Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921536K21Rik |
T |
C |
11: 3,844,987 (GRCm39) |
D34G |
probably benign |
Het |
Adam6a |
T |
C |
12: 113,508,337 (GRCm39) |
S237P |
probably damaging |
Het |
Adamts13 |
A |
C |
2: 26,871,092 (GRCm39) |
D235A |
probably benign |
Het |
Adgb |
T |
A |
10: 10,233,623 (GRCm39) |
M1259L |
probably benign |
Het |
Apbb1 |
T |
C |
7: 105,214,510 (GRCm39) |
Q529R |
probably damaging |
Het |
Bcl2 |
G |
A |
1: 106,640,292 (GRCm39) |
R107C |
probably damaging |
Het |
Camta1 |
T |
C |
4: 151,670,888 (GRCm39) |
T96A |
possibly damaging |
Het |
Ccdc148 |
A |
T |
2: 58,894,084 (GRCm39) |
|
probably null |
Het |
Cep170b |
T |
C |
12: 112,703,240 (GRCm39) |
Y568H |
probably damaging |
Het |
Clca4b |
A |
T |
3: 144,627,741 (GRCm39) |
I410N |
probably damaging |
Het |
Cnot10 |
G |
A |
9: 114,427,838 (GRCm39) |
T592I |
probably benign |
Het |
Col6a3 |
C |
T |
1: 90,755,771 (GRCm39) |
A173T |
probably damaging |
Het |
Ctcf |
T |
A |
8: 106,402,789 (GRCm39) |
C560* |
probably null |
Het |
Daglb |
G |
A |
5: 143,472,951 (GRCm39) |
V369I |
probably benign |
Het |
Defb19 |
G |
A |
2: 152,422,146 (GRCm39) |
L8F |
unknown |
Het |
Emcn |
G |
T |
3: 137,078,608 (GRCm39) |
E65* |
probably null |
Het |
Etl4 |
G |
T |
2: 20,782,940 (GRCm39) |
R753L |
probably damaging |
Het |
Fam151b |
T |
C |
13: 92,586,689 (GRCm39) |
Y248C |
probably benign |
Het |
Fmo1 |
T |
C |
1: 162,663,704 (GRCm39) |
D275G |
probably benign |
Het |
Gjd4 |
A |
G |
18: 9,280,964 (GRCm39) |
V38A |
possibly damaging |
Het |
Hivep1 |
T |
C |
13: 42,311,855 (GRCm39) |
V1365A |
possibly damaging |
Het |
Hivep2 |
T |
C |
10: 14,005,702 (GRCm39) |
S767P |
possibly damaging |
Het |
Hoxa6 |
T |
C |
6: 52,183,548 (GRCm39) |
T166A |
possibly damaging |
Het |
Ift80 |
G |
T |
3: 68,843,232 (GRCm39) |
L367I |
probably benign |
Het |
Igf2bp1 |
T |
C |
11: 95,859,719 (GRCm39) |
N369S |
possibly damaging |
Het |
Igsf11 |
C |
A |
16: 38,829,179 (GRCm39) |
D24E |
probably benign |
Het |
Ints5 |
C |
T |
19: 8,873,114 (GRCm39) |
L358F |
probably damaging |
Het |
Kbtbd3 |
A |
G |
9: 4,330,519 (GRCm39) |
T298A |
possibly damaging |
Het |
Kif28 |
C |
A |
1: 179,558,818 (GRCm39) |
V297F |
probably damaging |
Het |
Krt12 |
T |
C |
11: 99,308,771 (GRCm39) |
Y422C |
probably damaging |
Het |
Lig1 |
T |
A |
7: 13,043,122 (GRCm39) |
W856R |
probably damaging |
Het |
Liph |
C |
T |
16: 21,786,730 (GRCm39) |
|
probably null |
Het |
Lrig3 |
T |
A |
10: 125,849,317 (GRCm39) |
C1012* |
probably null |
Het |
Lrit1 |
A |
G |
14: 36,782,182 (GRCm39) |
E285G |
probably damaging |
Het |
Lrrc31 |
A |
G |
3: 30,743,377 (GRCm39) |
V196A |
probably benign |
Het |
Lrrn4 |
T |
C |
2: 132,712,363 (GRCm39) |
T487A |
probably benign |
Het |
Mllt10 |
T |
C |
2: 18,167,424 (GRCm39) |
Y372H |
probably damaging |
Het |
Mrpl50 |
A |
T |
4: 49,514,515 (GRCm39) |
V52E |
probably damaging |
Het |
Mthfd1l |
T |
C |
10: 4,006,766 (GRCm39) |
V676A |
probably damaging |
Het |
Ncl |
C |
T |
1: 86,284,362 (GRCm39) |
D245N |
possibly damaging |
Het |
Neil1 |
A |
T |
9: 57,054,065 (GRCm39) |
|
probably null |
Het |
Nfatc3 |
A |
G |
8: 106,818,827 (GRCm39) |
E515G |
probably damaging |
Het |
Nlrp4b |
A |
G |
7: 10,449,108 (GRCm39) |
E70G |
possibly damaging |
Het |
Nme3 |
A |
T |
17: 25,115,491 (GRCm39) |
I2F |
possibly damaging |
Het |
Nxpe3 |
T |
A |
16: 55,686,898 (GRCm39) |
