Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abat |
T |
C |
16: 8,418,805 (GRCm39) |
I102T |
possibly damaging |
Het |
Abca9 |
T |
C |
11: 110,054,206 (GRCm39) |
|
probably null |
Het |
Ago3 |
T |
C |
4: 126,244,115 (GRCm39) |
|
probably null |
Het |
Akap1 |
G |
T |
11: 88,735,099 (GRCm39) |
A75E |
probably damaging |
Het |
Atad2b |
C |
A |
12: 5,041,012 (GRCm39) |
A227E |
possibly damaging |
Het |
Bmpr1a |
G |
T |
14: 34,163,148 (GRCm39) |
H81N |
possibly damaging |
Het |
Camkv |
C |
T |
9: 107,824,296 (GRCm39) |
T236I |
probably damaging |
Het |
Ccdc30 |
T |
C |
4: 119,181,358 (GRCm39) |
E601G |
probably benign |
Het |
Ccin |
G |
A |
4: 43,984,064 (GRCm39) |
R157H |
probably damaging |
Het |
Cdkn3 |
C |
T |
14: 47,004,780 (GRCm39) |
P114L |
probably damaging |
Het |
Col6a2 |
C |
T |
10: 76,446,527 (GRCm39) |
G352D |
probably damaging |
Het |
Csf2rb |
A |
T |
15: 78,232,520 (GRCm39) |
D609V |
probably benign |
Het |
Ctc1 |
T |
G |
11: 68,917,175 (GRCm39) |
Y110* |
probably null |
Het |
D630023F18Rik |
T |
A |
1: 65,147,899 (GRCm39) |
N218I |
probably damaging |
Het |
Dchs1 |
A |
T |
7: 105,408,212 (GRCm39) |
H1873Q |
probably benign |
Het |
Dnah1 |
T |
C |
14: 31,012,396 (GRCm39) |
D1901G |
probably damaging |
Het |
Eddm3b |
T |
A |
14: 51,354,110 (GRCm39) |
S33T |
probably damaging |
Het |
Efcc1 |
A |
G |
6: 87,728,768 (GRCm39) |
T408A |
probably benign |
Het |
Epas1 |
A |
G |
17: 87,134,920 (GRCm39) |
T518A |
probably benign |
Het |
Ergic2 |
A |
T |
6: 148,104,005 (GRCm39) |
M84K |
probably damaging |
Het |
Ergic3 |
T |
C |
2: 155,853,160 (GRCm39) |
V201A |
probably benign |
Het |
Espn |
C |
A |
4: 152,223,278 (GRCm39) |
W258L |
probably damaging |
Het |
Gm45337 |
A |
G |
7: 141,697,817 (GRCm39) |
S156P |
unknown |
Het |
Hmcn2 |
T |
C |
2: 31,244,741 (GRCm39) |
Y733H |
probably damaging |
Het |
Itga2 |
C |
T |
13: 115,009,866 (GRCm39) |
G363D |
probably damaging |
Het |
Kcnk5 |
T |
C |
14: 20,192,046 (GRCm39) |
R372G |
probably benign |
Het |
Khdc4 |
G |
T |
3: 88,617,219 (GRCm39) |
S506I |
probably damaging |
Het |
Kif11 |
T |
A |
19: 37,386,602 (GRCm39) |
D387E |
probably damaging |
Het |
Lrrn2 |
A |
C |
1: 132,866,104 (GRCm39) |
I390L |
probably benign |
Het |
Map2 |
G |
T |
1: 66,419,684 (GRCm39) |
R5L |
probably damaging |
Het |
Muc16 |
C |
T |
9: 18,558,529 (GRCm39) |
R2588K |
unknown |
Het |
Or3a10 |
A |
G |
11: 73,935,782 (GRCm39) |
F106S |
possibly damaging |
Het |
Or5b99 |
A |
T |
19: 12,976,445 (GRCm39) |
I32F |
probably damaging |
Het |
Or7g29 |
A |
G |
9: 19,286,262 (GRCm39) |
I305T |
probably benign |
Het |
Osbpl8 |
T |
C |
10: 111,103,530 (GRCm39) |
I178T |
probably damaging |
Het |
Pak2 |
A |
T |
16: 31,852,729 (GRCm39) |
|
probably benign |
Het |
Perp |
A |
T |
10: 18,729,326 (GRCm39) |
I86F |
possibly damaging |
Het |
Polr1f |
T |
A |
12: 33,483,526 (GRCm39) |
Y93N |
probably damaging |
Het |
Preb |
A |
G |
5: 31,115,671 (GRCm39) |
S220P |
probably damaging |
Het |
Prrt4 |
T |
C |
6: 29,177,665 (GRCm39) |
T35A |
probably damaging |
Het |
Ror2 |
T |
A |
13: 53,286,032 (GRCm39) |
I73F |
possibly damaging |
Het |
Rpl36-ps4 |
A |
G |
17: 88,228,574 (GRCm39) |
T40A |
probably damaging |
Het |
Rsbn1 |
A |
T |
3: 103,868,830 (GRCm39) |
H623L |
possibly damaging |
Het |
Sap30 |
C |
A |
8: 57,940,456 (GRCm39) |
A49S |
possibly damaging |
