Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp10a |
G |
T |
7: 58,465,894 (GRCm39) |
|
probably benign |
Het |
B3gnt9 |
T |
C |
8: 105,980,956 (GRCm39) |
E144G |
probably null |
Het |
Bcl9 |
G |
T |
3: 97,113,042 (GRCm39) |
Q1138K |
possibly damaging |
Het |
C6 |
T |
C |
15: 4,769,231 (GRCm39) |
|
probably benign |
Het |
Ccl4 |
A |
G |
11: 83,554,402 (GRCm39) |
|
probably benign |
Het |
Cdc73 |
A |
G |
1: 143,578,230 (GRCm39) |
|
probably null |
Het |
Cemip |
A |
T |
7: 83,593,283 (GRCm39) |
L1140* |
probably null |
Het |
Col27a1 |
G |
A |
4: 63,175,351 (GRCm39) |
|
probably null |
Het |
Col9a1 |
G |
A |
1: 24,262,701 (GRCm39) |
|
probably null |
Het |
Colgalt1 |
C |
T |
8: 72,070,804 (GRCm39) |
T232I |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,939,974 (GRCm39) |
D1640G |
probably damaging |
Het |
Dot1l |
T |
G |
10: 80,621,859 (GRCm39) |
C504G |
probably benign |
Het |
Gm9892 |
T |
C |
8: 52,649,458 (GRCm39) |
T212A |
probably benign |
Het |
Hjurp |
G |
A |
1: 88,205,090 (GRCm39) |
|
probably benign |
Het |
Ifnar2 |
A |
G |
16: 91,200,809 (GRCm39) |
D350G |
possibly damaging |
Het |
Ift172 |
T |
C |
5: 31,419,210 (GRCm39) |
I1144V |
probably benign |
Het |
Ipo7 |
A |
T |
7: 109,629,011 (GRCm39) |
N94Y |
possibly damaging |
Het |
Irag1 |
T |
A |
7: 110,487,252 (GRCm39) |
M699L |
probably benign |
Het |
Mapkbp1 |
C |
A |
2: 119,829,015 (GRCm39) |
A57D |
possibly damaging |
Het |
Mmd |
T |
A |
11: 90,167,676 (GRCm39) |
I235N |
probably benign |
Het |
Naip2 |
T |
C |
13: 100,298,362 (GRCm39) |
E558G |
probably benign |
Het |
Naip2 |
C |
T |
13: 100,298,368 (GRCm39) |
G556D |
probably benign |
Het |
Palld |
A |
G |
8: 61,975,916 (GRCm39) |
|
probably null |
Het |
Parp4 |
G |
A |
14: 56,827,854 (GRCm39) |
E202K |
probably damaging |
Het |
Pclo |
C |
A |
5: 14,732,191 (GRCm39) |
|
probably benign |
Het |
Pde8a |
T |
C |
7: 80,952,042 (GRCm39) |
|
probably null |
Het |
Pdgfrb |
T |
A |
18: 61,198,952 (GRCm39) |
L370* |
probably null |
Het |
Phf2 |
A |
T |
13: 48,957,953 (GRCm39) |
S1020R |
unknown |
Het |
Pik3r4 |
T |
A |
9: 105,528,100 (GRCm39) |
|
probably null |
Het |
Plxnb1 |
C |
A |
9: 108,929,720 (GRCm39) |
P192Q |
possibly damaging |
Het |
Ppil3 |
A |
T |
1: 58,480,037 (GRCm39) |
I46N |
probably damaging |
Het |
Prr14l |
A |
C |
5: 32,987,604 (GRCm39) |
C630W |
probably damaging |
Het |
Rfx5 |
A |
G |
3: 94,865,723 (GRCm39) |
I341V |
probably benign |
Het |
Ryr3 |
T |
C |
2: 112,581,148 (GRCm39) |
K2895E |
probably damaging |
Het |
Slc5a12 |
T |
C |
2: 110,447,435 (GRCm39) |
|
probably null |
Het |
Slc8a3 |
T |
C |
12: 81,362,790 (GRCm39) |
T10A |
probably damaging |
Het |
Ss18 |
A |
G |
18: 14,769,595 (GRCm39) |
Y321H |
unknown |
Het |
Sspo |
A |
G |
6: 48,438,569 (GRCm39) |
N1546D |
probably benign |
Het |
Thbs4 |
G |
A |
13: 92,888,925 (GRCm39) |
L923F |
probably damaging |
Het |
Ulk1 |
C |
T |
5: 110,937,223 (GRCm39) |
R691Q |
probably benign |
Het |
|
Other mutations in Chd4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00573:Chd4
|
APN |
6 |
125,086,860 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00917:Chd4
|
APN |
6 |
125,081,909 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01088:Chd4
|
APN |
6 |
125,099,431 (GRCm39) |
unclassified |
probably benign |
|
IGL02005:Chd4
|
APN |
6 |
125,105,779 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02405:Chd4
|
APN |
6 |
125,074,190 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02707:Chd4
|
APN |
6 |
125,085,730 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02976:Chd4
|
APN |
6 |
125,098,331 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03001:Chd4
|
APN |
6 |
125,078,529 (GRCm39) |
missense |
possibly damaging |
0.93 |
FR4304:Chd4
|
UTSW |
6 |
125,099,107 (GRCm39) |
unclassified |
probably benign |
|
FR4589:Chd4
|
UTSW |
6 |
125,099,102 (GRCm39) |
unclassified |
probably benign |
|
FR4589:Chd4
|
UTSW |
6 |
125,099,096 (GRCm39) |
missense |
probably benign |
0.02 |
FR4737:Chd4
|
UTSW |
6 |
125,099,094 (GRCm39) |
unclassified |
probably benign |
|
FR4976:Chd4
|
UTSW |
6 |
125,099,094 (GRCm39) |
unclassified |
probably benign |
|
R0311:Chd4
|
UTSW |
6 |
125,078,628 (GRCm39) |
missense |
probably benign |
0.15 |
R0414:Chd4
|
UTSW |
6 |
125,084,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R0647:Chd4
|
UTSW |
6 |
