Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
A |
T |
14: 32,382,562 (GRCm39) |
D1134E |
probably benign |
Het |
Abca5 |
C |
T |
11: 110,182,911 (GRCm39) |
|
probably null |
Het |
Acp2 |
A |
G |
2: 91,036,409 (GRCm39) |
T169A |
probably damaging |
Het |
Agtpbp1 |
A |
T |
13: 59,622,429 (GRCm39) |
N932K |
probably benign |
Het |
Aldh5a1 |
G |
A |
13: 25,121,293 (GRCm39) |
R87C |
probably damaging |
Het |
Bpifa1 |
G |
T |
2: 153,985,843 (GRCm39) |
A53S |
unknown |
Het |
Cacna2d2 |
T |
C |
9: 107,396,384 (GRCm39) |
I667T |
probably benign |
Het |
Catsperg1 |
T |
A |
7: 28,889,751 (GRCm39) |
T784S |
probably benign |
Het |
Ccdc93 |
C |
T |
1: 121,369,584 (GRCm39) |
Q109* |
probably null |
Het |
Cd46 |
C |
G |
1: 194,767,720 (GRCm39) |
D114H |
probably damaging |
Het |
Cd82 |
A |
T |
2: 93,267,740 (GRCm39) |
L19Q |
probably damaging |
Het |
Celsr1 |
T |
C |
15: 85,806,535 (GRCm39) |
|
probably benign |
Het |
Cnksr1 |
A |
G |
4: 133,961,885 (GRCm39) |
I180T |
possibly damaging |
Het |
Drg2 |
T |
C |
11: 60,358,966 (GRCm39) |
V362A |
probably benign |
Het |
Eef2 |
T |
A |
10: 81,014,994 (GRCm39) |
M231K |
probably benign |
Het |
Egr2 |
T |
C |
10: 67,375,628 (GRCm39) |
Y75H |
probably damaging |
Het |
Exoc6 |
A |
C |
19: 37,585,545 (GRCm39) |
Q473H |
probably benign |
Het |
Focad |
T |
A |
4: 88,267,076 (GRCm39) |
M1029K |
unknown |
Het |
Fpr-rs4 |
T |
A |
17: 18,242,391 (GRCm39) |
S133T |
probably benign |
Het |
Gbf1 |
T |
C |
19: 46,268,432 (GRCm39) |
V1322A |
probably benign |
Het |
Gm572 |
T |
C |
4: 148,752,966 (GRCm39) |
S282P |
possibly damaging |
Het |
Gm7579 |
GGCTGTGGCTCCTGTGGGGGCTGCAAGGGAAGCTGTGGCTCCTGTGGGGGCTGCAAGGGAAGCTGTGGCTCCTGTGGGGGATGCAAGGGAGGCTGTGGCTCCTGTGGGGG |
GGCTGTGGCTCCTGTGGGGGCTGCAAGGGAAGCTGTGGCTCCTGTGGGGGATGCAAGGGAGGCTGTGGCTCCTGTGGGGG |
7: 141,765,782 (GRCm39) |
|
probably benign |
Het |
Golph3l |
T |
C |
3: 95,496,369 (GRCm39) |
V31A |
probably benign |
Het |
Iars2 |
A |
T |
1: 185,034,913 (GRCm39) |
V610D |
probably damaging |
Het |
Igsf6 |
T |
A |
7: 120,666,472 (GRCm39) |
I203F |
probably damaging |
Het |
Ildr2 |
A |
G |
1: 166,136,691 (GRCm39) |
Y510C |
probably damaging |
Het |
Iqcf4 |
C |
A |
9: 106,445,652 (GRCm39) |
R165L |
possibly damaging |
Het |
Itgb1bp1 |
T |
G |
12: 21,320,943 (GRCm39) |
I183L |
possibly damaging |
Het |
Itgb4 |
A |
C |
11: 115,895,855 (GRCm39) |
S1414R |
probably benign |
Het |
Kbtbd7 |
G |
T |
14: 79,664,944 (GRCm39) |
A259S |
probably benign |
Het |
Kif14 |
T |
A |
1: 136,401,174 (GRCm39) |
D508E |
possibly damaging |
Het |
Klc2 |
A |
T |
19: 5,159,662 (GRCm39) |
D484E |
possibly damaging |
Het |
Lamc2 |
T |
C |
1: 153,013,072 (GRCm39) |
S630G |
probably benign |
Het |
Myl6b |
G |
A |
10: 128,331,066 (GRCm39) |
T125M |
possibly damaging |
Het |
Nbea |
T |
A |
3: 55,943,309 (GRCm39) |
K655N |
possibly damaging |
Het |
Nkx3-2 |
T |
C |
5: 41,919,493 (GRCm39) |
D165G |
probably benign |
Het |
Npy |
A |
T |
6: 49,804,481 (GRCm39) |
R67S |
probably damaging |
Het |
Nrg3 |
A |
T |
14: 39,194,556 (GRCm39) |
