Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,281,687 (GRCm39) |
M3190L |
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,637,154 (GRCm39) |
L3429H |
probably damaging |
Het |
Ahnak |
A |
G |
19: 8,991,484 (GRCm39) |
D4256G |
probably damaging |
Het |
Ahnak |
A |
G |
19: 8,984,515 (GRCm39) |
N1933S |
probably benign |
Het |
Amacr |
A |
G |
15: 10,984,835 (GRCm39) |
D151G |
probably benign |
Het |
Ano9 |
A |
T |
7: 140,687,762 (GRCm39) |
H255Q |
possibly damaging |
Het |
Asphd2 |
A |
T |
5: 112,539,501 (GRCm39) |
Y111N |
possibly damaging |
Het |
Cage1 |
T |
A |
13: 38,209,334 (GRCm39) |
K214N |
probably benign |
Het |
Cdkn2c |
A |
G |
4: 109,518,606 (GRCm39) |
L116P |
probably damaging |
Het |
Cltc |
C |
T |
11: 86,624,490 (GRCm39) |
R148H |
probably damaging |
Het |
Cmbl |
A |
G |
15: 31,582,176 (GRCm39) |
N58D |
probably damaging |
Het |
Cpsf1 |
T |
A |
15: 76,481,202 (GRCm39) |
N1218I |
probably damaging |
Het |
Csf2rb |
T |
C |
15: 78,232,531 (GRCm39) |
S613P |
probably benign |
Het |
Ctnnd1 |
A |
G |
2: 84,439,411 (GRCm39) |
S761P |
probably damaging |
Het |
Cxcr6 |
A |
C |
9: 123,639,463 (GRCm39) |
I155L |
probably benign |
Het |
Ecpas |
A |
G |
4: 58,819,155 (GRCm39) |
V1265A |
probably damaging |
Het |
Fam216a |
A |
G |
5: 122,508,576 (GRCm39) |
|
probably null |
Het |
Fgf10 |
T |
A |
13: 118,918,147 (GRCm39) |
|
probably null |
Het |
Fgf17 |
T |
C |
14: 70,875,996 (GRCm39) |
T79A |
probably damaging |
Het |
G3bp1 |
T |
C |
11: 55,389,452 (GRCm39) |
F383L |
probably damaging |
Het |
Gm1527 |
G |
T |
3: 28,980,828 (GRCm39) |
V643L |
probably benign |
Het |
Hmcn2 |
A |
T |
2: 31,276,689 (GRCm39) |
Q1556L |
possibly damaging |
Het |
Hspa4l |
C |
T |
3: 40,738,758 (GRCm39) |
T616I |
possibly damaging |
Het |
Irag2 |
A |
G |
6: 145,110,986 (GRCm39) |
S264G |
probably benign |
Het |
Irgm1 |
T |
C |
11: 48,757,154 (GRCm39) |
D219G |
probably damaging |
Het |
Jcad |
A |
G |
18: 4,673,243 (GRCm39) |
D335G |
probably damaging |
Het |
Kcnh4 |
A |
G |
11: 100,641,084 (GRCm39) |
F455S |
probably damaging |
Het |
Khdrbs3 |
T |
C |
15: 68,889,210 (GRCm39) |
Y120H |
probably damaging |
Het |
Kndc1 |
A |
T |
7: 139,493,939 (GRCm39) |
T507S |
probably null |
Het |
Lepr |
G |
T |
4: 101,625,290 (GRCm39) |
E482* |
probably null |
Het |
Mcemp1 |
T |
A |
8: 3,717,507 (GRCm39) |
M146K |
probably benign |
Het |
Mllt10 |
A |
G |
2: 18,211,948 (GRCm39) |
T411A |
probably damaging |
Het |
Myh8 |
A |
T |
11: 67,192,837 (GRCm39) |
I1543L |
probably benign |
Het |
Myo1f |
T |
C |
17: 33,797,258 (GRCm39) |
S147P |
probably damaging |
Het |
Myrf |
G |
C |
19: 10,195,526 (GRCm39) |
T428S |
probably benign |
Het |
Or5j1 |
C |
T |
2: 86,878,837 (GRCm39) |
V248I |
probably damaging |
Het |
Plaat1 |
G |
A |
16: 29,039,331 (GRCm39) |
|
probably null |
Het |
Plch2 |
G |
A |
4: 155,093,469 (GRCm39) |
R57C |
probably damaging |
Het |
Rbm20 |
G |
A |
19: 53,839,626 (GRCm39) |
G872R |
probably damaging |
Het |
Retsat |
A |
T |
6: 72,583,414 (GRCm39) |
I373F |
probably damaging |
Het |
Rnf145 |
T |
C |
11: 44,446,056 (GRCm39) |
F297L |
probably benign |
Het |
Ros1 |
A |
T |
10: 52,031,204 (GRCm39) |
M479K |
possibly damaging |
Het |
Rubcnl |
T |
A |
14: 75,273,521 (GRCm39) |
N244K |
probably benign |
Het |
Samhd1 |
A |
G |
2: 156,952,535 (GRCm39) |
F406L |
probably damaging |
Het |
Sdsl |
A |
T |
5: 120,597,533 (GRCm39) |
V258D |
probably damaging |
Het |
Sec24c |
C |
