Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AW551984 |
T |
A |
9: 39,507,922 (GRCm39) |
R405* |
probably null |
Het |
AW551984 |
C |
T |
9: 39,504,624 (GRCm39) |
|
probably null |
Het |
Bdp1 |
T |
C |
13: 100,197,481 (GRCm39) |
E968G |
possibly damaging |
Het |
Ccdc87 |
T |
A |
19: 4,889,889 (GRCm39) |
L127H |
probably damaging |
Het |
Cdk5r1 |
G |
T |
11: 80,368,569 (GRCm39) |
A79S |
probably benign |
Het |
Cdyl |
A |
T |
13: 35,867,725 (GRCm39) |
|
probably benign |
Het |
Cfdp1 |
A |
G |
8: 112,580,766 (GRCm39) |
|
probably benign |
Het |
Chi3l1 |
A |
T |
1: 134,111,339 (GRCm39) |
I62F |
probably damaging |
Het |
Cnot1 |
A |
T |
8: 96,481,706 (GRCm39) |
I789K |
probably benign |
Het |
Cobl |
T |
C |
11: 12,204,371 (GRCm39) |
K695R |
probably damaging |
Het |
Cobl |
C |
A |
11: 12,204,370 (GRCm39) |
K752N |
probably damaging |
Het |
Cstdc5 |
G |
A |
16: 36,179,899 (GRCm39) |
P73S |
probably benign |
Het |
Dcaf6 |
T |
C |
1: 165,165,915 (GRCm39) |
|
probably null |
Het |
Ece2 |
A |
T |
16: 20,451,398 (GRCm39) |
I197F |
probably damaging |
Het |
Eif2b5 |
T |
G |
16: 20,321,536 (GRCm39) |
V363G |
possibly damaging |
Het |
Gca |
T |
C |
2: 62,502,702 (GRCm39) |
S37P |
probably benign |
Het |
Ghsr |
A |
C |
3: 27,426,645 (GRCm39) |
I234L |
probably damaging |
Het |
Grin3b |
A |
T |
10: 79,808,723 (GRCm39) |
I158F |
possibly damaging |
Het |
Gtf2h2 |
A |
T |
13: 100,617,747 (GRCm39) |
D178E |
probably damaging |
Het |
Herc2 |
A |
G |
7: 55,747,246 (GRCm39) |
E461G |
probably damaging |
Het |
Hsph1 |
T |
A |
5: 149,547,057 (GRCm39) |
N531I |
possibly damaging |
Het |
Insl6 |
G |
T |
19: 29,302,529 (GRCm39) |
Q63K |
probably benign |
Het |
Lrp1b |
T |
C |
2: 40,592,806 (GRCm39) |
N3771S |
probably benign |
Het |
Lrp8 |
T |
C |
4: 107,691,952 (GRCm39) |
|
probably null |
Het |
Lvrn |
C |
T |
18: 47,023,971 (GRCm39) |
Q773* |
probably null |
Het |
Mterf1b |
T |
C |
5: 4,246,478 (GRCm39) |
F40L |
possibly damaging |
Het |
Nrg1 |
G |
A |
8: 32,316,391 (GRCm39) |
|
probably benign |
Het |
Or10ak13 |
T |
A |
4: 118,639,117 (GRCm39) |
I222F |
possibly damaging |
Het |
Or1n1 |
T |
A |
2: 36,750,232 (GRCm39) |
I43F |
probably damaging |
Het |
Or5p79 |
T |
C |
7: 108,221,880 (GRCm39) |
I287T |
possibly damaging |
Het |
Pax5 |
C |
T |
4: 44,570,059 (GRCm39) |
V319I |
probably damaging |
Het |
Plcz1 |
T |
A |
6: 139,956,307 (GRCm39) |
T321S |
probably benign |
Het |
Plekha6 |
A |
G |
1: 133,212,676 (GRCm39) |
E660G |
probably damaging |
Het |
Prep |
T |
C |
10: 44,943,428 (GRCm39) |
M1T |
probably null |
Het |
Prickle1 |
C |
T |
15: 93,399,034 (GRCm39) |
S598N |
possibly damaging |
Het |
Prtn3 |
A |
G |
10: 79,716,932 (GRCm39) |
Q99R |
probably benign |
Het |
Rad50 |
A |
G |
11: 53,592,883 (GRCm39) |
V89A |
probably damaging |
Het |
Ret |
T |
C |
6: 118,153,213 (GRCm39) |
Y485C |
probably benign |
Het |
Setd2 |
T |
A |
9: 110,379,124 (GRCm39) |
F980I |
possibly damaging |
Het |
Slc44a4 |
A |
G |
17: 35,140,279 (GRCm39) |
