Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agap1 |
G |
T |
1: 89,770,876 (GRCm39) |
K622N |
probably damaging |
Het |
Ap3b2 |
A |
T |
7: 81,115,917 (GRCm39) |
|
probably null |
Het |
Arl5b |
T |
C |
2: 15,074,648 (GRCm39) |
V43A |
probably benign |
Het |
Astn1 |
T |
C |
1: 158,427,935 (GRCm39) |
V702A |
possibly damaging |
Het |
Bach1 |
T |
C |
16: 87,512,322 (GRCm39) |
V15A |
probably benign |
Het |
Cacna1c |
C |
T |
6: 118,589,586 (GRCm39) |
R1446H |
probably damaging |
Het |
Ccar2 |
C |
T |
14: 70,377,218 (GRCm39) |
V774M |
probably benign |
Het |
Dcaf5 |
T |
C |
12: 80,386,989 (GRCm39) |
D379G |
possibly damaging |
Het |
Dcpp1 |
T |
A |
17: 24,100,405 (GRCm39) |
I45K |
possibly damaging |
Het |
Ddx17 |
T |
A |
15: 79,425,288 (GRCm39) |
S128C |
probably damaging |
Het |
Eml3 |
A |
G |
19: 8,910,614 (GRCm39) |
N192S |
probably benign |
Het |
Epha3 |
T |
G |
16: 63,593,431 (GRCm39) |
D219A |
probably damaging |
Het |
Fhod3 |
C |
T |
18: 25,118,293 (GRCm39) |
A210V |
probably damaging |
Het |
Khdc4 |
C |
A |
3: 88,616,169 (GRCm39) |
P452Q |
probably damaging |
Het |
Klhl5 |
A |
G |
5: 65,298,683 (GRCm39) |
N154S |
probably benign |
Het |
Lrif1 |
A |
G |
3: 106,640,033 (GRCm39) |
N373D |
possibly damaging |
Het |
Map3k20 |
A |
G |
2: 72,271,864 (GRCm39) |
N664S |
probably benign |
Het |
Parp14 |
G |
A |
16: 35,677,130 (GRCm39) |
A946V |
probably benign |
Het |
Pdia3 |
G |
A |
2: 121,262,858 (GRCm39) |
G275S |
probably damaging |
Het |
Pglyrp4 |
T |
A |
3: 90,636,138 (GRCm39) |
|
probably null |
Het |
Pole |
A |
G |
5: 110,443,119 (GRCm39) |
E349G |
possibly damaging |
Het |
Ptprj |
A |
G |
2: 90,274,868 (GRCm39) |
Y1165H |
probably damaging |
Het |
Rasd1 |
T |
A |
11: 59,855,547 (GRCm39) |
I29F |
possibly damaging |
Het |
Scamp3 |
T |
C |
3: 89,088,505 (GRCm39) |
F237S |
probably damaging |
Het |
Sccpdh |
T |
G |
1: 179,511,775 (GRCm39) |
D82E |
probably benign |
Het |
Slc19a3 |
A |
C |
1: 83,000,413 (GRCm39) |
H201Q |
possibly damaging |
Het |
Slc5a4a |
G |
A |
10: 76,013,995 (GRCm39) |
A401T |
possibly damaging |
Het |
Snupn |
T |
G |
9: 56,864,389 (GRCm39) |
C29W |
probably benign |
Het |
Sorbs2 |
A |
G |
8: 46,223,613 (GRCm39) |
Y222C |
probably damaging |
Het |
Sox17 |
A |
T |
1: 4,562,075 (GRCm39) |
V310E |
probably damaging |
Het |
Srgap1 |
T |
A |
10: 121,691,382 (GRCm39) |
Y284F |
probably benign |
Het |
Srpk1 |
C |
A |
17: 28,818,748 (GRCm39) |
V363F |
probably benign |
Het |
Syt13 |
T |
A |
2: 92,773,387 (GRCm39) |
|
probably null |
Het |
Taf2 |
A |
G |
15: 54,934,793 (GRCm39) |
V45A |
probably benign |
Het |
Tal1 |
A |
T |
4: 114,925,813 (GRCm39) |
D294V |
probably damaging |
Het |
Tbl2 |
A |
G |
5: 135,188,246 (GRCm39) |
T347A |
probably benign |
Het |
Tet3 |
A |
G |
6: 83,381,434 (GRCm39) |
S110P |
probably benign |
Het |
Tmem132a |
A |
G |
19: 10,835,938 (GRCm39) |
V864A |
probably damaging |
Het |
Trak1 |
T |
C |
9: 121,221,073 (GRCm39) |
I80T |
probably benign |
Het |
Trappc6b |
G |
A |
12: 59,097,064 (GRCm39) |
T86I |
probably damaging |
Het |
Usf3 |
T |
A |
16: 44,038,910 (GRCm39) |
I1130N |
probably damaging |
Het |
Xirp2 |
T |
C |
2: 67,340,231 (GRCm39) |
V824A |
possibly damaging |
Het |
Zfp810 |
T |
C |
9: 22,189,828 (GRCm39) |
Y360C |
possibly damaging |
Het |
Zmiz1 |
T |
A |
14: 25,654,936 (GRCm39) |
V685E |
probably damaging |
Het |
Zp2 |
A |
T |
7: 119,735,268 (GRCm39) |
D368E |
probably damaging |
Het |
|
Other mutations in Or52z15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02547:Or52z15
|
APN |
7 |
103,331,973 (GRCm39) |
missense |
probably benign |
0.01 |
R1508:Or52z15
|
UTSW |
7 |
103,332,678 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1766:Or52z15
|
UTSW |
7 |
103,332,068 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1901:Or52z15
|
UTSW |
7 |
103,332,750 (GRCm39) |
missense |
probably damaging |
0.98 |
R2116:Or52z15
|
UTSW |
7 |
103,332,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R4701:Or52z15
|
UTSW |
7 |
103,332,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R4995:Or52z15
|
UTSW |
7 |
103,332,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R5198:Or52z15
|
UTSW |
7 |
103,331,936 (GRCm39) |
missense |
probably benign |
0.40 |
R5750:Or52z15
|
UTSW |
7 |
103,332,362 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5776:Or52z15
|
UTSW |
7 |
103,332,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R5905:Or52z15
|
UTSW |
7 |
103,332,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R5933:Or52z15
|
UTSW |
7 |
103,332,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R6488:Or52z15
|
UTSW |
7 |
103,332,285 (GRCm39) |
missense |
probably damaging |
0.98 |
R7846:Or52z15
|
UTSW |
7 |
103,332,407 (GRCm39) |
missense |
probably benign |
0.03 |
R7878:Or52z15
|
UTSW |
7 |
103,332,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R9170:Or52z15
|
UTSW |
7 |
103,332,404 (GRCm39) |
missense |
probably benign |
0.00 |
R9347:Or52z15
|
UTSW |
7 |
103,332,464 (GRCm39) |
missense |
probably damaging |
0.97 |
R9474:Or52z15
|
UTSW |
7 |
103,332,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R9781:Or52z15
|
UTSW |
7 |
103,332,246 (GRCm39) |
missense |
probably damaging |
1.00 |
RF040:Or52z15
|
UTSW |
7 |
103,332,145 (GRCm39) |
frame shift |
probably null |
|
Z1088:Or52z15
|
UTSW |
7 |
103,332,393 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Or52z15
|
UTSW |
7 |
103,332,312 (GRCm39) |
missense |
probably benign |
0.09 |
|