Other mutations in this stock |
Total: 17 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
A |
T |
11: 110,195,811 (GRCm39) |
D549E |
probably damaging |
Het |
Abcc9 |
A |
G |
6: 142,610,347 (GRCm39) |
F606L |
probably damaging |
Het |
Bltp3a |
C |
T |
17: 28,095,891 (GRCm39) |
|
probably benign |
Het |
Canx |
A |
G |
11: 50,191,823 (GRCm39) |
S363P |
possibly damaging |
Het |
Cdh6 |
T |
C |
15: 13,041,525 (GRCm39) |
D513G |
possibly damaging |
Het |
Cyp11a1 |
G |
T |
9: 57,926,596 (GRCm39) |
G111W |
probably damaging |
Het |
Dnm1l |
A |
G |
16: 16,151,691 (GRCm39) |
|
probably null |
Het |
Dsg1b |
T |
A |
18: 20,524,975 (GRCm39) |
L137* |
probably null |
Het |
Kcnh5 |
A |
T |
12: 75,160,963 (GRCm39) |
|
probably null |
Het |
Nlrp9b |
T |
A |
7: 19,757,111 (GRCm39) |
I116K |
possibly damaging |
Het |
Notch2 |
T |
C |
3: 98,018,991 (GRCm39) |
Y718H |
possibly damaging |
Het |
Prkdc |
T |
C |
16: 15,605,022 (GRCm39) |
L2980P |
probably benign |
Het |
Samm50 |
C |
T |
15: 84,084,576 (GRCm39) |
S171F |
possibly damaging |
Het |
Saraf |
T |
A |
8: 34,634,962 (GRCm39) |
S288T |
probably benign |
Het |
Ubr5 |
C |
T |
15: 38,018,528 (GRCm39) |
V865I |
possibly damaging |
Het |
Vnn3 |
G |
T |
10: 23,743,066 (GRCm39) |
K425N |
possibly damaging |
Het |
Zswim8 |
T |
C |
14: 20,766,969 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Kcnu1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Kcnu1
|
APN |
8 |
26,387,884 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00580:Kcnu1
|
APN |
8 |
26,355,691 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00928:Kcnu1
|
APN |
8 |
26,339,763 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01324:Kcnu1
|
APN |
8 |
26,339,735 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01346:Kcnu1
|
APN |
8 |
26,424,551 (GRCm39) |
splice site |
probably benign |
|
IGL01361:Kcnu1
|
APN |
8 |
26,376,796 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01651:Kcnu1
|
APN |
8 |
26,351,123 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01795:Kcnu1
|
APN |
8 |
26,403,733 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01800:Kcnu1
|
APN |
8 |
26,427,528 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01975:Kcnu1
|
APN |
8 |
26,424,525 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02103:Kcnu1
|
APN |
8 |
26,395,976 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02109:Kcnu1
|
APN |
8 |
26,427,727 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02127:Kcnu1
|
APN |
8 |
26,382,090 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02170:Kcnu1
|
APN |
8 |
26,427,588 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02217:Kcnu1
|
APN |
8 |
26,348,212 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02385:Kcnu1
|
APN |
8 |
26,422,298 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02493:Kcnu1
|
APN |
8 |
26,427,548 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02883:Kcnu1
|
APN |
8 |
26,339,855 (GRCm39) |
missense |
probably benign |
|
IGL02884:Kcnu1
|
APN |
8 |
26,411,556 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03022:Kcnu1
|
APN |
8 |
26,427,614 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03281:Kcnu1
|
APN |
8 |
26,382,105 (GRCm39) |
missense |
probably null |
1.00 |
IGL03345:Kcnu1
|
APN |
8 |
26,371,321 (GRCm39) |
splice site |
probably benign |
|
P0026:Kcnu1
|
UTSW |
8 |
26,382,150 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4677001:Kcnu1
|
UTSW |
8 |
26,396,021 (GRCm39) |
missense |
probably benign |
|
R0001:Kcnu1
|
UTSW |
8 |
26,349,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R0419:Kcnu1
|
UTSW |
8 |
26,427,646 (GRCm39) |
missense |
probably benign |
0.13 |
R0518:Kcnu1
|
UTSW |
8 |
26,400,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R0521:Kcnu1
|
UTSW |
8 |
26,400,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R0581:Kcnu1
|
UTSW |
8 |
26,427,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R0840:Kcnu1
|
UTSW |
8 |
26,403,712 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R1282:Kcnu1
|
UTSW |
8 |
26,395,985 (GRCm39) |
