Incidental Mutation 'R4995:Pygm'
ID |
385219 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Pygm
|
Ensembl Gene |
ENSMUSG00000032648 |
Gene Name |
muscle glycogen phosphorylase |
Synonyms |
PG |
MMRRC Submission |
042589-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4995 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
19 |
Chromosomal Location |
6384399-6398459 bp(+) (GRCm38) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 6398139 bp (GRCm38)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Threonine
at position 737
(I737T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000109111
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000035269]
[ENSMUST00000035716]
[ENSMUST00000113467]
[ENSMUST00000113468]
[ENSMUST00000113469]
[ENSMUST00000113471]
[ENSMUST00000113472]
[ENSMUST00000113475]
[ENSMUST00000113476]
[ENSMUST00000113483]
[ENSMUST00000139522]
[ENSMUST00000127021]
[ENSMUST00000146601]
[ENSMUST00000146831]
[ENSMUST00000150713]
[ENSMUST00000167240]
[ENSMUST00000138555]
|
AlphaFold |
Q9WUB3 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000035269
AA Change: I825T
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000047564 Gene: ENSMUSG00000032648 AA Change: I825T
Domain | Start | End | E-Value | Type |
Pfam:Phosphorylase
|
113 |
829 |
N/A |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000035716
|
SMART Domains |
Protein: ENSMUSP00000041135 Gene: ENSMUSG00000032946
Domain | Start | End | E-Value | Type |
RasGEFN
|
3 |
126 |
3.56e-29 |
SMART |
RasGEF
|
150 |
388 |
1.08e-100 |
SMART |
EFh
|
430 |
458 |
8.25e-3 |
SMART |
EFh
|
459 |
487 |
1.42e1 |
SMART |
C1
|
499 |
548 |
3.22e-14 |
SMART |
low complexity region
|
575 |
595 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113467
|
SMART Domains |
Protein: ENSMUSP00000109095 Gene: ENSMUSG00000032946
Domain | Start | End | E-Value | Type |
Blast:RasGEFN
|
3 |
24 |
9e-8 |
BLAST |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113468
|
SMART Domains |
Protein: ENSMUSP00000109096 Gene: ENSMUSG00000032946
Domain | Start | End | E-Value | Type |
RasGEFN
|
3 |
97 |
1.93e-7 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113469
|
SMART Domains |
Protein: ENSMUSP00000109097 Gene: ENSMUSG00000032946
Domain | Start | End | E-Value | Type |
Blast:RasGEFN
|
3 |
24 |
1e-7 |
BLAST |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113471
|
SMART Domains |
Protein: ENSMUSP00000109099 Gene: ENSMUSG00000032946
Domain | Start | End | E-Value | Type |
RasGEFN
|
3 |
126 |
7.2e-31 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113472
|
SMART Domains |
Protein: ENSMUSP00000109100 Gene: ENSMUSG00000032946
Domain | Start | End | E-Value | Type |
RasGEFN
|
3 |
126 |
7.2e-31 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113475
|
SMART Domains |
Protein: ENSMUSP00000109103 Gene: ENSMUSG00000032946
Domain | Start | End | E-Value | Type |
RasGEFN
|
3 |
126 |
7.2e-31 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113476
|
SMART Domains |
Protein: ENSMUSP00000109104 Gene: ENSMUSG00000032946
Domain | Start | End | E-Value | Type |
RasGEFN
|
3 |
126 |
3.56e-29 |
SMART |
RasGEF
|
150 |
388 |
1.08e-100 |
SMART |
EFh
|
430 |
458 |
8.25e-3 |
SMART |
EFh
|
459 |
487 |
1.42e1 |
SMART |
C1
|
499 |
548 |
