Incidental Mutation 'IGL02140:Vmn2r32'
ID 281481
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r32
Ensembl Gene ENSMUSG00000096743
Gene Name vomeronasal 2, receptor 32
Synonyms V2r5
Accession Numbers
Essential gene? Probably non essential (E-score: 0.249) question?
Stock # IGL02140
Quality Score
Status
Chromosome 7
Chromosomal Location 7466968-7482972 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 7479696 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Serine at position 159 (F159S)
Ref Sequence ENSEMBL: ENSMUSP00000092462 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094866]
AlphaFold K7N686
Predicted Effect probably damaging
Transcript: ENSMUST00000094866
AA Change: F159S

PolyPhen 2 Score 0.970 (Sensitivity: 0.77; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000092462
Gene: ENSMUSG00000096743
AA Change: F159S

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 73 470 3.6e-33 PFAM
Pfam:NCD3G 512 565 8.1e-21 PFAM
Pfam:7tm_3 598 833 9.5e-55 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700049A03Rik G A 12: 71,195,034 (GRCm39) V144I probably benign Het
B3gat1 A G 9: 26,669,043 (GRCm39) K325E possibly damaging Het
Cd36 T A 5: 18,033,766 (GRCm39) probably benign Het
Ces3a A G 8: 105,782,263 (GRCm39) E325G probably benign Het
Col1a2 G A 6: 4,515,639 (GRCm39) G136D unknown Het
Cyp3a25 T G 5: 145,946,273 (GRCm39) probably benign Het
Cyp3a59 T C 5: 146,039,690 (GRCm39) L321P probably damaging Het
Dag1 A G 9: 108,095,391 (GRCm39) S34P probably damaging Het
Defa27 A T 8: 21,805,674 (GRCm39) K13* probably null Het
Disp2 T C 2: 118,621,350 (GRCm39) F694S probably benign Het
Dnah12 G T 14: 26,437,732 (GRCm39) A454S probably benign Het
Dync2h1 A T 9: 7,147,791 (GRCm39) D946E probably benign Het
Fcgbp A G 7: 27,791,379 (GRCm39) E880G probably damaging Het
Fgfr4 T C 13: 55,308,992 (GRCm39) V371A probably benign Het
Frem3 G T 8: 81,340,736 (GRCm39) V1010F possibly damaging Het
Gm13283 G A 4: 88,679,272 (GRCm39) V88I probably benign Het
Gm5134 G A 10: 75,821,945 (GRCm39) V260I probably benign Het
Grhl2 A G 15: 37,270,830 (GRCm39) probably benign Het
Hectd1 A T 12: 51,820,920 (GRCm39) W1090R probably damaging Het
Hydin G A 8: 111,293,570 (GRCm39) V3506I probably benign Het
Igkc C T 6: 70,703,559 (GRCm39) R47* probably null Het
Iglv3 T A 16: 19,060,160 (GRCm39) Q56L probably damaging Het
Impg2 T A 16: 56,079,831 (GRCm39) M436K probably benign Het
Kcnma1 T A 14: 23,359,113 (GRCm39) K1110N probably damaging Het
Marf1 T C 16: 13,959,776 (GRCm39) E694G probably damaging Het
Nup37 A C 10: 87,994,791 (GRCm39) K118T probably benign Het
Or10al7 A G 17: 38,366,481 (GRCm39) M1T probably null Het
Or4a73 T C 2: 89,420,586 (GRCm39) E291G probably damaging Het
P3h1 A G 4: 119,095,062 (GRCm39) D273G probably damaging Het
Pcsk9 T C 4: 106,311,843 (GRCm39) D178G probably benign Het
Phyhipl T C 10: 70,406,660 (GRCm39) K53R probably damaging Het
