Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610042L04Rik |
G |
A |
14: 4,350,856 (GRCm38) |
G130D |
probably damaging |
Het |
Abca8b |
T |
A |
11: 109,862,589 (GRCm39) |
D392V |
probably damaging |
Het |
Cep43 |
A |
T |
17: 8,411,109 (GRCm39) |
D354V |
probably damaging |
Het |
Clptm1l |
T |
A |
13: 73,765,688 (GRCm39) |
|
probably benign |
Het |
Creb3l1 |
G |
A |
2: 91,823,678 (GRCm39) |
T178I |
probably benign |
Het |
Ctsd |
A |
G |
7: 141,930,336 (GRCm39) |
|
probably null |
Het |
Dcstamp |
A |
T |
15: 39,623,755 (GRCm39) |
I401F |
possibly damaging |
Het |
Dnah5 |
A |
G |
15: 28,370,682 (GRCm39) |
D2874G |
probably benign |
Het |
Fcsk |
A |
G |
8: 111,620,034 (GRCm39) |
F281S |
probably damaging |
Het |
Fli1 |
T |
A |
9: 32,335,503 (GRCm39) |
K310* |
probably null |
Het |
Fndc4 |
C |
T |
5: 31,452,556 (GRCm39) |
|
probably null |
Het |
Gc |
G |
A |
5: 89,569,981 (GRCm39) |
|
probably benign |
Het |
Obscn |
C |
T |
11: 58,911,367 (GRCm39) |
G6422S |
probably benign |
Het |
Or10d5 |
C |
A |
9: 39,861,536 (GRCm39) |
C177F |
probably damaging |
Het |
Or10j2 |
T |
A |
1: 173,097,919 (GRCm39) |
M59K |
probably damaging |
Het |
Or5b21 |
T |
A |
19: 12,839,746 (GRCm39) |
F202L |
probably benign |
Het |
Pgr |
C |
T |
9: 8,922,669 (GRCm39) |
P613L |
probably damaging |
Het |
Pnpla8 |
C |
A |
12: 44,342,816 (GRCm39) |
A524E |
possibly damaging |
Het |
Psma2 |
A |
T |
13: 14,793,948 (GRCm39) |
I105F |
probably damaging |
Het |
Ptprg |
A |
G |
14: 12,220,661 (GRCm38) |
R458G |
probably damaging |
Het |
Rbm44 |
A |
G |
1: 91,090,830 (GRCm39) |
I755V |
probably benign |
Het |
Rev3l |
A |
G |
10: 39,698,733 (GRCm39) |
K1077E |
possibly damaging |
Het |
Rps20 |
A |
C |
4: 3,834,494 (GRCm39) |
|
probably benign |
Het |
Sel1l3 |
A |
C |
5: 53,357,680 (GRCm39) |
V104G |
probably damaging |
Het |
Sirpb1c |
T |
C |
3: 15,892,937 (GRCm39) |
N89S |
probably benign |
Het |
Slc25a16 |
G |
A |
10: 62,766,220 (GRCm39) |
|
probably null |
Het |
Sulf1 |
C |
T |
1: 12,888,731 (GRCm39) |
R339C |
probably damaging |
Het |
Tedc2 |
C |
T |
17: 24,436,926 (GRCm39) |
A270T |
probably benign |
Het |
Trem3 |
T |
C |
17: 48,554,880 (GRCm39) |
S2P |
possibly damaging |
Het |
Vps37a |
G |
T |
8: 40,993,771 (GRCm39) |
Q255H |
probably damaging |
Het |
Zfp352 |
C |
T |
4: 90,112,391 (GRCm39) |
A177V |
possibly damaging |
Het |
|
Other mutations in Krtap26-1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00886:Krtap26-1
|
APN |
16 |
88,444,267 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01721:Krtap26-1
|
APN |
16 |
88,444,060 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02524:Krtap26-1
|
APN |
16 |
88,444,367 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0383:Krtap26-1
|
UTSW |
16 |
88,444,131 (GRCm39) |
nonsense |
probably null |
|
R2367:Krtap26-1
|
UTSW |
16 |
88,444,213 (GRCm39) |
missense |
probably benign |
0.28 |
R4694:Krtap26-1
|
UTSW |
16 |
88,444,108 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6699:Krtap26-1
|
UTSW |
16 |
88,444,603 (GRCm39) |
missense |
unknown |
|
R6884:Krtap26-1
|
UTSW |
16 |
88,444,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R7299:Krtap26-1
|
UTSW |
16 |
88,444,132 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7808:Krtap26-1
|
UTSW |
16 |
88,444,198 (GRCm39) |
missense |
not run |
|
R8824:Krtap26-1
|
UTSW |
16 |
88,444,324 (GRCm39) |
missense |
probably damaging |
0.99 |
R8824:Krtap26-1
|
UTSW |
16 |
88,444,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R9034:Krtap26-1
|
UTSW |
16 |
88,444,161 (GRCm39) |
missense |
probably benign |
0.14 |
R9186:Krtap26-1
|
UTSW |
16 |
88,444,609 (GRCm39) |
missense |
unknown |
|
R9279:Krtap26-1
|
UTSW |
16 |
88,444,342 (GRCm39) |
missense |
probably benign |
0.00 |
|