Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvr2b |
G |
T |
9: 119,256,587 (GRCm39) |
R40L |
probably benign |
Het |
Asph |
T |
C |
4: 9,517,668 (GRCm39) |
N402D |
possibly damaging |
Het |
Brip1 |
T |
C |
11: 85,968,776 (GRCm39) |
Y803C |
probably damaging |
Het |
Cenpc1 |
T |
C |
5: 86,170,234 (GRCm39) |
|
probably benign |
Het |
Dynlt5 |
A |
G |
4: 102,859,714 (GRCm39) |
T85A |
probably benign |
Het |
Fam110b |
A |
G |
4: 5,799,448 (GRCm39) |
M289V |
probably benign |
Het |
Fam193b |
T |
C |
13: 55,691,475 (GRCm39) |
N429S |
probably damaging |
Het |
Folh1 |
T |
C |
7: 86,395,379 (GRCm39) |
Y351C |
possibly damaging |
Het |
Fryl |
G |
A |
5: 73,216,726 (GRCm39) |
A2188V |
possibly damaging |
Het |
Gtf2f1 |
C |
T |
17: 57,317,971 (GRCm39) |
|
probably null |
Het |
Gucy1a1 |
T |
C |
3: 82,016,404 (GRCm39) |
K195E |
probably benign |
Het |
H2-Oa |
T |
C |
17: 34,313,023 (GRCm39) |
V100A |
probably damaging |
Het |
Mtss1 |
A |
G |
15: 58,825,439 (GRCm39) |
S254P |
probably damaging |
Het |
N4bp2l2 |
A |
G |
5: 150,566,761 (GRCm39) |
S516P |
probably benign |
Het |
Nrcam |
A |
G |
12: 44,645,225 (GRCm39) |
D1139G |
probably damaging |
Het |
Nxpe4 |
T |
C |
9: 48,304,548 (GRCm39) |
S212P |
probably damaging |
Het |
Or1ab2 |
A |
C |
8: 72,863,968 (GRCm39) |
K186T |
probably damaging |
Het |
Or5d47 |
C |
T |
2: 87,804,341 (GRCm39) |
V223I |
probably benign |
Het |
Or5p52 |
A |
T |
7: 107,502,188 (GRCm39) |
H88L |
probably benign |
Het |
Parp2 |
T |
C |
14: 51,058,553 (GRCm39) |
Y528H |
probably damaging |
Het |
Pdgfd |
T |
C |
9: 6,288,495 (GRCm39) |
Y50H |
probably damaging |
Het |
Prkaca |
A |
G |
8: 84,721,976 (GRCm39) |
D329G |
possibly damaging |
Het |
Rbbp8 |
A |
G |
18: 11,858,559 (GRCm39) |
|
probably benign |
Het |
Sele |
A |
G |
1: 163,882,248 (GRCm39) |
T578A |
probably benign |
Het |
Shroom2 |
A |
G |
X: 151,443,089 (GRCm39) |
V692A |
probably benign |
Het |
Stxbp3 |
G |
A |
3: 108,708,072 (GRCm39) |
L410F |
probably damaging |
Het |
Tcaf1 |
C |
A |
6: 42,655,060 (GRCm39) |
G553* |
probably null |
Het |
Ttn |
G |
A |
2: 76,576,862 (GRCm39) |
T24677M |
probably damaging |
Het |
Vmn2r24 |
T |
A |
6: 123,755,967 (GRCm39) |
L13H |
probably damaging |
Het |
Zfp106 |
C |
A |
2: 120,359,120 (GRCm39) |
|
probably benign |
Het |
Zfp616 |
A |
G |
11: 73,973,800 (GRCm39) |
D23G |
possibly damaging |
Het |
Zfp84 |
T |
C |
7: 29,474,759 (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 |
IGL00675:Kcnu1
|
APN |
8 |
26,341,877 (GRCm39) |
missense |
probably benign |
|
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 |
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 |
|