Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
A |
3: 121,932,261 (GRCm39) |
|
probably null |
Het |
Acadsb |
A |
C |
7: 131,042,922 (GRCm39) |
|
probably benign |
Het |
Ankk1 |
A |
G |
9: 49,333,166 (GRCm39) |
L106P |
probably benign |
Het |
Ankrd24 |
G |
A |
10: 81,474,483 (GRCm39) |
A72T |
probably benign |
Het |
Ankrd35 |
A |
T |
3: 96,592,117 (GRCm39) |
Q801L |
probably damaging |
Het |
Avil |
A |
G |
10: 126,852,193 (GRCm39) |
I659M |
probably benign |
Het |
Ccnc |
A |
G |
4: 21,742,683 (GRCm39) |
D170G |
possibly damaging |
Het |
Cfap57 |
T |
C |
4: 118,441,936 (GRCm39) |
K711E |
probably damaging |
Het |
Dctn1 |
T |
C |
6: 83,174,466 (GRCm39) |
|
probably benign |
Het |
Dpp6 |
T |
C |
5: 27,914,548 (GRCm39) |
|
probably null |
Het |
Efhb |
A |
T |
17: 53,706,087 (GRCm39) |
W817R |
probably damaging |
Het |
Emilin3 |
G |
A |
2: 160,750,649 (GRCm39) |
Q320* |
probably null |
Het |
Fer1l4 |
A |
G |
2: 155,881,286 (GRCm39) |
|
probably benign |
Het |
Fgf8 |
T |
C |
19: 45,725,667 (GRCm39) |
N137S |
probably damaging |
Het |
Fndc3b |
T |
C |
3: 27,521,576 (GRCm39) |
D533G |
probably benign |
Het |
Fshb |
A |
G |
2: 106,887,812 (GRCm39) |
V69A |
probably benign |
Het |
Galnt7 |
A |
T |
8: 57,979,223 (GRCm39) |
H633Q |
probably damaging |
Het |
Gm5458 |
A |
G |
14: 19,652,451 (GRCm39) |
|
probably null |
Het |
Hjv |
T |
A |
3: 96,435,922 (GRCm39) |
D393E |
probably benign |
Het |
Hpca |
A |
C |
4: 129,012,319 (GRCm39) |
F72L |
probably damaging |
Het |
Inpp5d |
A |
T |
1: 87,638,863 (GRCm39) |
D552V |
probably damaging |
Het |
Lepr |
C |
T |
4: 101,671,876 (GRCm39) |
Q967* |
probably null |
Het |
Lgr5 |
A |
G |
10: 115,288,937 (GRCm39) |
V497A |
probably benign |
Het |
Matr3 |
A |
G |
18: 35,705,471 (GRCm39) |
K132R |
probably damaging |
Het |
Mib1 |
T |
G |
18: 10,752,029 (GRCm39) |
|
probably null |
Het |
Mios |
T |
A |
6: 8,215,156 (GRCm39) |
N117K |
probably damaging |
Het |
Nab1 |
T |
C |
1: 52,529,429 (GRCm39) |
D156G |
probably benign |
Het |
Nfxl1 |
C |
T |
5: 72,698,005 (GRCm39) |
|
probably benign |
Het |
Nutm2 |
G |
A |
13: 50,621,480 (GRCm39) |
G15E |
probably damaging |
Het |
Oca2 |
A |
G |
7: 55,945,232 (GRCm39) |
H280R |
probably benign |
Het |
Or4d1 |
T |
C |
11: 87,804,914 (GRCm39) |
I273V |
probably benign |
Het |
P2ry1 |
A |
G |
3: 60,911,736 (GRCm39) |
T292A |
probably benign |
Het |
Pcna |
C |
T |
2: 132,093,673 (GRCm39) |
E109K |
probably benign |
Het |
Pidd1 |
A |
G |
7: 141,020,369 (GRCm39) |
|
probably null |
Het |
Pitpnm2 |
T |
C |
5: 124,271,445 (GRCm39) |
E376G |
possibly damaging |
Het |
Pkd1l2 |
G |
A |
8: 117,792,484 (GRCm39) |
T436I |
probably benign |
Het |
Polr2a |
T |
C |
11: 69,635,872 (GRCm39) |
|
probably null |
Het |
Sbno2 |
A |
T |
10: 79,893,368 (GRCm39) |
M1311K |
probably damaging |
Het |
Senp7 |
A |
G |
16: 55,992,228 (GRCm39) |
N701S |
probably benign |
Het |
Sirpa |
T |
A |
2: 129,471,848 (GRCm39) |
I211N |
probably damaging |
Het |
Slc9a4 |
A |
G |
1: 40,668,562 (GRCm39) |
E735G |
probably benign |
