Other mutations in this stock |
Total: 21 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp11b |
G |
T |
3: 35,881,222 (GRCm39) |
R593L |
probably damaging |
Het |
Axl |
A |
T |
7: 25,463,908 (GRCm39) |
D566E |
probably damaging |
Het |
Ccp110 |
A |
G |
7: 118,329,946 (GRCm39) |
D912G |
probably damaging |
Het |
Clca3b |
C |
T |
3: 144,544,923 (GRCm39) |
D355N |
probably benign |
Het |
Clock |
A |
C |
5: 76,402,260 (GRCm39) |
Y133* |
probably null |
Het |
Cntn4 |
T |
A |
6: 106,639,616 (GRCm39) |
V582E |
probably damaging |
Het |
Dnase2b |
G |
A |
3: 146,302,133 (GRCm39) |
T8I |
probably benign |
Het |
Ermard |
T |
C |
17: 15,208,328 (GRCm39) |
|
probably benign |
Het |
Gtf3c2 |
A |
G |
5: 31,331,752 (GRCm39) |
V22A |
probably damaging |
Het |
Ifi208 |
T |
C |
1: 173,510,427 (GRCm39) |
I194T |
possibly damaging |
Het |
Krt9 |
T |
A |
11: 100,080,832 (GRCm39) |
E340V |
probably damaging |
Het |
Nup58 |
G |
T |
14: 60,480,889 (GRCm39) |
T152K |
possibly damaging |
Het |
Otog |
A |
G |
7: 45,923,516 (GRCm39) |
S1050G |
probably damaging |
Het |
Prkdc |
A |
G |
16: 15,634,503 (GRCm39) |
N3580S |
probably benign |
Het |
Rsbn1 |
T |
C |
3: 103,836,137 (GRCm39) |
S392P |
probably damaging |
Het |
Sestd1 |
T |
C |
2: 77,018,866 (GRCm39) |
I647V |
probably benign |
Het |
Sugct |
A |
T |
13: 17,837,357 (GRCm39) |
S91R |
probably damaging |
Het |
Syne1 |
A |
G |
10: 5,344,922 (GRCm38) |
Y1227S |
possibly damaging |
Het |
Synpo |
C |
T |
18: 60,737,149 (GRCm39) |
V27I |
probably damaging |
Het |
Tcp11l2 |
T |
C |
10: 84,430,574 (GRCm39) |
I233T |
possibly damaging |
Het |
Vwde |
A |
G |
6: 13,187,411 (GRCm39) |
V692A |
probably benign |
Het |
|
Other mutations in Ddx1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00725:Ddx1
|
APN |
12 |
13,295,691 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00958:Ddx1
|
APN |
12 |
13,290,849 (GRCm39) |
splice site |
probably null |
|
IGL01786:Ddx1
|
APN |
12 |
13,279,137 (GRCm39) |
missense |
probably benign |
|
IGL02832:Ddx1
|
APN |
12 |
13,277,318 (GRCm39) |
nonsense |
probably null |
|
IGL02983:Ddx1
|
APN |
12 |
13,273,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R0201:Ddx1
|
UTSW |
12 |
13,273,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R0931:Ddx1
|
UTSW |
12 |
13,287,818 (GRCm39) |
splice site |
probably benign |
|
R1434:Ddx1
|
UTSW |
12 |
13,287,232 (GRCm39) |
missense |
probably benign |
0.01 |
R1558:Ddx1
|
UTSW |
12 |
13,289,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R1673:Ddx1
|
UTSW |
12 |
13,294,967 (GRCm39) |
critical splice donor site |
probably null |
|
R1854:Ddx1
|
UTSW |
12 |
13,279,332 (GRCm39) |
missense |
probably benign |
0.19 |
R2910:Ddx1
|
UTSW |
12 |
13,281,441 (GRCm39) |
splice site |
probably null |
|
R2911:Ddx1
|
UTSW |
12 |
13,281,441 (GRCm39) |
splice site |
probably null |
|
R4181:Ddx1
|
UTSW |
12 |
13,281,504 (GRCm39) |
nonsense |
probably null |
|
R4182:Ddx1
|
UTSW |
12 |
13,281,504 (GRCm39) |
nonsense |
probably null |
|
R4183:Ddx1
|
UTSW |
12 |
13,281,504 (GRCm39) |
nonsense |
probably null |
|
R4231:Ddx1
|
UTSW |
12 |
13,273,858 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4234:Ddx1
|
UTSW |
12 |
13,273,858 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4235:Ddx1
|
UTSW |
12 |
13,273,858 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4243:Ddx1
|
UTSW |
12 |
13,290,910 (GRCm39) |
nonsense |
probably null |
|
R4717:Ddx1
|
UTSW |
12 |
13,290,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R4821:Ddx1
|
UTSW |
12 |
13,289,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R5032:Ddx1
|
UTSW |
12 |
13,273,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R5082:Ddx1
|
UTSW |
12 |
13,270,436 (GRCm39) |
nonsense |
probably null |
|
R5528:Ddx1
|
UTSW |
12 |
13,279,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R5997:Ddx1
|
UTSW |
12 |
13,287,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R6398:Ddx1
|
UTSW |
12 |
13,295,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R6891:Ddx1
|
UTSW |
12 |
13,286,096 (GRCm39) |
missense |
probably benign |
0.25 |
R7085:Ddx1
|
UTSW |
12 |
13,279,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R7125:Ddx1
|
UTSW |
12 |
13,293,864 (GRCm39) |
missense |
probably benign |
0.18 |
R7307:Ddx1
|
UTSW |
12 |
13,273,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R7388:Ddx1
|
UTSW |
12 |
13,275,456 (GRCm39) |
missense |
probably null |
1.00 |
R7393:Ddx1
|
UTSW |
12 |
13,280,354 (GRCm39) |
missense |
probably benign |
0.03 |
R7460:Ddx1
|
UTSW |
12 |
13,281,440 (GRCm39) |
splice site |
probably null |
|
R8310:Ddx1
|
UTSW |
12 |
13,274,280 (GRCm39) |
intron |
probably benign |
|
R8479:Ddx1
|
UTSW |
12 |
13,270,749 (GRCm39) |
missense |
probably damaging |
0.97 |
R8712:Ddx1
|
UTSW |
12 |
13,293,859 (GRCm39) |
critical splice donor site |
probably benign |
|
R8790:Ddx1
|
UTSW |
12 |
13,273,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R8826:Ddx1
|
UTSW |
12 |
13,277,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R9120:Ddx1
|
UTSW |
12 |
13,275,458 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9214:Ddx1
|
UTSW |
12 |
13,286,119 (GRCm39) |
missense |
probably benign |
|
R9400:Ddx1
|
UTSW |
12 |
13,273,703 (GRCm39) |
missense |
probably damaging |
1.00 |
X0011:Ddx1
|
UTSW |
12 |
13,279,416 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Ddx1
|
UTSW |
12 |
13,293,867 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Ddx1
|
UTSW |
12 |
13,279,260 (GRCm39) |
missense |
probably damaging |
0.96 |
|