Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam2 |
A |
G |
14: 66,272,678 (GRCm39) |
|
probably benign |
Het |
Aldh1a7 |
T |
G |
19: 20,695,103 (GRCm39) |
Y154S |
probably damaging |
Het |
Casc3 |
A |
G |
11: 98,713,947 (GRCm39) |
D393G |
probably damaging |
Het |
Cd180 |
A |
G |
13: 102,842,936 (GRCm39) |
I661V |
probably benign |
Het |
Cdh1 |
T |
C |
8: 107,384,392 (GRCm39) |
S287P |
probably damaging |
Het |
Clnk |
T |
C |
5: 38,952,321 (GRCm39) |
N6S |
probably damaging |
Het |
Cstdc6 |
C |
A |
16: 36,154,625 (GRCm39) |
A11S |
probably damaging |
Het |
Cyp17a1 |
C |
T |
19: 46,659,531 (GRCm39) |
V100M |
possibly damaging |
Het |
Ddhd2 |
A |
G |
8: 26,238,621 (GRCm39) |
V53A |
probably damaging |
Het |
Elovl7 |
T |
A |
13: 108,410,927 (GRCm39) |
|
probably null |
Het |
Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
Gm14180 |
A |
G |
11: 99,625,053 (GRCm39) |
S22P |
unknown |
Het |
Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
Golga5 |
G |
A |
12: 102,446,061 (GRCm39) |
|
probably null |
Het |
Gpr162 |
A |
T |
6: 124,838,370 (GRCm39) |
F93L |
possibly damaging |
Het |
Lamp3 |
A |
T |
16: 19,492,169 (GRCm39) |
F358L |
probably damaging |
Het |
Mdn1 |
T |
G |
4: 32,669,591 (GRCm39) |
D409E |
probably damaging |
Het |
Ms4a10 |
T |
C |
19: 10,940,374 (GRCm39) |
D211G |
probably benign |
Het |
Ms4a3 |
T |
C |
19: 11,616,630 (GRCm39) |
E4G |
possibly damaging |
Het |
Myo15a |
A |
G |
11: 60,418,260 (GRCm39) |
|
probably benign |
Het |
Or2ag16 |
A |
G |
7: 106,351,752 (GRCm39) |
V281A |
possibly damaging |
Het |
Or4c10b |
A |
G |
2: 89,711,826 (GRCm39) |
I219V |
probably damaging |
Het |
Or51aa2 |
A |
T |
7: 103,188,177 (GRCm39) |
L88Q |
probably damaging |
Het |
Or51q1c |
A |
G |
7: 103,653,274 (GRCm39) |
H264R |
probably damaging |
Het |
Or5b12 |
T |
C |
19: 12,896,947 (GRCm39) |
H242R |
probably damaging |
Het |
Or6c217 |
A |
G |
10: 129,737,722 (GRCm39) |
F286L |
probably benign |
Het |
Penk |
T |
C |
4: 4,134,465 (GRCm39) |
I61V |
probably benign |
Het |
Pkhd1 |
T |
A |
1: 20,290,307 (GRCm39) |
K2860N |
probably benign |
Het |
Prtg |
C |
T |
9: 72,762,348 (GRCm39) |
P492S |
probably damaging |
Het |
Spata31e2 |
A |
G |
1: 26,721,665 (GRCm39) |
F1172L |
probably benign |
Het |
Tdrd7 |
T |
C |
4: 45,989,225 (GRCm39) |
|
probably benign |
Het |
Terf2ip |
A |
G |
8: 112,738,700 (GRCm39) |
N196S |
probably benign |
Het |
Tgtp1 |
T |
C |
11: 48,878,382 (GRCm39) |
N108D |
possibly damaging |
Het |
Thumpd3 |
A |
G |
6: 113,036,932 (GRCm39) |
H277R |
probably benign |
Het |
Tshz2 |
T |
A |
2: 169,727,456 (GRCm39) |
L215Q |
possibly damaging |
Het |
Ube3c |
T |
A |
5: 29,873,005 (GRCm39) |
V1015E |
probably damaging |
Het |
Utrn |
T |
A |
10: 12,516,672 (GRCm39) |
K2307N |
probably damaging |
Het |
Vmn1r75 |
A |
G |
7: 11,614,739 (GRCm39) |
Y157C |
probably damaging |
Het |
Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Kcnh8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01313:Kcnh8
|
APN |
17 |
53,141,708 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01959:Kcnh8
|
APN |
17 |
53,141,635 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02214:Kcnh8
|
APN |
17 |
53,184,939 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02528:Kcnh8
|
APN |
17 |
53,110,556 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02620:Kcnh8
|
APN |
17 |
53,205,525 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02688:Kcnh8
|
APN |
17 |
53,266,471 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02931:Kcnh8
|
APN |
17 |
53,263,650 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02950:Kcnh8
|
APN |
17 |
53,263,795 (GRCm39) |
missense |
probably benign |
0.22 |
Incompetent
|
UTSW |
17 |
53,201,129 (GRCm39) |
missense |
probably damaging |
1.00 |
leak
