Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
T |
A |
5: 8,984,320 (GRCm39) |
N683K |
probably benign |
Het |
Atad2b |
T |
A |
12: 5,060,351 (GRCm39) |
H915Q |
probably benign |
Het |
Bltp2 |
T |
C |
11: 78,160,367 (GRCm39) |
S609P |
probably damaging |
Het |
Camk1d |
G |
T |
2: 5,449,908 (GRCm39) |
P91Q |
probably benign |
Het |
Camk1d |
G |
C |
2: 5,449,910 (GRCm39) |
S90R |
probably damaging |
Het |
Card11 |
T |
C |
5: 140,885,524 (GRCm39) |
E345G |
probably damaging |
Het |
Ccpg1 |
G |
T |
9: 72,920,526 (GRCm39) |
V714L |
possibly damaging |
Het |
Chst9 |
T |
C |
18: 15,586,254 (GRCm39) |
E103G |
possibly damaging |
Het |
Cnga1 |
C |
T |
5: 72,762,615 (GRCm39) |
V300I |
probably benign |
Het |
Crb1 |
T |
C |
1: 139,159,337 (GRCm39) |
Y1295C |
probably damaging |
Het |
Dnah5 |
A |
G |
15: 28,402,014 (GRCm39) |
T3392A |
probably benign |
Het |
Elp3 |
C |
A |
14: 65,785,439 (GRCm39) |
R473L |
probably damaging |
Het |
Epgn |
T |
A |
5: 91,181,807 (GRCm39) |
I145N |
probably benign |
Het |
Fam107b |
G |
A |
2: 3,779,457 (GRCm39) |
G220D |
probably damaging |
Het |
Fbn2 |
A |
G |
18: 58,257,383 (GRCm39) |
V328A |
probably benign |
Het |
Fn1 |
A |
T |
1: 71,639,481 (GRCm39) |
I1770N |
probably damaging |
Het |
Fndc1 |
T |
A |
17: 7,988,585 (GRCm39) |
Y1159F |
unknown |
Het |
Frem2 |
A |
G |
3: 53,444,679 (GRCm39) |
L2484P |
probably damaging |
Het |
Grk2 |
C |
T |
19: 4,340,496 (GRCm39) |
R295H |
probably damaging |
Het |
Gtf3c1 |
A |
T |
7: 125,243,237 (GRCm39) |
V1789D |
possibly damaging |
Het |
Hmgcl |
T |
C |
4: 135,677,898 (GRCm39) |
V33A |
probably damaging |
Het |
Ighv7-1 |
A |
G |
12: 113,860,239 (GRCm39) |
F51S |
probably damaging |
Het |
Kcna6 |
A |
G |
6: 126,716,688 (GRCm39) |
L67P |
probably damaging |
Het |
Lamc1 |
A |
T |
1: 153,123,030 (GRCm39) |
V720E |
probably benign |
Het |
Lrch1 |
T |
C |
14: 75,054,558 (GRCm39) |
D312G |
probably damaging |
Het |
Mix23 |
A |
G |
16: 35,905,427 (GRCm39) |
N63S |
probably benign |
Het |
Nav2 |
A |
G |
7: 49,206,794 (GRCm39) |
T1540A |
probably damaging |
Het |
Nisch |
A |
T |
14: 30,913,373 (GRCm39) |
|
probably benign |
Het |
Nos1ap |
T |
A |
1: 170,176,968 (GRCm39) |
K145M |
probably damaging |
Het |
Npc1l1 |
A |
G |
11: 6,177,839 (GRCm39) |
Y524H |
probably damaging |
Het |
Nrap |
T |
C |
19: 56,377,916 (GRCm39) |
T25A |
possibly damaging |
Het |
Nusap1 |
A |
G |
2: 119,477,580 (GRCm39) |
K363R |
probably damaging |
Het |
Or5ar1 |
T |
C |
2: 85,671,656 (GRCm39) |
T160A |
probably damaging |
Het |
Or7e177 |
T |
A |
9: 20,212,390 (GRCm39) |
L298Q |
probably damaging |
Het |
Pde4d |
T |
C |
13: 110,074,547 (GRCm39) |
I384T |
probably damaging |
Het |
Pkhd1 |
T |
A |
1: 20,593,875 (GRCm39) |
R1413* |
probably null |
Het |
Plcd3 |
T |
A |
11: 102,964,592 (GRCm39) |
Y593F |
possibly damaging |
Het |
Plxna1 |
A |
T |
6: 89,310,087 (GRCm39) |
I1026N |
possibly damaging |
Het |
Podxl |
T |
A |
6: 31,501,329 (GRCm39) |
I409F |
probably damaging |
Het |
Polq |
A |
C |
16: 36,837,625 (GRCm39) |
Q179P |
probably benign |
Het |
Pomt1 |
T |
C |
2: 32,137,602 (GRCm39) |
V401A |
probably damaging |
Het |
Qdpr |
C |
T |
5: 45,596,727 (GRCm39) |
G146S |
probably damaging |
Het |
Shc4 |
T |
A |
2: 125,512,218 (GRCm39) |
Q2L |
probably damaging |
Het |
Skint8 |
T |
