Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc3 |
A |
G |
11: 94,236,818 (GRCm39) |
V1473A |
possibly damaging |
Het |
Akap9 |
T |
A |
5: 4,120,397 (GRCm39) |
C3604* |
probably null |
Het |
Alas1 |
A |
G |
9: 106,112,721 (GRCm39) |
I545T |
probably benign |
Het |
Anpep |
A |
C |
7: 79,491,646 (GRCm39) |
D118E |
probably benign |
Het |
Arhgef17 |
A |
T |
7: 100,579,062 (GRCm39) |
S629T |
probably damaging |
Het |
Arid2 |
C |
T |
15: 96,266,625 (GRCm39) |
R558C |
probably damaging |
Het |
Camk2n1 |
A |
G |
4: 138,184,056 (GRCm39) |
D65G |
probably damaging |
Het |
Cenpe |
ACTCTCT |
ACTCT |
3: 134,945,609 (GRCm39) |
|
probably null |
Het |
Crb1 |
T |
C |
1: 139,165,122 (GRCm39) |
I1062V |
probably benign |
Het |
Decr2 |
A |
G |
17: 26,301,962 (GRCm39) |
L256P |
probably damaging |
Het |
Dhx37 |
T |
C |
5: 125,501,739 (GRCm39) |
M507V |
probably benign |
Het |
Disp1 |
A |
G |
1: 182,870,803 (GRCm39) |
I539T |
probably damaging |
Het |
Dqx1 |
T |
A |
6: 83,036,788 (GRCm39) |
V264E |
probably damaging |
Het |
Enpp4 |
A |
G |
17: 44,413,136 (GRCm39) |
S133P |
possibly damaging |
Het |
Fam149a |
T |
C |
8: 45,802,048 (GRCm39) |
T476A |
probably benign |
Het |
Fam20b |
A |
G |
1: 156,533,407 (GRCm39) |
W70R |
probably damaging |
Het |
Fbxl13 |
T |
A |
5: 21,728,566 (GRCm39) |
N508Y |
probably damaging |
Het |
Fjx1 |
A |
G |
2: 102,280,720 (GRCm39) |
L405P |
probably damaging |
Het |
Fn1 |
G |
A |
1: 71,629,310 (GRCm39) |
Q2399* |
probably null |
Het |
Foxa2 |
G |
C |
2: 147,885,909 (GRCm39) |
T308S |
probably benign |
Het |
Gatad1 |
T |
C |
5: 3,693,540 (GRCm39) |
R210G |
probably benign |
Het |
Gm10521 |
A |
G |
1: 171,723,752 (GRCm39) |
D21G |
unknown |
Het |
Gstcd |
C |
T |
3: 132,787,868 (GRCm39) |
V277M |
probably damaging |
Het |
Herpud1 |
A |
G |
8: 95,119,014 (GRCm39) |
E256G |
probably damaging |
Het |
Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
Kctd13 |
A |
G |
7: 126,528,414 (GRCm39) |
D63G |
possibly damaging |
Het |
Lamp3 |
C |
A |
16: 19,519,809 (GRCm39) |
D125Y |
probably damaging |
Het |
Luzp2 |
A |
G |
7: 54,724,823 (GRCm39) |
D128G |
probably damaging |
Het |
Lyve1 |
A |
G |
7: 110,458,649 (GRCm39) |
C105R |
probably damaging |
Het |
Mlkl |
A |
T |
8: 112,060,086 (GRCm39) |
V100E |
probably damaging |
Het |
Muc5b |
T |
C |
7: 141,421,478 (GRCm39) |
S4323P |
possibly damaging |
Het |
Myoz3 |
T |
G |
18: 60,713,922 (GRCm39) |
|
probably null |
Het |
Nlrp9c |
T |
A |
7: 26,070,864 (GRCm39) |
N906Y |
possibly damaging |
Het |
Odad1 |
A |
G |
7: 45,592,276 (GRCm39) |
D352G |
probably benign |
Het |
Or10x4 |
A |
G |
1: 174,219,382 (GRCm39) |
H249R |
probably damaging |
Het |
Or51f23 |
A |
T |
7: 102,452,763 (GRCm39) |
H26L |
possibly damaging |
Het |
Or8b49 |
T |
C |
9: 38,506,186 (GRCm39) |
F223S |
probably benign |
Het |
Or8w1 |
C |
T |
2: 87,465,847 (GRCm39) |
M81I |
probably benign |
Het |
Pcsk9 |
G |
A |
4: 106,311,536 (GRCm39) |
H232Y |
possibly damaging |
Het |
Plec |
A |
G |
15: 76,063,380 (GRCm39) |
