Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aldh1l1 |
G |
A |
6: 90,574,028 (GRCm39) |
|
probably benign |
Het |
Ambn |
T |
C |
5: 88,615,810 (GRCm39) |
V413A |
possibly damaging |
Het |
Amotl1 |
T |
A |
9: 14,507,824 (GRCm39) |
D41V |
probably damaging |
Het |
Arhgef26 |
T |
C |
3: 62,247,468 (GRCm39) |
V184A |
probably benign |
Het |
Birc6 |
G |
T |
17: 74,925,497 (GRCm39) |
G936V |
possibly damaging |
Het |
Ccser1 |
T |
A |
6: 61,288,226 (GRCm39) |
S130T |
possibly damaging |
Het |
Cecr2 |
A |
G |
6: 120,697,868 (GRCm39) |
I56V |
probably damaging |
Het |
Cfap52 |
A |
G |
11: 67,821,570 (GRCm39) |
I486T |
probably damaging |
Het |
Col4a3 |
A |
G |
1: 82,694,050 (GRCm39) |
I1557V |
possibly damaging |
Het |
Col6a5 |
T |
A |
9: 105,823,046 (GRCm39) |
I104F |
unknown |
Het |
Cry2 |
A |
G |
2: 92,243,312 (GRCm39) |
S510P |
probably benign |
Het |
Csmd2 |
G |
C |
4: 128,439,944 (GRCm39) |
A3133P |
probably benign |
Het |
Cyld |
G |
T |
8: 89,459,621 (GRCm39) |
A611S |
probably damaging |
Het |
Dennd4c |
G |
A |
4: 86,743,749 (GRCm39) |
G1197E |
probably damaging |
Het |
Dnah10 |
T |
C |
5: 124,885,793 (GRCm39) |
F2969L |
probably benign |
Het |
Dnai1 |
A |
G |
4: 41,625,281 (GRCm39) |
K415R |
probably benign |
Het |
Dnmbp |
T |
A |
19: 43,842,610 (GRCm39) |
T1253S |
probably benign |
Het |
Dsp |
T |
C |
13: 38,379,678 (GRCm39) |
L1542P |
possibly damaging |
Het |
Duox1 |
T |
A |
2: 122,170,682 (GRCm39) |
L1234Q |
probably damaging |
Het |
Efr3b |
T |
A |
12: 4,018,590 (GRCm39) |
R585S |
possibly damaging |
Het |
Gpt |
A |
G |
15: 76,583,552 (GRCm39) |
|
probably null |
Het |
Heatr6 |
G |
A |
11: 83,644,544 (GRCm39) |
|
probably benign |
Het |
Kcns2 |
A |
G |
15: 34,839,930 (GRCm39) |
D431G |
probably benign |
Het |
Kdm3b |
A |
G |
18: 34,962,342 (GRCm39) |
N1543D |
probably damaging |
Het |
Man2a1 |
A |
G |
17: 64,932,375 (GRCm39) |
K154R |
probably benign |
Het |
Mical3 |
G |
A |
6: 120,935,232 (GRCm39) |
Q893* |
probably null |
Het |
Morc3 |
C |
T |
16: 93,663,341 (GRCm39) |
H515Y |
possibly damaging |
Het |
Mprip |
A |
T |
11: 59,648,547 (GRCm39) |
R750S |
probably damaging |
Het |
Mroh1 |
G |
A |
15: 76,335,691 (GRCm39) |
V1436M |
probably benign |
Het |
Muc5ac |
C |
T |
7: 141,344,406 (GRCm39) |
R69* |
probably null |
Het |
Muc5b |
A |
T |
7: 141,410,449 (GRCm39) |
Y1274F |
unknown |
Het |
Mybpc1 |
A |
G |
10: 88,378,318 (GRCm39) |
L674P |
probably damaging |
Het |
Mypn |
A |
G |
10: 62,966,802 (GRCm39) |
V958A |
probably benign |
Het |
Nipbl |
T |
C |
15: 8,326,302 (GRCm39) |
T2436A |
probably benign |
Het |
Or7g20 |
A |
G |
9: 18,946,443 (GRCm39) |
D8G |
probably benign |
Het |
Pcdhb5 |
T |
A |
18: 37,454,826 (GRCm39) |
L402Q |
probably damaging |
Het |
Pigp |
T |
A |
16: 94,171,053 (GRCm39) |
|
probably null |
Het |
Rp1 |
A |
G |
1: 4,418,685 (GRCm39) |
L809P |
probably benign |
Het |
Scn3a |
T |
A |
2: 65,325,125 (GRCm39) |
|
probably benign |
Het |
Sdf2 |
A |
T |
11: 78,136,906 (GRCm39) |
M29L |
probably benign |
Het |
Serpina3b |
T |
G |
12: 104,100,350 (GRCm39) |
L311V |
possibly damaging |
Het |
Snx31 |
A |
T |
15: 36,523,634 (GRCm39) |
Y349* |
probably null |
Het |
Spidr |
A |
C |
16: 15,932,733 (GRCm39) |
C182W |
probably damaging |
Het |
St13 |
A |
T |
15: 81,261,999 (GRCm39) |
