Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930579F01Rik |
A |
T |
3: 137,879,343 (GRCm39) |
L235Q |
probably damaging |
Het |
Aadacl4fm4 |
A |
T |
4: 144,412,790 (GRCm39) |
M50K |
possibly damaging |
Het |
Adam6b |
T |
A |
12: 113,454,275 (GRCm39) |
V364D |
probably benign |
Het |
Akap13 |
T |
C |
7: 75,259,677 (GRCm39) |
L767P |
probably benign |
Het |
Akap13 |
T |
A |
7: 75,380,248 (GRCm39) |
S2193T |
probably damaging |
Het |
Anapc11 |
T |
C |
11: 120,496,203 (GRCm39) |
V69A |
probably benign |
Het |
Ankmy1 |
C |
T |
1: 92,823,912 (GRCm39) |
R118Q |
probably damaging |
Het |
Ankrd27 |
T |
C |
7: 35,337,478 (GRCm39) |
S931P |
probably benign |
Het |
Atp6v1c2 |
G |
A |
12: 17,338,169 (GRCm39) |
R280C |
probably damaging |
Het |
Bbs10 |
T |
A |
10: 111,135,913 (GRCm39) |
I342N |
probably damaging |
Het |
Calhm2 |
T |
C |
19: 47,121,389 (GRCm39) |
D260G |
possibly damaging |
Het |
Camk2a |
A |
G |
18: 61,091,310 (GRCm39) |
E264G |
probably damaging |
Het |
Ccdc146 |
T |
A |
5: 21,524,543 (GRCm39) |
M270L |
probably benign |
Het |
Cdc16 |
A |
G |
8: 13,829,264 (GRCm39) |
T517A |
probably benign |
Het |
Ces1g |
T |
C |
8: 94,057,821 (GRCm39) |
H160R |
probably benign |
Het |
Chst4 |
T |
C |
8: 110,757,026 (GRCm39) |
N196S |
probably damaging |
Het |
Ciz1 |
A |
T |
2: 32,257,479 (GRCm39) |
N175Y |
probably damaging |
Het |
Cyb5r4 |
G |
A |
9: 86,909,093 (GRCm39) |
V57I |
probably damaging |
Het |
Cyth3 |
A |
G |
5: 143,670,181 (GRCm39) |
|
probably benign |
Het |
Def6 |
A |
G |
17: 28,439,154 (GRCm39) |
E255G |
probably damaging |
Het |
Dhtkd1 |
T |
G |
2: 5,916,681 (GRCm39) |
Q665P |
probably damaging |
Het |
Dsg3 |
A |
C |
18: 20,672,804 (GRCm39) |
D825A |
probably damaging |
Het |
Eif3m |
T |
C |
2: 104,835,345 (GRCm39) |
T242A |
probably benign |
Het |
Emilin3 |
A |
G |
2: 160,751,737 (GRCm39) |
F101L |
probably benign |
Het |
Epha7 |
A |
G |
4: 28,935,700 (GRCm39) |
|
probably null |
Het |
Fbxo45 |
A |
T |
16: 32,057,223 (GRCm39) |
Y224N |
probably damaging |
Het |
Fhod3 |
A |
T |
18: 25,223,161 (GRCm39) |
M836L |
possibly damaging |
Het |
Fut4 |
C |
A |
9: 14,662,506 (GRCm39) |
V263F |
probably damaging |
Het |
Ggt1 |
C |
T |
10: 75,415,104 (GRCm39) |
T206M |
probably benign |
Het |
Gls |
T |
C |
1: 52,227,858 (GRCm39) |
R79G |
probably damaging |
Het |
Grhl1 |
T |
C |
12: 24,631,514 (GRCm39) |
S156P |
probably benign |
Het |
Ipo8 |
C |
T |
6: 148,676,540 (GRCm39) |
S983N |
probably benign |
Het |
Kpnb1 |
A |
T |
11: 97,075,916 (GRCm39) |
L40Q |
probably damaging |
Het |
Matn1 |
A |
T |
4: 130,677,417 (GRCm39) |
S209C |
probably damaging |
Het |
Mcc |
A |
G |
18: 44,608,289 (GRCm39) |
I501T |
probably benign |
Het |
Mdp1 |
A |
T |
14: 55,896,832 (GRCm39) |
F104L |
probably damaging |
Het |
Mib2 |
A |
T |
4: 155,740,745 (GRCm39) |
N626K |
probably damaging |
Het |
Mrgprh |
T |
C |
17: 13,095,843 (GRCm39) |
S28P |
possibly damaging |
Het |
Mup-ps23 |
T |
A |
4: 61,774,386 (GRCm39) |
|
noncoding transcript |
Het |
Myh15 |
A |
G |
16: 49,003,322 (GRCm39) |
