Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
T |
C |
6: 23,075,828 (GRCm39) |
I770V |
probably benign |
Het |
Abtb3 |
C |
A |
10: 85,223,762 (GRCm39) |
N190K |
unknown |
Het |
Actr10 |
T |
C |
12: 70,989,073 (GRCm39) |
L64S |
probably damaging |
Het |
Adam22 |
T |
C |
5: 8,177,343 (GRCm39) |
T589A |
probably benign |
Het |
Akr1b7 |
T |
C |
6: 34,395,977 (GRCm39) |
S160P |
probably damaging |
Het |
Ankrd52 |
C |
T |
10: 128,217,850 (GRCm39) |
H277Y |
probably damaging |
Het |
Cc2d1b |
T |
A |
4: 108,482,062 (GRCm39) |
L112Q |
probably damaging |
Het |
Cd200r3 |
T |
A |
16: 44,773,750 (GRCm39) |
|
probably benign |
Het |
Clec3a |
A |
G |
8: 115,152,375 (GRCm39) |
D127G |
probably damaging |
Het |
Cnnm3 |
T |
C |
1: 36,551,962 (GRCm39) |
L324P |
probably damaging |
Het |
Cspp1 |
T |
C |
1: 10,147,469 (GRCm39) |
|
probably null |
Het |
Cwf19l1 |
C |
T |
19: 44,124,274 (GRCm39) |
|
probably benign |
Het |
Cyp26b1 |
G |
A |
6: 84,551,379 (GRCm39) |
T470I |
probably damaging |
Het |
Dedd2 |
A |
G |
7: 24,917,092 (GRCm39) |
V110A |
probably benign |
Het |
Dnah8 |
A |
G |
17: 30,975,729 (GRCm39) |
I2866M |
possibly damaging |
Het |
Dpp10 |
T |
C |
1: 123,360,667 (GRCm39) |
Y286C |
probably damaging |
Het |
Efna2 |
C |
T |
10: 80,024,524 (GRCm39) |
P177L |
probably damaging |
Het |
Fbxo46 |
A |
G |
7: 18,869,325 (GRCm39) |
|
probably benign |
Het |
Gdpd5 |
A |
T |
7: 99,108,048 (GRCm39) |
T542S |
probably benign |
Het |
Gm136 |
T |
G |
4: 34,750,928 (GRCm39) |
D115A |
possibly damaging |
Het |
Gm7356 |
T |
A |
17: 14,221,687 (GRCm39) |
K114I |
possibly damaging |
Het |
Grk4 |
T |
C |
5: 34,905,653 (GRCm39) |
I466T |
|
Het |
Hic1 |
A |
G |
11: 75,060,332 (GRCm39) |
M5T |
unknown |
Het |
Hmcn2 |
C |
A |
2: 31,303,685 (GRCm39) |
N3058K |
probably benign |
Het |
Htr5a |
T |
A |
5: 28,055,799 (GRCm39) |
H263Q |
probably benign |
Het |
Lrrc7 |
T |
C |
3: 157,946,138 (GRCm39) |
K187R |
probably benign |
Het |
Map3k8 |
A |
T |
18: 4,340,557 (GRCm39) |
H252Q |
probably benign |
Het |
Muc4 |
CAC |
CACTAC |
16: 32,575,367 (GRCm39) |
|
probably benign |
Het |
Naa16 |
A |
T |
14: 79,612,289 (GRCm39) |
M233K |
probably benign |
Het |
Napsa |
A |
T |
7: 44,235,223 (GRCm39) |
D336V |
probably damaging |
Het |
Neurod1 |
T |
A |
2: 79,285,218 (GRCm39) |
N55I |
possibly damaging |
Het |
Or10d5 |
A |
T |
9: 39,862,087 (GRCm39) |
|
probably benign |
Het |
Or4c115 |
A |
T |
2: 88,927,369 (GRCm39) |
C301S |
probably benign |
Het |
Or5an9 |
T |
C |
19: 12,187,703 (GRCm39) |
F258L |
probably damaging |
Het |
Or8b12 |
T |
A |
9: 37,657,963 (GRCm39) |
C178S |
probably damaging |
Het |
Pcdha8 |
G |
T |
18: 37,127,323 (GRCm39) |
G602C |
probably damaging |
Het |
Peg10 |
T |
TCCG |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Pigr |
G |
A |
1: 130,774,231 (GRCm39) |
V404M |
probably damaging |
Het |
Plch1 |
G |
A |
3: 63,612,036 (GRCm39) |
P803L |
probably damaging |
Het |
Ppp4r3b |
T |
A |
11: 29,159,396 (GRCm39) |
F583L |
probably benign |
Het |
Rit2 |
A |
T |
18: 31,108,468 (GRCm39) |
D172E |
possibly damaging |
Het |
Skint4 |
C |
T |
4: 112,022,932 (GRCm39) |
P476S |
possibly damaging |
Het |
Slco2b1 |
A |
G |
7: 99,320,171 (GRCm39) |
V353A |
probably benign |
Het |
Slit3 |
A |
G |
11: 35,574,917 (GRCm39) |
D1077G |
probably damaging |
Het |
Sun2 |
A |
G |
15: 79,612,252 (GRCm39) |
F478L |
probably benign |
Het |
Syt6 |
C |
