Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm4 |
C |
A |
7: 119,302,597 (GRCm39) |
H241N |
probably damaging |
Het |
Arhgap32 |
G |
A |
9: 32,168,095 (GRCm39) |
A693T |
probably damaging |
Het |
B4galnt3 |
G |
T |
6: 120,191,759 (GRCm39) |
A658D |
probably damaging |
Het |
Car12 |
G |
A |
9: 66,653,895 (GRCm39) |
E84K |
probably benign |
Het |
Crocc2 |
T |
A |
1: 93,133,624 (GRCm39) |
S969T |
probably damaging |
Het |
Crym |
A |
G |
7: 119,794,667 (GRCm39) |
V184A |
possibly damaging |
Het |
Cryzl2 |
T |
C |
1: 157,292,583 (GRCm39) |
C122R |
probably damaging |
Het |
Defb30 |
T |
C |
14: 63,273,463 (GRCm39) |
E49G |
probably benign |
Het |
Dnah3 |
A |
G |
7: 119,550,803 (GRCm39) |
L3161P |
probably damaging |
Het |
Dnajc5g |
A |
G |
5: 31,267,036 (GRCm39) |
N104S |
probably benign |
Het |
Fcgr1 |
T |
G |
3: 96,194,302 (GRCm39) |
K195T |
probably damaging |
Het |
Gal |
C |
T |
19: 3,461,167 (GRCm39) |
R89H |
probably damaging |
Het |
Gcfc2 |
C |
T |
6: 81,925,316 (GRCm39) |
A577V |
probably benign |
Het |
Gm5116 |
A |
C |
7: 32,195,379 (GRCm39) |
|
noncoding transcript |
Het |
Golga3 |
A |
T |
5: 110,340,806 (GRCm39) |
Q540L |
probably damaging |
Het |
Hectd1 |
T |
C |
12: 51,797,171 (GRCm39) |
E2184G |
probably damaging |
Het |
Hspa12a |
T |
C |
19: 58,787,977 (GRCm39) |
D615G |
probably damaging |
Het |
Igkv14-130 |
A |
T |
6: 67,768,465 (GRCm39) |
Y107F |
probably damaging |
Het |
Ldlr |
T |
A |
9: 21,657,203 (GRCm39) |
|
probably null |
Het |
Lin9 |
T |
A |
1: 180,496,763 (GRCm39) |
L351I |
probably benign |
Het |
Lrrc37a |
A |
T |
11: 103,389,066 (GRCm39) |
S2120T |
unknown |
Het |
Mtfmt |
G |
T |
9: 65,346,897 (GRCm39) |
V164F |
probably damaging |
Het |
Nampt |
T |
C |
12: 32,883,037 (GRCm39) |
V74A |
probably damaging |
Het |
Ndufc2 |
G |
T |
7: 97,056,871 (GRCm39) |
R120L |
probably damaging |
Het |
Neo1 |
A |
T |
9: 58,801,194 (GRCm39) |
V1156D |
possibly damaging |
Het |
Nlrp1b |
G |
A |
11: 71,050,898 (GRCm39) |
P1065S |
possibly damaging |
Het |
Or4k41 |
A |
T |
2: 111,279,934 (GRCm39) |
T150S |
probably benign |
Het |
Or6c75 |
A |
T |
10: 129,337,178 (GRCm39) |
M142L |
possibly damaging |
Het |
Pign |
A |
T |
1: 105,449,798 (GRCm39) |
N909K |
possibly damaging |
Het |
Prex1 |
A |
G |
2: 166,414,883 (GRCm39) |
V304A |
probably benign |
Het |
Racgap1 |
G |
A |
15: 99,526,643 (GRCm39) |
R307W |
probably damaging |
Het |
Rap1gds1 |
C |
A |
3: 138,661,181 (GRCm39) |
E399* |
probably null |
Het |
Rwdd4a |
G |
A |
8: 47,995,837 (GRCm39) |
|
probably null |
Het |
Sanbr |
A |
C |
11: 23,570,354 (GRCm39) |
M182R |
probably benign |
Het |
Scp2 |
T |
C |
4: 107,928,488 (GRCm39) |
T401A |
probably benign |
Het |
Sdha |
A |
G |
13: 74,475,452 (GRCm39) |
F526S |
probably damaging |
Het |
Shroom1 |
T |
A |
11: 53,354,872 (GRCm39) |
L264Q |
probably benign |
Het |
Sorl1 |
T |
C |
9: 41,907,590 (GRCm39) |
T1466A |
probably benign |
Het |
Trpm2 |
C |
T |
10: 77,801,852 (GRCm39) |
C71Y |
probably damaging |
Het |
Ugt2b34 |
G |
A |
5: 87,052,246 (GRCm39) |
S250L |
probably benign |
Het |
Vmn2r88 |
A |
G |
14: 51,650,638 (GRCm39) |
D117G |
probably benign |
Het |
Wdr73 |
A |
T |
7: 80,542,173 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Nop9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02156:Nop9
|
APN |
14 |
55,990,740 (GRCm39) |
nonsense |
probably null |
|
IGL02803:Nop9
|
APN |
14 |
55,987,533 (GRCm39) |
missense |
probably benign |
|
R0443:Nop9
|
UTSW |
14 |
55,991,205 (GRCm39) |
missense |
probably benign |
0.00 |
R1766:Nop9
|
UTSW |
14 |
55,989,591 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1785:Nop9
|
UTSW |
14 |
55,988,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R1786:Nop9
|
UTSW |
14 |
55,988,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R3015:Nop9
|
UTSW |
14 |
55,988,631 (GRCm39) |
missense |
probably benign |
0.00 |
R4784:Nop9
|
UTSW |
14 |
55,983,859 (GRCm39) |
small deletion |
probably benign |
|
R5787:Nop9
|
UTSW |
14 |
55,983,791 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6271:Nop9
|
UTSW |
14 |
55,991,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R6379:Nop9
|
UTSW |
14 |
55,983,249 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6943:Nop9
|
UTSW |
14 |
55,990,270 (GRCm39) |
missense |
probably benign |
0.25 |
R7562:Nop9
|
UTSW |
14 |
55,986,809 (GRCm39) |
missense |
probably benign |
0.01 |
R8916:Nop9
|
UTSW |
14 |
55,991,101 (GRCm39) |
missense |
probably benign |
0.17 |
R8992:Nop9
|
UTSW |
14 |
55,983,438 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9070:Nop9
|
UTSW |
14 |
55,990,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R9206:Nop9
|
UTSW |
14 |
55,987,592 (GRCm39) |
critical splice donor site |
probably null |
|
R9385:Nop9
|
UTSW |
14 |
55,988,584 (GRCm39) |
missense |
probably benign |
0.01 |
|