Incidental Mutation 'IGL02136:Vmn2r107'
ID 281313
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vmn2r107
Ensembl Gene ENSMUSG00000056910
Gene Name vomeronasal 2, receptor 107
Synonyms V2r6
Accession Numbers
Essential gene? Probably non essential (E-score: 0.117) question?
Stock # IGL02136
Quality Score
Status
Chromosome 17
Chromosomal Location 20565687-20596034 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 20595168 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Leucine at position 574 (V574L)
Ref Sequence ENSEMBL: ENSMUSP00000048706 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042090]
AlphaFold E9PZJ7
Predicted Effect probably benign
Transcript: ENSMUST00000042090
AA Change: V574L

PolyPhen 2 Score 0.017 (Sensitivity: 0.95; Specificity: 0.80)
SMART Domains Protein: ENSMUSP00000048706
Gene: ENSMUSG00000056910
AA Change: V574L

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
Pfam:ANF_receptor 83 466 3.6e-40 PFAM
Pfam:NCD3G 509 562 5.1e-21 PFAM
Pfam:7tm_3 593 830 8e-51 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca12 G T 1: 71,286,301 (GRCm39) T2511K probably damaging Het
Acta2 T A 19: 34,229,230 (GRCm39) D53V probably damaging Het
Banf1 G A 19: 5,415,098 (GRCm39) A71V probably benign Het
Cacng5 A T 11: 107,772,557 (GRCm39) I97N probably benign Het
Clec14a T A 12: 58,315,415 (GRCm39) E69V probably damaging Het
Cracr2a T C 6: 127,606,893 (GRCm39) probably benign Het
Dysf A G 6: 84,085,149 (GRCm39) R845G probably benign Het
Dzip3 T C 16: 48,747,945 (GRCm39) N949S possibly damaging Het
Eprs1 T G 1: 185,117,180 (GRCm39) W408G probably damaging Het
Fgf14 G A 14: 124,217,784 (GRCm39) P240S possibly damaging Het
Fpgt G T 3: 154,798,989 (GRCm39) A2E probably benign Het
Galntl5 T A 5: 25,425,060 (GRCm39) S392R probably benign Het
Gatd1 A G 7: 140,988,873 (GRCm39) *221Q probably null Het
Gcsam T A 16: 45,430,896 (GRCm39) M1K probably null Het
Ksr2 A G 5: 117,754,959 (GRCm39) N351S possibly damaging Het
Map1a T C 2: 121,130,693 (GRCm39) V503A probably damaging Het
Myl12a T A 17: 71,303,851 (GRCm39) K9* probably null Het
Ncapg2 A T 12: 116,424,203 (GRCm39) M1129L probably benign Het
Or11g2 T C 14: 50,855,708 (GRCm39) S10P possibly damaging Het
Or8k41 T C 2: 86,313,809 (GRCm39) I92M probably damaging Het
Otof T C 5: 30,531,336 (GRCm39) K1691E possibly damaging Het
Pdk4 A T 6: 5,486,715 (GRCm39) M353K probably damaging Het
Pkhd1 A T 1: 20,345,839 (GRCm39) W2730R probably damaging Het
Pkn2 T A 3: 142,559,351 (GRCm39) K58I probably damaging Het
Plk5 T C 10: 80,199,001 (GRCm39) probably null Het
Prkcq T C 2: 11,265,479 (GRCm39) F399L probably benign Het
Ptprz1 G A 6: 22,972,821 (GRCm39) V244M probably damaging Het
Rpusd2 T C 2: 118,868,659 (GRCm39) F361L probably damaging Het
Rttn T A 18: 89,064,252 (GRCm39) L1168I possibly damaging Het
S100a9 T C 3: 90,600,075 (GRCm39) H107R probably benign Het
Serpinb3a T A 1: 106,974,015 (GRCm39) M299L probably benign Het
Slfn8 G A 11: 82,894,291 (GRCm39) Q783* probably null Het
Smc3 T C 19: 53,624,147 (GRCm39) I721T probably benign Het
Top2b C A 14: 16,407,103 (GRCm38) probably benign Het
Uvssa T A 5: 33,549,192 (GRCm39) W351R probably damaging Het
Wdr3 G A 3: 100,046,041 (GRCm39) R931* probably null Het
Other mutations in Vmn2r107
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01402:Vmn2r107 APN 17 20,596,009 (GRCm39) missense probably damaging 0.98
IGL01768:Vmn2r107 APN 17 20,565,868 (GRCm39) missense probably benign 0.32
IGL02086:Vmn2r107 APN 17 20,578,062 (GRCm39) missense probably benign 0.00
IGL02266:Vmn2r107 APN 17 20,577,039 (GRCm39) missense probably damaging 1.00
IGL02285:Vmn2r107 APN 17 20,595,823 (GRCm39) missense probably damaging 1.00
IGL02724:Vmn2r107 APN 17 20,577,006 (GRCm39) missense possibly damaging 0.49
IGL02998:Vmn2r107 APN 17 20,578,017 (GRCm39) missense probably damaging 0.99
IGL03089:Vmn2r107 APN 17 20,595,974 (GRCm39) missense probably benign 0.05
IGL03284:Vmn2r107 APN 17 20,577,173 (GRCm39) missense probably benign 0.07
