Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563M21Rik |
T |
C |
9: 55,888,126 (GRCm39) |
D397G |
probably benign |
Het |
6820408C15Rik |
C |
T |
2: 152,270,873 (GRCm39) |
T32I |
possibly damaging |
Het |
Abca13 |
A |
G |
11: 9,384,188 (GRCm39) |
K3880R |
probably benign |
Het |
Ahnak |
C |
T |
19: 8,979,147 (GRCm39) |
L144F |
probably benign |
Het |
Antxr2 |
A |
T |
5: 98,086,266 (GRCm39) |
I447N |
probably damaging |
Het |
Cdc20 |
C |
T |
4: 118,290,257 (GRCm39) |
R468Q |
probably damaging |
Het |
Clip2 |
A |
G |
5: 134,564,051 (GRCm39) |
|
probably benign |
Het |
Cntnap2 |
A |
T |
6: 46,507,324 (GRCm39) |
|
probably benign |
Het |
Ddi1 |
A |
G |
9: 6,265,799 (GRCm39) |
M190T |
probably benign |
Het |
Dicer1 |
A |
G |
12: 104,695,487 (GRCm39) |
V148A |
possibly damaging |
Het |
Dpp8 |
A |
G |
9: 64,962,205 (GRCm39) |
D415G |
probably benign |
Het |
Galnt11 |
G |
A |
5: 25,470,258 (GRCm39) |
R569Q |
probably benign |
Het |
Gpr6 |
T |
C |
10: 40,946,604 (GRCm39) |
N326S |
probably damaging |
Het |
Hexb |
T |
C |
13: 97,313,259 (GRCm39) |
|
probably benign |
Het |
L3mbtl3 |
G |
A |
10: 26,216,846 (GRCm39) |
A181V |
unknown |
Het |
Lrrc37a |
G |
A |
11: 103,393,115 (GRCm39) |
T770I |
probably damaging |
Het |
Or12e8 |
T |
C |
2: 87,188,597 (GRCm39) |
S270P |
probably damaging |
Het |
Or2d2 |
A |
G |
7: 106,728,244 (GRCm39) |
S119P |
probably damaging |
Het |
Or6a2 |
T |
C |
7: 106,600,536 (GRCm39) |
N177S |
probably damaging |
Het |
Or7g32 |
C |
T |
9: 19,388,893 (GRCm39) |
V215I |
probably benign |
Het |
Phactr1 |
T |
A |
13: 43,248,363 (GRCm39) |
N437K |
possibly damaging |
Het |
Ppp1r13b |
T |
C |
12: 111,805,170 (GRCm39) |
T181A |
probably benign |
Het |
Prc1 |
G |
A |
7: 79,960,964 (GRCm39) |
|
probably benign |
Het |
Proca1 |
A |
G |
11: 78,095,752 (GRCm39) |
N128S |
probably benign |
Het |
Psmd8 |
G |
A |
7: 28,876,546 (GRCm39) |
P155L |
probably damaging |
Het |
Rad54l |
A |
G |
4: 115,956,646 (GRCm39) |
V500A |
probably damaging |
Het |
Scamp3 |
G |
A |
3: 89,089,234 (GRCm39) |
|
probably null |
Het |
Serpinb10 |
C |
T |
1: 107,466,179 (GRCm39) |
T55M |
probably benign |
Het |
Sipa1l2 |
T |
C |
8: 126,218,395 (GRCm39) |
E314G |
probably benign |
Het |
Slc14a2 |
G |
A |
18: 78,250,283 (GRCm39) |
R62C |
probably damaging |
Het |
Tdrd9 |
C |
T |
12: 112,034,059 (GRCm39) |
R1334* |
probably null |
Het |
Trank1 |
A |
G |
9: 111,196,103 (GRCm39) |
I1376V |
probably benign |
Het |
Trim28 |
T |
A |
7: 12,761,838 (GRCm39) |
H268Q |
possibly damaging |
Het |
Vmn2r76 |
T |
A |
7: 85,879,740 (GRCm39) |
I187L |
probably benign |
Het |
Wdr95 |
A |
T |
5: 149,486,802 (GRCm39) |
R160* |
probably null |
Het |
Wnt5a |
T |
C |
14: 28,244,823 (GRCm39) |
C357R |
probably damaging |
Het |
Zfp157 |
A |
G |
5: 138,445,803 (GRCm39) |
I53V |
probably damaging |
Het |
Zfp184 |
G |
A |
13: 22,142,948 (GRCm39) |
R218H |
probably damaging |
Het |
|
Other mutations in Ighv3-4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R3907:Ighv3-4
|
UTSW |
12 |
114,217,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R3957:Ighv3-4
|
UTSW |
12 |
114,217,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R4238:Ighv3-4
|
UTSW |
12 |
114,217,533 (GRCm39) |
missense |
probably benign |
0.00 |
R4239:Ighv3-4
|
UTSW |
12 |
114,217,533 (GRCm39) |
missense |
probably benign |
0.00 |
R4355:Ighv3-4
|
UTSW |
12 |
114,217,260 (GRCm39) |
missense |
probably benign |
0.01 |
R5026:Ighv3-4
|
UTSW |
12 |
114,217,382 (GRCm39) |
missense |
probably benign |
0.03 |
R5745:Ighv3-4
|
UTSW |
12 |
114,217,388 (GRCm39) |
missense |
probably benign |
0.00 |
R7068:Ighv3-4
|
UTSW |
12 |
114,217,274 (GRCm39) |
missense |
probably damaging |
0.98 |
R8472:Ighv3-4
|
UTSW |
12 |
114,217,649 (GRCm39) |
missense |
probably benign |
0.00 |
R8504:Ighv3-4
|
UTSW |
12 |
114,217,544 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8880:Ighv3-4
|
UTSW |
12 |
114,217,535 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8991:Ighv3-4
|
UTSW |
12 |
114,217,266 (GRCm39) |
missense |
probably benign |
0.40 |
R9523:Ighv3-4
|
UTSW |
12 |
114,217,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R9656:Ighv3-4
|
UTSW |
12 |
114,217,295 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9756:Ighv3-4
|
UTSW |
12 |
114,217,448 (GRCm39) |
missense |
probably damaging |
1.00 |
|