Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
A |
T |
17: 24,346,221 (GRCm38) |
L79* |
probably null |
Het |
Acot3 |
A |
G |
12: 84,053,474 (GRCm38) |
N8S |
probably benign |
Het |
Adora2a |
T |
C |
10: 75,333,608 (GRCm38) |
V302A |
probably benign |
Het |
Anpep |
A |
C |
7: 79,839,185 (GRCm38) |
|
probably null |
Het |
Arrb1 |
A |
G |
7: 99,601,150 (GRCm38) |
K392E |
probably benign |
Het |
Atp8a1 |
A |
T |
5: 67,751,049 (GRCm38) |
N444K |
probably benign |
Het |
Bltp3b |
T |
A |
10: 89,787,158 (GRCm38) |
N298K |
probably benign |
Het |
Brinp2 |
C |
T |
1: 158,266,590 (GRCm38) |
G181R |
probably benign |
Het |
Cacna1g |
A |
T |
11: 94,409,427 (GRCm38) |
C2184* |
probably null |
Het |
Cacna1h |
C |
T |
17: 25,381,550 (GRCm38) |
A1606T |
probably damaging |
Het |
Ccdc30 |
T |
C |
4: 119,356,718 (GRCm38) |
T205A |
probably benign |
Het |
Celsr1 |
A |
G |
15: 86,031,495 (GRCm38) |
I759T |
probably damaging |
Het |
Chaf1a |
A |
G |
17: 56,063,404 (GRCm38) |
D623G |
possibly damaging |
Het |
Col6a3 |
G |
T |
1: 90,779,045 (GRCm38) |
N2115K |
unknown |
Het |
Dync1h1 |
A |
T |
12: 110,651,653 (GRCm38) |
T3209S |
probably damaging |
Het |
Erich6 |
T |
C |
3: 58,616,566 (GRCm38) |
D629G |
possibly damaging |
Het |
Fahd1 |
G |
T |
17: 24,849,941 (GRCm38) |
A54E |
probably damaging |
Het |
Flrt3 |
C |
T |
2: 140,660,025 (GRCm38) |
R561Q |
probably damaging |
Het |
Grm6 |
A |
T |
11: 50,856,963 (GRCm38) |
D334V |
probably damaging |
Het |
Helb |
A |
T |
10: 120,105,468 (GRCm38) |
D438E |
probably damaging |
Het |
Hmgcs1 |
T |
C |
13: 119,695,049 (GRCm38) |
|
probably null |
Het |
Hnf4g |
C |
A |
3: 3,657,110 (GRCm38) |
Y441* |
probably null |
Het |
Hspa13 |
A |
T |
16: 75,765,037 (GRCm38) |
N91K |
possibly damaging |
Het |
Ilvbl |
T |
C |
10: 78,577,223 (GRCm38) |
I193T |
possibly damaging |
Het |
Itga7 |
T |
C |
10: 128,949,472 (GRCm38) |
V848A |
probably benign |
Het |
Kash5 |
C |
T |
7: 45,200,311 (GRCm38) |
V63I |
probably benign |
Het |
Lpin1 |
A |
G |
12: 16,565,528 (GRCm38) |
M341T |
probably benign |
Het |
Lypd5 |
G |
T |
7: 24,353,106 (GRCm38) |
|
probably null |
Het |
Mrgprb1 |
A |
C |
7: 48,447,897 (GRCm38) |
V89G |
possibly damaging |
Het |
Nsun7 |
T |
C |
5: 66,283,737 (GRCm38) |
|
probably null |
Het |
Oasl1 |
T |
A |
5: 114,937,183 (GRCm38) |
V434E |
probably damaging |
Het |
Or2ak6 |
G |
A |
11: 58,702,543 (GRCm38) |
V281I |
probably benign |
Het |
Or7g22 |
A |
G |
9: 19,137,478 (GRCm38) |
M162V |
probably benign |
Het |
Or8k16 |
T |
C |
2: 85,689,608 (GRCm38) |
Y60H |
probably damaging |
Het |
Otor |
T |
A |
2: 143,080,035 (GRCm38) |
|
probably null |
Het |
Pik3cg |
G |
A |
12: 32,194,758 (GRCm38) |
T899M |
probably damaging |
Het |
Plaat5 |
A |
G |
19: 7,613,330 (GRCm38) |
D74G |
probably benign |
Het |
Pld2 |
C |
A |
11: 70,541,107 (GRCm38) |
L52M |
probably damaging |
Het |
Pon3 |
A |
T |
6: 5,230,786 (GRCm38) |
M247K |
possibly damaging |
Het |
Ppfia2 |
C |
A |
10: 106,906,458 (GRCm38) |
Y1037* |
probably null |
Het |
Ppm1m |
A |
T |
9: 106,198,152 (GRCm38) |
C99* |
probably null |
Het |
Prss44 |
A |
T |
9: 110,815,293 (GRCm38) |
*145C |
probably null |
Het |
Ralgapb |
T |
G |
2: 158,476,136 (GRCm38) |
V866G |
probably damaging |
Het |
Rassf6 |
C |
A |
5: 90,609,774 (GRCm38) |
R109L |
possibly damaging |
Het |
Rbm4b |
A |
C |
19: 4,762,003 (GRCm38) |
T147P |
probably benign |
Het |
Rpl7l1 |
T |
C |
17: 46,779,396 (GRCm38) |
K104R |
probably benign |
Het |
Ryr1 |
A |
T |
7: 29,117,404 (GRCm38) |
I69N |
possibly damaging |
Het |
Scd1 |
G |
T |
19: 44,406,488 (GRCm38) |
F99L |
probably benign |
Het |
Semp2l1 |
A |
T |
1: 32,546,763 (GRCm38) |
I22N |
probably benign |
Het |
Spint2 |
A |
T |
7: 29,259,423 (GRCm38) |