missense |
probably benign |
0.02 |
R1556:Kcnu1
|
UTSW |
8 |
26,351,219 (GRCm39) |
critical splice donor site |
probably null |
|
R1600:Kcnu1
|
UTSW |
8 |
26,339,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R2011:Kcnu1
|
UTSW |
8 |
26,408,470 (GRCm39) |
missense |
probably benign |
0.03 |
R2035:Kcnu1
|
UTSW |
8 |
26,386,721 (GRCm39) |
missense |
probably benign |
0.35 |
R2082:Kcnu1
|
UTSW |
8 |
26,411,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Kcnu1
|
UTSW |
8 |
26,341,928 (GRCm39) |
missense |
probably damaging |
0.99 |
R2415:Kcnu1
|
UTSW |
8 |
26,400,906 (GRCm39) |
missense |
probably benign |
|
R2513:Kcnu1
|
UTSW |
8 |
26,395,994 (GRCm39) |
missense |
probably benign |
0.00 |
R3712:Kcnu1
|
UTSW |
8 |
26,371,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R3749:Kcnu1
|
UTSW |
8 |
26,376,798 (GRCm39) |
missense |
probably null |
0.01 |
R3840:Kcnu1
|
UTSW |
8 |
26,375,380 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3874:Kcnu1
|
UTSW |
8 |
26,375,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R4184:Kcnu1
|
UTSW |
8 |
26,352,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R4576:Kcnu1
|
UTSW |
8 |
26,380,048 (GRCm39) |
missense |
probably benign |
0.06 |
R4658:Kcnu1
|
UTSW |
8 |
26,427,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R4667:Kcnu1
|
UTSW |
8 |
26,400,949 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4791:Kcnu1
|
UTSW |
8 |
26,403,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R4940:Kcnu1
|
UTSW |
8 |
26,387,890 (GRCm39) |
splice site |
probably null |
|
R5120:Kcnu1
|
UTSW |
8 |
26,424,516 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5314:Kcnu1
|
UTSW |
8 |
26,352,486 (GRCm39) |
missense |
probably damaging |
0.97 |
R5712:Kcnu1
|
UTSW |
8 |
26,409,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R5807:Kcnu1
|
UTSW |
8 |
26,339,742 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6237:Kcnu1
|
UTSW |
8 |
26,422,362 (GRCm39) |
missense |
probably benign |
|
R6260:Kcnu1
|
UTSW |
8 |
26,341,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R6360:Kcnu1
|
UTSW |
8 |
26,351,208 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6612:Kcnu1
|
UTSW |
8 |
26,408,344 (GRCm39) |
missense |
probably benign |
0.10 |
R6708:Kcnu1
|
UTSW |
8 |
26,427,739 (GRCm39) |
missense |
probably benign |
|
R6765:Kcnu1
|
UTSW |
8 |
26,403,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R6816:Kcnu1
|
UTSW |
8 |
26,427,762 (GRCm39) |
nonsense |
probably null |
|
R7030:Kcnu1
|
UTSW |
8 |
26,408,491 (GRCm39) |
missense |
probably benign |
0.00 |
R7202:Kcnu1
|
UTSW |
8 |
26,409,609 (GRCm39) |
splice site |
probably null |
|
R7208:Kcnu1
|
UTSW |
8 |
26,409,665 (GRCm39) |
nonsense |
probably null |
|
R7411:Kcnu1
|
UTSW |
8 |
26,382,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R7520:Kcnu1
|
UTSW |
8 |
26,375,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R7579:Kcnu1
|
UTSW |
8 |
26,386,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R7968:Kcnu1
|
UTSW |
8 |
26,400,898 (GRCm39) |
missense |
probably benign |
|
R8305:Kcnu1
|
UTSW |
8 |
26,382,018 (GRCm39) |
missense |
probably benign |
0.21 |
R8443:Kcnu1
|
UTSW |
8 |
26,382,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R8694:Kcnu1
|
UTSW |
8 |
26,342,101 (GRCm39) |
unclassified |
probably benign |
|
R8730:Kcnu1
|
UTSW |
8 |
26,403,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R9173:Kcnu1
|
UTSW |
8 |
26,390,074 (GRCm39) |
critical splice donor site |
probably null |
|
R9285:Kcnu1
|
UTSW |
8 |
26,381,611 (GRCm39) |
missense |
probably damaging |
0.99 |
R9291:Kcnu1
|
UTSW |
8 |
26,390,041 (GRCm39) |
missense |
probably benign |
|
R9340:Kcnu1
|
UTSW |
8 |
26,376,786 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9470:Kcnu1
|
UTSW |
8 |
26,409,660 (GRCm39) |
missense |
probably benign |
0.13 |
R9556:Kcnu1
|
UTSW |
8 |
26,348,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R9616:Kcnu1
|
UTSW |
8 |
26,403,675 (GRCm39) |
frame shift |
probably null |
|
Z1177:Kcnu1
|
UTSW |
8 |
26,339,792 (GRCm39) |
missense |
probably damaging |
1.00 |
|