3.22e-14 |
SMART |
low complexity region
|
575 |
595 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000113483
AA Change: I737T
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000109111 Gene: ENSMUSG00000032648 AA Change: I737T
Domain | Start | End | E-Value | Type |
Pfam:Phosphorylase
|
62 |
742 |
N/A |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000122930
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000139775
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000123661
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000142755
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000145611
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000130480
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000133968
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000139522
|
SMART Domains |
Protein: ENSMUSP00000123036 Gene: ENSMUSG00000032946
Domain | Start | End | E-Value | Type |
RasGEFN
|
3 |
125 |
6.02e-27 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000127021
|
SMART Domains |
Protein: ENSMUSP00000119740 Gene: ENSMUSG00000032946
Domain | Start | End | E-Value | Type |
Blast:RasGEFN
|
3 |
24 |
1e-7 |
BLAST |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000146601
|
SMART Domains |
Protein: ENSMUSP00000117681 Gene: ENSMUSG00000032946
Domain | Start | End | E-Value | Type |
Blast:RasGEFN
|
3 |
58 |
1e-35 |
BLAST |
SCOP:d1bkds_
|
9 |
58 |
1e-8 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000146831
|
SMART Domains |
Protein: ENSMUSP00000120630 Gene: ENSMUSG00000032946
Domain | Start | End | E-Value | Type |
RasGEFN
|
3 |
126 |
3.56e-29 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000150713
|
SMART Domains |
Protein: ENSMUSP00000120949 Gene: ENSMUSG00000032946
Domain | Start | End | E-Value | Type |
RasGEFN
|
3 |
95 |
6.73e-7 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000167240
|
SMART Domains |
Protein: ENSMUSP00000129873 Gene: ENSMUSG00000032946
Domain | Start | End | E-Value | Type |
RasGEFN
|
3 |
126 |
3.56e-29 |
SMART |
RasGEF
|
150 |
388 |
1.08e-100 |
SMART |
EFh
|
430 |
458 |
8.25e-3 |
SMART |
EFh
|
459 |
487 |
1.42e1 |
SMART |
C1
|
499 |
548 |
3.22e-14 |
SMART |
low complexity region
|
575 |
595 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000138555
|
SMART Domains |
Protein: ENSMUSP00000121635 Gene: ENSMUSG00000032946
Domain | Start | End | E-Value | Type |
RasGEFN
|
3 |
126 |
3.56e-29 |
SMART |
Pfam:RasGEF
|
151 |
231 |
1.6e-15 |
PFAM |
|
Meta Mutation Damage Score |
0.9535  |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.7%
- 20x: 93.6%
|
Validation Efficiency |
99% (86/87) |
MGI Phenotype |
FUNCTION: This gene encodes a glycolysis enzyme found in muscle. Highly similar enzymes encoded by different genes are found in liver and brain. The encoded protein is involved in regulating the breakdown of glycogen to glucose-1-phosphate, which is necessary for ATP generation. [provided by RefSeq, Dec 2015] PHENOTYPE: Mice homozygous for a null mutation exhibit massive muscle glycogen accumulation, elevated creatine kinase levels in blood, and very poor exercise performance. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921504E06Rik |
G |
A |
2: 19,494,184 (GRCm38) |
Q333* |
probably null |
Het |
4930505A04Rik |