S66T |
probably benign |
Het |
Tarm1 |
T |
A |
7: 3,502,462 (GRCm38) |
I2F |
probably benign |
Het |
Tenm4 |
T |
C |
7: 96,892,860 (GRCm38) |
V1860A |
probably damaging |
Het |
Usp38 |
A |
G |
8: 81,014,291 (GRCm38) |
I49T |
possibly damaging |
Het |
Vars2 |
A |
G |
17: 35,660,402 (GRCm38) |
|
probably null |
Het |
Vmn2r27 |
T |
G |
6: 124,200,593 (GRCm38) |
H484P |
possibly damaging |
Het |
Wdr35 |
T |
A |
12: 9,003,982 (GRCm38) |
|
probably null |
Het |
Zfp937 |
A |
T |
2: 150,239,423 (GRCm38) |
K458* |
probably null |
Het |
|
Other mutations in Ptpro |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00334:Ptpro
|
APN |
6 |
137,394,909 (GRCm38) |
critical splice donor site |
probably null |
|
IGL00844:Ptpro
|
APN |
6 |
137,414,239 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00983:Ptpro
|
APN |
6 |
137,418,248 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01073:Ptpro
|
APN |
6 |
137,377,088 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01832:Ptpro
|
APN |
6 |
137,393,668 (GRCm38) |
missense |
possibly damaging |
0.93 |
IGL02308:Ptpro
|
APN |
6 |
137,454,700 (GRCm38) |
missense |
probably benign |
0.37 |
IGL02387:Ptpro
|
APN |
6 |
137,410,980 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL02605:Ptpro
|
APN |
6 |
137,380,318 (GRCm38) |
missense |
probably benign |
0.02 |
IGL02666:Ptpro
|
APN |
6 |
137,378,059 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL03275:Ptpro
|
APN |
6 |
137,450,006 (GRCm38) |
missense |
probably damaging |
1.00 |
Brau
|
UTSW |
6 |
137,454,598 (GRCm38) |
missense |
probably damaging |
1.00 |
court
|
UTSW |
6 |
137,393,675 (GRCm38) |
nonsense |
probably null |
|
Hoff
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
Jester
|
UTSW |
6 |
137,449,917 (GRCm38) |
missense |
probably damaging |
1.00 |
mann
|
UTSW |
6 |
137,411,116 (GRCm38) |
splice site |
probably null |
|
R0017:Ptpro
|
UTSW |
6 |
137,416,827 (GRCm38) |
missense |
probably benign |
0.03 |
R0017:Ptpro
|
UTSW |
6 |
137,416,827 (GRCm38) |
missense |
probably benign |
0.03 |
R0020:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0022:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0023:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0024:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0094:Ptpro
|
UTSW |
6 |
137,386,352 (GRCm38) |
missense |
probably benign |
0.08 |
R0094:Ptpro
|
UTSW |
6 |
137,386,352 (GRCm38) |
missense |
probably benign |
0.08 |
R0103:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0106:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0316:Ptpro
|
UTSW |
6 |
137,376,989 (GRCm38) |
missense |
possibly damaging |
0.81 |
R0427:Ptpro
|
UTSW |
6 |
137,368,296 (GRCm38) |
missense |
possibly damaging |
0.81 |
R0456:Ptpro
|
UTSW |
6 |
137,414,230 (GRCm38) |
missense |
probably benign |
0.04 |
R0536:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0537:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0552:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0555:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0664:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0708:Ptpro
|
UTSW |
6 |
137,386,253 (GRCm38) |
missense |
probably benign |
0.26 |
R0730:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0735:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0738:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0786:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0811:Ptpro
|
UTSW |
6 |
137,368,079 (GRCm38) |
missense |
probably benign |
0.00 |
R0812:Ptpro
|
UTSW |
6 |
137,368,079 (GRCm38) |
missense |
probably benign |
0.00 |
