Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930550C14Rik |
A |
G |
9: 53,319,372 (GRCm39) |
K4R |
possibly damaging |
Het |
A830018L16Rik |
G |
A |
1: 11,484,848 (GRCm39) |
G19D |
probably damaging |
Het |
Abca3 |
A |
T |
17: 24,583,916 (GRCm39) |
M102L |
probably benign |
Het |
Adam19 |
A |
T |
11: 46,022,544 (GRCm39) |
Y499F |
probably benign |
Het |
Adck2 |
T |
C |
6: 39,560,797 (GRCm39) |
V444A |
probably damaging |
Het |
Adck5 |
T |
C |
15: 76,478,016 (GRCm39) |
V214A |
probably damaging |
Het |
Agrn |
G |
A |
4: 156,262,966 (GRCm39) |
T437M |
probably damaging |
Het |
Aox3 |
A |
T |
1: 58,158,671 (GRCm39) |
I81F |
probably damaging |
Het |
Bcl6 |
G |
A |
16: 23,784,976 (GRCm39) |
R675* |
probably null |
Het |
Blmh |
A |
G |
11: 76,836,987 (GRCm39) |
Y23C |
unknown |
Het |
Cacnb1 |
A |
G |
11: 97,903,726 (GRCm39) |
V109A |
probably benign |
Het |
Ccdc27 |
C |
T |
4: 154,117,282 (GRCm39) |
R555H |
not run |
Het |
Cep170 |
A |
C |
1: 176,602,031 (GRCm39) |
S358R |
probably damaging |
Het |
Cfap46 |
A |
T |
7: 139,197,994 (GRCm39) |
|
probably null |
Het |
Dclk1 |
G |
T |
3: 55,163,549 (GRCm39) |
E214* |
probably null |
Het |
Dhrs1 |
A |
G |
14: 55,976,838 (GRCm39) |
L282P |
probably benign |
Het |
Dlgap5 |
A |
G |
14: 47,637,095 (GRCm39) |
L461P |
probably damaging |
Het |
Elp2 |
G |
T |
18: 24,747,503 (GRCm39) |
C185F |
probably benign |
Het |
Fbxw7 |
T |
C |
3: 84,832,892 (GRCm39) |
|
probably benign |
Het |
Fga |
T |
C |
3: 82,933,571 (GRCm39) |
V17A |
probably benign |
Het |
Gdi1 |
G |
A |
X: 73,350,461 (GRCm39) |
R55H |
probably benign |
Het |
Gm43302 |
T |
A |
5: 105,441,493 (GRCm39) |
|
probably null |
Het |
Gpatch8 |
TTCCTCCTCCTCCTCTTCCTCCTCCTC |
TTCCTCCTCCTCCTCCTCTTCCTCCTCCTC |
11: 102,371,014 (GRCm39) |
|
probably benign |
Het |
Hcn1 |
A |
T |
13: 118,062,083 (GRCm39) |
I450L |
unknown |
Het |
Hydin |
T |
A |
8: 111,329,968 (GRCm39) |
C4901S |
probably benign |
Het |
Ino80 |
A |
T |
2: 119,223,356 (GRCm39) |
I1186N |
probably damaging |
Het |
Ints7 |
T |
A |
1: 191,349,949 (GRCm39) |
I781N |
possibly damaging |
Het |
Irf2 |
T |
A |
8: 47,290,712 (GRCm39) |
V178E |
possibly damaging |
Het |
Iws1 |
T |
A |
18: 32,226,277 (GRCm39) |
S722T |
possibly damaging |
Het |
Jak1 |
G |
A |
4: 101,032,385 (GRCm39) |
S407F |
probably damaging |
Het |
Kdm3a |
G |
T |
6: 71,609,061 (GRCm39) |
D55E |
probably damaging |
Het |
Kdm5d |
T |
C |
Y: 899,940 (GRCm39) |
S169P |
probably damaging |
Het |
Kif15 |
A |
G |
9: 122,846,722 (GRCm39) |
N1348S |
probably damaging |
Het |
Kpna7 |
G |
A |
5: 144,939,206 (GRCm39) |
P187L |
unknown |
Het |
Krt35 |
A |
T |
11: 99,986,984 (GRCm39) |
F10Y |
probably damaging |
Het |
Lemd1 |
G |
T |
