Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arsk |
A |
G |
13: 76,246,487 (GRCm39) |
|
probably null |
Het |
As3mt |
A |
G |
19: 46,700,673 (GRCm39) |
I159V |
probably benign |
Het |
Atpsckmt |
T |
C |
15: 31,606,261 (GRCm39) |
V73A |
possibly damaging |
Het |
Ctsll3 |
C |
A |
13: 60,948,075 (GRCm39) |
V201L |
probably benign |
Het |
Dapk1 |
T |
C |
13: 60,909,211 (GRCm39) |
Y1275H |
probably damaging |
Het |
Erap1 |
G |
A |
13: 74,821,826 (GRCm39) |
R727H |
probably benign |
Het |
Fcrl6 |
T |
A |
1: 172,426,674 (GRCm39) |
T91S |
probably benign |
Het |
Gvin1 |
T |
C |
7: 105,757,377 (GRCm39) |
E2364G |
probably benign |
Het |
Hcls1 |
T |
A |
16: 36,776,383 (GRCm39) |
|
probably null |
Het |
Igf2r |
C |
T |
17: 12,902,754 (GRCm39) |
R2432H |
possibly damaging |
Het |
Kif27 |
C |
A |
13: 58,492,486 (GRCm39) |
V218F |
possibly damaging |
Het |
Klhl20 |
T |
C |
1: 160,918,076 (GRCm39) |
Y70C |
probably benign |
Het |
Krt86 |
C |
T |
15: 101,371,741 (GRCm39) |
H104Y |
probably benign |
Het |
Lcn12 |
G |
T |
2: 25,383,332 (GRCm39) |
N15K |
possibly damaging |
Het |
Mrgpra1 |
T |
C |
7: 46,985,326 (GRCm39) |
M118V |
probably benign |
Het |
Nacad |
G |
T |
11: 6,550,632 (GRCm39) |
T853K |
probably damaging |
Het |
Nos3 |
A |
T |
5: 24,574,860 (GRCm39) |
Q293L |
probably damaging |
Het |
Prkca |
C |
T |
11: 107,874,800 (GRCm39) |
V381M |
probably damaging |
Het |
Ptcd3 |
A |
G |
6: 71,884,828 (GRCm39) |
F37S |
possibly damaging |
Het |
Ptgs2 |
A |
G |
1: 149,980,175 (GRCm39) |
Y371C |
probably damaging |
Het |
Pygl |
T |
C |
12: 70,254,516 (GRCm39) |
Y143C |
probably damaging |
Het |
Samhd1 |
A |
G |
2: 156,949,343 (GRCm39) |
|
probably benign |
Het |
Scube1 |
T |
A |
15: 83,587,702 (GRCm39) |
H89L |
probably damaging |
Het |
Tmem59l |
G |
A |
8: 70,938,315 (GRCm39) |
|
probably benign |
Het |
Vmn2r108 |
A |
G |
17: 20,682,774 (GRCm39) |
V810A |
probably damaging |
Het |
Vmn2r61 |
T |
G |
7: 41,949,935 (GRCm39) |
F785C |
probably damaging |
Het |
Zfas1 |
G |
T |
2: 166,907,406 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Hacd3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01323:Hacd3
|
APN |
9 |
64,905,587 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02943:Hacd3
|
APN |
9 |
64,897,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R0145:Hacd3
|
UTSW |
9 |
64,911,524 (GRCm39) |
splice site |
probably benign |
|
R0390:Hacd3
|
UTSW |
9 |
64,908,304 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2403:Hacd3
|
UTSW |
9 |
64,908,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R3117:Hacd3
|
UTSW |
9 |
64,905,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R3740:Hacd3
|
UTSW |
9 |
64,928,755 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4972:Hacd3
|
UTSW |
9 |
64,897,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R6174:Hacd3
|
UTSW |
9 |
64,912,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R7085:Hacd3
|
UTSW |
9 |
64,905,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R9131:Hacd3
|
UTSW |
9 |
64,908,286 (GRCm39) |
missense |
probably damaging |
0.99 |
|