Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abl2 |
G |
A |
1: 156,450,189 (GRCm39) |
V119M |
probably damaging |
Het |
Acss2 |
T |
C |
2: 155,399,100 (GRCm39) |
V454A |
probably damaging |
Het |
Adam6b |
T |
A |
12: 113,453,784 (GRCm39) |
D200E |
probably benign |
Het |
Adarb1 |
T |
A |
10: 77,131,712 (GRCm39) |
|
probably null |
Het |
Aqp12 |
C |
T |
1: 92,934,088 (GRCm39) |
|
probably benign |
Het |
Atrnl1 |
T |
C |
19: 57,924,078 (GRCm39) |
V1281A |
possibly damaging |
Het |
Brdt |
A |
G |
5: 107,518,160 (GRCm39) |
E761G |
possibly damaging |
Het |
Bsn |
A |
T |
9: 107,987,718 (GRCm39) |
I2678N |
unknown |
Het |
C2cd2 |
A |
T |
16: 97,676,580 (GRCm39) |
C136S |
|
Het |
Camk4 |
A |
G |
18: 33,318,178 (GRCm39) |
D445G |
probably benign |
Het |
Cckar |
T |
C |
5: 53,864,624 (GRCm39) |
T26A |
probably damaging |
Het |
Cd209a |
T |
A |
8: 3,798,857 (GRCm39) |
|
probably null |
Het |
Cept1 |
A |
G |
3: 106,411,056 (GRCm39) |
F379S |
probably benign |
Het |
Crhr1 |
A |
G |
11: 104,054,719 (GRCm39) |
|
probably null |
Het |
Cryzl1 |
T |
C |
16: 91,509,085 (GRCm39) |
E72G |
probably benign |
Het |
Ctnnal1 |
T |
A |
4: 56,826,285 (GRCm39) |
E526V |
possibly damaging |
Het |
Cyp3a41a |
T |
C |
5: 145,650,374 (GRCm39) |
I90V |
possibly damaging |
Het |
Dek |
T |
C |
13: 47,259,053 (GRCm39) |
E51G |
unknown |
Het |
Dnaaf6rt |
A |
T |
1: 31,262,432 (GRCm39) |
D138V |
probably damaging |
Het |
Evc2 |
T |
A |
5: 37,544,477 (GRCm39) |
V742E |
probably damaging |
Het |
Fat4 |
G |
A |
3: 38,944,358 (GRCm39) |
V1084M |
probably damaging |
Het |
Fscb |
G |
A |
12: 64,518,598 (GRCm39) |
T956I |
unknown |
Het |
Glipr2 |
T |
C |
4: 43,968,184 (GRCm39) |
L29P |
probably damaging |
Het |
Gm19402 |
A |
T |
10: 77,526,261 (GRCm39) |
S111T |
unknown |
Het |
Gm4553 |
ACCCTTGCAGCCACCACAGGAGCCACAGCCCCCACAGGAGCTACAGCCTCCCTTGCAGCCACCACAGGAGCCACAGCCCCCACAGGAGCTACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCC |
ACCCTTGCAGCCACCACAGGAGCCACAGCCCCCACAGGAGCTACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCC |
7: 141,719,157 (GRCm39) |
|
probably benign |
Het |
Gnl3 |
T |
C |
14: 30,738,843 (GRCm39) |
K115E |
probably benign |
Het |
Gpn1 |
T |
A |
5: 31,658,465 (GRCm39) |
F147I |
probably damaging |
Het |
Gsdmd |
T |
A |
15: 75,737,618 (GRCm39) |
L232H |
probably benign |
Het |
Helz2 |
A |
G |
2: 180,880,216 (GRCm39) |
V500A |
possibly damaging |
Het |
Hemk1 |
T |
C |
9: 107,214,267 (GRCm39) |
E55G |
probably benign |
Het |
Hs2st1 |
A |
T |
3: 144,141,221 (GRCm39) |
|
probably null |
Het |
Ighv1-63 |
A |
G |
12: 115,459,486 (GRCm39) |
V37A |
probably damaging |
Het |
Iqsec3 |
C |
A |
6: 121,360,991 (GRCm39) |
E956* |
probably null |
Het |
Kif3c |
T |
A |
12: 3,437,592 (GRCm39) |
M531K |
probably benign |
Het |