C |
T |
11: 30,426,349 (GRCm38) |
V173M |
probably damaging |
Het |
Acvrl1 |
G |
A |
15: 101,135,860 (GRCm38) |
R141H |
probably benign |
Het |
Adprm |
A |
G |
11: 67,041,610 (GRCm38) |
F158L |
possibly damaging |
Het |
Aldoart2 |
C |
T |
12: 55,566,253 (GRCm38) |
T321M |
probably benign |
Het |
Ap3m2 |
A |
G |
8: 22,803,776 (GRCm38) |
V86A |
probably benign |
Het |
Arhgef19 |
T |
A |
4: 141,247,515 (GRCm38) |
|
probably null |
Het |
Armc4 |
G |
A |
18: 7,223,663 (GRCm38) |
T460M |
probably damaging |
Het |
Bcl2l12 |
T |
G |
7: 44,994,191 (GRCm38) |
|
probably null |
Het |
Bptf |
T |
C |
11: 107,054,565 (GRCm38) |
Q2501R |
probably damaging |
Het |
C230029F24Rik |
A |
T |
1: 49,338,136 (GRCm38) |
|
noncoding transcript |
Het |
C7 |
C |
T |
15: 5,049,592 (GRCm38) |
G78D |
probably damaging |
Het |
Caly |
T |
C |
7: 140,070,625 (GRCm38) |
T135A |
probably benign |
Het |
Cbl |
A |
G |
9: 44,153,811 (GRCm38) |
M740T |
possibly damaging |
Het |
Cbx4 |
A |
G |
11: 119,081,211 (GRCm38) |
V446A |
probably benign |
Het |
Celsr1 |
C |
A |
15: 85,937,911 (GRCm38) |
R1735L |
probably damaging |
Het |
Cep250 |
A |
G |
2: 155,988,316 (GRCm38) |
D135G |
probably damaging |
Het |
Cgn |
T |
C |
3: 94,779,936 (GRCm38) |
T19A |
probably damaging |
Het |
Chic2 |
A |
T |
5: 75,044,204 (GRCm38) |
V32D |
probably damaging |
Het |
Cntln |
A |
G |
4: 85,049,883 (GRCm38) |
K780E |
probably benign |
Het |
Col8a2 |
A |
T |
4: 126,310,788 (GRCm38) |
D197V |
probably damaging |
Het |
Crot |
A |
T |
5: 8,974,000 (GRCm38) |
V372E |
probably damaging |
Het |
Cyb561d2 |
C |
T |
9: 107,541,548 (GRCm38) |
V26M |
probably damaging |
Het |
Ddx5 |
G |
A |
11: 106,785,236 (GRCm38) |
T237I |
probably damaging |
Het |
Dmxl2 |
G |
T |
9: 54,501,441 (GRCm38) |
|
probably benign |
Het |
Dock8 |
T |
A |
19: 25,158,383 (GRCm38) |
S1188R |
probably benign |
Het |
Ehbp1 |
T |
A |
11: 22,101,073 (GRCm38) |
H493L |
probably damaging |
Het |
Eif5b |
T |
A |
1: 38,051,711 (GRCm38) |
*1217K |
probably null |
Het |
Eprs |
A |
G |
1: 185,410,139 (GRCm38) |
|
probably benign |
Het |
Etfdh |
T |
C |
3: 79,605,788 (GRCm38) |
D376G |
probably benign |
Het |
Fam186a |
T |
C |
15: 99,945,099 (GRCm38) |
Q1088R |
probably benign |
Het |
Fbxw16 |
G |
T |
9: 109,441,250 (GRCm38) |
T141N |
probably damaging |
Het |
Fgf11 |
G |
A |
11: 69,798,759 (GRCm38) |
H138Y |
probably damaging |
Het |
Gm1673 |
G |
A |
5: 33,984,926 (GRCm38) |
R79H |
probably damaging |
Het |
Htra3 |
T |
C |
5: 35,671,074 (GRCm38) |
E154G |
probably damaging |
Het |
Hydin |
T |
A |
8: 110,569,642 (GRCm38) |
V3601D |
probably damaging |
Het |
Jup |
G |
T |
11: 100,379,541 (GRCm38) |
S380* |
probably null |
Het |
Klrg1 |
T |
A |
6: 122,278,275 (GRCm38) |
D66V |
probably benign |
Het |
Llgl1 |
C |
T |
11: 60,709,724 (GRCm38) |
A633V |
probably benign |
Het |
Lmln |
T |
A |
16: 33,074,097 (GRCm38) |
Y203* |
probably null |
Het |
Lrrc58 |
T |
G |
16: 37,877,056 (GRCm38) |
C165G |
probably benign |
Het |
Lss |
T |
C |
10: 76,547,537 (GRCm38) |
V557A |
probably benign |
Het |
Mast4 |
T |
C |
13: 102,905,754 (GRCm38) |
|
probably benign |
Het |
Med13l |
C |
A |
5: 118,730,949 (GRCm38) |
P754Q |
possibly damaging |
Het |
Mga |
C |
T |
2: 119,932,582 (GRCm38) |
R1240* |
probably null |
Het |
Mgat5b |
