Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd13 |
T |
C |
8: 10,037,387 (GRCm39) |
|
probably benign |
Het |
Ap2a2 |
T |
A |
7: 141,178,689 (GRCm39) |
N105K |
probably benign |
Het |
Axin1 |
A |
G |
17: 26,407,012 (GRCm39) |
H535R |
probably damaging |
Het |
Ccnb3 |
T |
A |
X: 6,874,040 (GRCm39) |
E846D |
probably benign |
Het |
Cdca7 |
G |
A |
2: 72,315,631 (GRCm39) |
G365R |
probably damaging |
Het |
Clvs2 |
T |
A |
10: 33,498,967 (GRCm39) |
|
probably benign |
Het |
Coq10a |
A |
G |
10: 128,200,998 (GRCm39) |
V93A |
possibly damaging |
Het |
Ddx42 |
A |
G |
11: 106,138,636 (GRCm39) |
T812A |
probably benign |
Het |
Dnaaf6 |
T |
A |
X: 139,006,770 (GRCm39) |
N216K |
possibly damaging |
Het |
Eya1 |
T |
A |
1: 14,344,433 (GRCm39) |
|
probably null |
Het |
Fcna |
G |
C |
2: 25,517,505 (GRCm39) |
P49A |
probably damaging |
Het |
Gckr |
T |
A |
5: 31,458,211 (GRCm39) |
|
probably null |
Het |
Golgb1 |
A |
G |
16: 36,707,709 (GRCm39) |
K68E |
probably damaging |
Het |
Got1l1 |
A |
G |
8: 27,689,864 (GRCm39) |
|
probably null |
Het |
Hip1 |
T |
C |
5: 135,451,026 (GRCm39) |
E451G |
probably damaging |
Het |
Hs6st2 |
C |
T |
X: 50,770,332 (GRCm39) |
V50I |
possibly damaging |
Het |
Ighv1-23 |
C |
T |
12: 114,728,087 (GRCm39) |
V112I |
probably benign |
Het |
Map1s |
A |
G |
8: 71,365,163 (GRCm39) |
N107D |
probably damaging |
Het |
Mmel1 |
T |
A |
4: 154,974,043 (GRCm39) |
V361D |
probably damaging |
Het |
Myh15 |
A |
G |
16: 48,959,095 (GRCm39) |
D989G |
probably benign |
Het |
Myo1g |
G |
T |
11: 6,467,870 (GRCm39) |
H188Q |
possibly damaging |
Het |
Or14j3 |
A |
G |
17: 37,900,587 (GRCm39) |
V219A |
probably benign |
Het |
Or51q1c |
A |
G |
7: 103,653,039 (GRCm39) |
M186V |
probably damaging |
Het |
Plcz1 |
C |
T |
6: 139,947,807 (GRCm39) |
R525Q |
probably damaging |
Het |
Ppef2 |
T |
G |
5: 92,376,581 (GRCm39) |
S649R |
probably damaging |
Het |
Rusc2 |
T |
G |
4: 43,415,935 (GRCm39) |
S414A |
probably damaging |
Het |
Sez6l |
A |
G |
5: 112,623,227 (GRCm39) |
L108P |
possibly damaging |
Het |
Slc1a7 |
A |
G |
4: 107,868,191 (GRCm39) |
E497G |
probably benign |
Het |
Spag8 |
T |
A |
4: 43,651,606 (GRCm39) |
S423C |
probably damaging |
Het |
Sspo |
C |
T |
6: 48,457,631 (GRCm39) |
R3178C |
probably damaging |
Het |
St6galnac1 |
A |
G |
11: 116,656,682 (GRCm39) |
W486R |
probably damaging |
Het |
Syk |
A |
G |
13: 52,785,775 (GRCm39) |
D327G |
probably benign |
Het |
Tbc1d8b |
C |
T |
X: 138,614,140 (GRCm39) |
A391V |
probably benign |
Het |
Tmed9 |
A |
G |
13: 55,743,387 (GRCm39) |
E173G |
probably benign |
Het |
Top1mt |
T |
C |
15: 75,529,025 (GRCm39) |
N573S |
probably benign |
Het |
Tusc1 |
C |
A |
4: 93,223,173 (GRCm39) |
R162L |
probably damaging |
Het |
Ubn2 |
A |
G |
6: 38,475,674 (GRCm39) |
T1211A |
probably benign |
Het |
Unc80 |
G |
A |
1: 66,678,464 (GRCm39) |
V2082I |
probably benign |
Het |
Vmn2r63 |
A |
G |
7: 42,576,406 (GRCm39) |
F469S |
probably benign |
Het |
Zfp92 |
C |
T |
X: 72,463,900 (GRCm39) |
|
probably benign |
Het |
Zfyve28 |
C |
T |
5: 34,357,028 (GRCm39) |
M723I |
probably benign |
Het |
Zmynd8 |
A |
T |
2: 165,657,371 (GRCm39) |
M533K |
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 |
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 |
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 |
|
|