R0881:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R0973:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1145:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1145:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1146:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1146:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1147:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1147:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1259:Ptpro
|
UTSW |
6 |
137,392,741 (GRCm38) |
missense |
probably damaging |
0.98 |
R1340:Ptpro
|
UTSW |
6 |
137,441,081 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1381:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1382:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1385:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1396:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1401:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1416:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1422:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1448:Ptpro
|
UTSW |
6 |
137,441,116 (GRCm38) |
missense |
probably damaging |
1.00 |
R1513:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1518:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1526:Ptpro
|
UTSW |
6 |
137,461,726 (GRCm38) |
missense |
probably damaging |
1.00 |
R1540:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1571:Ptpro
|
UTSW |
6 |
137,378,130 (GRCm38) |
missense |
probably benign |
|
R1573:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1587:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1588:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1649:Ptpro
|
UTSW |
6 |
137,444,017 (GRCm38) |
nonsense |
probably null |
|
R1700:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1701:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1745:Ptpro
|
UTSW |
6 |
137,400,645 (GRCm38) |
missense |
probably benign |
0.03 |
R1772:Ptpro
|
UTSW |
6 |
137,430,743 (GRCm38) |
missense |
probably damaging |
1.00 |
R1911:Ptpro
|
UTSW |
6 |
137,400,619 (GRCm38) |
splice site |
probably benign |
|
R1958:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R1967:Ptpro
|
UTSW |
6 |
137,416,865 (GRCm38) |
missense |
probably benign |
0.38 |
R2025:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R2026:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R2040:Ptpro
|
UTSW |
6 |
137,386,164 (GRCm38) |
splice site |
probably benign |
|
R2115:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R2117:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R2130:Ptpro
|
UTSW |
6 |
137,411,116 (GRCm38) |
splice site |
probably null |
|
R2161:Ptpro
|
UTSW |
6 |
137,449,887 (GRCm38) |
missense |
probably benign |
0.01 |
R2431:Ptpro
|
UTSW |
6 |
137,443,585 (GRCm38) |
nonsense |
probably null |
|
R2915:Ptpro
|
UTSW |
6 |
137,414,241 (GRCm38) |
start gained |
probably benign |
|
R2988:Ptpro
|
UTSW |
6 |
137,443,599 (GRCm38) |
nonsense |
probably null |
|
R3772:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R3773:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R3795:Ptpro
|
UTSW |
6 |
137,380,309 (GRCm38) |
missense |
probably benign |
|
R3885:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R3886:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R3887:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R3888:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R3893:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R4032:Ptpro
|
UTSW |
6 |
137,461,742 (GRCm38) |
missense |
probably damaging |
1.00 |
R4133:Ptpro
|
UTSW |
6 |
137,420,372 (GRCm38) |
missense |
probably damaging |
1.00 |
R4377:Ptpro
|
UTSW |
6 |
137,380,266 (GRCm38) |
missense |
probably benign |
0.26 |
R4455:Ptpro
|
UTSW |
6 |
137,393,659 (GRCm38) |
missense |
probably damaging |
1.00 |
