Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933427D14Rik |
G |
A |
11: 72,093,308 (GRCm39) |
S8F |
probably damaging |
Het |
Alpk1 |
T |
A |
3: 127,522,931 (GRCm39) |
Q37L |
probably damaging |
Het |
Cfap43 |
T |
C |
19: 47,736,463 (GRCm39) |
T1343A |
probably benign |
Het |
Cmbl |
C |
A |
15: 31,585,554 (GRCm39) |
P146Q |
possibly damaging |
Het |
Cog2 |
A |
T |
8: 125,259,951 (GRCm39) |
|
probably null |
Het |
Dgkh |
C |
A |
14: 78,825,016 (GRCm39) |
V880L |
probably benign |
Het |
Dop1a |
T |
C |
9: 86,402,141 (GRCm39) |
S1114P |
probably damaging |
Het |
Eif5b |
T |
A |
1: 38,080,828 (GRCm39) |
V723D |
probably damaging |
Het |
Gdf11 |
A |
G |
10: 128,721,253 (GRCm39) |
Y314H |
probably damaging |
Het |
Gm10110 |
T |
C |
14: 90,135,031 (GRCm39) |
|
noncoding transcript |
Het |
Gria1 |
G |
A |
11: 57,127,750 (GRCm39) |
V320I |
probably benign |
Het |
H2-Q10 |
T |
A |
17: 35,784,463 (GRCm39) |
*326R |
probably null |
Het |
Irx6 |
T |
A |
8: 93,403,659 (GRCm39) |
L128Q |
probably damaging |
Het |
Kif21b |
T |
A |
1: 136,087,495 (GRCm39) |
L937Q |
probably damaging |
Het |
Lama5 |
A |
G |
2: 179,832,120 (GRCm39) |
|
probably benign |
Het |
Mios |
A |
G |
6: 8,231,269 (GRCm39) |
I718V |
probably benign |
Het |
Mroh8 |
A |
G |
2: 157,096,893 (GRCm39) |
V318A |
probably damaging |
Het |
Nags |
A |
G |
11: 102,039,897 (GRCm39) |
*528W |
probably null |
Het |
Nom1 |
T |
A |
5: 29,642,708 (GRCm39) |
V403D |
probably damaging |
Het |
Npffr2 |
C |
A |
5: 89,731,310 (GRCm39) |
N413K |
probably benign |
Het |
Olr1 |
C |
T |
6: 129,476,860 (GRCm39) |
R135K |
possibly damaging |
Het |
Or1e34 |
A |
T |
11: 73,779,121 (GRCm39) |
Y26N |
probably benign |
Het |
Or52e8 |
T |
A |
7: 104,624,665 (GRCm39) |
I176F |
possibly damaging |
Het |
Pkhd1 |
A |
G |
1: 20,140,600 (GRCm39) |
|
probably null |
Het |
Ptpro |
A |
G |
6: 137,431,698 (GRCm39) |
M1158V |
probably benign |
Het |
Sh3d19 |
A |
G |
3: 86,001,017 (GRCm39) |
K238E |
probably damaging |
Het |
Smarcc2 |
G |
T |
10: 128,318,641 (GRCm39) |
R641L |
probably damaging |
Het |
Th |
T |
C |
7: 142,451,794 (GRCm39) |
E75G |
possibly damaging |
Het |
Top6bl |
T |
C |
19: 4,713,583 (GRCm39) |
K132E |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,724,705 (GRCm39) |
R2107* |
probably null |
Het |
Ubr2 |
A |
T |
17: 47,245,119 (GRCm39) |
C1636S |
probably damaging |
Het |
Vmn2r100 |
T |
A |
17: 19,741,597 (GRCm39) |
I103K |
possibly damaging |
Het |
Vmn2r88 |
A |
G |
14: 51,655,437 (GRCm39) |
M558V |
possibly damaging |
Het |
Zzef1 |
G |
A |
11: 72,777,573 (GRCm39) |
M1801I |
probably benign |
Het |
|
Other mutations in Tlr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00571:Tlr1
|
APN |
5 |
65,083,777 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01324:Tlr1
|
APN |
5 |
65,082,522 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01564:Tlr1
|
APN |
5 |
65,083,189 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01663:Tlr1
|
APN |
5 |
65,082,416 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL01689:Tlr1
|
APN |
5 |
65,083,122 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01749:Tlr1
|
APN |
5 |
65,083,290 (GRCm39) |
nonsense |
probably null |
|
IGL01751:Tlr1
|
APN |
5 |
65,083,290 (GRCm39) |
nonsense |
probably null |
|
IGL01769:Tlr1
|
APN |
5 |
65,083,290 (GRCm39) |
nonsense |
probably null |
|
IGL01899:Tlr1
|
APN |
5 |
65,084,359 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02197:Tlr1
|
APN |
5 |
65,083,797 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02295:Tlr1
|
APN |
5 |
65,083,290 (GRCm39) |
nonsense |
probably null |
|
IGL02309:Tlr1
|
APN |
5 |
65,083,290 (GRCm39) |
nonsense |
probably null |
|
IGL02311:Tlr1
|
APN |
5 |
65,083,290 (GRCm39) |
nonsense |
probably null |
|
IGL02591:Tlr1
|
APN |
5 |
65,084,059 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02739:Tlr1
|
APN |
5 |
65,084,469 (GRCm39) |
missense |
probably benign |
0.41 |
IGL03206:Tlr1
|
APN |
5 |
65,082,400 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03055:Tlr1