A |
3: 103,494,825 (GRCm39) |
C263* |
probably null |
Het |
Tfpi |
C |
A |
2: 84,273,235 (GRCm39) |
L229F |
unknown |
Het |
Tmem131l |
A |
T |
3: 83,817,775 (GRCm39) |
C1242S |
probably benign |
Het |
Ttc3 |
T |
A |
16: 94,204,219 (GRCm39) |
W280R |
probably damaging |
Het |
Uncx |
A |
G |
5: 139,532,573 (GRCm39) |
K213E |
possibly damaging |
Het |
Usp24 |
T |
C |
4: 106,232,875 (GRCm39) |
L887P |
probably benign |
Het |
Vmn1r178 |
A |
T |
7: 23,593,404 (GRCm39) |
I151F |
probably damaging |
Het |
Vmn2r50 |
G |
T |
7: 9,772,061 (GRCm39) |
Q547K |
possibly damaging |
Het |
Vwf |
A |
G |
6: 125,625,792 (GRCm39) |
|
probably benign |
Het |
Wdfy3 |
A |
T |
5: 102,000,451 (GRCm39) |
V2973D |
probably benign |
Het |
Zbtb49 |
T |
C |
5: 38,358,289 (GRCm39) |
M655V |
probably benign |
Het |
Zc3h3 |
C |
T |
15: 75,711,499 (GRCm39) |
A321T |
probably benign |
Het |
Zeb2 |
T |
A |
2: 45,000,040 (GRCm39) |
R65W |
possibly damaging |
Het |
Zfp541 |
A |
G |
7: 15,812,376 (GRCm39) |
E343G |
probably damaging |
Het |
Zfp775 |
C |
A |
6: 48,597,151 (GRCm39) |
R342S |
probably damaging |
Het |
Zwilch |
A |
G |
9: 64,075,942 (GRCm39) |
F27L |
probably benign |
Het |
|
Other mutations in Gpr180 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02212:Gpr180
|
APN |
14 |
118,397,588 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02449:Gpr180
|
APN |
14 |
118,397,532 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02740:Gpr180
|
APN |
14 |
118,377,161 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03103:Gpr180
|
APN |
14 |
118,377,175 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0321:Gpr180
|
UTSW |
14 |
118,385,699 (GRCm39) |
critical splice donor site |
probably null |
|
R0545:Gpr180
|
UTSW |
14 |
118,397,458 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0688:Gpr180
|
UTSW |
14 |
118,385,596 (GRCm39) |
missense |
probably benign |
0.00 |
R0844:Gpr180
|
UTSW |
14 |
118,395,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R2566:Gpr180
|
UTSW |
14 |
118,377,185 (GRCm39) |
missense |
probably benign |
0.06 |
R5334:Gpr180
|
UTSW |
14 |
118,397,468 (GRCm39) |
missense |
probably damaging |
0.99 |
R5378:Gpr180
|
UTSW |
14 |
118,377,251 (GRCm39) |
missense |
probably benign |
|
R5583:Gpr180
|
UTSW |
14 |
118,400,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R6081:Gpr180
|
UTSW |
14 |
118,391,086 (GRCm39) |
missense |
probably benign |
0.02 |
R6851:Gpr180
|
UTSW |
14 |
118,391,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R7382:Gpr180
|
UTSW |
14 |
118,400,035 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7798:Gpr180
|
UTSW |
14 |
118,391,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R8159:Gpr180
|
UTSW |
14 |
118,391,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R8950:Gpr180
|
UTSW |
14 |
118,395,452 (GRCm39) |
missense |
probably benign |
0.24 |
R9231:Gpr180
|
UTSW |
14 |
118,395,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R9696:Gpr180
|
UTSW |
14 |
118,391,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R9697:Gpr180
|
UTSW |
14 |
118,391,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R9698:Gpr180
|
UTSW |
14 |
118,391,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R9701:Gpr180
|
UTSW |
14 |
118,391,302 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Gpr180
|
UTSW |
14 |
118,385,613 (GRCm39) |
missense |
probably damaging |
0.98 |
|