S146R |
probably damaging |
Het |
St8sia4 |
A |
G |
1: 95,581,307 (GRCm39) |
V145A |
probably damaging |
Het |
Stradb |
T |
C |
1: 59,019,175 (GRCm39) |
|
probably null |
Het |
Tfdp2 |
C |
T |
9: 96,199,627 (GRCm39) |
P74S |
unknown |
Het |
Tmprss15 |
C |
T |
16: 78,854,547 (GRCm39) |
R287H |
probably benign |
Het |
Trav10d |
T |
C |
14: 53,048,779 (GRCm39) |
Y57H |
probably damaging |
Het |
Vmn2r104 |
A |
G |
17: 20,249,733 (GRCm39) |
I846T |
probably benign |
Het |
Ywhah |
T |
A |
5: 33,184,292 (GRCm39) |
M165K |
possibly damaging |
Het |
Zfp324 |
C |
A |
7: 12,703,293 (GRCm39) |
P72T |
probably benign |
Het |
|
Other mutations in Tcp11l2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00725:Tcp11l2
|
APN |
10 |
84,430,574 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL00845:Tcp11l2
|
APN |
10 |
84,440,847 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02375:Tcp11l2
|
APN |
10 |
84,440,932 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02418:Tcp11l2
|
APN |
10 |
84,449,470 (GRCm39) |
nonsense |
probably null |
|
IGL03325:Tcp11l2
|
APN |
10 |
84,440,764 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0031:Tcp11l2
|
UTSW |
10 |
84,427,004 (GRCm39) |
missense |
probably damaging |
0.98 |
R0591:Tcp11l2
|
UTSW |
10 |
84,440,458 (GRCm39) |
missense |
probably benign |
0.05 |
R1563:Tcp11l2
|
UTSW |
10 |
84,420,808 (GRCm39) |
missense |
probably damaging |
0.96 |
R1607:Tcp11l2
|
UTSW |
10 |
84,449,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R1840:Tcp11l2
|
UTSW |
10 |
84,440,463 (GRCm39) |
missense |
probably damaging |
0.98 |
R2144:Tcp11l2
|
UTSW |
10 |
84,449,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R2251:Tcp11l2
|
UTSW |
10 |
84,440,933 (GRCm39) |
critical splice donor site |
probably null |
|
R4289:Tcp11l2
|
UTSW |
10 |
84,440,937 (GRCm39) |
splice site |
probably null |
|
R4639:Tcp11l2
|
UTSW |
10 |
84,420,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R4844:Tcp11l2
|
UTSW |
10 |
84,449,555 (GRCm39) |
missense |
probably benign |
0.00 |
R4973:Tcp11l2
|
UTSW |
10 |
84,427,027 (GRCm39) |
missense |
probably damaging |
0.98 |
R5264:Tcp11l2
|
UTSW |
10 |
84,449,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R6966:Tcp11l2
|
UTSW |
10 |
84,427,133 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7250:Tcp11l2
|
UTSW |
10 |
84,423,105 (GRCm39) |
critical splice donor site |
probably null |
|
R7535:Tcp11l2
|
UTSW |
10 |
84,430,523 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7565:Tcp11l2
|
UTSW |
10 |
84,422,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R7619:Tcp11l2
|
UTSW |
10 |
84,430,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R7774:Tcp11l2
|
UTSW |
10 |
84,440,847 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8145:Tcp11l2
|
UTSW |
10 |
84,444,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R8379:Tcp11l2
|
UTSW |
10 |
84,449,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R8458:Tcp11l2
|
UTSW |
10 |
84,449,396 (GRCm39) |
nonsense |
probably null |
|
R8821:Tcp11l2
|
UTSW |
10 |
84,449,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R8831:Tcp11l2
|
UTSW |
10 |
84,449,522 (GRCm39) |
missense |
probably damaging |
1.00 |
RF008:Tcp11l2
|
UTSW |
10 |
84,449,388 (GRCm39) |
missense |
probably damaging |
0.99 |
|