T37S |
probably benign |
Het |
Olfm1 |
T |
A |
2: 28,102,554 (GRCm39) |
M76K |
probably benign |
Het |
Pgbd5 |
A |
T |
8: 125,160,771 (GRCm39) |
V32E |
probably damaging |
Het |
Plcb4 |
T |
C |
2: 135,810,339 (GRCm39) |
M646T |
probably damaging |
Het |
Plekha7 |
G |
A |
7: 115,757,255 (GRCm39) |
P565L |
probably damaging |
Het |
Poc5 |
A |
G |
13: 96,535,374 (GRCm39) |
D213G |
probably null |
Het |
Poli |
A |
G |
18: 70,656,452 (GRCm39) |
I125T |
probably benign |
Het |
Ppm1f |
T |
C |
16: 16,721,254 (GRCm39) |
M1T |
probably null |
Het |
Psmd7 |
T |
C |
8: 108,307,523 (GRCm39) |
K320R |
unknown |
Het |
Rabggtb |
A |
G |
3: 153,615,954 (GRCm39) |
V128A |
probably damaging |
Het |
Rasa2 |
A |
T |
9: 96,454,012 (GRCm39) |
L308H |
probably damaging |
Het |
Serpina1d |
C |
T |
12: 103,730,034 (GRCm39) |
V383M |
probably benign |
Het |
Sipa1l1 |
T |
C |
12: 82,431,530 (GRCm39) |
|
probably null |
Het |
Sos1 |
T |
C |
17: 80,715,740 (GRCm39) |
T1006A |
probably benign |
Het |
Sugp1 |
T |
A |
8: 70,522,658 (GRCm39) |
Y453N |
probably damaging |
Het |
Taf3 |
A |
T |
2: 10,047,455 (GRCm39) |
D64E |
probably benign |
Het |
Tcf19 |
A |
T |
17: 35,826,801 (GRCm39) |
|
probably null |
Het |
Trim60 |
T |
A |
8: 65,453,868 (GRCm39) |
H127L |
probably damaging |
Het |
Tubb4a |
C |
T |
17: 57,387,770 (GRCm39) |
V419M |
probably damaging |
Het |
Vmn2r22 |
G |
T |
6: 123,614,684 (GRCm39) |
T302K |
probably damaging |
Het |
Vmn2r68 |
T |
G |
7: 84,870,884 (GRCm39) |
T800P |
possibly damaging |
Het |
Zfhx2 |
A |
C |
14: 55,300,965 (GRCm39) |
V2262G |
probably damaging |
Het |
|
Other mutations in Nup210 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01139:Nup210
|
APN |
6 |
91,007,079 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01532:Nup210
|
APN |
6 |
91,062,981 (GRCm39) |
splice site |
probably benign |
|
IGL01574:Nup210
|
APN |
6 |
91,017,546 (GRCm39) |
missense |
probably benign |
0.35 |
IGL01621:Nup210
|
APN |
6 |
91,007,099 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01976:Nup210
|
APN |
6 |
91,030,596 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02089:Nup210
|
APN |
6 |
91,053,680 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02291:Nup210
|
APN |
6 |
91,078,250 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03013:Nup210
|
APN |
6 |
91,030,361 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03046:Nup210
|
APN |
6 |
90,995,978 (GRCm39) |
splice site |
probably benign |
|
IGL03136:Nup210
|
APN |
6 |
91,005,843 (GRCm39) |
missense |
probably benign |
0.32 |
IGL03139:Nup210
|
APN |
6 |
90,997,221 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03195:Nup210
|
APN |
6 |
90,992,832 (GRCm39) |
missense |
probably benign |
0.32 |
IGL03344:Nup210
|
APN |
6 |
90,998,411 (GRCm39) |
missense |
possibly damaging |
0.53 |
brotherhood
|
UTSW |
6 |
91,013,451 (GRCm39) |
missense |
possibly damaging |
0.81 |
equality
|
UTSW |
6 |
90,998,377 (GRCm39) |
critical splice donor site |
probably null |
|
fraternity
|
UTSW |
6 |
91,019,235 (GRCm39) |
critical splice donor site |
probably null |
|
Liberty
|
UTSW |
6 |
90,997,162 (GRCm39) |
missense |
probably benign |
0.04 |
napoleonic
|
UTSW |
6 |
91,030,434 (GRCm39) |
missense |
probably damaging |
1.00 |
unity
|
UTSW |
6 |
91,008,650 (GRCm39) |
nonsense |
probably null |
|
IGL03134:Nup210
|
UTSW |
6 |
