Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akt1 |
T |
C |
12: 112,623,518 (GRCm39) |
E314G |
probably damaging |
Het |
Amtn |
C |
A |
5: 88,529,481 (GRCm39) |
Q106K |
probably benign |
Het |
Birc6 |
T |
C |
17: 74,916,184 (GRCm39) |
F1700S |
probably damaging |
Het |
Brdt |
T |
C |
5: 107,525,861 (GRCm39) |
S905P |
possibly damaging |
Het |
Ccdc68 |
C |
T |
18: 70,080,236 (GRCm39) |
Q194* |
probably null |
Het |
Cdc27 |
A |
G |
11: 104,417,807 (GRCm39) |
|
probably benign |
Het |
Cdh13 |
A |
G |
8: 119,401,897 (GRCm39) |
T100A |
probably benign |
Het |
Cdsn |
A |
G |
17: 35,866,791 (GRCm39) |
H440R |
possibly damaging |
Het |
Cenpf |
C |
A |
1: 189,390,227 (GRCm39) |
D1202Y |
probably damaging |
Het |
Chat |
C |
A |
14: 32,180,570 (GRCm39) |
V21L |
probably benign |
Het |
Clca4c-ps |
T |
A |
3: 144,585,493 (GRCm39) |
|
noncoding transcript |
Het |
Cst9 |
A |
G |
2: 148,677,203 (GRCm39) |
I25V |
probably benign |
Het |
Dennd1b |
C |
A |
1: 139,096,705 (GRCm39) |
|
probably benign |
Het |
Dnah9 |
A |
G |
11: 65,928,570 (GRCm39) |
|
probably benign |
Het |
Dpp3 |
T |
G |
19: 4,973,159 (GRCm39) |
Q145P |
probably benign |
Het |
Elovl5 |
C |
T |
9: 77,888,784 (GRCm39) |
T217M |
probably damaging |
Het |
Etl4 |
T |
C |
2: 20,812,840 (GRCm39) |
V906A |
possibly damaging |
Het |
Gm10647 |
C |
T |
9: 66,705,543 (GRCm39) |
|
probably benign |
Het |
Grm5 |
A |
G |
7: 87,723,918 (GRCm39) |
N736S |
probably damaging |
Het |
Hectd1 |
A |
G |
12: 51,814,423 (GRCm39) |
S1638P |
possibly damaging |
Het |
Hsd3b2 |
T |
G |
3: 98,623,740 (GRCm39) |
E46A |
possibly damaging |
Het |
Igkv15-103 |
A |
G |
6: 68,414,674 (GRCm39) |
T38A |
probably benign |
Het |
Itpr2 |
C |
A |
6: 146,287,477 (GRCm39) |
V450L |
probably damaging |
Het |
Kbtbd12 |
T |
C |
6: 88,595,311 (GRCm39) |
H173R |
probably benign |
Het |
Man1a |
G |
A |
10: 53,795,340 (GRCm39) |
R638W |
probably damaging |
Het |
Mterf2 |
A |
T |
10: 84,955,878 (GRCm39) |
S249T |
probably damaging |
Het |
Muc6 |
T |
C |
7: 141,234,627 (GRCm39) |
D700G |
probably damaging |
Het |
Myh13 |
A |
G |
11: 67,239,742 (GRCm39) |
H764R |
possibly damaging |
Het |
Myh7b |
A |
G |
2: 155,470,747 (GRCm39) |
D1065G |
probably damaging |
Het |
Naip1 |
C |
A |
13: 100,569,770 (GRCm39) |
W288L |
probably damaging |
Het |
Naip6 |
C |
A |
13: 100,437,168 (GRCm39) |
A452S |
probably benign |
Het |
Nop2 |
A |
C |
6: 125,121,048 (GRCm39) |
K610T |
possibly damaging |
Het |
Nop2 |
G |
T |
6: 125,121,033 (GRCm39) |
G605V |
probably benign |
Het |
Npvf |
G |
A |
6: 50,629,670 (GRCm39) |
R107W |
probably benign |
Het |
Or10h28 |
T |
A |
17: 33,488,328 (GRCm39) |
I210K |
probably benign |
Het |
Or2h2 |
T |
C |
17: 37,397,048 (GRCm39) |
|
probably null |
Het |
Os9 |
G |
A |
10: 126,935,262 (GRCm39) |
|
probably benign |
Het |
Parp4 |
T |
C |
14: 56,886,326 (GRCm39) |
S1802P |
unknown |
Het |
Piezo2 |
G |
A |
18: 63,153,704 (GRCm39) |
S2547F |
probably benign |
Het |
Plekha7 |
G |
T |
7: 115,734,413 (GRCm39) |
A1024E |
probably damaging |
Het |
R3hdm1 |
T |
C |
1: 128,102,677 (GRCm39) |
|
probably benign |
Het |
Robo4 |
T |
C |
9: 37,324,678 (GRCm39) |
S1022P |
probably damaging |
Het |
Sc5d |
T |
C |
9: 42,166,690 (GRCm39) |
N283S |
probably benign |
Het |
Scn10a |
C |
T |
9: 119,500,674 (GRCm39) |