G |
14: 20,733,467 (GRCm39) |
P166A |
probably benign |
Het |
Sele |
C |
A |
1: 163,881,184 (GRCm39) |
Y461* |
probably null |
Het |
Slc22a1 |
G |
T |
17: 12,881,487 (GRCm39) |
S334* |
probably null |
Het |
Spem1 |
T |
G |
11: 69,712,691 (GRCm39) |
|
probably null |
Het |
Stat3 |
T |
C |
11: 100,794,469 (GRCm39) |
E280G |
probably damaging |
Het |
Stxbp4 |
T |
C |
11: 90,483,186 (GRCm39) |
H280R |
probably benign |
Het |
Tas2r129 |
G |
A |
6: 132,928,906 (GRCm39) |
C281Y |
probably benign |
Het |
Tas2r129 |
T |
G |
6: 132,928,907 (GRCm39) |
C281W |
probably benign |
Het |
Tcp11 |
T |
A |
17: 28,298,897 (GRCm39) |
|
probably null |
Het |
Tnrc6b |
G |
A |
15: 80,764,876 (GRCm39) |
V793M |
probably benign |
Het |
Vmn2r59 |
A |
C |
7: 41,696,528 (GRCm39) |
Y71* |
probably null |
Het |
Wdr35 |
T |
C |
12: 9,062,743 (GRCm39) |
|
probably null |
Het |
Zan |
A |
G |
5: 137,411,620 (GRCm39) |
|
probably null |
Het |
Zap70 |
G |
T |
1: 36,818,365 (GRCm39) |
V351L |
probably damaging |
Het |
Zfp609 |
G |
T |
9: 65,609,916 (GRCm39) |
Q1016K |
unknown |
Het |
Zfp641 |
C |
A |
15: 98,187,060 (GRCm39) |
V188L |
probably benign |
Het |
Zpld2 |
A |
T |
4: 133,930,089 (GRCm39) |
L72Q |
probably damaging |
Het |
|
Other mutations in Cpa6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00858:Cpa6
|
APN |
1 |
10,554,219 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00933:Cpa6
|
APN |
1 |
10,407,595 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01710:Cpa6
|
APN |
1 |
10,395,497 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02211:Cpa6
|
APN |
1 |
10,665,861 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02504:Cpa6
|
APN |
1 |
10,559,144 (GRCm39) |
missense |
probably benign |
0.19 |
R1260:Cpa6
|
UTSW |
1 |
10,395,544 (GRCm39) |
splice site |
probably null |
|
R2154:Cpa6
|
UTSW |
1 |
10,407,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R4705:Cpa6
|
UTSW |
1 |
10,551,283 (GRCm39) |
missense |
probably benign |
0.03 |
R4788:Cpa6
|
UTSW |
1 |
10,478,502 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4872:Cpa6
|
UTSW |
1 |
10,665,843 (GRCm39) |
critical splice donor site |
probably null |
|
R4941:Cpa6
|
UTSW |
1 |
10,479,562 (GRCm39) |
missense |
probably benign |
0.25 |
R5656:Cpa6
|
UTSW |
1 |
10,399,739 (GRCm39) |
missense |
probably benign |
0.19 |
R5969:Cpa6
|
UTSW |
1 |
10,559,108 (GRCm39) |
missense |
probably benign |
0.15 |
R6019:Cpa6
|
UTSW |
1 |
10,665,868 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6322:Cpa6
|
UTSW |
1 |
10,547,346 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6958:Cpa6
|
UTSW |
1 |
10,665,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R7154:Cpa6
|
UTSW |
1 |
10,407,694 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7274:Cpa6
|
UTSW |
1 |
10,479,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R8140:Cpa6
|
UTSW |
1 |
10,395,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R8559:Cpa6
|
UTSW |
1 |
10,478,574 (GRCm39) |
nonsense |
probably null |
|
R9042:Cpa6
|
UTSW |
1 |
10,407,515 (GRCm39) |
missense |
probably benign |
0.05 |
R9297:Cpa6
|
UTSW |
1 |
10,554,273 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9355:Cpa6
|
UTSW |
1 |
10,479,520 (GRCm39) |
missense |
probably benign |
0.09 |
R9498:Cpa6
|
UTSW |
1 |
10,479,546 (GRCm39) |
missense |
possibly damaging |
0.73 |
Z1177:Cpa6
|
UTSW |
1 |
10,399,784 (GRCm39) |
critical splice acceptor site |
probably null |
|
|