Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl1 |
C |
T |
4: 86,342,477 (GRCm39) |
T1672I |
probably damaging |
Het |
Ahnak |
T |
G |
19: 8,990,266 (GRCm39) |
M3850R |
unknown |
Het |
Cacna1s |
T |
A |
1: 136,022,689 (GRCm39) |
L874Q |
possibly damaging |
Het |
Cacna2d4 |
A |
T |
6: 119,274,479 (GRCm39) |
D622V |
probably benign |
Het |
Ccdc150 |
T |
C |
1: 54,317,990 (GRCm39) |
S310P |
probably damaging |
Het |
Cecr2 |
A |
T |
6: 120,735,538 (GRCm39) |
N148Y |
|
Het |
Celsr2 |
T |
C |
3: 108,322,084 (GRCm39) |
T243A |
probably damaging |
Het |
Coro1b |
C |
T |
19: 4,201,473 (GRCm39) |
T279I |
probably damaging |
Het |
Cyp51 |
A |
G |
5: 4,150,198 (GRCm39) |
I175T |
probably damaging |
Het |
Dnajc21 |
T |
C |
15: 10,462,048 (GRCm39) |
I118V |
possibly damaging |
Het |
Dtna |
T |
C |
18: 23,780,112 (GRCm39) |
|
probably null |
Het |
Etl4 |
A |
G |
2: 20,748,784 (GRCm39) |
K374R |
probably benign |
Het |
Fance |
G |
A |
17: 28,537,327 (GRCm39) |
C53Y |
probably damaging |
Het |
Gm14496 |
G |
T |
2: 181,640,647 (GRCm39) |
C538F |
probably damaging |
Het |
Gon4l |
T |
A |
3: 88,803,538 (GRCm39) |
V1383D |
probably benign |
Het |
Gpr6 |
C |
A |
10: 40,946,944 (GRCm39) |
D213Y |
possibly damaging |
Het |
Has2 |
A |
G |
15: 56,531,684 (GRCm39) |
Y344H |
probably damaging |
Het |
Kcnh2 |
A |
T |
5: 24,537,964 (GRCm39) |
M133K |
probably benign |
Het |
Kdm5a |
A |
G |
6: 120,365,056 (GRCm39) |
H152R |
probably damaging |
Het |
Klhl33 |
C |
T |
14: 51,130,225 (GRCm39) |
R163H |
probably damaging |
Het |
Lax1 |
T |
A |
1: 133,611,752 (GRCm39) |
Q61L |
probably benign |
Het |
Lct |
T |
C |
1: 128,228,329 (GRCm39) |
T1055A |
possibly damaging |
Het |
Lrrc8c |
A |
G |
5: 105,756,163 (GRCm39) |
Y646C |
possibly damaging |
Het |
Mtarc1 |
T |
C |
1: 184,527,633 (GRCm39) |
T274A |
probably benign |
Het |
Myo1b |
A |
G |
1: 51,902,577 (GRCm39) |
V51A |
probably damaging |
Het |
Naip2 |
T |
A |
13: 100,298,243 (GRCm39) |
S598C |
probably damaging |
Het |
Neb |
A |
G |
2: 52,137,215 (GRCm39) |
S250P |
|
Het |
Nim1k |
A |
T |
13: 120,189,362 (GRCm39) |
C16S |
probably benign |
Het |
Oosp1 |
T |
C |
19: 11,664,769 (GRCm39) |
T96A |
probably damaging |
Het |
Or1e1c |
T |
C |
11: 73,265,790 (GRCm39) |
S75P |
probably damaging |
Het |
Or2q1 |
G |
T |
6: 42,795,197 (GRCm39) |
R264L |
probably benign |
Het |
Or8k17 |
T |
A |
2: 86,066,744 (GRCm39) |
Q138L |
probably damaging |
Het |
Pik3c2b |
C |
T |
1: 133,005,187 (GRCm39) |
R563C |
probably damaging |
Het |
Ppp1r18 |
CGAGGAGGAGGAGGAGGAGGAGGA |
CGAGGAGGAGGAGGAGGAGGA |
17: 36,184,743 (GRCm39) |
|
probably benign |
Het |
Prps1l1 |
T |
A |
12: 35,035,089 (GRCm39) |
M68K |
|
Het |
Prr11 |
A |
T |
11: 86,992,254 (GRCm39) |
L207* |
probably null |
Het |
Psme3 |
T |
C |
11: 101,211,559 (GRCm39) |
Y202H |
probably damaging |
Het |
Ptma |
A |
G |
1: 86,455,694 (GRCm39) |
S57G |
unknown |
Het |
Rab24 |
A |
G |
13: 55,468,049 (GRCm39) |
V33A |
unknown |
Het |
Reep6 |
A |
G |
10: 80,166,091 (GRCm39) |
T83A |
probably benign |
Het |
Shroom4 |
GCAACAACAACAACAACAACAACAACA |
GCAACAACAACAACAACAACAACA |
X: 6,536,131 (GRCm39) |
|
probably benign |
Het |
Siglec1 |
T |
C |
2: 130,925,390 (GRCm39) |
K357R |
