Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5530400C23Rik |
T |
C |
6: 133,269,205 (GRCm39) |
|
probably benign |
Het |
Ankrd1 |
A |
G |
19: 36,097,165 (GRCm39) |
V6A |
probably benign |
Het |
Apobr |
T |
A |
7: 126,185,779 (GRCm39) |
V430E |
probably benign |
Het |
Arhgap28 |
A |
G |
17: 68,203,084 (GRCm39) |
V123A |
probably benign |
Het |
Atp2b2 |
A |
G |
6: 113,790,903 (GRCm39) |
V167A |
probably damaging |
Het |
B3galnt2 |
A |
T |
13: 14,171,618 (GRCm39) |
*505C |
probably null |
Het |
Bcat2 |
T |
A |
7: 45,237,431 (GRCm39) |
L305Q |
probably damaging |
Het |
Coa8 |
T |
A |
12: 111,690,847 (GRCm39) |
|
probably benign |
Het |
Col9a1 |
T |
C |
1: 24,224,339 (GRCm39) |
S174P |
unknown |
Het |
Ddx41 |
A |
T |
13: 55,680,170 (GRCm39) |
D418E |
probably benign |
Het |
Defa40 |
A |
G |
8: 21,740,377 (GRCm39) |
D61G |
probably damaging |
Het |
Exoc6 |
T |
C |
19: 37,566,922 (GRCm39) |
F240L |
probably benign |
Het |
Fbln7 |
G |
A |
2: 128,737,477 (GRCm39) |
V431I |
probably benign |
Het |
Gfral |
T |
A |
9: 76,104,374 (GRCm39) |
N213Y |
probably damaging |
Het |
Golgb1 |
A |
G |
16: 36,706,562 (GRCm39) |
D22G |
probably benign |
Het |
H2-M1 |
G |
A |
17: 36,981,141 (GRCm39) |
T298I |
unknown |
Het |
Haus3 |
A |
T |
5: 34,323,580 (GRCm39) |
Y343* |
probably null |
Het |
Hid1 |
T |
C |
11: 115,243,446 (GRCm39) |
E534G |
probably damaging |
Het |
Il4ra |
T |
C |
7: 125,170,676 (GRCm39) |
V196A |
probably benign |
Het |
Itm2b |
C |
A |
14: 73,600,536 (GRCm39) |
E255* |
probably null |
Het |
Kidins220 |
A |
T |
12: 25,047,332 (GRCm39) |
|
probably benign |
Het |
Klhl22 |
T |
A |
16: 17,594,762 (GRCm39) |
F297Y |
possibly damaging |
Het |
Krt9 |
T |
C |
11: 100,082,041 (GRCm39) |
E253G |
probably damaging |
Het |
Man2a2 |
G |
A |
7: 80,009,388 (GRCm39) |
A822V |
probably damaging |
Het |
Map3k6 |
T |
A |
4: 132,973,932 (GRCm39) |
|
probably null |
Het |
Med29 |
C |
A |
7: 28,086,448 (GRCm39) |
R120L |
possibly damaging |
Het |
Napa |
C |
T |
7: 15,846,503 (GRCm39) |
|
probably benign |
Het |
Ncapd3 |
T |
A |
9: 26,961,624 (GRCm39) |
Y351N |
probably benign |
Het |
Nphs1 |
C |
T |
7: 30,181,060 (GRCm39) |
|
probably benign |
Het |
Or5b94 |
A |
G |
19: 12,651,899 (GRCm39) |
D110G |
probably benign |
Het |
Prss16 |
T |
C |
13: 22,193,697 (GRCm39) |
I33V |
probably benign |
Het |
Ripk1 |
A |
G |
13: 34,199,227 (GRCm39) |
Y193C |
probably damaging |
Het |
Rph3a |
C |
T |
5: 121,102,002 (GRCm39) |
R78H |
probably damaging |
Het |
Rrp9 |
T |
A |
9: 106,362,471 (GRCm39) |
I452N |
probably damaging |
Het |
Ryr2 |
A |
T |
13: 11,737,607 (GRCm39) |
|
probably benign |
Het |
Sec23a |
A |
G |
12: 59,048,813 (GRCm39) |
L103P |
probably damaging |
Het |
Slc17a9 |
A |
C |
2: 180,377,674 (GRCm39) |
D190A |
probably benign |
