Incidental Mutation 'IGL03181:Vmn2r100'
ID 412220
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r100
Ensembl Gene ENSMUSG00000091859
Gene Name vomeronasal 2, receptor 100
Synonyms EG627537
Accession Numbers
Essential gene? Probably non essential (E-score: 0.093) question?
Stock # IGL03181
Quality Score
Status
Chromosome 17
Chromosomal Location 19725073-19752322 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 19752207 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Asparagine at position 813 (I813N)
Ref Sequence ENSEMBL: ENSMUSP00000128350 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000166081] [ENSMUST00000231465]
AlphaFold E9QAZ9
Predicted Effect probably damaging
Transcript: ENSMUST00000166081
AA Change: I813N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000128350
Gene: ENSMUSG00000091859
AA Change: I813N

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
Pfam:ANF_receptor 83 456 7.4e-41 PFAM
Pfam:NCD3G 510 563 1.9e-21 PFAM
Pfam:7tm_3 594 831 2.6e-51 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000231465
AA Change: I750N

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700049A03Rik T C 12: 71,240,147 (GRCm39) V1319A possibly damaging Het
Abcb11 T A 2: 69,158,352 (GRCm39) probably benign Het
Acss3 G T 10: 106,889,249 (GRCm39) H190Q probably damaging Het
Adra2b C T 2: 127,205,903 (GRCm39) T140I probably benign Het
Arl1 T A 10: 88,578,921 (GRCm39) probably benign Het
Atp4a T G 7: 30,424,129 (GRCm39) C968G probably benign Het
Clec4n T C 6: 123,207,474 (GRCm39) C13R possibly damaging Het
Cnot3 T C 7: 3,656,247 (GRCm39) Y178H probably damaging Het
Col18a1 G A 10: 76,891,532 (GRCm39) R1560C probably damaging Het
Cyp2c66 T C 19: 39,130,483 (GRCm39) F106S probably benign Het
Dcn A C 10: 97,319,314 (GRCm39) E30D probably damaging Het
Dennd5a A T 7: 109,532,865 (GRCm39) F302I probably damaging Het
Dip2b T C 15: 100,113,088 (GRCm39) V1501A probably damaging Het
Dnah10 C T 5: 124,825,521 (GRCm39) P687S probably damaging Het
Drc7 A G 8: 95,794,755 (GRCm39) T387A probably benign Het
Dusp7 T A 9: 106,251,009 (GRCm39) M378K probably damaging Het
Ftmt T C 18: 52,464,953 (GRCm39) Y90H probably damaging Het
Glb1l3 T C 9: 26,739,659 (GRCm39) probably null Het
Gpatch3 T C 4: 133,305,433 (GRCm39) F223L probably damaging Het
Gpr158 T A 2: 21,787,972 (GRCm39) F538I probably benign Het
Gucy2e A G 11: 69,121,008 (GRCm39) probably benign Het
Hadha A G 5: 30,326,524 (GRCm39) V566A probably benign Het
Hectd4 A T 5: 121,492,021 (GRCm39) S3787C possibly damaging Het
Hnrnpk A T 13: 58,542,130 (GRCm39) D265E possibly damaging Het
Hspbp1 G A 7: 4,687,363 (GRCm39) R83W probably damaging Het
Hspg2 T A 4: 137,243,248 (GRCm39) L758Q probably damaging Het
Ippk A G 13: 49,595,463 (GRCm39) Y180C probably damaging Het
Itpr3 T A 17: 27,330,242 (GRCm39) M1620K probably benign Het
Klf7 T C 1: 64,074,885 (GRCm39) K298R possibly damaging Het
Ktn1 A T 14: 47,970,741 (GRCm39) T1229S probably benign Het
Lefty2 A G 1: 180,725,115 (GRCm39) N282D probably damaging Het
Lrrc37 A T 11: 103,507,242 (GRCm39) probably benign Het
Nsd1 G A 13: 55,394,858 (GRCm39) E820K probably damaging Het
Obsl1 C A 1: 75,469,228 (GRCm39) A1238S probably benign Het
Odr4 G T 1: 150,239,290 (GRCm39) P378T probably benign Het
Pias2 T C 18: 77,220,938 (GRCm39) I391T possibly damaging Het
Ppp1r10 G T 17: 36,241,516 (GRCm39) G764* probably null Het
Ptpra T C 2: 130,359,707 (GRCm39) F158L probably damaging Het
Recql T C 6: 142,323,918 (GRCm39) S59G probably benign Het
Rrp1b A T 17: 32,276,150 (GRCm39) I566F probably benign Het
