Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
T |
G |
14: 32,384,672 (GRCm39) |
D431A |
possibly damaging |
Het |
Adgrb1 |
T |
C |
15: 74,401,631 (GRCm39) |
M209T |
probably damaging |
Het |
Ano8 |
T |
C |
8: 71,937,486 (GRCm39) |
H86R |
probably damaging |
Het |
Camk1d |
G |
T |
2: 5,449,895 (GRCm39) |
Y87* |
probably null |
Het |
Capza3 |
A |
G |
6: 139,987,872 (GRCm39) |
D157G |
probably benign |
Het |
Ckmt2 |
A |
T |
13: 92,009,947 (GRCm39) |
D124E |
probably benign |
Het |
Col14a1 |
C |
A |
15: 55,284,231 (GRCm39) |
Q831K |
unknown |
Het |
Copb2 |
C |
T |
9: 98,469,605 (GRCm39) |
P829S |
probably benign |
Het |
Dlg5 |
A |
G |
14: 24,208,419 (GRCm39) |
V929A |
probably benign |
Het |
Dolk |
A |
G |
2: 30,175,991 (GRCm39) |
V18A |
probably benign |
Het |
Ecm2 |
G |
T |
13: 49,676,304 (GRCm39) |
L340F |
probably damaging |
Het |
Hacl1 |
A |
G |
14: 31,352,940 (GRCm39) |
L149P |
probably benign |
Het |
Higd2a |
A |
T |
13: 54,738,235 (GRCm39) |
|
probably null |
Het |
Hspa12a |
A |
T |
19: 58,816,730 (GRCm39) |
S28R |
probably benign |
Het |
Igkv5-37 |
A |
G |
6: 69,940,435 (GRCm39) |
Y70H |
probably damaging |
Het |
Iho1 |
G |
A |
9: 108,283,820 (GRCm39) |
T208I |
probably benign |
Het |
Kif11 |
T |
C |
19: 37,373,057 (GRCm39) |
V92A |
probably damaging |
Het |
Kif26a |
T |
C |
12: 112,141,284 (GRCm39) |
S696P |
probably damaging |
Het |
Kng1 |
A |
T |
16: 22,886,558 (GRCm39) |
N168Y |
probably damaging |
Het |
Krt26 |
C |
T |
11: 99,224,471 (GRCm39) |
R349Q |
probably benign |
Het |
Lepr |
A |
G |
4: 101,625,264 (GRCm39) |
D473G |
probably damaging |
Het |
Lipt1 |
G |
A |
1: 37,914,867 (GRCm39) |
E308K |
possibly damaging |
Het |
Luc7l3 |
A |
T |
11: 94,194,792 (GRCm39) |
F76Y |
probably benign |
Het |
Mapk1 |
A |
G |
16: 16,841,316 (GRCm39) |
I163V |
probably benign |
Het |
Matn3 |
A |
G |
12: 9,017,638 (GRCm39) |
E430G |
possibly damaging |
Het |
Med13 |
A |
T |
11: 86,177,591 (GRCm39) |
S1502T |
probably damaging |
Het |
Mlf1 |
A |
T |
3: 67,307,046 (GRCm39) |
H237L |
probably benign |
Het |
Mss51 |
A |
C |
14: 20,534,923 (GRCm39) |
Y282* |
probably null |
Het |
Ncoa3 |
A |
G |
2: 165,897,182 (GRCm39) |
T658A |
probably benign |
Het |
Or1p1c |
A |
T |
11: 74,160,544 (GRCm39) |
M110L |
probably benign |
Het |
Or7d11 |
A |
T |
9: 19,966,196 (GRCm39) |
S188T |
probably benign |
Het |
Phrf1 |
T |
A |
7: 140,839,196 (GRCm39) |
|
probably benign |
Het |
Ppme1 |
C |
T |
7: 99,983,139 (GRCm39) |
M335I |
probably damaging |
Het |
Ror2 |
C |
T |
13: 53,264,764 (GRCm39) |
S764N |
probably damaging |
Het |
Sntg2 |
T |
A |
12: 30,357,230 (GRCm39) |
|
probably null |
Het |
Spryd3 |
T |
C |
15: 102,027,354 (GRCm39) |
|
probably benign |
Het |
Srpx |
A |
G |
X: 9,933,662 (GRCm39) |
|
probably null |
Het |
St8sia1 |
G |
T |
6: 142,909,504 (GRCm39) |
|
probably benign |
Het |
Stab1 |
A |
G |
14: 30,865,470 (GRCm39) |
|
probably null |
Het |
Sycp2 |
A |
T |
2: 178,000,047 (GRCm39) |
S976R |
probably benign |
Het |
Sycp2 |
T |
A |
2: 178,043,783 (GRCm39) |
K108* |
probably null |
Het |
Tg |
C |
T |
15: 66,589,082 (GRCm39) |
T21I |
probably benign |
Het |
Tlr4 |
A |
T |
4: 66,759,202 (GRCm39) |
Y665F |
probably damaging |
Het |
Tmc8 |
T |
G |
11: 117,682,081 (GRCm39) |
S525A |
probably benign |
Het |
Tor4a |
A |
T |
2: 25,084,810 (GRCm39) |
D364E |
probably benign |
Het |
Trim44 |
T |
C |
2: 102,211,253 (GRCm39) |
I236V |
probably benign |
Het |
Ube2o |
A |
G |
11: 116,434,226 (GRCm39) |
|
probably benign |
Het |
Wdr38 |
A |
T |
2: 38,888,424 (GRCm39) |
N7I |
probably damaging |
Het |
Xirp2 |
A |
T |
2: 67,347,300 (GRCm39) |
R3180S |
probably benign |
Het |
Zfp335 |
A |
G |
2: 164,735,724 (GRCm39) |
C1077R |
probably damaging |
Het |
|
Other mutations in Tagap1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01384:Tagap1
|
APN |
17 |
7,224,282 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02475:Tagap1
|
APN |
17 |
7,223,826 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02955:Tagap1
|
APN |
17 |
7,223,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R1494:Tagap1
|
UTSW |
17 |
7,224,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Tagap1
|
UTSW |
17 |
7,223,425 (GRCm39) |
missense |
probably benign |
0.02 |
R1990:Tagap1
|
UTSW |
17 |
7,224,285 (GRCm39) |
missense |
probably benign |
0.00 |
R2067:Tagap1
|
UTSW |
17 |
7,224,259 (GRCm39) |
missense |
probably benign |
0.00 |
R2086:Tagap1
|
UTSW |
17 |
7,224,102 (GRCm39) |
missense |
probably benign |
0.00 |
R2111:Tagap1
|
UTSW |
17 |
7,224,259 (GRCm39) |
missense |
probably benign |
0.00 |
R4425:Tagap1
|
UTSW |
17 |
7,223,511 (GRCm39) |
missense |
probably benign |
0.00 |
R5271:Tagap1
|
UTSW |
17 |
7,223,495 (GRCm39) |
nonsense |
probably null |
|
R5728:Tagap1
|
UTSW |
17 |
7,224,420 (GRCm39) |
missense |
probably benign |
0.30 |
R7100:Tagap1
|
UTSW |
17 |
7,224,111 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8145:Tagap1
|
UTSW |
17 |
7,223,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R9627:Tagap1
|
UTSW |
17 |
7,224,327 (GRCm39) |
missense |
probably benign |
0.09 |
R9698:Tagap1
|
UTSW |
17 |
7,228,477 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Tagap1
|
UTSW |
17 |
7,224,016 (GRCm39) |
missense |
probably benign |
0.01 |
|