Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb3 |
C |
T |
10: 85,494,029 (GRCm39) |
A1049V |
possibly damaging |
Het |
Arhgap26 |
C |
T |
18: 39,243,504 (GRCm39) |
|
probably benign |
Het |
Asxl1 |
T |
C |
2: 153,234,860 (GRCm39) |
|
probably benign |
Het |
Atm |
A |
T |
9: 53,410,471 (GRCm39) |
V1037E |
probably benign |
Het |
Bmp6 |
A |
G |
13: 38,669,865 (GRCm39) |
N383S |
probably damaging |
Het |
Btf3l4 |
A |
C |
4: 108,676,394 (GRCm39) |
S103R |
probably damaging |
Het |
Cadps2 |
T |
C |
6: 23,587,440 (GRCm39) |
D321G |
probably damaging |
Het |
Col24a1 |
G |
A |
3: 145,244,319 (GRCm39) |
S1531N |
probably benign |
Het |
Cpb1 |
T |
A |
3: 20,303,969 (GRCm39) |
Y365F |
possibly damaging |
Het |
Dpp6 |
T |
C |
5: 27,762,599 (GRCm39) |
Y238H |
probably damaging |
Het |
Epha6 |
G |
A |
16: 59,476,100 (GRCm39) |
R1089* |
probably null |
Het |
Fga |
T |
C |
3: 82,940,059 (GRCm39) |
F571S |
probably damaging |
Het |
Focad |
A |
G |
4: 88,260,542 (GRCm39) |
T933A |
unknown |
Het |
Gm57858 |
T |
A |
3: 36,080,077 (GRCm39) |
M227L |
possibly damaging |
Het |
Gria2 |
A |
G |
3: 80,615,004 (GRCm39) |
|
probably null |
Het |
Hnrnpul1 |
T |
C |
7: 25,424,077 (GRCm39) |
N725S |
unknown |
Het |
Ik |
A |
T |
18: 36,889,974 (GRCm39) |
K534N |
probably damaging |
Het |
Itga8 |
T |
C |
2: 12,196,525 (GRCm39) |
T631A |
probably benign |
Het |
Kcnip1 |
G |
T |
11: 33,580,593 (GRCm39) |
D214E |
probably benign |
Het |
Kcnk10 |
A |
T |
12: 98,456,322 (GRCm39) |
Y170N |
probably damaging |
Het |
Lalba |
A |
G |
15: 98,379,948 (GRCm39) |
|
probably null |
Het |
Ly75 |
A |
T |
2: 60,152,036 (GRCm39) |
|
probably null |
Het |
Myh10 |
T |
C |
11: 68,698,045 (GRCm39) |
L1629P |
probably damaging |
Het |
Myo15b |
C |
A |
11: 115,760,330 (GRCm39) |
C1127* |
probably null |
Het |
Neurl4 |
T |
G |
11: 69,797,925 (GRCm39) |
N728K |
probably damaging |
Het |
Nrxn3 |
T |
A |
12: 89,477,128 (GRCm39) |
F801Y |
probably damaging |
Het |
Obscn |
G |
A |
11: 58,921,884 (GRCm39) |
R6624C |
probably damaging |
Het |
Or2g1 |
T |
C |
17: 38,106,413 (GRCm39) |
F26S |
probably damaging |
Het |
Pdk1 |
A |
G |
2: 71,726,123 (GRCm39) |
T344A |
probably benign |
Het |
Pitx2 |
C |
A |
3: 129,008,413 (GRCm39) |
S63Y |
probably damaging |
Het |
Ppara |
A |
C |
15: 85,661,844 (GRCm39) |
L28F |
probably damaging |
Het |
Rad54l |
G |
A |
4: 115,963,074 (GRCm39) |
T308I |
probably damaging |
Het |
Sbds |
T |
C |
5: 130,282,907 (GRCm39) |
E7G |
probably damaging |
Het |
Slc22a19 |
T |
C |
19: 7,688,495 (GRCm39) |
I22V |
probably benign |
Het |
Slfn10-ps |
T |
C |
11: 82,926,322 (GRCm39) |
|
noncoding transcript |
Het |
Spag4 |
T |
C |
2: 155,911,252 (GRCm39) |
S396P |
possibly damaging |
Het |
Spef2 |
C |
A |
15: 9,716,499 (GRCm39) |
L362F |
probably damaging |
Het |
Srebf2 |
A |
G |
15: 82,055,419 (GRCm39) |
T208A |
probably damaging |
Het |
Ssc5d |
A |
G |
7: 4,945,808 (GRCm39) |
T947A |
probably benign |
Het |
Tdp1 |
T |
C |
12: 99,875,940 (GRCm39) |
I297T |
possibly damaging |
Het |
Tent5c |
A |
T |
3: 100,380,485 (GRCm39) |
D90E |
probably damaging |
Het |
Tsen2 |
T |
C |
6: 115,536,555 (GRCm39) |
Y104H |
possibly damaging |
Het |
Was |
G |
A |
X: 7,954,055 (GRCm39) |
R229C |
probably damaging |
Het |
|
Other mutations in Nup214 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00490:Nup214
|
APN |
2 |
31,923,991 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00649:Nup214
|
APN |
2 |
31,896,733 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01149:Nup214
|
APN |
2 |
