Incidental Mutation 'IGL02621:Vmn1r168'
ID 300853
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn1r168
Ensembl Gene ENSMUSG00000074291
Gene Name vomeronasal 1 receptor 168
Synonyms Gm10659
Accession Numbers
Essential gene? Probably non essential (E-score: 0.103) question?
Stock # IGL02621
Quality Score
Status
Chromosome 7
Chromosomal Location 23240145-23241074 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 23240780 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Serine at position 212 (R212S)
Ref Sequence ENSEMBL: ENSMUSP00000096301 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098704]
AlphaFold K7N6B6
Predicted Effect probably damaging
Transcript: ENSMUST00000098704
AA Change: R212S

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000096301
Gene: ENSMUSG00000074291
AA Change: R212S

DomainStartEndE-ValueType
Pfam:TAS2R 8 296 1.1e-12 PFAM
Pfam:V1R 41 295 2.5e-14 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110002L01Rik C A 12: 3,476,688 (GRCm39) probably benign Het
2210408I21Rik T C 13: 77,408,150 (GRCm39) I159T possibly damaging Het
Agpat3 T A 10: 78,120,900 (GRCm39) I93F probably damaging Het
Armc8 T C 9: 99,409,122 (GRCm39) probably benign Het
Atr G A 9: 95,790,453 (GRCm39) A1598T probably benign Het
Bltp1 T A 3: 37,095,633 (GRCm39) probably benign Het
Clk1 T C 1: 58,453,614 (GRCm39) D324G probably damaging Het
Cntnap4 A T 8: 113,537,355 (GRCm39) D742V probably damaging Het
Esrrb A G 12: 86,468,735 (GRCm39) N16S probably benign Het
Grm1 A T 10: 10,564,755 (GRCm39) Y1184* probably null Het
Hint1 G T 11: 54,761,011 (GRCm39) probably benign Het
Itch A T 2: 155,014,504 (GRCm39) probably null Het
Lmod3 T C 6: 97,215,796 (GRCm39) probably benign Het
Map3k4 C A 17: 12,482,900 (GRCm39) A606S probably damaging Het
Mapk4 A T 18: 74,103,346 (GRCm39) S54R probably damaging Het
Megf11 A G 9: 64,601,214 (GRCm39) D807G probably benign Het
Mgat5 A G 1: 127,325,326 (GRCm39) T398A possibly damaging Het
Nme8 T G 13: 19,859,818 (GRCm39) K28N probably damaging Het
Pamr1 A G 2: 102,464,688 (GRCm39) N279S probably benign Het
Pcca A T 14: 122,922,391 (GRCm39) D384V probably damaging Het
Prkag1 A T 15: 98,711,909 (GRCm39) I239N probably damaging Het
Psme4 A G 11: 30,798,131 (GRCm39) T1375A probably benign Het
Ptk2 A C 15: 73,077,994 (GRCm39) L1024R probably damaging Het
Rere G A 4: 150,698,269 (GRCm39) probably benign Het
Scn2a A G 2: 65,579,223 (GRCm39) probably benign Het
Sema5a T A 15: 32,538,802 (GRCm39) probably benign Het
Shoc1 A T 4: 59,062,668 (GRCm39) W863R probably damaging Het
Slc9a1 T A 4: 133,097,879 (GRCm39) W9R probably benign Het
Slco1a5 T A 6: 142,187,741 (GRCm39) M533L probably benign Het
Ttll4 T A 1: 74,726,643 (GRCm39) S720T probably damaging Het
Vmn2r114 T C 17: 23,529,494 (GRCm39) I203V probably damaging Het
Wdr38 A T 2: 38,888,424 (GRCm39) N7I probably damaging Het
Other mutations in Vmn1r168
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01761:Vmn1r168 APN 7 23,241,070 (GRCm39) missense possibly damaging 0.73
IGL02650:Vmn1r168 APN 7 23,240,916 (GRCm39) missense probably benign 0.13
PIT4466001:Vmn1r168 UTSW 7 23,240,421 (GRCm39) missense probably damaging 1.00
R0320:Vmn1r168 UTSW 7 23,240,767 (GRCm39) missense probably benign 0.12
R1595:Vmn1r168 UTSW 7 23,240,620 (GRCm39) missense probably damaging 1.00
R1618:Vmn1r168 UTSW 7 23,240,725 (GRCm39) missense probably benign 0.02
R1808:Vmn1r168 UTSW 7 23,240,184 (GRCm39) missense probably benign 0.05
R2418:Vmn1r168 UTSW 7 23,240,824 (GRCm39) missense probably benign 0.05
R2419:Vmn1r168 UTSW 7 23,240,824 (GRCm39) missense probably benign 0.05
R4846:Vmn1r168 UTSW 7 23,240,490 (GRCm39) missense probably damaging 1.00
R4864:Vmn1r168 UTSW 7 23,240,907 (GRCm39) missense probably damaging 0.98
R5269:Vmn1r168 UTSW 7 23,240,839 (GRCm39) missense probably benign 0.40
R6265:Vmn1r168 UTSW 7 23,240,961 (GRCm39) missense probably benign
R6353:Vmn1r168 UTSW 7 23,240,944 (GRCm39) missense probably benign 0.02
R6768:Vmn1r168 UTSW 7 23,240,460 (GRCm39) missense probably damaging 1.00
R6921:Vmn1r168 UTSW 7 23,240,323 (GRCm39) missense probably damaging 1.00
R8247:Vmn1r168 UTSW 7 23,240,487 (GRCm39) missense possibly damaging 0.61
R8749:Vmn1r168 UTSW 7 23,240,428 (GRCm39) missense probably benign 0.10
R9749:Vmn1r168 UTSW 7 23,240,237 (GRCm39) missense probably damaging 0.98
R9768:Vmn1r168 UTSW 7 23,240,509 (GRCm39) missense probably benign 0.02
Posted On 2015-04-16