Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap9 |
G |
A |
5: 4,051,550 (GRCm39) |
S1439N |
probably benign |
Het |
Bcl9l |
A |
G |
9: 44,419,539 (GRCm39) |
T1069A |
possibly damaging |
Het |
Btaf1 |
T |
G |
19: 36,988,652 (GRCm39) |
|
probably benign |
Het |
Cdc40 |
A |
T |
10: 40,719,124 (GRCm39) |
V335E |
probably damaging |
Het |
Cenpj |
A |
T |
14: 56,802,420 (GRCm39) |
N48K |
possibly damaging |
Het |
Cfh |
A |
G |
1: 140,016,420 (GRCm39) |
W635R |
probably damaging |
Het |
Clca3a1 |
A |
G |
3: 144,714,719 (GRCm39) |
S633P |
possibly damaging |
Het |
Cnot6 |
T |
C |
11: 49,575,947 (GRCm39) |
M176V |
probably benign |
Het |
Cryz |
G |
T |
3: 154,324,163 (GRCm39) |
E51* |
probably null |
Het |
Dcc |
A |
G |
18: 71,589,954 (GRCm39) |
Y681H |
probably benign |
Het |
Dmxl1 |
T |
A |
18: 50,045,792 (GRCm39) |
N2412K |
probably benign |
Het |
Gpr137b |
C |
T |
13: 13,539,650 (GRCm39) |
W258* |
probably null |
Het |
Hnf1b |
A |
G |
11: 83,773,526 (GRCm39) |
T242A |
probably benign |
Het |
Hsd11b1 |
A |
T |
1: 192,905,952 (GRCm39) |
C213* |
probably null |
Het |
Igsf11 |
A |
T |
16: 38,829,279 (GRCm39) |
T117S |
probably damaging |
Het |
Inpp5b |
T |
C |
4: 124,677,787 (GRCm39) |
Y416H |
probably damaging |
Het |
Kcnq3 |
C |
A |
15: 65,876,575 (GRCm39) |
V523F |
probably damaging |
Het |
Krtap9-5 |
T |
C |
11: 99,839,291 (GRCm39) |
|
probably benign |
Het |
Lrig3 |
T |
C |
10: 125,832,984 (GRCm39) |
L286S |
probably damaging |
Het |
Myo18b |
C |
T |
5: 113,022,873 (GRCm39) |
|
probably benign |
Het |
Nup58 |
A |
G |
14: 60,466,365 (GRCm39) |
|
probably benign |
Het |
Or51b6b |
T |
A |
7: 103,310,274 (GRCm39) |
Y61F |
probably damaging |
Het |
Or5b94 |
T |
C |
19: 12,651,605 (GRCm39) |
L12P |
probably damaging |
Het |
Or5h18 |
A |
G |
16: 58,847,994 (GRCm39) |
I92T |
possibly damaging |
Het |
Or8k16 |
G |
A |
2: 85,520,007 (GRCm39) |
C78Y |
probably benign |
Het |
Pyroxd2 |
T |
C |
19: 42,719,877 (GRCm39) |
D443G |
possibly damaging |
Het |
Ttc28 |
A |
G |
5: 111,373,606 (GRCm39) |
D1014G |
probably benign |
Het |
Tubgcp5 |
T |
A |
7: 55,456,343 (GRCm39) |
S312T |
possibly damaging |
Het |
Uckl1 |
T |
C |
2: 181,211,410 (GRCm39) |
D473G |
probably benign |
Het |
Vmn2r76 |
G |
T |
7: 85,877,925 (GRCm39) |
H491N |
probably benign |
Het |
Wwc2 |
G |
A |
8: 48,299,193 (GRCm39) |
R1039W |
unknown |
Het |
Zc3h14 |
T |
A |
12: 98,725,102 (GRCm39) |
S255T |
probably benign |
Het |
Zfp369 |
T |
C |
13: 65,445,074 (GRCm39) |
V739A |
probably benign |
Het |
Zfyve21 |
A |
G |
12: 111,791,368 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Znhit6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00160:Znhit6
|
APN |
3 |
145,283,915 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01588:Znhit6
|
APN |
3 |
145,301,962 (GRCm39) |
splice site |
probably benign |
|
IGL01911:Znhit6
|
APN |
3 |
145,283,853 (GRCm39) |
splice site |
probably benign |
|
IGL02118:Znhit6
|
APN |
3 |
145,283,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R1066:Znhit6
|
UTSW |
3 |
145,284,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R1115:Znhit6
|
UTSW |
3 |
145,300,440 (GRCm39) |
splice site |
probably null |
|
R2278:Znhit6
|
UTSW |
3 |
145,281,991 (GRCm39) |
unclassified |
probably benign |
|
R2391:Znhit6
|
UTSW |
3 |
145,300,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R2656:Znhit6
|
UTSW |
3 |
145,283,924 (GRCm39) |
critical splice donor site |
probably null |
|
R2877:Znhit6
|
UTSW |
3 |
145,282,409 (GRCm39) |
missense |
probably benign |
0.31 |
R3825:Znhit6
|
UTSW |
3 |
145,284,099 (GRCm39) |
missense |
probably benign |
0.17 |
R4636:Znhit6
|
UTSW |
3 |
145,306,333 (GRCm39) |
splice site |
silent |
|
R4636:Znhit6
|
UTSW |
3 |
145,306,334 (GRCm39) |
missense |
probably null |
0.11 |
R5295:Znhit6
|
UTSW |
3 |
145,306,248 (GRCm39) |
missense |
probably benign |
0.41 |
R5964:Znhit6
|
UTSW |
3 |
145,282,688 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5965:Znhit6
|
UTSW |
3 |
145,284,103 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6537:Znhit6
|
UTSW |
3 |
145,300,374 (GRCm39) |
missense |
probably benign |
0.32 |
X0065:Znhit6
|
UTSW |
3 |
145,284,241 (GRCm39) |
missense |
probably benign |
|
|