Het |
Slc44a4 |
G |
A |
17: 35,146,686 (GRCm39) |
V422I |
probably benign |
Het |
Smc5 |
C |
T |
19: 23,191,996 (GRCm39) |
|
probably benign |
Het |
Tax1bp1 |
C |
T |
6: 52,730,351 (GRCm39) |
S611F |
probably benign |
Het |
Tmem38b |
G |
A |
4: 53,854,345 (GRCm39) |
M192I |
probably benign |
Het |
Unc45a |
G |
T |
7: 79,989,410 (GRCm39) |
C34* |
probably null |
Het |
Usp46 |
T |
A |
5: 74,190,014 (GRCm39) |
M6L |
probably benign |
Het |
Uspl1 |
G |
A |
5: 149,150,212 (GRCm39) |
V471M |
probably damaging |
Het |
Vmn1r35 |
T |
A |
6: 66,655,875 (GRCm39) |
Q265L |
probably damaging |
Het |
Vmn1r35 |
G |
T |
6: 66,655,876 (GRCm39) |
Q265K |
probably damaging |
Het |
Vmn1r50 |
A |
G |
6: 90,084,461 (GRCm39) |
I69V |
possibly damaging |
Het |
Vps33b |
A |
G |
7: 79,935,082 (GRCm39) |
|
probably null |
Het |
Xntrpc |
A |
C |
7: 101,742,802 (GRCm39) |
D604A |
probably damaging |
Het |
Yeats4 |
T |
A |
10: 117,051,716 (GRCm39) |
R180S |
probably benign |
Het |
|
Other mutations in Adap2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02442:Adap2
|
APN |
11 |
80,068,032 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02953:Adap2
|
APN |
11 |
80,045,126 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4283001:Adap2
|
UTSW |
11 |
80,068,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R0157:Adap2
|
UTSW |
11 |
80,056,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R0382:Adap2
|
UTSW |
11 |
80,069,211 (GRCm39) |
splice site |
probably benign |
|
R0499:Adap2
|
UTSW |
11 |
80,066,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R0722:Adap2
|
UTSW |
11 |
80,047,810 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0828:Adap2
|
UTSW |
11 |
80,056,490 (GRCm39) |
splice site |
probably benign |
|
R1938:Adap2
|
UTSW |
11 |
80,061,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R2268:Adap2
|
UTSW |
11 |
80,056,552 (GRCm39) |
missense |
probably damaging |
0.99 |
R3103:Adap2
|
UTSW |
11 |
80,047,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R4621:Adap2
|
UTSW |
11 |
80,064,899 (GRCm39) |
splice site |
probably null |
|
R5157:Adap2
|
UTSW |
11 |
80,047,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R6326:Adap2
|
UTSW |
11 |
80,045,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R6914:Adap2
|
UTSW |
11 |
80,045,891 (GRCm39) |
missense |
probably benign |
0.01 |
R6942:Adap2
|
UTSW |
11 |
80,045,891 (GRCm39) |
missense |
probably benign |
0.01 |
R7835:Adap2
|
UTSW |
11 |
80,051,057 (GRCm39) |
missense |
probably benign |
0.11 |
R8879:Adap2
|
UTSW |
11 |
80,047,785 (GRCm39) |
missense |
probably benign |
0.02 |
R9183:Adap2
|
UTSW |
11 |
80,045,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R9408:Adap2
|
UTSW |
11 |
80,045,942 (GRCm39) |
missense |
probably damaging |
1.00 |
|