C 13: 68,714,212 (GRCm39) D509G probably benign Het
Ncan C T 8: 70,560,090 (GRCm39) probably null Het
Or51aa2 T A 7: 103,187,781 (GRCm39) Y220F probably damaging Het
Pcdhb4 T C 18: 37,442,067 (GRCm39) V459A probably damaging Het
Phrf1 C A 7: 140,840,879 (GRCm39) P1274Q probably damaging Het
Slc4a2 T C 5: 24,645,205 (GRCm39) L1125P probably damaging Het
Synpo T C 18: 60,735,280 (GRCm39) I650V probably benign Het
Tsc1 G A 2: 28,552,519 (GRCm39) R86H probably damaging Het
Ugt2a3 A G 5: 87,473,414 (GRCm39) V501A probably benign Het
Vps13a A G 19: 16,687,650 (GRCm39) C933R probably damaging Het
Zfp142 A T 1: 74,615,184 (GRCm39) F342Y probably damaging Het
Other mutations in Vmn1r203
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01356:Vmn1r203 APN 13 22,708,947 (GRCm39) missense probably damaging 1.00
IGL01527:Vmn1r203 APN 13 22,708,447 (GRCm39) missense possibly damaging 0.89
IGL01887:Vmn1r203 APN 13 22,709,046 (GRCm39) missense probably benign 0.00
IGL02340:Vmn1r203 APN 13 22,708,997 (GRCm39) nonsense probably null
IGL02543:Vmn1r203 APN 13 22,709,074 (GRCm39) missense probably damaging 1.00
IGL02684:Vmn1r203 APN 13 22,708,539 (GRCm39) missense possibly damaging 0.95
BB005:Vmn1r203 UTSW 13 22,708,705 (GRCm39) missense probably benign 0.01
BB015:Vmn1r203 UTSW 13 22,708,705 (GRCm39) missense probably benign 0.01
PIT4519001:Vmn1r203 UTSW 13 22,708,765 (GRCm39) missense probably benign 0.01
R0544:Vmn1r203 UTSW 13 22,708,443 (GRCm39) missense possibly damaging 0.94
R1365:Vmn1r203 UTSW 13 22,708,756 (GRCm39) missense probably benign 0.00
R1396:Vmn1r203 UTSW 13 22,708,678 (GRCm39) missense probably benign 0.01
R1794:Vmn1r203 UTSW 13 22,708,521 (GRCm39) missense probably damaging 1.00
R2010:Vmn1r203 UTSW 13 22,708,617 (GRCm39) missense possibly damaging 0.56
R2169:Vmn1r203 UTSW 13 22,708,905 (GRCm39) nonsense probably null
R2333:Vmn1r203 UTSW 13 22,709,113 (GRCm39) missense probably damaging 1.00
R2418:Vmn1r203 UTSW 13 22,709,004 (GRCm39) missense possibly damaging 0.57
R2419:Vmn1r203 UTSW 13 22,709,004 (GRCm39) missense possibly damaging 0.57
R4322:Vmn1r203 UTSW 13 22,708,408 (GRCm39) missense probably damaging 1.00
R4460:Vmn1r203 UTSW 13 22,708,852 (GRCm39) missense probably damaging 0.98
R4686:Vmn1r203 UTSW 13 22,708,528 (GRCm39) missense probably damaging 1.00
R5526:Vmn1r203 UTSW 13 22,708,273 (GRCm39) missense probably benign 0.01
R6240:Vmn1r203 UTSW 13 22,708,899 (GRCm39) missense possibly damaging 0.89
R6607:Vmn1r203 UTSW 13 22,708,891 (GRCm39) missense probably benign 0.23
R7575:Vmn1r203 UTSW 13 22,708,588 (GRCm39) missense probably benign 0.12
R7928:Vmn1r203 UTSW 13 22,708,705 (GRCm39) missense probably benign 0.01
R8375:Vmn1r203 UTSW 13 22,709,154 (GRCm39) makesense probably null
R8421:Vmn1r203 UTSW 13 22,709,154 (GRCm39) makesense probably null
R8424:Vmn1r203 UTSW 13 22,709,004 (GRCm39) missense probably damaging 1.00
R8845:Vmn1r203 UTSW 13 22,708,720 (GRCm39) missense possibly damaging 0.81
R8933:Vmn1r203 UTSW 13 22,708,691 (GRCm39) missense possibly damaging 0.69
R8956:Vmn1r203 UTSW 13 22,709,004 (GRCm39) missense possibly damaging 0.57
R9493:Vmn1r203 UTSW 13 22,708,423 (GRCm39) missense probably damaging 1.00
Z1177:Vmn1r203 UTSW 13 22,708,579 (GRCm39) missense probably damaging 0.97
Posted On 2014-02-04