Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd35 |
A |
G |
3: 96,592,378 (GRCm39) |
E888G |
probably damaging |
Het |
Arhgef10 |
T |
C |
8: 15,004,918 (GRCm39) |
F150S |
probably damaging |
Het |
Atp10d |
G |
T |
5: 72,396,500 (GRCm39) |
R235L |
probably benign |
Het |
Cacna1b |
A |
G |
2: 24,653,055 (GRCm39) |
V2A |
possibly damaging |
Het |
Cand1 |
A |
T |
10: 119,075,102 (GRCm39) |
L15Q |
probably benign |
Het |
Cavin3 |
C |
A |
7: 105,130,350 (GRCm39) |
G154V |
probably benign |
Het |
Ccdc73 |
A |
T |
2: 104,821,830 (GRCm39) |
D593V |
probably damaging |
Het |
Cdk5rap2 |
T |
C |
4: 70,168,647 (GRCm39) |
K161E |
probably damaging |
Het |
Chil4 |
A |
T |
3: 106,111,056 (GRCm39) |
N279K |
probably benign |
Het |
Chst13 |
T |
G |
6: 90,295,245 (GRCm39) |
D56A |
probably damaging |
Het |
Cnn1 |
C |
A |
9: 22,010,664 (GRCm39) |
H5N |
probably benign |
Het |
Cpsf4l |
T |
A |
11: 113,593,319 (GRCm39) |
K88N |
probably damaging |
Het |
Ctnnbl1 |
G |
T |
2: 157,713,113 (GRCm39) |
|
probably null |
Het |
Dnah7a |
A |
C |
1: 53,657,275 (GRCm39) |
F834V |
probably damaging |
Het |
Fbxo41 |
A |
G |
6: 85,461,163 (GRCm39) |
S182P |
probably benign |
Het |
Fkbp5 |
T |
C |
17: 28,634,970 (GRCm39) |
T180A |
probably benign |
Het |
Flg2 |
T |
A |
3: 93,127,334 (GRCm39) |
I2082N |
unknown |
Het |
Gm4968 |
A |
G |
6: 127,210,725 (GRCm39) |
|
noncoding transcript |
Het |
Gpc5 |
T |
A |
14: 116,761,747 (GRCm39) |
H612Q |
probably benign |
Het |
Gsg1 |
A |
T |
6: 135,218,251 (GRCm39) |
V212D |
probably damaging |
Het |
Hipk1 |
A |
G |
3: 103,651,430 (GRCm39) |
V1111A |
probably damaging |
Het |
Hormad1 |
A |
T |
3: 95,483,596 (GRCm39) |
Q136L |
probably benign |
Het |
Ifi35 |
T |
A |
11: 101,348,511 (GRCm39) |
S147R |
probably benign |
Het |
Iqca1l |
A |
G |
5: 24,754,624 (GRCm39) |
|
probably null |
Het |
Iqgap3 |
C |
T |
3: 87,998,089 (GRCm39) |
A282V |
probably null |
Het |
Jmy |
T |
C |
13: 93,590,558 (GRCm39) |
D515G |
probably damaging |
Het |
Kctd10 |
G |
A |
5: 114,512,984 (GRCm39) |
R64C |
probably damaging |
Het |
Kidins220 |
T |
C |
12: 25,040,757 (GRCm39) |
V121A |
probably damaging |
Het |
Lcn3 |
G |
A |
2: 25,656,133 (GRCm39) |
V63M |
possibly damaging |
Het |
Lmx1b |
T |
A |
2: 33,529,543 (GRCm39) |
Y72F |
probably benign |
Het |
Lrp1 |
T |
C |
10: 127,389,424 (GRCm39) |
D3164G |
probably damaging |
Het |
Mdh1b |
C |
T |
1: 63,758,927 (GRCm39) |
V222M |
probably damaging |
Het |
Mst1 |
T |
C |
9: 107,958,702 (GRCm39) |
|
probably benign |
Het |
Myo7b |
C |
A |
18: 32,143,132 (GRCm39) |
V189F |
probably damaging |
Het |
Ndc1 |
T |
C |
4: 107,250,355 (GRCm39) |
S533P |
probably damaging |
Het |
Ndrg3 |
T |
C |
2: 156,785,947 (GRCm39) |
D164G |
probably damaging |
