Incidental Mutation 'IGL03236:Vmn1r66'
ID 414054
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r66
Ensembl Gene ENSMUSG00000043066
Gene Name vomeronasal 1 receptor 66
Synonyms V1re11
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # IGL03236
Quality Score
Status
Chromosome 7
Chromosomal Location 10007755-10009278 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 10008990 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Asparagine at position 14 (K14N)
Ref Sequence ENSEMBL: ENSMUSP00000153860 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000060374] [ENSMUST00000227719] [ENSMUST00000228086] [ENSMUST00000228622]
AlphaFold Q8K4I0
Predicted Effect probably damaging
Transcript: ENSMUST00000060374
AA Change: K14N

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000055861
Gene: ENSMUSG00000043066
AA Change: K14N

DomainStartEndE-ValueType
Pfam:V1R 39 295 4.5e-28 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000226202
Predicted Effect probably damaging
Transcript: ENSMUST00000227719
AA Change: K14N

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
Predicted Effect probably damaging
Transcript: ENSMUST00000228086
AA Change: K14N

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
Predicted Effect probably damaging
Transcript: ENSMUST00000228622
AA Change: K14N

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl4fm1 A G 4: 144,246,486 (GRCm39) T11A probably benign Het
Abca17 A G 17: 24,545,450 (GRCm39) probably benign Het
Aox1 G T 1: 58,349,156 (GRCm39) E641* probably null Het
Arhgef10l G T 4: 140,338,671 (GRCm39) D30E probably damaging Het
Arhgef37 A T 18: 61,656,897 (GRCm39) I56N probably damaging Het
Cwf19l1 T C 19: 44,115,887 (GRCm39) I181V probably benign Het
Dnai2 A G 11: 114,648,075 (GRCm39) probably benign Het
Elp2 A G 18: 24,755,300 (GRCm39) probably benign Het
Epb41l4a G A 18: 33,943,272 (GRCm39) S541L probably damaging Het
Ibsp A C 5: 104,453,871 (GRCm39) N70H probably benign Het
Ikzf1 A G 11: 11,657,848 (GRCm39) E35G probably damaging Het
Kdm5a T C 6: 120,415,949 (GRCm39) V1623A probably damaging Het
Kpna7 A T 5: 144,922,504 (GRCm39) V499E unknown Het
Krtap4-16 C A 11: 99,741,962 (GRCm39) R146L unknown Het
Map2k5 T A 9: 63,193,674 (GRCm39) probably benign Het
Mfn2 A G 4: 147,966,562 (GRCm39) F543S probably damaging Het
Mical3 A G 6: 120,946,345 (GRCm39) L1052P probably benign Het
Mycbp2 T C 14: 103,536,134 (GRCm39) N272S probably damaging Het
Ndel1 A G 11: 68,732,976 (GRCm39) Y87H probably benign Het
Ndnf G A 6: 65,673,156 (GRCm39) V45M possibly damaging Het
Nr3c1 A G 18: 39,619,444 (GRCm39) I281T probably benign Het
Ntm A G 9: 29,020,802 (GRCm39) V139A probably benign Het
Or5ac23 A C 16: 59,149,200 (GRCm39) V224G probably damaging Het
Pkhd1l1 T G 15: 44,445,222 (GRCm39) V3698G probably damaging Het
Plcb1 A G 2: 135,188,226 (GRCm39) Y773C probably damaging Het
Prkaca T A 8: 84,717,074 (GRCm39) F138Y probably damaging Het
Qser1 T C 2: 104,616,877 (GRCm39) T1312A probably benign Het
Slc47a2 T C 11: 61,204,505 (GRCm39) E282G probably damaging Het
Smchd1 G A 17: 71,698,425 (GRCm39) T1117I possibly damaging Het
Utp6 A G 11: 79,851,567 (GRCm39) probably benign Het
Vmn1r71 A T 7: 10,482,211 (GRCm39) V93E probably benign Het
Zfp768 G A 7: 126,943,142 (GRCm39) L329F possibly damaging Het
Other mutations in Vmn1r66
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02957:Vmn1r66 APN 7 10,008,737 (GRCm39) missense probably damaging 1.00
R0380:Vmn1r66 UTSW 7 10,008,670 (GRCm39) missense probably benign 0.02
R1625:Vmn1r66 UTSW 7 10,008,316 (GRCm39) missense probably benign 0.00
R3745:Vmn1r66 UTSW 7 10,008,248 (GRCm39) missense possibly damaging 0.64
R4081:Vmn1r66 UTSW 7 10,008,733 (GRCm39) missense probably damaging 1.00
R4389:Vmn1r66 UTSW 7 10,008,715 (GRCm39) nonsense probably null
R5081:Vmn1r66 UTSW 7 10,008,722 (GRCm39) missense probably damaging 1.00
R5909:Vmn1r66 UTSW 7 10,008,269 (GRCm39) missense probably benign 0.44
R6164:Vmn1r66 UTSW 7 10,008,329 (GRCm39) nonsense probably null
R6792:Vmn1r66 UTSW 7 10,008,412 (GRCm39) missense possibly damaging 0.78
R6843:Vmn1r66 UTSW 7 10,008,692 (GRCm39) missense probably damaging 1.00
R7013:Vmn1r66 UTSW 7 10,008,683 (GRCm39) missense possibly damaging 0.94
R7173:Vmn1r66 UTSW 7 10,008,482 (GRCm39) missense probably benign 0.00
R7400:Vmn1r66 UTSW 7 10,008,874 (GRCm39) missense probably damaging 0.99
R9092:Vmn1r66 UTSW 7 10,008,110 (GRCm39) missense possibly damaging 0.71
Z1176:Vmn1r66 UTSW 7 10,008,212 (GRCm39) missense probably benign 0.01
Posted On 2016-08-02