Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930111J21Rik2 |
A |
T |
11: 48,910,312 (GRCm39) |
I707N |
probably damaging |
Het |
Abca14 |
A |
G |
7: 119,815,489 (GRCm39) |
I246V |
probably benign |
Het |
Adam19 |
G |
A |
11: 46,015,850 (GRCm39) |
A337T |
possibly damaging |
Het |
Ankrd40 |
G |
T |
11: 94,225,662 (GRCm39) |
G231V |
probably damaging |
Het |
Arhgap5 |
G |
A |
12: 52,565,572 (GRCm39) |
V848I |
probably damaging |
Het |
Bmpr2 |
G |
A |
1: 59,906,515 (GRCm39) |
R536H |
probably damaging |
Het |
Casz1 |
T |
A |
4: 149,033,040 (GRCm39) |
S1310T |
probably benign |
Het |
Chi3l1 |
A |
T |
1: 134,117,280 (GRCm39) |
D367V |
probably damaging |
Het |
Cltc |
A |
G |
11: 86,598,392 (GRCm39) |
V990A |
probably benign |
Het |
Col6a3 |
A |
T |
1: 90,729,935 (GRCm39) |
S1790R |
probably damaging |
Het |
Comt |
C |
T |
16: 18,230,637 (GRCm39) |
W24* |
probably null |
Het |
Cyp2c70 |
T |
C |
19: 40,149,024 (GRCm39) |
E374G |
possibly damaging |
Het |
Dach1 |
T |
C |
14: 98,406,076 (GRCm39) |
T224A |
probably damaging |
Het |
Dapk1 |
G |
A |
13: 60,887,911 (GRCm39) |
E656K |
probably benign |
Het |
Dicer1 |
A |
G |
12: 104,668,936 (GRCm39) |
S1249P |
probably benign |
Het |
Dpp8 |
A |
C |
9: 64,988,037 (GRCm39) |
I861L |
probably benign |
Het |
Enam |
C |
T |
5: 88,651,209 (GRCm39) |
S906L |
possibly damaging |
Het |
Fbxo10 |
C |
A |
4: 45,041,809 (GRCm39) |
G807C |
possibly damaging |
Het |
Fcgbpl1 |
G |
T |
7: 27,843,346 (GRCm39) |
G745C |
probably damaging |
Het |
Fsip2 |
G |
C |
2: 82,808,963 (GRCm39) |
E1761Q |
probably damaging |
Het |
Ggnbp2 |
C |
T |
11: 84,728,815 (GRCm39) |
|
probably null |
Het |
Gm4353 |
G |
A |
7: 115,682,784 (GRCm39) |
P266S |
probably benign |
Het |
Gpr84 |
T |
C |
15: 103,217,963 (GRCm39) |
N38S |
probably damaging |
Het |
Guca1a |
A |
T |
17: 47,706,480 (GRCm39) |
I115N |
probably damaging |
Het |
Hic1 |
C |
T |
11: 75,057,096 (GRCm39) |
V598M |
possibly damaging |
Het |
Itga1 |
A |
T |
13: 115,143,604 (GRCm39) |
I309N |
probably damaging |
Het |
Itga11 |
T |
C |
9: 62,662,460 (GRCm39) |
S478P |
possibly damaging |
Het |
Kctd8 |
T |
C |
5: 69,497,713 (GRCm39) |
D311G |
probably damaging |
Het |
Klhl32 |
T |
C |
4: 24,682,203 (GRCm39) |
E127G |
possibly damaging |
Het |
Lama2 |
T |
A |
10: 27,298,559 (GRCm39) |
Y179F |
probably benign |
Het |
Lamb2 |
G |
T |
9: 108,365,563 (GRCm39) |
R1382L |
probably benign |
Het |
Mrpl1 |
C |
G |
5: 96,374,226 (GRCm39) |
A167G |
probably benign |
Het |
Muc17 |
A |
T |
5: 137,175,570 (GRCm39) |
N33K |
|
Het |
Myt1 |
A |
T |
2: 181,424,399 (GRCm39) |
R31* |
probably null |
Het |
Nectin2 |
T |
C |
7: 19,451,646 (GRCm39) |
T463A |
probably benign |
Het |
Nectin2 |
A |
T |
7: 19,472,003 (GRCm39) |
Y129N |
probably damaging |
Het |
Or12d13 |
A |
G |
17: 37,647,466 (GRCm39) |
I219T |
possibly damaging |
Het |
Or4k47 |
A |
T |
2: 111,451,849 (GRCm39) |
M190K |
probably benign |
Het |
Papolb |
T |
A |
5: 142,514,296 (GRCm39) |
N449I |
possibly damaging |
Het |
Parn |
T |
C |
16: 13,466,338 (GRCm39) |
K236R |
probably benign |
Het |
Pramel22 |
A |
G |
4: 143,382,997 (GRCm39) |
I74T |
probably damaging |
Het |
Prelid1 |
G |
A |
13: 55,470,698 (GRCm39) |
R42Q |
probably damaging |
Het |
Prelp |
A |
G |
1: 133,843,020 (GRCm39) |
F42L |
probably benign |
Het |
Pygo1 |
C |
T |
9: 72,852,380 (GRCm39) |
P189L |
probably damaging |
Het |
Rimbp3 |
T |
A |
16: 17,030,886 (GRCm39) |
S1437T |
probably damaging |
Het |
Slc37a2 |
T |
A |
9: 37,148,726 (GRCm39) |
D252V |
probably benign |
Het |
Socs7 |
A |
G |
11: 97,254,165 (GRCm39) |
K233R |
