Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930011G23Rik |
A |
T |
5: 99,391,067 (GRCm39) |
F97L |
probably benign |
Het |
Acad10 |
T |
C |
5: 121,764,145 (GRCm39) |
Y928C |
probably benign |
Het |
Aqp7 |
A |
G |
4: 41,045,326 (GRCm39) |
M18T |
probably benign |
Het |
Atxn7 |
T |
C |
14: 14,052,994 (GRCm38) |
V144A |
probably damaging |
Het |
Baiap2l2 |
T |
A |
15: 79,155,753 (GRCm39) |
N107I |
probably damaging |
Het |
Cd180 |
A |
G |
13: 102,842,924 (GRCm39) |
K657E |
probably damaging |
Het |
Cep192 |
T |
C |
18: 67,961,547 (GRCm39) |
|
probably null |
Het |
Cma2 |
A |
G |
14: 56,211,256 (GRCm39) |
I183V |
probably damaging |
Het |
Col18a1 |
C |
A |
10: 76,949,177 (GRCm39) |
A112S |
possibly damaging |
Het |
Ctu2 |
A |
G |
8: 123,205,446 (GRCm39) |
D100G |
possibly damaging |
Het |
Defb29 |
T |
C |
2: 152,380,812 (GRCm39) |
K66E |
probably damaging |
Het |
Dis3l |
T |
A |
9: 64,219,232 (GRCm39) |
D566V |
probably damaging |
Het |
Dtx1 |
C |
A |
5: 120,832,955 (GRCm39) |
R161L |
probably damaging |
Het |
Efcab6 |
T |
A |
15: 83,836,422 (GRCm39) |
L436F |
probably benign |
Het |
Fip1l1 |
A |
G |
5: 74,731,776 (GRCm39) |
I254V |
possibly damaging |
Het |
Gid8 |
C |
A |
2: 180,356,501 (GRCm39) |
A46E |
probably damaging |
Het |
Grm8 |
G |
T |
6: 27,618,649 (GRCm39) |
Q398K |
probably damaging |
Het |
Hsd17b7 |
C |
T |
1: 169,780,649 (GRCm39) |
E320K |
probably damaging |
Het |
Iigp1c |
T |
C |
18: 60,379,221 (GRCm39) |
V252A |
probably benign |
Het |
Kcnt1 |
T |
C |
2: 25,784,480 (GRCm39) |
|
probably benign |
Het |
Lrrc8a |
T |
C |
2: 30,145,683 (GRCm39) |
S166P |
probably damaging |
Het |
Map2k6 |
A |
T |
11: 110,387,299 (GRCm39) |
|
probably benign |
Het |
Mmab |
A |
G |
5: 114,571,405 (GRCm39) |
L157P |
probably damaging |
Het |
Mmrn1 |
A |
T |
6: 60,953,324 (GRCm39) |
E535V |
probably damaging |
Het |
Mup4 |
T |
C |
4: 59,958,482 (GRCm39) |
|
probably benign |
Het |
Or52b4 |
A |
G |
7: 102,184,517 (GRCm39) |
K188E |
possibly damaging |
Het |
Pik3cg |
T |
C |
12: 32,242,222 (GRCm39) |
I963V |
probably damaging |
Het |
Plcg1 |
T |
C |
2: 160,590,049 (GRCm39) |
|
probably null |
Het |
Plscr1 |
T |
C |
9: 92,148,438 (GRCm39) |
|
probably benign |
Het |
Prss36 |
C |
T |
7: 127,532,783 (GRCm39) |
G202E |
probably damaging |
Het |
Psen2 |
A |
T |
1: 180,068,350 (GRCm39) |
V101E |
probably damaging |
Het |
Saxo1 |
T |
C |
4: 86,405,999 (GRCm39) |
M67V |
possibly damaging |
Het |
Sfrp4 |
G |
A |
13: 19,807,728 (GRCm39) |
M42I |
probably damaging |
Het |
Strn3 |
C |
A |
12: 51,699,633 (GRCm39) |
|
probably benign |
Het |
Tgfb1i1 |
C |
A |
7: 127,848,476 (GRCm39) |
P197Q |
possibly damaging |
Het |
Thsd4 |
A |
G |
9: 59,904,456 (GRCm39) |
V580A |
probably benign |
Het |
Tjp1 |
C |
A |
7: 64,990,182 (GRCm39) |
|
probably benign |
Het |
Tprn |
C |
T |
2: 25,154,066 (GRCm39) |
A456V |
probably benign |
Het |
Ttc34 |
T |
C |
4: 154,945,727 (GRCm39) |
Y763H |
probably benign |
Het |
Ttn |
T |
C |
2: 76,601,507 (GRCm39) |
T18686A |
probably benign |
Het |
Uggt2 |
T |
A |
14: 119,332,722 (GRCm39) |
T71S |
probably benign |
Het |
Vmn2r120 |
T |
A |
17: 57,831,742 (GRCm39) |
Y349F |
probably benign |
Het |
Zbtb41 |
A |
G |
1: 139,351,576 (GRCm39) |
T230A |
probably benign |
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 |
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 |
R0348:Nup210
|
UTSW |
6 |
91,051,292 (GRCm39) |
missense |
probably benign |
0.27 |
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 |
|
|