Sh3yl1 G A 12: 30,991,979 (GRCm39) D145N possibly damaging Het
Slc35f5 T A 1: 125,512,922 (GRCm39) I52N probably damaging Het
Slc51b A G 9: 65,322,447 (GRCm39) probably null Het
Smpd4 C T 16: 17,443,671 (GRCm39) Q72* probably null Het
Spata6 A G 4: 111,679,963 (GRCm39) D391G probably benign Het
Tnc T A 4: 63,885,543 (GRCm39) D1853V possibly damaging Het
Tnks1bp1 C T 2: 84,893,058 (GRCm39) T333I probably benign Het
Vwa8 T A 14: 79,246,690 (GRCm39) H677Q probably benign Het
Washc4 T C 10: 83,426,883 (GRCm39) Y1064H probably damaging Het
Wdr82 T A 9: 106,063,614 (GRCm39) I272K probably benign Het
Zc3h12a T C 4: 125,013,097 (GRCm39) Y589C probably damaging Het
Other mutations in Vmn2r100
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00904:Vmn2r100 APN 17 19,746,262 (GRCm39) missense probably damaging 1.00
IGL00912:Vmn2r100 APN 17 19,751,654 (GRCm39) missense possibly damaging 0.95
IGL01107:Vmn2r100 APN 17 19,741,618 (GRCm39) missense probably damaging 1.00
IGL01517:Vmn2r100 APN 17 19,742,225 (GRCm39) missense probably benign 0.37
IGL01594:Vmn2r100 APN 17 19,751,495 (GRCm39) missense possibly damaging 0.52
IGL01657:Vmn2r100 APN 17 19,746,178 (GRCm39) missense possibly damaging 0.89
IGL01822:Vmn2r100 APN 17 19,725,100 (GRCm39) missense probably null 0.00
IGL02020:Vmn2r100 APN 17 19,725,200 (GRCm39) missense possibly damaging 0.78
IGL02060:Vmn2r100 APN 17 19,741,516 (GRCm39) missense possibly damaging 0.79
IGL02126:Vmn2r100 APN 17 19,741,504 (GRCm39) splice site probably benign
IGL02142:Vmn2r100 APN 17 19,742,583 (GRCm39) missense probably damaging 1.00
IGL02308:Vmn2r100 APN 17 19,741,597 (GRCm39) missense possibly damaging 0.90
IGL02407:Vmn2r100 APN 17 19,741,770 (GRCm39) missense probably damaging 0.98
IGL02469:Vmn2r100 APN 17 19,751,547 (GRCm39) nonsense probably null
IGL03088:Vmn2r100 APN 17 19,742,301 (GRCm39) missense probably benign 0.27
IGL03405:Vmn2r100 APN 17 19,752,186 (GRCm39) missense probably damaging 1.00
H8562:Vmn2r100 UTSW 17 19,741,752 (GRCm39) missense possibly damaging 0.87
R0012:Vmn2r100 UTSW 17 19,746,296 (GRCm39) missense probably damaging 0.99
R0012:Vmn2r100 UTSW 17 19,725,136 (GRCm39) missense probably benign
R0044:Vmn2r100 UTSW 17 19,742,441 (GRCm39) missense possibly damaging 0.46
R0109:Vmn2r100 UTSW 17 19,742,382 (GRCm39) missense possibly damaging 0.80
R0111:Vmn2r100 UTSW 17 19,742,382 (GRCm39) missense possibly damaging 0.80
R0112:Vmn2r100 UTSW 17 19,742,382 (GRCm39) missense possibly damaging 0.80
R0149:Vmn2r100 UTSW 17 19,741,509 (GRCm39) critical splice acceptor site probably null
R0355:Vmn2r100 UTSW 17 19,751,582 (GRCm39) missense probably benign 0.00
R0395:Vmn2r100 UTSW 17 19,742,382 (GRCm39) missense possibly damaging 0.80
R0396:Vmn2r100 UTSW 17 19,742,382 (GRCm39) missense possibly damaging 0.80
R0453:Vmn2r100 UTSW 17 19,742,382 (GRCm39) missense possibly damaging 0.80
R0465:Vmn2r100 UTSW 17 19,751,792 (GRCm39) missense probably damaging 0.98
R0477:Vmn2r100 UTSW 17 19,742,776 (GRCm39) missense probably benign 0.00
R0510:Vmn2r100 UTSW 17 19,742,382 (GRCm39) missense possibly damaging 0.80
R0512:Vmn2r100 UTSW 17 19,742,382 (GRCm39) missense possibly damaging 0.80
R0514:Vmn2r100 UTSW 17 19,742,382 (GRCm39) missense possibly damaging 0.80
R0518:Vmn2r100 UTSW 17 19,742,178 (GRCm39) missense probably damaging 1.00
R0521:Vmn2r100 UTSW 17 19,742,178 (GRCm39) missense probably damaging 1.00
R0555:Vmn2r100 UTSW 17 19,742,382 (GRCm39) missense possibly damaging 0.80
R0608:Vmn2r100 UTSW 17 19,742,382 (GRCm39) missense possibly damaging 0.80
R0959:Vmn2r100 UTSW 17 19,743,786 (GRCm39) missense possibly damaging 0.95