V202M |
probably damaging |
Het |
Slco1a8 |
C |
T |
6: 141,949,197 (GRCm39) |
G60R |
probably damaging |
Het |
Spag16 |
T |
C |
1: 70,304,067 (GRCm39) |
I366T |
possibly damaging |
Het |
Sptbn4 |
G |
A |
7: 27,126,258 (GRCm39) |
R222C |
possibly damaging |
Het |
Tlr9 |
C |
T |
9: 106,101,929 (GRCm39) |
Q407* |
probably null |
Het |
Trappc12 |
G |
A |
12: 28,741,405 (GRCm39) |
S768L |
probably damaging |
Het |
Vmn2r44 |
A |
T |
7: 8,386,050 (GRCm39) |
L63Q |
probably damaging |
Het |
|
Other mutations in Zfy2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02850:Zfy2
|
APN |
Y |
2,117,188 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02850:Zfy2
|
APN |
Y |
2,106,894 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02851:Zfy2
|
APN |
Y |
2,117,188 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02852:Zfy2
|
APN |
Y |
2,117,188 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02852:Zfy2
|
APN |
Y |
2,106,894 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4515001:Zfy2
|
UTSW |
Y |
2,117,096 (GRCm39) |
missense |
probably benign |
0.09 |
R0426:Zfy2
|
UTSW |
Y |
2,107,348 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0490:Zfy2
|
UTSW |
Y |
2,106,620 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1080:Zfy2
|
UTSW |
Y |
2,121,645 (GRCm39) |
missense |
probably benign |
0.00 |
R1513:Zfy2
|
UTSW |
Y |
2,116,185 (GRCm39) |
missense |
probably benign |
0.00 |
R1935:Zfy2
|
UTSW |
Y |
2,121,496 (GRCm39) |
missense |
probably benign |
0.02 |
R1936:Zfy2
|
UTSW |
Y |
2,121,496 (GRCm39) |
missense |
probably benign |
0.02 |
R2358:Zfy2
|
UTSW |
Y |
2,107,272 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4484:Zfy2
|
UTSW |
Y |
2,107,351 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4754:Zfy2
|
UTSW |
Y |
2,121,477 (GRCm39) |
missense |
probably benign |
0.02 |
R4777:Zfy2
|
UTSW |
Y |
2,116,194 (GRCm39) |
missense |
probably benign |
0.00 |
R4812:Zfy2
|
UTSW |
Y |
2,106,334 (GRCm39) |
missense |
probably benign |
0.08 |
R5045:Zfy2
|
UTSW |
Y |
2,107,159 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5363:Zfy2
|
UTSW |
Y |
2,106,555 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6256:Zfy2
|
UTSW |
Y |
2,116,267 (GRCm39) |
missense |
probably benign |
0.02 |
R6618:Zfy2
|
UTSW |
Y |
2,121,477 (GRCm39) |
missense |
probably benign |
0.10 |
R6941:Zfy2
|
UTSW |
Y |
2,121,491 (GRCm39) |
missense |
probably benign |
0.02 |
R7011:Zfy2
|
UTSW |
Y |
2,107,127 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7712:Zfy2
|
UTSW |
Y |
2,121,420 (GRCm39) |
missense |
probably benign |
0.05 |
R7759:Zfy2
|
UTSW |
Y |
2,117,083 (GRCm39) |
missense |
probably benign |
0.02 |
R7985:Zfy2
|
UTSW |
Y |
2,116,263 (GRCm39) |
missense |
probably benign |
0.00 |
R8051:Zfy2
|
UTSW |
Y |
2,117,380 (GRCm39) |
intron |
probably benign |
|
R8218:Zfy2
|
UTSW |
Y |
2,133,421 (GRCm39) |
missense |
unknown |
|
R8345:Zfy2
|
UTSW |
Y |
2,107,096 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8371:Zfy2
|
UTSW |
Y |
2,117,168 (GRCm39) |
missense |
probably benign |
0.00 |
R8830:Zfy2
|
UTSW |
Y |
2,106,600 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9448:Zfy2
|
UTSW |
Y |
2,109,904 (GRCm39) |
missense |
probably damaging |
0.98 |
R9537:Zfy2
|
UTSW |
Y |
2,108,596 (GRCm39) |
missense |
|
|
|