Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9530068E07Rik |
A |
G |
11: 52,294,193 (GRCm39) |
R145G |
probably damaging |
Het |
Akr1c21 |
T |
A |
13: 4,627,431 (GRCm39) |
M175K |
probably benign |
Het |
Apol7a |
C |
T |
15: 77,273,530 (GRCm39) |
A311T |
probably damaging |
Het |
Atxn10 |
G |
T |
15: 85,260,896 (GRCm39) |
E214* |
probably null |
Het |
Bmp2k |
C |
T |
5: 97,234,823 (GRCm39) |
Q749* |
probably null |
Het |
Ccdc141 |
G |
A |
2: 76,876,023 (GRCm39) |
A669V |
probably benign |
Het |
Cndp2 |
A |
C |
18: 84,689,036 (GRCm39) |
C249G |
probably benign |
Het |
Cnr1 |
A |
G |
4: 33,944,802 (GRCm39) |
I397V |
possibly damaging |
Het |
Col19a1 |
T |
C |
1: 24,345,331 (GRCm39) |
|
probably benign |
Het |
Dbn1 |
T |
C |
13: 55,630,117 (GRCm39) |
|
probably benign |
Het |
Dmgdh |
C |
T |
13: 93,845,803 (GRCm39) |
P486S |
probably damaging |
Het |
Dpys |
A |
G |
15: 39,656,702 (GRCm39) |
V455A |
possibly damaging |
Het |
Farp2 |
A |
G |
1: 93,546,702 (GRCm39) |
N907S |
probably benign |
Het |
Fndc3c1 |
C |
T |
X: 105,476,378 (GRCm39) |
E894K |
probably benign |
Het |
Gm6685 |
A |
T |
11: 28,289,473 (GRCm39) |
N114K |
probably damaging |
Het |
Golga3 |
A |
T |
5: 110,365,675 (GRCm39) |
|
probably null |
Het |
Grin2c |
A |
G |
11: 115,151,708 (GRCm39) |
L84P |
probably damaging |
Het |
Gucy2c |
A |
G |
6: 136,675,009 (GRCm39) |
F1001L |
probably benign |
Het |
Hcn4 |
A |
G |
9: 58,767,169 (GRCm39) |
H910R |
unknown |
Het |
Kdm4b |
T |
C |
17: 56,660,518 (GRCm39) |
|
probably benign |
Het |
Lrrfip2 |
A |
G |
9: 111,043,284 (GRCm39) |
T497A |
probably benign |
Het |
Man2c1 |
A |
G |
9: 57,048,884 (GRCm39) |
Y924C |
probably damaging |
Het |
Nkain2 |
T |
A |
10: 32,278,237 (GRCm39) |
T63S |
probably damaging |
Het |
Nlrp1a |
T |
A |
11: 71,013,742 (GRCm39) |
T503S |
probably benign |
Het |
Or52n3 |
T |
C |
7: 104,530,037 (GRCm39) |
V41A |
probably benign |
Het |
Or52n4 |
T |
A |
7: 104,294,136 (GRCm39) |
I146F |
possibly damaging |
Het |
Pitrm1 |
T |
A |
13: 6,623,078 (GRCm39) |
C780S |
probably damaging |
Het |
Plekha5 |
C |
T |
6: 140,516,042 (GRCm39) |
|
probably benign |
Het |
Rapgef4 |
C |
T |
2: 72,005,185 (GRCm39) |
R193* |
probably null |
Het |
Rbm20 |
A |
G |
19: 53,840,044 (GRCm39) |
E1011G |
possibly damaging |
Het |
Rfx3 |
A |
T |
19: 27,746,050 (GRCm39) |
D685E |
probably benign |
Het |
Ror1 |
T |
C |
4: 100,190,984 (GRCm39) |
S114P |
probably damaging |
Het |
Slc17a6 |
A |
G |
7: 51,318,863 (GRCm39) |
K502E |
probably benign |
Het |
Spink2 |
A |
T |
5: 77,359,174 (GRCm39) |
|
probably benign |
Het |
Sptb |
A |
T |
12: 76,659,921 (GRCm39) |
I993N |
possibly damaging |
Het |
Stxbp4 |
A |
G |
11: 90,512,475 (GRCm39) |
|
probably benign |
Het |
Tes |
A |
T |
6: 17,099,878 (GRCm39) |
Y291F |
probably damaging |
Het |
Tmtc4 |
G |
T |
14: 123,163,366 (GRCm39) |
|
probably benign |
Het |
Trpa1 |
T |
C |
