Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A230072I06Rik |
A |
G |
8: 12,329,665 (GRCm39) |
Q40R |
unknown |
Het |
A730015C16Rik |
C |
T |
4: 108,705,053 (GRCm39) |
V89I |
unknown |
Het |
Adam19 |
G |
T |
11: 46,022,570 (GRCm39) |
E508* |
probably null |
Het |
Arhgef33 |
C |
T |
17: 80,644,736 (GRCm39) |
Q22* |
probably null |
Het |
Arih2 |
C |
G |
9: 108,488,938 (GRCm39) |
R260P |
probably damaging |
Het |
Astn2 |
T |
A |
4: 66,184,492 (GRCm39) |
T202S |
unknown |
Het |
Bpifb5 |
T |
A |
2: 154,067,005 (GRCm39) |
L86Q |
possibly damaging |
Het |
Brpf3 |
G |
A |
17: 29,040,276 (GRCm39) |
S899N |
probably benign |
Het |
Ccl20 |
T |
C |
1: 83,095,586 (GRCm39) |
F49S |
|
Het |
Ctse |
A |
G |
1: 131,592,111 (GRCm39) |
T146A |
probably benign |
Het |
Dhx35 |
T |
C |
2: 158,671,444 (GRCm39) |
S292P |
possibly damaging |
Het |
Fut7 |
C |
T |
2: 25,314,993 (GRCm39) |
P84S |
possibly damaging |
Het |
Gm9736 |
A |
C |
10: 77,586,393 (GRCm39) |
S266A |
unknown |
Het |
Gsdma |
T |
A |
11: 98,566,771 (GRCm39) |
L366Q |
probably benign |
Het |
Igkv2-112 |
G |
A |
6: 68,197,678 (GRCm39) |
V117I |
probably benign |
Het |
Kcnh2 |
C |
T |
5: 24,538,003 (GRCm39) |
G120E |
probably damaging |
Het |
Kcnip1 |
T |
G |
11: 33,601,548 (GRCm39) |
Y29S |
probably benign |
Het |
Lrrc37a |
T |
G |
11: 103,388,454 (GRCm39) |
M2324L |
unknown |
Het |
Mettl5 |
T |
A |
2: 69,702,113 (GRCm39) |
D185V |
possibly damaging |
Het |
Mmp1b |
T |
A |
9: 7,369,271 (GRCm39) |
M359L |
probably benign |
Het |
Ndufa5 |
G |
A |
6: 24,522,749 (GRCm39) |
T31I |
probably benign |
Het |
Ngly1 |
T |
A |
14: 16,281,801 (GRCm38) |
C352* |
probably null |
Het |
Or14c45 |
A |
G |
7: 86,176,373 (GRCm39) |
H136R |
probably benign |
Het |
Or51a39 |
A |
T |
7: 102,362,875 (GRCm39) |
C248* |
probably null |
Het |
Pcdhac1 |
C |
T |
18: 37,224,021 (GRCm39) |
A278V |
possibly damaging |
Het |
Ppp2r3c |
T |
A |
12: 55,345,268 (GRCm39) |
K73N |
probably benign |
Het |
Rasgrf1 |
T |
C |
9: 89,884,460 (GRCm39) |
V975A |
probably damaging |
Het |
Rps27rt |
C |
T |
9: 114,811,673 (GRCm39) |
V35M |
probably benign |
Het |
Slc22a8 |
A |
G |
19: 8,571,469 (GRCm39) |
N67D |
probably benign |
Het |
Slc39a6 |
C |
A |
18: 24,718,493 (GRCm39) |
M521I |
probably benign |
Het |
Snx31 |
C |
T |
15: 36,555,430 (GRCm39) |
S39N |
probably damaging |
Het |
Speer1b |
C |
T |
5: 11,823,221 (GRCm39) |
T130I |
possibly damaging |
Het |
Sv2a |
T |
C |
3: 96,096,795 (GRCm39) |
|
probably null |
Het |
Thg1l |
G |
A |
11: 45,846,273 (GRCm39) |
A7V |
probably benign |
Het |
Ttc39c |
C |
T |
18: 12,822,932 (GRCm39) |
Q147* |
probably null |
Het |
Ube2u |
A |
G |
4: 100,407,194 (GRCm39) |
N352D |
unknown |
Het |
Uhrf1 |
T |
C |
17: 56,617,737 (GRCm39) |
V153A |
possibly damaging |
Het |
Wdfy4 |
A |
G |
14: 32,875,996 (GRCm39) |
S143P |
|
Het |
|
Other mutations in Ifna15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01575:Ifna15
|
APN |
4 |
88,476,044 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01757:Ifna15
|
APN |
4 |
88,476,322 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL01824:Ifna15
|
APN |
4 |
88,476,020 (GRCm39) |
missense |
probably benign |
0.00 |
R3853:Ifna15
|
UTSW |
4 |
88,476,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R4356:Ifna15
|
UTSW |
4 |
88,476,079 (GRCm39) |
missense |
probably benign |
0.09 |
R4357:Ifna15
|
UTSW |
4 |
88,476,079 (GRCm39) |
missense |
probably benign |
0.09 |
R4358:Ifna15
|
UTSW |
4 |
88,476,079 (GRCm39) |
missense |
probably benign |
0.09 |
R4359:Ifna15
|
UTSW |
4 |
88,476,079 (GRCm39) |
missense |
probably benign |
0.09 |
R5038:Ifna15
|
UTSW |
4 |
88,476,266 (GRCm39) |
missense |
probably benign |
0.03 |
R5372:Ifna15
|
UTSW |
4 |
88,476,338 (GRCm39) |
missense |
probably damaging |
0.97 |
R6036:Ifna15
|
UTSW |
4 |
88,476,310 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6036:Ifna15
|
UTSW |
4 |
88,476,310 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7347:Ifna15
|
UTSW |
4 |
88,476,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R8097:Ifna15
|
UTSW |
4 |
88,475,938 (GRCm39) |
missense |
probably benign |
0.01 |
R8132:Ifna15
|
UTSW |
4 |
88,475,920 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8824:Ifna15
|
UTSW |
4 |
88,475,998 (GRCm39) |
missense |
probably damaging |
1.00 |
|