Incidental Mutation 'R1970:Pik3c2g'
ID 219690
Institutional Source Beutler Lab
Gene Symbol Pik3c2g
Ensembl Gene ENSMUSG00000030228
Gene Name phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma
Synonyms
MMRRC Submission 039983-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.087) question?
Stock # R1970 (G1)
Quality Score 208
Status Validated
Chromosome 6
Chromosomal Location 139587221-139969284 bp(+) (GRCm38)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) T to A at 139900386 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000151281 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000087657] [ENSMUST00000087657] [ENSMUST00000111868] [ENSMUST00000218528]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000087657
SMART Domains Protein: ENSMUSP00000084939
Gene: ENSMUSG00000030228

DomainStartEndE-ValueType
PI3Kc 125 387 2.11e-109 SMART
PX 411 515 1.24e-21 SMART
C2 550 647 1.34e-7 SMART
Predicted Effect probably null
Transcript: ENSMUST00000087657
SMART Domains Protein: ENSMUSP00000084939
Gene: ENSMUSG00000030228

DomainStartEndE-ValueType
PI3Kc 125 387 2.11e-109 SMART
PX 411 515 1.24e-21 SMART
C2 550 647 1.34e-7 SMART
Predicted Effect probably null
Transcript: ENSMUST00000111868
SMART Domains Protein: ENSMUSP00000107499
Gene: ENSMUSG00000030228

DomainStartEndE-ValueType
SCOP:d1e8xa2 1 83 4e-16 SMART
PI3Ka 103 288 7.6e-29 SMART
PI3Kc 375 637 2.11e-109 SMART
PX 661 765 1.24e-21 SMART
C2 800 897 1.34e-7 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000187448
Predicted Effect noncoding transcript
Transcript: ENSMUST00000189374
SMART Domains Protein: ENSMUSP00000139763
Gene: ENSMUSG00000030228

DomainStartEndE-ValueType
PI3Kc 125 387 2.11e-109 SMART
PX 411 515 1.24e-21 SMART
C2 550 647 1.34e-7 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000206646
Predicted Effect probably null
Transcript: ENSMUST00000218528
Meta Mutation Damage Score 0.9480 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 96.8%
  • 20x: 94.2%
Validation Efficiency 97% (121/125)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the phosphoinositide 3-kinase (PI3K) family. PI3-kinases play roles in signaling pathways involved in cell proliferation, oncogenic transformation, cell survival, cell migration, and intracellular protein trafficking. This protein contains a lipid kinase catalytic domain as well as a C-terminal C2 domain, a characteristic of class II PI3-kinases. C2 domains act as calcium-dependent phospholipid binding motifs that mediate translocation of proteins to membranes, and may also mediate protein-protein interactions. This gene may play a role in several diseases, including type II diabetes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]
PHENOTYPE: Mice homozygous for a knock-out allelel exhibit reduced liver glucogen accumulation, hyperlipidemia, adiposity and insulin resistance with age or after consumption of a high-fat diet. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 121 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca17 A T 17: 24,307,575 (GRCm38) H578Q probably benign Het
