Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
A |
C |
17: 24,536,104 (GRCm39) |
I521S |
probably damaging |
Het |
Ace |
A |
T |
11: 105,870,376 (GRCm39) |
K265I |
probably benign |
Het |
Acss3 |
A |
G |
10: 106,889,187 (GRCm39) |
|
probably null |
Het |
Aldh3a2 |
A |
G |
11: 61,153,082 (GRCm39) |
Y215H |
probably damaging |
Het |
Clk2 |
A |
G |
3: 89,082,729 (GRCm39) |
M393V |
probably damaging |
Het |
Cyc1 |
A |
G |
15: 76,229,365 (GRCm39) |
I242V |
probably benign |
Het |
Evpl |
G |
A |
11: 116,118,727 (GRCm39) |
L657F |
probably benign |
Het |
Fbxw10 |
G |
A |
11: 62,764,327 (GRCm39) |
V675M |
probably damaging |
Het |
Fgf21 |
A |
G |
7: 45,264,597 (GRCm39) |
V45A |
probably damaging |
Het |
Gm5134 |
T |
C |
10: 75,836,255 (GRCm39) |
I412T |
possibly damaging |
Het |
Gnat3 |
T |
C |
5: 18,208,749 (GRCm39) |
|
probably benign |
Het |
Hk3 |
C |
T |
13: 55,162,239 (GRCm39) |
|
probably null |
Het |
Ipp |
A |
G |
4: 116,389,856 (GRCm39) |
M471V |
possibly damaging |
Het |
Kcnj1 |
G |
A |
9: 32,307,794 (GRCm39) |
V73I |
probably benign |
Het |
Kin |
G |
A |
2: 10,085,515 (GRCm39) |
R25H |
probably damaging |
Het |
Kin |
T |
C |
2: 10,085,517 (GRCm39) |
W26R |
probably damaging |
Het |
Mical2 |
T |
C |
7: 111,920,652 (GRCm39) |
|
probably benign |
Het |
Mllt1 |
A |
T |
17: 57,202,086 (GRCm39) |
S428R |
probably damaging |
Het |
Ppm1k |
T |
A |
6: 57,501,740 (GRCm39) |
H141L |
probably benign |
Het |
Septin4 |
G |
T |
11: 87,480,599 (GRCm39) |
C392F |
probably damaging |
Het |
Slc26a11 |
T |
C |
11: 119,270,727 (GRCm39) |
F550L |
probably benign |
Het |
Ssb |
T |
A |
2: 69,701,179 (GRCm39) |
|
probably null |
Het |
Stk36 |
T |
A |
1: 74,663,093 (GRCm39) |
M588K |
possibly damaging |
Het |
Ubqln4 |
G |
A |
3: 88,471,808 (GRCm39) |
A415T |
probably benign |
Het |
Zfp839 |
C |
A |
12: 110,827,382 (GRCm39) |
S424R |
probably damaging |
Het |
Zkscan6 |
G |
T |
11: 65,705,573 (GRCm39) |
G95W |
probably damaging |
Het |
|
Other mutations in Ifna12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02649:Ifna12
|
APN |
4 |
88,521,091 (GRCm39) |
missense |
probably damaging |
0.98 |
R1463:Ifna12
|
UTSW |
4 |
88,521,193 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2432:Ifna12
|
UTSW |
4 |
88,521,590 (GRCm39) |
start gained |
probably benign |
|
R4388:Ifna12
|
UTSW |
4 |
88,521,346 (GRCm39) |
missense |
probably benign |
0.05 |
R6033:Ifna12
|
UTSW |
4 |
88,521,154 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6033:Ifna12
|
UTSW |
4 |
88,521,154 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6154:Ifna12
|
UTSW |
4 |
88,521,531 (GRCm39) |
nonsense |
probably null |
|
R6189:Ifna12
|
UTSW |
4 |
88,521,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R7081:Ifna12
|
UTSW |
4 |
88,521,440 (GRCm39) |
missense |
probably damaging |
0.97 |
R7102:Ifna12
|
UTSW |
4 |
88,521,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R7467:Ifna12
|
UTSW |
4 |
88,521,502 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7754:Ifna12
|
UTSW |
4 |
88,521,415 (GRCm39) |
missense |
probably damaging |
0.99 |
R9056:Ifna12
|
UTSW |
4 |
88,521,079 (GRCm39) |
missense |
possibly damaging |
0.69 |
|