Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
C |
A |
11: 9,208,452 (GRCm39) |
|
probably benign |
Het |
Acnat2 |
A |
T |
4: 49,380,131 (GRCm39) |
S398T |
probably benign |
Het |
Adgrb2 |
G |
T |
4: 129,912,635 (GRCm39) |
E1296D |
possibly damaging |
Het |
Adh4 |
C |
T |
3: 138,134,788 (GRCm39) |
|
probably benign |
Het |
Anapc2 |
C |
A |
2: 25,164,725 (GRCm39) |
D322E |
probably benign |
Het |
Apobec1 |
A |
G |
6: 122,565,138 (GRCm39) |
|
probably benign |
Het |
Asic1 |
T |
C |
15: 99,595,353 (GRCm39) |
V393A |
probably benign |
Het |
Cfap65 |
A |
C |
1: 74,959,702 (GRCm39) |
F816C |
probably damaging |
Het |
Cfap69 |
A |
C |
5: 5,631,284 (GRCm39) |
L914R |
probably damaging |
Het |
Cgas |
A |
G |
9: 78,349,802 (GRCm39) |
S187P |
probably benign |
Het |
Cspg4 |
C |
T |
9: 56,805,762 (GRCm39) |
T2191I |
probably benign |
Het |
Cyp11a1 |
T |
A |
9: 57,928,106 (GRCm39) |
I210N |
probably damaging |
Het |
Dgkb |
T |
A |
12: 38,032,009 (GRCm39) |
Y24N |
probably benign |
Het |
Epc1 |
T |
C |
18: 6,449,136 (GRCm39) |
T504A |
possibly damaging |
Het |
Fam135a |
A |
T |
1: 24,094,992 (GRCm39) |
D125E |
probably damaging |
Het |
Fgd3 |
T |
C |
13: 49,433,664 (GRCm39) |
H345R |
possibly damaging |
Het |
Gm12253 |
T |
C |
11: 58,325,379 (GRCm39) |
V17A |
probably damaging |
Het |
Hars1 |
C |
T |
18: 36,903,265 (GRCm39) |
G355D |
probably damaging |
Het |
Hpgd |
A |
T |
8: 56,772,097 (GRCm39) |
I190F |
probably benign |
Het |
Ighv1-34 |
A |
T |
12: 114,815,003 (GRCm39) |
M53K |
probably benign |
Het |
Ildr2 |
A |
T |
1: 166,096,939 (GRCm39) |
T53S |
possibly damaging |
Het |
Ints5 |
T |
A |
19: 8,872,829 (GRCm39) |
C263S |
probably benign |
Het |
Lars2 |
T |
C |
9: 123,224,008 (GRCm39) |
|
probably benign |
Het |
Ldha |
G |
A |
7: 46,504,524 (GRCm39) |
A349T |
possibly damaging |
Het |
Map3k2 |
T |
A |
18: 32,359,684 (GRCm39) |
C512* |
probably null |
Het |
Parp4 |
G |
A |
14: 56,848,245 (GRCm39) |
R687Q |
possibly damaging |
Het |
Plk2 |
T |
C |
13: 110,535,731 (GRCm39) |
S518P |
probably damaging |
Het |
Prrc2b |
T |
G |
2: 32,114,057 (GRCm39) |
V2036G |
possibly damaging |
Het |
Psg16 |
T |
A |
7: 16,827,631 (GRCm39) |
S196T |
probably benign |
Het |
Psme3ip1 |
G |
T |
8: 95,302,380 (GRCm39) |
A217D |
possibly damaging |
Het |
Ranbp17 |
T |
C |
11: 33,450,770 (GRCm39) |
T56A |
possibly damaging |
Het |
Retsat |
T |
C |
6: 72,581,978 (GRCm39) |
|
probably benign |
Het |
Robo3 |
G |
T |
9: 37,335,949 (GRCm39) |
L484I |
probably damaging |
Het |
Septin4 |
G |
T |
11: 87,458,555 (GRCm39) |
G310W |
possibly damaging |
Het |
Slc17a6 |
T |
C |
7: 51,317,705 (GRCm39) |
M446T |
possibly damaging |
Het |
Slc38a1 |
G |
A |
15: 96,521,927 (GRCm39) |
T11M |
probably damaging |
Het |
Tmem138 |
T |
C |
19: 10,548,952 (GRCm39) |
N106S |
probably benign |
Het |
Traf1 |
G |
A |
2: 34,836,879 (GRCm39) |
|
probably benign |
Het |
Tspan8 |
T |
C |
10: 115,675,913 (GRCm39) |
|
probably benign |
Het |
Ubr5 |
T |
C |
15: 37,973,256 (GRCm39) |
E2615G |
probably damaging |
Het |
Vwde |
A |
G |
6: 13,219,977 (GRCm39) |
I58T |
possibly damaging |
Het |
Zc3h12c |
A |
G |
9: 52,027,611 (GRCm39) |
S603P |
probably damaging |
Het |
|
Other mutations in Zfp746 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0020:Zfp746
|
UTSW |
6 |
48,041,641 (GRCm39) |
missense |
probably benign |
0.05 |
R0020:Zfp746
|
UTSW |
6 |
48,041,641 (GRCm39) |
missense |
probably benign |
0.05 |
R0734:Zfp746
|
UTSW |
6 |
48,041,833 (GRCm39) |
missense |
probably damaging |
0.97 |
R1109:Zfp746
|
UTSW |
6 |
48,041,856 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1656:Zfp746
|
UTSW |
6 |
48,041,411 (GRCm39) |
missense |
probably damaging |
0.99 |
R1657:Zfp746
|
UTSW |
6 |
48,059,108 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2474:Zfp746
|
UTSW |
6 |
48,041,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R4748:Zfp746
|
UTSW |
6 |
48,041,490 (GRCm39) |
missense |
probably benign |
0.05 |
R5168:Zfp746
|
UTSW |
6 |
48,041,329 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5386:Zfp746
|
UTSW |
6 |
48,041,110 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5446:Zfp746
|
UTSW |
6 |
48,041,107 (GRCm39) |
missense |
probably damaging |
0.97 |
R5560:Zfp746
|
UTSW |
6 |
48,059,108 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7251:Zfp746
|
UTSW |
6 |
48,041,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R7524:Zfp746
|
UTSW |
6 |
48,041,823 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9502:Zfp746
|
UTSW |
6 |
48,041,397 (GRCm39) |
missense |
probably damaging |
0.97 |
|