Het |
Sf3b3 |
T |
C |
8: 111,550,075 (GRCm39) |
T648A |
probably benign |
Het |
Sh3pxd2a |
T |
C |
19: 47,361,882 (GRCm39) |
R83G |
probably damaging |
Het |
Slc35e1 |
A |
T |
8: 73,246,042 (GRCm39) |
I130N |
probably damaging |
Het |
Smchd1 |
C |
T |
17: 71,743,767 (GRCm39) |
R466Q |
probably damaging |
Het |
Smgc |
C |
T |
15: 91,722,565 (GRCm39) |
|
probably benign |
Het |
Stk32b |
A |
T |
5: 37,612,341 (GRCm39) |
N348K |
possibly damaging |
Het |
Sult2a1 |
A |
G |
7: 13,530,342 (GRCm39) |
F266L |
probably damaging |
Het |
Sult2a2 |
A |
T |
7: 13,467,484 (GRCm39) |
M1L |
probably damaging |
Het |
Telo2 |
A |
G |
17: 25,332,085 (GRCm39) |
V161A |
probably benign |
Het |
Tmed11 |
C |
T |
5: 108,925,293 (GRCm39) |
R173H |
probably damaging |
Het |
Trappc6a |
G |
A |
7: 19,249,923 (GRCm39) |
|
probably benign |
Het |
Vmn2r5 |
A |
T |
3: 64,398,522 (GRCm39) |
V819D |
probably damaging |
Het |
Vmn2r74 |
A |
G |
7: 85,606,569 (GRCm39) |
I259T |
probably damaging |
Het |
Vps13a |
A |
G |
19: 16,723,340 (GRCm39) |
I286T |
probably damaging |
Het |
Vsig10l |
A |
T |
7: 43,117,623 (GRCm39) |
I739F |
possibly damaging |
Het |
Zfyve1 |
A |
C |
12: 83,594,802 (GRCm39) |
V730G |
probably benign |
Het |
Zfyve9 |
A |
T |
4: 108,499,288 (GRCm39) |
D1284E |
possibly damaging |
Het |
Zmym4 |
C |
T |
4: 126,758,060 (GRCm39) |
R1498H |
probably damaging |
Het |
Znhit2 |
A |
T |
19: 6,111,803 (GRCm39) |
R183* |
probably null |
Het |
|
Other mutations in Plpp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00780:Plpp1
|
APN |
13 |
112,988,040 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02139:Plpp1
|
APN |
13 |
112,993,433 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02269:Plpp1
|
APN |
13 |
112,993,526 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4260001:Plpp1
|
UTSW |
13 |
112,993,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R0550:Plpp1
|
UTSW |
13 |
112,971,519 (GRCm39) |
missense |
probably benign |
0.02 |
R1301:Plpp1
|
UTSW |
13 |
112,971,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R1473:Plpp1
|
UTSW |
13 |
112,996,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R5224:Plpp1
|
UTSW |
13 |
112,988,046 (GRCm39) |
nonsense |
probably null |
|
R5306:Plpp1
|
UTSW |
13 |
112,988,089 (GRCm39) |
critical splice donor site |
probably null |
|
R6108:Plpp1
|
UTSW |
13 |
113,003,399 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6111:Plpp1
|
UTSW |
13 |
113,003,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R6500:Plpp1
|
UTSW |
13 |
113,003,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R7520:Plpp1
|
UTSW |
13 |
112,937,781 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7716:Plpp1
|
UTSW |
13 |
112,996,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R7716:Plpp1
|
UTSW |
13 |
112,993,323 (GRCm39) |
missense |
probably benign |
0.27 |
R8080:Plpp1
|
UTSW |
13 |
113,004,002 (GRCm39) |
missense |
probably benign |
0.19 |
R8209:Plpp1
|
UTSW |
13 |
113,003,465 (GRCm39) |
missense |
probably benign |
0.44 |
R8226:Plpp1
|
UTSW |
13 |
113,003,465 (GRCm39) |
missense |
probably benign |
0.44 |
R8514:Plpp1
|
UTSW |
13 |
112,971,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Plpp1
|
UTSW |
13 |
112,943,057 (GRCm39) |
intron |
probably benign |
|
R9130:Plpp1
|
UTSW |
13 |
112,988,038 (GRCm39) |
missense |
|
|
|