Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsf2 |
G |
T |
11: 94,453,700 (GRCm39) |
N420K |
probably benign |
Het |
Adam26a |
A |
T |
8: 44,022,229 (GRCm39) |
C420* |
probably null |
Het |
Afap1l1 |
T |
C |
18: 61,874,909 (GRCm39) |
Y424C |
probably damaging |
Het |
Agl |
A |
G |
3: 116,576,246 (GRCm39) |
V553A |
probably benign |
Het |
Akr7a5 |
T |
A |
4: 139,045,434 (GRCm39) |
M325K |
probably damaging |
Het |
Aldh7a1 |
C |
A |
18: 56,692,341 (GRCm39) |
E87* |
probably null |
Het |
Arhgap29 |
A |
G |
3: 121,767,578 (GRCm39) |
K7E |
probably damaging |
Het |
Brca2 |
T |
A |
5: 150,466,114 (GRCm39) |
D1959E |
probably benign |
Het |
Cdh20 |
G |
A |
1: 109,988,862 (GRCm39) |
V255I |
probably benign |
Het |
Chil5 |
G |
T |
3: 105,925,409 (GRCm39) |
Q171K |
probably benign |
Het |
Cul9 |
C |
G |
17: 46,833,101 (GRCm39) |
A1326P |
probably damaging |
Het |
Dhrs7c |
A |
T |
11: 67,702,476 (GRCm39) |
I155F |
probably damaging |
Het |
Dip2c |
A |
G |
13: 9,603,300 (GRCm39) |
|
probably null |
Het |
Fam124b |
T |
C |
1: 80,191,056 (GRCm39) |
Y109C |
possibly damaging |
Het |
Gak |
T |
A |
5: 108,739,011 (GRCm39) |
K156M |
probably damaging |
Het |
Gm17535 |
A |
G |
9: 3,035,804 (GRCm39) |
Y224C |
probably null |
Het |
Grm1 |
T |
C |
10: 10,955,879 (GRCm39) |
D135G |
probably benign |
Het |
Hrh3 |
T |
G |
2: 179,744,547 (GRCm39) |
D131A |
probably damaging |
Het |
Hspg2 |
C |
T |
4: 137,267,411 (GRCm39) |
L2042F |
possibly damaging |
Het |
Itpr1 |
A |
T |
6: 108,366,514 (GRCm39) |
Q979L |
probably null |
Het |
Klb |
G |
C |
5: 65,506,089 (GRCm39) |
R112P |
possibly damaging |
Het |
Lingo2 |
A |
T |
4: 35,709,420 (GRCm39) |
C187S |
possibly damaging |
Het |
Lrp1 |
T |
A |
10: 127,417,760 (GRCm39) |
|
probably null |
Het |
Ltbp4 |
T |
C |
7: 27,028,464 (GRCm39) |
N266S |
unknown |
Het |
Mgam |
G |
A |
6: 40,643,815 (GRCm39) |
S581N |
possibly damaging |
Het |
Mrgpra9 |
T |
A |
7: 46,885,386 (GRCm39) |
I94L |
probably benign |
Het |
Msantd4 |
A |
T |
9: 4,384,023 (GRCm39) |
I115F |
probably benign |
Het |
Nrxn1 |
A |
C |
17: 90,950,481 (GRCm39) |
L566R |
probably benign |
Het |
Or5p59 |
T |
A |
7: 107,702,822 (GRCm39) |
I102N |
probably benign |
Het |
Prl7d1 |
A |
T |
13: 27,893,180 (GRCm39) |
F243I |
possibly damaging |
Het |
Rbm27 |
T |
C |
18: 42,450,746 (GRCm39) |
S509P |
probably damaging |
Het |
Rnf44 |
C |
T |
13: 54,829,821 (GRCm39) |
E306K |
probably damaging |
Het |
Rp1 |
T |
C |
1: 4,416,520 (GRCm39) |
R1531G |
possibly damaging |
Het |
Sf3b4 |
A |
G |
3: 96,080,953 (GRCm39) |
|
probably null |
Het |
Sfi1 |
TCGC |
TC |
11: 3,096,254 (GRCm39) |
|
probably null |
Het |
Sfi1 |
CCTCTC |
CCTCTCTC |
11: 3,127,419 (GRCm39) |
|
probably benign |
Het |
Sp110 |
T |
G |
1: 85,506,800 (GRCm39) |
E421A |
probably benign |
Het |
Stk4 |
C |
T |
2: 163,942,448 (GRCm39) |
T360M |
probably benign |
Het |
Vcan |
T |
A |
13: 89,836,603 (GRCm39) |
E2980D |
probably benign |
Het |
Vwa2 |
C |
T |
19: 56,869,570 (GRCm39) |
P2S |
unknown |
Het |
Wdr77 |
G |
A |
3: 105,874,573 (GRCm39) |
V322I |
possibly damaging |
Het |
Zfp12 |
C |
A |
5: 143,230,535 (GRCm39) |
Y287* |
probably null |
Het |
Zfp937 |
T |
A |
2: 150,080,868 (GRCm39) |
Y299* |
probably null |
Het |
|
Other mutations in Got1l1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01392:Got1l1
|
APN |
8 |
27,688,019 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02094:Got1l1
|
APN |
8 |
27,689,873 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03155:Got1l1
|
APN |
8 |
27,689,360 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03395:Got1l1
|
APN |
8 |
27,690,885 (GRCm39) |
missense |
probably benign |
0.00 |
R0026:Got1l1
|
UTSW |
8 |
27,690,276 (GRCm39) |
missense |
probably benign |
0.00 |
R1086:Got1l1
|
UTSW |
8 |
27,688,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R1403:Got1l1
|
UTSW |
8 |
27,690,745 (GRCm39) |
splice site |
probably null |
|
R2349:Got1l1
|
UTSW |
8 |
27,687,959 (GRCm39) |
missense |
probably benign |
0.09 |
R3413:Got1l1
|
UTSW |
8 |
27,689,864 (GRCm39) |
critical splice donor site |
probably null |
|
R4513:Got1l1
|
UTSW |
8 |
27,688,513 (GRCm39) |
missense |
probably benign |
0.27 |
R4514:Got1l1
|
UTSW |
8 |
27,688,513 (GRCm39) |
missense |
probably benign |
0.27 |
R5686:Got1l1
|
UTSW |
8 |
27,688,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R5979:Got1l1
|
UTSW |
8 |
27,687,951 (GRCm39) |
splice site |
probably null |
|
R6023:Got1l1
|
UTSW |
8 |
27,689,932 (GRCm39) |
nonsense |
probably null |
|
R6229:Got1l1
|
UTSW |
8 |
27,688,464 (GRCm39) |
splice site |
probably null |
|
R7635:Got1l1
|
UTSW |
8 |
27,687,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R8101:Got1l1
|
UTSW |
8 |
27,690,330 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8104:Got1l1
|
UTSW |
8 |
27,687,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R8298:Got1l1
|
UTSW |
8 |
27,688,586 (GRCm39) |
missense |
probably benign |
0.09 |
R8792:Got1l1
|
UTSW |
8 |
27,690,749 (GRCm39) |
critical splice donor site |
probably null |
|
R9089:Got1l1
|
UTSW |
8 |
27,690,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R9526:Got1l1
|
UTSW |
8 |
27,688,503 (GRCm39) |
missense |
probably benign |
0.07 |
|