Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930474N05Rik |
A |
G |
14: 35,817,109 (GRCm39) |
D53G |
probably benign |
Het |
A1cf |
C |
T |
19: 31,909,945 (GRCm39) |
P330S |
probably benign |
Het |
Acta2 |
A |
G |
19: 34,225,941 (GRCm39) |
|
probably benign |
Het |
Actrt3 |
A |
G |
3: 30,651,985 (GRCm39) |
*370R |
probably null |
Het |
Aif1 |
G |
A |
17: 35,391,127 (GRCm39) |
P44L |
probably benign |
Het |
Btbd8 |
T |
C |
5: 107,658,440 (GRCm39) |
L1158S |
probably damaging |
Het |
Cadps2 |
C |
G |
6: 23,838,977 (GRCm39) |
|
probably benign |
Het |
Camsap3 |
C |
T |
8: 3,656,808 (GRCm39) |
R1048C |
probably damaging |
Het |
Cdkl2 |
C |
T |
5: 92,181,538 (GRCm39) |
A148T |
possibly damaging |
Het |
Dab2 |
T |
A |
15: 6,464,733 (GRCm39) |
I395K |
possibly damaging |
Het |
Dclk2 |
A |
G |
3: 86,706,324 (GRCm39) |
F589S |
probably damaging |
Het |
Ddx60 |
T |
C |
8: 62,465,470 (GRCm39) |
S1376P |
possibly damaging |
Het |
Eprs1 |
T |
C |
1: 185,148,005 (GRCm39) |
F1256L |
probably damaging |
Het |
Etaa1 |
A |
T |
11: 17,895,605 (GRCm39) |
|
probably null |
Het |
Fat2 |
T |
C |
11: 55,202,727 (GRCm39) |
T116A |
possibly damaging |
Het |
Fem1al |
C |
A |
11: 29,773,718 (GRCm39) |
A580S |
probably benign |
Het |
Fmnl3 |
T |
C |
15: 99,268,108 (GRCm39) |
T26A |
probably benign |
Het |
Foxp1 |
A |
G |
6: 98,980,254 (GRCm39) |
V158A |
possibly damaging |
Het |
G6pd2 |
T |
A |
5: 61,967,351 (GRCm39) |
D375E |
probably benign |
Het |
Gne |
C |
T |
4: 44,042,196 (GRCm39) |
A460T |
probably damaging |
Het |
Hecw2 |
T |
C |
1: 53,943,581 (GRCm39) |
M949V |
possibly damaging |
Het |
Herc1 |
G |
A |
9: 66,336,251 (GRCm39) |
V1599M |
possibly damaging |
Het |
Hk2 |
A |
C |
6: 82,708,096 (GRCm39) |
N628K |
probably damaging |
Het |
Hmcn1 |
T |
C |
1: 150,498,685 (GRCm39) |
T4065A |
possibly damaging |
Het |
Ipo8 |
T |
A |
6: 148,691,321 (GRCm39) |
Q683L |
probably benign |
Het |
Krt81 |
A |
G |
15: 101,361,217 (GRCm39) |
I121T |
probably benign |
Het |
Lamb2 |
T |
C |
9: 108,359,340 (GRCm39) |
L322P |
probably benign |
Het |
Lilrb4a |
A |
G |
10: 51,367,796 (GRCm39) |
M113V |
probably benign |
Het |
Mnat1 |
G |
A |
12: 73,265,917 (GRCm39) |
|
probably null |
Het |
Mucl1 |
T |
A |
15: 103,783,964 (GRCm39) |
T68S |
possibly damaging |
Het |
Npnt |
G |
T |
3: 132,597,170 (GRCm39) |
D461E |
probably damaging |
Het |
Nrp1 |
A |
T |
8: 129,224,385 (GRCm39) |
Q716L |
probably benign |
Het |
Or11g25 |
A |
G |
14: 50,723,097 (GRCm39) |
T61A |
possibly damaging |
Het |
Or12k5 |
T |
G |
2: 36,895,159 (GRCm39) |
S156R |
probably damaging |
Het |
Or51b6b |
A |
T |
7: 103,309,617 (GRCm39) |
I280N |
possibly damaging |
Het |
Podxl2 |
T |
C |
6: 88,826,178 (GRCm39) |
Q376R |
probably damaging |
Het |
Pudp |
T |
C |
18: 50,701,646 (GRCm39) |
D29G |
probably benign |
Het |
Rrs1 |
C |
A |
1: 9,616,026 (GRCm39) |
|
probably null |
Het |
S1pr3 |
T |
C |
13: 51,573,614 (GRCm39) |
I265T |
possibly damaging |
Het |
Scgb1b2 |
A |
T |
7: 30,991,038 (GRCm39) |
C23* |
probably null |
Het |
Spag8 |
G |
T |
4: 43,652,826 (GRCm39) |
R212S |
probably benign |
Het |
Tacc2 |
A |
G |
7: 130,335,299 (GRCm39) |
|
probably null |
Het |
Trmt1l |
C |
T |
1: 151,304,710 (GRCm39) |
|
probably benign |
Het |
Trpa1 |
A |
T |
1: 14,954,469 (GRCm39) |
L810Q |
