Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5430401F13Rik |
G |
T |
6: 131,529,742 (GRCm39) |
R112L |
unknown |
Het |
Abcd4 |
G |
T |
12: 84,658,507 (GRCm39) |
A232E |
probably damaging |
Het |
Acsm5 |
T |
A |
7: 119,140,123 (GRCm39) |
I508N |
probably damaging |
Het |
Adam22 |
T |
C |
5: 8,132,156 (GRCm39) |
Q263R |
probably damaging |
Het |
Ckap4 |
C |
T |
10: 84,363,384 (GRCm39) |
D560N |
probably damaging |
Het |
Crb3 |
T |
A |
17: 57,369,743 (GRCm39) |
L17Q |
probably damaging |
Het |
Fbxo21 |
G |
T |
5: 118,115,098 (GRCm39) |
R78L |
probably benign |
Het |
Gapvd1 |
A |
T |
2: 34,599,229 (GRCm39) |
C669S |
probably damaging |
Het |
Gria2 |
A |
T |
3: 80,629,331 (GRCm39) |
|
probably benign |
Het |
H2-M11 |
T |
C |
17: 36,859,829 (GRCm39) |
L274P |
probably benign |
Het |
Hmox1 |
A |
G |
8: 75,823,931 (GRCm39) |
T200A |
probably benign |
Het |
Hspa8 |
G |
A |
9: 40,713,920 (GRCm39) |
|
probably null |
Het |
Isy1 |
C |
A |
6: 87,796,094 (GRCm39) |
R281L |
probably benign |
Het |
Kiz |
C |
A |
2: 146,697,973 (GRCm39) |
|
probably benign |
Het |
Lrig2 |
T |
C |
3: 104,371,591 (GRCm39) |
K704R |
probably benign |
Het |
Lrp1 |
A |
T |
10: 127,375,147 (GRCm39) |
D4484E |
probably damaging |
Het |
Lrrc7 |
C |
A |
3: 157,869,903 (GRCm39) |
|
probably benign |
Het |
Mtmr14 |
T |
C |
6: 113,216,543 (GRCm39) |
|
probably null |
Het |
Mtmr3 |
A |
T |
11: 4,438,474 (GRCm39) |
V660E |
probably benign |
Het |
Mtor |
T |
C |
4: 148,570,513 (GRCm39) |
I1190T |
probably benign |
Het |
Mtrf1l |
T |
C |
10: 5,763,376 (GRCm39) |
R318G |
probably damaging |
Het |
Myh7 |
T |
C |
14: 55,210,596 (GRCm39) |
T1739A |
probably benign |
Het |
Ofcc1 |
C |
T |
13: 40,362,305 (GRCm39) |
G206R |
probably benign |
Het |
Or5h18 |
C |
T |
16: 58,847,791 (GRCm39) |
V160I |
probably benign |
Het |
Pcca |
A |
G |
14: 123,126,957 (GRCm39) |
E722G |
possibly damaging |
Het |
Pds5b |
T |
A |
5: 150,662,656 (GRCm39) |
|
probably benign |
Het |
Ralgapa2 |
A |
T |
2: 146,277,923 (GRCm39) |
F413I |
probably damaging |
Het |
Rbbp9 |
T |
C |
2: 144,392,628 (GRCm39) |
Y24C |
probably damaging |
Het |
Rgs2 |
A |
G |
1: 143,877,988 (GRCm39) |
S103P |
probably damaging |
Het |
Rtn1 |
G |
T |
12: 72,355,156 (GRCm39) |
Y263* |
probably null |
Het |
Slc22a1 |
T |
C |
17: 12,875,933 (GRCm39) |
E427G |
probably benign |
Het |
Speg |
A |
G |
1: 75,393,727 (GRCm39) |
T1695A |
probably damaging |
Het |
Tlx3 |
C |
A |
11: 33,153,315 (GRCm39) |
G49W |
probably damaging |
Het |
Tor1b |
A |
G |
2: 30,846,928 (GRCm39) |
M292V |
probably benign |
Het |
Tspyl3 |
A |
T |
2: 153,066,854 (GRCm39) |
L128Q |
probably damaging |
Het |
Zbtb14 |
C |
A |
17: 69,695,497 (GRCm39) |
F398L |
probably damaging |
Het |
Zfc3h1 |
G |
A |
10: 115,263,621 (GRCm39) |
V1821I |
probably benign |
Het |
Zfhx4 |
A |
T |
3: 5,477,272 (GRCm39) |
T3271S |
possibly damaging |
Het |
Zfp386 |
G |
T |
12: 116,018,329 (GRCm39) |
|
probably benign |
Het |
Zfp574 |
A |
T |
7: 24,779,323 (GRCm39) |
K115M |
probably damaging |
Het |
|
Other mutations in Ccdc88c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01112:Ccdc88c
|
APN |
12 |
100,883,062 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02016:Ccdc88c
|
APN |
12 |
100,907,466 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02031:Ccdc88c
|
APN |