1: 132,184,475 (GRCm39) |
V131F |
probably benign |
Het |
Mcf2l |
G |
A |
8: 12,965,439 (GRCm39) |
R4H |
probably benign |
Het |
Megf6 |
C |
T |
4: 154,351,898 (GRCm39) |
R1166C |
probably damaging |
Het |
Mmp11 |
T |
C |
10: 75,762,410 (GRCm39) |
I308V |
possibly damaging |
Het |
Mrgpra4 |
A |
G |
7: 47,631,238 (GRCm39) |
V121A |
probably benign |
Het |
Myl2 |
T |
A |
5: 122,239,885 (GRCm39) |
I26N |
probably damaging |
Het |
Myo15a |
A |
G |
11: 60,389,195 (GRCm39) |
M862V |
|
Het |
Nckap5l |
T |
C |
15: 99,331,354 (GRCm39) |
H64R |
probably damaging |
Het |
Nipsnap2 |
A |
C |
5: 129,821,774 (GRCm39) |
E90A |
probably benign |
Het |
Or2h2 |
T |
C |
17: 37,396,937 (GRCm39) |
N40S |
probably damaging |
Het |
Or2t48 |
C |
A |
11: 58,419,994 (GRCm39) |
E273* |
probably null |
Het |
Or5m11b |
T |
A |
2: 85,805,932 (GRCm39) |
L115Q |
probably damaging |
Het |
Or8c19-ps1 |
T |
C |
9: 38,220,345 (GRCm39) |
F85L |
probably damaging |
Het |
Or9e1 |
T |
C |
11: 58,732,012 (GRCm39) |
V24A |
probably benign |
Het |
Pcmt1 |
A |
T |
10: 7,513,922 (GRCm39) |
M249K |
probably benign |
Het |
Pde3a |
T |
C |
6: 141,433,270 (GRCm39) |
L767P |
probably damaging |
Het |
Pde8a |
T |
C |
7: 80,956,456 (GRCm39) |
V285A |
possibly damaging |
Het |
Pla2g4a |
T |
A |
1: 149,716,416 (GRCm39) |
K690* |
probably null |
Het |
Plxna4 |
T |
C |
6: 32,473,691 (GRCm39) |
H442R |
probably benign |
Het |
Polr1b |
A |
G |
2: 128,967,931 (GRCm39) |
D1108G |
probably benign |
Het |
Prkn |
G |
A |
17: 12,280,434 (GRCm39) |
C430Y |
probably damaging |
Het |
Sec23ip |
T |
C |
7: 128,364,257 (GRCm39) |
|
probably null |
Het |
Slc24a3 |
A |
G |
2: 145,086,911 (GRCm39) |
D57G |
probably benign |
Het |
Sprtn |
T |
G |
8: 125,625,044 (GRCm39) |
F50V |
probably damaging |
Het |
Srr |
A |
G |
11: 74,803,828 (GRCm39) |
F43S |
probably damaging |
Het |
Szt2 |
A |
G |
4: 118,262,727 (GRCm39) |
F17L |
possibly damaging |
Het |
Taar1 |
G |
T |
10: 23,796,918 (GRCm39) |
M205I |
probably benign |
Het |
Tas2r143 |
A |
G |
6: 42,377,202 (GRCm39) |
I11V |
probably benign |
Het |
Tlx1 |
T |
C |
19: 45,139,655 (GRCm39) |
S101P |
probably damaging |
Het |
Tmeff2 |
T |
C |
1: 50,977,503 (GRCm39) |
|
probably null |
Het |
Vhl |
A |
G |
6: 113,606,451 (GRCm39) |
D156G |
possibly damaging |
Het |
Washc4 |
T |
A |
10: 83,426,897 (GRCm39) |
D1068E |
probably damaging |
Het |
Zfp513 |
A |
G |
5: 31,358,076 (GRCm39) |
V101A |
probably benign |
Het |
Zfp82 |
T |
C |
7: 29,761,669 (GRCm39) |
R71G |
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 |
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 |
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 |
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 |
|
|