Incidental Mutation 'IGL02142:Vmn2r100'
ID 281599
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 # IGL02142
Quality Score
Status
Chromosome 17
Chromosomal Location 19725073-19752322 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 19742583 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Proline at position 319 (H319P)
Ref Sequence ENSEMBL: ENSMUSP00000156263 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000166081] [ENSMUST00000231465]
AlphaFold E9QAZ9
Predicted Effect probably damaging
Transcript: ENSMUST00000166081
AA Change: H319P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000128350
Gene: ENSMUSG00000091859
AA Change: H319P

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: H319P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca4 T C 3: 121,963,575 (GRCm39) S2060P probably benign Het
Abcg4 A G 9: 44,189,014 (GRCm39) F426S probably benign Het
Actn1 C T 12: 80,222,929 (GRCm39) probably null Het
Adgrd1 T A 5: 129,208,648 (GRCm39) H251Q probably benign Het
Adgrg3 C T 8: 95,766,483 (GRCm39) P385S probably damaging Het
Ampd2 G T 3: 107,987,660 (GRCm39) probably benign Het
Arhgap42 A G 9: 9,155,360 (GRCm39) S86P probably damaging Het
Art5 C T 7: 101,747,123 (GRCm39) E121K probably null Het
Atad5 G A 11: 79,985,023 (GRCm39) E37K probably benign Het
Atp13a5 A G 16: 29,053,315 (GRCm39) V1084A probably benign Het
Cfap44 T C 16: 44,241,507 (GRCm39) I626T probably benign Het
Col16a1 T A 4: 129,945,440 (GRCm39) probably null Het
Defa22 T G 8: 21,653,130 (GRCm39) C81G possibly damaging Het
Dnm2 A G 9: 21,411,649 (GRCm39) Y622C probably damaging Het
Efna5 T A 17: 62,914,340 (GRCm39) L201F unknown Het
Elac1 T C 18: 73,871,991 (GRCm39) R335G probably benign Het
Enpp5 T C 17: 44,396,468 (GRCm39) V460A probably benign Het
Esr2 A G 12: 76,169,969 (GRCm39) V453A probably benign Het
Fam210b T A 2: 172,194,497 (GRCm39) probably benign Het
Fcgr1 T C 3: 96,191,893 (GRCm39) Y305C probably benign Het
Fcrlb A G 1: 170,736,248 (GRCm39) V176A probably damaging Het
Gabrq T A X: 71,879,783 (GRCm39) V256E possibly damaging Het
Gba1 T C 3: 89,113,148 (GRCm39) L193P probably damaging Het
Gm10717 C T 9: 3,025,616 (GRCm39) S67L probably benign Het
Helq A G 5: 100,930,960 (GRCm39) F597L probably benign Het
Hrh1 A T 6: 114,457,204 (GRCm39) I162L probably damaging Het
Jph1 A T 1: 17,161,884 (GRCm39) F259L probably damaging Het
Kdm2b C T 5: 123,085,898 (GRCm39) E238K probably damaging Het
Kdm4c T A 4: 74,225,253 (GRCm39) probably null Het
Kif13a T C 13: 46,925,011 (GRCm39) T308A probably benign Het
Lars1 C T 18: 42,360,345 (GRCm39) V704M probably benign Het
Lcmt2 A G 2: 120,969,394 (GRCm39) L343P possibly damaging Het
Lhfpl1 A G X: 144,123,733 (GRCm39) F125L probably benign Het
Lmbrd2 C A 15: 9,186,772 (GRCm39) D582E probably damaging Het
Lrrn2 T A 1: 132,866,983 (GRCm39) S683T possibly damaging Het
Macf1 T C 4: 123,365,842 (GRCm39) D1408G probably benign Het
Magi3 T C 3: 103,923,219 (GRCm39) K1166R probably benign Het
Marchf5 T C 19: 37,197,892 (GRCm39) probably benign Het
Ms4a20 G A 19: 11,087,695 (GRCm39) Q79* probably null Het
Naa25 A G 5: 121,564,825 (GRCm39) Q555R possibly damaging Het
Npat A G 9: 53,481,207 (GRCm39) T1005A probably benign Het
Nt5c3 G A 6: 56,863,670 (GRCm39) A108V probably damaging Het
Ocrl T A X: 47,024,995 (GRCm39) M322K probably damaging Het
Odad2 C A 18: 7,214,601 (GRCm39) W733C probably damaging Het
Or8g2 A G 9: 39,821,935 (GRCm39) T279A possibly damaging Het
Psg23 A T 7: 18,344,345 (GRCm39) V370E probably benign Het
Rassf2 A T 2: 131,838,353 (GRCm39) M311K possibly damaging Het
Rhobtb3 A G 13: 76,025,614 (GRCm39) Y501H probably damaging Het
Rpl4 A G 9: 64,083,488 (GRCm39) D179G possibly damaging Het
Scn2a T A 2: 65,546,182 (GRCm39) I915N probably damaging Het
Scn3a T A 2: 65,356,965 (GRCm39) T160S possibly damaging Het
Slx4ip T G 2: 136,909,942 (GRCm39) N242K possibly damaging Het
Spidr T A 16: 15,865,945 (GRCm39) Q288L probably benign Het
Sun1 A T 5: 139,216,918 (GRCm39) H255L possibly damaging Het
Tacc1 C T 8: 25,665,233 (GRCm39) G51S probably damaging Het
Tet2 T A 3: 133,185,900 (GRCm39) N1179I possibly damaging Het
Tgfbrap1 T C 1: 43,101,752 (GRCm39) Y349C probably damaging Het
Tnrc6a T C 7: 122,751,414 (GRCm39) probably benign Het
Trim32 T C 4: 65,532,736 (GRCm39) L431P probably damaging Het
Vmn1r35 A G 6: 66,656,334 (GRCm39) L112S probably damaging Het
Wdr20rt A G 12: 65,274,039 (GRCm39) T328A probably benign Het
Zbtb17 T C 4: 141,192,293 (GRCm39) Y413H probably benign 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
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
IGL03181:Vmn2r100 APN 17 19,752,207 (GRCm39) missense probably damaging 1.00
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 2015-04-16