125,086,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R0656:Chd4
|
UTSW |
6 |
125,079,930 (GRCm39) |
missense |
probably damaging |
0.98 |
R1651:Chd4
|
UTSW |
6 |
125,100,547 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1850:Chd4
|
UTSW |
6 |
125,098,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R2190:Chd4
|
UTSW |
6 |
125,091,260 (GRCm39) |
missense |
probably benign |
0.18 |
R2192:Chd4
|
UTSW |
6 |
125,082,320 (GRCm39) |
missense |
probably damaging |
0.99 |
R2858:Chd4
|
UTSW |
6 |
125,081,849 (GRCm39) |
missense |
probably damaging |
0.99 |
R3406:Chd4
|
UTSW |
6 |
125,098,970 (GRCm39) |
missense |
probably benign |
0.09 |
R3431:Chd4
|
UTSW |
6 |
125,097,523 (GRCm39) |
splice site |
probably benign |
|
R4330:Chd4
|
UTSW |
6 |
125,078,565 (GRCm39) |
missense |
probably benign |
0.29 |
R4394:Chd4
|
UTSW |
6 |
125,098,581 (GRCm39) |
missense |
probably damaging |
0.99 |
R4538:Chd4
|
UTSW |
6 |
125,097,649 (GRCm39) |
missense |
probably damaging |
0.99 |
R4664:Chd4
|
UTSW |
6 |
125,078,465 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4805:Chd4
|
UTSW |
6 |
125,105,908 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5050:Chd4
|
UTSW |
6 |
125,084,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R5055:Chd4
|
UTSW |
6 |
125,077,949 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5232:Chd4
|
UTSW |
6 |
125,098,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R5314:Chd4
|
UTSW |
6 |
125,077,551 (GRCm39) |
missense |
probably damaging |
0.96 |
R5343:Chd4
|
UTSW |
6 |
125,097,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R5502:Chd4
|
UTSW |
6 |
125,082,239 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5613:Chd4
|
UTSW |
6 |
125,097,509 (GRCm39) |
missense |
probably damaging |
0.99 |
R6211:Chd4
|
UTSW |
6 |
125,078,248 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6606:Chd4
|
UTSW |
6 |
125,086,389 (GRCm39) |
missense |
probably damaging |
0.99 |
R6753:Chd4
|
UTSW |
6 |
125,091,263 (GRCm39) |
missense |
probably benign |
0.01 |
R6808:Chd4
|
UTSW |
6 |
125,099,086 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6939:Chd4
|
UTSW |
6 |
125,083,501 (GRCm39) |
missense |
probably damaging |
0.99 |
R6968:Chd4
|
UTSW |
6 |
125,085,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R6973:Chd4
|
UTSW |
6 |
125,099,825 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6992:Chd4
|
UTSW |
6 |
125,091,339 (GRCm39) |
missense |
probably benign |
0.14 |
R7058:Chd4
|
UTSW |
6 |
125,085,405 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7081:Chd4
|
UTSW |
6 |
125,106,948 (GRCm39) |
missense |
unknown |
|
R7253:Chd4
|
UTSW |
6 |
125,083,555 (GRCm39) |
splice site |
probably null |
|
R7423:Chd4
|
UTSW |
6 |
125,105,822 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7535:Chd4
|
UTSW |
6 |
125,105,836 (GRCm39) |
missense |
probably benign |
0.32 |
R7566:Chd4
|
UTSW |
6 |
125,078,866 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8053:Chd4
|
UTSW |
6 |
125,105,779 (GRCm39) |
nonsense |
probably null |
|
R8155:Chd4
|
UTSW |
6 |
125,082,287 (GRCm39) |
missense |
probably benign |
0.00 |
R8711:Chd4
|
UTSW |
6 |
125,100,485 (GRCm39) |
unclassified |
probably benign |
|
R8783:Chd4
|
UTSW |
6 |
125,100,347 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9020:Chd4
|
UTSW |
6 |
125,084,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R9093:Chd4
|
UTSW |
6 |
125,090,974 (GRCm39) |
missense |
probably benign |
0.13 |
R9417:Chd4
|
UTSW |
6 |
125,097,688 (GRCm39) |
missense |
probably damaging |
0.99 |
R9509:Chd4
|
UTSW |
6 |
125,099,485 (GRCm39) |
missense |
possibly damaging |
0.96 |
RF046:Chd4
|
UTSW |
6 |
125,099,094 (GRCm39) |
unclassified |
probably benign |
|
RF052:Chd4
|
UTSW |
6 |
125,099,108 (GRCm39) |
unclassified |
probably benign |
|
RF058:Chd4
|
UTSW |
6 |
125,099,094 (GRCm39) |
unclassified |
probably benign |
|
RF060:Chd4
|
UTSW |
6 |
125,099,108 (GRCm39) |
unclassified |
probably benign |
|
X0025:Chd4
|
UTSW |
6 |
125,083,430 (GRCm39) |
nonsense |
probably null |
|
X0027:Chd4
|
UTSW |
6 |
125,079,127 (GRCm39) |
missense |
probably damaging |
0.98 |
X0063:Chd4
|
UTSW |
6 |
125,090,978 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Chd4
|
UTSW |
6 |
125,078,561 (GRCm39) |
missense |
probably benign |
0.36 |
Z1176:Chd4
|
UTSW |
6 |
125,077,823 (GRCm39) |
missense |
possibly damaging |
0.93 |
|