Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5031439G07Rik |
C |
T |
15: 84,871,836 (GRCm39) |
S56N |
probably benign |
Het |
Atg16l2 |
T |
G |
7: 100,939,473 (GRCm39) |
D542A |
probably damaging |
Het |
Blm |
A |
G |
7: 80,105,032 (GRCm39) |
L1412P |
probably damaging |
Het |
Cela1 |
T |
A |
15: 100,573,213 (GRCm39) |
M39L |
probably benign |
Het |
Col12a1 |
T |
A |
9: 79,517,133 (GRCm39) |
D2849V |
probably damaging |
Het |
Fam53c |
A |
G |
18: 34,901,854 (GRCm39) |
E257G |
probably damaging |
Het |
Fmo9 |
A |
T |
1: 166,502,039 (GRCm39) |
N144K |
probably damaging |
Het |
Gabrd |
T |
A |
4: 155,470,148 (GRCm39) |
M354L |
probably benign |
Het |
Gm5773 |
A |
T |
3: 93,680,835 (GRCm39) |
D169V |
probably benign |
Het |
Gria2 |
A |
T |
3: 80,599,774 (GRCm39) |
F703L |
probably damaging |
Het |
Grm3 |
A |
T |
5: 9,561,726 (GRCm39) |
I708N |
probably benign |
Het |
Hlcs |
G |
A |
16: 94,063,617 (GRCm39) |
P481L |
possibly damaging |
Het |
Ifi206 |
T |
C |
1: 173,314,311 (GRCm39) |
Y43C |
|
Het |
Igf2r |
A |
G |
17: 12,928,328 (GRCm39) |
L1005P |
probably damaging |
Het |
Ighv2-6-8 |
T |
C |
12: 113,759,834 (GRCm39) |
N92D |
possibly damaging |
Het |
Invs |
A |
G |
4: 48,422,109 (GRCm39) |
K914E |
probably damaging |
Het |
Iqsec3 |
T |
C |
6: 121,389,813 (GRCm39) |
|
probably benign |
Het |
Klra6 |
T |
C |
6: 129,999,660 (GRCm39) |
T103A |
probably benign |
Het |
Lipo5 |
C |
T |
19: 33,441,849 (GRCm39) |
|
probably null |
Het |
Llgl1 |
T |
C |
11: 60,595,809 (GRCm39) |
|
probably null |
Het |
Lonrf1 |
T |
C |
8: 36,698,292 (GRCm39) |
E402G |
probably benign |
Het |
Lrp1b |
T |
A |
2: 41,396,791 (GRCm39) |
Y311F |
probably benign |
Het |
Lrrc8a |
T |
A |
2: 30,146,208 (GRCm39) |
W341R |
possibly damaging |
Het |
Lrriq1 |
A |
G |
10: 102,882,016 (GRCm39) |
I117T |
|
Het |
Mmp9 |
T |
C |
2: 164,795,486 (GRCm39) |
V668A |
possibly damaging |
Het |
Naip5 |
A |
C |
13: 100,359,220 (GRCm39) |
M672R |
probably damaging |
Het |
Ncam1 |
A |
T |
9: 49,431,445 (GRCm39) |
L664Q |
probably damaging |
Het |
Nol4l |
T |
C |
2: 153,278,266 (GRCm39) |
D234G |
probably damaging |
Het |
Or5t16 |
T |
C |
2: 86,818,822 (GRCm39) |
K233E |
probably damaging |
Het |
Oscp1 |
T |
A |
4: 125,971,203 (GRCm39) |
H170Q |
possibly damaging |
Het |
Pard3 |
T |
A |
8: 128,186,784 (GRCm39) |
M1021K |
probably damaging |
Het |
Pkd1l2 |
T |
A |
8: 117,774,302 (GRCm39) |
|
probably null |
Het |
Plcxd2 |
T |
C |
16: 45,800,949 (GRCm39) |
K92E |
probably damaging |
Het |
Ptpdc1 |
A |
T |
13: 48,739,759 (GRCm39) |
C557* |
probably null |
Het |
Robo2 |
G |
A |
16: 73,745,228 (GRCm39) |
T849I |
probably damaging |
Het |
Rp1 |
A |
T |
1: 4,416,813 (GRCm39) |
I1433N |
possibly damaging |
Het |
Scarb1 |
A |
G |
5: 125,371,227 (GRCm39) |
S282P |
probably damaging |
Het |
Schip1 |
G |
T |
3: 68,401,946 (GRCm39) |
G36C |
probably damaging |
