Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alms1 |
G |
T |
6: 85,605,735 (GRCm39) |
G2462C |
probably damaging |
Het |
Anapc5 |
T |
C |
5: 122,937,406 (GRCm39) |
E464G |
probably damaging |
Het |
Aoc3 |
T |
A |
11: 101,227,261 (GRCm39) |
V378E |
possibly damaging |
Het |
Atp13a5 |
T |
A |
16: 29,051,551 (GRCm39) |
K1152I |
possibly damaging |
Het |
Auh |
G |
A |
13: 52,989,532 (GRCm39) |
P308L |
probably benign |
Het |
Calcoco1 |
C |
A |
15: 102,627,988 (GRCm39) |
G49C |
probably damaging |
Het |
Cd70 |
T |
C |
17: 57,453,401 (GRCm39) |
T88A |
possibly damaging |
Het |
Cpeb1 |
C |
T |
7: 81,085,974 (GRCm39) |
R56Q |
probably benign |
Het |
Dglucy |
A |
G |
12: 100,808,938 (GRCm39) |
Y212C |
probably damaging |
Het |
Dnhd1 |
C |
A |
7: 105,364,127 (GRCm39) |
P4160T |
possibly damaging |
Het |
Ecel1 |
T |
C |
1: 87,082,143 (GRCm39) |
D190G |
probably benign |
Het |
Exoc6b |
A |
G |
6: 85,046,326 (GRCm39) |
L21P |
probably damaging |
Het |
Fam110c |
A |
G |
12: 31,124,394 (GRCm39) |
R119G |
unknown |
Het |
Gask1b |
T |
A |
3: 79,843,970 (GRCm39) |
N32K |
probably benign |
Het |
Gm42791 |
C |
A |
5: 148,896,311 (GRCm39) |
|
probably benign |
Het |
Hpcal4 |
A |
G |
4: 123,084,532 (GRCm39) |
I154V |
probably benign |
Het |
Itgb1 |
A |
G |
8: 129,452,519 (GRCm39) |
D728G |
probably damaging |
Het |
Kdm5d |
A |
T |
Y: 927,753 (GRCm39) |
D701V |
probably damaging |
Het |
Kif18a |
A |
G |
2: 109,133,227 (GRCm39) |
K448E |
probably damaging |
Het |
Kif26a |
T |
C |
12: 112,140,292 (GRCm39) |
F507S |
possibly damaging |
Het |
Kmt2c |
C |
T |
5: 25,520,003 (GRCm39) |
G2036R |
probably damaging |
Het |
Lrrc43 |
T |
A |
5: 123,630,276 (GRCm39) |
|
probably benign |
Het |
Map3k20 |
T |
C |
2: 72,219,836 (GRCm39) |
I256T |
probably damaging |
Het |
Med29 |
T |
A |
7: 28,092,130 (GRCm39) |
|
probably benign |
Het |
Mtf2 |
T |
C |
5: 108,235,936 (GRCm39) |
Y87H |
probably damaging |
Het |
Myo18a |
G |
A |
11: 77,744,140 (GRCm39) |
R1834K |
probably damaging |
Het |
Nlrc4 |
T |
A |
17: 74,748,903 (GRCm39) |
D779V |
probably damaging |
Het |
Or51q1c |
T |
C |
7: 103,652,518 (GRCm39) |
F18S |
probably damaging |
Het |
Otud3 |
T |
C |
4: 138,625,329 (GRCm39) |
T242A |
probably damaging |
Het |
Pcare |
A |
T |
17: 72,057,373 (GRCm39) |
F768Y |
probably damaging |
Het |
Pnliprp1 |
T |
A |
19: 58,720,574 (GRCm39) |
M150K |
possibly damaging |
Het |
Polm |
T |
A |
11: 5,784,776 (GRCm39) |
Q227L |
probably benign |
Het |
Poln |
A |
G |
5: 34,280,016 (GRCm39) |
V282A |
probably benign |
Het |
Ppfia2 |
T |
A |
10: 106,751,533 (GRCm39) |
|
probably null |
Het |
Rad51 |
T |
G |
2: 118,954,295 (GRCm39) |
M168R |
probably benign |
Het |
Senp2 |
A |
G |
16: 21,846,792 (GRCm39) |
T266A |
probably benign |
Het |
Sfswap |
A |
G |
