Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700056E22Rik |
A |
G |
1: 183,765,369 (GRCm39) |
V230A |
possibly damaging |
Het |
2010315B03Rik |
T |
C |
9: 124,056,631 (GRCm39) |
T123A |
possibly damaging |
Het |
Abca4 |
T |
C |
3: 121,899,019 (GRCm39) |
V667A |
probably damaging |
Het |
Abcb5 |
A |
G |
12: 118,929,040 (GRCm39) |
S4P |
possibly damaging |
Het |
Adam25 |
G |
T |
8: 41,207,163 (GRCm39) |
C143F |
probably damaging |
Het |
Ahnak |
C |
A |
19: 8,994,270 (GRCm39) |
H5185N |
probably benign |
Het |
Apobec4 |
A |
G |
1: 152,632,001 (GRCm39) |
T10A |
probably benign |
Het |
Ascc1 |
A |
G |
10: 59,885,624 (GRCm39) |
Y225C |
probably damaging |
Het |
Aspscr1 |
A |
T |
11: 120,579,771 (GRCm39) |
K39N |
possibly damaging |
Het |
Atf7ip |
C |
T |
6: 136,538,192 (GRCm39) |
P483L |
probably damaging |
Het |
Atp11a |
C |
G |
8: 12,863,118 (GRCm39) |
P99R |
probably damaging |
Het |
B4galnt1 |
G |
T |
10: 127,003,394 (GRCm39) |
V172F |
possibly damaging |
Het |
Bag6 |
C |
A |
17: 35,361,319 (GRCm39) |
P476H |
probably damaging |
Het |
Bltp1 |
C |
T |
3: 37,096,038 (GRCm39) |
T1108I |
probably benign |
Het |
C2cd3 |
A |
G |
7: 100,044,395 (GRCm39) |
K326E |
possibly damaging |
Het |
Casp1 |
A |
G |
9: 5,306,204 (GRCm39) |
D363G |
probably damaging |
Het |
Ccdc33 |
G |
T |
9: 58,024,840 (GRCm39) |
Q129K |
probably benign |
Het |
Ccdc88a |
T |
C |
11: 29,372,586 (GRCm39) |
I107T |
probably benign |
Het |
Cela2a |
T |
C |
4: 141,548,722 (GRCm39) |
N138S |
probably benign |
Het |
Cfap61 |
A |
C |
2: 145,877,122 (GRCm39) |
R460S |
probably damaging |
Het |
Clstn2 |
T |
C |
9: 97,345,612 (GRCm39) |
N579D |
possibly damaging |
Het |
Col13a1 |
C |
A |
10: 61,685,944 (GRCm39) |
G683W |
unknown |
Het |
Col4a2 |
G |
A |
8: 11,363,504 (GRCm39) |
R14Q |
possibly damaging |
Het |
Cpa6 |
A |
G |
1: 10,551,283 (GRCm39) |
S164P |
probably benign |
Het |
Cpq |
A |
G |
15: 33,497,484 (GRCm39) |
N408S |
probably benign |
Het |
Ctnnal1 |
T |
C |
4: 56,812,579 (GRCm39) |
T690A |
probably benign |
Het |
Cx3cl1 |
A |
T |
8: 95,506,835 (GRCm39) |
N280I |
probably benign |
Het |
Cyp2b19 |
C |
T |
7: 26,456,717 (GRCm39) |
R36C |
probably benign |
Het |
Ddx51 |
T |
C |
5: 110,803,174 (GRCm39) |
V269A |
probably damaging |
Het |
Dipk2a |
T |
C |
9: 94,402,688 (GRCm39) |
N325D |
possibly damaging |
Het |
Dlst |
G |
T |
12: 85,165,616 (GRCm39) |
|
probably null |
Het |
Dmkn |
G |
C |
7: 30,463,406 (GRCm39) |
A20P |
probably damaging |
Het |
Dnhd1 |
T |
C |
7: 105,304,948 (GRCm39) |
I330T |
probably damaging |
Het |
Dock3 |
G |
A |
9: 106,902,535 (GRCm39) |
H292Y |
probably damaging |
