Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700048O20Rik |
C |
A |
9: 121,769,833 (GRCm39) |
|
noncoding transcript |
Het |
4930579F01Rik |
C |
A |
3: 137,891,959 (GRCm39) |
|
probably benign |
Het |
Aurkc |
T |
A |
7: 6,999,547 (GRCm39) |
I18N |
probably damaging |
Het |
Bace1 |
T |
C |
9: 45,750,588 (GRCm39) |
|
probably null |
Het |
Chrne |
C |
T |
11: 70,506,588 (GRCm39) |
V311I |
probably benign |
Het |
Cimip2b |
G |
A |
4: 43,428,158 (GRCm39) |
R100W |
possibly damaging |
Het |
Cyp2c70 |
C |
T |
19: 40,156,020 (GRCm39) |
V177M |
probably damaging |
Het |
Dusp10 |
A |
G |
1: 183,801,328 (GRCm39) |
E365G |
probably benign |
Het |
Fcgbp |
C |
A |
7: 27,785,560 (GRCm39) |
N332K |
possibly damaging |
Het |
Irx4 |
T |
C |
13: 73,416,810 (GRCm39) |
V402A |
probably benign |
Het |
Kcnq4 |
G |
A |
4: 120,555,213 (GRCm39) |
Q657* |
probably null |
Het |
Kif14 |
G |
A |
1: 136,396,756 (GRCm39) |
S354N |
probably benign |
Het |
Lama3 |
A |
G |
18: 12,582,645 (GRCm39) |
|
probably benign |
Het |
Lhfpl7 |
A |
G |
5: 113,383,869 (GRCm39) |
R96G |
probably benign |
Het |
Lrrc8b |
T |
C |
5: 105,628,365 (GRCm39) |
I237T |
probably damaging |
Het |
Mepe |
G |
T |
5: 104,485,843 (GRCm39) |
G328C |
probably damaging |
Het |
Numb |
A |
G |
12: 83,854,906 (GRCm39) |
I129T |
probably damaging |
Het |
Or5h25 |
T |
C |
16: 58,930,961 (GRCm39) |
D4G |
probably benign |
Het |
Or6c209 |
T |
C |
10: 129,483,306 (GRCm39) |
I103T |
probably benign |
Het |
Osmr |
T |
C |
15: 6,866,504 (GRCm39) |
D390G |
probably benign |
Het |
Pglyrp3 |
G |
A |
3: 91,929,986 (GRCm39) |
V51I |
probably damaging |
Het |
Phactr2 |
T |
C |
10: 13,121,279 (GRCm39) |
T470A |
probably damaging |
Het |
Psmg1 |
G |
A |
16: 95,781,268 (GRCm39) |
T259I |
possibly damaging |
Het |
Rtl3 |
T |
C |
X: 105,882,543 (GRCm39) |
T240A |
probably benign |
Het |
Ryr1 |
C |
T |
7: 28,824,385 (GRCm39) |
|
probably null |
Het |
Slc1a6 |
T |
C |
10: 78,637,647 (GRCm39) |
L391P |
probably damaging |
Het |
Slc6a7 |
C |
T |
18: 61,134,681 (GRCm39) |
V465M |
possibly damaging |
Het |
Sost |
T |
C |
11: 101,857,705 (GRCm39) |
D32G |
probably damaging |
Het |
Sox4 |
C |
A |
13: 29,136,956 (GRCm39) |
G17W |
probably damaging |
Het |
Tifab |
A |
G |
13: 56,324,282 (GRCm39) |
S54P |
probably damaging |
Het |
Tnrc6a |
T |
A |
7: 122,770,003 (GRCm39) |
S598T |
probably benign |
Het |
Vmn2r1 |
T |
A |
3: 64,012,809 (GRCm39) |
I890N |
probably damaging |
Het |
Wapl |
A |
G |
14: 34,414,593 (GRCm39) |
D485G |
probably benign |
Het |
Wee2 |
A |
T |
6: 40,438,995 (GRCm39) |
I373F |
probably damaging |
Het |
Xkr6 |
A |
G |
14: 64,056,664 (GRCm39) |
T192A |
probably damaging |
Het |
Zfp638 |
A |
G |
6: 83,956,700 (GRCm39) |
D1769G |
probably damaging |
Het |
|
Other mutations in Slc10a6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00428:Slc10a6
|
APN |
5 |
103,760,362 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02893:Slc10a6
|
APN |
5 |
103,776,739 (GRCm39) |
missense |
probably benign |
0.39 |
R0681:Slc10a6
|
UTSW |
5 |
103,760,315 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1300:Slc10a6
|
UTSW |
5 |
103,754,550 (GRCm39) |
missense |
probably benign |
0.28 |
R1636:Slc10a6
|
UTSW |
5 |
103,777,012 (GRCm39) |
missense |
probably benign |
0.00 |
R2127:Slc10a6
|
UTSW |
5 |
103,756,922 (GRCm39) |
missense |
probably benign |
0.00 |
R2129:Slc10a6
|
UTSW |
5 |
103,756,922 (GRCm39) |
missense |
probably benign |
0.00 |
R4789:Slc10a6
|
UTSW |
5 |
103,776,848 (GRCm39) |
missense |
probably benign |
0.03 |
R4908:Slc10a6
|
UTSW |
5 |
103,754,493 (GRCm39) |
missense |
probably benign |
0.00 |
R4976:Slc10a6
|
UTSW |
5 |
103,754,470 (GRCm39) |
missense |
probably benign |
0.04 |
R5309:Slc10a6
|
UTSW |
5 |
103,756,958 (GRCm39) |
missense |
probably damaging |
0.96 |
R6784:Slc10a6
|
UTSW |
5 |
103,776,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R7362:Slc10a6
|
UTSW |
5 |
103,776,992 (GRCm39) |
missense |
probably damaging |
0.99 |
R7658:Slc10a6
|
UTSW |
5 |
103,777,056 (GRCm39) |
missense |
probably damaging |
0.99 |
R7708:Slc10a6
|
UTSW |
5 |
103,777,128 (GRCm39) |
start gained |
probably benign |
|
R8084:Slc10a6
|
UTSW |
5 |
103,760,327 (GRCm39) |
missense |
probably benign |
|
R9145:Slc10a6
|
UTSW |
5 |
103,776,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R9190:Slc10a6
|
UTSW |
5 |
103,765,571 (GRCm39) |
missense |
probably damaging |
0.96 |
R9345:Slc10a6
|
UTSW |
5 |
103,754,521 (GRCm39) |
missense |
probably benign |
0.01 |
RF009:Slc10a6
|
UTSW |
5 |
103,756,858 (GRCm39) |
missense |
probably damaging |
1.00 |
X0022:Slc10a6
|
UTSW |
5 |
103,760,291 (GRCm39) |
missense |
probably benign |
0.00 |
|