Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agbl3 |
T |
A |
6: 34,776,234 (GRCm39) |
L242M |
probably damaging |
Het |
Atad2b |
A |
T |
12: 5,040,949 (GRCm39) |
H206L |
probably damaging |
Het |
Bmp2k |
A |
G |
5: 97,235,937 (GRCm39) |
Q1120R |
probably benign |
Het |
Cdk18 |
G |
A |
1: 132,050,088 (GRCm39) |
T29I |
probably damaging |
Het |
Chrna3 |
T |
A |
9: 54,923,185 (GRCm39) |
I208F |
probably damaging |
Het |
Dhrs1 |
G |
A |
14: 55,978,729 (GRCm39) |
P140S |
possibly damaging |
Het |
Dnah14 |
C |
T |
1: 181,566,552 (GRCm39) |
R2775C |
probably damaging |
Het |
Fnip1 |
T |
G |
11: 54,393,437 (GRCm39) |
N600K |
probably benign |
Het |
Garin5b |
T |
C |
7: 4,761,464 (GRCm39) |
D416G |
probably benign |
Het |
Jmjd6 |
T |
C |
11: 116,733,326 (GRCm39) |
Y117C |
probably damaging |
Het |
Kbtbd4 |
T |
A |
2: 90,739,635 (GRCm39) |
V340E |
probably damaging |
Het |
Kif26b |
T |
C |
1: 178,755,871 (GRCm39) |
V1995A |
probably damaging |
Het |
Krt10 |
T |
C |
11: 99,278,221 (GRCm39) |
|
probably null |
Het |
Macf1 |
T |
C |
4: 123,326,074 (GRCm39) |
D3022G |
probably benign |
Het |
Map3k13 |
C |
T |
16: 21,740,527 (GRCm39) |
T618I |
probably benign |
Het |
Mat1a |
G |
A |
14: 40,843,379 (GRCm39) |
V302M |
probably damaging |
Het |
Med13l |
T |
C |
5: 118,859,539 (GRCm39) |
F242S |
probably damaging |
Het |
Npffr2 |
A |
T |
5: 89,730,871 (GRCm39) |
K267M |
probably damaging |
Het |
Nup58 |
A |
T |
14: 60,460,672 (GRCm39) |
|
probably null |
Het |
Papss2 |
A |
G |
19: 32,640,548 (GRCm39) |
Y440C |
possibly damaging |
Het |
Ppil4 |
T |
A |
10: 7,674,186 (GRCm39) |
I110N |
probably damaging |
Het |
Qrfpr |
G |
A |
3: 36,234,414 (GRCm39) |
T309I |
probably damaging |
Het |
Rbl2 |
C |
A |
8: 91,796,998 (GRCm39) |
S65R |
probably benign |
Het |
Rchy1 |
G |
A |
5: 92,105,817 (GRCm39) |
H44Y |
probably damaging |
Het |
Slc19a3 |
T |
C |
1: 83,004,081 (GRCm39) |
T7A |
probably benign |
Het |
St7 |
C |
T |
6: 17,852,313 (GRCm39) |
A233V |
probably damaging |
Het |
Syn2 |
T |
A |
6: 115,258,059 (GRCm39) |
S546T |
probably benign |
Het |
Syne1 |
A |
T |
10: 5,168,645 (GRCm39) |
Y5245* |
probably null |
Het |
Trmt6 |
A |
G |
2: 132,654,073 (GRCm39) |
W52R |
probably benign |
Het |
Ubr4 |
G |
A |
4: 139,141,705 (GRCm39) |
V1264M |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Vmn2r27 |
T |
A |
6: 124,169,369 (GRCm39) |
H587L |
possibly damaging |
Het |
Vmn2r79 |
A |
G |
7: 86,652,741 (GRCm39) |
R478G |
probably benign |
Het |
Zp2 |
T |
C |
7: 119,731,748 (GRCm39) |
E669G |
probably benign |
Het |
|
Other mutations in Ulk4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01122:Ulk4
|
APN |
9 |
120,997,358 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL01345:Ulk4
|
APN |
9 |
121,037,228 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL01432:Ulk4
|
APN |
9 |
121,095,367 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01807:Ulk4
|
APN |
9 |
121,084,251 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02139:Ulk4
|
APN |
9 |
120,970,897 (GRCm39) |
splice site |
probably null |
|
IGL02266:Ulk4
|
APN |
9 |
120,910,766 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02511:Ulk4
|
APN |