probably damaging |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Ugt3a1 |
T |
A |
15: 9,292,059 (GRCm39) |
|
probably benign |
Het |
Vmn2r23 |
T |
G |
6: 123,681,384 (GRCm39) |
I97M |
possibly damaging |
Het |
Vmn2r65 |
A |
T |
7: 84,590,051 (GRCm39) |
F622I |
possibly damaging |
Het |
Vps13a |
C |
T |
19: 16,697,817 (GRCm39) |
G766E |
probably damaging |
Het |
Wnk1 |
T |
C |
6: 119,946,495 (GRCm39) |
T553A |
probably benign |
Het |
Xirp2 |
T |
A |
2: 67,341,114 (GRCm39) |
D1118E |
probably damaging |
Het |
Zfyve9 |
A |
C |
4: 108,517,811 (GRCm39) |
D461E |
probably damaging |
Het |
|
Other mutations in Gprin1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01021:Gprin1
|
APN |
13 |
54,888,182 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02001:Gprin1
|
APN |
13 |
54,887,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03188:Gprin1
|
APN |
13 |
54,886,465 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03308:Gprin1
|
APN |
13 |
54,887,957 (GRCm39) |
missense |
probably benign |
0.05 |
R0980:Gprin1
|
UTSW |
13 |
54,888,214 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1638:Gprin1
|
UTSW |
13 |
54,887,689 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1942:Gprin1
|
UTSW |
13 |
54,887,752 (GRCm39) |
missense |
probably benign |
0.36 |
R2145:Gprin1
|
UTSW |
13 |
54,886,445 (GRCm39) |
missense |
probably damaging |
0.99 |
R2215:Gprin1
|
UTSW |
13 |
54,888,046 (GRCm39) |
missense |
probably damaging |
0.99 |
R3014:Gprin1
|
UTSW |
13 |
54,886,288 (GRCm39) |
missense |
probably benign |
0.34 |
R4634:Gprin1
|
UTSW |
13 |
54,885,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Gprin1
|
UTSW |
13 |
54,887,770 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4733:Gprin1
|
UTSW |
13 |
54,887,770 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4903:Gprin1
|
UTSW |
13 |
54,885,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R4915:Gprin1
|
UTSW |
13 |
54,885,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R5102:Gprin1
|
UTSW |
13 |
54,887,576 (GRCm39) |
missense |
probably benign |
0.06 |
R5979:Gprin1
|
UTSW |
13 |
54,887,791 (GRCm39) |
missense |
probably benign |
0.01 |
R6544:Gprin1
|
UTSW |
13 |
54,888,124 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7007:Gprin1
|
UTSW |
13 |
54,886,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R7022:Gprin1
|
UTSW |
13 |
54,886,855 (GRCm39) |
missense |
probably benign |
0.11 |
R7110:Gprin1
|
UTSW |
13 |
54,887,056 (GRCm39) |
missense |
probably benign |
0.01 |
R7385:Gprin1
|
UTSW |
13 |
54,886,423 (GRCm39) |
missense |
probably benign |
0.09 |
R7916:Gprin1
|
UTSW |
13 |
54,887,263 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8696:Gprin1
|
UTSW |
13 |
54,885,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R9151:Gprin1
|
UTSW |
13 |
54,886,778 (GRCm39) |
missense |
probably benign |
0.22 |
R9178:Gprin1
|
UTSW |
13 |
54,885,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R9285:Gprin1
|
UTSW |
13 |
54,886,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R9398:Gprin1
|
UTSW |
13 |
54,887,383 (GRCm39) |
missense |
probably damaging |
0.99 |
R9711:Gprin1
|
UTSW |
13 |
54,886,714 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Gprin1
|
UTSW |
13 |
54,888,210 (GRCm39) |
missense |
probably benign |
0.18 |
|