R1114:Vmn2r100 UTSW 17 19,752,261 (GRCm39) missense probably damaging 1.00
R2027:Vmn2r100 UTSW 17 19,742,334 (GRCm39) missense probably benign 0.02
R2049:Vmn2r100 UTSW 17 19,742,312 (GRCm39) missense probably benign 0.00
R2224:Vmn2r100 UTSW 17 19,742,634 (GRCm39) missense probably benign 0.03
R2226:Vmn2r100 UTSW 17 19,742,634 (GRCm39) missense probably benign 0.03
R3618:Vmn2r100 UTSW 17 19,743,692 (GRCm39) missense probably benign
R3715:Vmn2r100 UTSW 17 19,752,272 (GRCm39) missense probably damaging 0.99
R4120:Vmn2r100 UTSW 17 19,752,215 (GRCm39) missense probably damaging 1.00
R4152:Vmn2r100 UTSW 17 19,743,681 (GRCm39) frame shift probably null
R4153:Vmn2r100 UTSW 17 19,743,681 (GRCm39) frame shift probably null
R4154:Vmn2r100 UTSW 17 19,743,681 (GRCm39) frame shift probably null
R4200:Vmn2r100 UTSW 17 19,742,797 (GRCm39) missense probably benign 0.29
R4632:Vmn2r100 UTSW 17 19,752,216 (GRCm39) missense probably damaging 1.00
R4720:Vmn2r100 UTSW 17 19,742,788 (GRCm39) missense probably benign 0.02
R4761:Vmn2r100 UTSW 17 19,741,630 (GRCm39) missense possibly damaging 0.47
R4831:Vmn2r100 UTSW 17 19,741,672 (GRCm39) missense probably benign 0.28
R4951:Vmn2r100 UTSW 17 19,752,300 (GRCm39) missense probably benign 0.01
R5211:Vmn2r100 UTSW 17 19,746,257 (GRCm39) missense possibly damaging 0.67
R5553:Vmn2r100 UTSW 17 19,725,110 (GRCm39) missense possibly damaging 0.64
R5657:Vmn2r100 UTSW 17 19,725,178 (GRCm39) missense probably benign 0.31
R5883:Vmn2r100 UTSW 17 19,743,786 (GRCm39) missense probably benign
R5912:Vmn2r100 UTSW 17 19,752,071 (GRCm39) missense probably damaging 0.99
R6141:Vmn2r100 UTSW 17 19,742,576 (GRCm39) missense probably benign 0.07
R6146:Vmn2r100 UTSW 17 19,742,522 (GRCm39) missense probably benign 0.04
R6500:Vmn2r100 UTSW 17 19,742,355 (GRCm39) missense probably damaging 1.00
R6575:Vmn2r100 UTSW 17 19,741,671 (GRCm39) missense probably benign 0.12
R6647:Vmn2r100 UTSW 17 19,742,785 (GRCm39) missense probably benign 0.00
R7038:Vmn2r100 UTSW 17 19,725,263 (GRCm39) missense possibly damaging 0.76
R7052:Vmn2r100 UTSW 17 19,751,556 (GRCm39) missense possibly damaging 0.95
R7170:Vmn2r100 UTSW 17 19,752,233 (GRCm39) missense probably benign 0.00
R7209:Vmn2r100 UTSW 17 19,751,576 (GRCm39) missense not run
R7312:Vmn2r100 UTSW 17 19,742,296 (GRCm39) missense probably benign 0.01
R7734:Vmn2r100 UTSW 17 19,742,296 (GRCm39) missense probably benign 0.01
R7750:Vmn2r100 UTSW 17 19,742,726 (GRCm39) missense probably benign
R8103:Vmn2r100 UTSW 17 19,751,415 (GRCm39) splice site probably null
R8193:Vmn2r100 UTSW 17 19,725,102 (GRCm39) nonsense probably null
R8267:Vmn2r100 UTSW 17 19,742,752 (GRCm39) nonsense probably null
R8290:Vmn2r100 UTSW 17 19,751,612 (GRCm39) missense probably damaging 0.99
R8531:Vmn2r100 UTSW 17 19,742,459 (GRCm39) missense possibly damaging 0.66
R8786:Vmn2r100 UTSW 17 19,742,838 (GRCm39) missense probably damaging 1.00
R8920:Vmn2r100 UTSW 17 19,741,620 (GRCm39) missense probably damaging 1.00
R8938:Vmn2r100 UTSW 17 19,751,825 (GRCm39) missense probably benign 0.00
R9555:Vmn2r100 UTSW 17 19,743,857 (GRCm39) missense probably benign 0.00
R9572:Vmn2r100 UTSW 17 19,741,513 (GRCm39) missense probably benign 0.00
R9609:Vmn2r100 UTSW 17 19,743,732 (GRCm39) missense probably damaging 1.00
R9618:Vmn2r100 UTSW 17 19,742,583 (GRCm39) missense probably damaging 1.00
X0062:Vmn2r100 UTSW 17 19,751,652 (GRCm39) missense possibly damaging 0.89
Z1176:Vmn2r100 UTSW 17 19,741,792 (GRCm39) missense probably benign 0.00
Z1177:Vmn2r100 UTSW 17 19,725,251 (GRCm39) missense probably benign 0.00
Posted On 2016-08-02