9 |
121,017,420 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02546:Ulk4
|
APN |
9 |
120,981,373 (GRCm39) |
nonsense |
probably null |
|
IGL02687:Ulk4
|
APN |
9 |
121,021,728 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03220:Ulk4
|
APN |
9 |
120,974,402 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Ulk4
|
UTSW |
9 |
121,084,237 (GRCm39) |
missense |
probably benign |
0.02 |
R0031:Ulk4
|
UTSW |
9 |
121,102,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Ulk4
|
UTSW |
9 |
120,873,885 (GRCm39) |
missense |
probably benign |
0.27 |
R0513:Ulk4
|
UTSW |
9 |
120,981,391 (GRCm39) |
missense |
probably benign |
0.13 |
R0524:Ulk4
|
UTSW |
9 |
121,081,717 (GRCm39) |
critical splice donor site |
probably null |
|
R1268:Ulk4
|
UTSW |
9 |
121,086,140 (GRCm39) |
splice site |
probably benign |
|
R1439:Ulk4
|
UTSW |
9 |
121,095,324 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1470:Ulk4
|
UTSW |
9 |
120,910,722 (GRCm39) |
missense |
probably benign |
0.00 |
R1470:Ulk4
|
UTSW |
9 |
120,910,722 (GRCm39) |
missense |
probably benign |
0.00 |
R1531:Ulk4
|
UTSW |
9 |
120,873,841 (GRCm39) |
missense |
probably damaging |
0.97 |
R1595:Ulk4
|
UTSW |
9 |
120,873,904 (GRCm39) |
missense |
probably damaging |
0.96 |
R1620:Ulk4
|
UTSW |
9 |
121,033,871 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1835:Ulk4
|
UTSW |
9 |
120,997,250 (GRCm39) |
missense |
probably null |
1.00 |
R1966:Ulk4
|
UTSW |
9 |
121,086,182 (GRCm39) |
missense |
probably benign |
|
R2129:Ulk4
|
UTSW |
9 |
120,981,248 (GRCm39) |
missense |
probably benign |
0.03 |
R2329:Ulk4
|
UTSW |
9 |
121,101,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R2877:Ulk4
|
UTSW |
9 |
121,089,105 (GRCm39) |
missense |
probably benign |
0.11 |
R2878:Ulk4
|
UTSW |
9 |
121,089,105 (GRCm39) |
missense |
probably benign |
0.11 |
R3734:Ulk4
|
UTSW |
9 |
121,091,055 (GRCm39) |
missense |
probably benign |
0.21 |
R3769:Ulk4
|
UTSW |
9 |
121,092,766 (GRCm39) |
missense |
probably benign |
0.00 |
R4005:Ulk4
|
UTSW |
9 |
120,997,265 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4024:Ulk4
|
UTSW |
9 |
120,873,915 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4321:Ulk4
|
UTSW |
9 |
120,903,062 (GRCm39) |
missense |
probably benign |
0.00 |
R4461:Ulk4
|
UTSW |
9 |
120,985,950 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4537:Ulk4
|
UTSW |
9 |
121,092,704 (GRCm39) |
nonsense |
probably null |
|
R4542:Ulk4
|
UTSW |
9 |
121,092,704 (GRCm39) |
nonsense |
probably null |
|
R4572:Ulk4
|
UTSW |
9 |
121,021,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R4647:Ulk4
|
UTSW |
9 |
120,970,918 (GRCm39) |
missense |
probably benign |
0.15 |
R4712:Ulk4
|
UTSW |
9 |
121,073,436 (GRCm39) |
missense |
probably benign |
0.23 |
R4730:Ulk4
|
UTSW |
9 |
121,092,791 (GRCm39) |
missense |
probably benign |
0.05 |
R4731:Ulk4
|
UTSW |
9 |
121,092,704 (GRCm39) |
nonsense |
probably null |
|
R4732:Ulk4
|
UTSW |
9 |
121,092,704 (GRCm39) |
nonsense |
probably null |
|
R4733:Ulk4
|
UTSW |
9 |
121,092,704 (GRCm39) |
nonsense |
probably null |
|
R4737:Ulk4
|
UTSW |
9 |
120,902,938 (GRCm39) |
nonsense |
probably null |
|
R4781:Ulk4
|
UTSW |
9 |