31,924,712 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01360:Nup214
|
APN |
2 |
31,928,190 (GRCm39) |
unclassified |
probably benign |
|
IGL01530:Nup214
|
APN |
2 |
31,923,733 (GRCm39) |
missense |
probably benign |
|
IGL01554:Nup214
|
APN |
2 |
31,941,084 (GRCm39) |
nonsense |
probably null |
|
IGL01944:Nup214
|
APN |
2 |
31,924,971 (GRCm39) |
nonsense |
probably null |
|
IGL02296:Nup214
|
APN |
2 |
31,878,200 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02563:Nup214
|
APN |
2 |
31,867,872 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02688:Nup214
|
APN |
2 |
31,921,287 (GRCm39) |
missense |
probably benign |
|
IGL02858:Nup214
|
APN |
2 |
31,900,384 (GRCm39) |
splice site |
probably benign |
|
IGL02953:Nup214
|
APN |
2 |
31,878,241 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03090:Nup214
|
APN |
2 |
31,908,254 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03124:Nup214
|
APN |
2 |
31,886,452 (GRCm39) |
missense |
probably benign |
0.27 |
IGL03225:Nup214
|
APN |
2 |
31,924,423 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03375:Nup214
|
APN |
2 |
31,900,233 (GRCm39) |
missense |
probably damaging |
0.97 |
Des_moines
|
UTSW |
2 |
31,870,596 (GRCm39) |
splice site |
probably null |
|
ANU74:Nup214
|
UTSW |
2 |
31,924,978 (GRCm39) |
missense |
probably damaging |
0.99 |
R0035:Nup214
|
UTSW |
2 |
31,880,379 (GRCm39) |
splice site |
probably null |
|
R0243:Nup214
|
UTSW |
2 |
31,888,069 (GRCm39) |
splice site |
probably benign |
|
R0270:Nup214
|
UTSW |
2 |
31,924,826 (GRCm39) |
missense |
probably damaging |
0.96 |
R0358:Nup214
|
UTSW |
2 |
31,894,312 (GRCm39) |
splice site |
probably null |
|
R1168:Nup214
|
UTSW |
2 |
31,915,313 (GRCm39) |
missense |
probably benign |
|
R1242:Nup214
|
UTSW |
2 |
31,867,782 (GRCm39) |
missense |
probably benign |
0.00 |
R1481:Nup214
|
UTSW |
2 |
31,924,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R1482:Nup214
|
UTSW |
2 |
31,924,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R1579:Nup214
|
UTSW |
2 |
31,924,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R1580:Nup214
|
UTSW |
2 |
31,924,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R1581:Nup214
|
UTSW |
2 |
31,924,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R1610:Nup214
|
UTSW |
2 |
31,924,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R1894:Nup214
|
UTSW |
2 |
31,886,392 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2146:Nup214
|
UTSW |
2 |
31,924,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R2149:Nup214
|
UTSW |
2 |
31,924,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R2293:Nup214
|
UTSW |
2 |
31,916,887 (GRCm39) |
missense |
probably benign |
|
R2924:Nup214
|
UTSW |
2 |
31,888,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R2925:Nup214
|
UTSW |
2 |
31,888,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R3037:Nup214
|
UTSW |
2 |
31,866,632 (GRCm39) |
missense |
probably benign |
0.00 |
R3426:Nup214
|
UTSW |
2 |
31,923,415 (GRCm39) |
missense |
probably damaging |
0.97 |
R3799:Nup214
|
UTSW |
2 |
31,924,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R3843:Nup214
|
UTSW |
2 |
31,941,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R4323:Nup214
|
UTSW |
2 |
31,884,696 (GRCm39) |
missense |
probably benign |
|
R4353:Nup214
|
UTSW |
2 |
31,867,929 (GRCm39) |
critical splice donor site |
probably null |
|
R4601:Nup214
|
UTSW |
2 |
31,887,977 (GRCm39) |
missense |
probably benign |
0.36 |
R4626:Nup214
|
UTSW |
2 |
31,923,416 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4874:Nup214
