Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057M21Rik |
A |
T |
7: 130,964,331 (GRCm39) |
C24S |
probably benign |
Het |
2410137M14Rik |
A |
G |
17: 37,288,965 (GRCm39) |
|
probably benign |
Het |
Abhd18 |
G |
A |
3: 40,865,008 (GRCm39) |
G83D |
probably benign |
Het |
Adam34 |
T |
C |
8: 44,105,274 (GRCm39) |
I124V |
probably benign |
Het |
Adck2 |
A |
G |
6: 39,560,773 (GRCm39) |
D123G |
probably damaging |
Het |
Arhgef2 |
A |
G |
3: 88,537,221 (GRCm39) |
E37G |
probably damaging |
Het |
Axl |
T |
C |
7: 25,470,061 (GRCm39) |
Y466C |
probably damaging |
Het |
B4galt3 |
C |
A |
1: 171,101,613 (GRCm39) |
H196N |
probably damaging |
Het |
Bpifb9a |
A |
T |
2: 154,106,161 (GRCm39) |
|
probably null |
Het |
Brip1 |
A |
G |
11: 85,952,703 (GRCm39) |
V1026A |
probably benign |
Het |
Cacna1h |
A |
T |
17: 25,603,987 (GRCm39) |
S1282T |
probably benign |
Het |
Calcr |
T |
C |
6: 3,717,133 (GRCm39) |
Y109C |
probably damaging |
Het |
Col9a2 |
C |
G |
4: 120,911,455 (GRCm39) |
R599G |
probably damaging |
Het |
Crygs |
C |
T |
16: 22,624,301 (GRCm39) |
G102D |
possibly damaging |
Het |
Cst13 |
A |
T |
2: 148,665,202 (GRCm39) |
R66W |
probably damaging |
Het |
Cstf2t |
A |
G |
19: 31,061,175 (GRCm39) |
N237S |
probably benign |
Het |
Dhx8 |
A |
G |
11: 101,641,797 (GRCm39) |
T632A |
probably benign |
Het |
Disp2 |
G |
T |
2: 118,622,725 (GRCm39) |
Q1152H |
probably benign |
Het |
Dlg1 |
A |
G |
16: 31,672,664 (GRCm39) |
H599R |
probably benign |
Het |
Dmxl1 |
T |
C |
18: 50,027,161 (GRCm39) |
S2090P |
probably benign |
Het |
Dnajc13 |
C |
G |
9: 104,080,717 (GRCm39) |
V821L |
probably damaging |
Het |
Dop1a |
T |
A |
9: 86,403,652 (GRCm39) |
H1617Q |
probably benign |
Het |
Emilin1 |
C |
T |
5: 31,075,082 (GRCm39) |
P441L |
possibly damaging |
Het |
Ephb4 |
T |
C |
5: 137,355,981 (GRCm39) |
C197R |
probably damaging |
Het |
Foxn1 |
C |
A |
11: 78,249,630 (GRCm39) |
A632S |
probably benign |
Het |
Fpr3 |
A |
C |
17: 18,190,908 (GRCm39) |
T60P |
probably damaging |
Het |
Gja4 |
A |
T |
4: 127,206,410 (GRCm39) |
S118T |
probably benign |
Het |
Hivep2 |
C |
A |
10: 14,004,713 (GRCm39) |
T437K |
probably benign |
Het |
Itfg1 |
A |
T |
8: 86,502,827 (GRCm39) |
S246R |
probably benign |
Het |
Kazn |
A |
T |
4: 141,845,603 (GRCm39) |
|
probably null |
Het |
Mdn1 |
T |
C |
4: 32,716,271 (GRCm39) |
L2111P |
possibly damaging |
Het |
Myo6 |
A |
G |
9: 80,165,737 (GRCm39) |
Y374C |
probably benign |
Het |
Odad2 |
C |
A |
18: 7,223,676 (GRCm39) |
G456W |
probably benign |
Het |
Or1a1 |
G |
T |
11: 74,087,150 (GRCm39) |
V274L |
possibly damaging |
Het |
Or1j16 |
G |
T |
2: 36,530,201 (GRCm39) |
R50M |
possibly damaging |
Het |
Or5b99 |
A |
G |
19: 12,976,404 (GRCm39) |
D18G |
probably benign |
Het |
Or9m1b |
A |
G |
2: 87,836,579 (GRCm39) |
V181A |
probably benign |
Het |
Pcdhb15 |
A |
T |
18: 37,608,075 (GRCm39) |
T436S |
probably benign |
Het |
Pcdhb18 |
T |
A |
18: 37,624,342 (GRCm39) |
N557K |
probably damaging |
Het |
Pcdhb6 |
T |
C |
18: 37,468,633 (GRCm39) |
M518T |
probably benign |
Het |
Pcmtd1 |
A |
T |
1: 7,239,807 (GRCm39) |
I83L |
probably benign |
Het |
Pitrm1 |
T |
A |
13: 6,619,327 (GRCm39) |
Y721N |
probably damaging |
Het |
Prcp |
C |
T |
7: 92,577,820 (GRCm39) |
T328I |
probably damaging |
Het |
Psg27 |
C |
A |
7: 18,301,036 (GRCm39) |
E6* |
probably null |
Het |
Pth1r |
T |
A |
9: 110,552,655 (GRCm39) |
