Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
T |
C |
2: 25,331,590 (GRCm39) |
S1326P |
possibly damaging |
Het |
Adam22 |
T |
G |
5: 8,199,218 (GRCm39) |
D246A |
probably damaging |
Het |
Bmf |
T |
C |
2: 118,363,018 (GRCm39) |
|
probably benign |
Het |
Cd300lf |
T |
C |
11: 115,015,089 (GRCm39) |
Y160C |
possibly damaging |
Het |
Chuk |
G |
A |
19: 44,090,279 (GRCm39) |
A71V |
probably benign |
Het |
Col19a1 |
C |
T |
1: 24,309,473 (GRCm39) |
G1060E |
probably damaging |
Het |
Dock7 |
A |
G |
4: 98,904,973 (GRCm39) |
V634A |
probably benign |
Het |
Dpm3 |
A |
G |
3: 89,174,039 (GRCm39) |
|
probably benign |
Het |
Dqx1 |
A |
G |
6: 83,036,460 (GRCm39) |
T155A |
probably benign |
Het |
Dysf |
G |
A |
6: 84,163,491 (GRCm39) |
|
probably null |
Het |
Fam184b |
T |
C |
5: 45,697,106 (GRCm39) |
E686G |
probably benign |
Het |
Fhad1 |
T |
A |
4: 141,712,854 (GRCm39) |
D195V |
possibly damaging |
Het |
Glis2 |
T |
C |
16: 4,429,240 (GRCm39) |
S148P |
probably benign |
Het |
Gm8587 |
C |
T |
12: 88,056,516 (GRCm39) |
|
noncoding transcript |
Het |
Gon7 |
A |
G |
12: 102,720,363 (GRCm39) |
S90P |
probably benign |
Het |
Haus6 |
A |
T |
4: 86,501,811 (GRCm39) |
W687R |
probably benign |
Het |
Hivep2 |
C |
A |
10: 14,004,713 (GRCm39) |
T437K |
probably benign |
Het |
Idh3g |
A |
T |
X: 72,825,610 (GRCm39) |
|
probably null |
Het |
Ints9 |
T |
C |
14: 65,230,430 (GRCm39) |
L119P |
probably damaging |
Het |
Itga9 |
T |
C |
9: 118,436,146 (GRCm39) |
Y51H |
probably damaging |
Het |
Klf17 |
T |
A |
4: 117,616,383 (GRCm39) |
H316L |
probably benign |
Het |
Klf4 |
C |
T |
4: 55,530,884 (GRCm39) |
G26R |
possibly damaging |
Het |
Krt1 |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
15: 101,758,813 (GRCm39) |
|
probably benign |
Het |
Lhcgr |
A |
G |
17: 89,049,711 (GRCm39) |
V605A |
probably damaging |
Het |
Mafa |
T |
C |
15: 75,619,413 (GRCm39) |
Y120C |
possibly damaging |
Het |
Map3k20 |
A |
G |
2: 72,271,915 (GRCm39) |
Y681C |
probably damaging |
Het |
Nub1 |
T |
C |
5: 24,897,875 (GRCm39) |
I87T |
probably damaging |
Het |
Or1ak2 |
T |
A |
2: 36,827,242 (GRCm39) |
V37D |
probably damaging |
Het |
Pak2 |
C |
G |
16: 31,871,005 (GRCm39) |
G59A |
probably benign |
Het |
Pdzrn4 |
T |
A |
15: 92,299,898 (GRCm39) |
V256D |
possibly damaging |
Het |
Pkd2l1 |
T |
C |
19: 44,180,620 (GRCm39) |
N32D |
probably benign |
Het |
Plec |
T |
C |
15: 76,064,415 (GRCm39) |
K1953R |
possibly damaging |
Het |
Plekhg4 |
T |
A |
8: 106,108,030 (GRCm39) |
V1029E |
possibly damaging |
Het |
Prkcd |
A |
G |
14: 30,332,261 (GRCm39) |
|
probably benign |
Het |
Rgcc |
T |
C |
14: 79,538,155 (GRCm39) |
S79G |
probably benign |
Het |
Sspo |
T |
C |
6: 48,475,329 (GRCm39) |
|
probably null |
Het |
Stxbp5l |
A |
T |
16: 37,068,242 (GRCm39) |
C315S |
probably benign |
Het |
Tc2n |
A |
G |
12: 101,631,954 (GRCm39) |
L301P |
probably damaging |
Het |
Tcerg1l |
T |
C |
7: 137,878,405 (GRCm39) |
|
probably null |
Het |
Tex12 |
T |
C |
9: 50,470,587 (GRCm39) |
|
probably null |
Het |
Tgm5 |
T |
C |
2: 120,907,442 (GRCm39) |
I94V |
probably benign |
Het |
Tonsl |
A |
G |
15: 76,508,675 (GRCm39) |
L26P |
probably damaging |
Het |
Top2b |
T |
G |
14: 16,409,189 (GRCm38) |
I777M |
probably damaging |
Het |
Trbv4 |
A |
C |
6: 41,036,646 (GRCm39) |
D57A |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Tuba4a |
T |
C |
1: 75,192,426 (GRCm39) |
D396G |
probably benign |
Het |
Txnrd2 |
C |
G |
16: 18,245,175 (GRCm39) |
|
probably null |
Het |
Zfp445 |
T |
C |
9: 122,681,589 (GRCm39) |
N784S |
probably benign |
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 |
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 |
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 |
|