Incidental Mutation 'IGL01986:Vmn2r95'
ID 181894
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r95
Ensembl Gene ENSMUSG00000091631
Gene Name vomeronasal 2, receptor 95
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.067) question?
Stock # IGL01986
Quality Score
Status
Chromosome 17
Chromosomal Location 18644366-18672586 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 18660473 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Serine at position 295 (N295S)
Ref Sequence ENSEMBL: ENSMUSP00000156117 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000166327] [ENSMUST00000232090] [ENSMUST00000232464]
AlphaFold A0A338P6T0
Predicted Effect probably benign
Transcript: ENSMUST00000166327
AA Change: N295S

PolyPhen 2 Score 0.057 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000126106
Gene: ENSMUSG00000091631
AA Change: N295S

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:ANF_receptor 82 462 1.8e-35 PFAM
Pfam:NCD3G 509 562 3.2e-20 PFAM
Pfam:7tm_3 594 830 3.2e-51 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000232090
AA Change: N295S

PolyPhen 2 Score 0.057 (Sensitivity: 0.94; Specificity: 0.84)
Predicted Effect probably benign
Transcript: ENSMUST00000232464
AA Change: N295S

PolyPhen 2 Score 0.011 (Sensitivity: 0.96; Specificity: 0.78)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
6820408C15Rik A T 2: 152,282,956 (GRCm39) I245F possibly damaging Het
Abca3 G A 17: 24,627,088 (GRCm39) G1263D probably damaging Het
Arap2 A T 5: 62,779,265 (GRCm39) S1442T probably damaging Het
Arl15 C A 13: 114,058,902 (GRCm39) S56R possibly damaging Het
Ccdc38 A T 10: 93,415,705 (GRCm39) N415Y probably damaging Het
Ccny G A 18: 9,377,817 (GRCm39) R81C probably damaging Het
Cracd T A 5: 77,006,457 (GRCm39) S939R unknown Het
Csmd3 T C 15: 47,522,591 (GRCm39) T2693A possibly damaging Het
Fancm C T 12: 65,173,429 (GRCm39) Q1914* probably null Het
Fcsk T C 8: 111,609,889 (GRCm39) T1042A probably benign Het
Gm18856 G A 13: 14,139,413 (GRCm39) probably benign Het
Gramd1a A T 7: 30,833,434 (GRCm39) L610Q possibly damaging Het
Hsd17b4 C A 18: 50,293,193 (GRCm39) probably benign Het
Hspa12a A G 19: 58,787,834 (GRCm39) S663P probably benign Het
Insr C T 8: 3,208,817 (GRCm39) V1215I probably damaging Het
Kdr A G 5: 76,113,519 (GRCm39) V783A probably benign Het
Klhl9 T C 4: 88,640,016 (GRCm39) D75G probably damaging Het
Lmntd1 A G 6: 145,365,533 (GRCm39) S53P probably damaging Het
Lrrc41 T A 4: 115,946,519 (GRCm39) F411L probably benign Het
Lyst G A 13: 13,950,212 (GRCm39) probably null Het
Mmp17 A G 5: 129,673,692 (GRCm39) H257R probably damaging Het
Nkiras1 G A 14: 18,280,071 (GRCm38) R154Q probably damaging Het
Or10ag2 A G 2: 87,248,880 (GRCm39) I163V probably benign Het
Or2b4 A G 17: 38,116,957 (GRCm39) K307R probably damaging Het
Or4p21 C T 2: 88,276,839 (GRCm39) V148I probably benign Het
