Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd18 |
T |
A |
3: 40,859,338 (GRCm39) |
M1K |
probably null |
Het |
Adam34l |
A |
T |
8: 44,079,089 (GRCm39) |
C378* |
probably null |
Het |
Bdkrb2 |
T |
C |
12: 105,558,755 (GRCm39) |
V332A |
possibly damaging |
Het |
Cdc27 |
T |
C |
11: 104,398,026 (GRCm39) |
E778G |
probably damaging |
Het |
Chd4 |
C |
A |
6: 125,098,970 (GRCm39) |
T1586K |
probably benign |
Het |
Cnga3 |
A |
G |
1: 37,301,146 (GRCm39) |
E622G |
probably benign |
Het |
Dbh |
A |
G |
2: 27,064,977 (GRCm39) |
D396G |
possibly damaging |
Het |
Dhodh |
G |
A |
8: 110,330,107 (GRCm39) |
R86* |
probably null |
Het |
Dpt |
A |
C |
1: 164,624,500 (GRCm39) |
E67A |
probably damaging |
Het |
Eif2ak2 |
A |
G |
17: 79,166,068 (GRCm39) |
|
probably benign |
Het |
Esp4 |
T |
A |
17: 40,913,336 (GRCm39) |
L68M |
possibly damaging |
Het |
Exo1 |
A |
G |
1: 175,733,536 (GRCm39) |
K787E |
possibly damaging |
Het |
Fbxo38 |
T |
C |
18: 62,647,914 (GRCm39) |
T875A |
probably damaging |
Het |
Gsdma |
T |
C |
11: 98,563,964 (GRCm39) |
|
probably benign |
Het |
Hemk1 |
G |
A |
9: 107,214,415 (GRCm39) |
Q6* |
probably null |
Het |
Hmcn2 |
C |
T |
2: 31,323,284 (GRCm39) |
|
probably benign |
Het |
Hook2 |
A |
G |
8: 85,720,613 (GRCm39) |
|
probably benign |
Het |
Irx3 |
A |
G |
8: 92,525,555 (GRCm39) |
S507P |
unknown |
Het |
Kazn |
C |
A |
4: 141,966,506 (GRCm39) |
|
probably benign |
Het |
Kcne4 |
C |
T |
1: 78,795,688 (GRCm39) |
A112V |
possibly damaging |
Het |
Lamb1 |
C |
T |
12: 31,337,528 (GRCm39) |
R372C |
probably damaging |
Het |
Lrrc30 |
A |
G |
17: 67,939,175 (GRCm39) |
L135P |
probably damaging |
Het |
Lyst |
T |
A |
13: 13,809,815 (GRCm39) |
M495K |
possibly damaging |
Het |
Mki67 |
T |
A |
7: 135,309,204 (GRCm39) |
T416S |
probably benign |
Het |
Mlst8 |
A |
T |
17: 24,697,099 (GRCm39) |
M56K |
probably benign |
Het |
Mmp9 |
A |
G |
2: 164,791,310 (GRCm39) |
Y160C |
probably damaging |
Het |
Mslnl |
A |
G |
17: 25,965,155 (GRCm39) |
Y507C |
probably damaging |
Het |
Muc6 |
G |
A |
7: 141,218,313 (GRCm39) |
S2120F |
possibly damaging |
Het |
Myl12a |
A |
T |
17: 71,301,737 (GRCm39) |
M130K |
probably benign |
Het |
Nalf2 |
A |
G |
X: 98,889,109 (GRCm39) |
I325V |
probably benign |
Het |
Ncdn |
C |
T |
4: 126,642,388 (GRCm39) |
R423Q |
probably benign |
Het |
Ncf2 |
A |
G |
1: 152,701,698 (GRCm39) |
|
probably benign |
Het |
Nek8 |
G |
T |
11: 78,061,572 (GRCm39) |
S319* |
probably null |
Het |
Or11g7 |
G |
A |
14: 50,690,653 (GRCm39) |
C48Y |
probably benign |
Het |
Or52m2 |
T |
C |
7: 102,263,993 (GRCm39) |
M68V |
possibly damaging |
Het |
Pcdh17 |
T |
A |
14: 84,684,062 (GRCm39) |
D176E |
probably damaging |
Het |
Pcdhb15 |
C |
A |
18: 37,608,442 (GRCm39) |
A558E |
probably benign |
Het |
Plrg1 |
T |
A |
3: 82,978,526 (GRCm39) |
W431R |
probably damaging |
Het |
Rbfox3 |
T |
A |
11: 118,387,283 (GRCm39) |
Q277L |
possibly damaging |
Het |
Rpgrip1 |
G |
A |
14: 52,382,666 (GRCm39) |
D600N |
possibly damaging |
Het |
Siah3 |
A |
G |
14: 75,763,421 (GRCm39) |
D224G |
probably damaging |
Het |
Slc22a6 |
T |
C |
19: 8,598,675 (GRCm39) |
L244P |
probably damaging |
Het |
Stap2 |
A |
T |
17: 56,304,511 (GRCm39) |
W374R |
probably benign |
Het |
Tbck |
T |
A |
3: 132,432,845 (GRCm39) |
N418K |
probably benign |
Het |
Tcp11x2 |
T |
C |
X: 134,555,733 (GRCm39) |
N474S |
probably damaging |
Het |
Tenm3 |
A |
C |
8: 48,681,590 (GRCm39) |
V2680G |
probably damaging |
Het |
Thada |
A |
T |
17: 84,538,213 (GRCm39) |
|
probably benign |
Het |
Tlr6 |
C |
T |
5: 65,110,772 (GRCm39) |
V712M |
probably damaging |
Het |
Uvssa |
G |
T |
5: 33,547,162 (GRCm39) |
G243C |
probably damaging |
Het |
Vwa8 |
T |
A |
14: 79,401,660 (GRCm39) |
|
probably benign |
Het |
Znrf2 |
A |
T |
6: 54,861,776 (GRCm39) |
N229I |
probably damaging |
Het |
|
Other mutations in Mab21l3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00897:Mab21l3
|
APN |
3 |
101,730,771 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01123:Mab21l3
|
APN |
3 |
101,742,446 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01997:Mab21l3
|
APN |
3 |
101,725,955 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02423:Mab21l3
|
APN |
3 |
101,726,045 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02546:Mab21l3
|
APN |
3 |
101,730,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R1268:Mab21l3
|
UTSW |
3 |
101,742,363 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1803:Mab21l3
|
UTSW |
3 |
101,742,446 (GRCm39) |
missense |
probably benign |
0.06 |
R2056:Mab21l3
|
UTSW |
3 |
101,722,469 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2104:Mab21l3
|
UTSW |
3 |
101,730,744 (GRCm39) |
missense |
probably benign |
0.31 |
R3107:Mab21l3
|
UTSW |
3 |
101,734,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R3405:Mab21l3
|
UTSW |
3 |
101,730,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R5715:Mab21l3
|
UTSW |
3 |
101,730,723 (GRCm39) |
missense |
probably benign |
0.36 |
R6612:Mab21l3
|
UTSW |
3 |
101,725,961 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7183:Mab21l3
|
UTSW |
3 |
101,722,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R8933:Mab21l3
|
UTSW |
3 |
101,730,774 (GRCm39) |
missense |
probably benign |
|
R9187:Mab21l3
|
UTSW |
3 |
101,730,594 (GRCm39) |
missense |
probably benign |
0.00 |
R9342:Mab21l3
|
UTSW |
3 |
101,742,519 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9478:Mab21l3
|
UTSW |
3 |
101,725,987 (GRCm39) |
missense |
probably damaging |
1.00 |
|