Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921536K21Rik |
T |
C |
11: 3,844,987 (GRCm39) |
D34G |
probably benign |
Het |
Adam6a |
T |
C |
12: 113,508,337 (GRCm39) |
S237P |
probably damaging |
Het |
Adamts13 |
A |
C |
2: 26,871,092 (GRCm39) |
D235A |
probably benign |
Het |
Adgb |
T |
A |
10: 10,233,623 (GRCm39) |
M1259L |
probably benign |
Het |
Apbb1 |
T |
C |
7: 105,214,510 (GRCm39) |
Q529R |
probably damaging |
Het |
Bcl2 |
G |
A |
1: 106,640,292 (GRCm39) |
R107C |
probably damaging |
Het |
Camta1 |
T |
C |
4: 151,670,888 (GRCm39) |
T96A |
possibly damaging |
Het |
Cep170b |
T |
C |
12: 112,703,240 (GRCm39) |
Y568H |
probably damaging |
Het |
Clca4b |
A |
T |
3: 144,627,741 (GRCm39) |
I410N |
probably damaging |
Het |
Cnot10 |
G |
A |
9: 114,427,838 (GRCm39) |
T592I |
probably benign |
Het |
Col6a3 |
C |
T |
1: 90,755,771 (GRCm39) |
A173T |
probably damaging |
Het |
Ctcf |
T |
A |
8: 106,402,789 (GRCm39) |
C560* |
probably null |
Het |
Daglb |
G |
A |
5: 143,472,951 (GRCm39) |
V369I |
probably benign |
Het |
Defb19 |
G |
A |
2: 152,422,146 (GRCm39) |
L8F |
unknown |
Het |
Emcn |
G |
T |
3: 137,078,608 (GRCm39) |
E65* |
probably null |
Het |
Etl4 |
G |
T |
2: 20,782,940 (GRCm39) |
R753L |
probably damaging |
Het |
Fam151b |
T |
C |
13: 92,586,689 (GRCm39) |
Y248C |
probably benign |
Het |
Fmo1 |
T |
C |
1: 162,663,704 (GRCm39) |
D275G |
probably benign |
Het |
Gjd4 |
A |
G |
18: 9,280,964 (GRCm39) |
V38A |
possibly damaging |
Het |
Hivep1 |
T |
C |
13: 42,311,855 (GRCm39) |
V1365A |
possibly damaging |
Het |
Hivep2 |
T |
C |
10: 14,005,702 (GRCm39) |
S767P |
possibly damaging |
Het |
Hoxa6 |
T |
C |
6: 52,183,548 (GRCm39) |
T166A |
possibly damaging |
Het |
Ift80 |
G |
T |
3: 68,843,232 (GRCm39) |
L367I |
probably benign |
Het |
Igf2bp1 |
T |
C |
11: 95,859,719 (GRCm39) |
N369S |
possibly damaging |
Het |
Igsf11 |
C |
A |
16: 38,829,179 (GRCm39) |
D24E |
probably benign |
Het |
Ints5 |
C |
T |
19: 8,873,114 (GRCm39) |
L358F |
probably damaging |
Het |
Kbtbd3 |
A |
G |
9: 4,330,519 (GRCm39) |
T298A |
possibly damaging |
Het |
Kif28 |
C |
A |
1: 179,558,818 (GRCm39) |
V297F |
probably damaging |
Het |
Krt12 |
T |
C |
11: 99,308,771 (GRCm39) |
Y422C |
probably damaging |
Het |
Lig1 |
T |
A |
7: 13,043,122 (GRCm39) |
W856R |
probably damaging |
Het |
Liph |
C |
T |
16: 21,786,730 (GRCm39) |
|
probably null |
Het |
Lrig3 |
T |
A |
10: 125,849,317 (GRCm39) |
C1012* |
probably null |
Het |
Lrit1 |
A |
G |
14: 36,782,182 (GRCm39) |
E285G |
probably damaging |
Het |
Lrrc31 |
A |
G |
3: 30,743,377 (GRCm39) |
V196A |
probably benign |
Het |
Lrrn4 |
T |
C |
2: 132,712,363 (GRCm39) |
T487A |
probably benign |
Het |
Mllt10 |
T |
C |
2: 18,167,424 (GRCm39) |
Y372H |
probably damaging |
Het |
Mrpl50 |
A |
T |
4: 49,514,515 (GRCm39) |
V52E |
probably damaging |
Het |
Mthfd1l |
T |
C |
10: 4,006,766 (GRCm39) |
V676A |
probably damaging |
Het |
Ncl |
C |
T |
1: 86,284,362 (GRCm39) |
D245N |
possibly damaging |
Het |
Neil1 |
A |
T |
9: 57,054,065 (GRCm39) |
|
probably null |
Het |
Nfatc3 |
A |
G |
8: 106,818,827 (GRCm39) |
E515G |
probably damaging |
Het |
Nlrp4b |
A |
G |
7: 10,449,108 (GRCm39) |
E70G |
possibly damaging |
Het |
Nme3 |
A |
T |
17: 25,115,491 (GRCm39) |
I2F |
possibly damaging |
Het |
Nup210 |
G |
A |
6: 91,051,292 (GRCm39) |
H364Y |
probably benign |
Het |
Nxpe3 |
T |
A |
16: 55,686,898 (GRCm39) |
T37S |
probably benign |
Het |
Olfm1 |
T |
A |
2: 28,102,554 (GRCm39) |
M76K |
probably benign |
Het |
Pgbd5 |
A |
T |
8: 125,160,771 (GRCm39) |
V32E |
probably damaging |
Het |
Plcb4 |
T |
C |
2: 135,810,339 (GRCm39) |
M646T |
probably damaging |
Het |
Plekha7 |
G |
A |
7: 115,757,255 (GRCm39) |
P565L |
probably damaging |
Het |
Poc5 |
A |
G |
13: 96,535,374 (GRCm39) |
D213G |
probably null |
Het |
Poli |
A |
G |
18: 70,656,452 (GRCm39) |
I125T |
probably benign |
Het |
Ppm1f |
T |
C |
16: 16,721,254 (GRCm39) |
M1T |
probably null |
Het |
Psmd7 |
T |
C |
8: 108,307,523 (GRCm39) |
K320R |
unknown |
