Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410004B18Rik |
A |
G |
3: 145,649,558 (GRCm39) |
D159G |
probably benign |
Het |
Ahnak |
A |
G |
19: 8,992,579 (GRCm39) |
N4621S |
possibly damaging |
Het |
Ankrd16 |
C |
T |
2: 11,784,604 (GRCm39) |
A144V |
probably damaging |
Het |
Bhmt1b |
G |
A |
18: 87,775,046 (GRCm39) |
E190K |
probably benign |
Het |
Ccdc14 |
T |
C |
16: 34,511,176 (GRCm39) |
V2A |
probably damaging |
Het |
Ccdc187 |
C |
T |
2: 26,179,731 (GRCm39) |
V243I |
probably benign |
Het |
Cdk12 |
A |
T |
11: 98,132,525 (GRCm39) |
I985F |
unknown |
Het |
Cfap65 |
T |
C |
1: 74,971,058 (GRCm39) |
T87A |
possibly damaging |
Het |
Cilp2 |
G |
A |
8: 70,335,190 (GRCm39) |
P603S |
probably benign |
Het |
Cntnap5b |
A |
G |
1: 100,202,197 (GRCm39) |
E348G |
probably benign |
Het |
Cpa6 |
C |
T |
1: 10,665,913 (GRCm39) |
V42M |
probably damaging |
Het |
Cpsf4 |
A |
G |
5: 145,112,402 (GRCm39) |
I115V |
probably benign |
Het |
Dnah11 |
G |
T |
12: 117,897,544 (GRCm39) |
P3562Q |
probably damaging |
Het |
Dnah9 |
A |
G |
11: 65,967,167 (GRCm39) |
F1664L |
probably damaging |
Het |
Dpysl3 |
T |
C |
18: 43,571,067 (GRCm39) |
Q69R |
probably benign |
Het |
Ebf3 |
T |
C |
7: 136,800,994 (GRCm39) |
T455A |
possibly damaging |
Het |
Eif2ak3 |
T |
A |
6: 70,869,667 (GRCm39) |
C785S |
probably benign |
Het |
Elk4 |
T |
A |
1: 131,945,570 (GRCm39) |
F149L |
probably damaging |
Het |
Fgf14 |
A |
G |
14: 124,914,009 (GRCm39) |
W41R |
probably benign |
Het |
Fmnl1 |
T |
A |
11: 103,062,140 (GRCm39) |
M1K |
probably null |
Het |
Foxk2 |
A |
T |
11: 121,190,563 (GRCm39) |
Q568L |
probably benign |
Het |
Fryl |
T |
G |
5: 73,231,272 (GRCm39) |
I1602L |
possibly damaging |
Het |
Gfm2 |
A |
G |
13: 97,282,744 (GRCm39) |
I75V |
probably damaging |
Het |
Gm3233 |
T |
A |
10: 77,595,369 (GRCm39) |
|
probably benign |
Het |
Gnb1 |
G |
T |
4: 155,627,651 (GRCm39) |
|
probably null |
Het |
Gphn |
G |
T |
12: 78,727,073 (GRCm39) |
V662L |
possibly damaging |
Het |
Il3 |
A |
C |
11: 54,157,937 (GRCm39) |
V47G |
probably benign |
Het |
Iqgap3 |
A |
G |
3: 88,020,673 (GRCm39) |
D401G |
possibly damaging |
Het |
Kdm3b |
T |
A |
18: 34,941,336 (GRCm39) |
S276T |
probably benign |
Het |
Krtap6-2 |
A |
G |
16: 89,216,698 (GRCm39) |
S90P |
unknown |
Het |
Lars1 |
C |
T |
18: 42,369,704 (GRCm39) |
V394I |
probably damaging |
Het |
Lrit1 |
G |
C |
14: 36,782,052 (GRCm39) |
V242L |
probably damaging |
Het |
Lrp10 |
A |
G |
14: 54,707,278 (GRCm39) |
|
probably benign |
Het |
Ltn1 |
A |
T |
16: 87,194,679 (GRCm39) |
C1407S |
probably benign |
Het |
Lzts2 |
G |
T |
19: 45,012,582 (GRCm39) |
|
probably benign |
Het |
Msantd2 |
A |
G |
9: 37,434,753 (GRCm39) |
E331G |
probably damaging |
Het |
Myo15a |
G |
A |
11: 60,394,451 (GRCm39) |
G1218S |
probably benign |
Het |
Myom2 |
G |
A |
8: 15,167,741 (GRCm39) |
A1109T |
probably null |
Het |
Nhp2 |
A |
G |
11: 51,513,934 (GRCm39) |
T118A |
probably benign |
Het |
Nxpe2 |
A |
T |
9: 48,237,566 (GRCm39) |
C230S |
probably damaging |
Het |
Or12d13 |
T |
C |
17: 37,647,308 (GRCm39) |
I272V |
probably benign |
Het |
Or51g2 |
A |
G |
7: 102,623,091 (GRCm39) |
L36P |
possibly damaging |
Het |
Or5w8 |
T |
C |
2: 87,688,295 (GRCm39) |
Y259H |
probably damaging |
Het |
Pfkfb4 |
A |
T |