Het |
Ell |
A |
G |
8: 71,031,584 (GRCm39) |
D94G |
possibly damaging |
Het |
Enam |
T |
A |
5: 88,651,650 (GRCm39) |
L1053* |
probably null |
Het |
Fam3d |
T |
C |
14: 8,349,347 (GRCm38) |
E201G |
probably benign |
Het |
Fcgbp |
A |
G |
7: 27,806,721 (GRCm39) |
K2230E |
probably benign |
Het |
Frmd5 |
G |
T |
2: 121,393,344 (GRCm39) |
|
probably benign |
Het |
Gas2l1 |
G |
A |
11: 5,010,867 (GRCm39) |
S654L |
possibly damaging |
Het |
Gltpd2 |
G |
T |
11: 70,410,966 (GRCm39) |
E86* |
probably null |
Het |
Glyat |
T |
C |
19: 12,628,661 (GRCm39) |
L152P |
possibly damaging |
Het |
Gm17330 |
T |
C |
12: 24,018,783 (GRCm39) |
T22A |
probably damaging |
Het |
Gm9931 |
T |
A |
1: 147,157,591 (GRCm39) |
|
noncoding transcript |
Het |
Gpatch1 |
A |
T |
7: 34,998,730 (GRCm39) |
|
probably null |
Het |
Gpr4 |
T |
C |
7: 18,956,819 (GRCm39) |
L247P |
probably damaging |
Het |
Gtpbp3 |
G |
A |
8: 71,943,758 (GRCm39) |
E214K |
probably benign |
Het |
Hdac7 |
G |
T |
15: 97,709,468 (GRCm39) |
Q21K |
probably damaging |
Het |
Hivep3 |
A |
G |
4: 119,729,247 (GRCm39) |
|
probably benign |
Het |
Hk2 |
C |
T |
6: 82,716,631 (GRCm39) |
M300I |
possibly damaging |
Het |
Ighv1-61 |
T |
C |
12: 115,322,899 (GRCm39) |
Y71C |
probably damaging |
Het |
Il36b |
T |
C |
2: 24,044,630 (GRCm39) |
V10A |
probably benign |
Het |
Inpp5f |
G |
T |
7: 128,265,711 (GRCm39) |
S152I |
probably damaging |
Het |
Jag1 |
C |
A |
2: 136,938,229 (GRCm39) |
W257L |
probably damaging |
Het |
Jak2 |
T |
A |
19: 29,272,315 (GRCm39) |
N612K |
possibly damaging |
Het |
Kalrn |
T |
C |
16: 34,024,327 (GRCm39) |
D610G |
probably damaging |
Het |
Kbtbd6 |
A |
G |
14: 79,690,046 (GRCm39) |
D247G |
probably benign |
Het |
Kif15 |
A |
G |
9: 122,789,058 (GRCm39) |
|
probably null |
Het |
Kndc1 |
A |
G |
7: 139,510,036 (GRCm39) |
T1293A |
possibly damaging |
Het |
Lpar5 |
T |
C |
6: 125,059,170 (GRCm39) |
I297T |
possibly damaging |
Het |
Lpin2 |
T |
A |
17: 71,539,138 (GRCm39) |
|
probably benign |
Het |
Lypd10 |
T |
A |
7: 24,412,934 (GRCm39) |
L114Q |
probably damaging |
Het |
Mfsd4a |
A |
T |
1: 131,981,309 (GRCm39) |
L230Q |
probably damaging |
Het |
Mmp8 |
T |
C |
9: 7,565,550 (GRCm39) |
V313A |
probably benign |
Het |
Mrpl19 |
A |
T |
6: 81,941,266 (GRCm39) |
D98E |
probably damaging |
Het |
Mybl1 |
A |
G |
1: 9,760,340 (GRCm39) |
I86T |
probably damaging |
Het |
Nadk |
C |
A |
4: 155,669,684 (GRCm39) |
P157T |
probably benign |
Het |
Necab1 |
T |
C |
4: 15,052,628 (GRCm39) |
T117A |
probably damaging |
Het |
Nol11 |
A |
G |
11: 107,075,544 (GRCm39) |
|
probably benign |
Het |
Nucb2 |
G |
A |