|
UTSW |
5 |
65,083,939 (GRCm39) |
missense |
probably benign |
0.05 |
R0315:Tlr1
|
UTSW |
5 |
65,084,271 (GRCm39) |
missense |
probably damaging |
0.99 |
R0317:Tlr1
|
UTSW |
5 |
65,083,310 (GRCm39) |
nonsense |
probably null |
|
R0511:Tlr1
|
UTSW |
5 |
65,083,963 (GRCm39) |
missense |
probably damaging |
0.98 |
R1539:Tlr1
|
UTSW |
5 |
65,084,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R1552:Tlr1
|
UTSW |
5 |
65,084,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R1835:Tlr1
|
UTSW |
5 |
65,083,043 (GRCm39) |
missense |
probably benign |
0.01 |
R1933:Tlr1
|
UTSW |
5 |
65,082,781 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1956:Tlr1
|
UTSW |
5 |
65,082,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R2099:Tlr1
|
UTSW |
5 |
65,082,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R2507:Tlr1
|
UTSW |
5 |
65,082,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R2508:Tlr1
|
UTSW |
5 |
65,082,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R2937:Tlr1
|
UTSW |
5 |
65,083,251 (GRCm39) |
missense |
probably damaging |
0.96 |
R2938:Tlr1
|
UTSW |
5 |
65,083,251 (GRCm39) |
missense |
probably damaging |
0.96 |
R3033:Tlr1
|
UTSW |
5 |
65,082,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R4164:Tlr1
|
UTSW |
5 |
65,084,545 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4226:Tlr1
|
UTSW |
5 |
65,083,060 (GRCm39) |
missense |
probably damaging |
0.96 |
R4366:Tlr1
|
UTSW |
5 |
65,083,180 (GRCm39) |
missense |
probably benign |
0.00 |
R5009:Tlr1
|
UTSW |
5 |
65,083,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R5029:Tlr1
|
UTSW |
5 |
65,083,024 (GRCm39) |
missense |
probably damaging |
0.97 |
R5069:Tlr1
|
UTSW |
5 |
65,083,743 (GRCm39) |
missense |
probably benign |
0.01 |
R5186:Tlr1
|
UTSW |
5 |
65,082,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R5336:Tlr1
|
UTSW |
5 |
65,083,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R5500:Tlr1
|
UTSW |
5 |
65,084,441 (GRCm39) |
missense |
probably benign |
0.08 |
R5503:Tlr1
|
UTSW |
5 |
65,083,635 (GRCm39) |
missense |
probably damaging |
0.99 |
R5577:Tlr1
|
UTSW |
5 |
65,083,428 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6141:Tlr1
|
UTSW |
5 |
65,082,556 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6210:Tlr1
|
UTSW |
5 |
65,082,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R6238:Tlr1
|
UTSW |
5 |
65,084,472 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6284:Tlr1
|
UTSW |
5 |
65,084,442 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6311:Tlr1
|
UTSW |
5 |
65,084,188 (GRCm39) |
missense |
probably damaging |
0.99 |
R7021:Tlr1
|
UTSW |
5 |
65,083,056 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7140:Tlr1
|
UTSW |
5 |
65,083,021 (GRCm39) |
missense |
probably benign |
0.01 |
R7234:Tlr1
|
UTSW |
5 |
65,084,067 (GRCm39) |
missense |
probably damaging |
0.96 |
R7278:Tlr1
|
UTSW |
5 |
65,084,115 (GRCm39) |
missense |
probably benign |
0.03 |
R7378:Tlr1
|
UTSW |
5 |
65,082,571 (GRCm39) |
missense |
not run |
|
R7652:Tlr1
|
UTSW |
5 |
65,084,130 (GRCm39) |
nonsense |
probably null |
|
R7781:Tlr1
|
UTSW |
5 |
65,084,079 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7783:Tlr1
|
UTSW |
5 |
65,082,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R7851:Tlr1
|
UTSW |
5 |
65,082,307 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8546:Tlr1
|
UTSW |
5 |
65,084,374 (GRCm39) |
missense |
probably damaging |
0.99 |
R8696:Tlr1
|
UTSW |
5 |
65,084,094 (GRCm39) |
missense |
probably benign |
0.00 |
R8744:Tlr1
|
UTSW |
5 |
65,083,873 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9086:Tlr1
|
UTSW |
5 |
65,083,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R9160:Tlr1
|
UTSW |
5 |
65,083,653 (GRCm39) |
missense |
probably benign |
0.00 |
R9199:Tlr1
|
UTSW |
5 |
65,083,534 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9778:Tlr1
|
UTSW |
5 |
65,083,371 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Tlr1
|
UTSW |
5 |
65,083,918 (GRCm39) |
missense |
probably damaging |
1.00 |
|