Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatf |
A |
G |
11: 84,362,115 (GRCm39) |
|
probably benign |
Het |
Asap3 |
A |
T |
4: 135,966,548 (GRCm39) |
H542L |
probably benign |
Het |
Cyp4v3 |
A |
T |
8: 45,761,753 (GRCm39) |
L389H |
probably damaging |
Het |
Dnah17 |
C |
T |
11: 117,932,944 (GRCm39) |
E3605K |
probably damaging |
Het |
Fry |
C |
T |
5: 150,282,516 (GRCm39) |
T347M |
probably damaging |
Het |
Glul |
C |
A |
1: 153,782,862 (GRCm39) |
T191K |
probably benign |
Het |
Grsf1 |
A |
T |
5: 88,821,689 (GRCm39) |
L125Q |
probably damaging |
Het |
Hfm1 |
A |
G |
5: 107,022,118 (GRCm39) |
I976T |
probably damaging |
Het |
Itgb5 |
A |
G |
16: 33,740,275 (GRCm39) |
T462A |
probably benign |
Het |
Lmna |
G |
T |
3: 88,410,233 (GRCm39) |
R60S |
possibly damaging |
Het |
Mrpl10 |
T |
A |
11: 96,937,899 (GRCm39) |
V89D |
probably damaging |
Het |
Muc5b |
C |
T |
7: 141,411,449 (GRCm39) |
T1465I |
unknown |
Het |
Myh15 |
A |
C |
16: 48,937,628 (GRCm39) |
D743A |
possibly damaging |
Het |
Noxo1 |
C |
A |
17: 24,918,409 (GRCm39) |
L190I |
probably damaging |
Het |
Noxo1 |
T |
A |
17: 24,918,410 (GRCm39) |
L190Q |
probably damaging |
Het |
Nrn1 |
C |
A |
13: 36,914,080 (GRCm39) |
|
probably null |
Het |
Or2aj5 |
A |
T |
16: 19,425,050 (GRCm39) |
Y123N |
probably damaging |
Het |
Or4c121 |
T |
A |
2: 89,023,985 (GRCm39) |
Y131F |
probably damaging |
Het |
Or5m13 |
A |
G |
2: 85,748,460 (GRCm39) |
S64G |
probably benign |
Het |
Or8h8 |
A |
G |
2: 86,753,057 (GRCm39) |
V273A |
possibly damaging |
Het |
Pfkfb4 |
A |
G |
9: 108,836,364 (GRCm39) |
T131A |
probably null |
Het |
Phf20l1 |
T |
C |
15: 66,466,829 (GRCm39) |
|
probably null |
Het |
Pnliprp2 |
A |
G |
19: 58,759,878 (GRCm39) |
D363G |
probably benign |
Het |
Prpf6 |
C |
T |
2: 181,273,864 (GRCm39) |
T336I |
probably benign |
Het |
Rcc1 |
C |
T |
4: 132,065,067 (GRCm39) |
R139H |
probably benign |
Het |
Sae1 |
T |
G |
7: 16,093,043 (GRCm39) |
K221N |
probably damaging |
Het |
Slc45a1 |
T |
C |
4: 150,722,987 (GRCm39) |
K299R |
probably benign |
Het |
Slco1a8 |
T |
C |
6: 141,917,969 (GRCm39) |
R636G |
probably benign |
Het |
Smad2 |
C |
A |
18: 76,432,851 (GRCm39) |
|
probably null |
Het |
Tmem117 |
T |
C |
15: 94,777,306 (GRCm39) |
F152S |
probably damaging |
Het |
Tmem232 |
C |
T |
17: 65,757,365 (GRCm39) |
C276Y |
probably damaging |
Het |
Tor1b |
A |
T |
2: 30,843,865 (GRCm39) |
K47* |
probably null |
Het |
Ttn |
A |
G |
2: 76,740,147 (GRCm39) |
V3464A |
probably benign |
Het |
Ube3b |
A |
G |
5: 114,550,945 (GRCm39) |
T870A |
possibly damaging |
Het |
Zscan25 |
T |
G |
5: 145,227,296 (GRCm39) |
L320R |
probably benign |
Het |
|
Other mutations in 1700029H14Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03069:1700029H14Rik
|
APN |
8 |
13,607,704 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0242:1700029H14Rik
|
UTSW |
8 |
13,601,676 (GRCm39) |
missense |
probably benign |
|
R0242:1700029H14Rik
|
UTSW |
8 |
13,601,676 (GRCm39) |
missense |
probably benign |
|
R0243:1700029H14Rik
|
UTSW |
8 |
13,604,715 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0419:1700029H14Rik
|
UTSW |
8 |
13,601,842 (GRCm39) |
splice site |
probably benign |
|
R1747:1700029H14Rik
|
UTSW |
8 |
13,608,814 (GRCm39) |
missense |
probably damaging |
0.96 |
R1758:1700029H14Rik
|
UTSW |
8 |
13,612,237 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3890:1700029H14Rik
|
UTSW |
8 |
13,604,700 (GRCm39) |
missense |
probably damaging |
0.97 |
R5004:1700029H14Rik
|
UTSW |
8 |
13,605,927 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8067:1700029H14Rik
|
UTSW |
8 |
13,608,643 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9412:1700029H14Rik
|
UTSW |
8 |
13,604,695 (GRCm39) |
missense |
possibly damaging |
0.66 |
|