Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aopep |
G |
T |
13: 63,388,145 (GRCm39) |
K709N |
probably null |
Het |
Aste1 |
G |
A |
9: 105,273,880 (GRCm39) |
C40Y |
probably benign |
Het |
Atp6v0a2 |
G |
T |
5: 124,784,589 (GRCm39) |
A291S |
probably damaging |
Het |
Bcl9l |
G |
T |
9: 44,412,238 (GRCm39) |
V38L |
possibly damaging |
Het |
Bmp1 |
T |
C |
14: 70,727,630 (GRCm39) |
Y651C |
probably damaging |
Het |
Btnl9 |
T |
C |
11: 49,065,661 (GRCm39) |
E398G |
probably benign |
Het |
C2cd3 |
A |
T |
7: 100,040,286 (GRCm39) |
N285I |
possibly damaging |
Het |
Cavin1 |
T |
C |
11: 100,849,659 (GRCm39) |
T324A |
probably damaging |
Het |
Ccdc73 |
A |
G |
2: 104,821,712 (GRCm39) |
T554A |
probably benign |
Het |
Clcn1 |
A |
T |
6: 42,263,701 (GRCm39) |
M1L |
possibly damaging |
Het |
Clec18a |
A |
T |
8: 111,808,201 (GRCm39) |
S77T |
possibly damaging |
Het |
Dhx32 |
A |
G |
7: 133,323,876 (GRCm39) |
|
probably null |
Het |
Dmxl1 |
C |
G |
18: 50,072,639 (GRCm39) |
N2744K |
probably damaging |
Het |
Dnah10 |
A |
C |
5: 124,891,006 (GRCm39) |
E3199A |
probably damaging |
Het |
Dnah11 |
G |
T |
12: 117,987,718 (GRCm39) |
L2395I |
probably benign |
Het |
Dthd1 |
A |
T |
5: 63,007,096 (GRCm39) |
Y599F |
probably benign |
Het |
Dusp26 |
G |
A |
8: 31,586,367 (GRCm39) |
R196K |
unknown |
Het |
Dyrk1a |
A |
G |
16: 94,466,866 (GRCm39) |
Y140C |
probably damaging |
Het |
Elmo1 |
T |
A |
13: 20,766,438 (GRCm39) |
Y588* |
probably null |
Het |
Eml6 |
T |
A |
11: 29,703,110 (GRCm39) |
T1603S |
probably damaging |
Het |
Fam162b |
T |
C |
10: 51,466,469 (GRCm39) |
T17A |
probably benign |
Het |
Fnbp1 |
T |
A |
2: 30,995,346 (GRCm39) |
K29N |
probably damaging |
Het |
Fzd4 |
A |
T |
7: 89,056,792 (GRCm39) |
I280L |
possibly damaging |
Het |
G3bp2 |
G |
A |
5: 92,216,281 (GRCm39) |
T85I |
probably damaging |
Het |
Gm13283 |
C |
T |
4: 88,679,123 (GRCm39) |
A38V |
probably benign |
Het |
Hps3 |
T |
A |
3: 20,068,224 (GRCm39) |
H610L |
probably damaging |
Het |
Ifnlr1 |
T |
G |
4: 135,431,609 (GRCm39) |
L266R |
probably damaging |
Het |
Jak1 |
A |
T |
4: 101,020,109 (GRCm39) |
D683E |
probably benign |
Het |
Lrrc1 |
G |
A |
9: 77,342,373 (GRCm39) |
T412M |
probably damaging |
Het |
Mdga1 |
G |
T |
17: 30,058,959 (GRCm39) |
|
probably benign |
Het |
Med26 |
T |
C |
8: 73,250,934 (GRCm39) |
K55R |
probably benign |
Het |
Mturn |
C |
A |
6: 54,666,017 (GRCm39) |
C63* |
probably null |
Het |
Myo1h |
A |
C |
5: 114,470,784 (GRCm39) |
D381A |
probably damaging |
Het |
Nectin1 |
A |
G |
9: 43,703,237 (GRCm39) |
D165G |
probably benign |
Het |
Nktr |
T |
A |
9: 121,575,558 (GRCm39) |
D330E |
possibly damaging |
Het |
Oprm1 |
A |
T |
10: 6,782,644 (GRCm39) |
|
probably benign |
Het |
Papola |
T |
A |