Het |
Sorbs1 |
C |
T |
19: 40,302,820 (GRCm39) |
M790I |
probably damaging |
Het |
Sult1e1 |
T |
A |
5: 87,737,983 (GRCm39) |
M33L |
probably benign |
Het |
Tapbpl |
G |
A |
6: 125,205,191 (GRCm39) |
|
probably null |
Het |
Top1 |
A |
G |
2: 160,545,498 (GRCm39) |
T289A |
probably damaging |
Het |
Trim58 |
T |
A |
11: 58,542,216 (GRCm39) |
M392K |
probably benign |
Het |
Uaca |
A |
G |
9: 60,770,945 (GRCm39) |
I371V |
probably benign |
Het |
Vmn1r54 |
T |
C |
6: 90,246,854 (GRCm39) |
I256T |
possibly damaging |
Het |
Wdr19 |
T |
C |
5: 65,388,319 (GRCm39) |
I668T |
probably benign |
Het |
|
Other mutations in Or10al2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01300:Or10al2
|
APN |
17 |
37,983,778 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02456:Or10al2
|
APN |
17 |
37,983,340 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02750:Or10al2
|
APN |
17 |
37,983,500 (GRCm39) |
nonsense |
probably null |
|
IGL03339:Or10al2
|
APN |
17 |
37,983,448 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0032:Or10al2
|
UTSW |
17 |
37,983,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R1457:Or10al2
|
UTSW |
17 |
37,983,816 (GRCm39) |
nonsense |
probably null |
|
R1542:Or10al2
|
UTSW |
17 |
37,983,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R1771:Or10al2
|
UTSW |
17 |
37,983,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R1893:Or10al2
|
UTSW |
17 |
37,983,747 (GRCm39) |
nonsense |
probably null |
|
R2395:Or10al2
|
UTSW |
17 |
37,983,587 (GRCm39) |
nonsense |
probably null |
|
R3619:Or10al2
|
UTSW |
17 |
37,983,531 (GRCm39) |
missense |
probably benign |
0.05 |
R3917:Or10al2
|
UTSW |
17 |
37,983,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R3937:Or10al2
|
UTSW |
17 |
37,983,858 (GRCm39) |
missense |
probably benign |
0.01 |
R5600:Or10al2
|
UTSW |
17 |
37,983,176 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6415:Or10al2
|
UTSW |
17 |
37,983,448 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6462:Or10al2
|
UTSW |
17 |
37,983,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R7355:Or10al2
|
UTSW |
17 |
37,983,301 (GRCm39) |
missense |
probably benign |
0.02 |
R7861:Or10al2
|
UTSW |
17 |
37,983,408 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7913:Or10al2
|
UTSW |
17 |
37,982,999 (GRCm39) |
missense |
probably benign |
|
R7952:Or10al2
|
UTSW |
17 |
37,983,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R7969:Or10al2
|
UTSW |
17 |
37,983,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R8879:Or10al2
|
UTSW |
17 |
37,983,302 (GRCm39) |
nonsense |
probably null |
|
R8923:Or10al2
|
UTSW |
17 |
37,983,702 (GRCm39) |
missense |
probably benign |
0.00 |
R9253:Or10al2
|
UTSW |
17 |
37,983,637 (GRCm39) |
missense |
probably benign |
0.00 |
R9778:Or10al2
|
UTSW |
17 |
37,983,145 (GRCm39) |
missense |
probably damaging |
0.97 |
R9789:Or10al2
|
UTSW |
17 |
37,983,059 (GRCm39) |
missense |
probably damaging |
1.00 |
RF003:Or10al2
|
UTSW |
17 |
37,983,749 (GRCm39) |
missense |
probably damaging |
1.00 |
|