1: 14,959,637 (GRCm39) |
E683G |
probably benign |
Het |
Vmn2r73 |
T |
C |
7: 85,521,455 (GRCm39) |
D171G |
probably benign |
Het |
Wbp11 |
A |
G |
6: 136,791,612 (GRCm39) |
|
probably benign |
Het |
Wfdc12 |
A |
G |
2: 164,031,581 (GRCm39) |
*86R |
probably null |
Het |
|
Other mutations in Zfp281 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00531:Zfp281
|
APN |
1 |
136,555,648 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02037:Zfp281
|
APN |
1 |
136,555,185 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03233:Zfp281
|
APN |
1 |
136,554,567 (GRCm39) |
missense |
possibly damaging |
0.82 |
PIT4486001:Zfp281
|
UTSW |
1 |
136,554,741 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1514:Zfp281
|
UTSW |
1 |
136,554,435 (GRCm39) |
missense |
probably benign |
0.00 |
R1784:Zfp281
|
UTSW |
1 |
136,553,091 (GRCm39) |
small insertion |
probably benign |
|
R1785:Zfp281
|
UTSW |
1 |
136,553,091 (GRCm39) |
small insertion |
probably benign |
|
R2049:Zfp281
|
UTSW |
1 |
136,553,091 (GRCm39) |
small insertion |
probably benign |
|
R2142:Zfp281
|
UTSW |
1 |
136,553,091 (GRCm39) |
small insertion |
probably benign |
|
R4086:Zfp281
|
UTSW |
1 |
136,553,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R4087:Zfp281
|
UTSW |
1 |
136,553,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R4088:Zfp281
|
UTSW |
1 |
136,553,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R4090:Zfp281
|
UTSW |
1 |
136,553,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R4819:Zfp281
|
UTSW |
1 |
136,553,448 (GRCm39) |
missense |
probably benign |
|
R5380:Zfp281
|
UTSW |
1 |
136,553,676 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6033:Zfp281
|
UTSW |
1 |
136,554,464 (GRCm39) |
missense |
probably benign |
0.14 |
R6033:Zfp281
|
UTSW |
1 |
136,554,464 (GRCm39) |
missense |
probably benign |
0.14 |
R6056:Zfp281
|
UTSW |
1 |
136,553,178 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6213:Zfp281
|
UTSW |
1 |
136,553,250 (GRCm39) |
missense |
probably benign |
0.01 |
R7402:Zfp281
|
UTSW |
1 |
136,553,190 (GRCm39) |
missense |
probably damaging |
0.99 |
R7503:Zfp281
|
UTSW |
1 |
136,554,678 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7969:Zfp281
|
UTSW |
1 |
136,553,772 (GRCm39) |
missense |
probably benign |
0.06 |
R8343:Zfp281
|
UTSW |
1 |
136,555,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R8722:Zfp281
|
UTSW |
1 |
136,553,334 (GRCm39) |
missense |
probably benign |
0.00 |
R9199:Zfp281
|
UTSW |
1 |
136,553,643 (GRCm39) |
missense |
probably benign |
|
R9461:Zfp281
|
UTSW |
1 |
136,554,500 (GRCm39) |
missense |
probably benign |
0.28 |
R9487:Zfp281
|
UTSW |
1 |
136,555,143 (GRCm39) |
missense |
probably damaging |
0.96 |
R9532:Zfp281
|
UTSW |
1 |
136,554,894 (GRCm39) |
missense |
probably benign |
|
R9541:Zfp281
|
UTSW |
1 |
136,555,303 (GRCm39) |
missense |
probably damaging |
1.00 |
|