9: 108,839,615 (GRCm39) |
N244I |
probably damaging |
Het |
Pi4ka |
C |
T |
16: 17,143,091 (GRCm39) |
R24Q |
probably damaging |
Het |
Pkd2l2 |
C |
A |
18: 34,542,543 (GRCm39) |
Y8* |
probably null |
Het |
Pramel20 |
A |
T |
4: 143,297,829 (GRCm39) |
D83V |
probably damaging |
Het |
Ptprb |
T |
A |
10: 116,113,153 (GRCm39) |
N44K |
probably benign |
Het |
Sds |
G |
A |
5: 120,619,537 (GRCm39) |
V149M |
probably damaging |
Het |
Slc22a30 |
A |
G |
19: 8,364,065 (GRCm39) |
F204L |
probably damaging |
Het |
Slc26a7 |
C |
T |
4: 14,506,442 (GRCm39) |
A636T |
probably benign |
Het |
Slc27a1 |
C |
T |
8: 72,038,083 (GRCm39) |
A577V |
possibly damaging |
Het |
Spata13 |
A |
T |
14: 60,989,300 (GRCm39) |
T319S |
possibly damaging |
Het |
Styxl2 |
T |
A |
1: 165,935,565 (GRCm39) |
D211V |
probably damaging |
Het |
Tdrd3 |
A |
G |
14: 87,694,532 (GRCm39) |
D29G |
probably damaging |
Het |
Tex15 |
A |
T |
8: 34,060,899 (GRCm39) |
I110L |
probably benign |
Het |
Treml2 |
A |
G |
17: 48,615,180 (GRCm39) |
T222A |
probably damaging |
Het |
Trpd52l3 |
A |
T |
19: 29,981,546 (GRCm39) |
L100F |
probably damaging |
Het |
Ttf2 |
C |
T |
3: 100,853,248 (GRCm39) |
E975K |
probably benign |
Het |
Vmn1r193 |
T |
A |
13: 22,404,144 (GRCm39) |
|
probably benign |
Het |
Xpo1 |
A |
G |
11: 23,235,855 (GRCm39) |
T648A |
probably benign |
Het |
Zfp641 |
C |
T |
15: 98,190,832 (GRCm39) |
V71I |
possibly damaging |
Het |
|
Other mutations in Nup155 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00228:Nup155
|
APN |
15 |
8,150,939 (GRCm39) |
splice site |
probably benign |
|
IGL00426:Nup155
|
APN |
15 |
8,186,278 (GRCm39) |
makesense |
probably null |
|
IGL00765:Nup155
|
APN |
15 |
8,182,712 (GRCm39) |
missense |
probably benign |
0.16 |
IGL00936:Nup155
|
APN |
15 |
8,157,889 (GRCm39) |
splice site |
probably benign |
|
IGL01124:Nup155
|
APN |
15 |
8,183,163 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01739:Nup155
|
APN |
15 |
8,165,272 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02013:Nup155
|
APN |
15 |
8,143,132 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02066:Nup155
|
APN |
15 |
8,187,250 (GRCm39) |
unclassified |
probably benign |
|
IGL02231:Nup155
|
APN |
15 |
8,173,548 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02246:Nup155
|
APN |
15 |
8,172,486 (GRCm39) |
missense |
probably benign |
|
IGL02289:Nup155
|
APN |
15 |
8,160,977 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02608:Nup155
|
APN |
15 |
8,138,955 (GRCm39) |
missense |
probably benign |
|
IGL02749:Nup155
|
APN |
15 |
8,163,560 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02813:Nup155
|
APN |
15 |
8,159,605 (GRCm39) |
splice site |
probably benign |
|
IGL03102:Nup155
|
APN |
15 |
8,176,768 (GRCm39) |
missense |
probably benign |
0.00 |
H8930:Nup155
|
UTSW |
15 |
8,187,142 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02835:Nup155
|
UTSW |
15 |
8,172,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R0314:Nup155
|
UTSW |
15 |
8,176,736 (GRCm39) |
missense |
probably benign |
0.00 |
R0365:Nup155
|
UTSW |
15 |
8,161,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R0586:Nup155
|
UTSW |
15 |
8,159,716 (GRCm39) |
missense |
probably benign |
0.39 |
R0764:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R0839:Nup155
