Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
T |
A |
11: 110,051,359 (GRCm39) |
K112N |
probably benign |
Het |
Brwd1 |
A |
G |
16: 95,866,087 (GRCm39) |
S232P |
probably damaging |
Het |
Calm5 |
A |
T |
13: 3,904,629 (GRCm39) |
M108L |
possibly damaging |
Het |
Ces1g |
A |
T |
8: 94,055,094 (GRCm39) |
V201D |
probably damaging |
Het |
Cltc |
C |
A |
11: 86,598,312 (GRCm39) |
V1017L |
probably benign |
Het |
Cpt1c |
C |
T |
7: 44,616,516 (GRCm39) |
R245Q |
probably damaging |
Het |
Csrnp1 |
C |
A |
9: 119,806,158 (GRCm39) |
A39S |
probably benign |
Het |
Elf1 |
A |
G |
14: 79,808,322 (GRCm39) |
D258G |
possibly damaging |
Het |
Entrep1 |
A |
C |
19: 23,972,168 (GRCm39) |
S179A |
possibly damaging |
Het |
Gm4340 |
T |
C |
10: 104,031,820 (GRCm39) |
V188A |
probably benign |
Het |
Gsdma2 |
T |
C |
11: 98,540,375 (GRCm39) |
M98T |
probably benign |
Het |
Hars1 |
A |
T |
18: 36,903,476 (GRCm39) |
D315E |
probably benign |
Het |
Hsph1 |
A |
C |
5: 149,555,540 (GRCm39) |
Y89D |
probably damaging |
Het |
Ighv11-2 |
T |
A |
12: 114,012,008 (GRCm39) |
D69V |
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,995,528 (GRCm39) |
G438D |
possibly damaging |
Het |
Krt6a |
G |
T |
15: 101,600,187 (GRCm39) |
T355K |
possibly damaging |
Het |
Lce1m |
T |
C |
3: 92,925,177 (GRCm39) |
|
probably null |
Het |
Lmbrd1 |
A |
T |
1: 24,767,625 (GRCm39) |
|
probably null |
Het |
Lmtk3 |
A |
G |
7: 45,442,841 (GRCm39) |
E508G |
probably damaging |
Het |
Lrrc2 |
G |
A |
9: 110,809,899 (GRCm39) |
V312I |
probably benign |
Het |
Lyn |
A |
T |
4: 3,789,834 (GRCm39) |
K477* |
probably null |
Het |
Nfe2l2 |
T |
C |
2: 75,509,757 (GRCm39) |
D21G |
probably damaging |
Het |
Or14c45 |
G |
A |
7: 86,176,280 (GRCm39) |
C105Y |
probably benign |
Het |
Or4f14d |
T |
C |
2: 111,960,926 (GRCm39) |
T77A |
probably benign |
Het |
Or55b3 |
G |
A |
7: 102,126,472 (GRCm39) |
R202C |
possibly damaging |
Het |
Or8c15 |
T |
C |
9: 38,120,447 (GRCm39) |
F31L |
probably benign |
Het |
Pgap6 |
C |
A |
17: 26,336,865 (GRCm39) |
P261Q |
probably benign |
Het |
Pkm |
T |
A |
9: 59,585,441 (GRCm39) |
C474* |
probably null |
Het |
Prr36 |
T |
A |
8: 4,263,150 (GRCm39) |
I839F |
unknown |
Het |
Qtrt2 |
A |
G |
16: 43,689,303 (GRCm39) |
|
probably null |
Het |
Ripk4 |
A |
T |
16: 97,547,125 (GRCm39) |
V379E |
probably damaging |
Het |
Rreb1 |
C |
A |
13: 38,133,042 (GRCm39) |
P304Q |
|
Het |
Saxo2 |
A |
T |
7: 82,297,625 (GRCm39) |
C5S |
possibly damaging |
Het |
Scart2 |
G |
A |
7: 139,876,742 (GRCm39) |
G711D |
probably damaging |
Het |
Sema5a |
C |
A |
15: 32,609,378 (GRCm39) |
T428N |
possibly damaging |
Het |
Setd5 |
C |
A |
6: 113,121,010 (GRCm39) |
P1073Q |
possibly damaging |
Het |
Sh2d5 |
T |
G |
4: 137,984,150 (GRCm39) |
C173G |
probably benign |
Het |
Slc4a10 |
T |
G |
2: 62,080,823 (GRCm39) |
V350G |
probably damaging |
Het |
Slco1a6 |
A |
G |
6: 142,106,743 (GRCm39) |
C15R |
probably damaging |
Het |
Smg7 |
A |
T |
