Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
T |
A |
14: 32,382,908 (GRCm39) |
Y1019F |
probably benign |
Het |
4930455H04Rik |
T |
G |
3: 116,762,200 (GRCm39) |
|
probably benign |
Het |
9830107B12Rik |
A |
T |
17: 48,439,193 (GRCm39) |
|
probably benign |
Het |
Abcc8 |
A |
G |
7: 45,784,917 (GRCm39) |
V737A |
possibly damaging |
Het |
Adamts20 |
T |
A |
15: 94,229,329 (GRCm39) |
Y930F |
probably damaging |
Het |
Alkbh8 |
T |
A |
9: 3,369,825 (GRCm39) |
F365I |
probably damaging |
Het |
App |
G |
A |
16: 84,900,127 (GRCm39) |
H108Y |
probably damaging |
Het |
Bfsp1 |
T |
C |
2: 143,669,564 (GRCm39) |
|
probably benign |
Het |
Bltp3b |
T |
C |
10: 89,641,624 (GRCm39) |
S932P |
probably benign |
Het |
Cabin1 |
T |
C |
10: 75,578,263 (GRCm39) |
N478S |
probably damaging |
Het |
Camsap3 |
G |
A |
8: 3,654,795 (GRCm39) |
V796I |
probably damaging |
Het |
Carns1 |
A |
T |
19: 4,216,498 (GRCm39) |
|
probably null |
Het |
Clca3a1 |
C |
T |
3: 144,713,539 (GRCm39) |
M697I |
probably benign |
Het |
Cltc |
C |
T |
11: 86,593,074 (GRCm39) |
M1600I |
probably benign |
Het |
Cnot1 |
T |
A |
8: 96,467,637 (GRCm39) |
N1499Y |
probably damaging |
Het |
Crebbp |
T |
A |
16: 3,942,632 (GRCm39) |
I196L |
probably damaging |
Het |
Drc3 |
C |
A |
11: 60,249,475 (GRCm39) |
|
probably benign |
Het |
Fam161a |
T |
A |
11: 22,970,702 (GRCm39) |
Y234* |
probably null |
Het |
Il1r1 |
C |
A |
1: 40,352,330 (GRCm39) |
P500Q |
probably damaging |
Het |
Katnal1 |
G |
T |
5: 148,830,607 (GRCm39) |
|
probably benign |
Het |
Klhdc2 |
A |
G |
12: 69,343,827 (GRCm39) |
N20S |
probably benign |
Het |
Kmt2e |
A |
T |
5: 23,707,017 (GRCm39) |
T1527S |
possibly damaging |
Het |
Magi1 |
C |
T |
6: 93,724,205 (GRCm39) |
G270D |
probably damaging |
Het |
Mdn1 |
T |
A |
4: 32,715,922 (GRCm39) |
S2035T |
possibly damaging |
Het |
Mki67 |
A |
T |
7: 135,301,275 (GRCm39) |
M1253K |
probably benign |
Het |
Myh7 |
T |
C |
14: 55,226,336 (GRCm39) |
M435V |
possibly damaging |
Het |
Myh8 |
A |
G |
11: 67,183,505 (GRCm39) |
I739V |
probably benign |
Het |
Npnt |
T |
C |
3: 132,591,743 (GRCm39) |
K430R |
probably damaging |
Het |
Nrdc |
A |
G |
4: 108,904,857 (GRCm39) |
N696S |
probably benign |
Het |
Oit3 |
T |
C |
10: 59,261,306 (GRCm39) |
|
probably benign |
Het |
Or51a10 |
A |
G |
7: 103,699,376 (GRCm39) |
Y62H |
probably damaging |
Het |
Or51s1 |
A |
G |
7: 102,558,926 (GRCm39) |
I40T |
possibly damaging |
Het |
Or5bw2 |
A |
G |
7: 6,573,211 (GRCm39) |
T74A |
probably benign |
Het |
Or5p6 |
A |
T |
7: 107,631,328 (GRCm39) |
I74K |
possibly damaging |
Het |
Pkd1 |
G |
A |
17: 24,813,795 (GRCm39) |
|
probably null |
Het |
Plat |
A |
G |
8: 23,266,844 (GRCm39) |
M279V |
probably benign |
Het |
Prkd1 |
A |
T |
12: 50,439,693 (GRCm39) |
L378* |
probably null |
Het |
Rasgef1a |
C |
T |
6: 118,061,506 (GRCm39) |
T157I |
probably benign |
Het |
Rbm22 |
A |
G |
18: 60,693,929 (GRCm39) |
N11S |
probably damaging |
Het |
Ros1 |
T |
C |
10: 51,922,426 (GRCm39) |
|
probably benign |
Het |
Sema6d |
T |
A |
2: 124,495,562 (GRCm39) |
F3Y |
unknown |
Het |
Sis |
T |
C |
3: 72,868,354 (GRCm39) |
D112G |
probably benign |
Het |
Slit1 |
C |
A |
19: 41,599,483 (GRCm39) |
G1023C |
probably damaging |
Het |
Spata31h1 |
C |
A |
10: 82,120,568 (GRCm39) |
K4147N |
probably damaging |
Het |
Sptb |
T |
C |
12: 76,659,329 (GRCm39) |