|
UTSW |
15 |
8,175,071 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0844:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1066:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1067:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1085:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1137:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1162:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1166:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1202:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1203:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1219:Nup155
|
UTSW |
15 |
8,146,822 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1385:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1421:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1448:Nup155
|
UTSW |
15 |
8,141,890 (GRCm39) |
missense |
probably benign |
0.44 |
R1611:Nup155
|
UTSW |
15 |
8,159,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R1836:Nup155
|
UTSW |
15 |
8,184,464 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1863:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Nup155
|
UTSW |
15 |
8,145,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R1894:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R1976:Nup155
|
UTSW |
15 |
8,165,311 (GRCm39) |
missense |
probably benign |
0.01 |
R2024:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R2026:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R2027:Nup155
|
UTSW |
15 |
8,187,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R2077:Nup155
|
UTSW |
15 |
8,172,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R2111:Nup155
|
UTSW |
15 |
8,150,951 (GRCm39) |
missense |
probably benign |
0.45 |
R2921:Nup155
|
UTSW |
15 |
8,183,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R2936:Nup155
|
UTSW |
15 |
8,172,533 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3108:Nup155
|
UTSW |
15 |
8,146,790 (GRCm39) |
missense |
probably null |
1.00 |
R3161:Nup155
|
UTSW |
15 |
8,177,867 (GRCm39) |
missense |
possibly damaging |
0.56 |
R3162:Nup155
|
UTSW |
15 |
8,177,867 (GRCm39) |
missense |
possibly damaging |
0.56 |
R3162:Nup155
|
UTSW |
15 |
8,177,867 (GRCm39) |
missense |
possibly damaging |
0.56 |
R3522:Nup155
|
UTSW |
15 |
8,186,162 (GRCm39) |
splice site |
probably benign |
|
R4423:Nup155
|
UTSW |
15 |
8,150,948 (GRCm39) |
missense |
probably damaging |
0.99 |
R4451:Nup155
|
UTSW |
15 |
8,180,366 (GRCm39) |
missense |
probably benign |
0.02 |
R4498:Nup155
|
UTSW |
15 |
8,183,157 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4780:Nup155
|
UTSW |
15 |
8,187,187 (GRCm39) |
missense |
probably benign |
0.00 |
R4822:Nup155
|
UTSW |
15 |
8,158,010 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5013:Nup155
|
UTSW |
15 |
8,153,722 (GRCm39) |
missense |
probably benign |
0.00 |
R5064:Nup155
|
UTSW |
15 |
8,165,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R5172:Nup155
|
UTSW |
15 |
8,139,026 (GRCm39) |
missense |
probably benign |
0.06 |
R5406:Nup155
|
UTSW |
15 |
8,183,122 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5551:Nup155
|
UTSW |
15 |
8,177,817 (GRCm39) |
missense |
probably benign |
0.09 |
R5588:Nup155
|
UTSW |
15 |
8,148,737 (GRCm39) |
critical splice donor site |
