Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
A |
T |
11: 109,828,556 (GRCm39) |
D1447E |
probably damaging |
Het |
Atp2a3 |
T |
C |
11: 72,873,491 (GRCm39) |
I788T |
probably damaging |
Het |
Axin1 |
G |
A |
17: 26,409,015 (GRCm39) |
E672K |
probably damaging |
Het |
Ccno |
A |
G |
13: 113,125,561 (GRCm39) |
D175G |
probably damaging |
Het |
Cep83 |
C |
A |
10: 94,624,619 (GRCm39) |
T632K |
probably benign |
Het |
Ckmt1 |
A |
T |
2: 121,193,474 (GRCm39) |
I345F |
probably benign |
Het |
Cntnap1 |
G |
A |
11: 101,069,633 (GRCm39) |
|
probably benign |
Het |
Cstdc3 |
A |
G |
16: 36,128,426 (GRCm39) |
E7G |
probably benign |
Het |
Edem2 |
A |
G |
2: 155,550,948 (GRCm39) |
Y340H |
probably benign |
Het |
Erich3 |
A |
G |
3: 154,419,653 (GRCm39) |
K249R |
probably benign |
Het |
Fndc9 |
T |
C |
11: 46,128,526 (GRCm39) |
I15T |
probably benign |
Het |
Grip2 |
G |
T |
6: 91,759,878 (GRCm39) |
Q300K |
probably benign |
Het |
Herc2 |
T |
C |
7: 55,862,589 (GRCm39) |
V4050A |
possibly damaging |
Het |
Jup |
A |
T |
11: 100,277,075 (GRCm39) |
D44E |
probably benign |
Het |
Lingo3 |
G |
T |
10: 80,671,147 (GRCm39) |
P261Q |
probably damaging |
Het |
Lrrfip2 |
C |
T |
9: 111,048,783 (GRCm39) |
R311W |
probably damaging |
Het |
Mansc1 |
C |
A |
6: 134,598,748 (GRCm39) |
L56F |
probably benign |
Het |
Map1b |
A |
G |
13: 99,571,269 (GRCm39) |
I484T |
probably damaging |
Het |
Mpeg1 |
T |
A |
19: 12,440,149 (GRCm39) |
F536I |
probably damaging |
Het |
Mrgprb1 |
T |
G |
7: 48,097,775 (GRCm39) |
T46P |
probably benign |
Het |
Mug1 |
A |
G |
6: 121,847,458 (GRCm39) |
N612S |
probably benign |
Het |
Or5p56 |
T |
C |
7: 107,589,758 (GRCm39) |
F62S |
probably damaging |
Het |
Or6c212 |
T |
A |
10: 129,558,814 (GRCm39) |
I200L |
probably benign |
Het |
Pax8 |
A |
G |
2: 24,331,162 (GRCm39) |
S178P |
probably damaging |
Het |
Peak1 |
A |
G |
9: 56,165,811 (GRCm39) |
F706L |
probably benign |
Het |
Prkdc |
A |
G |
16: 15,544,568 (GRCm39) |
T1853A |
probably damaging |
Het |
Reln |
A |
C |
5: 22,174,031 (GRCm39) |
F2024C |
probably damaging |
Het |
Reln |
G |
T |
5: 22,124,067 (GRCm39) |
P2813Q |
probably damaging |
Het |
Riox1 |
A |
G |
12: 83,998,568 (GRCm39) |
Q368R |
probably damaging |
Het |
Rspry1 |
T |
C |
8: 95,376,483 (GRCm39) |
V335A |
probably benign |
Het |
Scn3a |
T |
C |
2: 65,325,457 (GRCm39) |
N1020S |
possibly damaging |
Het |
Scyl2 |
A |
G |
10: 89,476,497 (GRCm39) |
V876A |
probably benign |
Het |
Sdhaf3 |
T |
A |
6: 6,956,141 (GRCm39) |
F39I |
probably damaging |
Het |
Sfxn4 |
T |
C |
19: 60,839,452 (GRCm39) |
E202G |
possibly damaging |
Het |
Slc1a4 |
A |
T |
11: 20,258,644 (GRCm39) |
|
probably benign |
Het |
Sln |
A |
G |
9: 53,760,784 (GRCm39) |
I10V |
probably benign |
Het |
Ssh2 |
A |
G |
11: 77,340,552 (GRCm39) |
E568G |
probably damaging |
Het |
Supt7l |
G |
A |
5: 31,675,779 (GRCm39) |
P270S |
probably benign |
Het |
Tanc2 |
A |
G |
11: 105,777,300 (GRCm39) |
|
probably benign |
Het |
Tfip11 |
C |
T |
5: 112,477,369 (GRCm39) |
P117L |
possibly damaging |
Het |
Vpreb1a |
T |
C |
16: 16,686,951 (GRCm39) |
M9V |
probably benign |
Het |
|
Other mutations in Tatdn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03155:Tatdn1
|
APN |
15 |
58,788,045 (GRCm39) |
intron |
probably benign |
|
PIT4403001:Tatdn1
|
UTSW |
15 |
58,777,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R0417:Tatdn1
|
UTSW |
15 |
58,793,199 (GRCm39) |
missense |
probably benign |
0.00 |
R1605:Tatdn1
|
UTSW |
15 |
58,793,039 (GRCm39) |
intron |
probably benign |
|
R1823:Tatdn1
|
UTSW |
15 |
58,788,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R2267:Tatdn1
|
UTSW |
15 |
58,777,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R3923:Tatdn1
|
UTSW |
15 |
58,793,020 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6481:Tatdn1
|
UTSW |
15 |
58,795,760 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6912:Tatdn1
|
UTSW |
15 |
58,793,118 (GRCm39) |
splice site |
probably null |
|
R7827:Tatdn1
|
UTSW |
15 |
58,776,607 (GRCm39) |
missense |
probably benign |
0.00 |
R8374:Tatdn1
|
UTSW |
15 |
58,788,000 (GRCm39) |
critical splice donor site |
probably null |
|
R8788:Tatdn1
|
UTSW |
15 |
58,762,543 (GRCm39) |
makesense |
probably null |
|
|