Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahctf1 |
A |
G |
1: 179,596,599 (GRCm39) |
V126A |
probably damaging |
Het |
Akap9 |
T |
C |
5: 4,119,130 (GRCm39) |
Y3546H |
possibly damaging |
Het |
Ank2 |
C |
A |
3: 126,749,519 (GRCm39) |
E503D |
probably damaging |
Het |
Arhgap45 |
C |
A |
10: 79,853,768 (GRCm39) |
T94N |
probably benign |
Het |
Arid1b |
T |
C |
17: 5,392,166 (GRCm39) |
S1899P |
possibly damaging |
Het |
Atad5 |
T |
A |
11: 79,980,601 (GRCm39) |
V2E |
probably damaging |
Het |
Calr |
A |
T |
8: 85,571,528 (GRCm39) |
V155E |
probably benign |
Het |
Cckbr |
C |
T |
7: 105,083,238 (GRCm39) |
A147V |
probably damaging |
Het |
Ces1d |
C |
A |
8: 93,896,346 (GRCm39) |
|
probably null |
Het |
Cetn1 |
T |
C |
18: 9,619,422 (GRCm39) |
|
probably benign |
Het |
Chl1 |
A |
T |
6: 103,618,949 (GRCm39) |
L6F |
probably damaging |
Het |
Chrnb1 |
C |
T |
11: 69,675,935 (GRCm39) |
V436I |
possibly damaging |
Het |
Col4a4 |
T |
C |
1: 82,506,204 (GRCm39) |
E292G |
unknown |
Het |
Ddx56 |
A |
G |
11: 6,217,667 (GRCm39) |
L18P |
probably damaging |
Het |
Dhx36 |
A |
C |
3: 62,384,797 (GRCm39) |
|
probably benign |
Het |
Dnah5 |
A |
T |
15: 28,453,358 (GRCm39) |
R4376S |
possibly damaging |
Het |
Dnah6 |
T |
A |
6: 73,185,582 (GRCm39) |
D113V |
probably benign |
Het |
Dnah7a |
A |
G |
1: 53,512,118 (GRCm39) |
|
probably benign |
Het |
Dock7 |
T |
A |
4: 98,833,442 (GRCm39) |
K1920* |
probably null |
Het |
Dysf |
A |
G |
6: 84,076,471 (GRCm39) |
D628G |
probably benign |
Het |
Exoc3l2 |
A |
G |
7: 19,229,109 (GRCm39) |
I176V |
probably benign |
Het |
Fcrl1 |
A |
G |
3: 87,292,012 (GRCm39) |
Y57C |
probably damaging |
Het |
Fzd4 |
C |
T |
7: 89,057,162 (GRCm39) |
T403M |
probably damaging |
Het |
Gpr171 |
A |
T |
3: 59,005,288 (GRCm39) |
N162K |
probably benign |
Het |
Impdh1 |
T |
A |
6: 29,206,924 (GRCm39) |
K132* |
probably null |
Het |
Itgb2l |
A |
T |
16: 96,223,850 (GRCm39) |
W730R |
possibly damaging |
Het |
Jmjd8 |
T |
C |
17: 26,049,134 (GRCm39) |
F230S |
probably damaging |
Het |
Krt72 |
G |
A |
15: 101,690,556 (GRCm39) |
T232M |
probably damaging |
Het |
Lpin3 |
T |
C |
2: 160,740,540 (GRCm39) |
|
probably benign |
Het |
Or11g7 |
A |
T |
14: 50,690,507 (GRCm39) |
|
probably benign |
Het |
Or7d10 |
A |
G |
9: 19,831,747 (GRCm39) |
M81V |
probably damaging |
Het |
Or8c20 |
A |
G |
9: 38,260,469 (GRCm39) |
Q24R |
probably benign |
Het |
Or8g26 |
A |
G |
9: 39,095,822 (GRCm39) |
Y113C |
probably damaging |
Het |
Pdgfra |
T |
A |
5: 75,355,635 (GRCm39) |
S1048R |
probably damaging |
Het |
Sall3 |
G |
T |
18: 81,012,728 (GRCm39) |
A1236E |
probably damaging |
Het |
Sipa1 |
T |
C |
19: 5,705,736 (GRCm39) |
T411A |
probably damaging |
Het |
Thsd7a |
T |
G |
6: 12,500,994 (GRCm39) |
D471A |
probably benign |
Het |
Tm2d1 |
T |
A |
4: 98,263,192 (GRCm39) |
E100D |
probably damaging |
Het |
Tmcc1 |
A |
G |
6: 116,110,849 (GRCm39) |
V148A |
probably damaging |
Het |
Tubgcp6 |
A |
T |
15: 88,986,518 (GRCm39) |
Y19* |
probably null |
Het |
Ubr3 |
A |
G |
2: 69,783,203 (GRCm39) |
Y713C |
probably damaging |
Het |
Uevld |
A |
G |
7: 46,605,377 (GRCm39) |
V39A |
probably benign |
Het |
Vmn2r28 |
A |
T |
7: 5,484,003 (GRCm39) |
H732Q |
probably damaging |
Het |
Zfp629 |
A |
T |
7: 127,209,484 (GRCm39) |
F775Y |
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 |
|
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 |
|
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 |
|
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 |
|