Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9330159F19Rik |
G |
T |
10: 29,098,252 (GRCm39) |
L186F |
probably damaging |
Het |
Abce1 |
A |
C |
8: 80,412,572 (GRCm39) |
|
probably null |
Het |
Acvrl1 |
A |
T |
15: 101,035,002 (GRCm39) |
N254Y |
probably damaging |
Het |
Apip |
T |
A |
2: 102,918,916 (GRCm39) |
M72K |
possibly damaging |
Het |
Arg1 |
A |
G |
10: 24,792,356 (GRCm39) |
Y188H |
probably benign |
Het |
Armc3 |
A |
T |
2: 19,274,027 (GRCm39) |
N354Y |
probably damaging |
Het |
Arrdc5 |
A |
G |
17: 56,601,382 (GRCm39) |
F248L |
probably damaging |
Het |
Atp8b5 |
T |
C |
4: 43,302,576 (GRCm39) |
|
probably benign |
Het |
Bltp1 |
G |
T |
3: 36,971,922 (GRCm39) |
V552L |
probably benign |
Het |
Ccdc154 |
C |
T |
17: 25,389,606 (GRCm39) |
A490V |
probably benign |
Het |
Cdh6 |
T |
C |
15: 13,053,868 (GRCm39) |
|
probably benign |
Het |
Chmp2b |
G |
T |
16: 65,337,078 (GRCm39) |
T193K |
probably benign |
Het |
Clca3a1 |
A |
T |
3: 144,436,640 (GRCm39) |
N814K |
probably damaging |
Het |
Cmtr1 |
T |
C |
17: 29,916,098 (GRCm39) |
L576P |
probably damaging |
Het |
Fhl5 |
T |
C |
4: 25,213,624 (GRCm39) |
H104R |
probably benign |
Het |
Gm11596 |
T |
A |
11: 99,683,542 (GRCm39) |
T193S |
unknown |
Het |
Gm15217 |
A |
T |
14: 46,617,853 (GRCm39) |
|
probably benign |
Het |
Hic2 |
A |
G |
16: 17,075,377 (GRCm39) |
I69V |
probably benign |
Het |
Ivl |
T |
C |
3: 92,479,150 (GRCm39) |
D305G |
probably damaging |
Het |
Kcnn2 |
A |
G |
18: 45,725,472 (GRCm39) |
T323A |
probably damaging |
Het |
Krt7 |
C |
T |
15: 101,321,190 (GRCm39) |
Q336* |
probably null |
Het |
Krt73 |
T |
G |
15: 101,710,371 (GRCm39) |
D121A |
probably damaging |
Het |
Mok |
T |
C |
12: 110,774,539 (GRCm39) |
D216G |
probably damaging |
Het |
Muc17 |
A |
G |
5: 137,175,539 (GRCm39) |
C44R |
probably damaging |
Het |
Muc5b |
A |
G |
7: 141,395,132 (GRCm39) |
Y46C |
unknown |
Het |
Muc5b |
T |
C |
7: 141,396,995 (GRCm39) |
F223L |
unknown |
Het |
Noct |
A |
G |
3: 51,157,895 (GRCm39) |
D411G |
probably damaging |
Het |
Or2z8 |
C |
T |
8: 72,812,244 (GRCm39) |
T240M |
probably damaging |
Het |
Or5j1 |
T |
C |
2: 86,879,400 (GRCm39) |
Y60C |
probably damaging |
Het |
Or6c76b |
A |
T |
10: 129,692,906 (GRCm39) |
D173V |
probably damaging |
Het |
Pigv |
T |
C |
4: 133,393,062 (GRCm39) |
H36R |
probably damaging |
Het |
Plscr3 |
A |
G |
11: 69,740,880 (GRCm39) |
K239E |
probably damaging |
Het |
Prkag3 |
T |
C |
1: 74,780,330 (GRCm39) |
D445G |
probably benign |
Het |
Ramp1 |
A |
T |
1: 91,124,641 (GRCm39) |
|
probably benign |
Het |
Ror1 |
T |
A |
4: 100,266,942 (GRCm39) |
H214Q |
probably benign |
Het |
Selenbp2 |
A |
T |
