Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahcyl2 |
A |
G |
6: 29,903,266 (GRCm39) |
R516G |
probably damaging |
Het |
Ak9 |
T |
C |
10: 41,265,087 (GRCm39) |
F948S |
|
Het |
Aldh3b3 |
A |
G |
19: 4,014,549 (GRCm39) |
M95V |
probably benign |
Het |
Ankrd34a |
T |
C |
3: 96,505,816 (GRCm39) |
L340P |
possibly damaging |
Het |
Arid1a |
T |
A |
4: 133,412,482 (GRCm39) |
R1186W |
unknown |
Het |
Arpc4 |
T |
A |
6: 113,361,092 (GRCm39) |
M95K |
possibly damaging |
Het |
Atrnl1 |
A |
G |
19: 57,684,744 (GRCm39) |
E790G |
possibly damaging |
Het |
C130074G19Rik |
T |
C |
1: 184,606,624 (GRCm39) |
N103D |
probably damaging |
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
Camsap2 |
T |
C |
1: 136,198,678 (GRCm39) |
T782A |
|
Het |
Catsperd |
A |
G |
17: 56,971,055 (GRCm39) |
I706M |
probably benign |
Het |
Cbx2 |
T |
C |
11: 118,919,941 (GRCm39) |
V502A |
probably damaging |
Het |
Cd72 |
T |
G |
4: 43,454,515 (GRCm39) |
I5L |
possibly damaging |
Het |
Celsr3 |
A |
G |
9: 108,720,777 (GRCm39) |
Y2609C |
probably benign |
Het |
Col19a1 |
C |
T |
1: 24,356,788 (GRCm39) |
G632R |
probably damaging |
Het |
Efcc1 |
T |
C |
6: 87,707,972 (GRCm39) |
V33A |
probably damaging |
Het |
Eif4enif1 |
T |
A |
11: 3,177,709 (GRCm39) |
L367* |
probably null |
Het |
Eml2 |
T |
A |
7: 18,940,066 (GRCm39) |
L627* |
probably null |
Het |
F13b |
A |
G |
1: 139,435,433 (GRCm39) |
T193A |
probably benign |
Het |
Hif3a |
G |
A |
7: 16,776,560 (GRCm39) |
T462I |
possibly damaging |
Het |
Ifna7 |
T |
A |
4: 88,734,913 (GRCm39) |
I150N |
probably damaging |
Het |
Man2b2 |
G |
A |
5: 36,967,657 (GRCm39) |
H904Y |
probably damaging |
Het |
Midn |
A |
G |
10: 79,991,156 (GRCm39) |
T389A |
possibly damaging |
Het |
Myo19 |
A |
T |
11: 84,776,626 (GRCm39) |
H94L |
probably benign |
Het |
Naglu |
T |
C |
11: 100,962,725 (GRCm39) |
Y177H |
probably damaging |
Het |
Nek1 |
T |
A |
8: 61,583,179 (GRCm39) |
D1272E |
probably benign |
Het |
Nxn |
A |
T |
11: 76,152,378 (GRCm39) |
V372E |
probably damaging |
Het |
Obscn |
G |
A |
11: 58,984,242 (GRCm39) |
R1738C |
probably damaging |
Het |
Pcm1 |
A |
G |
8: 41,714,410 (GRCm39) |
E266G |
probably benign |
Het |
Pkd1l1 |
T |
C |
11: 8,879,441 (GRCm39) |
N920S |
|
Het |
Pkd1l3 |
C |
A |
8: 110,359,947 (GRCm39) |
T944K |
probably damaging |
Het |
Prl7d1 |
C |
A |
13: 27,894,168 (GRCm39) |
E133* |
probably null |
Het |
Qser1 |
G |
A |
2: 104,619,859 (GRCm39) |
L228F |
probably damaging |
Het |
Rasa3 |
A |
G |
8: 13,664,605 (GRCm39) |
I69T |
possibly damaging |
Het |
Rb1 |
A |
T |
14: 73,506,577 (GRCm39) |
S391T |
probably damaging |
Het |
Rnf220 |
T |
C |
4: 117,153,333 (GRCm39) |
Y301C |
possibly damaging |
Het |
Sertm1 |
A |
G |
3: 54,806,749 (GRCm39) |
V92A |
possibly damaging |
Het |
Slfn5 |
A |
G |
11: 82,851,442 (GRCm39) |
K580E |
probably damaging |
Het |
Stard4 |
T |
C |
18: 33,338,377 (GRCm39) |
Y111C |
unknown |
