Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310022A10Rik |
C |
T |
7: 27,278,198 (GRCm39) |
Q156* |
probably null |
Het |
2700097O09Rik |
A |
G |
12: 55,092,727 (GRCm39) |
I264T |
probably benign |
Het |
Arid3a |
G |
T |
10: 79,786,718 (GRCm39) |
M488I |
possibly damaging |
Het |
Auts2 |
A |
G |
5: 131,494,961 (GRCm39) |
F331S |
probably damaging |
Het |
Axdnd1 |
T |
C |
1: 156,158,532 (GRCm39) |
|
probably null |
Het |
Bpifb5 |
C |
A |
2: 154,066,876 (GRCm39) |
S43* |
probably null |
Het |
Carhsp1 |
A |
G |
16: 8,478,869 (GRCm39) |
V128A |
probably benign |
Het |
Ccdc141 |
A |
G |
2: 76,962,641 (GRCm39) |
V101A |
probably damaging |
Het |
Cdk6 |
C |
G |
5: 3,523,152 (GRCm39) |
L191V |
probably damaging |
Het |
Cgnl1 |
T |
G |
9: 71,632,416 (GRCm39) |
K312Q |
possibly damaging |
Het |
Col6a1 |
T |
C |
10: 76,557,277 (GRCm39) |
E225G |
probably damaging |
Het |
Copg1 |
T |
A |
6: 87,879,322 (GRCm39) |
L456Q |
probably damaging |
Het |
Ctif |
T |
A |
18: 75,570,279 (GRCm39) |
D540V |
possibly damaging |
Het |
Cyfip1 |
T |
C |
7: 55,569,241 (GRCm39) |
I917T |
probably benign |
Het |
Cyth1 |
T |
C |
11: 118,103,477 (GRCm39) |
D9G |
probably benign |
Het |
Dnajb1 |
T |
C |
8: 84,336,884 (GRCm39) |
I118T |
probably damaging |
Het |
Ebna1bp2 |
T |
A |
4: 118,480,575 (GRCm39) |
Y139* |
probably null |
Het |
Efcab3 |
A |
G |
11: 104,584,248 (GRCm39) |
T100A |
probably benign |
Het |
Fam162a |
A |
T |
16: 35,870,302 (GRCm39) |
V59E |
probably damaging |
Het |
Fhad1 |
CGG |
CG |
4: 141,645,602 (GRCm39) |
|
probably null |
Het |
Fmo6 |
C |
G |
1: 162,753,877 (GRCm39) |
R112T |
probably benign |
Het |
Gm17087 |
T |
A |
17: 8,785,304 (GRCm39) |
D133V |
probably benign |
Het |
Gm42669 |
A |
G |
5: 107,656,142 (GRCm39) |
I802V |
probably benign |
Het |
Gp2 |
T |
C |
7: 119,050,868 (GRCm39) |
N288D |
probably damaging |
Het |
Gstm7 |
C |
T |
3: 107,834,278 (GRCm39) |
D196N |
probably benign |
Het |
Hsph1 |
A |
T |
5: 149,553,865 (GRCm39) |
V201D |
probably damaging |
Het |
Il20ra |
T |
C |
10: 19,588,458 (GRCm39) |
L26P |
unknown |
Het |
Itpr1 |
T |
A |
6: 108,408,459 (GRCm39) |
|
probably null |
Het |
Kcns3 |
A |
T |
12: 11,141,688 (GRCm39) |
I337N |
probably damaging |
Het |
Kdm4d |
A |
G |
9: 14,375,475 (GRCm39) |
Y128H |
probably damaging |
Het |
Kirrel2 |
A |
G |
7: 30,153,999 (GRCm39) |
I200T |
probably benign |
Het |
Klhdc10 |
T |
A |
6: 30,450,502 (GRCm39) |
I294N |
probably damaging |
Het |
Map1a |
A |
C |
2: 121,130,720 (GRCm39) |
N512T |
probably damaging |
Het |
Marchf8 |
C |
G |
6: 116,380,504 (GRCm39) |
