Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aimp2 |
A |
G |
5: 143,841,509 (GRCm39) |
S110P |
possibly damaging |
Het |
Akap9 |
A |
G |
5: 3,998,783 (GRCm39) |
T51A |
probably benign |
Het |
Arhgef25 |
A |
G |
10: 127,019,650 (GRCm39) |
F430L |
possibly damaging |
Het |
Brap |
T |
C |
5: 121,813,342 (GRCm39) |
V235A |
probably damaging |
Het |
Cd69 |
C |
T |
6: 129,247,148 (GRCm39) |
G23D |
probably damaging |
Het |
Cecr2 |
C |
T |
6: 120,735,166 (GRCm39) |
R24* |
probably null |
Het |
Celsr2 |
T |
C |
3: 108,307,025 (GRCm39) |
D1974G |
possibly damaging |
Het |
Cps1 |
A |
G |
1: 67,234,358 (GRCm39) |
K915R |
probably benign |
Het |
Csmd1 |
T |
C |
8: 16,408,362 (GRCm39) |
D401G |
probably damaging |
Het |
Dusp13b |
A |
G |
14: 21,785,086 (GRCm39) |
F141S |
probably damaging |
Het |
Eif1ad19 |
A |
G |
12: 87,740,478 (GRCm39) |
V27A |
probably benign |
Het |
Fam162b |
A |
G |
10: 51,466,439 (GRCm39) |
W27R |
probably benign |
Het |
Focad |
A |
G |
4: 88,096,424 (GRCm39) |
T269A |
probably benign |
Het |
Ghr |
T |
A |
15: 3,357,544 (GRCm39) |
R241S |
possibly damaging |
Het |
Hirip3 |
AAGAG |
AAG |
7: 126,462,832 (GRCm39) |
|
probably null |
Het |
Ift70a1 |
A |
T |
2: 75,810,696 (GRCm39) |
N462K |
probably damaging |
Het |
Itgb2l |
A |
G |
16: 96,230,240 (GRCm39) |
Y357H |
possibly damaging |
Het |
Jrkl |
T |
C |
9: 13,244,938 (GRCm39) |
D241G |
possibly damaging |
Het |
Lmod1 |
A |
G |
1: 135,291,967 (GRCm39) |
D274G |
probably benign |
Het |
Lrrn2 |
A |
G |
1: 132,866,959 (GRCm39) |
S675G |
probably benign |
Het |
Ltbp4 |
G |
C |
7: 27,009,960 (GRCm39) |
P1200R |
probably damaging |
Het |
Mdn1 |
T |
C |
4: 32,735,576 (GRCm39) |
L3414P |
possibly damaging |
Het |
Myo16 |
T |
A |
8: 10,683,624 (GRCm39) |
S1856T |
probably damaging |
Het |
Neb |
A |
G |
2: 52,186,310 (GRCm39) |
Y921H |
probably damaging |
Het |
Or2n1c |
T |
A |
17: 38,520,074 (GRCm39) |
*313R |
probably null |
Het |
Pgap3 |
T |
C |
11: 98,281,960 (GRCm39) |
D117G |
probably damaging |
Het |
Ppp1r9b |
T |
C |
11: 94,892,812 (GRCm39) |
F671L |
possibly damaging |
Het |
Proser3 |
G |
A |
7: 30,245,572 (GRCm39) |
A144V |
probably benign |
Het |
Purg |
T |
G |
8: 33,876,897 (GRCm39) |
Y178* |
probably null |
Het |
Sfi1 |
TCGC |
TC |
11: 3,096,254 (GRCm39) |
|
probably null |
Het |
Sfi1 |
CCTCTC |
CCTCTCTC |
11: 3,127,419 (GRCm39) |
|
probably benign |
Het |
Sorbs1 |
T |
A |
19: 40,371,050 (GRCm39) |
D79V |
probably damaging |
Het |
Tcaf3 |
T |
C |
6: 42,568,368 (GRCm39) |
T663A |
probably damaging |
Het |
Timd4 |
C |
A |
11: 46,708,475 (GRCm39) |
T167K |
probably damaging |
Het |
Tjp2 |
A |
G |
19: 24,108,527 (GRCm39) |
L195P |
possibly damaging |
Het |
Tnr |
G |
A |
1: 159,679,856 (GRCm39) |
A277T |
probably benign |
Het |
Unc13a |
C |
T |
8: 72,114,477 (GRCm39) |
G181D |
probably benign |
Het |
Vmn1r11 |
T |
A |
6: 57,114,492 (GRCm39) |
L52Q |
possibly damaging |
Het |
Vmn2r125 |
C |
A |
4: 156,703,396 (GRCm39) |
A258D |
probably benign |
Het |
Zfp27 |
T |
C |
7: 29,595,254 (GRCm39) |
D237G |
possibly damaging |
Het |
Zfp39 |
T |
C |
11: 58,793,670 (GRCm39) |
T23A |
possibly damaging |
Het |
|
Other mutations in Zfp459 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03115:Zfp459
|
APN |
13 |
67,556,796 (GRCm39) |
nonsense |
probably null |
|
FR4304:Zfp459
|
UTSW |
13 |
67,556,393 (GRCm39) |
frame shift |
probably null |
|
FR4589:Zfp459
|
UTSW |
13 |
67,556,394 (GRCm39) |
frame shift |
probably null |
|
FR4976:Zfp459
|
UTSW |
13 |
67,556,395 (GRCm39) |
frame shift |
probably null |
|
FR4976:Zfp459
|
UTSW |
13 |
67,556,394 (GRCm39) |
frame shift |
probably null |
|
FR4976:Zfp459
|
UTSW |
13 |
67,556,393 (GRCm39) |
frame shift |
probably null |
|
R1185:Zfp459
|
UTSW |
13 |
67,556,600 (GRCm39) |
missense |
probably benign |
0.00 |
R1185:Zfp459
|
UTSW |
13 |
67,556,600 (GRCm39) |
missense |
probably benign |
0.00 |
R2130:Zfp459
|
UTSW |
13 |
67,556,395 (GRCm39) |
missense |
probably benign |
0.04 |
R2994:Zfp459
|
UTSW |
13 |
67,556,853 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4180:Zfp459
|
UTSW |
13 |
67,556,562 (GRCm39) |
missense |
probably benign |
0.41 |
R4306:Zfp459
|
UTSW |
13 |
67,561,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R5306:Zfp459
|
UTSW |
13 |
67,561,249 (GRCm39) |
missense |
probably damaging |
0.99 |
R5493:Zfp459
|
UTSW |
13 |
67,556,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R7683:Zfp459
|
UTSW |
13 |
67,556,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R9004:Zfp459
|
UTSW |
13 |
67,556,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R9145:Zfp459
|
UTSW |
13 |
67,556,735 (GRCm39) |
missense |
probably benign |
0.01 |
|