Abcc12 A G 8: 86,527,281 (GRCm38) I958T probably benign Het
Abcg5 AATCATTTG AG 17: 84,673,602 (GRCm38) probably null Het
Acap2 A G 16: 31,133,527 (GRCm38) probably null Het
Adgrb1 T C 15: 74,539,877 (GRCm38) probably benign Het
Akap6 T A 12: 52,938,475 (GRCm38) V897E probably damaging Het
Als2 A T 1: 59,215,169 (GRCm38) L343Q probably benign Het
Arhgap5 A G 12: 52,542,593 (GRCm38) I1275M probably damaging Het
Arnt C T 3: 95,448,393 (GRCm38) S16L possibly damaging Het
Bglap3 C T 3: 88,376,993 (GRCm38) probably benign Het
Blnk T C 19: 40,940,165 (GRCm38) probably benign Het
C1qtnf4 T C 2: 90,889,659 (GRCm38) M92T probably damaging Het
Ccdc177 G A 12: 80,758,712 (GRCm38) R263C unknown Het
Ccdc83 T A 7: 90,244,154 (GRCm38) S132C probably damaging Het
Cdc7 A G 5: 106,973,074 (GRCm38) probably benign Het
Cgnl1 T A 9: 71,725,535 (GRCm38) N178I probably benign Het
Col27a1 C T 4: 63,273,117 (GRCm38) probably benign Het
Col5a1 A T 2: 27,986,754 (GRCm38) M822L unknown Het
Coro7 T C 16: 4,633,756 (GRCm38) I451V probably benign Het
Csmd3 T C 15: 48,673,531 (GRCm38) T92A probably damaging Het
Ddc A G 11: 11,815,292 (GRCm38) V460A possibly damaging Het
Ddx4 C T 13: 112,600,013 (GRCm38) V608I probably damaging Het
Ddx60 A T 8: 61,972,206 (GRCm38) H676L possibly damaging Het
Dmtf1 T C 5: 9,148,989 (GRCm38) E48G probably benign Het
Dpf3 T A 12: 83,325,035 (GRCm38) probably null Het
Dydc2 A G 14: 41,061,903 (GRCm38) C88R probably benign Het
Elovl4 A G 9: 83,780,719 (GRCm38) Y163H probably damaging Het
Enpp2 T C 15: 54,882,982 (GRCm38) D296G probably damaging Het
Fam83h G T 15: 76,006,570 (GRCm38) probably benign Het
Fbf1 T A 11: 116,151,491 (GRCm38) Q511L possibly damaging Het
Fhdc1 A T 3: 84,454,851 (GRCm38) L323Q probably damaging Het
Fmnl2 T A 2: 53,105,576 (GRCm38) V437D possibly damaging Het
Foxo3 A G 10: 42,197,262 (GRCm38) S420P probably benign Het
Foxp4 C T 17: 47,875,871 (GRCm38) R378Q unknown Het
Garem2 G T 5: 30,117,174 (GRCm38) G844* probably null Het
Glmp T C 3: 88,327,870 (GRCm38) L269S probably damaging Het
Gm9915 T C 1: 42,230,721 (GRCm38) noncoding transcript Het
Gnb4 A T 3: 32,598,141 (GRCm38) D27E probably damaging Het
Gnb5 A G 9: 75,344,650 (GRCm38) probably null Het
Gpr161 T G 1: 165,306,358 (GRCm38) V63G probably damaging Het
Gsk3a T A 7: 25,229,721 (GRCm38) probably benign Het
Hapln2 T C 3: 88,024,120 (GRCm38) probably null Het
Incenp G T 19: 9,885,487 (GRCm38) T401N unknown Het
Kalrn A G 16: 33,977,524 (GRCm38) probably null Het
Kcnq3 A G 15: 66,028,623 (GRCm38) probably null Het
Kif21b T C 1: 136,171,156 (GRCm38) V1394A probably damaging Het
Klhl23 T C 2: 69,833,686 (GRCm38) C460R probably damaging Het
L3mbtl1 G A 2: 162,959,572 (GRCm38) A291T probably damaging Het
Lcp1 T C 14: 75,200,506 (GRCm38) S119P probably damaging Het