3: 94,607,008 (GRCm39) |
H156L |
probably benign |
Het |
Slc28a3 |
T |
C |
13: 58,721,314 (GRCm39) |
T284A |
probably benign |
Het |
Slc35a1 |
T |
C |
4: 34,668,962 (GRCm39) |
T284A |
probably benign |
Het |
Smco2 |
A |
T |
6: 146,763,244 (GRCm39) |
I184F |
probably damaging |
Het |
Son |
A |
G |
16: 91,453,472 (GRCm39) |
M740V |
possibly damaging |
Het |
Stil |
T |
A |
4: 114,880,882 (GRCm39) |
N475K |
possibly damaging |
Het |
Sval3 |
A |
G |
6: 41,949,839 (GRCm39) |
D122G |
probably damaging |
Het |
Tnks |
A |
G |
8: 35,328,701 (GRCm39) |
M623T |
probably benign |
Het |
Zfp142 |
A |
G |
1: 74,617,317 (GRCm39) |
V235A |
probably benign |
Het |
Zfp423 |
A |
T |
8: 88,500,262 (GRCm39) |
C1053* |
probably null |
Het |
Zfp648 |
T |
A |
1: 154,081,414 (GRCm39) |
D524E |
probably benign |
Het |
|
Other mutations in Foxk1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01331:Foxk1
|
APN |
5 |
142,439,344 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02122:Foxk1
|
APN |
5 |
142,437,184 (GRCm39) |
splice site |
probably benign |
|
IGL02686:Foxk1
|
APN |
5 |
142,439,340 (GRCm39) |
missense |
probably damaging |
0.99 |
R0027:Foxk1
|
UTSW |
5 |
142,436,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R0217:Foxk1
|
UTSW |
5 |
142,387,649 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0481:Foxk1
|
UTSW |
5 |
142,434,578 (GRCm39) |
missense |
probably benign |
0.09 |
R1941:Foxk1
|
UTSW |
5 |
142,442,429 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2128:Foxk1
|
UTSW |
5 |
142,420,943 (GRCm39) |
nonsense |
probably null |
|
R2129:Foxk1
|
UTSW |
5 |
142,420,943 (GRCm39) |
nonsense |
probably null |
|
R2356:Foxk1
|
UTSW |
5 |
142,441,164 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5156:Foxk1
|
UTSW |
5 |
142,434,588 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5958:Foxk1
|
UTSW |
5 |
142,442,429 (GRCm39) |
missense |
probably benign |
0.06 |
R7686:Foxk1
|
UTSW |
5 |
142,387,625 (GRCm39) |
missense |
probably damaging |
0.99 |
R8141:Foxk1
|
UTSW |
5 |
142,439,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R8406:Foxk1
|
UTSW |
5 |
142,387,528 (GRCm39) |
missense |
unknown |
|
R8433:Foxk1
|
UTSW |
5 |
142,434,539 (GRCm39) |
missense |
probably benign |
0.00 |
R9135:Foxk1
|
UTSW |
5 |
142,434,497 (GRCm39) |
missense |
probably benign |
0.34 |
R9487:Foxk1
|
UTSW |
5 |
142,437,389 (GRCm39) |
critical splice donor site |
probably null |
|
R9567:Foxk1
|
UTSW |
5 |
142,387,713 (GRCm39) |
nonsense |
probably null |
|
R9790:Foxk1
|
UTSW |
5 |
142,387,739 (GRCm39) |
missense |
probably damaging |
0.99 |
R9791:Foxk1
|
UTSW |
5 |
142,387,739 (GRCm39) |
missense |
probably damaging |
0.99 |
|