Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003H04Rik |
A |
G |
3: 124,373,527 (GRCm39) |
S23P |
possibly damaging |
Het |
Adam1a |
T |
C |
5: 121,657,439 (GRCm39) |
Y618C |
probably benign |
Het |
Amigo2 |
A |
C |
15: 97,143,107 (GRCm39) |
S438R |
probably benign |
Het |
Atp5me |
T |
C |
5: 108,581,922 (GRCm39) |
I21V |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,365,017 (GRCm39) |
|
probably benign |
Het |
Dock2 |
A |
G |
11: 34,260,390 (GRCm39) |
Y984H |
probably damaging |
Het |
Dpysl2 |
T |
A |
14: 67,045,367 (GRCm39) |
I469F |
possibly damaging |
Het |
Edem3 |
C |
T |
1: 151,694,379 (GRCm39) |
T886I |
probably benign |
Het |
Gart |
T |
C |
16: 91,422,400 (GRCm39) |
T706A |
probably benign |
Het |
Gfpt2 |
A |
T |
11: 49,698,517 (GRCm39) |
|
probably benign |
Het |
Gm11541 |
T |
G |
11: 94,586,495 (GRCm39) |
D84A |
unknown |
Het |
Gne |
T |
C |
4: 44,041,860 (GRCm39) |
|
probably null |
Het |
Gria4 |
A |
T |
9: 4,503,652 (GRCm39) |
D321E |
probably benign |
Het |
Ift122 |
T |
G |
6: 115,889,565 (GRCm39) |
|
probably null |
Het |
Lcp2 |
A |
T |
11: 33,997,345 (GRCm39) |
|
probably benign |
Het |
Mcm2 |
C |
T |
6: 88,868,948 (GRCm39) |
|
probably benign |
Het |
Or8b54 |
A |
G |
9: 38,687,225 (GRCm39) |
I225V |
probably benign |
Het |
Ptpru |
C |
A |
4: 131,496,803 (GRCm39) |
|
probably benign |
Het |
Rpap2 |
T |
C |
5: 107,751,492 (GRCm39) |
|
probably null |
Het |
Slc25a39 |
T |
C |
11: 102,295,726 (GRCm39) |
T138A |
probably damaging |
Het |
St6galnac1 |
A |
C |
11: 116,660,165 (GRCm39) |
S49R |
probably benign |
Het |
Stat1 |
T |
C |
1: 52,178,502 (GRCm39) |
L312P |
probably damaging |
Het |
Tmem198 |
T |
C |
1: 75,461,014 (GRCm39) |
|
probably benign |
Het |
Top2a |
A |
T |
11: 98,901,856 (GRCm39) |
L458Q |
probably damaging |
Het |
Treml4 |
T |
C |
17: 48,572,023 (GRCm39) |
|
probably benign |
Het |
Trpm6 |
A |
G |
19: 18,786,933 (GRCm39) |
D503G |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,775,617 (GRCm39) |
E1854D |
unknown |
Het |
Zfyve9 |
T |
C |
4: 108,539,457 (GRCm39) |
T939A |
probably damaging |
Het |
|
Other mutations in Ubqln3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00656:Ubqln3
|
APN |
7 |
103,790,984 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00766:Ubqln3
|
APN |
7 |
103,792,031 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01673:Ubqln3
|
APN |
7 |
103,791,605 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01705:Ubqln3
|
APN |
7 |
103,791,884 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01988:Ubqln3
|
APN |
7 |
103,792,089 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02008:Ubqln3
|
APN |
7 |
103,791,523 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02072:Ubqln3
|
APN |
7 |
103,790,506 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02546:Ubqln3
|
APN |
7 |
103,791,725 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02657:Ubqln3
|
APN |
7 |
103,791,170 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02682:Ubqln3
|
APN |
7 |
103,791,272 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02709:Ubqln3
|
APN |
7 |
103,790,543 (GRCm39) |
missense |
probably benign |
0.12 |
IGL03357:Ubqln3
|
APN |
7 |
103,791,763 (GRCm39) |
missense |
probably benign |
|
PIT4544001:Ubqln3
|
UTSW |
7 |
103,790,550 (GRCm39) |
missense |
probably damaging |
0.97 |
R0180:Ubqln3
|
UTSW |
7 |