Kif5c |
T |
A |
2: 49,648,671 (GRCm39) |
|
probably null |
Het |
Krt15 |
A |
T |
11: 100,026,386 (GRCm39) |
V100E |
possibly damaging |
Het |
Lcor |
T |
C |
19: 41,573,945 (GRCm39) |
L900P |
probably damaging |
Het |
Lrrc32 |
A |
G |
7: 98,149,014 (GRCm39) |
D598G |
probably benign |
Het |
Mug2 |
T |
C |
6: 122,060,425 (GRCm39) |
V1387A |
possibly damaging |
Het |
Nin |
T |
A |
12: 70,102,803 (GRCm39) |
E275V |
|
Het |
Or5p68 |
A |
G |
7: 107,945,703 (GRCm39) |
F162L |
probably benign |
Het |
Papolg |
A |
G |
11: 23,816,439 (GRCm39) |
I698T |
probably benign |
Het |
Pcdhb20 |
A |
G |
18: 37,639,840 (GRCm39) |
N789D |
probably benign |
Het |
Pik3cg |
C |
T |
12: 32,247,196 (GRCm39) |
M842I |
probably damaging |
Het |
Pnn |
T |
A |
12: 59,115,765 (GRCm39) |
D135E |
probably damaging |
Het |
Pold1 |
C |
A |
7: 44,192,847 (GRCm39) |
R5L |
possibly damaging |
Het |
Prl8a1 |
A |
T |
13: 27,758,089 (GRCm39) |
F207I |
probably damaging |
Het |
Prr11 |
A |
G |
11: 86,989,600 (GRCm39) |
V257A |
probably benign |
Het |
Prtg |
C |
T |
9: 72,758,848 (GRCm39) |
R401* |
probably null |
Het |
Rasgrp1 |
A |
G |
2: 117,115,635 (GRCm39) |
M651T |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,695,885 (GRCm39) |
H2994L |
probably damaging |
Het |
Snx13 |
A |
T |
12: 35,128,950 (GRCm39) |
I23L |
probably benign |
Het |
Snx7 |
A |
G |
3: 117,576,000 (GRCm39) |
L429P |
probably damaging |
Het |
Spta1 |
C |
T |
1: 174,025,201 (GRCm39) |
Q689* |
probably null |
Het |
Spty2d1 |
T |
C |
7: 46,648,692 (GRCm39) |
D79G |
probably damaging |
Het |
Tbc1d9b |
A |
G |
11: 50,059,515 (GRCm39) |
|
probably null |
Het |
Tnxb |
T |
C |
17: 34,936,228 (GRCm39) |
F2722L |
possibly damaging |
Het |
Tppp2 |
C |
T |
14: 52,156,865 (GRCm39) |
R81C |
probably benign |
Het |
Trim6 |
G |
T |
7: 103,881,843 (GRCm39) |
A391S |
probably benign |
Het |
Trim69 |
A |
C |
2: 122,009,064 (GRCm39) |
T375P |
possibly damaging |
Het |
Trim72 |
A |
G |
7: 127,603,858 (GRCm39) |
N68S |
possibly damaging |
Het |
Trrap |
G |
A |
5: 144,726,208 (GRCm39) |
V386I |
probably benign |
Het |
Ttn |
T |
C |
2: 76,778,275 (GRCm39) |
I1371V |
unknown |
Het |
Usp17lb |
A |
T |
7: 104,490,913 (GRCm39) |
|
probably null |
Het |
Vmn2r20 |
A |
T |
6: 123,362,468 (GRCm39) |
L772Q |
probably damaging |
Het |
Ypel3 |
A |
G |
7: 126,379,200 (GRCm39) |
E91G |
probably benign |
Het |
Zbtb21 |
C |
T |
16: 97,751,569 (GRCm39) |
E905K |
possibly damaging |
Het |
Zfp189 |
T |
A |
4: 49,530,417 (GRCm39) |
C507S |
possibly damaging |
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 |
IGL01901:Kcnh8
|
APN |
17 |
53,201,148 (GRCm39) |
splice site |
probably benign |
|
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 |
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 |
|