Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd18 |
T |
A |
3: 40,859,338 (GRCm39) |
M1K |
probably null |
Het |
Adam34l |
A |
T |
8: 44,079,089 (GRCm39) |
C378* |
probably null |
Het |
Bdkrb2 |
T |
C |
12: 105,558,755 (GRCm39) |
V332A |
possibly damaging |
Het |
Cdc27 |
T |
C |
11: 104,398,026 (GRCm39) |
E778G |
probably damaging |
Het |
Chd4 |
C |
A |
6: 125,098,970 (GRCm39) |
T1586K |
probably benign |
Het |
Cnga3 |
A |
G |
1: 37,301,146 (GRCm39) |
E622G |
probably benign |
Het |
Dbh |
A |
G |
2: 27,064,977 (GRCm39) |
D396G |
possibly damaging |
Het |
Dhodh |
G |
A |
8: 110,330,107 (GRCm39) |
R86* |
probably null |
Het |
Dpt |
A |
C |
1: 164,624,500 (GRCm39) |
E67A |
probably damaging |
Het |
Eif2ak2 |
A |
G |
17: 79,166,068 (GRCm39) |
|
probably benign |
Het |
Esp4 |
T |
A |
17: 40,913,336 (GRCm39) |
L68M |
possibly damaging |
Het |
Exo1 |
A |
G |
1: 175,733,536 (GRCm39) |
K787E |
possibly damaging |
Het |
Fbxo38 |
T |
C |
18: 62,647,914 (GRCm39) |
T875A |
probably damaging |
Het |
Hemk1 |
G |
A |
9: 107,214,415 (GRCm39) |
Q6* |
probably null |
Het |
Hmcn2 |
C |
T |
2: 31,323,284 (GRCm39) |
|
probably benign |
Het |
Hook2 |
A |
G |
8: 85,720,613 (GRCm39) |
|
probably benign |
Het |
Irx3 |
A |
G |
8: 92,525,555 (GRCm39) |
S507P |
unknown |
Het |
Kazn |
C |
A |
4: 141,966,506 (GRCm39) |
|
probably benign |
Het |
Kcne4 |
C |
T |
1: 78,795,688 (GRCm39) |
A112V |
possibly damaging |
Het |
Lamb1 |
C |
T |
12: 31,337,528 (GRCm39) |
R372C |
probably damaging |
Het |
Lrrc30 |
A |
G |
17: 67,939,175 (GRCm39) |
L135P |
probably damaging |
Het |
Lyst |
T |
A |
13: 13,809,815 (GRCm39) |
M495K |
possibly damaging |
Het |
Mab21l3 |
C |
A |
3: 101,730,847 (GRCm39) |
V131F |
probably damaging |
Het |
Mki67 |
T |
A |
7: 135,309,204 (GRCm39) |
T416S |
probably benign |
Het |
Mlst8 |
A |
T |
17: 24,697,099 (GRCm39) |
M56K |
probably benign |
Het |
Mmp9 |
A |
G |
2: 164,791,310 (GRCm39) |
Y160C |
probably damaging |
Het |
Mslnl |
A |
G |
17: 25,965,155 (GRCm39) |
Y507C |
probably damaging |
Het |
Muc6 |
G |
A |
7: 141,218,313 (GRCm39) |
S2120F |
possibly damaging |
Het |
Myl12a |
A |
T |
17: 71,301,737 (GRCm39) |
M130K |
probably benign |
Het |
Nalf2 |
A |
G |
X: 98,889,109 (GRCm39) |
I325V |
probably benign |
Het |
Ncdn |
C |
T |
4: 126,642,388 (GRCm39) |
R423Q |
probably benign |
Het |
Ncf2 |
A |
G |
1: 152,701,698 (GRCm39) |
|
probably benign |
Het |
Nek8 |
G |
T |
11: 78,061,572 (GRCm39) |
S319* |
probably null |
Het |
Or11g7 |
G |
A |
14: 50,690,653 (GRCm39) |
C48Y |
probably benign |
Het |
Or52m2 |
T |
C |
7: 102,263,993 (GRCm39) |
M68V |
possibly damaging |
Het |
Pcdh17 |
T |
A |
14: 84,684,062 (GRCm39) |
D176E |
probably damaging |
Het |
Pcdhb15 |
C |
A |
18: 37,608,442 (GRCm39) |
A558E |
probably benign |
Het |
Plrg1 |
T |
A |
3: 82,978,526 (GRCm39) |
W431R |
probably damaging |
Het |
Rbfox3 |
T |
A |
11: 118,387,283 (GRCm39) |
Q277L |
possibly damaging |
Het |
Rpgrip1 |
G |
A |
14: 52,382,666 (GRCm39) |
D600N |
