Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc3 |
T |
C |
11: 94,266,434 (GRCm39) |
Y52C |
probably damaging |
Het |
Acmsd |
C |
T |
1: 127,681,585 (GRCm39) |
R183* |
probably null |
Het |
Anxa2 |
T |
A |
9: 69,392,533 (GRCm39) |
D127E |
probably damaging |
Het |
Atrnl1 |
T |
A |
19: 57,673,945 (GRCm39) |
Y593* |
probably null |
Het |
Atxn2 |
C |
T |
5: 121,933,098 (GRCm39) |
|
probably null |
Het |
Ccl6 |
A |
T |
11: 83,480,169 (GRCm39) |
Y66N |
probably damaging |
Het |
Ccng1 |
A |
G |
11: 40,642,113 (GRCm39) |
V223A |
probably benign |
Het |
Cfap44 |
T |
C |
16: 44,269,556 (GRCm39) |
Y1187H |
probably benign |
Het |
Cfc1 |
A |
T |
1: 34,575,011 (GRCm39) |
I10F |
probably benign |
Het |
Chrne |
T |
A |
11: 70,506,352 (GRCm39) |
T365S |
probably benign |
Het |
Clec4b1 |
G |
T |
6: 123,048,414 (GRCm39) |
R183L |
probably benign |
Het |
Csmd2 |
A |
C |
4: 128,371,190 (GRCm39) |
Q1926P |
probably benign |
Het |
Dmpk |
C |
G |
7: 18,821,944 (GRCm39) |
L301V |
probably benign |
Het |
Dzip1 |
T |
A |
14: 119,124,563 (GRCm39) |
Q570L |
probably damaging |
Het |
Fam149a |
T |
A |
8: 45,797,690 (GRCm39) |
Q507L |
probably damaging |
Het |
Frem3 |
T |
C |
8: 81,339,195 (GRCm39) |
V496A |
probably benign |
Het |
Fryl |
A |
T |
5: 73,259,016 (GRCm39) |
D589E |
possibly damaging |
Het |
Hemk1 |
T |
C |
9: 107,206,631 (GRCm39) |
E4G |
possibly damaging |
Het |
Igkv4-80 |
A |
C |
6: 68,993,649 (GRCm39) |
S81A |
probably benign |
Het |
Kcnh7 |
T |
C |
2: 62,569,508 (GRCm39) |
D796G |
possibly damaging |
Het |
Lemd2 |
G |
T |
17: 27,414,356 (GRCm39) |
S326* |
probably null |
Het |
Mdc1 |
T |
C |
17: 36,163,982 (GRCm39) |
S1177P |
probably benign |
Het |
Mfsd4b4 |
A |
G |
10: 39,770,083 (GRCm39) |
F78S |
probably damaging |
Het |
Mmgt2 |
T |
A |
11: 62,555,954 (GRCm39) |
F101I |
possibly damaging |
Het |
Myo18a |
T |
C |
11: 77,714,924 (GRCm39) |
L785P |
probably damaging |
Het |
Or52r1c |
T |
C |
7: 102,734,884 (GRCm39) |
L48P |
probably damaging |
Het |
Or5w19 |
A |
G |
2: 87,699,171 (GRCm39) |
T279A |
probably benign |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pank1 |
A |
T |
19: 34,818,202 (GRCm39) |
C112* |
probably null |
Het |
Pcmtd1 |
T |
A |
1: 7,233,485 (GRCm39) |
M23K |
probably benign |
Het |
Rere |
A |
T |
4: 150,654,726 (GRCm39) |
R419S |
unknown |
Het |
Rpf1 |
T |
C |
3: 146,218,050 (GRCm39) |
R155G |
possibly damaging |
Het |
Sema7a |
A |
G |
9: 57,864,961 (GRCm39) |
T421A |
probably benign |
Het |
Sharpin |
A |
G |
15: 76,231,741 (GRCm39) |
S323P |
probably benign |
Het |
Slamf6 |
A |
G |
1: 171,764,147 (GRCm39) |
E180G |
probably benign |
Het |
Snd1 |
T |
G |
6: 28,886,615 (GRCm39) |
V874G |
possibly damaging |
Het |
Sult6b2 |
A |
T |
6: 142,743,657 (GRCm39) |
V123D |
probably damaging |
Het |
Tpk1 |
A |
T |
6: 43,536,951 (GRCm39) |
|
probably null |
Het |
Vmn1r160 |
A |
T |
7: 22,570,761 (GRCm39) |
N38I |
probably damaging |
Het |
Wdr93 |
T |
A |
7: 79,402,241 (GRCm39) |
I180N |
probably damaging |
Het |
Ythdf3 |
C |
T |
3: 16,258,198 (GRCm39) |
T119I |
probably damaging |
Het |
Zc3h18 |
T |
G |
8: 123,134,159 (GRCm39) |
|
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 |
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 |
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 |
|