Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl7b |
A |
G |
4: 56,741,173 (GRCm39) |
Y62H |
probably damaging |
Het |
Cfap52 |
A |
G |
11: 67,829,881 (GRCm39) |
I296T |
probably damaging |
Het |
Col14a1 |
A |
G |
15: 55,351,937 (GRCm39) |
|
probably null |
Het |
Daam2 |
G |
T |
17: 49,793,529 (GRCm39) |
D329E |
probably benign |
Het |
Fasn |
A |
T |
11: 120,703,621 (GRCm39) |
I1535N |
possibly damaging |
Het |
Fbxw15 |
A |
T |
9: 109,384,219 (GRCm39) |
Y431N |
probably benign |
Het |
Fbxw26 |
T |
G |
9: 109,575,087 (GRCm39) |
I13L |
probably damaging |
Het |
Fggy |
A |
T |
4: 95,710,301 (GRCm39) |
H300L |
probably damaging |
Het |
Fndc3c1 |
G |
A |
X: 105,464,307 (GRCm39) |
T1277I |
probably benign |
Het |
Gigyf1 |
G |
T |
5: 137,523,952 (GRCm39) |
V1041L |
possibly damaging |
Het |
Kif26b |
G |
A |
1: 178,742,946 (GRCm39) |
R567H |
probably benign |
Het |
Kpna6 |
G |
A |
4: 129,549,314 (GRCm39) |
T156M |
probably damaging |
Het |
Lrrc37a |
C |
T |
11: 103,388,499 (GRCm39) |
E2309K |
unknown |
Het |
Lyn |
T |
C |
4: 3,780,931 (GRCm39) |
Y357H |
possibly damaging |
Het |
Mki67 |
A |
G |
7: 135,297,219 (GRCm39) |
V2605A |
probably benign |
Het |
Mtmr3 |
T |
C |
11: 4,437,385 (GRCm39) |
D1023G |
probably damaging |
Het |
Muc5b |
G |
T |
7: 141,418,514 (GRCm39) |
R3820L |
probably benign |
Het |
Mus81 |
A |
G |
19: 5,534,991 (GRCm39) |
|
probably benign |
Het |
Nup188 |
A |
G |
2: 30,230,653 (GRCm39) |
Y1397C |
possibly damaging |
Het |
Pgd |
A |
T |
4: 149,249,685 (GRCm39) |
V29D |
probably damaging |
Het |
Plch2 |
T |
C |
4: 155,071,371 (GRCm39) |
S244G |
probably benign |
Het |
Rapgef5 |
C |
A |
12: 117,694,294 (GRCm39) |
T372K |
probably damaging |
Het |
Rb1 |
A |
G |
14: 73,520,306 (GRCm39) |
|
probably null |
Het |
Ryr3 |
A |
T |
2: 112,586,944 (GRCm39) |
V2680E |
possibly damaging |
Het |
Sgsm3 |
A |
C |
15: 80,895,855 (GRCm39) |
|
probably null |
Het |
Slc38a1 |
C |
T |
15: 96,477,228 (GRCm39) |
V362I |
possibly damaging |
Het |
Sun1 |
T |
A |
5: 139,216,886 (GRCm39) |
D308E |
probably damaging |
Het |
Tns1 |
C |
T |
1: 74,025,053 (GRCm39) |
V387M |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,582,083 (GRCm39) |
G22937C |
probably damaging |
Het |
Ubr1 |
C |
A |
2: 120,725,641 (GRCm39) |
A1258S |
probably benign |
Het |
Vmn2r74 |
A |
G |
7: 85,607,265 (GRCm39) |
F153L |
probably benign |
Het |
|
Other mutations in Defb26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02342:Defb26
|
APN |
2 |
152,350,121 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0078:Defb26
|
UTSW |
2 |
152,349,988 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0306:Defb26
|
UTSW |
2 |
152,349,888 (GRCm39) |
missense |
unknown |
|
R1351:Defb26
|
UTSW |
2 |
152,349,737 (GRCm39) |
missense |
unknown |
|
R1935:Defb26
|
UTSW |
2 |
152,350,195 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1936:Defb26
|
UTSW |
2 |
152,350,195 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4604:Defb26
|
UTSW |
2 |
152,350,104 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4888:Defb26
|
UTSW |
2 |
152,350,085 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5121:Defb26
|
UTSW |
2 |
152,350,085 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5262:Defb26
|
UTSW |
2 |
152,349,878 (GRCm39) |
missense |
unknown |
|
R5720:Defb26
|
UTSW |
2 |
152,350,122 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6257:Defb26
|
UTSW |
2 |
152,349,860 (GRCm39) |
missense |
unknown |
|
R7902:Defb26
|
UTSW |
2 |
152,350,156 (GRCm39) |
nonsense |
probably null |
|
Z1176:Defb26
|
UTSW |
2 |
152,350,221 (GRCm39) |
critical splice acceptor site |
probably null |
|
|