Other mutations in this stock |
Total: 20 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Flii |
T |
C |
11: 60,614,241 (GRCm39) |
N93D |
probably benign |
Het |
Gm8356 |
T |
C |
14: 17,693,287 (GRCm39) |
K24E |
probably damaging |
Het |
Hars1 |
G |
A |
18: 36,901,225 (GRCm39) |
T409M |
probably damaging |
Het |
Ivns1abp |
A |
G |
1: 151,226,863 (GRCm39) |
|
probably null |
Het |
Kdm4c |
T |
G |
4: 74,263,804 (GRCm39) |
V696G |
probably benign |
Het |
Klrb1f |
T |
A |
6: 129,030,138 (GRCm39) |
|
probably benign |
Het |
Lrp4 |
G |
A |
2: 91,325,371 (GRCm39) |
V1399I |
probably benign |
Het |
LTO1 |
G |
A |
7: 144,471,405 (GRCm39) |
G86D |
possibly damaging |
Het |
Mki67 |
A |
G |
7: 135,291,849 (GRCm39) |
V3168A |
probably benign |
Het |
Nf1 |
T |
A |
11: 79,286,731 (GRCm39) |
I177K |
probably damaging |
Het |
Nnt |
A |
T |
13: 119,506,533 (GRCm39) |
N371K |
probably damaging |
Het |
Or13a27 |
A |
G |
7: 139,925,123 (GRCm39) |
Y260H |
probably damaging |
Het |
Or5p52 |
C |
T |
7: 107,502,311 (GRCm39) |
P129L |
probably damaging |
Het |
Prkdc |
G |
T |
16: 15,627,508 (GRCm39) |
V3389L |
possibly damaging |
Het |
Prr16 |
T |
A |
18: 51,436,192 (GRCm39) |
Y224N |
possibly damaging |
Het |
Ptgs1 |
G |
A |
2: 36,127,231 (GRCm39) |
C39Y |
probably damaging |
Het |
Sla |
T |
C |
15: 66,654,479 (GRCm39) |
D269G |
possibly damaging |
Het |
Stk38l |
T |
A |
6: 146,659,971 (GRCm39) |
M1K |
probably null |
Het |
Trim24 |
T |
A |
6: 37,880,583 (GRCm39) |
N160K |
possibly damaging |
Het |
Zfp451 |
A |
G |
1: 33,825,621 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Kcnq4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00164:Kcnq4
|
APN |
4 |
120,555,213 (GRCm39) |
nonsense |
probably null |
|
IGL00228:Kcnq4
|
APN |
4 |
120,555,213 (GRCm39) |
nonsense |
probably null |
|
IGL00310:Kcnq4
|
APN |
4 |
120,555,213 (GRCm39) |
nonsense |
probably null |
|
IGL00330:Kcnq4
|
APN |
4 |
120,555,213 (GRCm39) |
nonsense |
probably null |
|
IGL00333:Kcnq4
|
APN |
4 |
120,555,213 (GRCm39) |
nonsense |
probably null |
|
IGL00335:Kcnq4
|
APN |
4 |
120,555,213 (GRCm39) |
nonsense |
probably null |
|
IGL00336:Kcnq4
|
APN |
4 |
120,555,213 (GRCm39) |
nonsense |
probably null |
|
IGL01143:Kcnq4
|
APN |
4 |
120,555,820 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01373:Kcnq4
|
APN |
4 |
120,574,229 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02095:Kcnq4
|
APN |
4 |
120,557,224 (GRCm39) |
splice site |
probably benign |
|
IGL02335:Kcnq4
|
APN |
4 |
120,573,051 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03188:Kcnq4
|
APN |
4 |
120,561,623 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0045:Kcnq4
|
UTSW |
4 |
120,555,152 (GRCm39) |
missense |
probably damaging |
0.99 |
R0045:Kcnq4
|
UTSW |
4 |
120,555,152 (GRCm39) |
missense |
probably damaging |
0.99 |
R0423:Kcnq4
|
UTSW |
4 |
120,574,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R0483:Kcnq4
|
UTSW |
4 |
120,573,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R0837:Kcnq4
|
UTSW |
4 |
120,604,058 (GRCm39) |
missense |
probably benign |
0.00 |
R1722:Kcnq4
|
UTSW |
4 |
120,559,624 (GRCm39) |
missense |
probably benign |
0.00 |
R1826:Kcnq4
|
UTSW |
4 |
120,561,701 (GRCm39) |
missense |
probably benign |
0.00 |
R2059:Kcnq4
|
UTSW |
4 |
120,555,199 (GRCm39) |
missense |
probably benign |
0.00 |
R4327:Kcnq4
|
UTSW |
4 |
120,568,561 (GRCm39) |
missense |
probably benign |
0.00 |
R4690:Kcnq4
|
UTSW |
4 |
120,574,208 (GRCm39) |
missense |
probably damaging |
0.99 |
R4706:Kcnq4
|
UTSW |
4 |
120,561,683 (GRCm39) |
missense |
probably benign |
|
R4729:Kcnq4
|
UTSW |
4 |
120,570,271 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4806:Kcnq4
|
UTSW |
4 |
120,570,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R4859:Kcnq4
|
UTSW |
4 |
120,573,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R4885:Kcnq4
|
UTSW |
4 |
120,570,260 (GRCm39) |
missense |
probably benign |
0.01 |
R5073:Kcnq4
|
UTSW |
4 |
120,574,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R5517:Kcnq4
|
UTSW |
4 |
120,573,006 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5590:Kcnq4
|
UTSW |
4 |
120,573,082 (GRCm39) |
missense |
probably damaging |
0.98 |
R5653:Kcnq4
|
UTSW |
4 |
120,559,608 (GRCm39) |
missense |
probably benign |
0.00 |
R5750:Kcnq4
|
UTSW |
4 |
120,572,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R6141:Kcnq4
|
UTSW |
4 |
120,573,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R6160:Kcnq4
|
UTSW |
4 |
120,573,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R7087:Kcnq4
|
UTSW |
4 |
120,561,596 (GRCm39) |
missense |
probably damaging |
0.96 |
R7088:Kcnq4
|
UTSW |
4 |
120,561,596 (GRCm39) |
missense |
probably damaging |
0.96 |
R7143:Kcnq4
|
UTSW |
4 |
120,568,436 (GRCm39) |
missense |
probably benign |
0.05 |
R7225:Kcnq4
|
UTSW |
4 |
120,604,111 (GRCm39) |
missense |
probably benign |
0.03 |
R7479:Kcnq4
|
UTSW |
4 |
120,573,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R7574:Kcnq4
|
UTSW |
4 |
120,568,565 (GRCm39) |
missense |
probably benign |
|
R7879:Kcnq4
|
UTSW |
4 |
120,559,632 (GRCm39) |
missense |
probably benign |
0.13 |
R7980:Kcnq4
|
UTSW |
4 |
120,568,494 (GRCm39) |
missense |
probably benign |
0.02 |
R9007:Kcnq4
|
UTSW |
4 |
120,555,150 (GRCm39) |
missense |
probably benign |
0.01 |
R9421:Kcnq4
|
UTSW |
4 |
120,573,868 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9468:Kcnq4
|
UTSW |
4 |
120,568,494 (GRCm39) |
missense |
probably benign |
0.02 |
R9774:Kcnq4
|
UTSW |
4 |
120,573,076 (GRCm39) |
missense |
probably damaging |
0.99 |
X0020:Kcnq4
|
UTSW |
4 |
120,572,524 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Kcnq4
|
UTSW |
4 |
120,555,694 (GRCm39) |
critical splice donor site |
probably null |
|
|