Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
C |
T |
6: 23,093,895 (GRCm39) |
S142N |
probably null |
Het |
Aida |
A |
G |
1: 183,103,346 (GRCm39) |
Y275C |
probably damaging |
Het |
Arrdc4 |
A |
G |
7: 68,398,594 (GRCm39) |
I74T |
probably benign |
Het |
C1ql4 |
A |
G |
15: 98,985,290 (GRCm39) |
V107A |
probably benign |
Het |
Ccnh |
T |
C |
13: 85,360,884 (GRCm39) |
V284A |
probably benign |
Het |
Cd180 |
A |
G |
13: 102,839,213 (GRCm39) |
E32G |
probably damaging |
Het |
Chd6 |
T |
C |
2: 160,808,174 (GRCm39) |
D1680G |
probably damaging |
Het |
Cog7 |
A |
T |
7: 121,563,516 (GRCm39) |
|
probably null |
Het |
Cyp2j6 |
T |
A |
4: 96,423,741 (GRCm39) |
Q209L |
possibly damaging |
Het |
Dars1 |
A |
T |
1: 128,319,084 (GRCm39) |
V116E |
probably damaging |
Het |
Dnah10 |
A |
G |
5: 124,854,890 (GRCm39) |
K1932E |
probably damaging |
Het |
Dock9 |
A |
G |
14: 121,780,926 (GRCm39) |
S2086P |
probably damaging |
Het |
Espl1 |
C |
G |
15: 102,207,660 (GRCm39) |
R375G |
probably benign |
Het |
Fer1l6 |
C |
T |
15: 58,443,275 (GRCm39) |
S526L |
possibly damaging |
Het |
Galnt9 |
G |
A |
5: 110,768,465 (GRCm39) |
R587H |
probably damaging |
Het |
Gigyf2 |
G |
T |
1: 87,371,396 (GRCm39) |
V1170L |
probably damaging |
Het |
Gm14412 |
G |
T |
2: 177,009,133 (GRCm39) |
T41K |
probably benign |
Het |
Gm45861 |
A |
G |
8: 27,990,086 (GRCm39) |
|
probably null |
Het |
H2bc4 |
T |
C |
13: 23,868,483 (GRCm39) |
I90T |
probably damaging |
Het |
Hoxc5 |
A |
G |
15: 102,922,322 (GRCm39) |
|
probably benign |
Het |
Jkampl |
A |
T |
6: 73,445,918 (GRCm39) |
Y210* |
probably null |
Het |
Klra1 |
T |
C |
6: 130,349,817 (GRCm39) |
D207G |
probably benign |
Het |
Lancl2 |
A |
G |
6: 57,680,240 (GRCm39) |
N57D |
probably benign |
Het |
Map2k4 |
T |
C |
11: 65,582,577 (GRCm39) |
|
probably benign |
Het |
Mgat3 |
G |
T |
15: 80,096,401 (GRCm39) |
Q409H |
probably damaging |
Het |
Mpp3 |
T |
A |
11: 101,892,974 (GRCm39) |
|
probably null |
Het |
Myh1 |
T |
A |
11: 67,105,396 (GRCm39) |
L1062Q |
probably damaging |
Het |
Nebl |
T |
A |
2: 17,439,725 (GRCm39) |
K183* |
probably null |
Het |
Npat |
G |
C |
9: 53,469,458 (GRCm39) |
D315H |
probably damaging |
Het |
Nt5c2 |
A |
G |
19: 46,912,766 (GRCm39) |
V63A |
probably damaging |
Het |
Opn1sw |
T |
A |
6: 29,379,846 (GRCm39) |
E129D |
probably damaging |
Het |
Or10ag2 |
C |
T |
2: 87,248,796 (GRCm39) |
R135C |
probably benign |
Het |
Or1e29 |
T |
G |
11: 73,667,676 (GRCm39) |
H159P |
probably damaging |
Het |
Or51t4 |
A |
T |
7: 102,597,722 (GRCm39) |
T17S |
possibly damaging |
Het |
Or5p1 |
A |
T |
7: 107,916,989 (GRCm39) |
D296V |
probably damaging |
Het |
Prdm16 |
T |
C |
4: 154,407,764 (GRCm39) |
Y1153C |
probably damaging |
Het |
Prdm6 |
T |
A |
18: 53,669,698 (GRCm39) |
D105E |
probably benign |
Het |
Pwwp4c |
C |
T |
X: 73,684,021 (GRCm39) |
R355H |
probably damaging |
Homo |
Rbm27 |
T |
C |
18: 42,434,929 (GRCm39) |
M331T |
probably benign |
Het |
S1pr1 |
A |
G |
3: 115,505,710 (GRCm39) |
Y295H |
probably damaging |
Het |
Sgpp1 |
G |
C |
12: 75,782,243 (GRCm39) |
P32R |
probably benign |
Het |
Sla2 |
C |
T |
2: 156,725,589 (GRCm39) |
S3N |
unknown |
Het |
Slc5a1 |
T |
C |
5: 33,315,460 (GRCm39) |
F493S |
probably benign |
Het |
Snx14 |
A |
T |
9: 88,263,845 (GRCm39) |
Y847N |
probably benign |
Het |
Tmc1 |
A |
G |
19: 20,805,015 (GRCm39) |
|
probably null |
Het |
Vps8 |
C |
A |
16: 21,381,957 (GRCm39) |
Q1130K |
probably benign |
Het |
|
Other mutations in Slc10a6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00335:Slc10a6
|
APN |
5 |
103,756,991 (GRCm39) |
missense |
probably benign |
0.16 |
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 |
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 |
|