Pkp3 T G 7: 140,669,249 (GRCm39) L697R probably damaging Het
Rab11fip3 A G 17: 26,286,866 (GRCm39) V429A probably benign Het
Rgl2 A G 17: 34,152,098 (GRCm39) N295S probably damaging Het
Spag5 A T 11: 78,206,459 (GRCm39) D817V possibly damaging Het
Tas2r117 C A 6: 132,780,558 (GRCm39) T232K probably benign Het
Thumpd1 A G 7: 119,316,232 (GRCm39) V239A possibly damaging Het
Timd4 T A 11: 46,710,841 (GRCm39) S248T possibly damaging Het
Tmem207 A T 16: 26,335,490 (GRCm39) N82K probably benign Het
Ttn T A 2: 76,538,557 (GRCm39) T34714S possibly damaging Het
Vmn1r194 G A 13: 22,428,706 (GRCm39) V108I probably benign Het
Vmn2r24 T A 6: 123,757,631 (GRCm39) S166R probably damaging Het
Wdr72 A T 9: 74,117,505 (GRCm39) Q739L probably benign Het
Other mutations in Vmn2r32
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02333:Vmn2r32 APN 7 7,467,143 (GRCm39) missense probably damaging 1.00
IGL02406:Vmn2r32 APN 7 7,479,709 (GRCm39) missense probably benign
IGL02428:Vmn2r32 APN 7 7,477,283 (GRCm39) missense probably benign 0.02
IGL02484:Vmn2r32 APN 7 7,467,116 (GRCm39) missense probably damaging 1.00
IGL03277:Vmn2r32 APN 7 7,477,251 (GRCm39) missense probably benign 0.23
IGL03366:Vmn2r32 APN 7 7,467,029 (GRCm39) missense probably damaging 0.99
R1055:Vmn2r32 UTSW 7 7,477,326 (GRCm39) nonsense probably null
R1695:Vmn2r32 UTSW 7 7,466,991 (GRCm39) missense probably benign 0.01
R2172:Vmn2r32 UTSW 7 7,477,614 (GRCm39) missense probably damaging 0.99
R2262:Vmn2r32 UTSW 7 7,477,618 (GRCm39) missense probably benign
R3150:Vmn2r32 UTSW 7 7,475,554 (GRCm39) missense probably benign
R4362:Vmn2r32 UTSW 7 7,482,857 (GRCm39) nonsense probably null
R4432:Vmn2r32 UTSW 7 7,482,918 (GRCm39) missense probably damaging 0.98
R4851:Vmn2r32 UTSW 7 7,482,953 (GRCm39) missense possibly damaging 0.59
R4949:Vmn2r32 UTSW 7 7,467,083 (GRCm39) missense probably benign 0.22
R5990:Vmn2r32 UTSW 7 7,482,809 (GRCm39) missense probably damaging 0.97
R6083:Vmn2r32 UTSW 7 7,467,209 (GRCm39) missense probably benign 0.15
R6084:Vmn2r32 UTSW 7 7,467,209 (GRCm39) missense probably benign 0.15
R6116:Vmn2r32 UTSW 7 7,467,092 (GRCm39) missense probably damaging 1.00
R6263:Vmn2r32 UTSW 7 7,479,691 (GRCm39) missense possibly damaging 0.90
R6889:Vmn2r32 UTSW 7 7,475,573 (GRCm39) missense possibly damaging 0.82
R7286:Vmn2r32 UTSW 7 7,482,807 (GRCm39) missense probably benign 0.21
R7390:Vmn2r32 UTSW 7 7,482,851 (GRCm39) missense probably benign 0.00
R7412:Vmn2r32 UTSW 7 7,477,212 (GRCm39) missense possibly damaging 0.53
R7508:Vmn2r32 UTSW 7 7,470,373 (GRCm39) missense possibly damaging 0.87
R8812:Vmn2r32 UTSW 7 7,477,669 (GRCm39) missense probably damaging 1.00
R8968:Vmn2r32 UTSW 7 7,477,204 (GRCm39) missense probably benign 0.00
R9331:Vmn2r32 UTSW 7 7,467,402 (GRCm39) nonsense probably null
R9358:Vmn2r32 UTSW 7 7,477,197 (GRCm39) missense probably damaging 1.00
Z1177:Vmn2r32 UTSW 7 7,477,160 (GRCm39) missense probably damaging 0.98
Posted On 2015-04-16