C68S |
possibly damaging |
Het |
Nup160 |
C |
T |
2: 90,560,138 (GRCm39) |
P1288S |
probably damaging |
Het |
Or8g33 |
A |
G |
9: 39,337,506 (GRCm39) |
L287P |
probably benign |
Het |
Pam |
T |
A |
1: 97,822,144 (GRCm39) |
I287L |
probably benign |
Het |
Phf10 |
T |
C |
17: 15,165,387 (GRCm39) |
R490G |
probably benign |
Het |
Prim2 |
T |
C |
1: 33,523,876 (GRCm39) |
Y345C |
probably damaging |
Het |
Ptchd3 |
C |
T |
11: 121,721,646 (GRCm39) |
A173V |
probably benign |
Het |
Rab8b |
G |
A |
9: 66,755,912 (GRCm39) |
R167W |
probably damaging |
Het |
S100a3 |
A |
G |
3: 90,509,502 (GRCm39) |
E49G |
probably benign |
Het |
Slc41a1 |
T |
A |
1: 131,766,896 (GRCm39) |
V138E |
probably damaging |
Het |
Slit1 |
C |
A |
19: 41,591,764 (GRCm39) |
|
probably null |
Het |
Sntg1 |
T |
A |
1: 8,433,814 (GRCm39) |
H479L |
probably damaging |
Het |
Stam |
T |
A |
2: 14,120,801 (GRCm39) |
C72S |
probably damaging |
Het |
Sval2 |
G |
T |
6: 41,840,795 (GRCm39) |
A93S |
probably benign |
Het |
Tas2r103 |
T |
A |
6: 133,013,686 (GRCm39) |
K127* |
probably null |
Het |
Trank1 |
C |
T |
9: 111,193,890 (GRCm39) |
T638M |
probably benign |
Het |
Utrn |
T |
A |
10: 12,519,173 (GRCm39) |
I2260F |
probably damaging |
Het |
Zfp268 |
G |
C |
4: 145,349,045 (GRCm39) |
E161Q |
|
Het |
Zfp280d |
T |
C |
9: 72,226,599 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Or52e15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01302:Or52e15
|
APN |
7 |
104,645,928 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4151001:Or52e15
|
UTSW |
7 |
104,645,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R0396:Or52e15
|
UTSW |
7 |
104,645,913 (GRCm39) |
missense |
probably damaging |
0.99 |
R0632:Or52e15
|
UTSW |
7 |
104,645,910 (GRCm39) |
missense |
probably benign |
0.00 |
R1490:Or52e15
|
UTSW |
7 |
104,645,700 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1781:Or52e15
|
UTSW |
7 |
104,645,315 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2251:Or52e15
|
UTSW |
7 |
104,645,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R3419:Or52e15
|
UTSW |
7 |
104,645,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R3625:Or52e15
|
UTSW |
7 |
104,645,191 (GRCm39) |
missense |
probably benign |
0.17 |
R4093:Or52e15
|
UTSW |
7 |
104,645,842 (GRCm39) |
missense |
probably benign |
0.01 |
R4620:Or52e15
|
UTSW |
7 |
104,645,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R4890:Or52e15
|
UTSW |
7 |
104,645,311 (GRCm39) |
missense |
probably benign |
0.15 |
R5338:Or52e15
|
UTSW |
7 |
104,645,514 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5934:Or52e15
|
UTSW |
7 |
104,645,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R6712:Or52e15
|
UTSW |
7 |
104,645,625 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7620:Or52e15
|
UTSW |
7 |
104,645,962 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9088:Or52e15
|
UTSW |
7 |
104,645,301 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Or52e15
|
UTSW |
7 |
104,645,661 (GRCm39) |
missense |
probably benign |
0.00 |
|