Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arap3 |
G |
A |
18: 38,123,889 (GRCm39) |
R377C |
probably damaging |
Het |
Arhgap20 |
A |
G |
9: 51,750,187 (GRCm39) |
M316V |
probably benign |
Het |
Chd7 |
T |
G |
4: 8,859,285 (GRCm39) |
N2458K |
possibly damaging |
Het |
Clpb |
G |
A |
7: 101,436,712 (GRCm39) |
V596I |
probably damaging |
Het |
Col9a3 |
T |
C |
2: 180,251,109 (GRCm39) |
|
probably benign |
Het |
D130043K22Rik |
G |
A |
13: 25,060,020 (GRCm39) |
|
probably null |
Het |
Drd4 |
T |
C |
7: 140,873,744 (GRCm39) |
|
probably benign |
Het |
Fam228b |
A |
T |
12: 4,813,055 (GRCm39) |
I105N |
probably damaging |
Het |
Gm20939 |
A |
T |
17: 95,181,721 (GRCm39) |
|
probably benign |
Het |
Gm4952 |
A |
G |
19: 12,595,771 (GRCm39) |
T54A |
possibly damaging |
Het |
Hbs1l |
T |
C |
10: 21,183,655 (GRCm39) |
V132A |
probably benign |
Het |
Kpna2 |
T |
A |
11: 106,882,027 (GRCm39) |
E266D |
probably benign |
Het |
Lars1 |
T |
C |
18: 42,347,892 (GRCm39) |
E977G |
probably benign |
Het |
Lrrn4 |
T |
C |
2: 132,721,392 (GRCm39) |
T142A |
probably benign |
Het |
Myo19 |
T |
C |
11: 84,800,372 (GRCm39) |
L919P |
probably damaging |
Het |
Nhlrc1 |
A |
T |
13: 47,167,607 (GRCm39) |
F217I |
probably damaging |
Het |
Or10q12 |
T |
C |
19: 13,745,901 (GRCm39) |
F65S |
probably damaging |
Het |
Plch1 |
T |
C |
3: 63,639,070 (GRCm39) |
I468V |
probably damaging |
Het |
Rergl |
T |
A |
6: 139,470,496 (GRCm39) |
|
probably null |
Het |
Sctr |
A |
G |
1: 119,972,499 (GRCm39) |
|
probably benign |
Het |
Sdhb |
T |
C |
4: 140,700,278 (GRCm39) |
V126A |
probably benign |
Het |
Smad3 |
C |
T |
9: 63,562,868 (GRCm39) |
R214Q |
probably damaging |
Het |
Spmip3 |
A |
G |
1: 177,570,950 (GRCm39) |
T95A |
possibly damaging |
Het |
Tdrd9 |
T |
C |
12: 112,013,423 (GRCm39) |
M1219T |
possibly damaging |
Het |
Tmem167b |
A |
T |
3: 108,466,222 (GRCm39) |
N75K |
possibly damaging |
Het |
Vmn2r83 |
T |
C |
10: 79,314,846 (GRCm39) |
S365P |
probably benign |
Het |
Vps16 |
T |
C |
2: 130,280,314 (GRCm39) |
F153L |
probably damaging |
Het |
|
Other mutations in Clock |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00598:Clock
|
APN |
5 |
76,377,311 (GRCm39) |
missense |
probably benign |
0.17 |
IGL00725:Clock
|
APN |
5 |
76,402,260 (GRCm39) |
nonsense |
probably null |
|
IGL01304:Clock
|
APN |
5 |
76,414,202 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01369:Clock
|
APN |
5 |
76,384,933 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02541:Clock
|
APN |
5 |
76,410,519 (GRCm39) |
splice site |
probably null |
|
IGL02602:Clock
|
APN |
5 |
76,402,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02602:Clock
|
APN |
5 |
76,402,273 (GRCm39) |
missense |
probably null |
1.00 |
IGL03186:Clock
|
APN |
5 |
76,390,929 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03309:Clock
|
APN |
5 |
76,379,241 (GRCm39) |
critical splice donor site |
probably null |
|
R6760_Clock_188
|
UTSW |
5 |
76,374,823 (GRCm39) |
missense |
unknown |
|
uhr
|
UTSW |
5 |
76,377,401 (GRCm39) |
nonsense |
probably null |
|
R0304:Clock
|
UTSW |
5 |
76,374,832 (GRCm39) |
missense |
unknown |
|
R0593:Clock
|
UTSW |
5 |
76,413,683 (GRCm39) |
missense |
probably benign |
0.25 |
R0654:Clock
|
UTSW |
5 |
76,374,976 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0684:Clock
|
UTSW |
5 |
76,393,365 (GRCm39) |
missense |
probably damaging |
0.96 |
R0707:Clock
|
UTSW |
5 |
76,374,976 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0751:Clock
|
UTSW |
5 |
76,377,208 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0865:Clock
|
UTSW |
5 |
76,414,271 (GRCm39) |
splice site |
probably benign |
|
R0920:Clock
|
UTSW |
5 |
76,378,167 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1396:Clock
|
UTSW |
5 |
76,414,649 (GRCm39) |
missense |
probably benign |
0.00 |
R1450:Clock
|
UTSW |
5 |
76,410,578 (GRCm39) |
nonsense |
probably null |
|
R1487:Clock
|
UTSW |
5 |
76,414,201 (GRCm39) |
splice site |
probably null |
|
R1574:Clock
|
UTSW |
5 |
76,390,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:Clock
|
UTSW |
5 |
76,390,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:Clock
|
UTSW |
5 |
76,388,756 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1872:Clock
