Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930431F12Rik |
A |
T |
5: 45,125,156 (GRCm39) |
|
noncoding transcript |
Het |
Abca12 |
A |
T |
1: 71,323,315 (GRCm39) |
I1589N |
probably benign |
Het |
Abca8a |
T |
G |
11: 109,950,801 (GRCm39) |
D888A |
probably benign |
Het |
Adam5 |
C |
T |
8: 25,232,150 (GRCm39) |
|
probably benign |
Het |
Amer1 |
A |
T |
X: 94,470,716 (GRCm39) |
N467K |
probably benign |
Het |
Atp6v0a2 |
A |
G |
5: 124,783,968 (GRCm39) |
D272G |
probably damaging |
Het |
Cacna1b |
A |
T |
2: 24,575,794 (GRCm39) |
N751K |
probably damaging |
Het |
Cfi |
T |
A |
3: 129,652,080 (GRCm39) |
N250K |
probably damaging |
Het |
Cndp2 |
G |
T |
18: 84,689,002 (GRCm39) |
P260Q |
possibly damaging |
Het |
Cnnm3 |
A |
G |
1: 36,551,956 (GRCm39) |
D322G |
probably benign |
Het |
Crybg1 |
A |
T |
10: 43,851,054 (GRCm39) |
S1606T |
possibly damaging |
Het |
Crybg1 |
A |
G |
10: 43,879,596 (GRCm39) |
S531P |
probably damaging |
Het |
Espnl |
A |
T |
1: 91,268,333 (GRCm39) |
K320* |
probably null |
Het |
Glt1d1 |
A |
G |
5: 127,709,384 (GRCm39) |
T13A |
possibly damaging |
Het |
Gpam |
C |
T |
19: 55,066,764 (GRCm39) |
A584T |
possibly damaging |
Het |
Gpr19 |
A |
G |
6: 134,846,705 (GRCm39) |
I289T |
probably damaging |
Het |
Grm8 |
T |
C |
6: 27,363,800 (GRCm39) |
I572V |
probably damaging |
Het |
Gtpbp4 |
A |
T |
13: 9,027,308 (GRCm39) |
N502K |
probably benign |
Het |
Herpud2 |
T |
C |
9: 25,062,247 (GRCm39) |
M6V |
probably benign |
Het |
Igdcc3 |
T |
C |
9: 65,085,724 (GRCm39) |
V263A |
probably damaging |
Het |
Il33 |
G |
A |
19: 29,930,156 (GRCm39) |
A65T |
probably benign |
Het |
Itga9 |
T |
A |
9: 118,598,227 (GRCm39) |
M1K |
probably null |
Het |
Izumo3 |
T |
C |
4: 92,035,217 (GRCm39) |
|
probably benign |
Het |
Kdr |
G |
A |
5: 76,110,261 (GRCm39) |
P909S |
probably damaging |
Het |
Kirrel1 |
C |
T |
3: 86,997,182 (GRCm39) |
E262K |
probably benign |
Het |
Lgi2 |
G |
T |
5: 52,711,807 (GRCm39) |
P195Q |
probably benign |
Het |
Lpcat3 |
T |
C |
6: 124,676,301 (GRCm39) |
F120S |
possibly damaging |
Het |
Nalcn |
C |
T |
14: 123,554,661 (GRCm39) |
R910Q |
probably benign |
Het |
Nrxn1 |
A |
G |
17: 90,366,902 (GRCm39) |
|
probably null |
Het |
Nuf2 |
A |
T |
1: 169,326,431 (GRCm39) |
V440E |
probably benign |
Het |
Or10ag60 |
T |
A |
2: 87,437,852 (GRCm39) |
I40N |
possibly damaging |
Het |
Or4f14 |
C |
T |
2: 111,742,652 (GRCm39) |
V208M |
probably benign |
Het |
Or51ah3 |
C |
T |
7: 103,210,008 (GRCm39) |
S108F |
probably benign |
Het |
Or6c205 |
T |
C |
10: 129,086,865 (GRCm39) |
I154T |
possibly damaging |
Het |
Pfpl |
A |
G |
19: 12,405,974 (GRCm39) |
D75G |
probably damaging |
Het |
Pgm5 |
A |
G |
19: 24,812,130 (GRCm39) |
V134A |
possibly damaging |
Het |
Prkch |
A |
G |
12: 73,805,787 (GRCm39) |
I521V |
possibly damaging |
Het |
Rps6kc1 |
T |
A |
1: 190,515,822 (GRCm39) |
E968V |
probably benign |
Het |
Slc25a30 |
T |
C |
14: 76,007,037 (GRCm39) |
Y153C |
probably damaging |
Het |
Smtnl2 |
T |
A |
11: 72,292,171 (GRCm39) |
