Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ac165356.1 |
C |
T |
7: 105,682,686 (GRCm39) |
A190T |
probably benign |
Het |
Aimp2 |
A |
G |
5: 143,841,509 (GRCm39) |
S110P |
possibly damaging |
Het |
Akap9 |
A |
G |
5: 3,998,783 (GRCm39) |
T51A |
probably benign |
Het |
Arhgef25 |
A |
G |
10: 127,019,650 (GRCm39) |
F430L |
possibly damaging |
Het |
Brap |
T |
C |
5: 121,813,342 (GRCm39) |
V235A |
probably damaging |
Het |
Cd69 |
C |
T |
6: 129,247,148 (GRCm39) |
G23D |
probably damaging |
Het |
Cecr2 |
C |
T |
6: 120,735,166 (GRCm39) |
R24* |
probably null |
Het |
Celsr2 |
T |
C |
3: 108,307,025 (GRCm39) |
D1974G |
possibly damaging |
Het |
Cps1 |
A |
G |
1: 67,234,358 (GRCm39) |
K915R |
probably benign |
Het |
Csmd1 |
T |
C |
8: 16,408,362 (GRCm39) |
D401G |
probably damaging |
Het |
Dusp13b |
A |
G |
14: 21,785,086 (GRCm39) |
F141S |
probably damaging |
Het |
Fam162b |
A |
G |
10: 51,466,439 (GRCm39) |
W27R |
probably benign |
Het |
Focad |
A |
G |
4: 88,096,424 (GRCm39) |
T269A |
probably benign |
Het |
Ghr |
T |
A |
15: 3,357,544 (GRCm39) |
R241S |
possibly damaging |
Het |
Hirip3 |
AAGAG |
AAG |
7: 126,462,832 (GRCm39) |
|
probably null |
Het |
Itgb2l |
A |
G |
16: 96,230,240 (GRCm39) |
Y357H |
possibly damaging |
Het |
Jrkl |
T |
C |
9: 13,244,938 (GRCm39) |
D241G |
possibly damaging |
Het |
Lmod1 |
A |
G |
1: 135,291,967 (GRCm39) |
D274G |
probably benign |
Het |
Lrrn2 |
A |
G |
1: 132,866,959 (GRCm39) |
S675G |
probably benign |
Het |
Ltbp4 |
G |
C |
7: 27,009,960 (GRCm39) |
P1200R |
probably damaging |
Het |
Mdn1 |
T |
C |
4: 32,735,576 (GRCm39) |
L3414P |
possibly damaging |
Het |
Muc19 |
A |
G |
15: 91,762,743 (GRCm39) |
|
noncoding transcript |
Het |
Neb |
A |
G |
2: 52,186,310 (GRCm39) |
Y921H |
probably damaging |
Het |
Or2n1c |
T |
A |
17: 38,520,074 (GRCm39) |
*313R |
probably null |
Het |
Pgap3 |
T |
C |
11: 98,281,960 (GRCm39) |
D117G |
probably damaging |
Het |
Ppp1r9b |
T |
C |
11: 94,892,812 (GRCm39) |
F671L |
possibly damaging |
Het |
Purg |
T |
G |
8: 33,876,897 (GRCm39) |
Y178* |
probably null |
Het |
Rsph10b |
G |
A |
5: 143,903,280 (GRCm39) |
|
probably benign |
Het |
Sorbs1 |
T |
A |
19: 40,371,050 (GRCm39) |
D79V |
probably damaging |
Het |
Tcaf3 |
T |
C |
6: 42,568,368 (GRCm39) |
T663A |
probably damaging |
Het |
Timd4 |
C |
A |
11: 46,708,475 (GRCm39) |
T167K |
probably damaging |
Het |
Tjp2 |
A |
G |
19: 24,108,527 (GRCm39) |
L195P |
possibly damaging |
Het |
Tnr |
G |
A |
1: 159,679,856 (GRCm39) |
A277T |
probably benign |
Het |
Trpm3 |
G |
A |
19: 22,891,781 (GRCm39) |
|
probably benign |
Het |
Unc13a |
C |
T |
8: 72,114,477 (GRCm39) |
G181D |
probably benign |
Het |
Vmn1r11 |
T |
A |
6: 57,114,492 (GRCm39) |
L52Q |
possibly damaging |
Het |
Vmn2r125 |
C |
A |
4: 156,703,396 (GRCm39) |
A258D |
probably benign |
Het |
Zfp27 |
T |
C |
7: 29,595,254 (GRCm39) |
D237G |
possibly damaging |
Het |
Zfp39 |
T |
C |
11: 58,793,670 (GRCm39) |
T23A |
possibly damaging |
Het |
Zfp459 |
T |
G |
13: 67,556,600 (GRCm39) |
N161T |
probably benign |
Het |
|
Other mutations in Eif1ad19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01118:Eif1ad19
|
APN |
12 |
87,740,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R0089:Eif1ad19
|
UTSW |
12 |
87,740,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R0559:Eif1ad19
|
UTSW |
12 |
87,740,223 (GRCm39) |
missense |
probably benign |
|
R1185:Eif1ad19
|
UTSW |
12 |
87,740,478 (GRCm39) |
missense |
probably benign |
0.14 |
R1185:Eif1ad19
|
UTSW |
12 |
87,740,478 (GRCm39) |
missense |
probably benign |
0.14 |
R3800:Eif1ad19
|
UTSW |
12 |
87,740,491 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4531:Eif1ad19
|
UTSW |
12 |
87,740,314 (GRCm39) |
nonsense |
probably null |
|
R5013:Eif1ad19
|
UTSW |
12 |
87,740,512 (GRCm39) |
nonsense |
probably null |
|
R5817:Eif1ad19
|
UTSW |
12 |
87,740,201 (GRCm39) |
missense |
probably benign |
0.01 |
R7137:Eif1ad19
|
UTSW |
12 |
87,740,316 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7187:Eif1ad19
|
UTSW |
12 |
87,740,708 (GRCm39) |
start gained |
probably benign |
|
R7403:Eif1ad19
|
UTSW |
12 |
87,740,314 (GRCm39) |
missense |
probably benign |
0.10 |
R7505:Eif1ad19
|
UTSW |
12 |
87,740,270 (GRCm39) |
missense |
probably benign |
0.20 |
R8711:Eif1ad19
|
UTSW |
12 |
87,740,130 (GRCm39) |
missense |
unknown |
|
R8966:Eif1ad19
|
UTSW |
12 |
87,740,273 (GRCm39) |
nonsense |
probably null |
|
R9751:Eif1ad19
|
UTSW |
12 |
87,740,526 (GRCm39) |
missense |
possibly damaging |
0.90 |
|