5: 129,616,758 (GRCm39) |
T401A |
probably benign |
Het |
Slc35a4 |
C |
A |
18: 36,815,788 (GRCm39) |
T206K |
possibly damaging |
Het |
Slc40a1 |
A |
G |
1: 45,963,921 (GRCm39) |
S23P |
probably damaging |
Het |
Spef2 |
T |
C |
15: 9,614,295 (GRCm39) |
K1217R |
probably damaging |
Het |
St18 |
A |
C |
1: 6,880,909 (GRCm39) |
|
probably benign |
Het |
Tdrd6 |
T |
C |
17: 43,939,218 (GRCm39) |
D610G |
possibly damaging |
Het |
Tmem163 |
C |
A |
1: 127,479,108 (GRCm39) |
R137L |
probably damaging |
Het |
Tmem94 |
T |
A |
11: 115,685,574 (GRCm39) |
D942E |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,580,754 (GRCm39) |
I23380F |
possibly damaging |
Het |
Uckl1 |
T |
A |
2: 181,212,393 (GRCm39) |
|
probably null |
Het |
Vav2 |
T |
C |
2: 27,208,976 (GRCm39) |
D99G |
possibly damaging |
Het |
Vmn2r30 |
T |
A |
7: 7,337,259 (GRCm39) |
I126F |
probably benign |
Het |
Zbtb41 |
A |
T |
1: 139,351,301 (GRCm39) |
Q138L |
probably benign |
Het |
Zfp599 |
T |
C |
9: 22,169,361 (GRCm39) |
Y37C |
probably damaging |
Het |
Zfp784 |
T |
A |
7: 5,038,782 (GRCm39) |
T259S |
possibly damaging |
Het |
Zfp954 |
T |
C |
7: 7,118,837 (GRCm39) |
S236G |
probably benign |
Het |
Zng1 |
A |
G |
19: 24,925,458 (GRCm39) |
V166A |
possibly damaging |
Het |
|
Other mutations in Mob3b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02198:Mob3b
|
APN |
4 |
35,083,983 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02991:Mob3b
|
UTSW |
4 |
35,083,805 (GRCm39) |
missense |
probably benign |
0.01 |
R0016:Mob3b
|
UTSW |
4 |
35,083,947 (GRCm39) |
missense |
probably benign |
0.02 |
R0408:Mob3b
|
UTSW |
4 |
35,083,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R1542:Mob3b
|
UTSW |
4 |
35,084,046 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1686:Mob3b
|
UTSW |
4 |
34,985,910 (GRCm39) |
splice site |
probably benign |
|
R1726:Mob3b
|
UTSW |
4 |
34,954,028 (GRCm39) |
missense |
probably benign |
0.09 |
R2013:Mob3b
|
UTSW |
4 |
35,083,922 (GRCm39) |
missense |
probably benign |
0.00 |
R2112:Mob3b
|
UTSW |
4 |
35,083,795 (GRCm39) |
missense |
probably damaging |
0.97 |
R5992:Mob3b
|
UTSW |
4 |
35,084,069 (GRCm39) |
missense |
probably benign |
0.43 |
R6043:Mob3b
|
UTSW |
4 |
34,985,993 (GRCm39) |
missense |
probably benign |
0.05 |
R6418:Mob3b
|
UTSW |
4 |
34,954,049 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7117:Mob3b
|
UTSW |
4 |
34,985,914 (GRCm39) |
critical splice donor site |
probably null |
|
R7170:Mob3b
|
UTSW |
4 |
35,083,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R7714:Mob3b
|
UTSW |
4 |
35,083,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R8385:Mob3b
|
UTSW |
4 |
34,985,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R9232:Mob3b
|
UTSW |
4 |
34,986,101 (GRCm39) |
missense |
probably benign |
|
|