IGL03307:Vmn2r107 APN 17 20,577,038 (GRCm39) missense probably benign 0.09
IGL03399:Vmn2r107 APN 17 20,578,220 (GRCm39) splice site probably benign
3-1:Vmn2r107 UTSW 17 20,565,766 (GRCm39) missense probably benign
BB006:Vmn2r107 UTSW 17 20,565,706 (GRCm39) missense probably null 0.96
BB016:Vmn2r107 UTSW 17 20,565,706 (GRCm39) missense probably null 0.96
R0285:Vmn2r107 UTSW 17 20,565,873 (GRCm39) missense probably benign 0.00
R0455:Vmn2r107 UTSW 17 20,595,085 (GRCm39) splice site probably benign
R0497:Vmn2r107 UTSW 17 20,595,394 (GRCm39) missense probably damaging 1.00
R0506:Vmn2r107 UTSW 17 20,578,021 (GRCm39) missense probably benign
R0621:Vmn2r107 UTSW 17 20,595,252 (GRCm39) missense probably benign 0.01
R0667:Vmn2r107 UTSW 17 20,575,916 (GRCm39) missense possibly damaging 0.91
R1118:Vmn2r107 UTSW 17 20,576,860 (GRCm39) missense probably benign 0.03
R1204:Vmn2r107 UTSW 17 20,578,031 (GRCm39) missense probably benign
R1237:Vmn2r107 UTSW 17 20,576,947 (GRCm39) nonsense probably null
R1485:Vmn2r107 UTSW 17 20,595,109 (GRCm39) missense possibly damaging 0.95
R1783:Vmn2r107 UTSW 17 20,576,775 (GRCm39) missense possibly damaging 0.51
R1873:Vmn2r107 UTSW 17 20,565,840 (GRCm39) missense probably benign 0.10
R1974:Vmn2r107 UTSW 17 20,575,879 (GRCm39) splice site probably null
R2009:Vmn2r107 UTSW 17 20,595,729 (GRCm39) missense probably benign 0.01
R2029:Vmn2r107 UTSW 17 20,595,549 (GRCm39) missense probably benign 0.01
R2164:Vmn2r107 UTSW 17 20,595,904 (GRCm39) missense probably damaging 1.00
R2269:Vmn2r107 UTSW 17 20,595,817 (GRCm39) missense possibly damaging 0.58
R3087:Vmn2r107 UTSW 17 20,580,607 (GRCm39) missense probably benign 0.03
R3740:Vmn2r107 UTSW 17 20,595,151 (GRCm39) missense probably benign 0.00
R3961:Vmn2r107 UTSW 17 20,595,717 (GRCm39) missense probably damaging 1.00
R4031:Vmn2r107 UTSW 17 20,595,483 (GRCm39) missense probably benign 0.00
R4270:Vmn2r107 UTSW 17 20,576,041 (GRCm39) missense probably benign
R4963:Vmn2r107 UTSW 17 20,595,403 (GRCm39) missense probably damaging 1.00
R5121:Vmn2r107 UTSW 17 20,576,015 (GRCm39) missense probably benign 0.01
R5640:Vmn2r107 UTSW 17 20,595,426 (GRCm39) missense probably damaging 1.00
R6007:Vmn2r107 UTSW 17 20,595,316 (GRCm39) missense probably benign 0.19
R6238:Vmn2r107 UTSW 17 20,565,849 (GRCm39) missense probably benign 0.43
R6298:Vmn2r107 UTSW 17 20,576,044 (GRCm39) missense probably benign 0.00
R6467:Vmn2r107 UTSW 17 20,595,939 (GRCm39) missense probably damaging 0.99
R6726:Vmn2r107 UTSW 17 20,595,637 (GRCm39) missense probably damaging 0.96
R6782:Vmn2r107 UTSW 17 20,577,141 (GRCm39) missense probably damaging 1.00
R7299:Vmn2r107 UTSW 17 20,565,878 (GRCm39) missense probably benign 0.01
R7301:Vmn2r107 UTSW 17 20,565,878 (GRCm39) missense probably benign 0.01
R7375:Vmn2r107 UTSW 17 20,576,138 (GRCm39) missense probably benign
R7448:Vmn2r107 UTSW 17 20,595,994 (GRCm39) missense probably benign 0.00
R7495:Vmn2r107 UTSW 17 20,595,271 (GRCm39) missense possibly damaging 0.71
R7589:Vmn2r107 UTSW 17 20,595,634 (GRCm39) missense probably benign 0.05
R7594:Vmn2r107 UTSW 17 20,580,635 (GRCm39) missense probably benign 0.03
R7678:Vmn2r107 UTSW 17 20,576,901 (GRCm39) missense probably benign 0.01
R7929:Vmn2r107 UTSW 17 20,565,706 (GRCm39) missense probably null 0.96
R7974:Vmn2r107 UTSW 17 20,577,270 (GRCm39) missense probably benign 0.00
R8040:Vmn2r107 UTSW 17 20,595,808 (GRCm39) missense probably damaging 1.00
R8263:Vmn2r107 UTSW 17 20,580,614 (GRCm39) missense probably damaging 1.00
R8426:Vmn2r107 UTSW 17 20,577,239 (GRCm39) missense possibly damaging 0.91
R9175:Vmn2r107 UTSW 17 20,577,051 (GRCm39) missense possibly damaging 0.79
R9537:Vmn2r107 UTSW 17 20,595,149 (GRCm39) missense probably benign 0.00
R9642:Vmn2r107 UTSW 17 20,580,661 (GRCm39) missense probably damaging 1.00
R9711:Vmn2r107 UTSW 17 20,577,262 (GRCm39) missense probably damaging 1.00
X0022:Vmn2r107 UTSW 17 20,577,230 (GRCm39) missense possibly damaging 0.85
Posted On 2015-04-16