Het |
Tagap |
C |
A |
17: 8,152,422 (GRCm39) |
Q536K |
possibly damaging |
Het |
Tank |
T |
C |
2: 61,480,513 (GRCm39) |
C351R |
probably damaging |
Het |
Tarbp2 |
A |
T |
15: 102,430,169 (GRCm39) |
M144L |
probably benign |
Het |
Tdrd9 |
T |
C |
12: 111,951,476 (GRCm39) |
Y89H |
probably damaging |
Het |
Tecpr2 |
C |
A |
12: 110,934,873 (GRCm39) |
T1373K |
probably benign |
Het |
Tle1 |
G |
A |
4: 72,055,349 (GRCm39) |
P434L |
probably damaging |
Het |
Tmed5 |
A |
G |
5: 108,272,495 (GRCm39) |
V201A |
probably benign |
Het |
Ust |
A |
G |
10: 8,266,650 (GRCm39) |
|
probably null |
Het |
Vmn2r94 |
T |
C |
17: 18,477,767 (GRCm39) |
T215A |
probably benign |
Het |
Zfp764l1 |
C |
T |
7: 126,992,496 (GRCm39) |
C38Y |
probably null |
Het |
|
Other mutations in Zfp273 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03115:Zfp273
|
APN |
13 |
67,973,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R1969:Zfp273
|
UTSW |
13 |
67,973,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R2679:Zfp273
|
UTSW |
13 |
67,973,895 (GRCm39) |
missense |
probably benign |
0.39 |
R3736:Zfp273
|
UTSW |
13 |
67,973,626 (GRCm39) |
nonsense |
probably null |
|
R4832:Zfp273
|
UTSW |
13 |
67,973,484 (GRCm39) |
missense |
probably benign |
0.01 |
R4896:Zfp273
|
UTSW |
13 |
67,973,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Zfp273
|
UTSW |
13 |
67,973,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R5223:Zfp273
|
UTSW |
13 |
67,974,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R5748:Zfp273
|
UTSW |
13 |
67,973,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R5948:Zfp273
|
UTSW |
13 |
67,973,918 (GRCm39) |
missense |
probably benign |
0.43 |
R6102:Zfp273
|
UTSW |
13 |
67,970,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R6668:Zfp273
|
UTSW |
13 |
67,973,243 (GRCm39) |
missense |
probably damaging |
0.99 |
R7192:Zfp273
|
UTSW |
13 |
67,973,183 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7792:Zfp273
|
UTSW |
13 |
67,974,135 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7874:Zfp273
|
UTSW |
13 |
67,973,558 (GRCm39) |
missense |
probably benign |
0.00 |
R8261:Zfp273
|
UTSW |
13 |
67,974,070 (GRCm39) |
missense |
probably benign |
0.12 |
R8424:Zfp273
|
UTSW |
13 |
67,970,471 (GRCm39) |
missense |
probably benign |
0.17 |
R8716:Zfp273
|
UTSW |
13 |
67,974,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R8843:Zfp273
|
UTSW |
13 |
67,970,387 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9010:Zfp273
|
UTSW |
13 |
67,974,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R9131:Zfp273
|
UTSW |
13 |
67,973,685 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Zfp273
|
UTSW |
13 |
67,971,261 (GRCm39) |
missense |
probably benign |
0.20 |
Z1088:Zfp273
|
UTSW |
13 |
67,973,513 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1176:Zfp273
|
UTSW |
13 |
67,971,265 (GRCm39) |
missense |
probably null |
|
|