I2230T |
possibly damaging |
Het |
Pou2f3 |
T |
A |
9: 43,058,205 (GRCm39) |
T47S |
probably damaging |
Het |
Rab8a |
A |
T |
8: 72,928,439 (GRCm39) |
I106F |
probably damaging |
Het |
Relch |
A |
T |
1: 105,605,902 (GRCm39) |
I181F |
probably damaging |
Het |
Ros1 |
A |
T |
10: 52,041,439 (GRCm39) |
S295T |
probably benign |
Het |
Sh3yl1 |
T |
A |
12: 30,992,098 (GRCm39) |
N222K |
possibly damaging |
Het |
Slc6a9 |
C |
T |
4: 117,725,083 (GRCm39) |
A559V |
possibly damaging |
Het |
Spata20 |
T |
G |
11: 94,369,963 (GRCm39) |
I778L |
probably benign |
Het |
Taar1 |
A |
T |
10: 23,797,033 (GRCm39) |
T244S |
probably benign |
Het |
Tmem229b |
C |
A |
12: 79,011,862 (GRCm39) |
C23F |
probably damaging |
Het |
Ttll4 |
A |
G |
1: 74,718,389 (GRCm39) |
Y80C |
probably benign |
Het |
Ube2m |
G |
A |
7: 12,769,566 (GRCm39) |
T176I |
probably benign |
Het |
Zfp790 |
G |
A |
7: 29,528,346 (GRCm39) |
A344T |
possibly damaging |
Het |
Zfp90 |
G |
A |
8: 107,145,760 (GRCm39) |
V31M |
probably benign |
Het |
Zswim4 |
C |
T |
8: 84,949,918 (GRCm39) |
R659Q |
probably benign |
Het |
|
Other mutations in Ccdc177 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01598:Ccdc177
|
APN |
12 |
80,805,519 (GRCm39) |
missense |
unknown |
|
IGL02433:Ccdc177
|
APN |
12 |
80,804,372 (GRCm39) |
missense |
unknown |
|
R0829:Ccdc177
|
UTSW |
12 |
80,806,253 (GRCm39) |
missense |
probably damaging |
0.96 |
R1739:Ccdc177
|
UTSW |
12 |
80,806,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Ccdc177
|
UTSW |
12 |
80,805,486 (GRCm39) |
missense |
unknown |
|
R2337:Ccdc177
|
UTSW |
12 |
80,805,465 (GRCm39) |
missense |
unknown |
|
R5001:Ccdc177
|
UTSW |
12 |
80,804,160 (GRCm39) |
missense |
unknown |
|
R5164:Ccdc177
|
UTSW |
12 |
80,805,336 (GRCm39) |
missense |
unknown |
|
R5249:Ccdc177
|
UTSW |
12 |
80,805,282 (GRCm39) |
missense |
unknown |
|
R5461:Ccdc177
|
UTSW |
12 |
80,804,816 (GRCm39) |
missense |
unknown |
|
R6802:Ccdc177
|
UTSW |
12 |
80,806,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R7051:Ccdc177
|
UTSW |
12 |
80,805,927 (GRCm39) |
missense |
probably damaging |
0.98 |
R7412:Ccdc177
|
UTSW |
12 |
80,805,792 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7510:Ccdc177
|
UTSW |
12 |
80,804,457 (GRCm39) |
missense |
unknown |
|
R7511:Ccdc177
|
UTSW |
12 |
80,804,457 (GRCm39) |
missense |
unknown |
|
R7712:Ccdc177
|
UTSW |
12 |
80,804,712 (GRCm39) |
nonsense |
probably null |
|
R8693:Ccdc177
|
UTSW |
12 |
80,804,582 (GRCm39) |
missense |
unknown |
|
R8708:Ccdc177
|
UTSW |
12 |
80,805,891 (GRCm39) |
missense |
probably benign |
0.08 |
R8862:Ccdc177
|
UTSW |
12 |
80,804,208 (GRCm39) |
missense |
unknown |
|
R8894:Ccdc177
|
UTSW |
12 |
80,806,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R9423:Ccdc177
|
UTSW |
12 |
80,804,162 (GRCm39) |
missense |
unknown |
|
R9727:Ccdc177
|
UTSW |
12 |
80,806,044 (GRCm39) |
missense |
probably benign |
0.04 |
Z1177:Ccdc177
|
UTSW |
12 |
80,804,510 (GRCm39) |
missense |
unknown |
|
|