Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp4b |
A |
G |
8: 13,438,810 (GRCm39) |
F189L |
probably damaging |
Het |
Atp8a1 |
A |
T |
5: 67,922,221 (GRCm39) |
Y372N |
probably benign |
Het |
Bves |
T |
C |
10: 45,245,389 (GRCm39) |
V354A |
probably benign |
Het |
Cd79b |
A |
T |
11: 106,202,836 (GRCm39) |
Y195* |
probably null |
Het |
Cog6 |
A |
C |
3: 52,920,362 (GRCm39) |
D131E |
probably benign |
Het |
Elp3 |
C |
T |
14: 65,785,539 (GRCm39) |
E421K |
possibly damaging |
Het |
Fbxw28 |
A |
T |
9: 109,157,378 (GRCm39) |
F237Y |
probably damaging |
Het |
Fezf1 |
T |
C |
6: 23,247,709 (GRCm39) |
N122S |
probably benign |
Het |
Galnt2 |
A |
G |
8: 125,051,042 (GRCm39) |
K157E |
probably damaging |
Het |
Git2 |
T |
C |
5: 114,871,970 (GRCm39) |
E141G |
possibly damaging |
Het |
Gm26888 |
T |
C |
11: 119,044,853 (GRCm39) |
|
silent |
Het |
Gnrhr |
T |
C |
5: 86,330,108 (GRCm39) |
|
probably null |
Het |
Hoxd13 |
A |
T |
2: 74,500,359 (GRCm39) |
D300V |
probably damaging |
Het |
Hspg2 |
G |
A |
4: 137,275,433 (GRCm39) |
A2748T |
probably benign |
Het |
Hyal2 |
A |
G |
9: 107,448,052 (GRCm39) |
N235S |
probably damaging |
Het |
Itgam |
T |
G |
7: 127,680,830 (GRCm39) |
L253R |
probably damaging |
Het |
Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
Matr3 |
A |
T |
18: 35,716,969 (GRCm39) |
K591N |
possibly damaging |
Het |
Mep1a |
T |
A |
17: 43,785,897 (GRCm39) |
I731F |
possibly damaging |
Het |
Mrtfa |
G |
A |
15: 80,905,124 (GRCm39) |
Q103* |
probably null |
Het |
Muc5b |
A |
G |
7: 141,415,124 (GRCm39) |
D2690G |
possibly damaging |
Het |
Nlrc5 |
A |
G |
8: 95,220,981 (GRCm39) |
Q1140R |
probably benign |
Het |
Or14c39 |
A |
G |
7: 86,343,798 (GRCm39) |
I45V |
probably benign |
Het |
Or5ac23 |
C |
T |
16: 59,148,961 (GRCm39) |
V304I |
probably benign |
Het |
Or6b6 |
A |
G |
7: 106,571,209 (GRCm39) |
L114P |
probably damaging |
Het |
Plcl1 |
T |
C |
1: 55,754,736 (GRCm39) |
F1028L |
probably damaging |
Het |
Plpp2 |
A |
G |
10: 79,363,327 (GRCm39) |
V106A |
possibly damaging |
Het |
Prpf8 |
A |
G |
11: 75,381,528 (GRCm39) |
T255A |
possibly damaging |
Het |
Shoc2 |
A |
G |
19: 54,019,660 (GRCm39) |
I568V |
probably benign |
Het |
Spopl |
C |
T |
2: 23,407,957 (GRCm39) |
V241M |
probably damaging |
Het |
Ssrp1 |
A |
T |
2: 84,868,285 (GRCm39) |
D9V |
probably damaging |
Het |
Strn3 |
A |
T |
12: 51,694,883 (GRCm39) |
D293E |
possibly damaging |
Het |
Tbx3 |
G |
T |
5: 119,818,636 (GRCm39) |
D404Y |
probably damaging |
Het |
Tdrd7 |
T |
C |
4: 46,005,540 (GRCm39) |
S416P |
possibly damaging |
Het |
Tspoap1 |
T |
C |
11: 87,666,429 (GRCm39) |
S947P |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,612,739 (GRCm39) |
S17113R |
probably damaging |
Het |
Ubqln1 |
T |
A |
13: 58,341,202 (GRCm39) |
N183I |
probably damaging |
Het |
Ubr4 |
A |
G |
4: 139,189,167 (GRCm39) |
N3917D |
possibly damaging |
Het |
Ucp2 |
A |
G |
7: 100,148,557 (GRCm39) |
*310W |
probably null |
Het |
Wdr76 |
A |
G |
2: 121,359,314 (GRCm39) |
M218V |
probably damaging |
Het |
Zranb3 |
A |
C |
1: 127,884,392 (GRCm39) |
L998R |
possibly damaging |
Het |
Zxdc |
G |
A |
6: 90,346,792 (GRCm39) |
G51E |
probably damaging |
Het |
|
Other mutations in Trim60 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00467:Trim60
|
APN |
8 |
65,453,371 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL03145:Trim60
|
APN |
8 |
65,453,224 (GRCm39) |
missense |
probably damaging |
0.99 |
R0054:Trim60
|
UTSW |
8 |
65,453,973 (GRCm39) |
missense |
probably benign |
0.05 |
R0054:Trim60
|
UTSW |
8 |
65,453,973 (GRCm39) |
missense |
probably benign |
0.05 |
R0080:Trim60
|
UTSW |
8 |
65,453,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R0244:Trim60
|
UTSW |
8 |
65,453,700 (GRCm39) |
missense |
probably benign |
0.07 |
R0348:Trim60
|
UTSW |
8 |
65,453,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R1104:Trim60
|
UTSW |
8 |
65,454,071 (GRCm39) |
missense |
probably benign |
0.04 |
R1615:Trim60
|
UTSW |
8 |
65,453,162 (GRCm39) |
nonsense |
probably null |
|
R1667:Trim60
|
UTSW |
8 |
65,454,116 (GRCm39) |
missense |
probably benign |
0.00 |
R1944:Trim60
|
UTSW |
8 |
65,453,964 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2009:Trim60
|
UTSW |
8 |
65,453,975 (GRCm39) |
missense |
probably damaging |
0.99 |
R4093:Trim60
|
UTSW |
8 |
65,454,030 (GRCm39) |
missense |
probably benign |
0.05 |
R5171:Trim60
|
UTSW |
8 |
65,453,176 (GRCm39) |
missense |
probably benign |
0.05 |
R5898:Trim60
|
UTSW |
8 |
65,453,016 (GRCm39) |
nonsense |
probably null |
|
R6586:Trim60
|
UTSW |
8 |
65,453,248 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7012:Trim60
|
UTSW |
8 |
65,453,043 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7092:Trim60
|
UTSW |
8 |
65,453,700 (GRCm39) |
missense |
probably benign |
0.07 |
R7274:Trim60
|
UTSW |
8 |
65,453,133 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7567:Trim60
|
UTSW |
8 |
65,454,177 (GRCm39) |
missense |
probably damaging |
0.97 |
R7761:Trim60
|
UTSW |
8 |
65,453,964 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9063:Trim60
|
UTSW |
8 |
65,453,465 (GRCm39) |
missense |
possibly damaging |
0.80 |
|