Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
T |
C |
11: 110,071,439 (GRCm39) |
K1471R |
probably benign |
Het |
Add1 |
A |
G |
5: 34,777,467 (GRCm39) |
S77G |
probably damaging |
Het |
Atm |
G |
T |
9: 53,364,863 (GRCm39) |
N2642K |
probably damaging |
Het |
Atp6v0a2 |
T |
A |
5: 124,767,267 (GRCm39) |
M10K |
possibly damaging |
Het |
Btd |
T |
A |
14: 31,389,193 (GRCm39) |
S305T |
probably damaging |
Het |
Cmya5 |
C |
T |
13: 93,229,065 (GRCm39) |
V2008I |
probably benign |
Het |
Cpd |
T |
G |
11: 76,681,814 (GRCm39) |
|
probably benign |
Het |
Dis3l |
A |
G |
9: 64,217,766 (GRCm39) |
F772L |
probably damaging |
Het |
Dlg5 |
A |
T |
14: 24,222,091 (GRCm39) |
I517N |
probably damaging |
Het |
Fig4 |
G |
A |
10: 41,161,661 (GRCm39) |
T34M |
probably damaging |
Het |
Flna |
C |
T |
X: 73,270,816 (GRCm39) |
V2235I |
probably damaging |
Het |
Flot2 |
T |
C |
11: 77,950,031 (GRCm39) |
I371T |
possibly damaging |
Het |
Fsip2 |
G |
A |
2: 82,813,398 (GRCm39) |
S3239N |
probably benign |
Het |
Gbp3 |
A |
G |
3: 142,273,343 (GRCm39) |
I297V |
probably benign |
Het |
Gcnt3 |
T |
C |
9: 69,942,235 (GRCm39) |
E111G |
probably benign |
Het |
Gdi1 |
G |
T |
X: 73,351,331 (GRCm39) |
A148S |
probably benign |
Het |
Heatr5b |
G |
A |
17: 79,060,502 (GRCm39) |
H2058Y |
probably benign |
Het |
Hsp90aa1 |
A |
G |
12: 110,662,113 (GRCm39) |
M1T |
probably null |
Het |
Il22b |
A |
G |
10: 118,130,762 (GRCm39) |
S45P |
probably damaging |
Het |
Inppl1 |
C |
A |
7: 101,477,478 (GRCm39) |
V715F |
possibly damaging |
Het |
Kansl1 |
T |
C |
11: 104,225,991 (GRCm39) |
Y975C |
probably damaging |
Het |
Kif18b |
A |
G |
11: 102,807,338 (GRCm39) |
|
probably benign |
Het |
Krt40 |
T |
A |
11: 99,432,492 (GRCm39) |
R175W |
probably damaging |
Het |
Map3k19 |
T |
C |
1: 127,751,803 (GRCm39) |
D516G |
probably damaging |
Het |
Mfsd3 |
A |
G |
15: 76,587,352 (GRCm39) |
H345R |
probably benign |
Het |
Mtnr1a |
A |
T |
8: 45,522,419 (GRCm39) |
N58I |
probably damaging |
Het |
Nsmf |
T |
C |
2: 24,951,774 (GRCm39) |
V499A |
probably damaging |
Het |
Nudt6 |
A |
G |
3: 37,473,655 (GRCm39) |
L22P |
probably damaging |
Het |
Nxf7 |
T |
G |
X: 134,490,159 (GRCm39) |
E35A |
probably damaging |
Het |
Or11h23 |
A |
C |
14: 50,948,653 (GRCm39) |
I289L |
probably damaging |
Het |
Paf1 |
T |
C |
7: 28,095,629 (GRCm39) |
|
probably null |
Het |
Pcdhb11 |
G |
T |
18: 37,557,021 (GRCm39) |
V784L |
probably benign |
Het |
Pglyrp2 |
T |
C |
17: 32,637,560 (GRCm39) |
D156G |
probably benign |
Het |
Pnpt1 |
A |
G |
11: 29,106,939 (GRCm39) |
D670G |
probably damaging |
Het |
Polr1b |
T |
A |
2: 128,967,443 (GRCm39) |
H945Q |
probably benign |
Het |
Ptk6 |
C |
T |
2: 180,840,861 (GRCm39) |
|
probably benign |
Het |
Rftn1 |
C |
T |
17: 50,362,280 (GRCm39) |
E273K |
probably benign |
Het |
Rnf125 |
A |
G |
18: 21,116,168 (GRCm39) |
I117V |
probably benign |
Het |
Robo4 |
A |
G |
9: 37,321,765 (GRCm39) |
K742R |
possibly damaging |
Het |
Sez6l |
T |
C |
5: 112,623,440 (GRCm39) |
E37G |
probably damaging |
Het |
Skint4 |
A |
T |
4: 111,993,218 (GRCm39) |
I306L |
probably benign |
Het |
Sntb1 |
A |
T |
15: 55,506,081 (GRCm39) |
Y497* |
probably null |
Het |
Snx27 |
C |
A |
3: 94,489,733 (GRCm39) |
V42L |
