Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
G |
12: 71,231,197 (GRCm39) |
V985G |
possibly damaging |
Het |
Acr |
T |
G |
15: 89,458,057 (GRCm39) |
M246R |
probably damaging |
Het |
Adgrf5 |
G |
T |
17: 43,763,989 (GRCm39) |
V1304L |
possibly damaging |
Het |
Ago4 |
A |
T |
4: 126,387,043 (GRCm39) |
D853E |
probably benign |
Het |
Arvcf |
C |
A |
16: 18,222,203 (GRCm39) |
D790E |
probably benign |
Het |
Atp8a2 |
A |
C |
14: 60,162,545 (GRCm39) |
D725E |
probably damaging |
Het |
C2cd5 |
A |
G |
6: 143,028,946 (GRCm39) |
Y98H |
probably benign |
Het |
Camkk2 |
T |
C |
5: 122,891,820 (GRCm39) |
Y234C |
probably damaging |
Het |
Ccdc106 |
A |
G |
7: 5,062,570 (GRCm39) |
D192G |
probably benign |
Het |
Ccm2l |
T |
C |
2: 152,916,788 (GRCm39) |
Y340H |
probably damaging |
Het |
Chd1l |
A |
G |
3: 97,477,685 (GRCm39) |
F690S |
probably benign |
Het |
Chuk |
A |
G |
19: 44,076,407 (GRCm39) |
S435P |
possibly damaging |
Het |
Cisd3 |
T |
A |
11: 97,576,703 (GRCm39) |
S10T |
probably benign |
Het |
Cnppd1 |
A |
G |
1: 75,113,063 (GRCm39) |
S402P |
probably damaging |
Het |
Cped1 |
A |
G |
6: 22,215,620 (GRCm39) |
D718G |
probably damaging |
Het |
Crtc1 |
A |
G |
8: 70,840,805 (GRCm39) |
S474P |
probably damaging |
Het |
Dcpp3 |
G |
T |
17: 24,138,123 (GRCm39) |
E94* |
probably null |
Het |
Dhx38 |
A |
T |
8: 110,289,361 (GRCm39) |
L13* |
probably null |
Het |
Dmbt1 |
T |
C |
7: 130,642,853 (GRCm39) |
Y120H |
unknown |
Het |
Fntb |
T |
A |
12: 76,934,826 (GRCm39) |
V201E |
possibly damaging |
Het |
Gga3 |
T |
C |
11: 115,481,244 (GRCm39) |
D242G |
probably benign |
Het |
Hif3a |
A |
T |
7: 16,774,912 (GRCm39) |
M562K |
probably benign |
Het |
Irf5 |
G |
A |
6: 29,535,997 (GRCm39) |
R337H |
probably damaging |
Het |
Kcnmb3 |
A |
G |
3: 32,526,624 (GRCm39) |
V189A |
possibly damaging |
Het |
Letmd1 |
A |
G |
15: 100,373,247 (GRCm39) |
T241A |
probably benign |
Het |
Lrrc14b |
T |
A |
13: 74,509,408 (GRCm39) |
D333V |
probably damaging |
Het |
Meaf6 |
T |
A |
4: 124,979,990 (GRCm39) |
L48Q |
probably damaging |
Het |
Miip |
T |
A |
4: 147,950,839 (GRCm39) |
|
probably benign |
Het |
Muc4 |
A |
G |
16: 32,569,461 (GRCm39) |
T236A |
possibly damaging |
Het |
Myh4 |
T |
A |
11: 67,132,335 (GRCm39) |
I155N |
probably damaging |
Het |
Obscn |
C |
T |
11: 58,898,440 (GRCm39) |
R6607Q |
unknown |
Het |
Or2ak7 |
C |
T |
11: 58,574,966 (GRCm39) |
T89I |
probably benign |
Het |
Or5v1 |
G |
A |
17: 37,810,321 (GRCm39) |
V260M |
probably benign |
Het |
Otof |
T |
C |
5: 30,529,044 (GRCm39) |
N1788S |
possibly damaging |
Het |
Psapl1 |
T |
C |
5: 36,362,314 (GRCm39) |
L302S |
probably damaging |
Het |
Rdh8 |
A |
C |
9: 20,734,021 (GRCm39) |
N69T |
probably benign |
Het |
Ryr3 |
T |
C |
2: 112,624,844 (GRCm39) |
E2212G |
probably damaging |
Het |
Septin7 |
A |
T |
9: 25,163,980 (GRCm39) |
N16Y |
possibly damaging |
Het |
Slc22a17 |
A |
T |
14: 55,146,436 (GRCm39) |
L60Q |
probably damaging |
Het |
Snrnp200 |
T |
C |
2: 127,060,349 (GRCm39) |
I531T |
probably damaging |
Het |
Ssh3 |
A |
T |
19: 4,317,992 (GRCm39) |
V41E |
probably damaging |
Het |
Tars1 |
G |
T |
15: 11,393,348 (GRCm39) |
N115K |
probably benign |
Het |
Tomm6 |
G |
C |
17: 47,998,850 (GRCm39) |
F34L |
possibly damaging |
Het |
Txnrd2 |
G |
A |
16: 18,259,601 (GRCm39) |
V173M |
possibly damaging |
Het |
Uba6 |
T |
A |
5: 86,289,454 (GRCm39) |
I450F |
possibly damaging |
Het |
Vmn2r95 |
G |
T |
17: 18,664,113 (GRCm39) |
S516I |
possibly damaging |
Het |
Vps4b |
A |
G |
1: 106,710,414 (GRCm39) |
F156L |
possibly damaging |
Het |
Zfp354c |
T |
A |
11: 50,706,019 (GRCm39) |
H352L |
probably damaging |
Het |
Zfp521 |
T |
C |
18: 14,072,150 (GRCm39) |
D30G |
probably benign |
Het |
Zic2 |
A |
T |
14: 122,713,530 (GRCm39) |
H148L |
possibly damaging |
Het |
|
Other mutations in Gsx2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01152:Gsx2
|
APN |
5 |
75,236,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R0018:Gsx2
|
UTSW |
5 |
75,237,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R0018:Gsx2
|
UTSW |
5 |
75,237,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R0265:Gsx2
|
UTSW |
5 |
75,237,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R0496:Gsx2
|
UTSW |
5 |
75,237,726 (GRCm39) |
missense |
probably benign |
0.26 |
R1017:Gsx2
|
UTSW |
5 |
75,237,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R2372:Gsx2
|
UTSW |
5 |
75,237,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R7226:Gsx2
|
UTSW |
5 |
75,236,621 (GRCm39) |
nonsense |
probably null |
|
R7362:Gsx2
|
UTSW |
5 |
75,236,765 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7504:Gsx2
|
UTSW |
5 |
75,237,060 (GRCm39) |
splice site |
probably null |
|
R8153:Gsx2
|
UTSW |
5 |
75,237,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Gsx2
|
UTSW |
5 |
75,236,755 (GRCm39) |
missense |
probably benign |
0.00 |
|