probably null |
|
R5977:Nup155
|
UTSW |
15 |
8,159,721 (GRCm39) |
critical splice donor site |
probably null |
|
R6035:Nup155
|
UTSW |
15 |
8,173,577 (GRCm39) |
missense |
probably benign |
|
R6035:Nup155
|
UTSW |
15 |
8,173,577 (GRCm39) |
missense |
probably benign |
|
R6036:Nup155
|
UTSW |
15 |
8,157,895 (GRCm39) |
missense |
probably benign |
0.16 |
R6036:Nup155
|
UTSW |
15 |
8,157,895 (GRCm39) |
missense |
probably benign |
0.16 |
R6085:Nup155
|
UTSW |
15 |
8,177,842 (GRCm39) |
missense |
probably damaging |
0.98 |
R6188:Nup155
|
UTSW |
15 |
8,139,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R6232:Nup155
|
UTSW |
15 |
8,138,963 (GRCm39) |
missense |
probably benign |
0.02 |
R6257:Nup155
|
UTSW |
15 |
8,180,282 (GRCm39) |
nonsense |
probably null |
|
R6262:Nup155
|
UTSW |
15 |
8,186,225 (GRCm39) |
missense |
probably benign |
0.03 |
R6267:Nup155
|
UTSW |
15 |
8,182,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R6296:Nup155
|
UTSW |
15 |
8,182,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R6299:Nup155
|
UTSW |
15 |
8,157,922 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6303:Nup155
|
UTSW |
15 |
8,147,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R6304:Nup155
|
UTSW |
15 |
8,147,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R6763:Nup155
|
UTSW |
15 |
8,165,379 (GRCm39) |
nonsense |
probably null |
|
R7088:Nup155
|
UTSW |
15 |
8,186,177 (GRCm39) |
missense |
probably benign |
0.11 |
R7313:Nup155
|
UTSW |
15 |
8,184,406 (GRCm39) |
missense |
probably damaging |
0.96 |
R7451:Nup155
|
UTSW |
15 |
8,175,091 (GRCm39) |
nonsense |
probably null |
|
R7560:Nup155
|
UTSW |
15 |
8,184,531 (GRCm39) |
missense |
probably benign |
0.39 |
R7633:Nup155
|
UTSW |
15 |
8,138,937 (GRCm39) |
missense |
probably damaging |
0.99 |
R7670:Nup155
|
UTSW |
15 |
8,183,180 (GRCm39) |
missense |
probably damaging |
0.99 |
R7726:Nup155
|
UTSW |
15 |
8,151,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R7752:Nup155
|
UTSW |
15 |
8,145,926 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7889:Nup155
|
UTSW |
15 |
8,150,991 (GRCm39) |
missense |
probably damaging |
0.98 |
R7899:Nup155
|
UTSW |
15 |
8,148,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R7901:Nup155
|
UTSW |
15 |
8,145,926 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8429:Nup155
|
UTSW |
15 |
8,141,904 (GRCm39) |
missense |
probably damaging |
0.96 |
R8467:Nup155
|
UTSW |
15 |
8,151,015 (GRCm39) |
missense |
probably benign |
0.00 |
R8507:Nup155
|
UTSW |
15 |
8,177,044 (GRCm39) |
nonsense |
probably null |
|
R8860:Nup155
|
UTSW |
15 |
8,159,640 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8994:Nup155
|
UTSW |
15 |
8,172,645 (GRCm39) |
critical splice donor site |
probably null |
|
R9046:Nup155
|
UTSW |
15 |
8,157,919 (GRCm39) |
frame shift |
probably null |
|
R9086:Nup155
|
UTSW |
15 |
8,177,830 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9500:Nup155
|
UTSW |
15 |
8,141,800 (GRCm39) |
missense |
probably damaging |
1.00 |
RF003:Nup155
|
UTSW |
15 |
8,148,660 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF048:Nup155
|
UTSW |
15 |
8,148,660 (GRCm39) |
critical splice acceptor site |
probably benign |
|
Z1177:Nup155
|
UTSW |
15 |
8,149,973 (GRCm39) |
missense |
probably benign |
0.23 |
|