Or8s16 T C 15: 98,210,660 (GRCm39) Y257C probably damaging Het
Pcsk6 G A 7: 65,577,625 (GRCm39) R60H probably damaging Het
Polk T C 13: 96,620,331 (GRCm39) D623G probably benign Het
Rlf A T 4: 121,005,303 (GRCm39) C1226S probably damaging Het
Rpa2 C T 4: 132,499,191 (GRCm39) P87S probably benign Het
Rpa2 C T 4: 132,499,192 (GRCm39) P87L probably benign Het
Sema5a T C 15: 32,682,506 (GRCm39) probably benign Het
Sis A T 3: 72,852,545 (GRCm39) M529K probably damaging Het
Sspo T C 6: 48,460,237 (GRCm39) M3375T probably benign Het
Syne3 A T 12: 104,934,259 (GRCm39) L83Q probably damaging Het
Tec A T 5: 72,939,348 (GRCm39) Y222* probably null Het
Tfap2d C T 1: 19,189,383 (GRCm39) probably benign Het
Trak1 G A 9: 121,302,033 (GRCm39) A930T probably benign Het
Ugt2b34 G T 5: 87,049,111 (GRCm39) H305N probably benign Het
Other mutations in Vmn2r95
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01024:Vmn2r95 APN 17 18,672,590 (GRCm39) utr 3 prime probably benign
IGL01479:Vmn2r95 APN 17 18,664,124 (GRCm39) missense probably damaging 1.00
IGL01890:Vmn2r95 APN 17 18,671,737 (GRCm39) missense probably damaging 1.00
IGL02113:Vmn2r95 APN 17 18,660,169 (GRCm39) missense possibly damaging 0.47
IGL02154:Vmn2r95 APN 17 18,672,248 (GRCm39) missense probably benign 0.16
IGL02190:Vmn2r95 APN 17 18,672,038 (GRCm39) missense probably benign 0.00
IGL02412:Vmn2r95 APN 17 18,660,218 (GRCm39) missense probably damaging 1.00
IGL02550:Vmn2r95 APN 17 18,671,994 (GRCm39) missense probably damaging 1.00
IGL02679:Vmn2r95 APN 17 18,664,116 (GRCm39) missense probably damaging 1.00
IGL02691:Vmn2r95 APN 17 18,672,120 (GRCm39) missense probably benign 0.07
IGL02990:Vmn2r95 APN 17 18,672,298 (GRCm39) nonsense probably null
IGL03032:Vmn2r95 APN 17 18,672,575 (GRCm39) missense probably benign 0.00
R0416:Vmn2r95 UTSW 17 18,661,664 (GRCm39) missense probably damaging 1.00
R0448:Vmn2r95 UTSW 17 18,672,005 (GRCm39) missense possibly damaging 0.92
R0514:Vmn2r95 UTSW 17 18,671,844 (GRCm39) missense probably benign
R0519:Vmn2r95 UTSW 17 18,659,765 (GRCm39) missense probably damaging 1.00
R0539:Vmn2r95 UTSW 17 18,672,362 (GRCm39) missense probably damaging 1.00
R1501:Vmn2r95 UTSW 17 18,660,118 (GRCm39) missense probably damaging 0.99
R1598:Vmn2r95 UTSW 17 18,672,575 (GRCm39) missense probably benign 0.03
R1613:Vmn2r95 UTSW 17 18,660,901 (GRCm39) splice site probably benign
R1861:Vmn2r95 UTSW 17 18,672,530 (GRCm39) missense probably damaging 1.00
R1921:Vmn2r95 UTSW 17 18,644,575 (GRCm39) missense probably benign 0.11
R1986:Vmn2r95 UTSW 17 18,671,805 (GRCm39) missense probably benign
R2031:Vmn2r95 UTSW 17 18,659,717 (GRCm39) missense possibly damaging 0.94
R2040:Vmn2r95 UTSW 17 18,661,561 (GRCm39) missense probably damaging 1.00
R3608:Vmn2r95 UTSW 17 18,660,235 (GRCm39) missense possibly damaging 0.47
