Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acox3 |
T |
C |
5: 35,758,865 (GRCm39) |
Y359H |
possibly damaging |
Het |
Actn2 |
A |
G |
13: 12,291,433 (GRCm39) |
|
probably benign |
Het |
Actr8 |
T |
C |
14: 29,704,728 (GRCm39) |
|
probably null |
Het |
Aldh16a1 |
G |
A |
7: 44,795,459 (GRCm39) |
P400L |
probably damaging |
Het |
Aldob |
T |
A |
4: 49,538,790 (GRCm39) |
K243* |
probably null |
Het |
Arfgap1 |
T |
C |
2: 180,622,237 (GRCm39) |
F274S |
possibly damaging |
Het |
Brd8 |
C |
T |
18: 34,735,780 (GRCm39) |
S899N |
probably damaging |
Het |
Cask |
T |
C |
X: 13,425,634 (GRCm39) |
I471V |
probably damaging |
Het |
Cdc42ep4 |
C |
T |
11: 113,619,942 (GRCm39) |
G150S |
probably benign |
Het |
Cpne1 |
T |
G |
2: 155,919,563 (GRCm39) |
D278A |
possibly damaging |
Het |
Gcn1 |
A |
G |
5: 115,748,938 (GRCm39) |
E1856G |
probably damaging |
Het |
Gm8362 |
A |
T |
14: 18,149,595 (GRCm39) |
V159E |
probably damaging |
Het |
Golga5 |
A |
G |
12: 102,462,011 (GRCm39) |
I700V |
possibly damaging |
Het |
Ifi206 |
T |
C |
1: 173,309,334 (GRCm39) |
T221A |
probably benign |
Het |
Ighv2-6-8 |
T |
C |
12: 113,760,037 (GRCm39) |
K24R |
possibly damaging |
Het |
Morc1 |
T |
C |
16: 48,407,467 (GRCm39) |
L661P |
probably benign |
Het |
Per2 |
G |
A |
1: 91,352,031 (GRCm39) |
T825I |
probably damaging |
Het |
Plscr1l1 |
A |
T |
9: 92,233,011 (GRCm39) |
K45* |
probably null |
Het |
Pramel20 |
A |
T |
4: 143,297,726 (GRCm39) |
T49S |
probably benign |
Het |
Prkar2b |
A |
G |
12: 32,025,963 (GRCm39) |
V19A |
probably damaging |
Het |
Psmb8 |
T |
A |
17: 34,420,198 (GRCm39) |
D263E |
probably damaging |
Het |
Pum2 |
T |
C |
12: 8,779,117 (GRCm39) |
I563T |
probably benign |
Het |
Retreg1 |
T |
G |
15: 25,966,709 (GRCm39) |
|
probably null |
Het |
Rfx7 |
A |
G |
9: 72,524,486 (GRCm39) |
T559A |
probably benign |
Het |
Rnf31 |
T |
G |
14: 55,836,569 (GRCm39) |
I801S |
probably damaging |
Het |
Rom1 |
G |
T |
19: 8,906,386 (GRCm39) |
T51N |
possibly damaging |
Het |
Sema6b |
G |
T |
17: 56,439,821 (GRCm39) |
P7T |
probably benign |
Het |
Stpg1 |
A |
G |
4: 135,235,375 (GRCm39) |
|
probably benign |
Het |
Sugct |
A |
T |
13: 17,627,105 (GRCm39) |
Y249* |
probably null |
Het |
Tcea2 |
A |
G |
2: 181,327,628 (GRCm39) |
I125V |
probably benign |
Het |
Ttc39b |
T |
A |
4: 83,216,186 (GRCm39) |
D19V |
probably damaging |
Het |
Tti2 |
T |
A |
8: 31,645,537 (GRCm39) |
|
probably null |
Het |
Usp32 |
A |
T |
11: 84,923,003 (GRCm39) |
Y142* |
probably null |
Het |
Vill |
A |
G |
9: 118,889,466 (GRCm39) |
Y134C |
probably benign |
Het |
Vmn2r9 |
G |
A |
5: 108,991,502 (GRCm39) |
L620F |
probably damaging |
Het |
Zfp398 |
A |
G |
6: 47,835,879 (GRCm39) |
D14G |
probably damaging |
Het |
Zfp598 |
T |
C |
17: 24,896,591 (GRCm39) |
Y223H |
probably damaging |
Het |
Znhit6 |
G |
T |
3: 145,283,859 (GRCm39) |
C43F |
probably damaging |
Het |
|
Other mutations in Tbc1d21 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00845:Tbc1d21
|
APN |
9 |
58,269,745 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02651:Tbc1d21
|
APN |
9 |
58,270,384 (GRCm39) |
nonsense |
probably null |
|
R0693:Tbc1d21
|
UTSW |
9 |
58,268,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R0730:Tbc1d21
|
UTSW |
9 |
58,267,160 (GRCm39) |
missense |
probably benign |
0.00 |
R1454:Tbc1d21
|
UTSW |
9 |
58,270,096 (GRCm39) |
critical splice donor site |
probably null |
|
R1776:Tbc1d21
|
UTSW |
9 |
58,274,011 (GRCm39) |
splice site |
probably benign |
|
R2230:Tbc1d21
|
UTSW |
9 |
58,270,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R2512:Tbc1d21
|
UTSW |
9 |
58,270,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R3052:Tbc1d21
|
UTSW |
9 |
58,270,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R3053:Tbc1d21
|
UTSW |
9 |
58,270,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R6348:Tbc1d21
|
UTSW |
9 |
58,268,501 (GRCm39) |
missense |
probably benign |
|
R6805:Tbc1d21
|
UTSW |
9 |
58,268,571 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7032:Tbc1d21
|
UTSW |
9 |
58,274,134 (GRCm39) |
critical splice donor site |
probably null |
|
R7153:Tbc1d21
|
UTSW |
9 |
58,270,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R7640:Tbc1d21
|
UTSW |
9 |
58,268,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R7753:Tbc1d21
|
UTSW |
9 |
58,269,306 (GRCm39) |
critical splice donor site |
probably null |
|
R8835:Tbc1d21
|
UTSW |
9 |
58,273,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R9316:Tbc1d21
|
UTSW |
9 |
58,274,215 (GRCm39) |
missense |
probably benign |
0.03 |
R9498:Tbc1d21
|
UTSW |
9 |
58,273,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R9606:Tbc1d21
|
UTSW |
9 |
58,268,487 (GRCm39) |
missense |
possibly damaging |
0.64 |
|