Incidental Mutation 'IGL03161:Vmn1r32'
ID 411403
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r32
Ensembl Gene ENSMUSG00000062905
Gene Name vomeronasal 1 receptor 32
Synonyms V1rc15
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # IGL03161
Quality Score
Status
Chromosome 6
Chromosomal Location 66529167-66536692 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 66530204 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Leucine at position 191 (M191L)
Ref Sequence ENSEMBL: ENSMUSP00000153723 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000079584] [ENSMUST00000227014]
AlphaFold Q8R2D9
Predicted Effect possibly damaging
Transcript: ENSMUST00000079584
AA Change: M191L

PolyPhen 2 Score 0.650 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000078536
Gene: ENSMUSG00000062905
AA Change: M191L

DomainStartEndE-ValueType
Pfam:V1R 28 293 9.7e-56 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000227014
AA Change: M191L

PolyPhen 2 Score 0.650 (Sensitivity: 0.87; Specificity: 0.91)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930579G24Rik T C 3: 79,536,493 (GRCm39) probably benign Het
Abtb2 G T 2: 103,397,799 (GRCm39) R243L probably benign Het
Adamts12 A G 15: 11,292,168 (GRCm39) E871G possibly damaging Het
Ascc3 A T 10: 50,494,168 (GRCm39) N201I probably damaging Het
Aste1 A T 9: 105,273,871 (GRCm39) H37L probably damaging Het
Atp1a2 T A 1: 172,106,429 (GRCm39) probably benign Het
Cand2 C A 6: 115,769,698 (GRCm39) T836K probably benign Het
Dnah7c G A 1: 46,506,456 (GRCm39) A178T probably benign Het
Dnm2 A G 9: 21,397,020 (GRCm39) probably benign Het
Dock3 T C 9: 106,900,987 (GRCm39) D326G probably damaging Het
Fignl1 A C 11: 11,752,680 (GRCm39) M125R probably benign Het
Gabarapl2 T A 8: 112,669,168 (GRCm39) V42D probably benign Het
Hivep2 T C 10: 14,019,100 (GRCm39) V1957A probably damaging Het
Hps1 T C 19: 42,755,710 (GRCm39) E172G probably damaging Het
Il16 T C 7: 83,371,707 (GRCm39) D33G probably damaging Het
Lamb1 A G 12: 31,376,255 (GRCm39) N1542D probably benign Het
Mllt6 T C 11: 97,557,977 (GRCm39) Y179H probably benign Het
Muc4 T C 16: 32,570,766 (GRCm39) S609P possibly damaging Het
Nacad G A 11: 6,550,378 (GRCm39) Q938* probably null Het
Odad3 A G 9: 21,913,611 (GRCm39) S54P probably benign Het
Or4k45 T C 2: 111,395,676 (GRCm39) I38V possibly damaging Het
Or4p22 G A 2: 88,317,792 (GRCm39) A239T probably benign Het
Pik3c3 C T 18: 30,426,760 (GRCm39) T292I probably benign Het
Prss3b A T 6: 41,011,240 (GRCm39) H47Q probably damaging Het
Slit3 T C 11: 35,591,241 (GRCm39) V1351A probably benign Het
Spg7 T C 8: 123,814,070 (GRCm39) M443T probably damaging Het
Spmip9 T C 6: 70,890,519 (GRCm39) E91G probably benign Het
Tcof1 A G 18: 60,966,560 (GRCm39) S344P possibly damaging Het
Tm4sf5 T A 11: 70,401,098 (GRCm39) S105T probably benign Het
Tmem119 A G 5: 113,932,961 (GRCm39) V280A possibly damaging Het
Trbv20 A T 6: 41,165,757 (GRCm39) I61L probably benign Het
Trip12 T C 1: 84,738,853 (GRCm39) probably benign Het
Vta1 A T 10: 14,543,716 (GRCm39) H219Q possibly damaging Het
Other mutations in Vmn1r32
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01449:Vmn1r32 APN 6 66,529,916 (GRCm39) missense probably benign
IGL02399:Vmn1r32 APN 6 66,529,913 (GRCm39) missense probably benign 0.18
IGL02964:Vmn1r32 APN 6 66,529,922 (GRCm39) missense probably benign 0.37
IGL03244:Vmn1r32 APN 6 66,530,489 (GRCm39) missense probably damaging 1.00
IGL03248:Vmn1r32 APN 6 66,529,897 (GRCm39) missense possibly damaging 0.82
R0668:Vmn1r32 UTSW 6 66,530,644 (GRCm39) missense possibly damaging 0.90
R0732:Vmn1r32 UTSW 6 66,530,690 (GRCm39) missense probably benign 0.01
R1205:Vmn1r32 UTSW 6 66,530,539 (GRCm39) missense probably benign 0.01
R1638:Vmn1r32 UTSW 6 66,529,939 (GRCm39) missense possibly damaging 0.53
R1732:Vmn1r32 UTSW 6 66,530,285 (GRCm39) missense probably benign 0.19
R2049:Vmn1r32 UTSW 6 66,530,545 (GRCm39) missense probably damaging 1.00
R2127:Vmn1r32 UTSW 6 66,530,533 (GRCm39) missense probably benign 0.09
R3773:Vmn1r32 UTSW 6 66,530,351 (GRCm39) missense probably benign 0.01
R3834:Vmn1r32 UTSW 6 66,530,647 (GRCm39) missense probably benign 0.02
R3980:Vmn1r32 UTSW 6 66,530,698 (GRCm39) missense probably damaging 0.98
R4737:Vmn1r32 UTSW 6 66,530,629 (GRCm39) missense probably damaging 1.00
R5569:Vmn1r32 UTSW 6 66,530,156 (GRCm39) missense probably damaging 0.98
R6382:Vmn1r32 UTSW 6 66,530,345 (GRCm39) missense probably benign 0.07
R6894:Vmn1r32 UTSW 6 66,530,345 (GRCm39) missense possibly damaging 0.94
R7394:Vmn1r32 UTSW 6 66,530,173 (GRCm39) missense probably benign 0.06
R7980:Vmn1r32 UTSW 6 66,530,305 (GRCm39) nonsense probably null
R8833:Vmn1r32 UTSW 6 66,530,623 (GRCm39) missense possibly damaging 0.53
R8867:Vmn1r32 UTSW 6 66,530,651 (GRCm39) missense probably damaging 0.98
R8975:Vmn1r32 UTSW 6 66,530,189 (GRCm39) missense probably benign 0.03
R9131:Vmn1r32 UTSW 6 66,530,020 (GRCm39) missense probably benign 0.30
R9135:Vmn1r32 UTSW 6 66,530,120 (GRCm39) nonsense probably null
R9429:Vmn1r32 UTSW 6 66,530,237 (GRCm39) missense probably benign 0.03
Posted On 2016-08-02