|
probably null |
Het |
Spmip4 |
C |
A |
6: 50,551,175 (GRCm39) |
V425L |
probably benign |
Het |
Tbc1d14 |
T |
A |
5: 36,700,544 (GRCm39) |
K275* |
probably null |
Het |
Tnc |
T |
C |
4: 63,931,314 (GRCm39) |
T799A |
probably benign |
Het |
Trdn |
A |
T |
10: 33,181,094 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
C |
2: 76,706,879 (GRCm39) |
|
probably benign |
Het |
Uaca |
T |
C |
9: 60,779,507 (GRCm39) |
M1296T |
probably benign |
Het |
Ubash3a |
A |
C |
17: 31,434,116 (GRCm39) |
I154L |
probably benign |
Het |
Vmn2r4 |
T |
A |
3: 64,317,200 (GRCm39) |
|
probably null |
Het |
Xpc |
T |
C |
6: 91,467,089 (GRCm39) |
K915E |
probably benign |
Het |
Zfp318 |
T |
C |
17: 46,724,153 (GRCm39) |
I2052T |
possibly damaging |
Het |
|
Other mutations in Krt25 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02415:Krt25
|
APN |
11 |
99,213,398 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02816:Krt25
|
APN |
11 |
99,208,977 (GRCm39) |
missense |
probably benign |
0.10 |
Plush
|
UTSW |
11 |
99,213,461 (GRCm39) |
missense |
probably damaging |
1.00 |
Sinuous
|
UTSW |
11 |
99,213,456 (GRCm39) |
missense |
probably damaging |
0.99 |
R0138:Krt25
|
UTSW |
11 |
99,213,524 (GRCm39) |
missense |
probably benign |
0.00 |
R0219:Krt25
|
UTSW |
11 |
99,208,885 (GRCm39) |
missense |
probably benign |
0.01 |
R0932:Krt25
|
UTSW |
11 |
99,212,109 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1733:Krt25
|
UTSW |
11 |
99,207,378 (GRCm39) |
nonsense |
probably null |
|
R1855:Krt25
|
UTSW |
11 |
99,209,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R2120:Krt25
|
UTSW |
11 |
99,212,023 (GRCm39) |
missense |
probably benign |
0.01 |
R2504:Krt25
|
UTSW |
11 |
99,208,122 (GRCm39) |
nonsense |
probably null |
|
R3615:Krt25
|
UTSW |
11 |
99,208,124 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3616:Krt25
|
UTSW |
11 |
99,208,124 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4590:Krt25
|
UTSW |
11 |
99,208,854 (GRCm39) |
intron |
probably benign |
|
R6250:Krt25
|
UTSW |
11 |
99,211,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R6331:Krt25
|
UTSW |
11 |
99,208,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R6927:Krt25
|
UTSW |
11 |
99,208,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R7067:Krt25
|
UTSW |
11 |
99,208,209 (GRCm39) |
missense |
probably benign |
0.01 |
R7289:Krt25
|
UTSW |
11 |
99,212,098 (GRCm39) |
missense |
probably benign |
0.15 |
R7360:Krt25
|
UTSW |
11 |
99,208,232 (GRCm39) |
missense |
probably benign |
0.01 |
R8057:Krt25
|
UTSW |
11 |
99,208,169 (GRCm39) |
missense |
probably benign |
0.44 |
R8090:Krt25
|
UTSW |
11 |
99,207,416 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8933:Krt25
|
UTSW |
11 |
99,212,064 (GRCm39) |
missense |
probably benign |
0.31 |
R8995:Krt25
|
UTSW |
11 |
99,207,382 (GRCm39) |
missense |
probably benign |
|
R9040:Krt25
|
UTSW |
11 |
99,207,379 (GRCm39) |
missense |
probably benign |
|
Z1176:Krt25
|
UTSW |
11 |
99,213,648 (GRCm39) |
missense |
probably benign |
0.44 |
|