probably benign |
Het |
Slc2a4 |
T |
A |
11: 69,836,728 (GRCm39) |
H167L |
probably benign |
Het |
Slc8a3 |
T |
A |
12: 81,361,838 (GRCm39) |
H327L |
probably benign |
Het |
Slf1 |
G |
A |
13: 77,194,656 (GRCm39) |
L890F |
|
Het |
Smchd1 |
A |
C |
17: 71,701,791 (GRCm39) |
I1067R |
probably benign |
Het |
Stk33 |
T |
A |
7: 108,940,689 (GRCm39) |
N7I |
probably benign |
Het |
Tex47 |
T |
C |
5: 7,355,194 (GRCm39) |
M125T |
possibly damaging |
Het |
Thada |
A |
T |
17: 84,766,292 (GRCm39) |
L38* |
probably null |
Het |
Thbs1 |
A |
G |
2: 117,947,983 (GRCm39) |
D381G |
probably benign |
Het |
Uggt1 |
A |
T |
1: 36,203,603 (GRCm39) |
V1009D |
|
Het |
Usp17la |
A |
T |
7: 104,508,531 (GRCm39) |
|
probably benign |
Het |
Zfp438 |
A |
T |
18: 5,214,054 (GRCm39) |
N301K |
probably benign |
Het |
Zfp606 |
T |
A |
7: 12,227,907 (GRCm39) |
I676N |
possibly damaging |
Het |
|
Other mutations in Semp2l2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02001:Semp2l2b
|
APN |
10 |
21,943,176 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02546:Semp2l2b
|
APN |
10 |
21,942,826 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02885:Semp2l2b
|
APN |
10 |
21,943,057 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0543:Semp2l2b
|
UTSW |
10 |
21,942,823 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1762:Semp2l2b
|
UTSW |
10 |
21,943,411 (GRCm39) |
missense |
probably benign |
0.02 |
R2249:Semp2l2b
|
UTSW |
10 |
21,943,015 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2354:Semp2l2b
|
UTSW |
10 |
21,943,155 (GRCm39) |
missense |
probably benign |
0.19 |
R2870:Semp2l2b
|
UTSW |
10 |
21,943,278 (GRCm39) |
missense |
probably benign |
|
R2870:Semp2l2b
|
UTSW |
10 |
21,943,278 (GRCm39) |
missense |
probably benign |
|
R3777:Semp2l2b
|
UTSW |
10 |
21,942,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R4117:Semp2l2b
|
UTSW |
10 |
21,943,615 (GRCm39) |
missense |
probably benign |
|
R4644:Semp2l2b
|
UTSW |
10 |
21,942,660 (GRCm39) |
missense |
probably benign |
0.02 |
R5002:Semp2l2b
|
UTSW |
10 |
21,943,716 (GRCm39) |
missense |
probably damaging |
0.99 |
R5667:Semp2l2b
|
UTSW |
10 |
21,942,742 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5671:Semp2l2b
|
UTSW |
10 |
21,942,742 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6694:Semp2l2b
|
UTSW |
10 |
21,943,620 (GRCm39) |
missense |
probably damaging |
0.99 |
R6810:Semp2l2b
|
UTSW |
10 |
21,942,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R6923:Semp2l2b
|
UTSW |
10 |
21,943,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R6942:Semp2l2b
|
UTSW |
10 |
21,943,160 (GRCm39) |
missense |
probably benign |
|
R7065:Semp2l2b
|
UTSW |
10 |
21,943,197 (GRCm39) |
missense |
probably benign |
0.00 |
R7204:Semp2l2b
|
UTSW |
10 |
21,943,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R8778:Semp2l2b
|
UTSW |
10 |
21,943,356 (GRCm39) |
missense |
probably damaging |
0.99 |
R9403:Semp2l2b
|
UTSW |
10 |
21,943,840 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9508:Semp2l2b
|
UTSW |
10 |
21,942,816 (GRCm39) |
missense |
probably damaging |
0.99 |
R9615:Semp2l2b
|
UTSW |
10 |
21,943,611 (GRCm39) |
missense |
probably benign |
0.29 |
|