Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810055G02Rik |
T |
C |
19: 3,766,608 (GRCm39) |
V65A |
possibly damaging |
Het |
4930402F06Rik |
A |
T |
2: 35,275,680 (GRCm39) |
S38T |
possibly damaging |
Het |
Adam4 |
A |
G |
12: 81,468,537 (GRCm39) |
L28S |
probably damaging |
Het |
Agmo |
T |
A |
12: 37,407,709 (GRCm39) |
F198I |
probably damaging |
Het |
Akap7 |
A |
G |
10: 25,047,062 (GRCm39) |
V45A |
probably damaging |
Het |
Amotl1 |
G |
T |
9: 14,486,465 (GRCm39) |
N476K |
probably benign |
Het |
Apcs |
A |
G |
1: 172,722,100 (GRCm39) |
L82P |
probably damaging |
Het |
Armc3 |
C |
A |
2: 19,253,444 (GRCm39) |
P195Q |
probably damaging |
Het |
Astn2 |
A |
T |
4: 66,322,491 (GRCm39) |
L36Q |
unknown |
Het |
Atad2 |
A |
T |
15: 57,961,962 (GRCm39) |
S870T |
possibly damaging |
Het |
Bmp10 |
A |
T |
6: 87,411,062 (GRCm39) |
D285V |
probably benign |
Het |
Caskin1 |
T |
C |
17: 24,724,128 (GRCm39) |
V972A |
probably benign |
Het |
Ccdc141 |
T |
A |
2: 76,861,015 (GRCm39) |
N921Y |
probably damaging |
Het |
Cntnap5b |
A |
T |
1: 100,318,297 (GRCm39) |
D1019V |
probably damaging |
Het |
Eml5 |
T |
C |
12: 98,810,205 (GRCm39) |
|
probably benign |
Het |
Evi5l |
T |
C |
8: 4,243,195 (GRCm39) |
Y360H |
probably damaging |
Het |
Ewsr1 |
A |
G |
11: 5,041,450 (GRCm39) |
|
probably benign |
Het |
Fn3k |
A |
T |
11: 121,339,712 (GRCm39) |
N158I |
probably damaging |
Het |
Galnt17 |
C |
T |
5: 130,935,540 (GRCm39) |
R381Q |
probably damaging |
Het |
Golga3 |
A |
T |
5: 110,335,227 (GRCm39) |
K180N |
probably damaging |
Het |
Hipk1 |
A |
G |
3: 103,667,854 (GRCm39) |
L571P |
probably damaging |
Het |
Hormad2 |
T |
A |
11: 4,374,808 (GRCm39) |
K69* |
probably null |
Het |
Hspg2 |
A |
T |
4: 137,244,915 (GRCm39) |
D880V |
probably damaging |
Het |
Ido2 |
T |
A |
8: 25,030,652 (GRCm39) |
D226V |
probably damaging |
Het |
Irs3 |
A |
G |
5: 137,642,961 (GRCm39) |
F159S |
probably damaging |
Het |
Itgb1bp1 |
T |
C |
12: 21,326,860 (GRCm39) |
T38A |
probably damaging |
Het |
Kif11 |
A |
G |
19: 37,399,062 (GRCm39) |
I749V |
probably benign |
Het |
Lrp1b |
T |
G |
2: 40,769,567 (GRCm39) |
M2811L |
probably benign |
Het |
Lysmd3 |
A |
G |
13: 81,817,737 (GRCm39) |
Y238C |
probably damaging |
Het |
Mdga2 |
C |
T |
12: 66,736,155 (GRCm39) |
V358I |
possibly damaging |
Het |
Muc4 |
C |
T |
16: 32,754,563 (GRCm38) |
T1479I |
probably benign |
Het |
Myom1 |
T |
C |
17: 71,371,592 (GRCm39) |
V578A |
possibly damaging |
Het |
Nek10 |
T |
G |
14: 14,885,047 (GRCm38) |
|
probably null |
Het |
Nid2 |
G |
A |
14: 19,828,111 (GRCm39) |
G516S |
probably benign |
Het |
Or2t47 |
T |
A |
11: 58,442,768 (GRCm39) |
Q99L |
probably damaging |
Het |
Or4k1 |
T |
A |
14: 50,377,580 (GRCm39) |
N172I |
probably damaging |
Het |
Or51a24 |
T |
G |
7: 103,734,033 (GRCm39) |
T85P |
probably benign |
Het |
Or51v14 |
G |
C |
7: 103,261,443 (GRCm39) |
T39R |
possibly damaging |
Het |
Or52a5b |
G |
T |
7: 103,417,168 (GRCm39) |
C145* |
probably null |
Het |
Or8d23 |
T |
C |
9: 38,841,875 (GRCm39) |
M136T |
probably damaging |
Het |
Pde4dip |
A |
T |
3: 97,664,937 (GRCm39) |
C333S |
probably benign |
