Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd11 |
T |
A |
5: 135,040,230 (GRCm39) |
V202D |
probably damaging |
Het |
Afdn |
A |
G |
17: 14,030,743 (GRCm39) |
N218S |
probably damaging |
Het |
Arhgef1 |
G |
A |
7: 24,625,208 (GRCm39) |
|
probably null |
Het |
Atp1a2 |
G |
T |
1: 172,103,754 (GRCm39) |
T959K |
probably damaging |
Het |
Atp6v0a2 |
A |
G |
5: 124,774,043 (GRCm39) |
E96G |
probably benign |
Het |
B9d1 |
A |
T |
11: 61,403,205 (GRCm39) |
M52L |
probably benign |
Het |
Col6a6 |
T |
A |
9: 105,661,108 (GRCm39) |
I334F |
probably damaging |
Het |
Drd3 |
T |
C |
16: 43,638,671 (GRCm39) |
F259L |
probably benign |
Het |
Drosha |
T |
G |
15: 12,889,805 (GRCm39) |
L891R |
probably damaging |
Het |
Ecpas |
G |
T |
4: 58,861,544 (GRCm39) |
T345K |
probably benign |
Het |
Garin5b |
T |
C |
7: 4,773,694 (GRCm39) |
N67S |
possibly damaging |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Greb1l |
T |
C |
18: 10,557,280 (GRCm39) |
V1760A |
possibly damaging |
Het |
Il36b |
T |
A |
2: 24,045,291 (GRCm39) |
W48R |
probably damaging |
Het |
Ipo9 |
C |
A |
1: 135,333,624 (GRCm39) |
V353F |
probably damaging |
Het |
Kmt2a |
A |
T |
9: 44,761,064 (GRCm39) |
F126I |
probably damaging |
Het |
Mmrn1 |
T |
C |
6: 60,948,167 (GRCm39) |
|
probably null |
Het |
Or9g19 |
A |
G |
2: 85,600,384 (GRCm39) |
I80V |
probably damaging |
Het |
Pcdh17 |
G |
T |
14: 84,684,960 (GRCm39) |
V476L |
probably benign |
Het |
Pcdh17 |
T |
A |
14: 84,684,961 (GRCm39) |
V476E |
probably damaging |
Het |
Prpf38b |
A |
T |
3: 108,811,991 (GRCm39) |
S291R |
probably benign |
Het |
Rap1gap |
T |
C |
4: 137,452,931 (GRCm39) |
S601P |
probably damaging |
Het |
Rnf213 |
T |
C |
11: 119,307,283 (GRCm39) |
Y648H |
probably benign |
Het |
Slfn3 |
A |
G |
11: 83,103,974 (GRCm39) |
T282A |
possibly damaging |
Het |
Ttll3 |
C |
T |
6: 113,391,076 (GRCm39) |
T887I |
probably benign |
Het |
Vmn1r197 |
A |
G |
13: 22,512,508 (GRCm39) |
N143S |
possibly damaging |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
Xpo4 |
T |
C |
14: 57,841,855 (GRCm39) |
I487V |
probably benign |
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 |
|
IGL01409:Nup214
|
APN |
2 |
31,916,943 (GRCm39) |
splice site |
probably null |
|
IGL01530:Nup214
|
APN |
2 |
31,923,733 (GRCm39) |
missense |
probably benign |
|
IGL01554:Nup214
|
APN |
2 |
31,941,084 (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 |
|