Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam4 |
T |
G |
12: 81,468,228 (GRCm39) |
D131A |
probably damaging |
Het |
Ank3 |
T |
C |
10: 69,826,074 (GRCm39) |
|
probably benign |
Het |
Atp1a4 |
T |
C |
1: 172,085,617 (GRCm39) |
|
probably benign |
Het |
Bmal2 |
T |
A |
6: 146,720,398 (GRCm39) |
D187E |
probably damaging |
Het |
Ccdc162 |
T |
C |
10: 41,520,637 (GRCm39) |
N673S |
probably benign |
Het |
Cd84 |
G |
A |
1: 171,700,344 (GRCm39) |
V154M |
probably damaging |
Het |
Celsr1 |
C |
A |
15: 85,790,115 (GRCm39) |
|
probably null |
Het |
Cfap57 |
A |
C |
4: 118,441,914 (GRCm39) |
L718R |
probably damaging |
Het |
Cntnap5b |
G |
A |
1: 100,406,211 (GRCm39) |
V803M |
probably damaging |
Het |
Col6a2 |
C |
T |
10: 76,450,392 (GRCm39) |
V180I |
probably damaging |
Het |
Coq4 |
A |
T |
2: 29,678,297 (GRCm39) |
|
probably benign |
Het |
Cyp2a4 |
A |
G |
7: 26,012,983 (GRCm39) |
T389A |
probably benign |
Het |
Dennd1c |
T |
C |
17: 57,373,802 (GRCm39) |
D587G |
probably benign |
Het |
Dnaja4 |
A |
G |
9: 54,607,038 (GRCm39) |
D9G |
probably damaging |
Het |
Hes2 |
T |
G |
4: 152,244,834 (GRCm39) |
L101R |
probably damaging |
Het |
Icam2 |
A |
G |
11: 106,273,307 (GRCm39) |
S2P |
probably damaging |
Het |
Krt31 |
A |
G |
11: 99,939,254 (GRCm39) |
L221P |
probably damaging |
Het |
Lipm |
A |
T |
19: 34,098,665 (GRCm39) |
N380Y |
probably benign |
Het |
Lrp2bp |
G |
A |
8: 46,473,600 (GRCm39) |
|
probably null |
Het |
Mbd2 |
T |
A |
18: 70,713,819 (GRCm39) |
M216K |
probably damaging |
Het |
Mrps33 |
T |
C |
6: 39,782,599 (GRCm39) |
|
probably benign |
Het |
Nbeal2 |
T |
C |
9: 110,462,060 (GRCm39) |
D1459G |
probably damaging |
Het |
Ncapd3 |
T |
C |
9: 26,998,852 (GRCm39) |
S1281P |
probably benign |
Het |
Nt5c1b |
T |
A |
12: 10,422,874 (GRCm39) |
Y56N |
possibly damaging |
Het |
Nthl1 |
A |
G |
17: 24,853,008 (GRCm39) |
K71E |
probably benign |
Het |
Or4f62 |
T |
A |
2: 111,987,227 (GRCm39) |
N310K |
probably benign |
Het |
Parvb |
C |
T |
15: 84,182,180 (GRCm39) |
R237W |
probably damaging |
Het |
Pde4a |
G |
A |
9: 21,122,521 (GRCm39) |
A806T |
probably damaging |
Het |
Pde4d |
C |
A |
13: 109,769,432 (GRCm39) |
S40* |
probably null |
Het |
Pde4dip |
G |
A |
3: 97,625,555 (GRCm39) |
R1348* |
probably null |
Het |
Pdx1 |
C |
T |
5: 147,207,310 (GRCm39) |
P88S |
probably damaging |
Het |
Pnisr |
T |
A |
4: 21,859,165 (GRCm39) |
V120D |
probably damaging |
Het |
Prss51 |
G |
T |
14: 64,332,508 (GRCm39) |
C65F |
probably damaging |
Het |
Pus10 |
G |
A |
11: 23,652,975 (GRCm39) |
E195K |
possibly damaging |
Het |
Pzp |
T |
A |
6: 128,464,917 (GRCm39) |
Q1319L |
probably damaging |
Het |
Rbpms |
G |
T |
8: 34,324,421 (GRCm39) |
T101K |
probably damaging |
Het |
Rundc3a |
A |
G |
11: 102,290,775 (GRCm39) |
N281S |
possibly damaging |
Het |
Scml4 |
C |
T |
10: 42,736,728 (GRCm39) |
|
probably benign |
Het |
Sez6 |
T |
C |
11: 77,844,528 (GRCm39) |
V117A |
probably damaging |
Het |
Sgsm2 |
A |
C |