R4613:Ptpro
|
UTSW |
6 |
137,416,836 (GRCm38) |
nonsense |
probably null |
|
R4827:Ptpro
|
UTSW |
6 |
137,442,710 (GRCm38) |
missense |
probably damaging |
1.00 |
R4863:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R4870:Ptpro
|
UTSW |
6 |
137,377,132 (GRCm38) |
missense |
probably damaging |
0.96 |
R4910:Ptpro
|
UTSW |
6 |
137,368,338 (GRCm38) |
missense |
probably damaging |
0.99 |
R4932:Ptpro
|
UTSW |
6 |
137,411,105 (GRCm38) |
nonsense |
probably null |
|
R4941:Ptpro
|
UTSW |
6 |
137,392,765 (GRCm38) |
missense |
probably damaging |
1.00 |
R4989:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R5009:Ptpro
|
UTSW |
6 |
137,377,132 (GRCm38) |
missense |
probably damaging |
0.96 |
R5032:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R5033:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R5162:Ptpro
|
UTSW |
6 |
137,443,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R5393:Ptpro
|
UTSW |
6 |
137,380,224 (GRCm38) |
missense |
probably benign |
0.04 |
R5423:Ptpro
|
UTSW |
6 |
137,442,707 (GRCm38) |
missense |
probably damaging |
1.00 |
R5782:Ptpro
|
UTSW |
6 |
137,399,498 (GRCm38) |
missense |
possibly damaging |
0.80 |
R6103:Ptpro
|
UTSW |
6 |
137,400,706 (GRCm38) |
missense |
possibly damaging |
0.76 |
R6239:Ptpro
|
UTSW |
6 |
137,380,608 (GRCm38) |
missense |
probably benign |
0.28 |
R6488:Ptpro
|
UTSW |
6 |
137,393,675 (GRCm38) |
nonsense |
probably null |
|
R6494:Ptpro
|
UTSW |
6 |
137,382,642 (GRCm38) |
missense |
probably benign |
0.20 |
R6763:Ptpro
|
UTSW |
6 |
137,418,281 (GRCm38) |
splice site |
probably null |
|
R6888:Ptpro
|
UTSW |
6 |
137,380,200 (GRCm38) |
missense |
probably benign |
0.30 |
R6983:Ptpro
|
UTSW |
6 |
137,449,917 (GRCm38) |
missense |
probably damaging |
1.00 |
R7019:Ptpro
|
UTSW |
6 |
137,380,478 (GRCm38) |
missense |
probably benign |
|
R7218:Ptpro
|
UTSW |
6 |
137,454,598 (GRCm38) |
missense |
probably damaging |
1.00 |
R7236:Ptpro
|
UTSW |
6 |
137,368,337 (GRCm38) |
missense |
probably damaging |
1.00 |
R7299:Ptpro
|
UTSW |
6 |
137,441,144 (GRCm38) |
critical splice donor site |
probably null |
|
R7381:Ptpro
|
UTSW |
6 |
137,399,561 (GRCm38) |
missense |
possibly damaging |
0.93 |
R7493:Ptpro
|
UTSW |
6 |
137,382,649 (GRCm38) |
missense |
probably benign |
0.01 |
R7733:Ptpro
|
UTSW |
6 |
137,414,286 (GRCm38) |
nonsense |
probably null |
|
R7793:Ptpro
|
UTSW |
6 |
137,416,820 (GRCm38) |
missense |
probably damaging |
0.99 |
R7804:Ptpro
|
UTSW |
6 |
137,399,601 (GRCm38) |
splice site |
probably null |
|
R7833:Ptpro
|
UTSW |
6 |
137,416,863 (GRCm38) |
nonsense |
probably null |
|
R7859:Ptpro
|
UTSW |
6 |
137,392,807 (GRCm38) |
critical splice donor site |
probably null |
|
R7873:Ptpro
|
UTSW |
6 |
137,430,739 (GRCm38) |
missense |
probably benign |
0.44 |
R8042:Ptpro
|
UTSW |
6 |
137,416,883 (GRCm38) |
missense |
possibly damaging |
0.71 |
R8859:Ptpro
|
UTSW |
6 |
137,426,784 (GRCm38) |
nonsense |
probably null |
|
R8979:Ptpro
|
UTSW |
6 |
137,368,142 (GRCm38) |
missense |
probably benign |
|
R9138:Ptpro
|
UTSW |
6 |
137,411,115 (GRCm38) |
critical splice donor site |
probably null |
|
R9309:Ptpro
|
UTSW |
6 |
137,454,658 (GRCm38) |
missense |
probably damaging |
1.00 |
R9420:Ptpro
|
UTSW |
6 |
137,443,935 (GRCm38) |
missense |
probably benign |
0.08 |
R9612:Ptpro
|
UTSW |
6 |
137,414,320 (GRCm38) |
missense |
probably benign |
0.31 |
R9625:Ptpro
|
UTSW |
6 |
137,394,875 (GRCm38) |
missense |
probably damaging |
1.00 |
R9697:Ptpro
|
UTSW |
6 |
137,386,290 (GRCm38) |
missense |
probably damaging |
1.00 |
R9715:Ptpro
|
UTSW |
6 |
137,368,110 (GRCm38) |
missense |
probably damaging |
0.96 |
Z1177:Ptpro
|
UTSW |
6 |
137,378,140 (GRCm38) |
missense |
probably damaging |
1.00 |
|