Het |
Rabggtb |
A |
G |
3: 153,615,954 (GRCm39) |
V128A |
probably damaging |
Het |
Rasa2 |
A |
T |
9: 96,454,012 (GRCm39) |
L308H |
probably damaging |
Het |
Serpina1d |
C |
T |
12: 103,730,034 (GRCm39) |
V383M |
probably benign |
Het |
Sipa1l1 |
T |
C |
12: 82,431,530 (GRCm39) |
|
probably null |
Het |
Sos1 |
T |
C |
17: 80,715,740 (GRCm39) |
T1006A |
probably benign |
Het |
Sugp1 |
T |
A |
8: 70,522,658 (GRCm39) |
Y453N |
probably damaging |
Het |
Taf3 |
A |
T |
2: 10,047,455 (GRCm39) |
D64E |
probably benign |
Het |
Tcf19 |
A |
T |
17: 35,826,801 (GRCm39) |
|
probably null |
Het |
Trim60 |
T |
A |
8: 65,453,868 (GRCm39) |
H127L |
probably damaging |
Het |
Tubb4a |
C |
T |
17: 57,387,770 (GRCm39) |
V419M |
probably damaging |
Het |
Vmn2r22 |
G |
T |
6: 123,614,684 (GRCm39) |
T302K |
probably damaging |
Het |
Vmn2r68 |
T |
G |
7: 84,870,884 (GRCm39) |
T800P |
possibly damaging |
Het |
Zfhx2 |
A |
C |
14: 55,300,965 (GRCm39) |
V2262G |
probably damaging |
Het |
|
Other mutations in Ccdc148 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01362:Ccdc148
|
APN |
2 |
58,719,811 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02056:Ccdc148
|
APN |
2 |
58,894,081 (GRCm39) |
splice site |
probably benign |
|
IGL02470:Ccdc148
|
APN |
2 |
58,891,911 (GRCm39) |
missense |
probably damaging |
0.96 |
PIT4585001:Ccdc148
|
UTSW |
2 |
58,872,988 (GRCm39) |
missense |
probably benign |
0.01 |
R0068:Ccdc148
|
UTSW |
2 |
58,717,629 (GRCm39) |
missense |
probably benign |
|
R0068:Ccdc148
|
UTSW |
2 |
58,717,629 (GRCm39) |
missense |
probably benign |
|
R1464:Ccdc148
|
UTSW |
2 |
58,824,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Ccdc148
|
UTSW |
2 |
58,824,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Ccdc148
|
UTSW |
2 |
58,796,374 (GRCm39) |
nonsense |
probably null |
|
R1464:Ccdc148
|
UTSW |
2 |
58,796,374 (GRCm39) |
nonsense |
probably null |
|
R1675:Ccdc148
|
UTSW |
2 |
58,870,566 (GRCm39) |
missense |
probably damaging |
0.96 |
R1677:Ccdc148
|
UTSW |
2 |
58,892,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R1832:Ccdc148
|
UTSW |
2 |
58,891,911 (GRCm39) |
missense |
probably damaging |
0.96 |
R1918:Ccdc148
|
UTSW |
2 |
58,872,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R2114:Ccdc148
|
UTSW |
2 |
58,892,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R2115:Ccdc148
|
UTSW |
2 |
58,892,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R4657:Ccdc148
|
UTSW |
2 |
58,891,900 (GRCm39) |
missense |
probably benign |
0.04 |
R4921:Ccdc148
|
UTSW |
2 |
58,719,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R5022:Ccdc148
|
UTSW |
2 |
58,717,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R5809:Ccdc148
|
UTSW |
2 |
58,713,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R6164:Ccdc148
|
UTSW |
2 |
58,713,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R6952:Ccdc148
|
UTSW |
2 |
58,713,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R6987:Ccdc148
|
UTSW |
2 |
58,872,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R7121:Ccdc148
|
UTSW |
2 |
58,717,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R7452:Ccdc148
|
UTSW |
2 |
58,717,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R7493:Ccdc148
|
UTSW |
2 |
58,899,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Ccdc148
|
UTSW |
2 |
58,713,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R7666:Ccdc148
|
UTSW |
2 |
58,824,512 (GRCm39) |
missense |
probably damaging |
0.99 |
R7763:Ccdc148
|
UTSW |
2 |
58,713,648 (GRCm39) |
missense |
probably benign |
|
R8045:Ccdc148
|
UTSW |
2 |
58,892,083 (GRCm39) |
critical splice donor site |
probably null |
|
R8865:Ccdc148
|
UTSW |
2 |
58,719,832 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8932:Ccdc148
|
UTSW |
2 |
58,894,054 (GRCm39) |
missense |
probably benign |
0.40 |
R9597:Ccdc148
|
UTSW |
2 |
58,893,397 (GRCm39) |
missense |
probably benign |
0.08 |
X0062:Ccdc148
|
UTSW |
2 |
58,893,460 (GRCm39) |
missense |
probably damaging |
0.98 |
|