Ldhc A G 7: 46,869,751 (GRCm38) I133V probably benign Het
Lmntd2 G A 7: 141,212,059 (GRCm38) probably benign Het
Lpl A T 8: 68,896,802 (GRCm38) K327* probably null Het
Lrp1b T C 2: 40,875,069 (GRCm38) D2801G probably damaging Het
Mppe1 C A 18: 67,229,772 (GRCm38) A131S probably benign Het
Msh3 T A 13: 92,249,820 (GRCm38) probably benign Het
Msh5 A G 17: 35,033,600 (GRCm38) I377T probably damaging Het
Myo1e T C 9: 70,368,773 (GRCm38) F757L probably benign Het
Myof A T 19: 37,945,634 (GRCm38) D955E probably damaging Het
Nckap1 C T 2: 80,517,942 (GRCm38) S889N probably benign Het
Ncor2 T C 5: 125,038,918 (GRCm38) D858G probably damaging Het
Neb A T 2: 52,263,905 (GRCm38) V2398D possibly damaging Het
Nefl C G 14: 68,086,672 (GRCm38) T453R probably benign Het
Nf1 A G 11: 79,553,961 (GRCm38) N371D probably benign Het
Nhsl3 A G 4: 129,226,017 (GRCm38) probably benign Het
Nlrp4f T C 13: 65,194,091 (GRCm38) Y580C probably damaging Het
Nme8 A C 13: 19,652,322 (GRCm38) L228R probably damaging Het
Numa1 C T 7: 102,009,322 (GRCm38) A1605V probably damaging Het
Ofd1 T C X: 166,427,214 (GRCm38) Y205C probably benign Het
Olfr1532-ps1 G A 7: 106,914,246 (GRCm38) G16D probably damaging Het
Or2ag12 T A 7: 106,677,670 (GRCm38) N272I probably damaging Het
Or4k77 C T 2: 111,369,076 (GRCm38) S148L probably benign Het
Or8g55 T A 9: 39,873,938 (GRCm38) I221N probably damaging Het
Or8k3 T A 2: 86,228,252 (GRCm38) T240S probably damaging Het
Pclo A G 5: 14,713,473 (GRCm38) T3987A unknown Het
Pdgfrb G A 18: 61,066,494 (GRCm38) probably benign Het
Pdxk G A 10: 78,441,154 (GRCm38) T270I probably damaging Het
Pex5 T C 6: 124,414,405 (GRCm38) E10G probably damaging Het
Pkhd1 T A 1: 20,381,523 (GRCm38) I2183F probably damaging Het
Plppr2 T C 9: 21,941,126 (GRCm38) V102A probably damaging Het
Plxnd1 T C 6: 115,962,517 (GRCm38) T1449A probably damaging Het
Pnkd T A 1: 74,285,910 (GRCm38) probably null Het
Pom121l2 A G 13: 21,983,472 (GRCm38) I638V probably damaging Het
Prag1 A G 8: 36,129,160 (GRCm38) probably null Het
Ranbp10 A G 8: 105,786,708 (GRCm38) F191L probably damaging Het
Rapgef1 T C 2: 29,733,711 (GRCm38) L824P probably damaging Het
Rec8 T C 14: 55,624,142 (GRCm38) L418P probably damaging Het
Rimbp2 T A 5: 128,797,241 (GRCm38) N429Y probably damaging Het
Rpe65 C A 3: 159,615,670 (GRCm38) T373K probably benign Het
Rpl35rt T G 1: 156,366,447 (GRCm38) *124G probably null Het
Rrn3 T C 16: 13,789,074 (GRCm38) S151P probably damaging Het
Scn7a A G 2: 66,684,289 (GRCm38) V1047A possibly damaging Het
Scn9a G T 2: 66,515,380 (GRCm38) P1123Q probably damaging Het
Secisbp2l T C 2: 125,747,510 (GRCm38) D706G probably damaging Het
Serpina5 A T 12: 104,103,857 (GRCm38) T338S probably benign Het
Sez6 G A 11: 77,954,068 (GRCm38) probably null Het
Shisa4 C T 1: 135,372,274 (GRCm38) G157D probably damaging Het
Slc1a7 G T 4: 107,968,585 (GRCm38) D14Y probably benign Het
Slc25a11 A C 11: 70,646,173 (GRCm38) L51V probably benign Het
