Incidental Mutation 'IGL01646:Vmn2r99'
ID 102691
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r99
Ensembl Gene ENSMUSG00000090304
Gene Name vomeronasal 2, receptor 99
Synonyms EG665376
Accession Numbers
Essential gene? Probably non essential (E-score: 0.122) question?
Stock # IGL01646
Quality Score
Status
Chromosome 17
Chromosomal Location 19582397-19614852 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) C to A at 19613920 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000156067 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000176107] [ENSMUST00000231989]
AlphaFold H3BK37
Predicted Effect probably benign
Transcript: ENSMUST00000176107
SMART Domains Protein: ENSMUSP00000135236
Gene: ENSMUSG00000090304

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:ANF_receptor 81 448 5.7e-33 PFAM
Pfam:NCD3G 508 561 1.8e-21 PFAM
Pfam:7tm_3 593 829 4.6e-52 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000231989
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ambp C T 4: 63,066,977 (GRCm39) V188I probably benign Het
Bbs9 G T 9: 22,582,221 (GRCm39) E638* probably null Het
Bmp6 A G 13: 38,682,904 (GRCm39) M465V probably damaging Het
Ccdc192 T A 18: 57,800,417 (GRCm39) C171* probably null Het
Cemip T C 7: 83,632,440 (GRCm39) E374G possibly damaging Het
Cnbd1 A T 4: 18,895,141 (GRCm39) Y200* probably null Het
Cox6b1 G T 7: 30,323,929 (GRCm39) Y34* probably null Het
Cyp2d26 A C 15: 82,675,619 (GRCm39) I303M probably benign Het
Diaph1 T A 18: 38,026,469 (GRCm39) probably null Het
Dmp1 T C 5: 104,359,731 (GRCm39) S136P probably damaging Het
Dpy19l1 C T 9: 24,396,365 (GRCm39) R117Q probably damaging Het
Eea1 A G 10: 95,832,877 (GRCm39) T241A probably damaging Het
Erap1 C A 13: 74,814,291 (GRCm39) T25K probably damaging Het
Fras1 A G 5: 96,906,007 (GRCm39) E3137G probably benign Het
Fryl C T 5: 73,179,844 (GRCm39) probably null Het
Gldc T G 19: 30,078,165 (GRCm39) D944A possibly damaging Het
Grm5 A G 7: 87,689,267 (GRCm39) Y546C probably damaging Het
Igkv1-122 G A 6: 67,993,728 (GRCm39) M1I probably null Het
Jag2 G A 12: 112,879,969 (GRCm39) P380S possibly damaging Het
Kcnc2 T C 10: 112,108,311 (GRCm39) probably null Het
Kmt2a T C 9: 44,736,781 (GRCm39) probably benign Het
Lrrc55 A G 2: 85,022,333 (GRCm39) V286A probably damaging Het
Mllt10 C A 2: 18,127,128 (GRCm39) H82N probably damaging Het
Myh11 C A 16: 14,039,639 (GRCm39) R837L probably damaging Het
Nsg1 C A 5: 38,313,035 (GRCm39) D55Y probably damaging Het
Nup107 C A 10: 117,617,247 (GRCm39) R221M probably damaging Het
Nup153 G T 13: 46,837,583 (GRCm39) A1213D possibly damaging Het
Ovgp1 G A 3: 105,885,665 (GRCm39) G174S probably damaging Het
Papss2 C T 19: 32,629,482 (GRCm39) A357V probably benign Het
Pclo A G 5: 14,763,881 (GRCm39) K4118R unknown Het
Pde2a T C 7: 101,156,918 (GRCm39) I628T possibly damaging Het
Pla2r1 A G 2: 60,325,708 (GRCm39) W521R probably damaging Het
Pld1 A T 3: 28,153,813 (GRCm39) Q744L probably damaging Het
Pnpo T A 11: 96,829,775 (GRCm39) E251V possibly damaging Het
Rdh10 C T 1: 16,178,246 (GRCm39) H173Y possibly damaging Het
Sgpp2 A T 1: 78,393,533 (GRCm39) I179F probably damaging Het
Slc11a1 C T 1: 74,423,899 (GRCm39) P409L probably damaging Het
Slc35b4 T A 6: 34,135,364 (GRCm39) N316I probably benign Het
Snrnp200 A G 2: 127,064,148 (GRCm39) I712V probably benign Het
Spr T C 6: 85,111,222 (GRCm39) D216G possibly damaging Het
Sri G A 5: 8,113,755 (GRCm39) probably null Het
Tas2r124 T C 6: 132,732,332 (GRCm39) S214P probably damaging Het
Tg T A 15: 66,549,936 (GRCm39) S233T probably damaging Het
Tgfbr3 A T 5: 107,269,279 (GRCm39) probably benign Het
Vmn2r45 A G 7: 8,486,337 (GRCm39) F317S probably benign Het
Zfp957 T C 14: 79,451,331 (GRCm39) E156G probably benign Het
Other mutations in Vmn2r99
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00503:Vmn2r99 APN 17 19,599,116 (GRCm39) missense probably benign 0.01
