Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2 |
A |
G |
3: 59,932,169 (GRCm39) |
H228R |
probably benign |
Het |
Amotl2 |
C |
T |
9: 102,600,968 (GRCm39) |
T345I |
probably benign |
Het |
Arhgef1 |
G |
A |
7: 24,616,306 (GRCm39) |
D317N |
probably damaging |
Het |
Atp11b |
C |
A |
3: 35,895,192 (GRCm39) |
T910K |
probably benign |
Het |
Babam1 |
T |
A |
8: 71,856,999 (GRCm39) |
L320Q |
probably damaging |
Het |
C530025M09Rik |
G |
A |
2: 149,672,974 (GRCm39) |
R54C |
unknown |
Het |
Cfap251 |
G |
A |
5: 123,421,579 (GRCm39) |
R644H |
possibly damaging |
Het |
Cilp |
A |
T |
9: 65,185,494 (GRCm39) |
I530F |
possibly damaging |
Het |
Dgkh |
A |
G |
14: 78,857,256 (GRCm39) |
V302A |
probably benign |
Het |
Eps8l3 |
A |
G |
3: 107,798,604 (GRCm39) |
K497E |
possibly damaging |
Het |
Evl |
C |
T |
12: 108,647,783 (GRCm39) |
R295* |
probably null |
Het |
Exosc10 |
A |
G |
4: 148,649,121 (GRCm39) |
D337G |
probably damaging |
Het |
Fabp3 |
A |
T |
4: 130,207,781 (GRCm39) |
H94L |
probably damaging |
Het |
Flrt3 |
T |
A |
2: 140,501,811 (GRCm39) |
K606* |
probably null |
Het |
Grm5 |
A |
G |
7: 87,624,569 (GRCm39) |
T379A |
probably damaging |
Het |
Hecw1 |
T |
A |
13: 14,552,332 (GRCm39) |
Y89F |
probably damaging |
Het |
Hoxd8 |
T |
C |
2: 74,536,378 (GRCm39) |
S163P |
probably damaging |
Het |
Itih4 |
T |
A |
14: 30,614,370 (GRCm39) |
I440N |
probably damaging |
Het |
Jmjd1c |
A |
G |
10: 67,085,461 (GRCm39) |
D2236G |
probably damaging |
Het |
Kctd17 |
CAGCTGGAGGAGC |
CAGC |
15: 78,321,113 (GRCm39) |
|
probably benign |
Het |
Klhl31 |
G |
A |
9: 77,557,430 (GRCm39) |
E49K |
probably damaging |
Het |
Mmp10 |
A |
G |
9: 7,504,116 (GRCm39) |
Y185C |
probably damaging |
Het |
Mtus2 |
A |
T |
5: 148,014,656 (GRCm39) |
E483V |
probably benign |
Het |
Myh7b |
A |
G |
2: 155,456,119 (GRCm39) |
|
probably null |
Het |
Or12e13 |
C |
T |
2: 87,663,863 (GRCm39) |
P160L |
possibly damaging |
Het |
Orc3 |
A |
T |
4: 34,598,645 (GRCm39) |
M187K |
probably damaging |
Het |
Pcdhb15 |
A |
G |
18: 37,607,902 (GRCm39) |
N378S |
probably damaging |
Het |
Pgm2l1 |
A |
C |
7: 99,910,854 (GRCm39) |
H266P |
probably damaging |
Het |
Pld5 |
A |
T |
1: 176,102,264 (GRCm39) |
D59E |
probably benign |
Het |
Ppp2r2c |
A |
G |
5: 37,097,450 (GRCm39) |
D212G |
possibly damaging |
Het |
Prorp |
G |
A |
12: 55,350,979 (GRCm39) |
G96D |
probably benign |
Het |
Rccd1 |
G |
A |
7: 79,968,657 (GRCm39) |
S301L |
possibly damaging |
Het |
Shbg |
T |
A |
11: 69,505,813 (GRCm39) |
D398V |
probably benign |
Het |
St6gal1 |
G |
A |
16: 23,176,585 (GRCm39) |
A393T |
probably benign |
Het |
Tecta |
G |
A |
9: 42,289,251 (GRCm39) |
T438M |
possibly damaging |
Het |
Trpm6 |
A |
T |
19: 18,756,023 (GRCm39) |
I89F |
probably damaging |
Het |
Tubg1 |
G |
T |
11: 101,014,854 (GRCm39) |
A199S |
probably benign |
Het |
Ugt2b36 |
C |
A |
5: 87,214,236 (GRCm39) |
M469I |
probably damaging |
Het |
Zfp599 |
A |
G |
9: 22,160,830 (GRCm39) |
V445A |
possibly damaging |
Het |
Zmym6 |
T |
C |
4: 127,016,453 (GRCm39) |
C745R |
probably benign |
Het |
|
Other mutations in Clpsl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1055:Clpsl2
|
UTSW |
17 |
28,768,500 (GRCm39) |
nonsense |
probably null |
|
R7587:Clpsl2
|
UTSW |
17 |
28,768,515 (GRCm39) |
missense |
probably benign |
0.03 |
R7970:Clpsl2
|
UTSW |
17 |
28,769,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R7972:Clpsl2
|
UTSW |
17 |
28,769,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R8017:Clpsl2
|
UTSW |
17 |
28,769,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R8017:Clpsl2
|
UTSW |
17 |
28,769,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R8019:Clpsl2
|
UTSW |
17 |
28,769,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R8020:Clpsl2
|
UTSW |
17 |
28,769,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R8045:Clpsl2
|
UTSW |
17 |
28,769,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R8046:Clpsl2
|
UTSW |
17 |
28,769,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R8105:Clpsl2
|
UTSW |
17 |
28,769,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R8123:Clpsl2
|
UTSW |
17 |
28,769,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R8124:Clpsl2
|
UTSW |
17 |
28,769,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R8125:Clpsl2
|
UTSW |
17 |
28,769,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R8126:Clpsl2
|
UTSW |
17 |
28,769,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R8172:Clpsl2
|
UTSW |
17 |
28,768,556 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8894:Clpsl2
|
UTSW |
17 |
28,769,645 (GRCm39) |
missense |
possibly damaging |
0.86 |
|