T1794A |
possibly damaging |
Het |
Myo18a |
C |
G |
11: 77,711,868 (GRCm39) |
P680A |
probably benign |
Het |
Myom2 |
G |
T |
8: 15,148,419 (GRCm39) |
D532Y |
possibly damaging |
Het |
Ndufaf5 |
A |
G |
2: 140,012,801 (GRCm39) |
N57S |
probably benign |
Het |
Nectin3 |
C |
T |
16: 46,278,550 (GRCm39) |
V282M |
probably damaging |
Het |
Nup188 |
G |
T |
2: 30,221,000 (GRCm39) |
D997Y |
probably damaging |
Het |
Olfm3 |
T |
C |
3: 114,916,454 (GRCm39) |
V462A |
probably damaging |
Het |
Opcml |
A |
G |
9: 28,724,694 (GRCm39) |
H164R |
possibly damaging |
Het |
Or14a259 |
A |
T |
7: 86,013,013 (GRCm39) |
C177* |
probably null |
Het |
Or4c120 |
A |
T |
2: 89,000,757 (GRCm39) |
F266L |
probably benign |
Het |
Or8u9 |
A |
C |
2: 86,002,050 (GRCm39) |
F37C |
probably damaging |
Het |
Pacrg |
A |
G |
17: 10,622,347 (GRCm39) |
I209T |
probably damaging |
Het |
Pcf11 |
T |
C |
7: 92,310,423 (GRCm39) |
M522V |
probably benign |
Het |
Pck1 |
T |
A |
2: 172,995,183 (GRCm39) |
M1K |
probably null |
Het |
Pcm1 |
G |
T |
8: 41,729,148 (GRCm39) |
E707* |
probably null |
Het |
Pcsk5 |
G |
A |
19: 17,632,213 (GRCm39) |
R318W |
probably damaging |
Het |
Phf11d |
A |
T |
14: 59,590,793 (GRCm39) |
M188K |
possibly damaging |
Het |
Ppip5k2 |
A |
T |
1: 97,668,262 (GRCm39) |
C615* |
probably null |
Het |
Prkdc |
T |
A |
16: 15,609,791 (GRCm39) |
S3132T |
probably damaging |
Het |
Prl2c5 |
A |
T |
13: 13,357,609 (GRCm39) |
|
probably benign |
Het |
Prpsap2 |
A |
G |
11: 61,631,826 (GRCm39) |
I177T |
possibly damaging |
Het |
Rad50 |
A |
G |
11: 53,541,346 (GRCm39) |
S1297P |
probably damaging |
Het |
Rasip1 |
T |
A |
7: 45,284,668 (GRCm39) |
N678K |
possibly damaging |
Het |
Rubcn |
A |
G |
16: 32,656,350 (GRCm39) |
S544P |
probably damaging |
Het |
Rwdd2a |
A |
T |
9: 86,456,453 (GRCm39) |
T210S |
possibly damaging |
Het |
Scd2 |
A |
G |
19: 44,291,479 (GRCm39) |
D306G |
probably damaging |
Het |
Sema3b |
T |
C |
9: 107,480,117 (GRCm39) |
N207S |
probably benign |
Het |
Sf3b2 |
C |
T |
19: 5,324,852 (GRCm39) |
D845N |
probably damaging |
Het |
Sipa1l2 |
C |
A |
8: 126,191,149 (GRCm39) |
C947F |
probably damaging |
Het |
Slc12a1 |
A |
T |
2: 125,067,951 (GRCm39) |
T1013S |
probably damaging |
Het |
Slc18a2 |
A |
T |
19: 59,275,799 (GRCm39) |
I461L |
probably benign |
Het |
Slc1a6 |
C |
A |
10: 78,637,756 (GRCm39) |
Y427* |
probably null |
Het |
Slc30a4 |
A |
T |
2: 122,531,319 (GRCm39) |
I231K |
probably damaging |
Het |
Sos1 |
G |
T |
17: 80,761,192 (GRCm39) |
A168D |
probably damaging |
Het |
Spata31f1a |
T |
C |
4: 42,851,161 (GRCm39) |
I332V |
probably benign |
Het |
Sptb |
T |
C |
12: 76,668,145 (GRCm39) |
S651G |
probably benign |
Het |
Stk36 |
T |
C |
1: 74,672,779 (GRCm39) |
L1007P |
probably damaging |
Het |
Tek |
A |
T |
4: 94,692,578 (GRCm39) |
N229Y |
probably damaging |
Het |
Tep1 |
A |
G |
14: 51,074,225 (GRCm39) |
F1887L |
possibly damaging |
Het |
Tet1 |
A |
T |
10: 62,713,988 (GRCm39) |
C602* |
probably null |
Het |
Tnfrsf19 |
A |
G |
14: 61,209,485 (GRCm39) |