Slit3 A G 11: 35,630,841 (GRCm38) probably null Het
Spata13 G T 14: 60,691,463 (GRCm38) G157W probably damaging Het
Spta1 T C 1: 174,240,367 (GRCm38) V2120A possibly damaging Het
Srpra T C 9: 35,213,538 (GRCm38) probably null Het
Syt6 A G 3: 103,587,420 (GRCm38) I234V probably benign Het
Thada G T 17: 84,310,042 (GRCm38) P1349T probably damaging Het
Tmem161a C T 8: 70,176,909 (GRCm38) R58W probably damaging Het
Top3b A G 16: 16,883,519 (GRCm38) I232V probably damaging Het
Tspan1 T A 4: 116,163,629 (GRCm38) Q197L possibly damaging Het
Ttc28 A C 5: 111,235,635 (GRCm38) Y1334S probably benign Het
Ubxn6 G T 17: 56,073,077 (GRCm38) N28K possibly damaging Het
Uggt1 T C 1: 36,151,781 (GRCm38) D1366G probably damaging Het
Ugp2 A G 11: 21,328,942 (GRCm38) S415P probably damaging Het
Vcan A T 13: 89,689,038 (GRCm38) S2796T probably damaging Het
Vipr2 T C 12: 116,136,206 (GRCm38) V231A probably benign Het
Vmn1r176 T C 7: 23,834,948 (GRCm38) N260S probably benign Het
Vmn1r59 A T 7: 5,454,039 (GRCm38) Y241N probably damaging Het
Vmn2r67 A T 7: 85,151,805 (GRCm38) Y308N probably benign Het
Vmn2r75 A T 7: 86,148,262 (GRCm38) M781K probably damaging Het
Vwa3a A T 7: 120,780,171 (GRCm38) I500F probably damaging Het
Zfp609 A G 9: 65,795,277 (GRCm38) V31A probably damaging Het
Zfp689 G T 7: 127,444,787 (GRCm38) Q224K probably damaging Het
Zfp81 A T 17: 33,335,501 (GRCm38) L113H probably benign Het
Other mutations in Pik3c2g
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00159:Pik3c2g APN 6 139,896,125 (GRCm38) missense probably damaging 1.00
IGL01355:Pik3c2g APN 6 139,852,857 (GRCm38) missense probably damaging 0.98
IGL01579:Pik3c2g APN 6 139,754,741 (GRCm38) nonsense probably null
IGL01580:Pik3c2g APN 6 139,622,516 (GRCm38) missense probably damaging 0.99
IGL01587:Pik3c2g APN 6 139,754,741 (GRCm38) nonsense probably null
IGL01813:Pik3c2g APN 6 139,622,409 (GRCm38) missense possibly damaging 0.55
IGL02218:Pik3c2g APN 6 139,860,355 (GRCm38) missense probably damaging 1.00
IGL02479:Pik3c2g APN 6 139,918,004 (GRCm38) missense probably benign 0.40
IGL02480:Pik3c2g APN 6 139,852,800 (GRCm38) missense probably damaging 1.00
IGL02721:Pik3c2g APN 6 139,736,973 (GRCm38) missense probably benign 0.15
IGL02967:Pik3c2g APN 6 139,967,828 (GRCm38) missense probably damaging 0.98
IGL03221:Pik3c2g APN 6 139,772,407 (GRCm38) critical splice acceptor site probably null
FR4304:Pik3c2g UTSW 6 139,635,656 (GRCm38) frame shift probably null
FR4340:Pik3c2g UTSW 6 139,635,656 (GRCm38) frame shift probably null
FR4976:Pik3c2g UTSW 6 139,635,654 (GRCm38) frame shift probably null
IGL02837:Pik3c2g UTSW 6 139,626,564 (GRCm38) nonsense probably null
PIT4531001:Pik3c2g UTSW 6 139,859,370 (GRCm38) missense
R0002:Pik3c2g UTSW 6 139,768,745 (GRCm38) missense probably benign 0.08
R0081:Pik3c2g UTSW 6 139,957,793 (GRCm38) missense probably benign 0.05
R0098:Pik3c2g UTSW 6 139,662,443 (GRCm38) missense unknown