C118W |
probably damaging |
Het |
Marchf8 |
T |
G |
6: 116,380,505 (GRCm39) |
C119G |
probably damaging |
Het |
Mrpl38 |
G |
T |
11: 116,025,741 (GRCm39) |
P195Q |
probably damaging |
Het |
Ms4a4d |
A |
T |
19: 11,525,947 (GRCm39) |
Q27L |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,569,532 (GRCm39) |
T996S |
unknown |
Het |
Mug1 |
C |
T |
6: 121,838,084 (GRCm39) |
A438V |
probably benign |
Het |
Mup7 |
T |
A |
4: 60,069,866 (GRCm39) |
I33F |
probably damaging |
Het |
Ndufa5 |
C |
T |
6: 24,519,190 (GRCm39) |
|
probably null |
Het |
Or2b7 |
A |
G |
13: 21,740,108 (GRCm39) |
F28S |
probably benign |
Het |
Or2l5 |
A |
T |
16: 19,334,206 (GRCm39) |
F60Y |
probably benign |
Het |
Or5w17 |
T |
C |
2: 87,584,215 (GRCm39) |
I41V |
probably benign |
Het |
Or5w1b |
A |
T |
2: 87,476,320 (GRCm39) |
L49Q |
probably damaging |
Het |
Or7e177 |
T |
A |
9: 20,211,959 (GRCm39) |
C154* |
probably null |
Het |
Parp9 |
T |
A |
16: 35,780,433 (GRCm39) |
|
probably null |
Het |
Pate8 |
C |
A |
9: 36,493,854 (GRCm39) |
W26C |
unknown |
Het |
Pbx1 |
T |
A |
1: 168,258,949 (GRCm39) |
D42V |
probably damaging |
Het |
Pde4dip |
G |
T |
3: 97,622,738 (GRCm39) |
N1490K |
possibly damaging |
Het |
Pdzd2 |
T |
C |
15: 12,372,647 (GRCm39) |
N2496S |
probably benign |
Het |
Pdzd2 |
A |
G |
15: 12,373,061 (GRCm39) |
M2358T |
probably benign |
Het |
Pglyrp2 |
C |
A |
17: 32,634,904 (GRCm39) |
C486F |
probably damaging |
Het |
Pi4ka |
A |
G |
16: 17,114,931 (GRCm39) |
|
probably benign |
Het |
Pknox2 |
T |
A |
9: 36,820,963 (GRCm39) |
T300S |
probably damaging |
Het |
Plekhm3 |
A |
G |
1: 64,922,429 (GRCm39) |
I582T |
probably damaging |
Het |
Prtg |
T |
C |
9: 72,799,267 (GRCm39) |
Y766H |
possibly damaging |
Het |
Prxl2a |
T |
C |
14: 40,724,451 (GRCm39) |
E71G |
probably benign |
Het |
Rabgap1 |
A |
G |
2: 37,450,575 (GRCm39) |
E901G |
probably benign |
Het |
Rabgap1l |
A |
T |
1: 160,169,642 (GRCm39) |
N60K |
probably damaging |
Het |
Rnf150 |
C |
T |
8: 83,769,292 (GRCm39) |
T359I |
probably benign |
Het |
Rps6ka2 |
C |
T |
17: 7,523,331 (GRCm39) |
H236Y |
probably benign |
Het |
Rrp1b |
T |
A |
17: 32,268,401 (GRCm39) |
L120Q |
probably damaging |
Het |
Scn7a |
C |
A |
2: 66,572,303 (GRCm39) |
G223C |
probably null |
Het |
Sema6a |
T |
A |
18: 47,431,284 (GRCm39) |
N138I |
probably damaging |
Het |
Septin5 |
T |
A |
16: 18,443,659 (GRCm39) |
I97F |
probably damaging |
Het |
Shcbp1 |
T |
A |
8: 4,804,234 (GRCm39) |
E225D |
probably damaging |
Het |
Slc25a19 |
A |
G |
11: 115,511,792 (GRCm39) |
C124R |
probably damaging |