possibly damaging |
Het |
Siah3 |
A |
G |
14: 75,763,421 (GRCm39) |
D224G |
probably damaging |
Het |
Slc22a6 |
T |
C |
19: 8,598,675 (GRCm39) |
L244P |
probably damaging |
Het |
Stap2 |
A |
T |
17: 56,304,511 (GRCm39) |
W374R |
probably benign |
Het |
Tbck |
T |
A |
3: 132,432,845 (GRCm39) |
N418K |
probably benign |
Het |
Tcp11x2 |
T |
C |
X: 134,555,733 (GRCm39) |
N474S |
probably damaging |
Het |
Tenm3 |
A |
C |
8: 48,681,590 (GRCm39) |
V2680G |
probably damaging |
Het |
Thada |
A |
T |
17: 84,538,213 (GRCm39) |
|
probably benign |
Het |
Tlr6 |
C |
T |
5: 65,110,772 (GRCm39) |
V712M |
probably damaging |
Het |
Uvssa |
G |
T |
5: 33,547,162 (GRCm39) |
G243C |
probably damaging |
Het |
Vwa8 |
T |
A |
14: 79,401,660 (GRCm39) |
|
probably benign |
Het |
Znrf2 |
A |
T |
6: 54,861,776 (GRCm39) |
N229I |
probably damaging |
Het |
|
Other mutations in Gsdma |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01650:Gsdma
|
APN |
11 |
98,564,513 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02573:Gsdma
|
APN |
11 |
98,561,577 (GRCm39) |
splice site |
probably benign |
|
IGL03005:Gsdma
|
APN |
11 |
98,567,085 (GRCm39) |
missense |
probably damaging |
0.97 |
R0143:Gsdma
|
UTSW |
11 |
98,557,080 (GRCm39) |
missense |
probably damaging |
0.96 |
R1337:Gsdma
|
UTSW |
11 |
98,560,533 (GRCm39) |
nonsense |
probably null |
|
R1533:Gsdma
|
UTSW |
11 |
98,567,210 (GRCm39) |
missense |
unknown |
|
R1605:Gsdma
|
UTSW |
11 |
98,557,319 (GRCm39) |
missense |
probably damaging |
0.98 |
R1929:Gsdma
|
UTSW |
11 |
98,562,193 (GRCm39) |
critical splice donor site |
probably null |
|
R1998:Gsdma
|
UTSW |
11 |
98,564,520 (GRCm39) |
missense |
probably damaging |
0.99 |
R2043:Gsdma
|
UTSW |
11 |
98,557,046 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2114:Gsdma
|
UTSW |
11 |
98,563,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R3404:Gsdma
|
UTSW |
11 |
98,563,964 (GRCm39) |
splice site |
probably benign |
|
R3405:Gsdma
|
UTSW |
11 |
98,563,964 (GRCm39) |
splice site |
probably benign |
|
R3711:Gsdma
|
UTSW |
11 |
98,557,045 (GRCm39) |
nonsense |
probably null |
|
R3764:Gsdma
|
UTSW |
11 |
98,561,593 (GRCm39) |
missense |
probably damaging |
0.98 |
R4656:Gsdma
|
UTSW |
11 |
98,563,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R5384:Gsdma
|
UTSW |
11 |
98,557,275 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5943:Gsdma
|
UTSW |
11 |
98,563,852 (GRCm39) |
missense |
probably benign |
0.30 |
R7620:Gsdma
|
UTSW |
11 |
98,557,429 (GRCm39) |
missense |
probably benign |
0.06 |
R8340:Gsdma
|
UTSW |
11 |
98,557,421 (GRCm39) |
missense |
probably benign |
0.07 |
R9349:Gsdma
|
UTSW |
11 |
98,566,771 (GRCm39) |
missense |
probably benign |
0.36 |
R9736:Gsdma
|
UTSW |
11 |
98,567,169 (GRCm39) |
missense |
probably damaging |
1.00 |
X0017:Gsdma
|
UTSW |
11 |
98,557,096 (GRCm39) |
critical splice donor site |
probably benign |
|
Z1176:Gsdma
|
UTSW |
11 |
98,560,585 (GRCm39) |
missense |
probably damaging |
1.00 |
|