Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933412E24Rik |
A |
G |
15: 59,888,212 (GRCm39) |
V76A |
possibly damaging |
Het |
Aif1 |
G |
A |
17: 35,391,127 (GRCm39) |
P44L |
probably benign |
Het |
Anapc4 |
T |
C |
5: 52,999,279 (GRCm39) |
|
probably benign |
Het |
Anxa4 |
A |
G |
6: 86,720,135 (GRCm39) |
S144P |
probably benign |
Het |
Bcr |
A |
G |
10: 74,966,944 (GRCm39) |
E517G |
probably damaging |
Het |
Ccdc57 |
T |
C |
11: 120,751,349 (GRCm39) |
E907G |
probably benign |
Het |
Chd6 |
TG |
T |
2: 160,807,679 (GRCm39) |
|
probably null |
Het |
Dock6 |
A |
G |
9: 21,750,782 (GRCm39) |
|
probably benign |
Het |
Dock8 |
A |
G |
19: 25,177,757 (GRCm39) |
K2031E |
probably damaging |
Het |
Gm5444 |
T |
C |
13: 4,884,344 (GRCm39) |
|
noncoding transcript |
Het |
Hlx |
G |
T |
1: 184,464,184 (GRCm39) |
A52D |
probably damaging |
Het |
Ino80d |
T |
C |
1: 63,104,985 (GRCm39) |
N364D |
possibly damaging |
Het |
Ltbp2 |
T |
C |
12: 84,855,937 (GRCm39) |
T769A |
probably benign |
Het |
Ms4a20 |
T |
A |
19: 11,083,157 (GRCm39) |
M88L |
probably benign |
Het |
Mug1 |
T |
C |
6: 121,861,588 (GRCm39) |
V1350A |
probably benign |
Het |
Nedd9 |
A |
G |
13: 41,469,987 (GRCm39) |
S389P |
probably damaging |
Het |
Or10ag57 |
A |
T |
2: 87,218,084 (GRCm39) |
I12F |
probably benign |
Het |
Or4c11b |
A |
G |
2: 88,624,989 (GRCm39) |
N88D |
probably benign |
Het |
Or8h8 |
T |
C |
2: 86,752,982 (GRCm39) |
K298R |
possibly damaging |
Het |
Pole |
A |
T |
5: 110,478,829 (GRCm39) |
I28F |
possibly damaging |
Het |
Prkce |
C |
A |
17: 86,781,870 (GRCm39) |
P180T |
probably damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,723,909 (GRCm39) |
H1995R |
possibly damaging |
Het |
Rnf144b |
A |
G |
13: 47,373,976 (GRCm39) |
K58E |
probably benign |
Het |
Rnf43 |
A |
G |
11: 87,622,851 (GRCm39) |
R651G |
probably damaging |
Het |
Scel |
A |
T |
14: 103,845,606 (GRCm39) |
L580F |
possibly damaging |
Het |
Scn4b |
G |
A |
9: 45,059,127 (GRCm39) |
V133M |
probably damaging |
Het |
Sipa1l3 |
T |
C |
7: 29,077,060 (GRCm39) |
N904S |
probably damaging |
Het |
Sun5 |
A |
G |
2: 153,709,422 (GRCm39) |
|
probably benign |
Het |
Tanc2 |
T |
C |
11: 105,725,877 (GRCm39) |
V347A |
probably benign |
Het |
Tmem245 |
T |
C |
4: 56,937,957 (GRCm39) |
Y197C |
probably damaging |
Het |
Usp30 |
C |
T |
5: 114,249,241 (GRCm39) |
R182* |
probably null |
Het |
Vmn2r112 |
T |
A |
17: 22,822,096 (GRCm39) |
V258E |
probably damaging |
Het |
Vps35 |
T |
C |
8: 86,001,443 (GRCm39) |
|
probably benign |
Het |
Xkr7 |
G |
A |
2: 152,896,318 (GRCm39) |
V391M |
possibly damaging |
Het |
Ythdf3 |
A |
T |
3: 16,257,379 (GRCm39) |
|
probably benign |
Het |
Zfp110 |
T |
C |
7: 12,583,113 (GRCm39) |
V587A |
probably benign |
Het |
|
Other mutations in Ifna16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01085:Ifna16
|
APN |
4 |
88,594,969 (GRCm39) |
missense |
probably benign |
|
IGL01779:Ifna16
|
APN |
4 |
88,594,882 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02717:Ifna16
|
APN |
4 |
88,594,777 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03226:Ifna16
|
APN |
4 |
88,594,741 (GRCm39) |
missense |
probably benign |
0.18 |
R0040:Ifna16
|
UTSW |
4 |
88,594,867 (GRCm39) |
missense |
probably benign |
0.35 |
R0040:Ifna16
|
UTSW |
4 |
88,594,867 (GRCm39) |
missense |
probably benign |
0.35 |
R1514:Ifna16
|
UTSW |
4 |
88,594,979 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4877:Ifna16
|
UTSW |
4 |
88,594,681 (GRCm39) |
missense |
probably benign |
0.00 |
R8989:Ifna16
|
UTSW |
4 |
88,594,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R9619:Ifna16
|
UTSW |
4 |
88,594,762 (GRCm39) |
missense |
probably benign |
0.30 |
R9648:Ifna16
|
UTSW |
4 |
88,595,060 (GRCm39) |
missense |
probably benign |
0.18 |
R9688:Ifna16
|
UTSW |
4 |
88,594,874 (GRCm39) |
nonsense |
probably null |
|
R9743:Ifna16
|
UTSW |
4 |
88,594,930 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Ifna16
|
UTSW |
4 |
88,594,615 (GRCm39) |
missense |
probably damaging |
1.00 |
|