7: 116,139,262 (GRCm39) |
|
probably null |
Het |
Odf2 |
T |
A |
2: 29,794,046 (GRCm39) |
L301Q |
probably damaging |
Het |
Oog4 |
T |
C |
4: 143,165,445 (GRCm39) |
Y234C |
probably benign |
Het |
Or11j4 |
A |
G |
14: 50,630,257 (GRCm39) |
I15V |
probably benign |
Het |
Or1ab2 |
T |
A |
8: 72,864,044 (GRCm39) |
F211L |
probably damaging |
Het |
Papln |
T |
C |
12: 83,823,982 (GRCm39) |
|
probably null |
Het |
Paqr6 |
C |
T |
3: 88,273,236 (GRCm39) |
A76V |
probably benign |
Het |
Pclo |
A |
G |
5: 14,726,494 (GRCm39) |
|
probably benign |
Het |
Pdzd8 |
T |
C |
19: 59,333,743 (GRCm39) |
T93A |
possibly damaging |
Het |
Pkdrej |
A |
T |
15: 85,705,368 (GRCm39) |
Y189* |
probably null |
Het |
Pknox2 |
A |
T |
9: 36,834,934 (GRCm39) |
N178K |
possibly damaging |
Het |
Pla2g15 |
T |
A |
8: 106,889,691 (GRCm39) |
M321K |
probably benign |
Het |
Plxnd1 |
A |
C |
6: 115,935,581 (GRCm39) |
L1735R |
probably damaging |
Het |
Polm |
T |
A |
11: 5,787,663 (GRCm39) |
D30V |
possibly damaging |
Het |
Rap1gap2 |
T |
A |
11: 74,328,265 (GRCm39) |
I100F |
probably damaging |
Het |
Rasgef1c |
T |
A |
11: 49,869,294 (GRCm39) |
W414R |
probably benign |
Het |
Rassf1 |
A |
G |
9: 107,435,066 (GRCm39) |
D187G |
probably benign |
Het |
Rhag |
T |
C |
17: 41,147,329 (GRCm39) |
I397T |
probably benign |
Het |
Rnft2 |
A |
G |
5: 118,366,928 (GRCm39) |
F269S |
probably damaging |
Het |
Rnmt |
T |
C |
18: 68,447,196 (GRCm39) |
F360S |
probably damaging |
Het |
Ror2 |
C |
T |
13: 53,271,333 (GRCm39) |
A329T |
probably benign |
Het |
Slc4a1 |
T |
A |
11: 102,247,084 (GRCm39) |
N501I |
possibly damaging |
Het |
Slc4a7 |
T |
A |
14: 14,733,856 (GRCm38) |
S89T |
probably damaging |
Het |
Sptbn1 |
G |
A |
11: 30,050,660 (GRCm39) |
H2310Y |
probably benign |
Het |
Tbc1d9b |
C |
A |
11: 50,031,289 (GRCm39) |
N103K |
probably benign |
Het |
Tbxas1 |
T |
C |
6: 39,060,791 (GRCm39) |
|
probably null |
Het |
Tmem100 |
C |
T |
11: 89,926,389 (GRCm39) |
T72I |
probably damaging |
Het |
Ttc38 |
A |
G |
15: 85,737,164 (GRCm39) |
T350A |
probably benign |
Het |
Ubr4 |
C |
T |
4: 139,177,840 (GRCm39) |
T3241M |
probably damaging |
Het |
Unc13d |
A |
T |
11: 115,964,214 (GRCm39) |
M350K |
possibly damaging |
Het |
Vit |
T |
C |
17: 78,932,543 (GRCm39) |
I550T |
probably damaging |
Het |
Vmn1r31 |
C |
A |
6: 58,448,953 (GRCm39) |
*304L |
probably null |
Het |
Zbtb12 |
T |
A |
17: 35,115,377 (GRCm39) |
H387Q |
possibly 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 |
R4626:Nup58
|
UTSW |
14 |
60,476,004 (GRCm39) |
missense |
probably benign |
0.24 |
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 |
|
|