R3727:Vmn2r95 UTSW 17 18,661,744 (GRCm39) nonsense probably null
R3953:Vmn2r95 UTSW 17 18,660,358 (GRCm39) missense possibly damaging 0.79
R3955:Vmn2r95 UTSW 17 18,660,358 (GRCm39) missense possibly damaging 0.79
R3957:Vmn2r95 UTSW 17 18,660,358 (GRCm39) missense possibly damaging 0.79
R4474:Vmn2r95 UTSW 17 18,672,507 (GRCm39) missense probably damaging 1.00
R4672:Vmn2r95 UTSW 17 18,672,413 (GRCm39) missense probably damaging 1.00
R4850:Vmn2r95 UTSW 17 18,671,915 (GRCm39) missense probably damaging 1.00
R5054:Vmn2r95 UTSW 17 18,671,708 (GRCm39) missense possibly damaging 0.63
R5178:Vmn2r95 UTSW 17 18,660,337 (GRCm39) missense probably benign 0.01
R5980:Vmn2r95 UTSW 17 18,661,624 (GRCm39) missense probably benign
R6183:Vmn2r95 UTSW 17 18,664,192 (GRCm39) missense probably damaging 0.99
R6276:Vmn2r95 UTSW 17 18,671,732 (GRCm39) missense possibly damaging 0.96
R6651:Vmn2r95 UTSW 17 18,660,622 (GRCm39) missense probably damaging 1.00
R6682:Vmn2r95 UTSW 17 18,660,489 (GRCm39) missense probably damaging 1.00
R6797:Vmn2r95 UTSW 17 18,672,551 (GRCm39) utr 3 prime probably benign
R6799:Vmn2r95 UTSW 17 18,659,555 (GRCm39) missense probably damaging 1.00
R6849:Vmn2r95 UTSW 17 18,664,182 (GRCm39) missense probably damaging 1.00
R6849:Vmn2r95 UTSW 17 18,664,181 (GRCm39) missense probably damaging 1.00
R6982:Vmn2r95 UTSW 17 18,672,323 (GRCm39) missense probably damaging 1.00
R7203:Vmn2r95 UTSW 17 18,661,577 (GRCm39) missense probably benign 0.01
R7226:Vmn2r95 UTSW 17 18,672,245 (GRCm39) missense possibly damaging 0.90
R7240:Vmn2r95 UTSW 17 18,672,225 (GRCm39) missense probably benign 0.15
R7383:Vmn2r95 UTSW 17 18,660,734 (GRCm39) missense probably benign 0.06
R7614:Vmn2r95 UTSW 17 18,660,352 (GRCm39) missense probably benign
R7755:Vmn2r95 UTSW 17 18,644,367 (GRCm39) start codon destroyed probably null 0.99
R7942:Vmn2r95 UTSW 17 18,660,529 (GRCm39) missense possibly damaging 0.74
R8355:Vmn2r95 UTSW 17 18,660,352 (GRCm39) missense probably benign
R8455:Vmn2r95 UTSW 17 18,660,352 (GRCm39) missense probably benign
R8478:Vmn2r95 UTSW 17 18,672,544 (GRCm39) missense probably damaging 1.00
R8547:Vmn2r95 UTSW 17 18,664,161 (GRCm39) missense probably damaging 1.00
R8752:Vmn2r95 UTSW 17 18,661,738 (GRCm39) missense probably damaging 0.98
R8788:Vmn2r95 UTSW 17 18,671,790 (GRCm39) missense probably benign 0.09
R8852:Vmn2r95 UTSW 17 18,664,113 (GRCm39) missense possibly damaging 0.95
R9098:Vmn2r95 UTSW 17 18,660,167 (GRCm39) missense possibly damaging 0.88
R9202:Vmn2r95 UTSW 17 18,644,394 (GRCm39) missense probably benign 0.00
R9244:Vmn2r95 UTSW 17 18,672,189 (GRCm39) missense possibly damaging 0.91
R9546:Vmn2r95 UTSW 17 18,661,721 (GRCm39) missense probably benign 0.01
R9665:Vmn2r95 UTSW 17 18,660,607 (GRCm39) missense probably damaging 0.99
Z1088:Vmn2r95 UTSW 17 18,660,663 (GRCm39) missense probably benign 0.01
Posted On 2014-05-07