Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts17 |
A |
T |
7: 66,770,636 (GRCm39) |
Y915F |
probably benign |
Het |
Adap2 |
T |
A |
11: 80,045,848 (GRCm39) |
F43I |
probably damaging |
Het |
Adprs |
A |
T |
4: 126,210,406 (GRCm39) |
L358Q |
possibly damaging |
Het |
Akap9 |
A |
C |
5: 4,012,061 (GRCm39) |
Q921H |
probably damaging |
Het |
Amigo2 |
A |
G |
15: 97,143,256 (GRCm39) |
S389P |
probably benign |
Het |
Atg2b |
A |
T |
12: 105,627,351 (GRCm39) |
C545* |
probably null |
Het |
C2cd3 |
A |
G |
7: 100,065,635 (GRCm39) |
E807G |
probably benign |
Het |
Ccdc110 |
A |
G |
8: 46,395,078 (GRCm39) |
E323G |
probably damaging |
Het |
Cdk5rap2 |
T |
A |
4: 70,153,691 (GRCm39) |
S1711C |
probably damaging |
Het |
Cebpzos |
T |
G |
17: 79,226,486 (GRCm39) |
D39E |
probably damaging |
Het |
Cenpe |
A |
G |
3: 134,945,539 (GRCm39) |
N1018D |
probably benign |
Het |
Cfap68 |
T |
G |
9: 50,676,057 (GRCm39) |
N87T |
probably damaging |
Het |
Clspn |
C |
A |
4: 126,459,532 (GRCm39) |
H141Q |
probably damaging |
Het |
Cluh |
C |
T |
11: 74,557,068 (GRCm39) |
A1010V |
probably benign |
Het |
Col27a1 |
G |
T |
4: 63,242,678 (GRCm39) |
|
probably benign |
Het |
Cpt2 |
T |
C |
4: 107,771,513 (GRCm39) |
M61V |
probably benign |
Het |
Ddr2 |
T |
A |
1: 169,814,709 (GRCm39) |
H578L |
probably damaging |
Het |
Dnah14 |
T |
A |
1: 181,611,121 (GRCm39) |
I3749N |
probably damaging |
Het |
Dnajc18 |
T |
C |
18: 35,813,978 (GRCm39) |
T264A |
possibly damaging |
Het |
Ecpas |
T |
A |
4: 58,827,068 (GRCm39) |
T1022S |
probably benign |
Het |
Eml6 |
T |
C |
11: 29,769,066 (GRCm39) |
N693S |
probably damaging |
Het |
Ephx4 |
A |
G |
5: 107,553,977 (GRCm39) |
E9G |
probably damaging |
Het |
Eps15l1 |
G |
A |
8: 73,095,278 (GRCm39) |
Q747* |
probably null |
Het |
Flrt1 |
C |
T |
19: 7,073,974 (GRCm39) |
S191N |
probably damaging |
Het |
Gm5114 |
C |
T |
7: 39,057,579 (GRCm39) |
R680H |
probably benign |
Het |
Gm5431 |
T |
C |
11: 48,780,172 (GRCm39) |
H250R |
probably damaging |
Het |
Gm7233 |
T |
C |
14: 43,040,342 (GRCm39) |
C198R |
possibly damaging |
Het |
Herc2 |
C |
G |
7: 55,872,682 (GRCm39) |
Q4407E |
probably damaging |
Het |
Hmx3 |
C |
G |
7: 131,144,734 (GRCm39) |
|
probably benign |
Het |
Hoxb7 |
C |
A |
11: 96,177,909 (GRCm39) |
A119E |
probably benign |
Het |
Ifi207 |
A |
T |
1: 173,557,532 (GRCm39) |
M402K |
probably benign |
Het |
Ints14 |
T |
C |
9: 64,871,719 (GRCm39) |
V19A |
probably benign |
Het |
Itgae |
T |
A |
11: 73,022,519 (GRCm39) |
N911K |
possibly damaging |
Het |
Kif1a |
T |
C |
1: 93,004,048 (GRCm39) |
S145G |
probably damaging |
Het |
Klhdc4 |
A |
G |
8: 122,531,793 (GRCm39) |
W187R |
probably damaging |
Het |
Krt1 |
A |
T |
15: 101,758,684 (GRCm39) |
I160N |
probably damaging |
Het |
Krt12 |
T |
C |
11: 99,307,745 (GRCm39) |
T448A |
probably benign |
Het |
Lcmt2 |
G |
A |
2: 120,969,938 (GRCm39) |
R382* |
probably null |