T |
A |
11: 116,974,199 (GRCm38) |
|
probably null |
Het |
Mtor |
A |
G |
4: 148,525,752 (GRCm38) |
D1572G |
probably damaging |
Het |
Muc4 |
T |
A |
16: 32,754,041 (GRCm38) |
S1306T |
probably benign |
Het |
Muc4 |
T |
A |
16: 32,754,214 (GRCm38) |
S1363T |
probably benign |
Het |
Myo18b |
A |
G |
5: 112,760,392 (GRCm38) |
V2005A |
probably damaging |
Het |
Myo1e |
G |
A |
9: 70,353,272 (GRCm38) |
D571N |
probably benign |
Het |
Mypn |
T |
C |
10: 63,119,968 (GRCm38) |
|
probably null |
Het |
Ndufb10 |
T |
C |
17: 24,722,757 (GRCm38) |
|
probably null |
Het |
Nelfb |
G |
T |
2: 25,206,196 (GRCm38) |
D300E |
probably benign |
Het |
Olfr1389 |
T |
A |
11: 49,430,655 (GRCm38) |
Y60N |
probably damaging |
Het |
Olfr1507 |
A |
T |
14: 52,490,531 (GRCm38) |
C61* |
probably null |
Het |
Olfr625-ps1 |
T |
A |
7: 103,683,367 (GRCm38) |
D206E |
probably damaging |
Het |
Olfr668 |
T |
A |
7: 104,925,735 (GRCm38) |
T10S |
probably benign |
Het |
Pcdha11 |
C |
T |
18: 37,011,027 (GRCm38) |
T57M |
probably benign |
Het |
Pkp1 |
A |
T |
1: 135,880,855 (GRCm38) |
I458N |
possibly damaging |
Het |
Prr12 |
T |
A |
7: 45,051,229 (GRCm38) |
|
probably benign |
Het |
Prrc2c |
A |
T |
1: 162,705,310 (GRCm38) |
|
probably benign |
Het |
Psd4 |
T |
C |
2: 24,397,247 (GRCm38) |
F397S |
probably benign |
Het |
Rfx1 |
T |
A |
8: 84,080,114 (GRCm38) |
|
probably null |
Het |
Rsl1 |
A |
G |
13: 67,182,249 (GRCm38) |
T254A |
possibly damaging |
Het |
Sh3rf3 |
A |
G |
10: 59,086,824 (GRCm38) |
Q574R |
probably benign |
Het |
Spire1 |
T |
C |
18: 67,552,779 (GRCm38) |
|
probably null |
Het |
St6galnac4 |
G |
A |
2: 32,594,063 (GRCm38) |
G91D |
probably damaging |
Het |
Sytl2 |
T |
C |
7: 90,382,257 (GRCm38) |
|
probably benign |
Het |
Tbpl2 |
T |
A |
2: 24,093,860 (GRCm38) |
K188N |
possibly damaging |
Het |
Tenm3 |
A |
T |
8: 48,229,137 (GRCm38) |
M2486K |
possibly damaging |
Het |
Tgoln1 |
A |
C |
6: 72,616,140 (GRCm38) |
V119G |
possibly damaging |
Het |
Tpgs1 |
A |
T |
10: 79,669,491 (GRCm38) |
N28Y |
probably benign |
Het |
U2surp |
A |
C |
9: 95,462,794 (GRCm38) |
|
probably benign |
Het |
Vmn2r103 |
A |
G |
17: 19,773,511 (GRCm38) |
H50R |
probably benign |
Het |
Vmn2r19 |
A |
G |
6: 123,329,910 (GRCm38) |
N459S |
probably benign |
Het |
Vmn2r72 |
T |
C |
7: 85,738,485 (GRCm38) |
S624G |
probably damaging |
Het |
Vps13c |
A |
G |
9: 67,919,321 (GRCm38) |
T1415A |
probably benign |
Het |
Vwa5b1 |
G |
A |
4: 138,608,843 (GRCm38) |
P147S |
probably damaging |
Het |
|
Other mutations in Pygm |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01123:Pygm
|
APN |
19 |
6,391,394 (GRCm38) |
missense |
probably benign |
|
IGL01743:Pygm
|
APN |
19 |
6,392,994 (GRCm38) |
splice site |
probably null |
|
IGL01827:Pygm
|
APN |
19 |
6,390,377 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02032:Pygm
|
APN |
19 |
6,388,087 (GRCm38) |
missense |
probably benign |
0.23 |
IGL02261:Pygm
|
APN |
19 |
6,388,271 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02431:Pygm
|
APN |
19 |
6,388,118 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02511:Pygm
|
APN |
19 |
6,385,688 (GRCm38) |
missense |
probably benign |
0.22 |
IGL02967:Pygm
|
APN |
19 |
6,393,838 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03081:Pygm
|
