Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
C |
T |
10: 79,844,598 (GRCm39) |
P1461L |
probably damaging |
Het |
Abhd14a |
T |
C |
9: 106,321,472 (GRCm39) |
Y10C |
probably damaging |
Het |
Adcy2 |
C |
T |
13: 68,816,671 (GRCm39) |
V772M |
possibly damaging |
Het |
Apob |
A |
G |
12: 8,059,077 (GRCm39) |
M2487V |
probably damaging |
Het |
B4galnt1 |
T |
C |
10: 127,007,662 (GRCm39) |
|
probably null |
Het |
Cabp7 |
C |
T |
11: 4,690,396 (GRCm39) |
V76I |
probably benign |
Het |
Cbr3 |
A |
G |
16: 93,487,399 (GRCm39) |
Y194C |
probably damaging |
Het |
Cryba4 |
T |
C |
5: 112,394,628 (GRCm39) |
D167G |
probably damaging |
Het |
Czib |
T |
G |
4: 107,752,119 (GRCm39) |
I130S |
probably damaging |
Het |
Dner |
T |
C |
1: 84,373,428 (GRCm39) |
N588S |
probably damaging |
Het |
Dnm1l |
T |
C |
16: 16,147,737 (GRCm39) |
I343V |
probably benign |
Het |
Eif1ad16 |
A |
G |
12: 87,985,460 (GRCm39) |
F28L |
probably benign |
Het |
Fam168b |
C |
A |
1: 34,875,822 (GRCm39) |
G21V |
probably damaging |
Het |
Fbxw17 |
G |
A |
13: 50,577,255 (GRCm39) |
R49Q |
probably damaging |
Het |
Garin2 |
T |
A |
12: 78,762,060 (GRCm39) |
D241E |
probably damaging |
Het |
Gm10332 |
T |
A |
14: 55,057,616 (GRCm39) |
F59I |
probably damaging |
Het |
Gnai3 |
A |
G |
3: 108,030,852 (GRCm39) |
|
probably null |
Het |
Helz |
T |
A |
11: 107,523,087 (GRCm39) |
M75K |
possibly damaging |
Het |
Hnrnph3 |
C |
T |
10: 62,854,672 (GRCm39) |
|
probably benign |
Het |
Ifi211 |
C |
T |
1: 173,733,118 (GRCm39) |
C181Y |
probably benign |
Het |
Immp1l |
A |
G |
2: 105,767,390 (GRCm39) |
K83R |
probably damaging |
Het |
Itga6 |
G |
A |
2: 71,671,468 (GRCm39) |
G740R |
probably damaging |
Het |
Klhl1 |
T |
C |
14: 96,755,354 (GRCm39) |
T134A |
probably benign |
Het |
Klhl7 |
A |
G |
5: 24,354,244 (GRCm39) |
D353G |
probably damaging |
Het |
Map3k1 |
A |
G |
13: 111,888,983 (GRCm39) |
S1325P |
probably benign |
Het |
Map3k4 |
A |
G |
17: 12,451,297 (GRCm39) |
|
probably null |
Het |
Meioc |
G |
A |
11: 102,559,286 (GRCm39) |
|
probably null |
Het |
Mfap5 |
T |
C |
6: 122,497,555 (GRCm39) |
F26L |
probably damaging |
Het |
Myo5a |
A |
G |
9: 75,054,249 (GRCm39) |
T386A |
probably damaging |
Het |
Npc1l1 |
A |
T |
11: 6,164,013 (GRCm39) |
L1266Q |
probably damaging |
Het |
Npc1l1 |
G |
T |
11: 6,164,014 (GRCm39) |
L1266M |
probably damaging |
Het |
Or4c116 |
A |
G |
2: 88,942,325 (GRCm39) |
M177T |
probably benign |
Het |
Or51aa2 |
C |
A |
7: 103,188,265 (GRCm39) |
V59F |
possibly damaging |
Het |
Pbld1 |
T |
A |
10: 62,910,842 (GRCm39) |
S233T |
probably damaging |
Het |
Phf12 |
A |
G |
11: 77,916,918 (GRCm39) |
*789W |
probably null |
Het |
Sf3b2 |
A |
T |
19: 5,329,992 (GRCm39) |
|
probably null |
Het |
Slc23a3 |
A |
G |
1: 75,105,191 (GRCm39) |
I459T |
probably damaging |
Het |
Spata31e4 |
A |
G |
13: 50,856,071 (GRCm39) |
T570A |
possibly damaging |
Het |
Sptbn2 |
C |
G |
19: 4,799,040 (GRCm39) |
R2037G |
probably benign |
Het |
Stard9 |
A |
C |
2: 120,526,253 (GRCm39) |
M837L |
probably benign |
