Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca3 |
T |
C |
17: 24,603,500 (GRCm39) |
L564P |
probably damaging |
Het |
Arsb |
T |
A |
13: 93,998,615 (GRCm39) |
S308T |
probably benign |
Het |
Atxn10 |
A |
G |
15: 85,346,526 (GRCm39) |
D428G |
probably benign |
Het |
Cd300a |
T |
C |
11: 114,784,165 (GRCm39) |
Y58H |
probably benign |
Het |
Cemip2 |
T |
A |
19: 21,809,539 (GRCm39) |
I973N |
possibly damaging |
Het |
Crkl |
T |
A |
16: 17,286,960 (GRCm39) |
M172K |
probably damaging |
Het |
Cyfip1 |
T |
C |
7: 55,549,774 (GRCm39) |
I647T |
probably damaging |
Het |
Dlgap1 |
A |
G |
17: 70,823,683 (GRCm39) |
T223A |
probably benign |
Het |
Dmtf1 |
T |
C |
5: 9,178,044 (GRCm39) |
S372G |
probably damaging |
Het |
Dock8 |
G |
A |
19: 25,160,934 (GRCm39) |
V1814M |
probably damaging |
Het |
Dusp22 |
A |
C |
13: 30,892,737 (GRCm39) |
K171N |
probably benign |
Het |
Evi2a |
T |
C |
11: 79,418,452 (GRCm39) |
S53G |
probably benign |
Het |
Ipcef1 |
T |
A |
10: 6,840,569 (GRCm39) |
D376V |
probably damaging |
Het |
Kndc1 |
A |
T |
7: 139,500,880 (GRCm39) |
D723V |
possibly damaging |
Het |
Kti12 |
A |
C |
4: 108,705,443 (GRCm39) |
E119A |
probably benign |
Het |
Kti12 |
G |
T |
4: 108,705,444 (GRCm39) |
E119D |
probably benign |
Het |
Mcur1 |
G |
A |
13: 43,713,485 (GRCm39) |
R40* |
probably null |
Het |
Mgam |
T |
A |
6: 40,717,113 (GRCm39) |
N265K |
possibly damaging |
Het |
Muc6 |
G |
A |
7: 141,231,687 (GRCm39) |
T1069I |
probably damaging |
Het |
Myh2 |
T |
C |
11: 67,077,526 (GRCm39) |
L887P |
probably damaging |
Het |
Myo1d |
T |
G |
11: 80,575,203 (GRCm39) |
D171A |
probably damaging |
Het |
Nat2 |
T |
A |
8: 67,954,002 (GRCm39) |
F37L |
probably damaging |
Het |
Nkx2-2 |
A |
G |
2: 147,019,730 (GRCm39) |
C236R |
unknown |
Het |
Nrl |
G |
A |
14: 55,759,582 (GRCm39) |
S115L |
probably benign |
Het |
Nrsn1 |
A |
C |
13: 25,446,254 (GRCm39) |
S41A |
probably damaging |
Het |
Or5b12 |
T |
A |
19: 12,897,346 (GRCm39) |
E109V |
probably damaging |
Het |
Pax8 |
T |
A |
2: 24,311,567 (GRCm39) |
H456L |
possibly damaging |
Het |
Pkd1 |
T |
A |
17: 24,790,254 (GRCm39) |
I979K |
probably damaging |
Het |
Prex2 |
A |
G |
1: 11,150,274 (GRCm39) |
N149D |
probably damaging |
Het |
Psg28 |
A |
T |
7: 18,160,149 (GRCm39) |
V349D |
probably damaging |
Het |
Ptpro |
G |
A |
6: 137,369,805 (GRCm39) |
|
probably null |
Het |
Sema4d |
T |
A |
13: 51,876,387 (GRCm39) |
K94N |
probably benign |
Het |
Slc22a22 |
A |
T |
15: 57,114,348 (GRCm39) |
D326E |
probably benign |
Het |
Slc25a29 |
G |
A |
12: 108,792,756 (GRCm39) |
T274I |
probably benign |
Het |
Slc43a1 |
T |
C |
2: 84,687,220 (GRCm39) |
F374L |
possibly damaging |
Het |
Syne1 |
G |
T |
10: 5,107,683 (GRCm39) |
Q520K |
possibly damaging |
Het |
Taar4 |
T |
C |
10: 23,837,032 (GRCm39) |
V214A |
probably benign |
Het |
Tex22 |
T |
A |
12: 113,052,103 (GRCm39) |