103,791,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R0845:Ubqln3
|
UTSW |
7 |
103,791,275 (GRCm39) |
missense |
probably damaging |
0.98 |
R1019:Ubqln3
|
UTSW |
7 |
103,790,593 (GRCm39) |
missense |
probably benign |
0.00 |
R1280:Ubqln3
|
UTSW |
7 |
103,791,283 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1448:Ubqln3
|
UTSW |
7 |
103,791,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R1550:Ubqln3
|
UTSW |
7 |
103,790,753 (GRCm39) |
missense |
probably damaging |
0.98 |
R1617:Ubqln3
|
UTSW |
7 |
103,792,067 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1650:Ubqln3
|
UTSW |
7 |
103,790,228 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2060:Ubqln3
|
UTSW |
7 |
103,791,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R2246:Ubqln3
|
UTSW |
7 |
103,791,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R2263:Ubqln3
|
UTSW |
7 |
103,790,842 (GRCm39) |
nonsense |
probably null |
|
R2366:Ubqln3
|
UTSW |
7 |
103,790,256 (GRCm39) |
missense |
probably damaging |
0.99 |
R4232:Ubqln3
|
UTSW |
7 |
103,791,010 (GRCm39) |
missense |
probably benign |
0.00 |
R4447:Ubqln3
|
UTSW |
7 |
103,792,021 (GRCm39) |
missense |
probably benign |
0.31 |
R4509:Ubqln3
|
UTSW |
7 |
103,790,651 (GRCm39) |
missense |
probably damaging |
0.97 |
R4604:Ubqln3
|
UTSW |
7 |
103,791,698 (GRCm39) |
missense |
probably benign |
0.00 |
R5416:Ubqln3
|
UTSW |
7 |
103,790,879 (GRCm39) |
missense |
probably benign |
0.34 |
R5617:Ubqln3
|
UTSW |
7 |
103,791,640 (GRCm39) |
missense |
probably damaging |
0.99 |
R5648:Ubqln3
|
UTSW |
7 |
103,790,117 (GRCm39) |
missense |
probably damaging |
0.99 |
R5722:Ubqln3
|
UTSW |
7 |
103,790,674 (GRCm39) |
missense |
probably benign |
0.00 |
R5723:Ubqln3
|
UTSW |
7 |
103,790,674 (GRCm39) |
missense |
probably benign |
0.00 |
R5724:Ubqln3
|
UTSW |
7 |
103,790,674 (GRCm39) |
missense |
probably benign |
0.00 |
R5819:Ubqln3
|
UTSW |
7 |
103,790,674 (GRCm39) |
missense |
probably benign |
0.00 |
R5820:Ubqln3
|
UTSW |
7 |
103,790,674 (GRCm39) |
missense |
probably benign |
0.00 |
R5966:Ubqln3
|
UTSW |
7 |
103,790,906 (GRCm39) |
missense |
probably benign |
0.03 |
R6260:Ubqln3
|
UTSW |
7 |
103,791,524 (GRCm39) |
nonsense |
probably null |
|
R6272:Ubqln3
|
UTSW |
7 |
103,791,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R6542:Ubqln3
|
UTSW |
7 |
103,790,824 (GRCm39) |
missense |
probably benign |
0.00 |
R6936:Ubqln3
|
UTSW |
7 |
103,791,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R7023:Ubqln3
|
UTSW |
7 |
103,790,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R7025:Ubqln3
|
UTSW |
7 |
103,790,482 (GRCm39) |
missense |
probably benign |
0.01 |
R7079:Ubqln3
|
UTSW |
7 |
103,790,578 (GRCm39) |
missense |
probably benign |
0.12 |
R7733:Ubqln3
|
UTSW |
7 |
103,790,283 (GRCm39) |
missense |
probably damaging |
0.98 |
R7764:Ubqln3
|
UTSW |
7 |
103,790,443 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7919:Ubqln3
|
UTSW |
7 |
103,790,399 (GRCm39) |
missense |
probably benign |
0.03 |
R7961:Ubqln3
|
UTSW |
7 |
103,791,797 (GRCm39) |
missense |
probably benign |
0.00 |
R8009:Ubqln3
|
UTSW |
7 |
103,791,797 (GRCm39) |
missense |
probably benign |
0.00 |
R9619:Ubqln3
|
UTSW |
7 |
103,791,053 (GRCm39) |
missense |
probably benign |
0.05 |
R9652:Ubqln3
|
UTSW |
7 |
103,791,962 (GRCm39) |
missense |
probably damaging |
1.00 |
RF054:Ubqln3
|
UTSW |
7 |
103,790,385 (GRCm39) |
frame shift |
probably null |
|
|