Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700024B05Rik |
A |
T |
14: 41,820,060 (GRCm39) |
I107F |
probably benign |
Het |
Adam20 |
G |
A |
8: 41,248,490 (GRCm39) |
R200H |
probably benign |
Het |
Ahnak |
GATCTCTAT |
GAT |
19: 8,984,393 (GRCm39) |
|
probably benign |
Het |
Arfgef3 |
A |
T |
10: 18,528,556 (GRCm39) |
I277N |
probably damaging |
Het |
Atp11b |
A |
T |
3: 35,885,560 (GRCm39) |
Y851F |
probably damaging |
Het |
Cdhr1 |
A |
G |
14: 36,801,751 (GRCm39) |
S731P |
probably damaging |
Het |
Csf2rb2 |
A |
G |
15: 78,176,730 (GRCm39) |
S221P |
possibly damaging |
Het |
Dact3 |
A |
T |
7: 16,620,292 (GRCm39) |
I596F |
unknown |
Het |
Eya4 |
A |
T |
10: 23,027,870 (GRCm39) |
Y287* |
probably null |
Het |
Folr2 |
T |
C |
7: 101,489,809 (GRCm39) |
D153G |
probably benign |
Het |
Gal3st2b |
A |
T |
1: 93,866,409 (GRCm39) |
I37L |
probably benign |
Het |
H2ac8 |
G |
A |
13: 23,755,041 (GRCm39) |
P81L |
probably damaging |
Het |
Hectd1 |
A |
G |
12: 51,823,328 (GRCm39) |
M1027T |
probably benign |
Het |
Hectd4 |
A |
T |
5: 121,448,744 (GRCm39) |
Y364F |
probably benign |
Het |
Hsd17b2 |
A |
T |
8: 118,485,342 (GRCm39) |
|
probably null |
Het |
Igkv4-74 |
A |
G |
6: 69,161,993 (GRCm39) |
Y59H |
probably damaging |
Het |
Ilvbl |
T |
C |
10: 78,412,489 (GRCm39) |
V70A |
probably benign |
Het |
Klrh1 |
A |
G |
6: 129,752,359 (GRCm39) |
V52A |
possibly damaging |
Het |
Ly9 |
A |
C |
1: 171,428,756 (GRCm39) |
I288S |
probably damaging |
Het |
Muc5b |
A |
G |
7: 141,416,678 (GRCm39) |
E3208G |
probably benign |
Het |
Myo1b |
G |
A |
1: 51,818,766 (GRCm39) |
T503I |
possibly damaging |
Het |
Ntm |
T |
A |
9: 29,090,327 (GRCm39) |
I131F |
possibly damaging |
Het |
Odad1 |
T |
G |
7: 45,578,562 (GRCm39) |
V45G |
probably damaging |
Het |
Or1p4-ps1 |
A |
G |
11: 74,208,078 (GRCm39) |
T76A |
probably damaging |
Het |
Or51f23c-ps1 |
T |
C |
7: 102,431,633 (GRCm39) |
*317Q |
probably null |
Het |
Or52ae7 |
C |
T |
7: 103,119,914 (GRCm39) |
L223F |
possibly damaging |
Het |
Or5b108 |
A |
T |
19: 13,168,727 (GRCm39) |
Y232F |
probably benign |
Het |
Or8k38 |
T |
C |
2: 86,488,041 (GRCm39) |
T254A |
possibly damaging |
Het |
Pbrm1 |
T |
C |
14: 30,828,123 (GRCm39) |
S1317P |
probably damaging |
Het |
Spaca6 |
T |
A |
17: 18,058,498 (GRCm39) |
Y39* |
probably null |
Het |
Spen |
G |
A |
4: 141,244,331 (GRCm39) |
R235C |
unknown |
Het |
Sycp2l |
C |
A |
13: 41,326,183 (GRCm39) |
A746D |
probably damaging |
Het |
Tgm3 |
A |
G |
2: 129,867,229 (GRCm39) |
E158G |
possibly damaging |
Het |
Trim26 |
A |
T |
17: 37,168,307 (GRCm39) |
D324V |
probably damaging |
Het |
Ttc9b |
T |
C |
7: 27,353,475 (GRCm39) |
S42P |
probably benign |
Het |
Ttn |
C |
A |
2: 76,682,434 (GRCm39) |
E952* |
probably null |
Het |
Vmn1r85 |
A |
T |
7: 12,818,458 (GRCm39) |
S229T |
probably damaging |
Het |
Wwc1 |
C |
A |
11: 35,766,576 (GRCm39) |
A560S |
probably benign |
Het |
Zfp787 |
A |
G |
7: 6,146,059 (GRCm39) |
|
probably null |
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 |
|
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 |
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 |
|