Incidental Mutation 'IGL01527:Vmn1r203'
ID 89585
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 # IGL01527
Quality Score
Status
Chromosome 13
Chromosomal Location 22708221-22709156 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 22708447 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 76 (I76T)
Ref Sequence ENSEMBL: ENSMUSP00000154399 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000091729] [ENSMUST00000227520] [ENSMUST00000228889]
AlphaFold Q8R273
Predicted Effect possibly damaging
Transcript: ENSMUST00000091729
AA Change: I76T

PolyPhen 2 Score 0.895 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000089322
Gene: ENSMUSG00000069289
AA Change: I76T

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 possibly damaging
Transcript: ENSMUST00000227520
AA Change: I76T

PolyPhen 2 Score 0.895 (Sensitivity: 0.82; Specificity: 0.94)
Predicted Effect possibly damaging
Transcript: ENSMUST00000228889
AA Change: I76T

PolyPhen 2 Score 0.895 (Sensitivity: 0.82; Specificity: 0.94)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2300002M23Rik G T 17: 35,878,730 (GRCm39) probably null Het
Abca13 T A 11: 9,240,788 (GRCm39) W884R possibly damaging Het
Ahi1 T C 10: 20,835,984 (GRCm39) probably benign Het
Ankfn1 G T 11: 89,282,465 (GRCm39) P394Q probably benign Het
Cacnb2 T C 2: 14,989,081 (GRCm39) I393T possibly damaging Het
Ces1a G T 8: 93,771,726 (GRCm39) P24T probably damaging Het
Col22a1 T C 15: 71,778,880 (GRCm39) E269G probably damaging Het
Cyp24a1 A G 2: 170,338,486 (GRCm39) L70P probably damaging Het
Cyp8b1 T C 9: 121,744,061 (GRCm39) K424E probably damaging Het
Dicer1 G A 12: 104,657,869 (GRCm39) Q1902* probably null Het
Dst T A 1: 34,286,734 (GRCm39) L544Q probably damaging Het
Esrp2 T C 8: 106,858,865 (GRCm39) T591A probably benign Het
Gap43 C T 16: 42,112,516 (GRCm39) E82K probably benign Het
Ift70a1 T C 2: 75,810,860 (GRCm39) I408V probably benign Het
Kif17 G A 4: 137,996,397 (GRCm39) V125I probably benign Het
Lancl2 T C 6: 57,709,307 (GRCm39) S370P probably damaging Het
Macf1 T C 4: 123,386,953 (GRCm39) I203V possibly damaging Het
Mphosph9 A G 5: 124,421,687 (GRCm39) probably benign Het
Ncapg A G 5: 45,829,726 (GRCm39) I143V possibly damaging Het
Nr3c1 A G 18: 39,619,690 (GRCm39) V199A probably benign Het
Obscn T A 11: 58,955,243 (GRCm39) N3890I possibly damaging Het
Or2g7 A G 17: 38,378,986 (GRCm39) N308S probably benign Het
Or2h2c A T 17: 37,422,701 (GRCm39) Y58N probably damaging Het
Or52n5 T A 7: 104,588,198 (GRCm39) V155E possibly damaging Het
Or8g32 A G 9: 39,305,114 (GRCm39) H6R probably benign Het
Palmd C A 3: 116,720,837 (GRCm39) E166* probably null Het
Pdzd2 T C 15: 12,445,750 (GRCm39) E327G probably damaging Het
Pex13 T C 11: 23,606,111 (GRCm39) T40A probably benign Het
Pkd2 T C 5: 104,646,750 (GRCm39) probably benign Het
Plb1 A G 5: 32,474,467 (GRCm39) T643A probably damaging Het
Prlr T A 15: 10,329,257 (GRCm39) D577E probably benign Het
Rimoc1 T C 15: 4,018,165 (GRCm39) Y170C probably damaging Het
Slc44a3 A G 3: 121,320,777 (GRCm39) C75R probably damaging Het
Susd6 A T 12: 80,921,093 (GRCm39) N230I possibly damaging Het
Tbx10 A G 19: 4,048,227 (GRCm39) R251G probably damaging Het
Uap1l1 A G 2: 25,253,816 (GRCm39) probably null Het
Ugt2b5 A G 5: 87,284,068 (GRCm39) V308A possibly damaging Het
Usp28 C A 9: 48,937,173 (GRCm39) H147Q probably benign Het
Vmn2r104 A G 17: 20,263,158 (GRCm39) I101T possibly damaging Het
Vmn2r17 T A 5: 109,601,006 (GRCm39) L768H probably damaging Het
Other mutations in Vmn1r203
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01356:Vmn1r203 APN 13 22,708,947 (GRCm39) missense probably damaging 1.00
IGL01808:Vmn1r203 APN 13 22,708,717 (GRCm39) missense probably benign 0.02
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 2013-12-03