C54S |
possibly damaging |
Het |
Tpo |
T |
A |
12: 30,150,573 (GRCm39) |
I436F |
probably damaging |
Het |
Usp53 |
T |
C |
3: 122,743,415 (GRCm39) |
H507R |
possibly damaging |
Het |
Usp54 |
T |
C |
14: 20,638,204 (GRCm39) |
E255G |
probably benign |
Het |
Vmn2r109 |
G |
T |
17: 20,761,436 (GRCm39) |
F640L |
probably damaging |
Het |
Vmn2r124 |
A |
G |
17: 18,282,212 (GRCm39) |
Y80C |
probably damaging |
Het |
Vmn2r27 |
A |
T |
6: 124,201,201 (GRCm39) |
I252K |
probably benign |
Het |
Zfp457 |
A |
G |
13: 67,454,445 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in BB014433 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00309:BB014433
|
APN |
8 |
15,092,510 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01595:BB014433
|
APN |
8 |
15,092,499 (GRCm39) |
splice site |
probably null |
|
IGL02056:BB014433
|
APN |
8 |
15,092,435 (GRCm39) |
nonsense |
probably null |
|
IGL02470:BB014433
|
APN |
8 |
15,092,803 (GRCm39) |
missense |
unknown |
|
R0359:BB014433
|
UTSW |
8 |
15,092,540 (GRCm39) |
nonsense |
probably null |
|
R1066:BB014433
|
UTSW |
8 |
15,092,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R1837:BB014433
|
UTSW |
8 |
15,092,629 (GRCm39) |
missense |
unknown |
|
R1838:BB014433
|
UTSW |
8 |
15,092,629 (GRCm39) |
missense |
unknown |
|
R2227:BB014433
|
UTSW |
8 |
15,091,717 (GRCm39) |
missense |
probably benign |
0.34 |
R4508:BB014433
|
UTSW |
8 |
15,092,095 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4882:BB014433
|
UTSW |
8 |
15,092,016 (GRCm39) |
missense |
probably benign |
0.05 |
R4996:BB014433
|
UTSW |
8 |
15,092,166 (GRCm39) |
missense |
probably benign |
0.10 |
R5988:BB014433
|
UTSW |
8 |
15,091,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R6051:BB014433
|
UTSW |
8 |
15,092,179 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6483:BB014433
|
UTSW |
8 |
15,092,208 (GRCm39) |
missense |
probably benign |
0.10 |
R6505:BB014433
|
UTSW |
8 |
15,092,304 (GRCm39) |
missense |
probably benign |
0.10 |
R7237:BB014433
|
UTSW |
8 |
15,091,765 (GRCm39) |
missense |
probably benign |
0.13 |
R7771:BB014433
|
UTSW |
8 |
15,092,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R7847:BB014433
|
UTSW |
8 |
15,092,160 (GRCm39) |
small deletion |
probably benign |
|
R8377:BB014433
|
UTSW |
8 |
15,092,160 (GRCm39) |
small deletion |
probably benign |
|
R8560:BB014433
|
UTSW |
8 |
15,092,160 (GRCm39) |
small deletion |
probably benign |
|
R8993:BB014433
|
UTSW |
8 |
15,092,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R9204:BB014433
|
UTSW |
8 |
15,092,623 (GRCm39) |
missense |
unknown |
|
R9446:BB014433
|
UTSW |
8 |
15,091,810 (GRCm39) |
small deletion |
probably benign |
|
R9542:BB014433
|
UTSW |
8 |
15,092,160 (GRCm39) |
small deletion |
probably benign |
|
X0066:BB014433
|
UTSW |
8 |
15,092,833 (GRCm39) |
missense |
unknown |
|
|