Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatf |
A |
C |
11: 84,313,784 (GRCm39) |
*527G |
probably null |
Het |
Abca17 |
A |
T |
17: 24,540,058 (GRCm39) |
I390N |
probably damaging |
Het |
Adamts18 |
C |
T |
8: 114,499,800 (GRCm39) |
W371* |
probably null |
Het |
Akr1c13 |
G |
T |
13: 4,247,869 (GRCm39) |
V214F |
probably damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Ankrd49 |
A |
C |
9: 14,693,936 (GRCm39) |
L77R |
probably damaging |
Het |
Ap3b1 |
T |
A |
13: 94,540,586 (GRCm39) |
N169K |
possibly damaging |
Het |
Arhgap39 |
A |
C |
15: 76,621,837 (GRCm39) |
F255V |
possibly damaging |
Het |
Atp1a3 |
T |
A |
7: 24,698,193 (GRCm39) |
N171I |
possibly damaging |
Het |
Atp9a |
T |
C |
2: 168,481,863 (GRCm39) |
D953G |
probably damaging |
Het |
Atxn1 |
T |
C |
13: 45,720,575 (GRCm39) |
Y440C |
probably damaging |
Het |
Bccip |
T |
C |
7: 133,322,457 (GRCm39) |
Y268H |
possibly damaging |
Het |
Brms1l |
C |
A |
12: 55,909,958 (GRCm39) |
P243T |
probably benign |
Het |
Btbd10 |
T |
C |
7: 112,927,605 (GRCm39) |
E250G |
probably damaging |
Het |
Cacna1e |
T |
C |
1: 154,358,294 (GRCm39) |
|
probably null |
Het |
Cfhr2 |
A |
T |
1: 139,741,314 (GRCm39) |
N220K |
probably damaging |
Het |
Csnk1g2 |
C |
A |
10: 80,475,648 (GRCm39) |
A405E |
probably damaging |
Het |
D5Ertd579e |
T |
C |
5: 36,771,903 (GRCm39) |
I831V |
possibly damaging |
Het |
F2 |
T |
A |
2: 91,461,015 (GRCm39) |
N239I |
probably benign |
Het |
Fbln5 |
T |
A |
12: 101,727,086 (GRCm39) |
D301V |
probably damaging |
Het |
Fbn2 |
A |
T |
18: 58,146,819 (GRCm39) |
C2692* |
probably null |
Het |
Fhdc1 |
C |
T |
3: 84,381,557 (GRCm39) |
D34N |
probably damaging |
Het |
Galnt13 |
T |
A |
2: 54,747,878 (GRCm39) |
M253K |
probably damaging |
Het |
Gpc6 |
C |
A |
14: 118,202,255 (GRCm39) |
Y488* |
probably null |
Het |
Grm5 |
G |
T |
7: 87,779,361 (GRCm39) |
G934C |
probably damaging |
Het |
Gys1 |
T |
C |
7: 45,088,958 (GRCm39) |
L119S |
probably damaging |
Het |
H2-T15 |
CTGGGTG |
CTG |
17: 36,368,788 (GRCm39) |
|
probably null |
Het |
Htra4 |
T |
C |
8: 25,527,130 (GRCm39) |
N222D |
probably benign |
Het |
Iba57 |
A |
G |
11: 59,049,287 (GRCm39) |
V294A |
probably benign |
Het |
Kctd21 |
A |
G |
7: 96,996,782 (GRCm39) |
D85G |
probably damaging |
Het |
Krt1 |
C |
T |
15: 101,754,622 (GRCm39) |
G543S |
unknown |
Het |
Lama5 |
G |
A |
2: 179,826,253 (GRCm39) |
T2330M |
probably damaging |
Het |
Lrguk |
G |
A |
6: 34,106,158 (GRCm39) |
E728K |
probably benign |
Het |
Mcm6 |
T |
C |
1: 128,279,285 (GRCm39) |
D167G |
probably benign |
Het |
Mettl18 |
T |
A |
1: 163,824,045 (GRCm39) |
V122E |
probably damaging |
Het |
Mindy2 |
G |
A |
9: 70,534,063 (GRCm39) |
S378L |
probably damaging |
Het |
Mis18bp1 |
G |
T |
12: 65,187,540 (GRCm39) |
F854L |
probably damaging |
Het |
Mtdh |
C |
T |
15: 34,114,980 (GRCm39) |
R106* |
probably null |
Het |
Nup214 |
T |
A |
2: 31,923,416 (GRCm39) |
V1315E |
possibly damaging |
Het |
Or1j1 |
A |
G |
2: 36,702,271 (GRCm39) |
Y278H |
probably damaging |
Het |
Or4c101 |
T |
C |
2: 88,390,176 (GRCm39) |
V121A |
possibly damaging |
Het |
Or6f2 |
T |
C |
7: 139,756,359 (GRCm39) |
S109P |
probably damaging |
Het |
Orc5 |
G |
T |
5: 22,753,003 (GRCm39) |
F10L |
probably benign |
Het |
Pcdha11 |
A |
T |
18: 37,140,051 (GRCm39) |
N560I |
probably damaging |
Het |
Pcdhb9 |
T |
A |
18: 37,535,302 (GRCm39) |
F432Y |
probably benign |
Het |
Peg10 |
GGATCC |
GGATCCCCATCAAGATCC |
6: 4,756,460 (GRCm39) |
|
probably benign |
Het |
Poll |
C |
A |
19: 45,543,563 (GRCm39) |
M385I |
probably benign |
Het |
Pomt1 |
A |
G |
2: 32,144,424 (GRCm39) |
K737E |
possibly damaging |
Het |
Prr16 |
C |
T |
18: 51,435,911 (GRCm39) |
T130I |
probably damaging |
Het |
Ptpn18 |
A |
G |
1: 34,510,873 (GRCm39) |
|
probably null |
Het |
Ranbp6 |
A |
T |
19: 29,788,263 (GRCm39) |
Y696* |
probably null |
Het |
Rmi1 |
A |
G |
13: 58,556,950 (GRCm39) |
R400G |
probably benign |