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R0282:Kcnh8
|
UTSW |
17 |
53,032,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R0448:Kcnh8
|
UTSW |
17 |
53,284,648 (GRCm39) |
splice site |
probably null |
|
R0496:Kcnh8
|
UTSW |
17 |
53,032,886 (GRCm39) |
missense |
probably benign |
0.19 |
R0601:Kcnh8
|
UTSW |
17 |
53,201,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R0671:Kcnh8
|
UTSW |
17 |
53,285,141 (GRCm39) |
nonsense |
probably null |
|
R0891:Kcnh8
|
UTSW |
17 |
53,212,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R0971:Kcnh8
|
UTSW |
17 |
53,032,927 (GRCm39) |
missense |
probably benign |
0.00 |
R1054:Kcnh8
|
UTSW |
17 |
53,110,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R1237:Kcnh8
|
UTSW |
17 |
53,200,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R1237:Kcnh8
|
UTSW |
17 |
53,200,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R1565:Kcnh8
|
UTSW |
17 |
53,263,909 (GRCm39) |
missense |
probably benign |
|
R1657:Kcnh8
|
UTSW |
17 |
53,146,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R1669:Kcnh8
|
UTSW |
17 |
53,200,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R1786:Kcnh8
|
UTSW |
17 |
53,200,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R1803:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R1804:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R1929:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R1980:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R1981:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R1982:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2016:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2017:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2132:Kcnh8
|
UTSW |
17 |
53,200,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R2133:Kcnh8
|
UTSW |
17 |
53,200,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R2208:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2265:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2266:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2267:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2303:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2309:Kcnh8
|
UTSW |
17 |
53,285,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R2760:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2764:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2857:Kcnh8
|
UTSW |
17 |
53,284,961 (GRCm39) |
missense |
probably benign |
|
R2898:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2987:Kcnh8
|
UTSW |
17 |
53,263,763 (GRCm39) |
missense |
probably benign |
0.05 |
R3031:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R3157:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R3158:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4080:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4081:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4082:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4087:Kcnh8
|
UTSW |
17 |
53,110,428 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4132:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4158:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4213:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4301:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4302:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4383:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4385:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4400:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4490:Kcnh8
|
UTSW |
17 |
53,268,905 (GRCm39) |
critical splice donor site |
probably null |
|
R4493:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4494:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4611:Kcnh8
|
UTSW |
17 |
52,909,864 (GRCm39) |
missense |
probably benign |
0.22 |
R4728:Kcnh8
|
UTSW |
17 |
