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 |
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 |
Rsl1 |
A |
G |
13: 67,330,892 (GRCm39) |
T447A |
probably benign |
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 Adck2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01356:Adck2
|
APN |
6 |
39,560,854 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02369:Adck2
|
APN |
6 |
39,551,678 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02956:Adck2
|
APN |
6 |
39,553,436 (GRCm39) |
missense |
probably benign |
0.11 |
R0240:Adck2
|
UTSW |
6 |
39,560,752 (GRCm39) |
missense |
probably benign |
0.10 |
R0240:Adck2
|
UTSW |
6 |
39,560,752 (GRCm39) |
missense |
probably benign |
0.10 |
R0241:Adck2
|
UTSW |
6 |
39,560,752 (GRCm39) |
missense |
probably benign |
0.10 |
R0241:Adck2
|
UTSW |
6 |
39,560,752 (GRCm39) |
missense |
probably benign |
0.10 |
R1107:Adck2
|
UTSW |
6 |
39,562,719 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1691:Adck2
|
UTSW |
6 |
39,551,902 (GRCm39) |
nonsense |
probably null |
|
R2125:Adck2
|
UTSW |
6 |
39,552,076 (GRCm39) |
missense |
probably benign |
0.00 |
R2422:Adck2
|
UTSW |
6 |
39,560,932 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4795:Adck2
|
UTSW |
6 |
39,553,327 (GRCm39) |
missense |
probably benign |
0.02 |
R5556:Adck2
|
UTSW |
6 |
39,560,869 (GRCm39) |
missense |
probably benign |
0.02 |
R6402:Adck2
|
UTSW |
6 |
39,563,803 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6824:Adck2
|
UTSW |
6 |
39,552,058 (GRCm39) |
missense |
probably benign |
0.00 |
R6927:Adck2
|
UTSW |
6 |
39,560,998 (GRCm39) |
critical splice donor site |
probably null |
|
R7163:Adck2
|
UTSW |
6 |
39,560,797 (GRCm39) |
missense |
probably damaging |
0.99 |
R8249:Adck2
|
UTSW |
6 |
39,562,667 (GRCm39) |
nonsense |
probably null |
|
R8775:Adck2
|
UTSW |
6 |
39,552,142 (GRCm39) |
critical splice donor site |
probably null |
|
R8775-TAIL:Adck2
|
UTSW |
6 |
39,552,142 (GRCm39) |
critical splice donor site |
probably null |
|
R8958:Adck2
|
UTSW |
6 |
39,560,848 (GRCm39) |
missense |
probably benign |
0.01 |
R8964:Adck2
|
UTSW |
6 |
39,551,083 (GRCm39) |
unclassified |
probably benign |
|
R9446:Adck2
|
UTSW |
6 |
39,551,221 (GRCm39) |
unclassified |
probably benign |
|
Z1177:Adck2
|
UTSW |
6 |
39,551,022 (GRCm39) |
unclassified |
probably benign |
|
|