1: 152,717,295 (GRCm39) |
F940Y |
possibly damaging |
Het |
Spata17 |
T |
A |
1: 186,854,833 (GRCm39) |
|
probably null |
Het |
Specc1 |
A |
G |
11: 62,019,210 (GRCm39) |
N603S |
possibly damaging |
Het |
Tbc1d1 |
A |
G |
5: 64,421,673 (GRCm39) |
D355G |
probably damaging |
Het |
Thbs2 |
T |
C |
17: 14,894,426 (GRCm39) |
D807G |
probably benign |
Het |
Usp53 |
T |
C |
3: 122,754,934 (GRCm39) |
T174A |
probably benign |
Het |
Vmn2r52 |
A |
G |
7: 9,907,274 (GRCm39) |
Y151H |
probably benign |
Het |
Wdr12 |
G |
A |
1: 60,136,748 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Glipr1l1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00467:Glipr1l1
|
APN |
10 |
111,914,286 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01660:Glipr1l1
|
APN |
10 |
111,908,184 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01893:Glipr1l1
|
APN |
10 |
111,912,074 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02576:Glipr1l1
|
APN |
10 |
111,896,224 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL03309:Glipr1l1
|
APN |
10 |
111,908,141 (GRCm39) |
splice site |
probably benign |
|
P0031:Glipr1l1
|
UTSW |
10 |
111,896,292 (GRCm39) |
missense |
probably benign |
|
R0987:Glipr1l1
|
UTSW |
10 |
111,914,340 (GRCm39) |
missense |
probably benign |
|
R0992:Glipr1l1
|
UTSW |
10 |
111,898,230 (GRCm39) |
missense |
probably benign |
|
R2136:Glipr1l1
|
UTSW |
10 |
111,896,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R2248:Glipr1l1
|
UTSW |
10 |
111,898,192 (GRCm39) |
missense |
probably benign |
0.09 |
R4297:Glipr1l1
|
UTSW |
10 |
111,898,252 (GRCm39) |
missense |
probably benign |
0.05 |
R4298:Glipr1l1
|
UTSW |
10 |
111,898,252 (GRCm39) |
missense |
probably benign |
0.05 |
R4569:Glipr1l1
|
UTSW |
10 |
111,898,317 (GRCm39) |
missense |
probably benign |
0.00 |
R5015:Glipr1l1
|
UTSW |
10 |
111,914,279 (GRCm39) |
missense |
probably benign |
0.00 |
R5552:Glipr1l1
|
UTSW |
10 |
111,898,243 (GRCm39) |
missense |
probably benign |
0.00 |
R5629:Glipr1l1
|
UTSW |
10 |
111,914,308 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6061:Glipr1l1
|
UTSW |
10 |
111,912,075 (GRCm39) |
missense |
probably benign |
0.32 |
R6237:Glipr1l1
|
UTSW |
10 |
111,896,332 (GRCm39) |
nonsense |
probably null |
|
R6519:Glipr1l1
|
UTSW |
10 |
111,898,153 (GRCm39) |
missense |
probably benign |
0.02 |
R6913:Glipr1l1
|
UTSW |
10 |
111,898,339 (GRCm39) |
critical splice donor site |
probably null |
|
R8171:Glipr1l1
|
UTSW |
10 |
111,914,289 (GRCm39) |
missense |
probably benign |
0.01 |
R9182:Glipr1l1
|
UTSW |
10 |
111,912,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R9319:Glipr1l1
|
UTSW |
10 |
111,898,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R9508:Glipr1l1
|
UTSW |
10 |
111,912,015 (GRCm39) |
missense |
probably damaging |
0.98 |
X0023:Glipr1l1
|
UTSW |
10 |
111,914,344 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Glipr1l1
|
UTSW |
10 |
111,914,295 (GRCm39) |
missense |
probably benign |
0.00 |
|