Het |
Map3k8 |
C |
T |
18: 4,340,651 (GRCm39) |
S221N |
probably damaging |
Het |
Med17 |
T |
C |
9: 15,190,854 (GRCm39) |
D79G |
probably benign |
Het |
Mlf1 |
A |
T |
3: 67,307,060 (GRCm39) |
I257F |
probably damaging |
Het |
Mov10l1 |
T |
A |
15: 88,879,098 (GRCm39) |
F153I |
probably damaging |
Het |
Msto1 |
A |
C |
3: 88,819,405 (GRCm39) |
V149G |
probably damaging |
Het |
Mybl1 |
T |
C |
1: 9,748,732 (GRCm39) |
|
probably null |
Het |
Myoc |
A |
G |
1: 162,476,580 (GRCm39) |
Y428C |
probably damaging |
Het |
Nin |
A |
G |
12: 70,091,955 (GRCm39) |
S785P |
possibly damaging |
Het |
Oit3 |
A |
T |
10: 59,264,061 (GRCm39) |
F358I |
probably damaging |
Het |
Or5t15 |
C |
T |
2: 86,681,338 (GRCm39) |
V235I |
probably benign |
Het |
Or6c88 |
A |
G |
10: 129,406,571 (GRCm39) |
T16A |
possibly damaging |
Het |
Paip1 |
A |
G |
13: 119,566,753 (GRCm39) |
N29S |
probably benign |
Het |
Pcdhgb4 |
T |
C |
18: 37,855,509 (GRCm39) |
S635P |
probably benign |
Het |
Pcsk1 |
A |
G |
13: 75,280,298 (GRCm39) |
N708D |
possibly damaging |
Het |
Plch1 |
C |
T |
3: 63,688,811 (GRCm39) |
W131* |
probably null |
Het |
Prag1 |
A |
T |
8: 36,569,860 (GRCm39) |
M148L |
possibly damaging |
Het |
Ptch1 |
A |
G |
13: 63,691,359 (GRCm39) |
L176P |
probably damaging |
Het |
Ralgapa1 |
A |
T |
12: 55,793,931 (GRCm39) |
V568D |
probably damaging |
Het |
Rb1 |
A |
T |
14: 73,435,974 (GRCm39) |
M897K |
probably benign |
Het |
Resf1 |
T |
A |
6: 149,230,493 (GRCm39) |
Y1180N |
probably damaging |
Het |
Robo3 |
T |
A |
9: 37,338,323 (GRCm39) |
Q386L |
probably damaging |
Het |
Rtn4rl1 |
T |
C |
11: 75,156,828 (GRCm39) |
V420A |
possibly damaging |
Het |
Sall1 |
A |
T |
8: 89,756,896 (GRCm39) |
N1069K |
probably benign |
Het |
Sipa1l1 |
A |
G |
12: 82,419,242 (GRCm39) |
E640G |
probably damaging |
Het |
Slc22a2 |
C |
A |
17: 12,831,297 (GRCm39) |
Y362* |
probably null |
Het |
Slc5a9 |
T |
C |
4: 111,737,450 (GRCm39) |
E603G |
probably benign |
Het |
Slc6a17 |
A |
T |
3: 107,407,722 (GRCm39) |
I83N |
probably damaging |
Het |
Snx29 |
G |
T |
16: 11,221,430 (GRCm39) |
M285I |
probably benign |
Het |
Spata2 |
T |
C |
2: 167,326,094 (GRCm39) |
T242A |
possibly damaging |
Het |
Stard13 |
A |
G |
5: 150,970,384 (GRCm39) |
L733P |
possibly damaging |
Het |
Svep1 |
A |
G |
4: 58,073,045 (GRCm39) |
V2088A |
possibly damaging |
Het |
Tdp2 |
A |
G |
13: 25,024,540 (GRCm39) |
E279G |
probably damaging |
Het |
Tnfrsf8 |
T |
G |
4: 144,995,794 (GRCm39) |
I422L |
probably damaging |
Het |
Tpk1 |
T |
A |
6: 43,323,736 (GRCm39) |
T189S |
possibly damaging |
Het |
Trhde |
A |
T |
10: 114,403,129 (GRCm39) |
M498K |
probably damaging |
Het |
Trim35 |
T |
A |
14: 66,540,653 (GRCm39) |
H168Q |
possibly damaging |
Het |
Tubb5 |
T |
C |
17: 36,147,347 (GRCm39) |
|
probably benign |
Het |
Tut4 |
C |
T |
4: 108,336,177 (GRCm39) |
T6I |
probably benign |
Het |
Vmn1r181 |
G |
A |
7: 23,684,183 (GRCm39) |
