Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrf5 |
G |
T |
17: 43,733,400 (GRCm39) |
D75Y |
possibly damaging |
Het |
Aen |
G |
A |
7: 78,557,050 (GRCm39) |
M299I |
probably damaging |
Het |
Ahi1 |
A |
G |
10: 20,950,332 (GRCm39) |
T128A |
probably benign |
Het |
Bves |
T |
A |
10: 45,229,944 (GRCm39) |
F249L |
probably damaging |
Het |
Capns1 |
T |
C |
7: 29,889,558 (GRCm39) |
I214V |
probably benign |
Het |
Cgnl1 |
G |
T |
9: 71,631,843 (GRCm39) |
Q503K |
possibly damaging |
Het |
Ep300 |
A |
G |
15: 81,514,207 (GRCm39) |
|
probably benign |
Het |
Fam117b |
T |
A |
1: 60,008,177 (GRCm39) |
F337Y |
probably damaging |
Het |
Fam178b |
A |
T |
1: 36,683,435 (GRCm39) |
V95E |
probably damaging |
Het |
Gak |
T |
A |
5: 108,740,236 (GRCm39) |
M560L |
probably damaging |
Het |
Gna11 |
C |
A |
10: 81,366,718 (GRCm39) |
A331S |
probably damaging |
Het |
Gtf3c3 |
A |
C |
1: 54,468,035 (GRCm39) |
F201V |
possibly damaging |
Het |
Kat6b |
G |
A |
14: 21,710,928 (GRCm39) |
R734H |
probably benign |
Het |
Lag3 |
T |
C |
6: 124,886,380 (GRCm39) |
D191G |
probably damaging |
Het |
Mttp |
T |
A |
3: 137,839,758 (GRCm39) |
|
probably null |
Het |
Nlgn3 |
A |
T |
X: 100,363,698 (GRCm39) |
T790S |
probably benign |
Het |
Or11g27 |
A |
G |
14: 50,771,406 (GRCm39) |
D179G |
probably damaging |
Het |
Or5b123 |
G |
A |
19: 13,597,110 (GRCm39) |
E195K |
probably damaging |
Het |
Pkd2l2 |
T |
A |
18: 34,550,068 (GRCm39) |
Y238N |
probably damaging |
Het |
Plg |
A |
T |
17: 12,615,586 (GRCm39) |
|
probably benign |
Het |
Ptprm |
A |
T |
17: 67,349,096 (GRCm39) |
C376S |
probably damaging |
Het |
Rexo1 |
T |
C |
10: 80,385,573 (GRCm39) |
D495G |
probably benign |
Het |
Rims1 |
A |
T |
1: 22,573,256 (GRCm39) |
V315D |
probably damaging |
Het |
Ros1 |
G |
A |
10: 52,018,424 (GRCm39) |
Q745* |
probably null |
Het |
Satb1 |
A |
G |
17: 52,112,317 (GRCm39) |
V99A |
probably damaging |
Het |
Sema3e |
C |
T |
5: 14,282,129 (GRCm39) |
P422S |
probably damaging |
Het |
Stkld1 |
G |
T |
2: 26,841,483 (GRCm39) |
W476L |
probably benign |
Het |
Syna |
T |
C |
5: 134,588,334 (GRCm39) |
D205G |
probably damaging |
Het |
Tas2r134 |
G |
T |
2: 51,517,671 (GRCm39) |
C50F |
probably damaging |
Het |
Togaram1 |
A |
G |
12: 65,027,650 (GRCm39) |
T880A |
probably benign |
Het |
Uckl1 |
T |
C |
2: 181,212,130 (GRCm39) |
E363G |
probably damaging |
Het |
Yeats2 |
T |
A |
16: 19,980,718 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in 1110038F14Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01060:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01063:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01065:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01066:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01067:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01069:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01070:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01131:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01132:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01133:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01134:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01135:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01154:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01155:1110038F14Rik
|
APN |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02472:1110038F14Rik
|
APN |
15 |
76,834,578 (GRCm39) |
missense |
probably damaging |
0.98 |
ANU05:1110038F14Rik
|
UTSW |
15 |
76,834,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R1845:1110038F14Rik
|
UTSW |
15 |
76,833,863 (GRCm39) |
small insertion |
probably benign |
|
R4023:1110038F14Rik
|
UTSW |
15 |
76,833,863 (GRCm39) |
small insertion |
probably benign |
|
|