|
UTSW |
2 |
31,870,596 (GRCm39) |
splice site |
probably null |
|
R4938:Nup214
|
UTSW |
2 |
31,873,171 (GRCm39) |
missense |
probably benign |
0.00 |
R4939:Nup214
|
UTSW |
2 |
31,873,171 (GRCm39) |
missense |
probably benign |
0.00 |
R5027:Nup214
|
UTSW |
2 |
31,881,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R5358:Nup214
|
UTSW |
2 |
31,907,158 (GRCm39) |
missense |
unknown |
|
R5406:Nup214
|
UTSW |
2 |
31,892,619 (GRCm39) |
missense |
probably damaging |
0.96 |
R5507:Nup214
|
UTSW |
2 |
31,878,188 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5695:Nup214
|
UTSW |
2 |
31,924,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R5744:Nup214
|
UTSW |
2 |
31,900,308 (GRCm39) |
missense |
probably damaging |
0.97 |
R5908:Nup214
|
UTSW |
2 |
31,881,353 (GRCm39) |
missense |
probably benign |
0.03 |
R5967:Nup214
|
UTSW |
2 |
31,869,790 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6140:Nup214
|
UTSW |
2 |
31,941,808 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6243:Nup214
|
UTSW |
2 |
31,892,944 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6488:Nup214
|
UTSW |
2 |
31,881,384 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6934:Nup214
|
UTSW |
2 |
31,872,683 (GRCm39) |
nonsense |
probably null |
|
R6970:Nup214
|
UTSW |
2 |
31,941,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R7028:Nup214
|
UTSW |
2 |
31,924,168 (GRCm39) |
missense |
probably benign |
0.22 |
R7114:Nup214
|
UTSW |
2 |
31,915,256 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7120:Nup214
|
UTSW |
2 |
31,941,054 (GRCm39) |
missense |
probably benign |
0.07 |
R7249:Nup214
|
UTSW |
2 |
31,878,245 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7821:Nup214
|
UTSW |
2 |
31,916,917 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8026:Nup214
|
UTSW |
2 |
31,923,362 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8264:Nup214
|
UTSW |
2 |
31,884,738 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8284:Nup214
|
UTSW |
2 |
31,886,458 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8356:Nup214
|
UTSW |
2 |
31,929,372 (GRCm39) |
missense |
probably benign |
0.05 |
R8397:Nup214
|
UTSW |
2 |
31,880,266 (GRCm39) |
missense |
probably damaging |
0.96 |
R8456:Nup214
|
UTSW |
2 |
31,929,372 (GRCm39) |
missense |
probably benign |
0.05 |
R8785:Nup214
|
UTSW |
2 |
31,924,465 (GRCm39) |
missense |
probably damaging |
0.97 |
R9257:Nup214
|
UTSW |
2 |
31,923,347 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9291:Nup214
|
UTSW |
2 |
31,867,806 (GRCm39) |
missense |
probably benign |
0.00 |
R9376:Nup214
|
UTSW |
2 |
31,924,244 (GRCm39) |
missense |
probably benign |
0.00 |
R9408:Nup214
|
UTSW |
2 |
31,937,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R9613:Nup214
|
UTSW |
2 |
31,901,035 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9789:Nup214
|
UTSW |
2 |
31,907,227 (GRCm39) |
missense |
possibly damaging |
0.46 |
RF015:Nup214
|
UTSW |
2 |
31,924,718 (GRCm39) |
missense |
probably benign |
0.00 |
X0026:Nup214
|
UTSW |
2 |
31,910,318 (GRCm39) |
missense |
possibly damaging |
0.46 |
X0065:Nup214
|
UTSW |
2 |
31,932,488 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Nup214
|
UTSW |
2 |
31,901,235 (GRCm39) |
missense |
probably benign |
0.27 |
Z1176:Nup214
|
UTSW |
2 |
31,924,237 (GRCm39) |
nonsense |
probably null |
|
Z1176:Nup214
|
UTSW |
2 |
31,900,270 (GRCm39) |
missense |
possibly damaging |
0.66 |
Z1177:Nup214
|
UTSW |
2 |
31,887,971 (GRCm39) |
missense |
possibly damaging |
0.83 |
|