R216Q |
probably benign |
Het |
Vmn2r77 |
G |
A |
7: 86,451,031 (GRCm39) |
G306R |
probably benign |
Het |
Xkr4 |
C |
T |
1: 3,741,261 (GRCm39) |
R104H |
possibly damaging |
Het |
|
Other mutations in Zfp398 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01420:Zfp398
|
APN |
6 |
47,842,868 (GRCm39) |
missense |
probably benign |
|
IGL01543:Zfp398
|
APN |
6 |
47,842,997 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01822:Zfp398
|
APN |
6 |
47,843,205 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02118:Zfp398
|
APN |
6 |
47,835,879 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02454:Zfp398
|
APN |
6 |
47,817,301 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02725:Zfp398
|
APN |
6 |
47,842,737 (GRCm39) |
missense |
probably benign |
0.00 |
R0453:Zfp398
|
UTSW |
6 |
47,842,782 (GRCm39) |
missense |
probably benign |
0.01 |
R0635:Zfp398
|
UTSW |
6 |
47,840,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R1759:Zfp398
|
UTSW |
6 |
47,836,412 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2366:Zfp398
|
UTSW |
6 |
47,840,143 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2696:Zfp398
|
UTSW |
6 |
47,843,879 (GRCm39) |
makesense |
probably null |
|
R4090:Zfp398
|
UTSW |
6 |
47,843,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R4157:Zfp398
|
UTSW |
6 |
47,812,843 (GRCm39) |
missense |
probably benign |
|
R4610:Zfp398
|
UTSW |
6 |
47,817,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R4784:Zfp398
|
UTSW |
6 |
47,817,186 (GRCm39) |
missense |
probably benign |
|
R4849:Zfp398
|
UTSW |
6 |
47,836,446 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5166:Zfp398
|
UTSW |
6 |
47,842,838 (GRCm39) |
missense |
probably benign |
|
R5289:Zfp398
|
UTSW |
6 |
47,840,115 (GRCm39) |
missense |
probably benign |
|
R5877:Zfp398
|
UTSW |
6 |
47,817,638 (GRCm39) |
intron |
probably benign |
|
R6383:Zfp398
|
UTSW |
6 |
47,843,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R6825:Zfp398
|
UTSW |
6 |
47,843,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R6882:Zfp398
|
UTSW |
6 |
47,843,016 (GRCm39) |
missense |
probably damaging |
0.99 |
R7038:Zfp398
|
UTSW |
6 |
47,843,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R7114:Zfp398
|
UTSW |
6 |
47,842,910 (GRCm39) |
missense |
probably benign |
0.00 |
R7386:Zfp398
|
UTSW |
6 |
47,835,884 (GRCm39) |
missense |
probably benign |
0.05 |
R7519:Zfp398
|
UTSW |
6 |
47,836,407 (GRCm39) |
missense |
probably benign |
0.00 |
R7525:Zfp398
|
UTSW |
6 |
47,842,752 (GRCm39) |
missense |
probably benign |
|
R7571:Zfp398
|
UTSW |
6 |
47,843,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R8374:Zfp398
|
UTSW |
6 |
47,836,468 (GRCm39) |
critical splice donor site |
probably null |
|
R9055:Zfp398
|
UTSW |
6 |
47,843,319 (GRCm39) |
missense |
possibly damaging |
0.73 |
Z1176:Zfp398
|
UTSW |
6 |
47,843,789 (GRCm39) |
missense |
probably benign |
|
|