Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
T |
C |
14: 32,381,988 (GRCm39) |
T1326A |
possibly damaging |
Het |
Afg3l1 |
C |
T |
8: 124,221,592 (GRCm39) |
R484C |
probably benign |
Het |
Atg2a |
C |
A |
19: 6,302,514 (GRCm39) |
Q946K |
probably benign |
Het |
Cdh20 |
T |
C |
1: 104,921,895 (GRCm39) |
Y731H |
probably benign |
Het |
Ctnnd2 |
T |
C |
15: 31,005,164 (GRCm39) |
S1073P |
probably damaging |
Het |
Dnah2 |
T |
C |
11: 69,355,889 (GRCm39) |
|
probably benign |
Het |
Evi2a |
T |
A |
11: 79,417,978 (GRCm39) |
R211W |
probably damaging |
Het |
Fmo1 |
T |
A |
1: 162,661,168 (GRCm39) |
I372F |
probably benign |
Het |
Glyctk |
T |
C |
9: 106,032,471 (GRCm39) |
D514G |
probably damaging |
Het |
Gmnc |
G |
A |
16: 26,779,069 (GRCm39) |
Q313* |
probably null |
Het |
Grik1 |
T |
C |
16: 87,743,623 (GRCm39) |
T520A |
probably damaging |
Het |
Gtsf2 |
A |
T |
15: 103,353,340 (GRCm39) |
C9S |
probably damaging |
Het |
Ift80 |
T |
G |
3: 68,870,996 (GRCm39) |
N200T |
possibly damaging |
Het |
Ints1 |
A |
G |
5: 139,742,047 (GRCm39) |
S1771P |
probably benign |
Het |
Lrba |
A |
G |
3: 86,683,484 (GRCm39) |
T2769A |
possibly damaging |
Het |
Lrfn2 |
G |
T |
17: 49,377,425 (GRCm39) |
V169L |
possibly damaging |
Het |
Mei1 |
G |
A |
15: 81,973,753 (GRCm39) |
R80H |
probably damaging |
Het |
Nbeal2 |
A |
T |
9: 110,473,746 (GRCm39) |
V31E |
probably damaging |
Het |
Ncapd2 |
G |
T |
6: 125,154,835 (GRCm39) |
P546T |
probably benign |
Het |
Or52l1 |
A |
G |
7: 104,829,929 (GRCm39) |
V212A |
probably damaging |
Het |
Pan3 |
T |
C |
5: 147,390,052 (GRCm39) |
|
probably benign |
Het |
Rab3b |
T |
A |
4: 108,781,223 (GRCm39) |
|
probably null |
Het |
Rabl2 |
T |
C |
15: 89,467,615 (GRCm39) |
K119E |
probably benign |
Het |
Reln |
A |
G |
5: 22,101,928 (GRCm39) |
V3334A |
probably damaging |
Het |
Rfx1 |
A |
G |
8: 84,819,601 (GRCm39) |
|
probably null |
Het |
Rhod |
T |
C |
19: 4,476,247 (GRCm39) |
Y168C |
probably damaging |
Het |
Sag |
T |
C |
1: 87,733,071 (GRCm39) |
I13T |
probably damaging |
Het |
Sat2 |
T |
C |
11: 69,513,789 (GRCm39) |
|
probably null |
Het |
Scn5a |
A |
T |
9: 119,315,091 (GRCm39) |
D1872E |
possibly damaging |
Het |
Sh2b2 |
T |
G |
5: 136,260,656 (GRCm39) |
I187L |
probably benign |
Het |
Slit3 |
G |
A |
11: 35,591,211 (GRCm39) |
G1341D |
possibly damaging |
Het |
Tmed11 |
A |
T |
5: 108,927,750 (GRCm39) |
S95T |
possibly damaging |
Het |
Tmem186 |
A |
G |
16: 8,453,733 (GRCm39) |
V176A |
possibly damaging |
Het |
Trim12c |
A |
T |
7: 103,997,422 (GRCm39) |
S45T |
possibly damaging |
Het |
Ube4b |
C |
A |
4: 149,468,275 (GRCm39) |
R167L |
probably damaging |
Het |
Zfp335 |
A |
T |
2: 164,752,540 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Cdk15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01307:Cdk15
|
APN |
1 |
59,326,955 (GRCm39) |
missense |
probably benign |
0.37 |
IGL02179:Cdk15
|
APN |
1 |
59,370,100 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03228:Cdk15
|
APN |
1 |
59,297,912 (GRCm39) |
missense |
possibly damaging |
0.95 |
FR4449:Cdk15
|
UTSW |
1 |
59,296,982 (GRCm39) |
small insertion |
probably benign |
|
R0270:Cdk15
|
UTSW |
1 |
59,349,965 (GRCm39) |
missense |
probably damaging |
0.99 |
R1720:Cdk15
|
UTSW |
1 |
59,328,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R1958:Cdk15
|
UTSW |
1 |
59,383,475 (GRCm39) |
missense |
probably damaging |
0.99 |
R1969:Cdk15
|
UTSW |
1 |
59,370,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R3159:Cdk15
|
UTSW |
1 |
59,340,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R6000:Cdk15
|
UTSW |
1 |
59,328,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R6226:Cdk15
|
UTSW |
1 |
59,304,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Cdk15
|
UTSW |
1 |
59,296,264 (GRCm39) |
critical splice donor site |
probably null |
|
R7184:Cdk15
|
UTSW |
1 |
59,304,814 (GRCm39) |
missense |
probably benign |
0.33 |
R7446:Cdk15
|
UTSW |
1 |
59,328,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R7467:Cdk15
|
UTSW |
1 |
59,328,938 (GRCm39) |
missense |
probably null |
0.96 |
R7588:Cdk15
|
UTSW |
1 |
59,383,458 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8540:Cdk15
|
UTSW |
1 |
59,349,992 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9024:Cdk15
|
UTSW |
1 |
59,326,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R9372:Cdk15
|
UTSW |
1 |
59,370,142 (GRCm39) |
missense |
probably benign |
0.00 |
R9404:Cdk15
|
UTSW |
1 |
59,328,914 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9493:Cdk15
|
UTSW |
1 |
59,326,943 (GRCm39) |
missense |
probably damaging |
1.00 |
|