Het |
Sf3a1 |
T |
A |
11: 4,125,039 (GRCm39) |
S357T |
probably benign |
Het |
Sh3glb2 |
A |
T |
2: 30,249,216 (GRCm39) |
M1K |
probably null |
Het |
Slc1a3 |
T |
C |
15: 8,671,853 (GRCm39) |
T368A |
probably damaging |
Het |
Slc66a1 |
A |
G |
4: 139,027,440 (GRCm39) |
|
probably benign |
Het |
Taf11 |
A |
T |
17: 28,121,594 (GRCm39) |
I138N |
probably damaging |
Het |
Tnfaip8l1 |
C |
T |
17: 56,478,749 (GRCm39) |
A13V |
probably damaging |
Het |
Trav6-2 |
T |
G |
14: 52,905,092 (GRCm39) |
F38V |
probably benign |
Het |
Vmn2r73 |
A |
G |
7: 85,519,638 (GRCm39) |
V440A |
probably benign |
Het |
Zfp292 |
A |
G |
4: 34,826,691 (GRCm39) |
|
probably null |
Het |
Zfp429 |
A |
T |
13: 67,538,828 (GRCm39) |
C205* |
probably null |
Het |
Zfp735 |
C |
G |
11: 73,601,811 (GRCm39) |
L252V |
possibly damaging |
Het |
Zfyve26 |
A |
T |
12: 79,334,454 (GRCm39) |
L188Q |
probably damaging |
Het |
|
Other mutations in Cdc37 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01943:Cdc37
|
APN |
9 |
21,054,409 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02448:Cdc37
|
APN |
9 |
21,051,147 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02547:Cdc37
|
APN |
9 |
21,051,262 (GRCm39) |
unclassified |
probably benign |
|
R0137:Cdc37
|
UTSW |
9 |
21,053,426 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0195:Cdc37
|
UTSW |
9 |
21,053,576 (GRCm39) |
missense |
probably benign |
0.01 |
R0523:Cdc37
|
UTSW |
9 |
21,054,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R0611:Cdc37
|
UTSW |
9 |
21,053,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R0629:Cdc37
|
UTSW |
9 |
21,052,064 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0755:Cdc37
|
UTSW |
9 |
21,051,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R1512:Cdc37
|
UTSW |
9 |
21,053,712 (GRCm39) |
splice site |
probably benign |
|
R2127:Cdc37
|
UTSW |
9 |
21,061,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R2238:Cdc37
|
UTSW |
9 |
21,053,829 (GRCm39) |
nonsense |
probably null |
|
R2239:Cdc37
|
UTSW |
9 |
21,053,829 (GRCm39) |
nonsense |
probably null |
|
R3031:Cdc37
|
UTSW |
9 |
21,054,487 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5068:Cdc37
|
UTSW |
9 |
21,061,099 (GRCm39) |
missense |
probably damaging |
0.98 |
R5169:Cdc37
|
UTSW |
9 |
21,052,413 (GRCm39) |
missense |
probably benign |
0.00 |
R5308:Cdc37
|
UTSW |
9 |
21,052,060 (GRCm39) |
missense |
probably benign |
0.00 |
R5333:Cdc37
|
UTSW |
9 |
21,054,457 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5595:Cdc37
|
UTSW |
9 |
21,054,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R7040:Cdc37
|
UTSW |
9 |
21,053,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R7819:Cdc37
|
UTSW |
9 |
21,052,260 (GRCm39) |
missense |
probably damaging |
0.97 |
R8066:Cdc37
|
UTSW |
9 |
21,054,437 (GRCm39) |
missense |
probably benign |
0.01 |
|