Het |
Stx5a |
A |
T |
19: 8,732,612 (GRCm39) |
|
probably benign |
Het |
Tmc7 |
A |
G |
7: 118,137,385 (GRCm39) |
V719A |
probably benign |
Het |
Trank1 |
T |
A |
9: 111,193,902 (GRCm39) |
I642K |
possibly damaging |
Het |
Trim34a |
T |
C |
7: 103,910,244 (GRCm39) |
Y349H |
probably damaging |
Het |
Uba7 |
A |
G |
9: 107,858,671 (GRCm39) |
Y834C |
possibly damaging |
Het |
Ube2d1 |
A |
G |
10: 71,092,530 (GRCm39) |
S105P |
possibly damaging |
Het |
Vps13a |
A |
G |
19: 16,722,283 (GRCm39) |
V343A |
possibly damaging |
Het |
Zbtb37 |
G |
A |
1: 160,859,643 (GRCm39) |
Q221* |
probably null |
Het |
Zfp119b |
T |
C |
17: 56,246,148 (GRCm39) |
N346S |
probably benign |
Het |
Zfp708 |
G |
T |
13: 67,218,785 (GRCm39) |
T358K |
possibly damaging |
Het |
|
Other mutations in Cdk18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00519:Cdk18
|
APN |
1 |
132,043,226 (GRCm39) |
missense |
probably benign |
0.36 |
IGL00929:Cdk18
|
APN |
1 |
132,046,257 (GRCm39) |
critical splice donor site |
probably null |
|
R0184:Cdk18
|
UTSW |
1 |
132,046,276 (GRCm39) |
missense |
probably benign |
0.00 |
R0606:Cdk18
|
UTSW |
1 |
132,045,355 (GRCm39) |
unclassified |
probably benign |
|
R0624:Cdk18
|
UTSW |
1 |
132,046,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R1295:Cdk18
|
UTSW |
1 |
132,047,698 (GRCm39) |
unclassified |
probably benign |
|
R1296:Cdk18
|
UTSW |
1 |
132,047,698 (GRCm39) |
unclassified |
probably benign |
|
R1298:Cdk18
|
UTSW |
1 |
132,050,189 (GRCm39) |
start gained |
probably benign |
|
R1611:Cdk18
|
UTSW |
1 |
132,050,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Cdk18
|
UTSW |
1 |
132,045,559 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2184:Cdk18
|
UTSW |
1 |
132,043,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R2279:Cdk18
|
UTSW |
1 |
132,043,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R2391:Cdk18
|
UTSW |
1 |
132,043,212 (GRCm39) |
missense |
probably benign |
|
R4601:Cdk18
|
UTSW |
1 |
132,044,657 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5001:Cdk18
|
UTSW |
1 |
132,046,587 (GRCm39) |
critical splice donor site |
probably null |
|
R5208:Cdk18
|
UTSW |
1 |
132,045,218 (GRCm39) |
critical splice donor site |
probably null |
|
R5818:Cdk18
|
UTSW |
1 |
132,046,836 (GRCm39) |
critical splice donor site |
probably null |
|
R6282:Cdk18
|
UTSW |
1 |
132,047,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R6546:Cdk18
|
UTSW |
1 |
132,050,088 (GRCm39) |
missense |
probably damaging |
0.99 |
R6892:Cdk18
|
UTSW |
1 |
132,049,848 (GRCm39) |
missense |
probably benign |
0.01 |
R6965:Cdk18
|
UTSW |
1 |
132,045,319 (GRCm39) |
missense |
probably damaging |
0.98 |
R7698:Cdk18
|
UTSW |
1 |
132,050,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R7828:Cdk18
|
UTSW |
1 |
132,044,642 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9386:Cdk18
|
UTSW |
1 |
132,044,183 (GRCm39) |
critical splice donor site |
probably null |
|
R9488:Cdk18
|
UTSW |
1 |
132,049,260 (GRCm39) |
missense |
probably benign |
0.01 |
|