Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
T |
A |
2: 69,104,356 (GRCm39) |
S777C |
probably damaging |
Het |
Ano5 |
T |
A |
7: 51,187,458 (GRCm39) |
|
probably null |
Het |
Arhgap17 |
T |
A |
7: 122,893,896 (GRCm39) |
H508L |
probably benign |
Het |
Arhgap29 |
T |
A |
3: 121,803,709 (GRCm39) |
|
probably null |
Het |
Atp12a |
T |
C |
14: 56,624,435 (GRCm39) |
F961S |
probably damaging |
Het |
B4galnt4 |
C |
A |
7: 140,647,975 (GRCm39) |
P497Q |
probably benign |
Het |
Camsap1 |
A |
G |
2: 25,834,568 (GRCm39) |
S364P |
probably damaging |
Het |
Ccdc150 |
C |
A |
1: 54,302,636 (GRCm39) |
D85E |
probably benign |
Het |
Cdc45 |
A |
G |
16: 18,613,930 (GRCm39) |
Y291H |
probably benign |
Het |
Comp |
A |
C |
8: 70,829,290 (GRCm39) |
N289T |
probably damaging |
Het |
Cops3 |
T |
A |
11: 59,708,856 (GRCm39) |
|
probably benign |
Het |
Crybg1 |
G |
A |
10: 43,874,208 (GRCm39) |
H967Y |
possibly damaging |
Het |
Csmd1 |
A |
T |
8: 16,039,090 (GRCm39) |
F2423I |
probably damaging |
Het |
Dact1 |
C |
A |
12: 71,365,347 (GRCm39) |
C709* |
probably null |
Het |
Dcxr |
T |
G |
11: 120,617,273 (GRCm39) |
Q90P |
probably damaging |
Het |
Ell |
A |
G |
8: 71,043,349 (GRCm39) |
Y494C |
probably damaging |
Het |
Emilin2 |
T |
C |
17: 71,581,727 (GRCm39) |
E333G |
possibly damaging |
Het |
Eml2 |
T |
C |
7: 18,913,372 (GRCm39) |
|
probably null |
Het |
Fam186b |
T |
A |
15: 99,178,682 (GRCm39) |
M215L |
probably damaging |
Het |
Gm17078 |
T |
A |
14: 51,848,699 (GRCm39) |
R13W |
probably null |
Het |
Gm4787 |
G |
C |
12: 81,424,604 (GRCm39) |
T518S |
probably benign |
Het |
Hspa14 |
A |
G |
2: 3,499,206 (GRCm39) |
F196S |
possibly damaging |
Het |
Ier5 |
A |
G |
1: 154,974,849 (GRCm39) |
S110P |
possibly damaging |
Het |
Kif1a |
T |
A |
1: 92,982,049 (GRCm39) |
I793F |
possibly damaging |
Het |
Lrrc43 |
T |
C |
5: 123,646,176 (GRCm39) |
I643T |
probably damaging |
Het |
Map3k19 |
A |
T |
1: 127,750,969 (GRCm39) |
L794Q |
probably benign |
Het |
Meox2 |
A |
T |
12: 37,158,935 (GRCm39) |
M36L |
probably benign |
Het |
Mgat5b |
T |
A |
11: 116,875,855 (GRCm39) |
L693Q |
probably damaging |
Het |
Mup4 |
T |
A |
4: 59,958,124 (GRCm39) |
E148V |
possibly damaging |
Het |
Napb |
T |
C |
2: 148,545,057 (GRCm39) |
N162S |
possibly damaging |
Het |
Nlgn2 |
T |
C |
11: 69,718,563 (GRCm39) |
D339G |
probably benign |
Het |
Nucks1 |
C |
T |
1: 131,855,840 (GRCm39) |
R90C |
possibly damaging |
Het |
Or11g7 |
T |
C |
14: 50,691,196 (GRCm39) |
V229A |
probably damaging |
Het |
Or5an9 |
T |
A |
19: 12,187,518 (GRCm39) |
V196E |
possibly damaging |
Het |
Plekhd1 |
A |
T |
12: 80,739,723 (GRCm39) |
D24V |
probably damaging |
Het |
Prpf4b |
C |
T |
13: 35,083,958 (GRCm39) |
P909L |
probably damaging |
Het |
Rasgrp1 |
T |
A |
2: 117,132,485 (GRCm39) |
K116* |
probably null |
Het |
Ror1 |
A |
G |
4: 100,269,133 (GRCm39) |
T324A |
possibly damaging |
Het |
Slc24a4 |
G |
A |
12: 102,230,629 (GRCm39) |
G505R |
probably damaging |
Het |
Slc8a1 |
A |
G |
17: 81,956,702 (GRCm39) |
I112T |
possibly damaging |