12 |
100,899,570 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02133:Ccdc88c
|
APN |
12 |
100,906,349 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02427:Ccdc88c
|
APN |
12 |
100,887,851 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02494:Ccdc88c
|
APN |
12 |
100,911,734 (GRCm39) |
missense |
probably benign |
|
IGL02496:Ccdc88c
|
APN |
12 |
100,919,552 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02549:Ccdc88c
|
APN |
12 |
100,895,191 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02618:Ccdc88c
|
APN |
12 |
100,879,812 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02626:Ccdc88c
|
APN |
12 |
100,934,059 (GRCm39) |
unclassified |
probably benign |
|
IGL03142:Ccdc88c
|
APN |
12 |
100,913,457 (GRCm39) |
missense |
probably damaging |
1.00 |
BB010:Ccdc88c
|
UTSW |
12 |
100,911,749 (GRCm39) |
missense |
possibly damaging |
0.93 |
BB020:Ccdc88c
|
UTSW |
12 |
100,911,749 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0127:Ccdc88c
|
UTSW |
12 |
100,901,999 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0533:Ccdc88c
|
UTSW |
12 |
100,920,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R0545:Ccdc88c
|
UTSW |
12 |
100,913,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R1230:Ccdc88c
|
UTSW |
12 |
100,914,747 (GRCm39) |
missense |
probably benign |
0.00 |
R1434:Ccdc88c
|
UTSW |
12 |
100,905,425 (GRCm39) |
splice site |
probably benign |
|
R1614:Ccdc88c
|
UTSW |
12 |
100,879,243 (GRCm39) |
missense |
probably benign |
0.00 |
R1644:Ccdc88c
|
UTSW |
12 |
100,879,733 (GRCm39) |
missense |
probably damaging |
0.98 |
R1712:Ccdc88c
|
UTSW |
12 |
100,905,284 (GRCm39) |
missense |
probably benign |
0.14 |
R2107:Ccdc88c
|
UTSW |
12 |
100,887,808 (GRCm39) |
missense |
probably benign |
|
R3612:Ccdc88c
|
UTSW |
12 |
100,905,332 (GRCm39) |
missense |
probably damaging |
0.99 |
R3724:Ccdc88c
|
UTSW |
12 |
100,896,783 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3737:Ccdc88c
|
UTSW |
12 |
100,896,783 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3743:Ccdc88c
|
UTSW |
12 |
100,914,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R3772:Ccdc88c
|
UTSW |
12 |
100,932,359 (GRCm39) |
unclassified |
probably benign |
|
R3776:Ccdc88c
|
UTSW |
12 |
100,913,438 (GRCm39) |
missense |
probably damaging |
0.97 |
R3917:Ccdc88c
|
UTSW |
12 |
100,907,366 (GRCm39) |
critical splice donor site |
probably null |
|
R4034:Ccdc88c
|
UTSW |
12 |
100,896,783 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4035:Ccdc88c
|
UTSW |
12 |
100,896,783 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4110:Ccdc88c
|
UTSW |
12 |
100,911,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R4113:Ccdc88c
|
UTSW |
12 |
100,911,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R4270:Ccdc88c
|
UTSW |
12 |
100,913,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R4271:Ccdc88c
|
UTSW |
12 |
100,913,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R4520:Ccdc88c
|
UTSW |
12 |
100,879,591 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4521:Ccdc88c
|
UTSW |
12 |
100,879,591 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4522:Ccdc88c
|
UTSW |
12 |
100,879,591 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4523:Ccdc88c
|
UTSW |
12 |
100,879,591 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4524:Ccdc88c