Het |
Pglyrp2 |
T |
A |
17: 32,637,222 (GRCm39) |
I269F |
probably benign |
Het |
Plch1 |
A |
G |
3: 63,628,655 (GRCm39) |
V536A |
probably benign |
Het |
Popdc2 |
T |
A |
16: 38,183,188 (GRCm39) |
L57Q |
probably damaging |
Het |
Pramel14 |
T |
C |
4: 143,720,885 (GRCm39) |
R19G |
possibly damaging |
Het |
Riox1 |
A |
G |
12: 83,997,709 (GRCm39) |
K82E |
probably benign |
Het |
Rnasel |
G |
A |
1: 153,630,647 (GRCm39) |
V388M |
probably damaging |
Het |
Smc1b |
A |
G |
15: 85,006,052 (GRCm39) |
|
probably benign |
Het |
Snx25 |
A |
G |
8: 46,494,444 (GRCm39) |
S814P |
probably damaging |
Het |
Spta1 |
A |
T |
1: 174,056,824 (GRCm39) |
H1859L |
probably benign |
Het |
Strc |
T |
C |
2: 121,196,343 (GRCm39) |
I1562V |
probably benign |
Het |
Taar5 |
T |
A |
10: 23,846,986 (GRCm39) |
I128N |
probably damaging |
Het |
Ttc28 |
C |
T |
5: 111,325,483 (GRCm39) |
|
probably benign |
Het |
Vcan |
A |
T |
13: 89,851,648 (GRCm39) |
M1104K |
possibly damaging |
Het |
Vnn1 |
C |
T |
10: 23,776,653 (GRCm39) |
Q335* |
probably null |
Het |
Zic1 |
T |
C |
9: 91,246,946 (GRCm39) |
D42G |
possibly damaging |
Het |
|
Other mutations in Mapk11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01744:Mapk11
|
APN |
15 |
89,031,046 (GRCm39) |
splice site |
probably benign |
|
IGL02164:Mapk11
|
APN |
15 |
89,029,651 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02825:Mapk11
|
APN |
15 |
89,030,585 (GRCm39) |
missense |
probably damaging |
1.00 |
E0370:Mapk11
|
UTSW |
15 |
89,030,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R1764:Mapk11
|
UTSW |
15 |
89,028,594 (GRCm39) |
critical splice donor site |
probably null |
|
R3149:Mapk11
|
UTSW |
15 |
89,029,653 (GRCm39) |
splice site |
probably null |
|
R3150:Mapk11
|
UTSW |
15 |
89,029,653 (GRCm39) |
splice site |
probably null |
|
R3730:Mapk11
|
UTSW |
15 |
89,029,318 (GRCm39) |
missense |
probably benign |
0.27 |
R4319:Mapk11
|
UTSW |
15 |
89,030,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R4424:Mapk11
|
UTSW |
15 |
89,029,576 (GRCm39) |
critical splice donor site |
probably null |
|
R4632:Mapk11
|
UTSW |
15 |
89,030,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R4783:Mapk11
|
UTSW |
15 |
89,033,691 (GRCm39) |
missense |
probably damaging |
0.98 |
R4937:Mapk11
|
UTSW |
15 |
89,030,685 (GRCm39) |
missense |
probably benign |
|
R5422:Mapk11
|
UTSW |
15 |
89,030,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R5511:Mapk11
|
UTSW |
15 |
89,029,380 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5914:Mapk11
|
UTSW |
15 |
89,030,038 (GRCm39) |
missense |
probably benign |
0.21 |
R5972:Mapk11
|
UTSW |
15 |
89,028,387 (GRCm39) |
missense |
probably benign |
0.34 |
R7290:Mapk11
|
UTSW |
15 |
89,028,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R8244:Mapk11
|
UTSW |
15 |
89,030,007 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8974:Mapk11
|
UTSW |
15 |
89,028,014 (GRCm39) |
missense |
probably benign |
0.00 |
R9276:Mapk11
|
UTSW |
15 |
89,029,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R9432:Mapk11
|
UTSW |
15 |
89,028,631 (GRCm39) |
missense |
probably benign |
0.01 |
|