Het |
Slc37a2 |
C |
T |
9: 37,145,183 (GRCm39) |
A428T |
probably damaging |
Het |
Slc5a12 |
A |
G |
2: 110,474,709 (GRCm39) |
I538V |
probably benign |
Het |
Slco4c1 |
A |
T |
1: 96,751,506 (GRCm39) |
|
probably null |
Het |
Smarcad1 |
T |
C |
6: 65,029,654 (GRCm39) |
S81P |
probably damaging |
Het |
Smyd1 |
T |
C |
6: 71,215,611 (GRCm39) |
D116G |
probably damaging |
Het |
Themis |
T |
C |
10: 28,665,703 (GRCm39) |
Y589H |
probably benign |
Het |
Trim30d |
T |
C |
7: 104,132,543 (GRCm39) |
K248R |
probably benign |
Het |
Tspan12 |
C |
T |
6: 21,772,918 (GRCm39) |
M210I |
probably benign |
Het |
Vmn2r11 |
T |
C |
5: 109,201,289 (GRCm39) |
Y405C |
probably damaging |
Het |
Wdfy3 |
A |
G |
5: 102,042,775 (GRCm39) |
|
probably null |
Het |
Wiz |
C |
A |
17: 32,580,840 (GRCm39) |
A83S |
probably damaging |
Het |
Zmym6 |
T |
A |
4: 127,017,337 (GRCm39) |
Y947* |
probably null |
Het |
|
Other mutations in Zfp1002 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R6648_Gm21994_337
|
UTSW |
2 |
150,097,097 (GRCm39) |
missense |
probably benign |
0.01 |
R0853:Zfp1002
|
UTSW |
2 |
150,097,398 (GRCm39) |
missense |
probably benign |
0.30 |
R5135:Zfp1002
|
UTSW |
2 |
150,097,410 (GRCm39) |
nonsense |
probably null |
|
R5161:Zfp1002
|
UTSW |
2 |
150,097,135 (GRCm39) |
missense |
probably damaging |
0.99 |
R5782:Zfp1002
|
UTSW |
2 |
150,097,438 (GRCm39) |
missense |
probably benign |
0.41 |
R6019:Zfp1002
|
UTSW |
2 |
150,097,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R6284:Zfp1002
|
UTSW |
2 |
150,097,198 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6476:Zfp1002
|
UTSW |
2 |
150,097,246 (GRCm39) |
missense |
probably benign |
0.00 |
R6479:Zfp1002
|
UTSW |
2 |
150,096,511 (GRCm39) |
missense |
probably damaging |
0.99 |
R6648:Zfp1002
|
UTSW |
2 |
150,097,097 (GRCm39) |
missense |
probably benign |
0.01 |
R6736:Zfp1002
|
UTSW |
2 |
150,097,198 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6963:Zfp1002
|
UTSW |
2 |
150,097,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R7138:Zfp1002
|
UTSW |
2 |
150,097,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R7625:Zfp1002
|
UTSW |
2 |
150,096,520 (GRCm39) |
missense |
probably benign |
0.05 |
R7855:Zfp1002
|
UTSW |
2 |
150,097,066 (GRCm39) |
missense |
probably benign |
0.00 |
R8145:Zfp1002
|
UTSW |
2 |
150,096,455 (GRCm39) |
missense |
probably benign |
0.00 |
R8284:Zfp1002
|
UTSW |
2 |
150,097,276 (GRCm39) |
unclassified |
probably benign |
|
R9712:Zfp1002
|
UTSW |
2 |
150,096,496 (GRCm39) |
missense |
probably benign |
0.04 |
|