probably benign |
Het |
Spopfm2 |
T |
C |
3: 94,082,921 (GRCm39) |
I297V |
probably benign |
Het |
Stat4 |
A |
G |
1: 52,137,637 (GRCm39) |
D476G |
possibly damaging |
Het |
Tesmin |
A |
G |
19: 3,439,077 (GRCm39) |
D43G |
probably benign |
Het |
Thap1 |
C |
A |
8: 26,648,502 (GRCm39) |
Y8* |
probably null |
Het |
Tln1 |
A |
G |
4: 43,536,397 (GRCm39) |
L1965P |
probably damaging |
Het |
Tmprss11d |
A |
G |
5: 86,457,165 (GRCm39) |
S303P |
probably damaging |
Het |
Tomm40 |
C |
T |
7: 19,435,759 (GRCm39) |
V324M |
probably damaging |
Het |
Vmn1r202 |
A |
T |
13: 22,685,985 (GRCm39) |
I144K |
probably damaging |
Het |
|
Other mutations in Eral1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01478:Eral1
|
APN |
11 |
77,966,558 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01643:Eral1
|
APN |
11 |
77,965,104 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02240:Eral1
|
APN |
11 |
77,968,687 (GRCm39) |
nonsense |
probably null |
|
IGL03085:Eral1
|
APN |
11 |
77,969,093 (GRCm39) |
missense |
probably damaging |
1.00 |
K3955:Eral1
|
UTSW |
11 |
77,966,847 (GRCm39) |
missense |
probably damaging |
1.00 |
P0038:Eral1
|
UTSW |
11 |
77,966,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Eral1
|
UTSW |
11 |
77,966,884 (GRCm39) |
splice site |
probably benign |
|
R1084:Eral1
|
UTSW |
11 |
77,965,324 (GRCm39) |
missense |
probably damaging |
0.96 |
R1563:Eral1
|
UTSW |
11 |
77,966,232 (GRCm39) |
missense |
probably benign |
0.39 |
R1881:Eral1
|
UTSW |
11 |
77,966,875 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1995:Eral1
|
UTSW |
11 |
77,965,315 (GRCm39) |
missense |
probably benign |
|
R2189:Eral1
|
UTSW |
11 |
77,966,657 (GRCm39) |
missense |
probably benign |
0.15 |
R2870:Eral1
|
UTSW |
11 |
77,967,104 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2870:Eral1
|
UTSW |
11 |
77,967,104 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4049:Eral1
|
UTSW |
11 |
77,966,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R4585:Eral1
|
UTSW |
11 |
77,969,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R4586:Eral1
|
UTSW |
11 |
77,969,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R4758:Eral1
|
UTSW |
11 |
77,966,425 (GRCm39) |
missense |
probably benign |
0.20 |
R5450:Eral1
|
UTSW |
11 |
77,969,183 (GRCm39) |
missense |
probably benign |
0.23 |
R5613:Eral1
|
UTSW |
11 |
77,965,230 (GRCm39) |
intron |
probably benign |
|
R5987:Eral1
|
UTSW |
11 |
77,971,059 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6048:Eral1
|
UTSW |
11 |
77,966,609 (GRCm39) |
missense |
probably benign |
0.03 |
R6363:Eral1
|
UTSW |
11 |
77,965,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R6891:Eral1
|
UTSW |
11 |
77,966,559 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7384:Eral1
|
UTSW |
11 |
77,964,927 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7468:Eral1
|
UTSW |
11 |
77,966,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R7762:Eral1
|
UTSW |
11 |
77,965,359 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8304:Eral1
|
UTSW |
11 |
77,966,828 (GRCm39) |
missense |
probably damaging |
0.96 |
R8433:Eral1
|
UTSW |
11 |
77,966,309 (GRCm39) |
missense |
probably benign |
|
R9136:Eral1
|
UTSW |
11 |
77,964,960 (GRCm39) |
missense |
|
|
R9384:Eral1
|
UTSW |
11 |
77,969,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R9670:Eral1
|
UTSW |
11 |
77,965,410 (GRCm39) |
missense |
|
|
X0066:Eral1
|
UTSW |
11 |
77,966,591 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Eral1
|
UTSW |
11 |
77,966,446 (GRCm39) |
missense |
probably damaging |
1.00 |
|