Other mutations in this stock |
Total: 20 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5031439G07Rik |
A |
G |
15: 84,840,020 (GRCm39) |
L109P |
probably damaging |
Het |
Aacs |
T |
A |
5: 125,585,772 (GRCm39) |
M316K |
probably benign |
Het |
Adarb2 |
T |
C |
13: 8,722,469 (GRCm39) |
V375A |
probably damaging |
Het |
Adgra2 |
C |
A |
8: 27,576,011 (GRCm39) |
A13E |
possibly damaging |
Het |
Ankrd34c |
A |
T |
9: 89,611,079 (GRCm39) |
S421T |
probably benign |
Het |
Bpifa6 |
A |
T |
2: 153,832,386 (GRCm39) |
M298L |
probably benign |
Het |
Casq2 |
T |
C |
3: 102,017,547 (GRCm39) |
|
probably benign |
Het |
Ckap5 |
A |
G |
2: 91,406,395 (GRCm39) |
T762A |
probably benign |
Het |
Dnah7b |
A |
T |
1: 46,105,889 (GRCm39) |
|
probably benign |
Het |
Dnajc7 |
A |
T |
11: 100,490,017 (GRCm39) |
F79L |
possibly damaging |
Het |
Dyrk3 |
A |
G |
1: 131,064,073 (GRCm39) |
I3T |
possibly damaging |
Het |
Fchsd2 |
T |
C |
7: 100,926,833 (GRCm39) |
I641T |
probably benign |
Het |
Furin |
A |
G |
7: 80,040,744 (GRCm39) |
V698A |
probably benign |
Het |
Lratd1 |
T |
C |
12: 14,200,527 (GRCm39) |
S67G |
probably benign |
Het |
Prl2c5 |
G |
A |
13: 13,364,061 (GRCm39) |
|
probably null |
Het |
Ryr3 |
A |
T |
2: 112,559,279 (GRCm39) |
|
probably benign |
Het |
Serpina6 |
G |
T |
12: 103,618,224 (GRCm39) |
|
probably benign |
Het |
Slc6a2 |
A |
G |
8: 93,722,728 (GRCm39) |
Y575C |
probably damaging |
Het |
Trim9 |
T |
C |
12: 70,393,887 (GRCm39) |
E19G |
probably damaging |
Het |
Tsfm |
G |
T |
10: 126,864,228 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Dhx38 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00508:Dhx38
|
APN |
8 |
110,283,566 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL00821:Dhx38
|
APN |
8 |
110,282,286 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01011:Dhx38
|
APN |
8 |
110,289,323 (GRCm39) |
missense |
probably benign |
|
IGL01401:Dhx38
|
APN |
8 |
110,278,746 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02133:Dhx38
|
APN |
8 |
110,284,873 (GRCm39) |
nonsense |
probably null |
|
IGL02529:Dhx38
|
APN |
8 |
110,285,645 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02652:Dhx38
|
APN |
8 |
110,282,761 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03241:Dhx38
|
APN |
8 |
110,289,288 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03378:Dhx38
|
APN |
8 |
110,285,722 (GRCm39) |
splice site |
probably null |
|
R0358:Dhx38
|
UTSW |
8 |
110,279,094 (GRCm39) |
missense |
probably benign |
0.13 |
R0375:Dhx38
|
UTSW |
8 |
110,281,813 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0437:Dhx38
|
UTSW |
8 |
110,285,261 (GRCm39) |
splice site |
probably benign |
|
R0481:Dhx38
|
UTSW |
8 |
110,282,848 (GRCm39) |
splice site |
probably benign |
|
R0492:Dhx38
|
UTSW |
8 |
110,288,576 (GRCm39) |
splice site |
probably benign |
|
R0528:Dhx38
|
UTSW |
8 |
110,289,293 (GRCm39) |
missense |
probably benign |
0.00 |
R0607:Dhx38
|
UTSW |
8 |
110,285,575 (GRCm39) |
missense |
probably benign |
0.07 |
R1638:Dhx38
|
UTSW |
8 |
110,280,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R2020:Dhx38
|
UTSW |
8 |
110,283,501 (GRCm39) |
splice site |
probably benign |
|
R2056:Dhx38
|
UTSW |
8 |
110,289,352 (GRCm39) |
unclassified |
probably benign |
|
R2096:Dhx38
|
UTSW |
8 |
110,280,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R2152:Dhx38
|
UTSW |
8 |
110,287,306 (GRCm39) |
missense |
probably benign |
0.00 |
R2154:Dhx38
|
UTSW |
8 |
110,287,306 (GRCm39) |
missense |
probably benign |
0.00 |
R2382:Dhx38
|
UTSW |
8 |
110,282,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R4367:Dhx38
|
UTSW |
8 |
110,279,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4368:Dhx38
|
UTSW |
8 |
110,279,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4369:Dhx38
|
UTSW |
8 |
110,279,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R5250:Dhx38
|
UTSW |
8 |
110,283,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R5354:Dhx38
|
UTSW |
8 |
110,282,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R5668:Dhx38
|
UTSW |
8 |
110,280,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R5777:Dhx38
|
UTSW |
8 |
110,283,534 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5784:Dhx38
|
UTSW |
8 |
110,286,245 (GRCm39) |
nonsense |
probably null |
|
R6799:Dhx38
|
UTSW |
8 |
110,279,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R6915:Dhx38
|
UTSW |
8 |
110,286,231 (GRCm39) |
missense |
probably benign |
0.15 |
R6932:Dhx38
|
UTSW |
8 |
110,279,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R7042:Dhx38
|
UTSW |
8 |
110,283,617 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7248:Dhx38
|
UTSW |
8 |
110,285,559 (GRCm39) |
missense |
probably benign |
0.15 |
R7394:Dhx38
|
UTSW |
8 |
110,283,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R7513:Dhx38
|
UTSW |
8 |
110,287,221 (GRCm39) |
missense |
probably benign |
0.00 |
R7569:Dhx38
|
UTSW |
8 |
110,287,327 (GRCm39) |
missense |
probably damaging |
0.98 |
R8003:Dhx38
|
UTSW |
8 |
110,282,772 (GRCm39) |
missense |
probably damaging |
0.99 |
R8071:Dhx38
|
UTSW |
8 |
110,285,333 (GRCm39) |
missense |
probably benign |
0.10 |
R8537:Dhx38
|
UTSW |
8 |
110,280,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R8852:Dhx38
|
UTSW |
8 |
110,289,361 (GRCm39) |
nonsense |
probably null |
|
R8860:Dhx38
|
UTSW |
8 |
110,289,361 (GRCm39) |
nonsense |
probably null |
|
R8937:Dhx38
|
UTSW |
8 |
110,283,098 (GRCm39) |
missense |
probably damaging |
0.96 |
R9099:Dhx38
|
UTSW |
8 |
110,282,783 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dhx38
|
UTSW |
8 |
110,282,717 (GRCm39) |
missense |
probably benign |
0.00 |
|