S262P |
possibly damaging |
Het |
Trim5 |
T |
C |
7: 103,914,891 (GRCm39) |
I393V |
probably benign |
Het |
Trpm6 |
A |
G |
19: 18,830,951 (GRCm39) |
E1272G |
probably benign |
Het |
Ttc21b |
A |
T |
2: 66,018,670 (GRCm39) |
Y1246N |
probably damaging |
Het |
Ttll3 |
T |
A |
6: 113,375,738 (GRCm39) |
L151H |
probably damaging |
Het |
U2surp |
C |
T |
9: 95,366,496 (GRCm39) |
V470I |
probably benign |
Het |
Ubr1 |
A |
T |
2: 120,777,138 (GRCm39) |
Y276N |
probably benign |
Het |
Uggt1 |
A |
G |
1: 36,218,751 (GRCm39) |
S59P |
probably benign |
Het |
Unc45a |
T |
C |
7: 79,976,092 (GRCm39) |
T796A |
probably damaging |
Het |
Unc5b |
C |
A |
10: 60,614,719 (GRCm39) |
V193F |
possibly damaging |
Het |
Upp1 |
G |
T |
11: 9,079,590 (GRCm39) |
M50I |
probably benign |
Het |
Vps18 |
C |
T |
2: 119,124,386 (GRCm39) |
R438C |
probably damaging |
Het |
Zfp715 |
T |
C |
7: 42,948,760 (GRCm39) |
Y400C |
possibly damaging |
Het |
Zfp955b |
T |
C |
17: 33,521,496 (GRCm39) |
Y322H |
probably benign |
Het |
|
Other mutations in Kcna7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01534:Kcna7
|
APN |
7 |
45,055,935 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02477:Kcna7
|
APN |
7 |
45,059,047 (GRCm39) |
missense |
probably benign |
0.01 |
R0624:Kcna7
|
UTSW |
7 |
45,059,114 (GRCm39) |
missense |
probably null |
1.00 |
R0850:Kcna7
|
UTSW |
7 |
45,058,855 (GRCm39) |
missense |
probably damaging |
0.99 |
R1721:Kcna7
|
UTSW |
7 |
45,056,345 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1727:Kcna7
|
UTSW |
7 |
45,058,930 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3040:Kcna7
|
UTSW |
7 |
45,056,212 (GRCm39) |
frame shift |
probably null |
|
R3755:Kcna7
|
UTSW |
7 |
45,058,369 (GRCm39) |
missense |
probably benign |
0.00 |
R5024:Kcna7
|
UTSW |
7 |
45,056,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R5054:Kcna7
|
UTSW |
7 |
45,056,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R5055:Kcna7
|
UTSW |
7 |
45,056,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R5056:Kcna7
|
UTSW |
7 |
45,056,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R5549:Kcna7
|
UTSW |
7 |
45,056,063 (GRCm39) |
missense |
probably damaging |
0.98 |
R6669:Kcna7
|
UTSW |
7 |
45,058,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R7284:Kcna7
|
UTSW |
7 |
45,058,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R7309:Kcna7
|
UTSW |
7 |
45,058,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R8028:Kcna7
|
UTSW |
7 |
45,058,947 (GRCm39) |
nonsense |
probably null |
|
R8326:Kcna7
|
UTSW |
7 |
45,058,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R9719:Kcna7
|
UTSW |
7 |
45,056,390 (GRCm39) |
missense |
probably benign |
|
R9744:Kcna7
|
UTSW |
7 |
45,056,402 (GRCm39) |
missense |
probably benign |
|
Z1088:Kcna7
|
UTSW |
7 |
45,058,529 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Kcna7
|
UTSW |
7 |
45,056,383 (GRCm39) |
missense |
probably benign |
0.21 |
Z1177:Kcna7
|
UTSW |
7 |
45,058,607 (GRCm39) |
missense |
probably damaging |
0.99 |
|