Y228C |
probably damaging |
Het |
Tex10 |
C |
T |
4: 48,435,028 (GRCm39) |
C779Y |
possibly damaging |
Het |
Tfdp2 |
T |
G |
9: 96,199,592 (GRCm39) |
S285A |
probably benign |
Het |
Thsd4 |
T |
A |
9: 59,896,380 (GRCm39) |
|
probably benign |
Het |
Tmem106a |
A |
C |
11: 101,481,219 (GRCm39) |
E242D |
probably benign |
Het |
Ttc22 |
T |
C |
4: 106,495,669 (GRCm39) |
V341A |
probably benign |
Het |
Ubr4 |
T |
A |
4: 139,138,095 (GRCm39) |
S1151T |
probably damaging |
Het |
Ubr4 |
G |
A |
4: 139,120,470 (GRCm39) |
|
probably null |
Het |
Vmn1r206 |
A |
T |
13: 22,805,060 (GRCm39) |
L49* |
probably null |
Het |
Vmn1r233 |
A |
T |
17: 21,214,887 (GRCm39) |
F21Y |
probably benign |
Het |
Vmn1r233 |
A |
T |
17: 21,214,886 (GRCm39) |
F21L |
probably benign |
Het |
Vmn2r15 |
A |
T |
5: 109,441,134 (GRCm39) |
C241* |
probably null |
Het |
Zmym6 |
T |
A |
4: 127,003,764 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Ccdc68 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01595:Ccdc68
|
APN |
18 |
70,089,117 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02851:Ccdc68
|
APN |
18 |
70,080,236 (GRCm39) |
nonsense |
probably null |
|
R0412:Ccdc68
|
UTSW |
18 |
70,093,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R0617:Ccdc68
|
UTSW |
18 |
70,079,623 (GRCm39) |
splice site |
probably null |
|
R1302:Ccdc68
|
UTSW |
18 |
70,072,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R1497:Ccdc68
|
UTSW |
18 |
70,093,585 (GRCm39) |
intron |
probably benign |
|
R1553:Ccdc68
|
UTSW |
18 |
70,073,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R1590:Ccdc68
|
UTSW |
18 |
70,073,251 (GRCm39) |
missense |
probably benign |
0.07 |
R1748:Ccdc68
|
UTSW |
18 |
70,089,062 (GRCm39) |
missense |
probably benign |
0.27 |
R5589:Ccdc68
|
UTSW |
18 |
70,079,577 (GRCm39) |
missense |
probably benign |
|
R6766:Ccdc68
|
UTSW |
18 |
70,099,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R7096:Ccdc68
|
UTSW |
18 |
70,073,241 (GRCm39) |
missense |
probably damaging |
0.96 |
R7359:Ccdc68
|
UTSW |
18 |
70,089,123 (GRCm39) |
missense |
probably benign |
0.02 |
R7485:Ccdc68
|
UTSW |
18 |
70,102,084 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7849:Ccdc68
|
UTSW |
18 |
70,080,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R8256:Ccdc68
|
UTSW |
18 |
70,072,018 (GRCm39) |
nonsense |
probably null |
|
R9229:Ccdc68
|
UTSW |
18 |
70,080,203 (GRCm39) |
missense |
probably benign |
0.31 |
R9374:Ccdc68
|
UTSW |
18 |
70,089,113 (GRCm39) |
missense |
probably damaging |
0.98 |
R9551:Ccdc68
|
UTSW |
18 |
70,089,113 (GRCm39) |
missense |
probably damaging |
0.98 |
R9552:Ccdc68
|
UTSW |
18 |
70,089,113 (GRCm39) |
missense |
probably damaging |
0.98 |
R9599:Ccdc68
|
UTSW |
18 |
70,093,492 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Ccdc68
|
UTSW |
18 |
70,094,532 (GRCm39) |
missense |
probably benign |
0.17 |
Z1177:Ccdc68
|
UTSW |
18 |
70,080,121 (GRCm39) |
critical splice acceptor site |
probably null |
|
|