IGL01113:Vmn2r99 APN 17 19,614,518 (GRCm39) missense probably benign 0.20
IGL01138:Vmn2r99 APN 17 19,602,885 (GRCm39) missense probably damaging 0.97
IGL01769:Vmn2r99 APN 17 19,600,377 (GRCm39) missense probably damaging 1.00
IGL02112:Vmn2r99 APN 17 19,600,494 (GRCm39) missense probably null 0.99
IGL02891:Vmn2r99 APN 17 19,598,952 (GRCm39) nonsense probably null
IGL03132:Vmn2r99 APN 17 19,598,485 (GRCm39) nonsense probably null
FR4548:Vmn2r99 UTSW 17 19,614,547 (GRCm39) missense probably damaging 0.97
FR4976:Vmn2r99 UTSW 17 19,614,547 (GRCm39) missense probably damaging 0.97
PIT4382001:Vmn2r99 UTSW 17 19,614,605 (GRCm39) missense probably damaging 1.00
R0196:Vmn2r99 UTSW 17 19,614,835 (GRCm39) missense probably benign 0.00
R0720:Vmn2r99 UTSW 17 19,599,305 (GRCm39) missense probably benign 0.00
R1501:Vmn2r99 UTSW 17 19,582,521 (GRCm39) missense possibly damaging 0.93
R1519:Vmn2r99 UTSW 17 19,600,322 (GRCm39) missense probably benign 0.00
R1670:Vmn2r99 UTSW 17 19,582,514 (GRCm39) missense probably benign 0.37
R1682:Vmn2r99 UTSW 17 19,598,207 (GRCm39) missense probably damaging 0.97
R1873:Vmn2r99 UTSW 17 19,582,415 (GRCm39) missense probably benign 0.25
R1967:Vmn2r99 UTSW 17 19,599,077 (GRCm39) missense probably benign 0.01
R2101:Vmn2r99 UTSW 17 19,598,253 (GRCm39) missense probably damaging 1.00
R2474:Vmn2r99 UTSW 17 19,598,891 (GRCm39) missense probably benign 0.04
R2519:Vmn2r99 UTSW 17 19,598,970 (GRCm39) missense probably damaging 0.99
R3911:Vmn2r99 UTSW 17 19,614,635 (GRCm39) missense possibly damaging 0.92
R3947:Vmn2r99 UTSW 17 19,599,252 (GRCm39) missense probably benign 0.40
R3949:Vmn2r99 UTSW 17 19,599,252 (GRCm39) missense probably benign 0.40
R4016:Vmn2r99 UTSW 17 19,598,832 (GRCm39) missense possibly damaging 0.86
R4413:Vmn2r99 UTSW 17 19,599,522 (GRCm39) missense probably damaging 1.00
R4594:Vmn2r99 UTSW 17 19,613,924 (GRCm39) missense probably damaging 1.00
R4999:Vmn2r99 UTSW 17 19,582,397 (GRCm39) start codon destroyed probably null 0.96
R5206:Vmn2r99 UTSW 17 19,598,868 (GRCm39) missense probably benign 0.40
R5362:Vmn2r99 UTSW 17 19,599,601 (GRCm39) missense probably benign 0.00
R5377:Vmn2r99 UTSW 17 19,599,531 (GRCm39) missense probably damaging 1.00
R5455:Vmn2r99 UTSW 17 19,614,408 (GRCm39) nonsense probably null
R6021:Vmn2r99 UTSW 17 19,598,210 (GRCm39) missense probably damaging 1.00
R6059:Vmn2r99 UTSW 17 19,599,242 (GRCm39) missense probably benign 0.00
R6214:Vmn2r99 UTSW 17 19,602,820 (GRCm39) missense probably benign 0.19
R6215:Vmn2r99 UTSW 17 19,602,820 (GRCm39) missense probably benign 0.19
R6313:Vmn2r99 UTSW 17 19,602,867 (GRCm39) missense probably damaging 1.00
R6646:Vmn2r99 UTSW 17 19,600,293 (GRCm39) missense probably damaging 1.00
R6810:Vmn2r99 UTSW 17 19,600,296 (GRCm39) missense probably benign 0.20
R6885:Vmn2r99 UTSW 17 19,600,457 (GRCm39) missense possibly damaging 0.52
R6991:Vmn2r99 UTSW 17 19,598,372 (GRCm39) missense probably benign 0.03
R7060:Vmn2r99 UTSW 17 19,614,826 (GRCm39) nonsense probably null
R7090:Vmn2r99 UTSW 17 19,613,972 (GRCm39) missense possibly damaging 0.83
R7094:Vmn2r99 UTSW 17 19,599,573 (GRCm39) missense probably benign 0.00
R7449:Vmn2r99 UTSW 17 19,599,407 (GRCm39) missense probably benign 0.01
R7789:Vmn2r99 UTSW 17 19,614,079 (GRCm39) missense possibly damaging 0.91
R8039:Vmn2r99 UTSW 17 19,600,302 (GRCm39) missense probably benign 0.00
R8493:Vmn2r99 UTSW 17 19,614,020 (GRCm39) missense probably benign 0.15
R8511:Vmn2r99 UTSW 17 19,614,443 (GRCm39) missense probably damaging 1.00
R8715:Vmn2r99 UTSW 17 19,613,922 (GRCm39) critical splice acceptor site probably benign
R9462:Vmn2r99 UTSW 17 19,598,388 (GRCm39) nonsense probably null
R9681:Vmn2r99 UTSW 17 19,598,889 (GRCm39) missense probably damaging 1.00
R9737:Vmn2r99 UTSW 17 19,582,563 (GRCm39) missense probably benign
Z1088:Vmn2r99 UTSW 17 19,599,563 (GRCm39) missense probably benign 0.18
Posted On 2014-01-21