120,932,642 (GRCm39) |
missense |
probably benign |
0.00 |
R4860:Ulk4
|
UTSW |
9 |
121,079,968 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4926:Ulk4
|
UTSW |
9 |
121,087,798 (GRCm39) |
missense |
probably benign |
0.00 |
R4990:Ulk4
|
UTSW |
9 |
121,021,852 (GRCm39) |
missense |
probably benign |
0.01 |
R6056:Ulk4
|
UTSW |
9 |
121,102,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R6448:Ulk4
|
UTSW |
9 |
120,932,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R6668:Ulk4
|
UTSW |
9 |
121,017,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R6915:Ulk4
|
UTSW |
9 |
121,087,886 (GRCm39) |
missense |
probably benign |
|
R6929:Ulk4
|
UTSW |
9 |
120,903,081 (GRCm39) |
missense |
probably benign |
0.02 |
R7069:Ulk4
|
UTSW |
9 |
121,095,583 (GRCm39) |
missense |
probably benign |
0.25 |
R7069:Ulk4
|
UTSW |
9 |
121,087,876 (GRCm39) |
missense |
probably benign |
0.01 |
R7293:Ulk4
|
UTSW |
9 |
121,084,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R7299:Ulk4
|
UTSW |
9 |
120,974,125 (GRCm39) |
missense |
probably benign |
0.32 |
R7301:Ulk4
|
UTSW |
9 |
120,974,125 (GRCm39) |
missense |
probably benign |
0.32 |
R7337:Ulk4
|
UTSW |
9 |
121,077,993 (GRCm39) |
missense |
probably benign |
0.44 |
R7395:Ulk4
|
UTSW |
9 |
121,084,178 (GRCm39) |
missense |
probably benign |
|
R7423:Ulk4
|
UTSW |
9 |
120,932,687 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7545:Ulk4
|
UTSW |
9 |
120,970,904 (GRCm39) |
missense |
probably benign |
0.00 |
R7753:Ulk4
|
UTSW |
9 |
121,095,578 (GRCm39) |
critical splice donor site |
probably null |
|
R7790:Ulk4
|
UTSW |
9 |
121,092,734 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7791:Ulk4
|
UTSW |
9 |
121,092,734 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7793:Ulk4
|
UTSW |
9 |
121,092,734 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7834:Ulk4
|
UTSW |
9 |
121,092,734 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7836:Ulk4
|
UTSW |
9 |
120,873,885 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7960:Ulk4
|
UTSW |
9 |
121,102,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R8087:Ulk4
|
UTSW |
9 |
121,095,317 (GRCm39) |
missense |
probably damaging |
0.99 |
R8203:Ulk4
|
UTSW |
9 |
120,997,274 (GRCm39) |
missense |
probably damaging |
0.96 |
R8246:Ulk4
|
UTSW |
9 |
120,985,941 (GRCm39) |
makesense |
probably null |
|
R8430:Ulk4
|
UTSW |
9 |
121,086,144 (GRCm39) |
critical splice donor site |
probably null |
|
R8841:Ulk4
|
UTSW |
9 |
121,033,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R9014:Ulk4
|
UTSW |
9 |
121,017,294 (GRCm39) |
missense |
probably benign |
0.00 |
R9092:Ulk4
|
UTSW |
9 |
120,903,003 (GRCm39) |
missense |
|
|
R9126:Ulk4
|
UTSW |
9 |
121,090,988 (GRCm39) |
missense |
probably damaging |
0.99 |
R9176:Ulk4
|
UTSW |
9 |
120,974,128 (GRCm39) |
missense |
probably benign |
|
R9235:Ulk4
|
UTSW |
9 |
120,981,217 (GRCm39) |
missense |
probably benign |
0.13 |
R9713:Ulk4
|
UTSW |
9 |
120,873,862 (GRCm39) |
nonsense |
probably null |
|
X0024:Ulk4
|
UTSW |
9 |
121,021,819 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Ulk4
|
UTSW |
9 |
121,091,672 (GRCm39) |
missense |
probably damaging |
1.00 |
|