Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts13 |
A |
T |
2: 26,896,275 (GRCm39) |
R1223* |
probably null |
Het |
Adgrb3 |
A |
T |
1: 25,150,852 (GRCm39) |
L1127* |
probably null |
Het |
Ankrd17 |
A |
T |
5: 90,433,384 (GRCm39) |
V727D |
possibly damaging |
Het |
Ankub1 |
A |
T |
3: 57,572,854 (GRCm39) |
C289* |
probably null |
Het |
C2 |
T |
A |
17: 35,083,323 (GRCm39) |
I242F |
possibly damaging |
Het |
C2cd3 |
T |
C |
7: 100,100,826 (GRCm39) |
L653P |
probably damaging |
Het |
Cacna1b |
A |
G |
2: 24,522,022 (GRCm39) |
V1696A |
probably damaging |
Het |
Cep295 |
A |
G |
9: 15,244,358 (GRCm39) |
I1366T |
probably damaging |
Het |
Chd9 |
T |
C |
8: 91,769,573 (GRCm39) |
L2553P |
probably damaging |
Het |
Cited4 |
C |
A |
4: 120,524,244 (GRCm39) |
T82K |
probably benign |
Het |
Dnah6 |
A |
T |
6: 73,021,756 (GRCm39) |
M3470K |
probably damaging |
Het |
Exosc3 |
G |
T |
4: 45,320,482 (GRCm39) |
P37Q |
probably damaging |
Het |
Fam120b |
C |
A |
17: 15,643,290 (GRCm39) |
Q690K |
possibly damaging |
Het |
Fyb1 |
T |
C |
15: 6,668,388 (GRCm39) |
I527T |
probably damaging |
Het |
Gm32742 |
A |
G |
9: 51,065,579 (GRCm39) |
L459P |
probably benign |
Het |
Gm45861 |
A |
G |
8: 28,014,462 (GRCm39) |
D655G |
unknown |
Het |
Ifi203 |
A |
G |
1: 173,756,340 (GRCm39) |
|
probably benign |
Het |
Ifnar2 |
T |
A |
16: 91,190,766 (GRCm39) |
L93* |
probably null |
Het |
Kdr |
A |
G |
5: 76,138,764 (GRCm39) |
V22A |
probably benign |
Het |
Llgl1 |
C |
T |
11: 60,601,179 (GRCm39) |
Q706* |
probably null |
Het |
Lrrc9 |
A |
T |
12: 72,497,546 (GRCm39) |
K121N |
probably benign |
Het |
Lyst |
T |
C |
13: 13,917,909 (GRCm39) |
F3323S |
probably damaging |
Het |
Mc4r |
A |
G |
18: 66,992,253 (GRCm39) |
Y287H |
probably damaging |
Het |
Nlrp4e |
A |
C |
7: 23,036,156 (GRCm39) |
|
probably null |
Het |
Or52z12 |
A |
T |
7: 103,233,651 (GRCm39) |
I141F |
probably damaging |
Het |
Or8b42 |
A |
G |
9: 38,342,444 (GRCm39) |
I289V |
probably benign |
Het |
Pear1 |
T |
A |
3: 87,666,872 (GRCm39) |
K38* |
probably null |
Het |
Pik3c2g |
G |
A |
6: 139,903,502 (GRCm39) |
R585Q |
possibly damaging |
Het |
Prpf40a |
A |
G |
2: 53,034,875 (GRCm39) |
V771A |
possibly damaging |
Het |
Rnd3 |
G |
T |
2: 51,027,187 (GRCm39) |
D103E |
probably damaging |
Het |
Sfpq |
GCCGCCGCAGCAGCCTCCGCCGCAGCAGCC |
GCCGCCGCAGCAGCC |
4: 126,915,419 (GRCm39) |
|
probably benign |
Het |
Spats2l |
A |
T |
1: 57,918,695 (GRCm39) |
N43I |
probably damaging |
Het |
Tmem202 |
C |
A |
9: 59,426,504 (GRCm39) |
G221C |
probably benign |
Het |
Ubiad1 |
T |
C |
4: 148,528,579 (GRCm39) |
D110G |
probably damaging |
Het |
Vmn2r118 |
C |
T |
17: 55,917,440 (GRCm39) |
M357I |
probably benign |
Het |
Zfp663 |
G |
C |
2: 165,195,178 (GRCm39) |
P347R |
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 |
R6546:Ulk4
|
UTSW |
9 |
120,970,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R6668:Ulk4
|
UTSW |
9 |
121,017,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R6915:Ulk4
|
UTSW |
9 |
121,087,886 (GRCm39) |
missense |
probably benign |
|
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 |
|