Het |
Scn10a |
A |
G |
9: 119,460,571 (GRCm39) |
I1101T |
possibly damaging |
Het |
Slc22a22 |
T |
C |
15: 57,126,734 (GRCm39) |
T93A |
probably damaging |
Het |
Snx10 |
A |
G |
6: 51,565,270 (GRCm39) |
D129G |
probably damaging |
Het |
Stub1 |
A |
G |
17: 26,050,845 (GRCm39) |
|
probably null |
Het |
Tfr2 |
T |
C |
5: 137,569,954 (GRCm39) |
V120A |
probably benign |
Het |
Trmu |
T |
C |
15: 85,779,186 (GRCm39) |
Y278H |
possibly damaging |
Het |
Ugt2b36 |
A |
C |
5: 87,239,947 (GRCm39) |
F146C |
probably damaging |
Het |
Vav2 |
T |
C |
2: 27,160,172 (GRCm39) |
I692V |
possibly damaging |
Het |
Wdfy3 |
A |
G |
5: 102,091,800 (GRCm39) |
L513P |
probably damaging |
Het |
Zfhx4 |
T |
A |
3: 5,467,699 (GRCm39) |
V2619D |
probably damaging |
Het |
Zfyve26 |
T |
A |
12: 79,315,844 (GRCm39) |
N1211Y |
possibly damaging |
Het |
Zp3r |
A |
G |
1: 130,542,912 (GRCm39) |
F142L |
probably damaging |
Het |
|
Other mutations in Nup58 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Nup58
|
APN |
14 |
60,480,026 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00693:Nup58
|
APN |
14 |
60,475,969 (GRCm39) |
missense |
probably benign |
0.10 |
IGL00725:Nup58
|
APN |
14 |
60,480,889 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL00969:Nup58
|
APN |
14 |
60,466,365 (GRCm39) |
splice site |
probably benign |
|
IGL03243:Nup58
|
APN |
14 |
60,459,065 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03351:Nup58
|
APN |
14 |
60,466,224 (GRCm39) |
missense |
probably benign |
0.19 |
R0056:Nup58
|
UTSW |
14 |
60,476,924 (GRCm39) |
splice site |
probably null |
|
R0113:Nup58
|
UTSW |
14 |
60,488,740 (GRCm39) |
start gained |
probably benign |
|
R0201:Nup58
|
UTSW |
14 |
60,482,065 (GRCm39) |
missense |
probably benign |
0.32 |
R0830:Nup58
|
UTSW |
14 |
60,480,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R0925:Nup58
|
UTSW |
14 |
60,457,590 (GRCm39) |
missense |
probably damaging |
0.99 |
R1004:Nup58
|
UTSW |
14 |
60,484,930 (GRCm39) |
splice site |
probably benign |
|
R1178:Nup58
|
UTSW |
14 |
60,482,119 (GRCm39) |
splice site |
probably benign |
|
R1181:Nup58
|
UTSW |
14 |
60,482,119 (GRCm39) |
splice site |
probably benign |
|
R1268:Nup58
|
UTSW |
14 |
60,482,119 (GRCm39) |
splice site |
probably benign |
|
R1388:Nup58
|
UTSW |
14 |
60,482,119 (GRCm39) |
splice site |
probably benign |
|
R1411:Nup58
|
UTSW |
14 |
60,482,119 (GRCm39) |
splice site |
probably benign |
|
R1442:Nup58
|
UTSW |
14 |
60,469,992 (GRCm39) |
splice site |
probably benign |
|
R1626:Nup58
|
UTSW |
14 |
60,480,076 (GRCm39) |
nonsense |
probably null |
|
R1697:Nup58
|
UTSW |
14 |
60,482,119 (GRCm39) |
splice site |
probably benign |
|
R1756:Nup58
|
UTSW |
14 |
60,482,119 (GRCm39) |
splice site |
probably benign |
|
R1853:Nup58
|
UTSW |
14 |
60,481,996 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1915:Nup58
|
UTSW |
14 |
60,475,980 (GRCm39) |
missense |
probably benign |
0.00 |
R2160:Nup58
|
UTSW |
14 |
60,476,957 (GRCm39) |
missense |
probably benign |
0.15 |
R2211:Nup58
|
UTSW |
14 |
60,470,089 (GRCm39) |
missense |
probably damaging |
0.99 |
R2213:Nup58
|
UTSW |
14 |
60,476,945 (GRCm39) |
missense |
probably benign |
0.01 |
R2518:Nup58
|
UTSW |
14 |
60,470,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R2519:Nup58
|
UTSW |
14 |
60,460,808 (GRCm39) |
missense |
probably benign |
0.23 |
R3914:Nup58
|
UTSW |
14 |
60,469,596 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4302:Nup58
|
UTSW |
14 |
60,484,875 (GRCm39) |
missense |
probably benign |
0.44 |
R4705:Nup58
|
UTSW |
14 |
60,488,664 (GRCm39) |
missense |
unknown |
|
R4772:Nup58
|
UTSW |
14 |
60,457,471 (GRCm39) |
missense |
probably benign |
0.00 |
R6151:Nup58
|
UTSW |
14 |
60,482,065 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6187:Nup58
|
UTSW |
14 |
60,478,256 (GRCm39) |
splice site |
probably null |
|
R6546:Nup58
|
UTSW |
14 |
60,460,672 (GRCm39) |
splice site |
probably null |
|
|