probably damaging |
Het |
Sorbs1 |
T |
A |
19: 40,365,187 (GRCm39) |
T199S |
probably benign |
Het |
Sorcs2 |
A |
G |
5: 36,235,301 (GRCm39) |
Y72H |
probably benign |
Het |
Spef2 |
G |
T |
15: 9,725,192 (GRCm39) |
|
probably benign |
Het |
Sucla2 |
G |
T |
14: 73,816,871 (GRCm39) |
V204L |
probably benign |
Het |
Tescl |
C |
A |
7: 24,033,098 (GRCm39) |
V76F |
probably damaging |
Het |
Tnxb |
T |
A |
17: 34,928,628 (GRCm39) |
Y2681N |
possibly damaging |
Het |
Usp42 |
T |
C |
5: 143,713,769 (GRCm39) |
T2A |
probably damaging |
Het |
Vdac3-ps1 |
T |
A |
13: 18,205,431 (GRCm39) |
|
noncoding transcript |
Het |
Wapl |
T |
A |
14: 34,461,181 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Mlkl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Mlkl
|
APN |
8 |
112,046,060 (GRCm39) |
nonsense |
probably null |
|
IGL01376:Mlkl
|
APN |
8 |
112,046,379 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02801:Mlkl
|
APN |
8 |
112,043,064 (GRCm39) |
missense |
probably benign |
0.18 |
IGL03121:Mlkl
|
APN |
8 |
112,041,612 (GRCm39) |
missense |
probably damaging |
1.00 |
Ghoulish
|
UTSW |
8 |
112,049,380 (GRCm39) |
missense |
probably damaging |
1.00 |
mecro
|
UTSW |
8 |
112,046,348 (GRCm39) |
critical splice donor site |
probably null |
|
necro
|
UTSW |
8 |
112,038,732 (GRCm39) |
intron |
probably benign |
|
secro
|
UTSW |
8 |
112,042,199 (GRCm39) |
intron |
probably benign |
|
R0133:Mlkl
|
UTSW |
8 |
112,054,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R0230:Mlkl
|
UTSW |
8 |
112,041,694 (GRCm39) |
missense |
probably benign |
0.07 |
R0387:Mlkl
|
UTSW |
8 |
112,059,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R0497:Mlkl
|
UTSW |
8 |
112,054,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R0735:Mlkl
|
UTSW |
8 |
112,054,433 (GRCm39) |
unclassified |
probably benign |
|
R1733:Mlkl
|
UTSW |
8 |
112,049,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R1761:Mlkl
|
UTSW |
8 |
112,060,355 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1911:Mlkl
|
UTSW |
8 |
112,038,732 (GRCm39) |
intron |
probably benign |
|
R2057:Mlkl
|
UTSW |
8 |
112,060,242 (GRCm39) |
missense |
probably benign |
0.07 |
R2921:Mlkl
|
UTSW |
8 |
112,043,079 (GRCm39) |
missense |
probably benign |
0.02 |
R3745:Mlkl
|
UTSW |
8 |
112,042,199 (GRCm39) |
intron |
probably benign |
|
R4760:Mlkl
|
UTSW |
8 |
112,046,348 (GRCm39) |
critical splice donor site |
probably null |
|
R5377:Mlkl
|
UTSW |
8 |
112,054,569 (GRCm39) |
missense |
probably benign |
0.23 |
R7052:Mlkl
|
UTSW |
8 |
112,046,074 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7155:Mlkl
|
UTSW |
8 |
112,046,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R7459:Mlkl
|
UTSW |
8 |
112,060,162 (GRCm39) |
missense |
probably benign |
0.36 |
R7728:Mlkl
|
UTSW |
8 |
112,060,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R8036:Mlkl
|
UTSW |
8 |
112,060,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R8064:Mlkl
|
UTSW |
8 |
112,038,700 (GRCm39) |
missense |
probably benign |
0.38 |
R9088:Mlkl
|
UTSW |
8 |
112,049,365 (GRCm39) |
missense |
|
|
R9152:Mlkl
|
UTSW |
8 |
112,046,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R9275:Mlkl
|
UTSW |
8 |
112,043,055 (GRCm39) |
missense |
probably benign |
0.07 |
|