Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aurka |
T |
C |
2: 172,199,117 (GRCm39) |
M318V |
probably benign |
Het |
Cacna2d1 |
T |
A |
5: 16,531,342 (GRCm39) |
D560E |
probably damaging |
Het |
Ccdc148 |
T |
A |
2: 58,872,988 (GRCm39) |
T202S |
probably benign |
Het |
Cdc42bpb |
T |
C |
12: 111,271,412 (GRCm39) |
D1149G |
probably damaging |
Het |
Clasp1 |
T |
A |
1: 118,390,285 (GRCm39) |
N156K |
probably damaging |
Het |
Cox18 |
G |
A |
5: 90,365,434 (GRCm39) |
T255I |
possibly damaging |
Het |
Cse1l |
A |
G |
2: 166,783,394 (GRCm39) |
T783A |
probably damaging |
Het |
Dnajc16 |
T |
C |
4: 141,491,996 (GRCm39) |
Y609C |
probably damaging |
Het |
Doc2g |
A |
G |
19: 4,056,630 (GRCm39) |
T339A |
probably benign |
Het |
Eif5a |
T |
C |
11: 69,808,896 (GRCm39) |
|
probably benign |
Het |
Epha3 |
A |
G |
16: 63,386,940 (GRCm39) |
|
probably null |
Het |
Esco1 |
A |
T |
18: 10,594,355 (GRCm39) |
C310* |
probably null |
Het |
Fam222a |
A |
G |
5: 114,749,101 (GRCm39) |
Y99C |
probably damaging |
Het |
Fzd2 |
T |
C |
11: 102,496,573 (GRCm39) |
L339P |
probably damaging |
Het |
Gfral |
A |
T |
9: 76,104,576 (GRCm39) |
N145K |
probably damaging |
Het |
Gga1 |
T |
A |
15: 78,777,990 (GRCm39) |
N618K |
probably benign |
Het |
Gpatch3 |
T |
A |
4: 133,310,397 (GRCm39) |
H447Q |
probably damaging |
Het |
Gpn1 |
A |
T |
5: 31,666,747 (GRCm39) |
R346* |
probably null |
Het |
Gsg1 |
T |
C |
6: 135,214,558 (GRCm39) |
E317G |
probably benign |
Het |
Gsk3b |
A |
G |
16: 38,004,816 (GRCm39) |
N129S |
probably damaging |
Het |
Hmg20b |
G |
T |
10: 81,184,789 (GRCm39) |
D94E |
possibly damaging |
Het |
Kash5 |
C |
T |
7: 44,849,695 (GRCm39) |
G76D |
probably benign |
Het |
Klhdc9 |
T |
A |
1: 171,187,386 (GRCm39) |
H204L |
possibly damaging |
Het |
Klhl24 |
A |
G |
16: 19,925,638 (GRCm39) |
I55M |
probably benign |
Het |
Kmt2c |
T |
C |
5: 25,520,104 (GRCm39) |
D2002G |
probably benign |
Het |
Lama4 |
A |
G |
10: 38,950,742 (GRCm39) |
N1015S |
probably damaging |
Het |
Lpp |
T |
C |
16: 24,580,697 (GRCm39) |
C263R |
probably benign |
Het |
Lrp1b |
T |
C |
2: 41,159,216 (GRCm39) |
I1689V |
|
Het |
Mipep |
C |
A |
14: 61,022,284 (GRCm39) |
Q50K |
probably benign |
Het |
Mx1 |
T |
C |
16: 97,257,454 (GRCm39) |
D101G |
probably benign |
Het |
Nabp2 |
C |
G |
10: 128,244,676 (GRCm39) |
E37Q |
possibly damaging |
Het |
Nme6 |
A |
G |
9: 109,671,104 (GRCm39) |
I115V |
possibly damaging |
Het |
Nup93 |
A |
T |
8: 94,970,355 (GRCm39) |
T85S |
probably benign |
Het |
Oit3 |
T |
A |
10: 59,266,835 (GRCm39) |
I224F |
possibly damaging |
Het |
Parp14 |
T |
C |
16: 35,678,975 (GRCm39) |
K331R |
probably benign |
Het |
Pls1 |
T |
A |
9: 95,643,443 (GRCm39) |
T519S |
probably benign |
Het |
Rcn3 |
A |
G |
7: 44,736,118 (GRCm39) |
F197L |
probably benign |
Het |
Rnf213 |
C |
T |
11: 119,349,218 (GRCm39) |
T3773I |
|
Het |
Rprd1b |
A |
T |
2: 157,889,877 (GRCm39) |
I153L |
probably benign |
Het |
Scel |
A |
G |
14: 103,829,804 (GRCm39) |
D462G |
possibly damaging |
Het |
Sh3bp1 |
C |
T |
15: 78,794,276 (GRCm39) |
S548L |
possibly damaging |
Het |
Sim1 |
T |
A |
10: 50,860,284 (GRCm39) |