A |
4: 111,807,387 (GRCm39) |
C358S |
probably benign |
Het |
Smc5 |
T |
C |
19: 23,221,467 (GRCm39) |
E354G |
possibly damaging |
Het |
Snx30 |
T |
C |
4: 59,868,275 (GRCm39) |
V129A |
probably damaging |
Het |
Sp110 |
G |
C |
1: 85,504,923 (GRCm39) |
|
probably benign |
Het |
Spag6 |
T |
A |
2: 18,703,613 (GRCm39) |
|
probably benign |
Het |
Trim28 |
T |
A |
7: 12,763,036 (GRCm39) |
Y450N |
probably benign |
Het |
Trip11 |
C |
T |
12: 101,851,924 (GRCm39) |
W428* |
probably null |
Het |
Umodl1 |
T |
A |
17: 31,213,761 (GRCm39) |
V966E |
probably damaging |
Het |
Utf1 |
A |
G |
7: 139,524,704 (GRCm39) |
|
probably benign |
Het |
Vmn1r72 |
T |
C |
7: 11,403,776 (GRCm39) |
Y224C |
probably damaging |
Het |
Whrn |
A |
G |
4: 63,334,825 (GRCm39) |
S748P |
probably damaging |
Het |
Zbtb41 |
T |
A |
1: 139,359,816 (GRCm39) |
|
probably null |
Het |
Zfhx3 |
T |
C |
8: 109,526,964 (GRCm39) |
F954L |
probably damaging |
Het |
Zfp456 |
A |
T |
13: 67,514,359 (GRCm39) |
I449K |
probably benign |
Het |
|
Other mutations in Or5b124 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00236:Or5b124
|
APN |
19 |
13,610,903 (GRCm39) |
missense |
probably benign |
0.25 |
IGL03052:Or5b124
|
UTSW |
19 |
13,611,090 (GRCm39) |
missense |
probably benign |
0.00 |
R0179:Or5b124
|
UTSW |
19 |
13,610,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R0270:Or5b124
|
UTSW |
19 |
13,611,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R0633:Or5b124
|
UTSW |
19 |
13,610,700 (GRCm39) |
missense |
probably damaging |
0.99 |
R4466:Or5b124
|
UTSW |
19 |
13,610,801 (GRCm39) |
missense |
probably damaging |
0.97 |
R4884:Or5b124
|
UTSW |
19 |
13,611,391 (GRCm39) |
missense |
probably benign |
0.14 |
R5247:Or5b124
|
UTSW |
19 |
13,610,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R5332:Or5b124
|
UTSW |
19 |
13,610,729 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6165:Or5b124
|
UTSW |
19 |
13,610,952 (GRCm39) |
missense |
probably benign |
0.02 |
R6165:Or5b124
|
UTSW |
19 |
13,610,507 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6221:Or5b124
|
UTSW |
19 |
13,610,830 (GRCm39) |
nonsense |
probably null |
|
R6486:Or5b124
|
UTSW |
19 |
13,611,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R7008:Or5b124
|
UTSW |
19 |
13,610,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R7076:Or5b124
|
UTSW |
19 |
13,611,244 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7539:Or5b124
|
UTSW |
19 |
13,610,933 (GRCm39) |
nonsense |
probably null |
|
R8278:Or5b124
|
UTSW |
19 |
13,610,958 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8708:Or5b124
|
UTSW |
19 |
13,611,401 (GRCm39) |
missense |
probably benign |
0.00 |
R9169:Or5b124
|
UTSW |
19 |
13,610,903 (GRCm39) |
missense |
probably benign |
|
R9185:Or5b124
|
UTSW |
19 |
13,610,765 (GRCm39) |
missense |
probably benign |
0.03 |
R9200:Or5b124
|
UTSW |
19 |
13,610,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R9229:Or5b124
|
UTSW |
19 |
13,611,414 (GRCm39) |
missense |
probably damaging |
0.98 |
R9381:Or5b124
|
UTSW |
19 |
13,610,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R9708:Or5b124
|
UTSW |
19 |
13,610,760 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Or5b124
|
UTSW |
19 |
13,610,817 (GRCm39) |
missense |
probably damaging |
1.00 |
|