R0719:Pik3c2g UTSW 6 139,629,725 (GRCm38) missense probably damaging 1.00
R0740:Pik3c2g UTSW 6 139,633,793 (GRCm38) critical splice donor site probably null
R0837:Pik3c2g UTSW 6 139,957,699 (GRCm38) splice site probably benign
R0840:Pik3c2g UTSW 6 139,896,072 (GRCm38) missense probably damaging 1.00
R1306:Pik3c2g UTSW 6 139,772,428 (GRCm38) missense probably benign
R1501:Pik3c2g UTSW 6 139,844,070 (GRCm38) critical splice donor site probably null
R1591:Pik3c2g UTSW 6 139,748,178 (GRCm38) missense probably benign 0.00
R1666:Pik3c2g UTSW 6 139,635,636 (GRCm38) intron probably benign
R1907:Pik3c2g UTSW 6 139,844,042 (GRCm38) missense probably damaging 1.00
R1982:Pik3c2g UTSW 6 139,622,548 (GRCm38) missense probably damaging 0.97
R2171:Pik3c2g UTSW 6 139,855,286 (GRCm38) nonsense probably null
R2188:Pik3c2g UTSW 6 139,852,874 (GRCm38) missense probably damaging 1.00
R3777:Pik3c2g UTSW 6 139,622,387 (GRCm38) missense probably damaging 1.00
R3778:Pik3c2g UTSW 6 139,622,387 (GRCm38) missense probably damaging 1.00
R3965:Pik3c2g UTSW 6 139,855,292 (GRCm38) missense possibly damaging 0.90
R4076:Pik3c2g UTSW 6 139,852,863 (GRCm38) missense probably damaging 1.00
R4078:Pik3c2g UTSW 6 139,635,610 (GRCm38) intron probably benign
R4108:Pik3c2g UTSW 6 139,730,370 (GRCm38) missense probably benign 0.00
R4461:Pik3c2g UTSW 6 139,841,681 (GRCm38) intron probably benign
R4474:Pik3c2g UTSW 6 139,633,751 (GRCm38) missense probably damaging 0.99
R4509:Pik3c2g UTSW 6 139,720,006 (GRCm38) missense probably benign 0.25
R4646:Pik3c2g UTSW 6 139,720,018 (GRCm38) missense probably benign 0.05
R4732:Pik3c2g UTSW 6 139,935,985 (GRCm38) missense probably benign 0.28
R4733:Pik3c2g UTSW 6 139,935,985 (GRCm38) missense probably benign 0.28
R4854:Pik3c2g UTSW 6 139,768,779 (GRCm38) missense probably damaging 1.00
R4928:Pik3c2g UTSW 6 139,967,802 (GRCm38) missense possibly damaging 0.88
R4959:Pik3c2g UTSW 6 139,843,931 (GRCm38) missense possibly damaging 0.65
R4973:Pik3c2g UTSW 6 139,843,931 (GRCm38) missense possibly damaging 0.65
R5032:Pik3c2g UTSW 6 139,896,202 (GRCm38) missense probably benign 0.00
R5071:Pik3c2g UTSW 6 139,720,147 (GRCm38) missense probably null 0.00
R5072:Pik3c2g UTSW 6 139,720,147 (GRCm38) missense probably null 0.00
R5073:Pik3c2g UTSW 6 139,720,147 (GRCm38) missense probably null 0.00
R5074:Pik3c2g UTSW 6 139,720,147 (GRCm38) missense probably null 0.00
R5107:Pik3c2g UTSW 6 139,635,625 (GRCm38) intron probably benign
R5186:Pik3c2g UTSW 6 139,622,018 (GRCm38) missense probably damaging 1.00
R5253:Pik3c2g UTSW 6 139,896,257 (GRCm38) critical splice donor site probably null
R5359:Pik3c2g UTSW 6 139,622,123 (GRCm38) missense probably damaging 1.00
R5394:Pik3c2g UTSW 6 139,720,082 (GRCm38) missense probably benign
R5417:Pik3c2g UTSW 6 139,736,943 (GRCm38) missense probably benign
R5435:Pik3c2g UTSW 6 139,715,855 (GRCm38) splice site probably null
R5580:Pik3c2g UTSW 6 139,626,533 (GRCm38) missense probably damaging 0.99