91,007,172 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4810001:Nup210
|
UTSW |
6 |
91,007,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R0100:Nup210
|
UTSW |
6 |
91,046,175 (GRCm39) |
missense |
probably benign |
0.04 |
R0385:Nup210
|
UTSW |
6 |
91,005,777 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0551:Nup210
|
UTSW |
6 |
90,998,466 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0606:Nup210
|
UTSW |
6 |
91,003,911 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1053:Nup210
|
UTSW |
6 |
91,005,793 (GRCm39) |
missense |
probably benign |
0.41 |
R1301:Nup210
|
UTSW |
6 |
91,019,329 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1381:Nup210
|
UTSW |
6 |
91,052,942 (GRCm39) |
missense |
probably damaging |
0.99 |
R1464:Nup210
|
UTSW |
6 |
91,030,551 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1464:Nup210
|
UTSW |
6 |
91,030,551 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1487:Nup210
|
UTSW |
6 |
91,019,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R1522:Nup210
|
UTSW |
6 |
91,046,148 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1529:Nup210
|
UTSW |
6 |
91,013,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R1531:Nup210
|
UTSW |
6 |
91,011,823 (GRCm39) |
missense |
probably benign |
0.05 |
R1668:Nup210
|
UTSW |
6 |
91,005,787 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1694:Nup210
|
UTSW |
6 |
91,039,785 (GRCm39) |
missense |
probably benign |
0.09 |
R1803:Nup210
|
UTSW |
6 |
91,051,264 (GRCm39) |
missense |
probably damaging |
0.99 |
R1851:Nup210
|
UTSW |
6 |
90,993,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R2145:Nup210
|
UTSW |
6 |
91,005,858 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2196:Nup210
|
UTSW |
6 |
91,032,226 (GRCm39) |
missense |
probably benign |
0.02 |
R2308:Nup210
|
UTSW |
6 |
91,017,850 (GRCm39) |
missense |
probably benign |
0.19 |
R2419:Nup210
|
UTSW |
6 |
90,994,538 (GRCm39) |
splice site |
probably benign |
|
R2912:Nup210
|
UTSW |
6 |
91,003,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R3413:Nup210
|
UTSW |
6 |
91,002,224 (GRCm39) |
missense |
probably benign |
0.00 |
R3718:Nup210
|
UTSW |
6 |
90,997,162 (GRCm39) |
missense |
probably benign |
0.04 |
R3753:Nup210
|
UTSW |
6 |
90,998,377 (GRCm39) |
critical splice donor site |
probably null |
|
R4058:Nup210
|
UTSW |
6 |
91,037,602 (GRCm39) |
missense |
probably benign |
0.02 |
R4840:Nup210
|
UTSW |
6 |
91,008,650 (GRCm39) |
nonsense |
probably null |
|
R4912:Nup210
|
UTSW |
6 |
90,994,511 (GRCm39) |
missense |
probably benign |
0.01 |
R4967:Nup210
|
UTSW |
6 |
91,013,451 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4996:Nup210
|
UTSW |
6 |
91,030,418 (GRCm39) |
missense |
probably benign |
0.16 |
R5074:Nup210
|
UTSW |
6 |
91,032,309 (GRCm39) |
missense |
probably benign |
0.16 |
R5233:Nup210
|
UTSW |
6 |
91,003,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R5352:Nup210
|
UTSW |
6 |
91,046,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R5490:Nup210
|
UTSW |
6 |
91,062,970 (GRCm39) |
missense |
probably damaging |
0.98 |
R5511:Nup210
|
UTSW |
6 |
91,003,945 (GRCm39) |
missense |
probably damaging |
0.97 |
R5773:Nup210
|
UTSW |
6 |
91,062,865 (GRCm39) |
missense |
probably damaging |
0.96 |
R6064:Nup210
|
UTSW |
6 |
91,032,273 (GRCm39) |
missense |
probably benign |
0.01 |
R6209:Nup210
|
UTSW |
6 |
91,002,337 (GRCm39) |
missense |