|
UTSW |
12 |
100,879,591 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4717:Ccdc88c
|
UTSW |
12 |
100,882,925 (GRCm39) |
missense |
probably benign |
0.00 |
R4821:Ccdc88c
|
UTSW |
12 |
100,904,338 (GRCm39) |
missense |
probably benign |
0.00 |
R4823:Ccdc88c
|
UTSW |
12 |
100,896,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R5090:Ccdc88c
|
UTSW |
12 |
100,920,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R5510:Ccdc88c
|
UTSW |
12 |
100,911,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R5514:Ccdc88c
|
UTSW |
12 |
100,879,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R5903:Ccdc88c
|
UTSW |
12 |
100,896,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R5999:Ccdc88c
|
UTSW |
12 |
100,934,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R6131:Ccdc88c
|
UTSW |
12 |
100,907,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R6164:Ccdc88c
|
UTSW |
12 |
100,919,642 (GRCm39) |
missense |
probably damaging |
0.98 |
R6971:Ccdc88c
|
UTSW |
12 |
100,920,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R6998:Ccdc88c
|
UTSW |
12 |
100,883,111 (GRCm39) |
missense |
probably damaging |
0.96 |
R7031:Ccdc88c
|
UTSW |
12 |
100,911,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R7240:Ccdc88c
|
UTSW |
12 |
100,911,198 (GRCm39) |
missense |
probably benign |
0.17 |
R7366:Ccdc88c
|
UTSW |
12 |
100,911,209 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7604:Ccdc88c
|
UTSW |
12 |
100,896,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R7674:Ccdc88c
|
UTSW |
12 |
100,911,491 (GRCm39) |
missense |
probably benign |
0.00 |
R7795:Ccdc88c
|
UTSW |
12 |
100,889,570 (GRCm39) |
missense |
probably benign |
0.32 |
R7933:Ccdc88c
|
UTSW |
12 |
100,911,749 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7990:Ccdc88c
|
UTSW |
12 |
100,934,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R8339:Ccdc88c
|
UTSW |
12 |
100,907,399 (GRCm39) |
nonsense |
probably null |
|
R8734:Ccdc88c
|
UTSW |
12 |
100,906,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R8778:Ccdc88c
|
UTSW |
12 |
100,911,483 (GRCm39) |
missense |
probably benign |
0.25 |
R8925:Ccdc88c
|
UTSW |
12 |
100,932,676 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8927:Ccdc88c
|
UTSW |
12 |
100,932,676 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9014:Ccdc88c
|
UTSW |
12 |
100,879,323 (GRCm39) |
missense |
probably benign |
0.09 |
R9204:Ccdc88c
|
UTSW |
12 |
100,904,322 (GRCm39) |
missense |
unknown |
|
R9257:Ccdc88c
|
UTSW |
12 |
100,889,474 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9326:Ccdc88c
|
UTSW |
12 |
100,995,109 (GRCm39) |
start gained |
probably benign |
|
R9424:Ccdc88c
|
UTSW |
12 |
100,911,749 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9439:Ccdc88c
|
UTSW |
12 |
100,884,597 (GRCm39) |
missense |
probably benign |
0.25 |
R9539:Ccdc88c
|
UTSW |
12 |
100,901,993 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9576:Ccdc88c
|
UTSW |
12 |
100,911,749 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1176:Ccdc88c
|
UTSW |
12 |
100,912,029 (GRCm39) |
missense |
possibly damaging |
0.69 |
Z1177:Ccdc88c
|
UTSW |
12 |
100,911,414 (GRCm39) |
missense |
probably benign |
|
Z1190:Ccdc88c
|
UTSW |
12 |
100,889,591 (GRCm39) |
missense |
probably benign |
|
|