R5664:Pik3c2g UTSW 6 139,737,007 (GRCm38) missense probably damaging 0.98
R5908:Pik3c2g UTSW 6 139,768,710 (GRCm38) missense
R5914:Pik3c2g UTSW 6 139,622,479 (GRCm38) missense probably benign 0.00
R6046:Pik3c2g UTSW 6 139,896,792 (GRCm38) missense probably damaging 1.00
R6046:Pik3c2g UTSW 6 139,622,139 (GRCm38) missense probably damaging 0.96
R6298:Pik3c2g UTSW 6 139,626,563 (GRCm38) missense probably damaging 1.00
R6382:Pik3c2g UTSW 6 139,719,998 (GRCm38) missense possibly damaging 0.88
R6480:Pik3c2g UTSW 6 139,730,469 (GRCm38) missense probably benign 0.27
R6917:Pik3c2g UTSW 6 139,896,173 (GRCm38) missense probably benign 0.00
R6929:Pik3c2g UTSW 6 139,957,776 (GRCm38) missense possibly damaging 0.67
R7022:Pik3c2g UTSW 6 139,622,063 (GRCm38) missense possibly damaging 0.82
R7144:Pik3c2g UTSW 6 139,629,870 (GRCm38) missense probably damaging 1.00
R7213:Pik3c2g UTSW 6 139,860,264 (GRCm38) missense
R7215:Pik3c2g UTSW 6 139,754,863 (GRCm38) missense
R7332:Pik3c2g UTSW 6 139,896,255 (GRCm38) missense
R7357:Pik3c2g UTSW 6 139,633,793 (GRCm38) critical splice donor site probably null
R7359:Pik3c2g UTSW 6 139,967,894 (GRCm38) missense unknown
R7385:Pik3c2g UTSW 6 139,855,353 (GRCm38) missense
R7455:Pik3c2g UTSW 6 139,967,917 (GRCm38) missense unknown
R7651:Pik3c2g UTSW 6 139,622,072 (GRCm38) missense possibly damaging 0.85
R7888:Pik3c2g UTSW 6 139,896,744 (GRCm38) missense
R7923:Pik3c2g UTSW 6 139,633,793 (GRCm38) critical splice donor site probably null
R7964:Pik3c2g UTSW 6 139,882,060 (GRCm38) missense
R8005:Pik3c2g UTSW 6 139,622,069 (GRCm38) missense probably benign 0.01
R8371:Pik3c2g UTSW 6 139,936,056 (GRCm38) missense unknown
R8724:Pik3c2g UTSW 6 139,967,893 (GRCm38) missense unknown
R8733:Pik3c2g UTSW 6 139,768,700 (GRCm38) nonsense probably null
R8809:Pik3c2g UTSW 6 139,768,710 (GRCm38) missense
R8888:Pik3c2g UTSW 6 139,730,366 (GRCm38) nonsense probably null
R8931:Pik3c2g UTSW 6 139,875,367 (GRCm38) missense probably benign 0.02
R9188:Pik3c2g UTSW 6 139,622,403 (GRCm38) missense possibly damaging 0.94
R9336:Pik3c2g UTSW 6 139,875,435 (GRCm38) missense
R9383:Pik3c2g UTSW 6 139,882,016 (GRCm38) nonsense probably null
R9524:Pik3c2g UTSW 6 139,629,770 (GRCm38) missense probably damaging 0.99
R9531:Pik3c2g UTSW 6 139,896,200 (GRCm38) missense
R9630:Pik3c2g UTSW 6 139,622,239 (GRCm38) missense possibly damaging 0.66
R9697:Pik3c2g UTSW 6 139,967,791 (GRCm38) missense unknown
R9708:Pik3c2g UTSW 6 139,629,867 (GRCm38) missense probably benign
R9717:Pik3c2g UTSW 6 139,896,184 (GRCm38) missense
RF015:Pik3c2g UTSW 6 139,754,771 (GRCm38) missense
RF032:Pik3c2g UTSW 6 139,635,658 (GRCm38) frame shift probably null
X0024:Pik3c2g UTSW 6 139,860,258 (GRCm38) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CAGGTGACTTTGTTACCAGCC -3'
(R):5'- GTACAGTGGTGCACATCTAGGC -3'

Sequencing Primer
(F):5'- CTTTGTTACCAGCCAAAGGAG -3'
(R):5'- GTGCACATCTAGGCAATGTG -3'
Posted On 2014-08-25