53,032,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R4810:Kcnh8
|
UTSW |
17 |
53,212,248 (GRCm39) |
splice site |
probably null |
|
R4927:Kcnh8
|
UTSW |
17 |
53,185,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R4984:Kcnh8
|
UTSW |
17 |
53,184,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R5017:Kcnh8
|
UTSW |
17 |
53,200,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R5214:Kcnh8
|
UTSW |
17 |
53,205,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R5272:Kcnh8
|
UTSW |
17 |
53,212,043 (GRCm39) |
missense |
probably damaging |
0.97 |
R5386:Kcnh8
|
UTSW |
17 |
53,033,023 (GRCm39) |
missense |
probably benign |
0.10 |
R5472:Kcnh8
|
UTSW |
17 |
53,284,844 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5500:Kcnh8
|
UTSW |
17 |
53,033,008 (GRCm39) |
missense |
probably benign |
0.00 |
R5714:Kcnh8
|
UTSW |
17 |
53,285,150 (GRCm39) |
missense |
probably benign |
0.31 |
R5866:Kcnh8
|
UTSW |
17 |
53,263,804 (GRCm39) |
missense |
probably benign |
0.05 |
R5903:Kcnh8
|
UTSW |
17 |
53,110,364 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6969:Kcnh8
|
UTSW |
17 |
53,184,971 (GRCm39) |
nonsense |
probably null |
|
R6994:Kcnh8
|
UTSW |
17 |
53,284,723 (GRCm39) |
missense |
probably benign |
0.02 |
R7101:Kcnh8
|
UTSW |
17 |
53,212,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R7189:Kcnh8
|
UTSW |
17 |
53,201,145 (GRCm39) |
splice site |
probably null |
|
R7228:Kcnh8
|
UTSW |
17 |
53,263,744 (GRCm39) |
missense |
probably benign |
0.01 |
R7372:Kcnh8
|
UTSW |
17 |
53,201,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R7751:Kcnh8
|
UTSW |
17 |
53,268,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R7819:Kcnh8
|
UTSW |
17 |
53,263,743 (GRCm39) |
missense |
probably benign |
|
R7952:Kcnh8
|
UTSW |
17 |
53,266,493 (GRCm39) |
missense |
probably benign |
0.02 |
R8176:Kcnh8
|
UTSW |
17 |
53,285,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R8190:Kcnh8
|
UTSW |
17 |
53,263,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R8407:Kcnh8
|
UTSW |
17 |
53,212,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R8473:Kcnh8
|
UTSW |
17 |
53,285,320 (GRCm39) |
missense |
probably benign |
|
R8716:Kcnh8
|
UTSW |
17 |
53,284,780 (GRCm39) |
missense |
probably benign |
0.02 |
R8943:Kcnh8
|
UTSW |
17 |
53,104,486 (GRCm39) |
missense |
probably benign |
0.00 |
R9051:Kcnh8
|
UTSW |
17 |
53,141,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R9211:Kcnh8
|
UTSW |
17 |
53,146,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R9233:Kcnh8
|
UTSW |
17 |
53,285,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R9243:Kcnh8
|
UTSW |
17 |
53,205,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R9327:Kcnh8
|
UTSW |
17 |
53,146,084 (GRCm39) |
missense |
probably damaging |
0.99 |
R9640:Kcnh8
|
UTSW |
17 |
53,185,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R9646:Kcnh8
|
UTSW |
17 |
53,104,573 (GRCm39) |
missense |
probably benign |
0.25 |
RF009:Kcnh8
|
UTSW |
17 |
53,285,267 (GRCm39) |
missense |
probably benign |
0.00 |
RF010:Kcnh8
|
UTSW |
17 |
53,285,267 (GRCm39) |
missense |
probably benign |
0.00 |
RF011:Kcnh8
|
UTSW |
17 |
53,285,267 (GRCm39) |
missense |
probably benign |
0.00 |
RF021:Kcnh8
|
UTSW |
17 |
53,285,267 (GRCm39) |
missense |
probably benign |
0.00 |
RF022:Kcnh8
|
UTSW |
17 |
53,285,267 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Kcnh8
|
UTSW |
17 |
53,285,320 (GRCm39) |
missense |
probably benign |
|
Z1088:Kcnh8
|
UTSW |
17 |
53,032,918 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Kcnh8
|
UTSW |
17 |
53,201,089 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Kcnh8
|
UTSW |
17 |
53,285,121 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1177:Kcnh8
|
UTSW |
17 |
53,110,499 (GRCm39) |
missense |
probably damaging |
1.00 |
|