Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
A |
T |
14: 32,384,956 (GRCm39) |
C336* |
probably null |
Het |
Adgrv1 |
T |
C |
13: 81,688,238 (GRCm39) |
D994G |
probably damaging |
Het |
Arhgap36 |
G |
T |
X: 48,586,631 (GRCm39) |
Q421H |
probably damaging |
Het |
Arhgef17 |
A |
G |
7: 100,578,656 (GRCm39) |
V764A |
probably benign |
Het |
Atf7ip |
T |
C |
6: 136,537,679 (GRCm39) |
V304A |
probably benign |
Het |
Babam2 |
T |
A |
5: 32,164,651 (GRCm39) |
F299L |
probably damaging |
Het |
Ceacam11 |
T |
G |
7: 17,707,595 (GRCm39) |
D126E |
possibly damaging |
Het |
Dlg3 |
C |
A |
X: 99,850,199 (GRCm39) |
H197Q |
probably damaging |
Het |
Dnmt3a |
T |
A |
12: 3,955,622 (GRCm39) |
L590Q |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,682,712 (GRCm39) |
|
probably benign |
Het |
Gabarapl1 |
T |
C |
6: 129,515,598 (GRCm39) |
F79L |
probably benign |
Het |
Gabbr2 |
A |
G |
4: 46,875,711 (GRCm39) |
V137A |
probably damaging |
Het |
Gphn |
T |
C |
12: 78,711,342 (GRCm39) |
|
probably benign |
Het |
Hnrnpr |
A |
G |
4: 136,066,516 (GRCm39) |
I399M |
probably benign |
Het |
Madd |
A |
C |
2: 90,998,213 (GRCm39) |
S636A |
probably damaging |
Het |
Pi15 |
T |
C |
1: 17,691,764 (GRCm39) |
|
probably benign |
Het |
Ppp3cb |
A |
T |
14: 20,581,754 (GRCm39) |
M87K |
possibly damaging |
Het |
Ptpro |
C |
A |
6: 137,391,237 (GRCm39) |
H786N |
probably damaging |
Het |
Sirt4 |
A |
G |
5: 115,617,685 (GRCm39) |
|
probably null |
Het |
Stab1 |
T |
C |
14: 30,869,023 (GRCm39) |
D1534G |
probably damaging |
Het |
Sulf2 |
A |
G |
2: 165,936,412 (GRCm39) |
S185P |
possibly damaging |
Het |
Svs6 |
A |
C |
2: 164,159,507 (GRCm39) |
K90T |
possibly damaging |
Het |
Tdrd6 |
A |
G |
17: 43,928,087 (GRCm39) |
M2102T |
probably benign |
Het |
Ttll5 |
T |
C |
12: 85,890,600 (GRCm39) |
V77A |
probably damaging |
Het |
Usp9x |
T |
G |
X: 12,994,685 (GRCm39) |
S959A |
probably benign |
Het |
Vps50 |
C |
T |
6: 3,532,177 (GRCm39) |
Q227* |
probably null |
Het |
Zfp57 |
C |
A |
17: 37,320,514 (GRCm39) |
Q120K |
possibly damaging |
Het |
Zswim2 |
T |
C |
2: 83,754,115 (GRCm39) |
N182D |
probably benign |
Het |
|
Other mutations in Rnase11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01024:Rnase11
|
APN |
14 |
51,287,321 (GRCm39) |
missense |
probably benign |
0.05 |
R1638:Rnase11
|
UTSW |
14 |
51,287,058 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1809:Rnase11
|
UTSW |
14 |
51,287,184 (GRCm39) |
missense |
probably benign |
0.00 |
R2844:Rnase11
|
UTSW |
14 |
51,287,227 (GRCm39) |
missense |
probably damaging |
0.99 |
R5478:Rnase11
|
UTSW |
14 |
51,287,332 (GRCm39) |
missense |
probably damaging |
0.99 |
R7607:Rnase11
|
UTSW |
14 |
51,287,029 (GRCm39) |
missense |
probably damaging |
0.99 |
R8077:Rnase11
|
UTSW |
14 |
51,287,398 (GRCm39) |
missense |
probably damaging |
0.99 |
R9743:Rnase11
|
UTSW |
14 |
51,287,370 (GRCm39) |
missense |
probably benign |
0.36 |
Z1176:Rnase11
|
UTSW |
14 |
51,287,345 (GRCm39) |
missense |
possibly damaging |
0.94 |
|