12: 105,775,946 (GRCm39) |
|
probably benign |
Het |
Pdcl2 |
A |
T |
5: 76,465,675 (GRCm39) |
C134S |
probably damaging |
Het |
Plch1 |
T |
C |
3: 63,639,039 (GRCm39) |
Y478C |
probably benign |
Het |
Rev1 |
A |
T |
1: 38,122,824 (GRCm39) |
W465R |
probably damaging |
Het |
Rp1 |
T |
A |
1: 4,419,817 (GRCm39) |
I432F |
probably benign |
Het |
Samd14 |
A |
C |
11: 94,912,027 (GRCm39) |
D168A |
probably damaging |
Het |
Sdk1 |
G |
T |
5: 141,598,935 (GRCm39) |
C200F |
probably benign |
Het |
Spmip2 |
A |
G |
3: 79,252,812 (GRCm39) |
H9R |
probably benign |
Het |
Spsb1 |
T |
C |
4: 149,991,475 (GRCm39) |
Y31C |
possibly damaging |
Het |
Spz1 |
T |
C |
13: 92,711,499 (GRCm39) |
K326E |
possibly damaging |
Het |
Tcaf1 |
C |
T |
6: 42,663,307 (GRCm39) |
S191N |
probably benign |
Het |
Tex15 |
A |
G |
8: 34,064,724 (GRCm39) |
S1385G |
probably benign |
Het |
Tmem38a |
C |
T |
8: 73,338,570 (GRCm39) |
A194V |
probably damaging |
Het |
Trappc9 |
T |
C |
15: 72,929,945 (GRCm39) |
N137S |
probably benign |
Het |
Tshr |
T |
C |
12: 91,504,997 (GRCm39) |
L645P |
probably damaging |
Het |
Unc13a |
T |
A |
8: 72,100,597 (GRCm39) |
I1064F |
probably damaging |
Het |
Utp20 |
G |
A |
10: 88,628,532 (GRCm39) |
Q921* |
probably null |
Het |
Vps13a |
A |
T |
19: 16,642,114 (GRCm39) |
I2171N |
probably damaging |
Het |
Zfp40 |
A |
G |
17: 23,401,201 (GRCm39) |
V14A |
probably benign |
Het |
|
Other mutations in Tspyl4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02437:Tspyl4
|
APN |
10 |
34,174,228 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03353:Tspyl4
|
APN |
10 |
34,174,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R0576:Tspyl4
|
UTSW |
10 |
34,174,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R1471:Tspyl4
|
UTSW |
10 |
34,174,107 (GRCm39) |
missense |
probably damaging |
0.98 |
R1757:Tspyl4
|
UTSW |
10 |
34,173,576 (GRCm39) |
nonsense |
probably null |
|
R4787:Tspyl4
|
UTSW |
10 |
34,173,760 (GRCm39) |
missense |
probably benign |
0.39 |
R4817:Tspyl4
|
UTSW |
10 |
34,173,734 (GRCm39) |
nonsense |
probably null |
|
R5044:Tspyl4
|
UTSW |
10 |
34,173,933 (GRCm39) |
missense |
probably benign |
|
R6966:Tspyl4
|
UTSW |
10 |
34,173,673 (GRCm39) |
missense |
probably benign |
0.03 |
R7841:Tspyl4
|
UTSW |
10 |
34,174,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R7869:Tspyl4
|
UTSW |
10 |
34,174,096 (GRCm39) |
missense |
probably damaging |
0.98 |
R8445:Tspyl4
|
UTSW |
10 |
34,173,742 (GRCm39) |
missense |
probably benign |
0.19 |
R8558:Tspyl4
|
UTSW |
10 |
34,174,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R9206:Tspyl4
|
UTSW |
10 |
34,173,568 (GRCm39) |
missense |
probably benign |
|
R9208:Tspyl4
|
UTSW |
10 |
34,173,568 (GRCm39) |
missense |
probably benign |
|
|