E465V |
probably damaging |
Het |
Pus7l |
T |
C |
15: 94,421,471 (GRCm39) |
Y613C |
probably damaging |
Het |
Setd3 |
C |
T |
12: 108,073,544 (GRCm39) |
V578M |
probably benign |
Het |
Slc10a1 |
T |
C |
12: 81,014,402 (GRCm39) |
N106S |
probably damaging |
Het |
Slc29a3 |
T |
C |
10: 60,551,686 (GRCm39) |
M453V |
possibly damaging |
Het |
Slc4a8 |
T |
C |
15: 100,705,326 (GRCm39) |
V844A |
probably damaging |
Het |
Sorcs1 |
T |
C |
19: 50,218,655 (GRCm39) |
H609R |
possibly damaging |
Het |
Spata31d1e |
A |
G |
13: 59,890,920 (GRCm39) |
V300A |
probably benign |
Het |
Tmppe |
C |
G |
9: 114,234,640 (GRCm39) |
P313R |
probably benign |
Het |
Tnxb |
A |
C |
17: 34,928,391 (GRCm39) |
T2602P |
possibly damaging |
Het |
Trip11 |
T |
C |
12: 101,839,701 (GRCm39) |
N1643S |
probably benign |
Het |
Trmt1l |
T |
C |
1: 151,311,594 (GRCm39) |
|
probably null |
Het |
Vmn1r177 |
A |
T |
7: 23,565,556 (GRCm39) |
C107S |
probably damaging |
Het |
Vmn1r225 |
A |
G |
17: 20,722,611 (GRCm39) |
I17M |
possibly damaging |
Het |
Vmn1r232 |
A |
G |
17: 21,134,465 (GRCm39) |
L45P |
probably benign |
Het |
Wdr7 |
T |
A |
18: 63,910,678 (GRCm39) |
V690E |
possibly damaging |
Het |
Xaf1 |
A |
T |
11: 72,194,228 (GRCm39) |
E36D |
possibly damaging |
Het |
Zbtb40 |
G |
A |
4: 136,744,596 (GRCm39) |
Q275* |
probably null |
Het |
Zfp513 |
T |
G |
5: 31,357,767 (GRCm39) |
K202T |
probably damaging |
Het |
|
Other mutations in Rsl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00972:Rsl1
|
APN |
13 |
67,329,862 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01120:Rsl1
|
APN |
13 |
67,325,230 (GRCm39) |
splice site |
probably benign |
|
IGL02041:Rsl1
|
APN |
13 |
67,324,612 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02316:Rsl1
|
APN |
13 |
67,325,120 (GRCm39) |
splice site |
probably null |
|
IGL02632:Rsl1
|
APN |
13 |
67,330,227 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02645:Rsl1
|
APN |
13 |
67,330,273 (GRCm39) |
missense |
probably benign |
0.00 |
R0097:Rsl1
|
UTSW |
13 |
67,329,966 (GRCm39) |
missense |
probably damaging |
0.99 |
R1644:Rsl1
|
UTSW |
13 |
67,325,229 (GRCm39) |
splice site |
probably benign |
|
R2040:Rsl1
|
UTSW |
13 |
67,330,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R2207:Rsl1
|
UTSW |
13 |
67,330,892 (GRCm39) |
missense |
probably benign |
|
R4235:Rsl1
|
UTSW |
13 |
67,325,226 (GRCm39) |
critical splice donor site |
probably null |
|
R4995:Rsl1
|
UTSW |
13 |
67,330,313 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5118:Rsl1
|
UTSW |
13 |
67,330,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R6733:Rsl1
|
UTSW |
13 |
67,325,206 (GRCm39) |
missense |
probably benign |
|
R6748:Rsl1
|
UTSW |
13 |
67,330,688 (GRCm39) |
missense |
probably benign |
0.00 |
R7397:Rsl1
|
UTSW |
13 |
67,330,101 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7531:Rsl1
|
UTSW |
13 |
67,324,566 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7729:Rsl1
|
UTSW |
13 |
67,330,284 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7963:Rsl1
|
UTSW |
13 |
67,330,173 (GRCm39) |
missense |
probably damaging |
0.98 |
R9188:Rsl1
|
UTSW |
13 |
67,330,185 (GRCm39) |
missense |
probably benign |
0.06 |
R9310:Rsl1
|
UTSW |
13 |
67,324,510 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9653:Rsl1
|
UTSW |
13 |
67,330,106 (GRCm39) |
missense |
probably damaging |
1.00 |
|