Y715* |
probably null |
Het |
Slc18a2 |
A |
T |
19: 59,282,293 (GRCm39) |
Q500L |
possibly damaging |
Het |
Slc5a8 |
T |
G |
10: 88,722,365 (GRCm39) |
M66R |
probably damaging |
Het |
Slco1a6 |
T |
C |
6: 142,055,246 (GRCm39) |
T233A |
probably damaging |
Het |
Tas2r104 |
T |
C |
6: 131,662,521 (GRCm39) |
T63A |
possibly damaging |
Het |
Tasor2 |
G |
A |
13: 3,624,979 (GRCm39) |
A1657V |
possibly damaging |
Het |
Top2a |
C |
T |
11: 98,892,199 (GRCm39) |
A1088T |
probably benign |
Het |
Ucp1 |
T |
C |
8: 84,020,577 (GRCm39) |
F129S |
probably damaging |
Het |
Unc13b |
T |
A |
4: 43,091,298 (GRCm39) |
D41E |
probably benign |
Het |
Usp10 |
T |
G |
8: 120,681,631 (GRCm39) |
V696G |
probably benign |
Het |
Xylt2 |
C |
T |
11: 94,557,066 (GRCm39) |
V745M |
probably damaging |
Het |
Zbtb49 |
A |
T |
5: 38,373,820 (GRCm39) |
N41K |
probably damaging |
Het |
Zfp109 |
T |
A |
7: 23,928,779 (GRCm39) |
D218V |
probably benign |
Het |
Zfp420 |
G |
A |
7: 29,575,430 (GRCm39) |
R550Q |
probably benign |
Het |
|
Other mutations in Smu1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02992:Smu1
|
APN |
4 |
40,739,550 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03271:Smu1
|
APN |
4 |
40,738,408 (GRCm39) |
missense |
probably benign |
0.11 |
IGL03329:Smu1
|
APN |
4 |
40,739,568 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0172:Smu1
|
UTSW |
4 |
40,738,439 (GRCm39) |
missense |
probably benign |
0.00 |
R1109:Smu1
|
UTSW |
4 |
40,755,722 (GRCm39) |
missense |
probably benign |
0.12 |
R1552:Smu1
|
UTSW |
4 |
40,748,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R1799:Smu1
|
UTSW |
4 |
40,745,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R2093:Smu1
|
UTSW |
4 |
40,738,438 (GRCm39) |
missense |
probably benign |
0.12 |
R2143:Smu1
|
UTSW |
4 |
40,744,073 (GRCm39) |
missense |
probably damaging |
0.99 |
R3082:Smu1
|
UTSW |
4 |
40,745,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R3083:Smu1
|
UTSW |
4 |
40,745,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R3113:Smu1
|
UTSW |
4 |
40,748,658 (GRCm39) |
missense |
probably benign |
0.03 |
R3157:Smu1
|
UTSW |
4 |
40,754,529 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3158:Smu1
|
UTSW |
4 |
40,754,529 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3159:Smu1
|
UTSW |
4 |
40,754,529 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3409:Smu1
|
UTSW |
4 |
40,752,008 (GRCm39) |
missense |
probably benign |
|
R3411:Smu1
|
UTSW |
4 |
40,752,008 (GRCm39) |
missense |
probably benign |
|
R4581:Smu1
|
UTSW |
4 |
40,737,401 (GRCm39) |
splice site |
probably null |
|
R5106:Smu1
|
UTSW |
4 |
40,743,104 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7747:Smu1
|
UTSW |
4 |
40,748,600 (GRCm39) |
missense |
probably benign |
0.44 |
R9029:Smu1
|
UTSW |
4 |
40,738,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R9069:Smu1
|
UTSW |
4 |
40,745,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R9537:Smu1
|
UTSW |
4 |
40,755,671 (GRCm39) |
missense |
probably benign |
0.01 |
R9797:Smu1
|
UTSW |
4 |
40,739,538 (GRCm39) |
missense |
possibly damaging |
0.69 |
|