Het |
Smarcc2 |
A |
G |
10: 128,297,314 (GRCm39) |
S69G |
probably damaging |
Het |
Smc2 |
A |
T |
4: 52,458,447 (GRCm39) |
E429D |
probably damaging |
Het |
Sry |
T |
C |
Y: 2,663,312 (GRCm39) |
D116G |
probably damaging |
Het |
Tcea3 |
T |
A |
4: 135,985,246 (GRCm39) |
V154E |
possibly damaging |
Het |
Tigd2 |
G |
A |
6: 59,188,205 (GRCm39) |
W357* |
probably null |
Het |
Tmem177 |
T |
A |
1: 119,838,419 (GRCm39) |
T87S |
probably benign |
Het |
Treh |
A |
T |
9: 44,594,186 (GRCm39) |
E144V |
probably null |
Het |
Trpm6 |
T |
A |
19: 18,764,124 (GRCm39) |
D243E |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,608,394 (GRCm39) |
D17843G |
probably damaging |
Het |
Vars2 |
A |
C |
17: 35,970,365 (GRCm39) |
|
probably null |
Het |
Vmn1r201 |
G |
A |
13: 22,659,530 (GRCm39) |
W248* |
probably null |
Het |
Yap1 |
T |
C |
9: 8,001,690 (GRCm39) |
T99A |
probably benign |
Het |
Zfp882 |
A |
G |
8: 72,668,498 (GRCm39) |
T442A |
possibly damaging |
Het |
Zxdc |
G |
T |
6: 90,359,320 (GRCm39) |
G651C |
probably benign |
Het |
|
Other mutations in Zbtb8b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01358:Zbtb8b
|
APN |
4 |
129,327,052 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01989:Zbtb8b
|
APN |
4 |
129,326,181 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03332:Zbtb8b
|
APN |
4 |
129,322,361 (GRCm39) |
missense |
probably damaging |
1.00 |
N/A:Zbtb8b
|
UTSW |
4 |
129,326,361 (GRCm39) |
missense |
probably benign |
|
PIT4131001:Zbtb8b
|
UTSW |
4 |
129,321,308 (GRCm39) |
makesense |
probably null |
|
R0391:Zbtb8b
|
UTSW |
4 |
129,326,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R2389:Zbtb8b
|
UTSW |
4 |
129,327,066 (GRCm39) |
missense |
probably benign |
0.25 |
R2392:Zbtb8b
|
UTSW |
4 |
129,326,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R2760:Zbtb8b
|
UTSW |
4 |
129,326,293 (GRCm39) |
missense |
probably benign |
0.04 |
R5572:Zbtb8b
|
UTSW |
4 |
129,322,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R6029:Zbtb8b
|
UTSW |
4 |
129,322,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R6671:Zbtb8b
|
UTSW |
4 |
129,321,577 (GRCm39) |
missense |
probably damaging |
0.99 |
R6714:Zbtb8b
|
UTSW |
4 |
129,326,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R7039:Zbtb8b
|
UTSW |
4 |
129,321,478 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7392:Zbtb8b
|
UTSW |
4 |
129,326,683 (GRCm39) |
missense |
probably benign |
0.01 |
R7454:Zbtb8b
|
UTSW |
4 |
129,326,562 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7634:Zbtb8b
|
UTSW |
4 |
129,326,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R8017:Zbtb8b
|
UTSW |
4 |
129,322,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R8444:Zbtb8b
|
UTSW |
4 |
129,326,424 (GRCm39) |
missense |
probably benign |
|
R9366:Zbtb8b
|
UTSW |
4 |
129,326,151 (GRCm39) |
missense |
probably benign |
0.01 |
R9417:Zbtb8b
|
UTSW |
4 |
129,326,517 (GRCm39) |
missense |
probably benign |
0.00 |
R9467:Zbtb8b
|
UTSW |
4 |
129,326,319 (GRCm39) |
missense |
probably benign |
0.41 |
|