|
UTSW |
5 |
76,396,309 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1905:Clock
|
UTSW |
5 |
76,414,735 (GRCm39) |
splice site |
probably benign |
|
R1937:Clock
|
UTSW |
5 |
76,377,340 (GRCm39) |
missense |
probably damaging |
0.99 |
R2411:Clock
|
UTSW |
5 |
76,379,360 (GRCm39) |
missense |
probably benign |
0.08 |
R2887:Clock
|
UTSW |
5 |
76,393,120 (GRCm39) |
missense |
probably damaging |
0.99 |
R3410:Clock
|
UTSW |
5 |
76,377,401 (GRCm39) |
nonsense |
probably null |
|
R4514:Clock
|
UTSW |
5 |
76,378,046 (GRCm39) |
missense |
probably benign |
0.00 |
R4598:Clock
|
UTSW |
5 |
76,383,657 (GRCm39) |
missense |
probably benign |
0.00 |
R4599:Clock
|
UTSW |
5 |
76,383,657 (GRCm39) |
missense |
probably benign |
0.00 |
R4795:Clock
|
UTSW |
5 |
76,413,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4796:Clock
|
UTSW |
5 |
76,413,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4973:Clock
|
UTSW |
5 |
76,402,258 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5204:Clock
|
UTSW |
5 |
76,391,017 (GRCm39) |
splice site |
probably null |
|
R5271:Clock
|
UTSW |
5 |
76,389,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R5547:Clock
|
UTSW |
5 |
76,378,185 (GRCm39) |
missense |
probably benign |
0.02 |
R5630:Clock
|
UTSW |
5 |
76,378,185 (GRCm39) |
missense |
probably benign |
0.02 |
R5631:Clock
|
UTSW |
5 |
76,378,185 (GRCm39) |
missense |
probably benign |
0.02 |
R5632:Clock
|
UTSW |
5 |
76,378,185 (GRCm39) |
missense |
probably benign |
0.02 |
R5787:Clock
|
UTSW |
5 |
76,384,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R6274:Clock
|
UTSW |
5 |
76,385,000 (GRCm39) |
missense |
probably benign |
0.45 |
R6578:Clock
|
UTSW |
5 |
76,364,556 (GRCm39) |
missense |
unknown |
|
R6622:Clock
|
UTSW |
5 |
76,389,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R6760:Clock
|
UTSW |
5 |
76,374,823 (GRCm39) |
missense |
unknown |
|
R6793:Clock
|
UTSW |
5 |
76,384,967 (GRCm39) |
frame shift |
probably null |
|
R7406:Clock
|
UTSW |
5 |
76,414,692 (GRCm39) |
start codon destroyed |
probably null |
0.26 |
R7414:Clock
|
UTSW |
5 |
76,410,611 (GRCm39) |
missense |
probably benign |
0.00 |
R7560:Clock
|
UTSW |
5 |
76,390,738 (GRCm39) |
splice site |
probably null |
|
R7593:Clock
|
UTSW |
5 |
76,384,145 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7640:Clock
|
UTSW |
5 |
76,396,225 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7708:Clock
|
UTSW |
5 |
76,414,256 (GRCm39) |
missense |
probably benign |
0.00 |
R7713:Clock
|
UTSW |
5 |
76,393,267 (GRCm39) |
critical splice donor site |
probably null |
|
R7807:Clock
|
UTSW |
5 |
76,390,982 (GRCm39) |
missense |
probably benign |
0.01 |
R8171:Clock
|
UTSW |
5 |
76,414,261 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8190:Clock
|
UTSW |
5 |
76,375,051 (GRCm39) |
missense |
probably damaging |
0.98 |
R8225:Clock
|
UTSW |
5 |
76,389,759 (GRCm39) |
missense |
probably damaging |
0.99 |
R8309:Clock
|
UTSW |
5 |
76,402,269 (GRCm39) |
missense |
probably benign |
0.07 |
R8557:Clock
|
UTSW |
5 |
76,377,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R8792:Clock
|
UTSW |
5 |
76,410,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R8869:Clock
|
UTSW |
5 |
76,374,889 (GRCm39) |
small deletion |
probably benign |
|
R8870:Clock
|
UTSW |
5 |
76,383,632 (GRCm39) |
missense |
probably benign |
0.17 |
R8980:Clock
|
UTSW |
5 |
76,402,286 (GRCm39) |
missense |
probably benign |
0.01 |
R8982:Clock
|
UTSW |
5 |
76,364,559 (GRCm39) |
missense |
unknown |
|
R9177:Clock
|
UTSW |
5 |
76,377,256 (GRCm39) |
missense |
probably benign |
0.00 |
R9208:Clock
|
UTSW |
5 |
76,384,871 (GRCm39) |
missense |
probably benign |
0.00 |
R9213:Clock
|
UTSW |
5 |
76,393,376 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9307:Clock
|
UTSW |
5 |
76,364,671 (GRCm39) |
missense |
unknown |
|
R9446:Clock
|
UTSW |
5 |
76,396,288 (GRCm39) |
missense |
probably benign |
0.00 |
R9516:Clock
|
UTSW |
5 |
76,377,227 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9572:Clock
|
UTSW |
5 |
76,377,338 (GRCm39) |
missense |
probably benign |
0.00 |
R9630:Clock
|
UTSW |
5 |
76,393,281 (GRCm39) |
missense |
probably benign |
0.03 |
|