Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
T |
C |
7: 45,631,661 (GRCm39) |
|
probably benign |
Het |
Cdkl2 |
A |
G |
5: 92,181,585 (GRCm39) |
I132T |
probably damaging |
Het |
Ckap4 |
A |
T |
10: 84,364,469 (GRCm39) |
I198N |
probably damaging |
Het |
Col6a3 |
C |
T |
1: 90,737,898 (GRCm39) |
R600H |
probably damaging |
Het |
Dnah7a |
A |
G |
1: 53,686,433 (GRCm39) |
I239T |
probably benign |
Het |
Ei24 |
A |
G |
9: 36,691,405 (GRCm39) |
*359R |
probably null |
Het |
Elk3 |
A |
T |
10: 93,090,683 (GRCm39) |
|
probably null |
Het |
Eps8l2 |
T |
A |
7: 140,922,875 (GRCm39) |
M46K |
probably damaging |
Het |
Frem2 |
G |
T |
3: 53,479,729 (GRCm39) |
T1988N |
probably benign |
Het |
Gm5431 |
T |
C |
11: 48,785,548 (GRCm39) |
K276E |
probably benign |
Het |
Gm8220 |
T |
A |
14: 44,525,729 (GRCm39) |
C133S |
possibly damaging |
Het |
Hectd2 |
T |
C |
19: 36,562,926 (GRCm39) |
L168P |
probably damaging |
Het |
Hydin |
A |
T |
8: 111,217,228 (GRCm39) |
D1372V |
probably damaging |
Het |
Isl1 |
T |
C |
13: 116,441,985 (GRCm39) |
S83G |
probably benign |
Het |
Lrp1b |
A |
G |
2: 40,490,279 (GRCm39) |
I107T |
probably benign |
Het |
Mlc1 |
A |
T |
15: 88,858,934 (GRCm39) |
V117D |
possibly damaging |
Het |
Ndc1 |
A |
G |
4: 107,237,856 (GRCm39) |
E220G |
possibly damaging |
Het |
Nlrp4b |
T |
A |
7: 10,448,427 (GRCm39) |
M210K |
probably benign |
Het |
Or2z8 |
A |
T |
8: 72,811,920 (GRCm39) |
Y132F |
probably damaging |
Het |
Plch1 |
T |
C |
3: 63,691,423 (GRCm39) |
E60G |
possibly damaging |
Het |
Pld1 |
G |
A |
3: 28,142,814 (GRCm39) |
R674H |
probably benign |
Het |
Ppp1r13l |
G |
A |
7: 19,102,794 (GRCm39) |
|
probably benign |
Het |
Rchy1 |
G |
T |
5: 92,110,502 (GRCm39) |
A26D |
probably benign |
Het |
Rrm1 |
T |
C |
7: 102,106,413 (GRCm39) |
F311L |
probably damaging |
Het |
Scrn1 |
G |
A |
6: 54,525,322 (GRCm39) |
R16* |
probably null |
Het |
Slc24a4 |
T |
C |
12: 102,189,084 (GRCm39) |
L173P |
probably damaging |
Het |
Srgap1 |
T |
C |
10: 121,640,826 (GRCm39) |
|
probably null |
Het |
Tube1 |
T |
A |
10: 39,010,977 (GRCm39) |
|
probably benign |
Het |
Utp20 |
C |
T |
10: 88,653,188 (GRCm39) |
|
probably null |
Het |
Vmn2r55 |
T |
C |
7: 12,405,120 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Ppp2cb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01566:Ppp2cb
|
APN |
8 |
34,101,791 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02985:Ppp2cb
|
APN |
8 |
34,105,474 (GRCm39) |
unclassified |
probably benign |
|
Breakthrough
|
UTSW |
8 |
34,105,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R0940:Ppp2cb
|
UTSW |
8 |
34,105,689 (GRCm39) |
splice site |
probably null |
|
R1688:Ppp2cb
|
UTSW |
8 |
34,105,480 (GRCm39) |
missense |
probably benign |
0.02 |
R2187:Ppp2cb
|
UTSW |
8 |
34,100,705 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2350:Ppp2cb
|
UTSW |
8 |
34,101,855 (GRCm39) |
missense |
probably null |
1.00 |
R4418:Ppp2cb
|
UTSW |
8 |
34,107,077 (GRCm39) |
missense |
probably benign |
|
R4566:Ppp2cb
|
UTSW |
8 |
34,100,723 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6187:Ppp2cb
|
UTSW |
8 |
34,105,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R6990:Ppp2cb
|
UTSW |
8 |
34,109,161 (GRCm39) |
missense |
probably benign |
0.01 |
R7477:Ppp2cb
|
UTSW |
8 |
34,105,502 (GRCm39) |
missense |
probably benign |
0.01 |
R9018:Ppp2cb
|
UTSW |
8 |
34,105,787 (GRCm39) |
missense |
probably benign |
0.17 |
R9301:Ppp2cb
|
UTSW |
8 |
34,090,038 (GRCm39) |
missense |
possibly damaging |
0.68 |
|