probably benign |
|
R6299:Nup210
|
UTSW |
6 |
91,051,270 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6705:Nup210
|
UTSW |
6 |
91,064,942 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6855:Nup210
|
UTSW |
6 |
91,017,835 (GRCm39) |
missense |
probably benign |
0.13 |
R6856:Nup210
|
UTSW |
6 |
91,064,895 (GRCm39) |
nonsense |
probably null |
|
R6911:Nup210
|
UTSW |
6 |
91,007,112 (GRCm39) |
missense |
probably damaging |
0.98 |
R6955:Nup210
|
UTSW |
6 |
91,064,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R7045:Nup210
|
UTSW |
6 |
91,031,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R7081:Nup210
|
UTSW |
6 |
91,037,647 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7163:Nup210
|
UTSW |
6 |
91,050,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R7305:Nup210
|
UTSW |
6 |
91,064,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R7387:Nup210
|
UTSW |
6 |
90,998,378 (GRCm39) |
critical splice donor site |
probably null |
|
R7404:Nup210
|
UTSW |
6 |
91,050,227 (GRCm39) |
missense |
probably benign |
0.01 |
R7469:Nup210
|
UTSW |
6 |
90,995,874 (GRCm39) |
missense |
probably benign |
0.08 |
R7603:Nup210
|
UTSW |
6 |
91,053,679 (GRCm39) |
missense |
probably benign |
0.00 |
R7731:Nup210
|
UTSW |
6 |
91,048,870 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7822:Nup210
|
UTSW |
6 |
90,995,759 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7944:Nup210
|
UTSW |
6 |
91,050,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R8032:Nup210
|
UTSW |
6 |
91,051,331 (GRCm39) |
missense |
probably benign |
0.02 |
R8039:Nup210
|
UTSW |
6 |
91,047,215 (GRCm39) |
missense |
probably benign |
0.09 |
R8081:Nup210
|
UTSW |
6 |
91,053,657 (GRCm39) |
missense |
probably benign |
0.00 |
R8177:Nup210
|
UTSW |
6 |
90,991,470 (GRCm39) |
missense |
probably benign |
|
R8331:Nup210
|
UTSW |
6 |
91,030,648 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8356:Nup210
|
UTSW |
6 |
91,051,330 (GRCm39) |
missense |
probably benign |
0.32 |
R8530:Nup210
|
UTSW |
6 |
91,053,627 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8896:Nup210
|
UTSW |
6 |
91,019,235 (GRCm39) |
critical splice donor site |
probably null |
|
R8926:Nup210
|
UTSW |
6 |
91,030,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R9093:Nup210
|
UTSW |
6 |
91,066,872 (GRCm39) |
missense |
probably benign |
0.16 |
R9130:Nup210
|
UTSW |
6 |
91,020,799 (GRCm39) |
missense |
probably benign |
0.08 |
R9136:Nup210
|
UTSW |
6 |
91,020,830 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9260:Nup210
|
UTSW |
6 |
91,039,785 (GRCm39) |
missense |
probably benign |
0.09 |
R9292:Nup210
|
UTSW |
6 |
91,051,235 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9444:Nup210
|
UTSW |
6 |
91,048,885 (GRCm39) |
missense |
probably benign |
|
R9482:Nup210
|
UTSW |
6 |
91,019,608 (GRCm39) |
missense |
probably damaging |
0.96 |
R9506:Nup210
|
UTSW |
6 |
91,048,856 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9621:Nup210
|
UTSW |
6 |
90,994,375 (GRCm39) |
missense |
probably benign |
0.18 |
R9735:Nup210
|
UTSW |
6 |
91,030,630 (GRCm39) |
missense |
probably benign |
0.42 |
X0067:Nup210
|
UTSW |
6 |
91,051,262 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Nup210
|
UTSW |
6 |
91,064,889 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1177:Nup210
|
UTSW |
6 |
90,997,167 (GRCm39) |
missense |
probably benign |
|
|