APN |
19 |
6,388,821 (GRCm38) |
missense |
possibly damaging |
0.53 |
R0336:Pygm
|
UTSW |
19 |
6,388,758 (GRCm38) |
missense |
probably damaging |
1.00 |
R0415:Pygm
|
UTSW |
19 |
6,391,366 (GRCm38) |
missense |
probably benign |
0.06 |
R0799:Pygm
|
UTSW |
19 |
6,386,018 (GRCm38) |
intron |
probably benign |
|
R1445:Pygm
|
UTSW |
19 |
6,389,887 (GRCm38) |
missense |
probably benign |
0.20 |
R1752:Pygm
|
UTSW |
19 |
6,391,034 (GRCm38) |
missense |
probably damaging |
0.99 |
R1828:Pygm
|
UTSW |
19 |
6,397,607 (GRCm38) |
missense |
possibly damaging |
0.72 |
R2054:Pygm
|
UTSW |
19 |
6,388,155 (GRCm38) |
missense |
probably benign |
0.02 |
R2086:Pygm
|
UTSW |
19 |
6,391,481 (GRCm38) |
critical splice donor site |
probably null |
|
R2116:Pygm
|
UTSW |
19 |
6,386,408 (GRCm38) |
missense |
probably damaging |
0.98 |
R2431:Pygm
|
UTSW |
19 |
6,393,785 (GRCm38) |
missense |
probably damaging |
1.00 |
R2516:Pygm
|
UTSW |
19 |
6,397,601 (GRCm38) |
missense |
probably benign |
0.20 |
R3938:Pygm
|
UTSW |
19 |
6,392,950 (GRCm38) |
missense |
probably benign |
0.42 |
R4609:Pygm
|
UTSW |
19 |
6,391,409 (GRCm38) |
missense |
possibly damaging |
0.92 |
R4924:Pygm
|
UTSW |
19 |
6,393,724 (GRCm38) |
missense |
probably damaging |
1.00 |
R5225:Pygm
|
UTSW |
19 |
6,389,464 (GRCm38) |
missense |
probably benign |
0.01 |
R5296:Pygm
|
UTSW |
19 |
6,384,579 (GRCm38) |
missense |
probably damaging |
1.00 |
R5437:Pygm
|
UTSW |
19 |
6,390,382 (GRCm38) |
missense |
probably damaging |
1.00 |
R5994:Pygm
|
UTSW |
19 |
6,398,043 (GRCm38) |
critical splice acceptor site |
probably null |
|
R6030:Pygm
|
UTSW |
19 |
6,388,812 (GRCm38) |
missense |
possibly damaging |
0.78 |
R6030:Pygm
|
UTSW |
19 |
6,388,812 (GRCm38) |
missense |
possibly damaging |
0.78 |
R6188:Pygm
|
UTSW |
19 |
6,397,937 (GRCm38) |
splice site |
probably null |
|
R6266:Pygm
|
UTSW |
19 |
6,398,139 (GRCm38) |
missense |
probably damaging |
1.00 |
R6799:Pygm
|
UTSW |
19 |
6,398,127 (GRCm38) |
missense |
probably damaging |
1.00 |
R6855:Pygm
|
UTSW |
19 |
6,393,757 (GRCm38) |
missense |
probably damaging |
1.00 |
R6856:Pygm
|
UTSW |
19 |
6,393,757 (GRCm38) |
missense |
probably damaging |
1.00 |
R6857:Pygm
|
UTSW |
19 |
6,393,757 (GRCm38) |
missense |
probably damaging |
1.00 |
R7223:Pygm
|
UTSW |
19 |
6,388,863 (GRCm38) |
missense |
probably benign |
|
R7256:Pygm
|
UTSW |
19 |
6,385,896 (GRCm38) |
missense |
probably benign |
0.01 |
R7263:Pygm
|
UTSW |
19 |
6,388,327 (GRCm38) |
missense |
probably damaging |
1.00 |
R7398:Pygm
|
UTSW |
19 |
6,385,936 (GRCm38) |
missense |
probably damaging |
1.00 |
R8093:Pygm
|
UTSW |
19 |
6,386,042 (GRCm38) |
missense |
probably damaging |
1.00 |
R8351:Pygm
|
UTSW |
19 |
6,388,087 (GRCm38) |
missense |
possibly damaging |
0.83 |
R8499:Pygm
|
UTSW |
19 |
6,390,362 (GRCm38) |
missense |
probably damaging |
0.99 |
R8967:Pygm
|
UTSW |
19 |
6,384,714 (GRCm38) |
missense |
probably damaging |
1.00 |
R9331:Pygm
|
UTSW |
19 |
6,398,099 (GRCm38) |
missense |
probably damaging |
1.00 |
R9656:Pygm
|
UTSW |
19 |
6,388,157 (GRCm38) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TTGTACAAGGTGAGGGGTCC -3'
(R):5'- TAGGCATCAGGACCTAGAGAC -3'
Sequencing Primer
(F):5'- CTGGCAGGGCTTTGACTC -3'
(R):5'- ACTGGGGAAAGTGGGTTCC -3'
|
Posted On |
2016-05-10 |