11: 74,756,250 (GRCm39) |
C366W |
probably damaging |
Het |
Slc12a4 |
T |
C |
8: 106,670,882 (GRCm39) |
|
probably null |
Het |
Smg5 |
C |
T |
3: 88,260,332 (GRCm39) |
R641C |
probably damaging |
Het |
Stxbp3 |
A |
G |
3: 108,723,762 (GRCm39) |
Y150H |
probably benign |
Het |
Thoc2l |
T |
A |
5: 104,668,145 (GRCm39) |
M889K |
probably damaging |
Het |
Tkt |
T |
C |
14: 30,291,041 (GRCm39) |
F351S |
probably damaging |
Het |
Tln1 |
A |
G |
4: 43,547,618 (GRCm39) |
L781P |
probably damaging |
Het |
Triobp |
G |
A |
15: 78,885,765 (GRCm39) |
E1823K |
probably damaging |
Het |
Ttll4 |
T |
C |
1: 74,720,948 (GRCm39) |
V538A |
possibly damaging |
Het |
Uba52rt |
A |
G |
4: 3,973,386 (GRCm39) |
Y59H |
probably benign |
Het |
Vmn1r61 |
T |
A |
7: 5,613,687 (GRCm39) |
N209I |
possibly damaging |
Het |
Wdr75 |
T |
A |
1: 45,844,512 (GRCm39) |
|
probably null |
Het |
Zfp985 |
T |
C |
4: 147,667,528 (GRCm39) |
V132A |
probably benign |
Het |
Zswim3 |
T |
A |
2: 164,662,544 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Castor2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01370:Castor2
|
APN |
5 |
134,167,111 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01924:Castor2
|
APN |
5 |
134,164,441 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02302:Castor2
|
APN |
5 |
134,164,482 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0733:Castor2
|
UTSW |
5 |
134,165,054 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1485:Castor2
|
UTSW |
5 |
134,165,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R1522:Castor2
|
UTSW |
5 |
134,154,726 (GRCm39) |
missense |
probably damaging |
0.97 |
R2130:Castor2
|
UTSW |
5 |
134,164,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Castor2
|
UTSW |
5 |
134,164,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Castor2
|
UTSW |
5 |
134,164,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R2133:Castor2
|
UTSW |
5 |
134,164,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R4211:Castor2
|
UTSW |
5 |
134,154,783 (GRCm39) |
critical splice donor site |
probably null |
|
R6422:Castor2
|
UTSW |
5 |
134,164,549 (GRCm39) |
missense |
probably benign |
0.04 |
R6959:Castor2
|
UTSW |
5 |
134,164,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R7161:Castor2
|
UTSW |
5 |
134,164,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R8157:Castor2
|
UTSW |
5 |
134,165,936 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8348:Castor2
|
UTSW |
5 |
134,166,955 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8448:Castor2
|
UTSW |
5 |
134,166,955 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8821:Castor2
|
UTSW |
5 |
134,164,092 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9489:Castor2
|
UTSW |
5 |
134,164,536 (GRCm39) |
missense |
probably benign |
0.01 |
X0028:Castor2
|
UTSW |
5 |
134,166,902 (GRCm39) |
missense |
possibly damaging |
0.92 |
X0064:Castor2
|
UTSW |
5 |
134,164,420 (GRCm39) |
missense |
probably benign |
0.40 |
|