|
probably benign |
Het |
Sspo |
T |
C |
6: 48,475,277 (GRCm39) |
I4881T |
probably benign |
Het |
Supt6 |
C |
A |
11: 78,111,969 (GRCm39) |
D1038Y |
probably damaging |
Het |
Tbc1d2b |
A |
T |
9: 90,087,144 (GRCm39) |
L945Q |
probably damaging |
Het |
Tgfbr3 |
G |
T |
5: 107,297,764 (GRCm39) |
A212E |
probably damaging |
Het |
Tipin |
A |
G |
9: 64,211,690 (GRCm39) |
T259A |
probably benign |
Het |
Traip |
T |
C |
9: 107,847,671 (GRCm39) |
S365P |
probably benign |
Het |
Tst |
T |
C |
15: 78,283,967 (GRCm39) |
T287A |
probably benign |
Het |
Tube1 |
C |
T |
10: 39,021,718 (GRCm39) |
|
probably benign |
Het |
Vmn1r37 |
T |
A |
6: 66,708,393 (GRCm39) |
N6K |
probably damaging |
Het |
Vmn2r111 |
C |
A |
17: 22,790,966 (GRCm39) |
E111* |
probably null |
Het |
Vmn2r17 |
C |
T |
5: 109,600,898 (GRCm39) |
T732I |
probably benign |
Het |
Vmn2r69 |
A |
T |
7: 85,055,836 (GRCm39) |
D767E |
possibly damaging |
Het |
|
Other mutations in Ccdc121 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02009:Ccdc121
|
APN |
5 |
31,644,835 (GRCm39) |
missense |
probably benign |
0.00 |
FR4304:Ccdc121
|
UTSW |
5 |
31,644,717 (GRCm39) |
small deletion |
probably benign |
|
FR4340:Ccdc121
|
UTSW |
5 |
31,644,717 (GRCm39) |
small deletion |
probably benign |
|
FR4342:Ccdc121
|
UTSW |
5 |
31,644,717 (GRCm39) |
small deletion |
probably benign |
|
FR4589:Ccdc121
|
UTSW |
5 |
31,644,717 (GRCm39) |
small deletion |
probably benign |
|
LCD18:Ccdc121
|
UTSW |
5 |
31,644,717 (GRCm39) |
small deletion |
probably benign |
|
PIT4486001:Ccdc121
|
UTSW |
5 |
31,645,087 (GRCm39) |
missense |
probably damaging |
0.99 |
R0650:Ccdc121
|
UTSW |
5 |
31,643,312 (GRCm39) |
unclassified |
probably benign |
|
R1366:Ccdc121
|
UTSW |
5 |
31,644,861 (GRCm39) |
missense |
probably benign |
0.07 |
R2050:Ccdc121
|
UTSW |
5 |
31,643,402 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2070:Ccdc121
|
UTSW |
5 |
31,644,727 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2862:Ccdc121
|
UTSW |
5 |
31,643,255 (GRCm39) |
unclassified |
probably benign |
|
R3965:Ccdc121
|
UTSW |
5 |
31,645,335 (GRCm39) |
missense |
probably benign |
0.02 |
R4299:Ccdc121
|
UTSW |
5 |
31,644,870 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4634:Ccdc121
|
UTSW |
5 |
31,645,435 (GRCm39) |
missense |
probably benign |
0.01 |
R4635:Ccdc121
|
UTSW |
5 |
31,645,435 (GRCm39) |
missense |
probably benign |
0.01 |
R4637:Ccdc121
|
UTSW |
5 |
31,645,435 (GRCm39) |
missense |
probably benign |
0.01 |
R4887:Ccdc121
|
UTSW |
5 |
31,643,596 (GRCm39) |
missense |
probably benign |
0.19 |
R5587:Ccdc121
|
UTSW |
5 |
31,643,428 (GRCm39) |
missense |
probably benign |
|
R5897:Ccdc121
|
UTSW |
5 |
31,643,308 (GRCm39) |
unclassified |
probably benign |
|
R6181:Ccdc121
|
UTSW |
5 |
31,645,399 (GRCm39) |
missense |
probably damaging |
0.98 |
R6183:Ccdc121
|
UTSW |
5 |
31,645,320 (GRCm39) |
missense |
probably damaging |
0.99 |
R8028:Ccdc121
|
UTSW |
5 |
31,645,266 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8231:Ccdc121
|
UTSW |
5 |
31,643,551 (GRCm39) |
missense |
probably benign |
0.35 |
R9535:Ccdc121
|
UTSW |
5 |
31,644,954 (GRCm39) |
missense |
probably benign |
0.01 |
R9655:Ccdc121
|
UTSW |
5 |
31,644,976 (GRCm39) |
missense |
probably benign |
0.00 |
RF006:Ccdc121
|
UTSW |
5 |
31,644,894 (GRCm39) |
nonsense |
probably null |
|
|