Het |
Nol11 |
C |
T |
11: 107,064,454 (GRCm39) |
C500Y |
possibly damaging |
Het |
Nsd3 |
A |
G |
8: 26,196,642 (GRCm39) |
N1208D |
probably benign |
Het |
Or5ak20 |
A |
T |
2: 85,183,347 (GRCm39) |
C308S |
probably benign |
Het |
Or6c38 |
A |
G |
10: 128,929,711 (GRCm39) |
I44T |
possibly damaging |
Het |
Or8b47 |
A |
G |
9: 38,435,081 (GRCm39) |
T18A |
probably damaging |
Het |
Or8b54 |
A |
T |
9: 38,687,016 (GRCm39) |
D155V |
possibly damaging |
Het |
Phf3 |
A |
G |
1: 30,844,684 (GRCm39) |
L1425P |
probably damaging |
Het |
Pla2r1 |
A |
G |
2: 60,279,250 (GRCm39) |
Y777H |
probably damaging |
Het |
Pld1 |
A |
G |
3: 28,085,396 (GRCm39) |
E184G |
probably damaging |
Het |
Plxna1 |
T |
C |
6: 89,314,335 (GRCm39) |
|
probably null |
Het |
Ptgfrn |
T |
C |
3: 100,950,718 (GRCm39) |
E865G |
probably damaging |
Het |
Ptpn13 |
G |
T |
5: 103,737,720 (GRCm39) |
|
probably benign |
Het |
Pygb |
G |
T |
2: 150,670,473 (GRCm39) |
V763F |
probably benign |
Het |
Ros1 |
A |
C |
10: 51,967,091 (GRCm39) |
Y1705* |
probably null |
Het |
Sec61a2 |
A |
G |
2: 5,898,027 (GRCm39) |
F5L |
probably benign |
Het |
Skint5 |
A |
G |
4: 113,614,102 (GRCm39) |
|
probably null |
Het |
Sntg2 |
A |
G |
12: 30,362,566 (GRCm39) |
V60A |
probably damaging |
Het |
Sppl2a |
A |
G |
2: 126,762,242 (GRCm39) |
C280R |
possibly damaging |
Het |
Srrm4 |
A |
C |
5: 116,584,603 (GRCm39) |
M1R |
probably null |
Het |
Sult1c2 |
T |
C |
17: 54,279,043 (GRCm39) |
E91G |
probably damaging |
Het |
Themis2 |
C |
G |
4: 132,512,906 (GRCm39) |
R440P |
probably damaging |
Het |
Tmem229a |
A |
G |
6: 24,955,058 (GRCm39) |
L232P |
probably benign |
Het |
Trappc1 |
T |
C |
11: 69,215,248 (GRCm39) |
F43L |
probably damaging |
Het |
Trappc11 |
A |
T |
8: 47,951,708 (GRCm39) |
Y982N |
possibly damaging |
Het |
Trpv6 |
A |
T |
6: 41,604,339 (GRCm39) |
M139K |
probably damaging |
Het |
Txnrd3 |
A |
G |
6: 89,640,057 (GRCm39) |
|
probably null |
Het |
Vmn1r184 |
T |
A |
7: 25,967,008 (GRCm39) |
Y251* |
probably null |
Het |
Vmn1r216 |
A |
G |
13: 23,283,544 (GRCm39) |
N76D |
possibly damaging |
Het |
Vmn1r71 |
C |
A |
7: 10,481,792 (GRCm39) |
V233F |
probably benign |
Het |
Vps13a |
A |
C |
19: 16,743,857 (GRCm39) |
|
probably benign |
Het |
Vwa5b2 |
A |
G |
16: 20,420,358 (GRCm39) |
S756G |
probably damaging |
Het |
Wdr36 |
T |
A |
18: 32,994,538 (GRCm39) |
|
probably null |
Het |
Wdr86 |
A |
G |
5: 24,923,305 (GRCm39) |
V129A |
probably benign |
Het |
Zfyve9 |
A |
G |
4: 108,576,940 (GRCm39) |
L47S |
probably benign |
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 |
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 |
|
R6958:Nup155
|
UTSW |
15 |
8,176,638 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|