Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl9 |
A |
T |
17: 33,652,098 (GRCm39) |
I53F |
probably damaging |
Het |
Apol7b |
T |
A |
15: 77,308,873 (GRCm39) |
D75V |
probably damaging |
Het |
Brd8 |
C |
T |
18: 34,741,528 (GRCm39) |
A387T |
probably damaging |
Het |
Cacybp |
T |
C |
1: 160,036,169 (GRCm39) |
|
probably null |
Het |
Calcoco1 |
T |
C |
15: 102,618,875 (GRCm39) |
K444E |
probably damaging |
Het |
Cers2 |
G |
A |
3: 95,228,320 (GRCm39) |
R120H |
probably benign |
Het |
Col11a1 |
A |
T |
3: 113,888,593 (GRCm39) |
K286N |
possibly damaging |
Het |
Creld2 |
A |
G |
15: 88,709,413 (GRCm39) |
N308S |
probably damaging |
Het |
Cyp2d12 |
T |
C |
15: 82,440,934 (GRCm39) |
S151P |
probably damaging |
Het |
Dlec1 |
A |
G |
9: 118,955,242 (GRCm39) |
H642R |
probably benign |
Het |
Eif6 |
T |
C |
2: 155,665,206 (GRCm39) |
Y151C |
probably damaging |
Het |
Erbb4 |
A |
T |
1: 68,079,462 (GRCm39) |
M1206K |
probably benign |
Het |
Fam178b |
G |
A |
1: 36,639,216 (GRCm39) |
T361M |
probably damaging |
Het |
Fbxo10 |
A |
G |
4: 45,059,035 (GRCm39) |
F234S |
probably benign |
Het |
Gcc2 |
A |
T |
10: 58,094,064 (GRCm39) |
E13D |
probably damaging |
Het |
Gm19410 |
C |
A |
8: 36,239,733 (GRCm39) |
A143E |
probably damaging |
Het |
Gtf3c5 |
T |
C |
2: 28,460,499 (GRCm39) |
K367E |
probably damaging |
Het |
Ifi204 |
T |
C |
1: 173,589,269 (GRCm39) |
E54G |
probably benign |
Het |
Kalrn |
A |
T |
16: 33,848,346 (GRCm39) |
I492N |
probably damaging |
Het |
Kifbp |
T |
C |
10: 62,410,923 (GRCm39) |
N140S |
possibly damaging |
Het |
Map2k5 |
A |
G |
9: 63,229,528 (GRCm39) |
Y168H |
probably benign |
Het |
Mbip |
A |
C |
12: 56,384,383 (GRCm39) |
|
probably null |
Het |
Mcmdc2 |
C |
T |
1: 10,004,242 (GRCm39) |
T574I |
probably damaging |
Het |
Or10a3b |
T |
C |
7: 108,444,747 (GRCm39) |
T157A |
probably benign |
Het |
Or52j3 |
T |
G |
7: 102,836,511 (GRCm39) |
D234E |
probably benign |
Het |
Or5w22 |
A |
T |
2: 87,363,285 (GRCm39) |
M303L |
probably benign |
Het |
Or8d2 |
T |
A |
9: 38,760,085 (GRCm39) |
I225N |
probably damaging |
Het |
Or8g33 |
T |
C |
9: 39,337,836 (GRCm39) |
Y177C |
probably damaging |
Het |
Or9s27 |
A |
T |
1: 92,516,768 (GRCm39) |
R239W |
probably damaging |
Het |
Pdzd8 |
A |
G |
19: 59,287,957 (GRCm39) |
*1148Q |
probably null |
Het |
Phactr1 |
T |
A |
13: 43,286,445 (GRCm39) |
I582N |
probably damaging |
Het |
Phf20l1 |
T |
G |
15: 66,502,762 (GRCm39) |
L714R |
probably damaging |
Het |
Pramel32 |
T |
C |
4: 88,548,291 (GRCm39) |
E38G |
probably damaging |
Het |
Rcor3 |
T |
C |
1: 191,822,179 (GRCm39) |
E6G |
possibly damaging |
Het |
Skic3 |
T |
C |
13: 76,333,298 (GRCm39) |
S1516P |
probably damaging |
Het |
Sptlc2 |
G |
A |
12: 87,397,069 (GRCm39) |
T239I |
possibly damaging |
Het |
Tmc1 |
A |
T |
19: 20,772,880 (GRCm39) |
V707D |
probably damaging |
Het |
Tmem63b |
T |
A |
17: 45,971,734 (GRCm39) |
E827V |
probably benign |
Het |
Triml1 |
A |
G |
8: 43,594,258 (GRCm39) |
S58P |
probably damaging |
Het |
Zdbf2 |
A |
G |
1: 63,347,687 (GRCm39) |
H2022R |
possibly damaging |
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 |
R1342:Chd4
|
UTSW |
6 |
125,074,151 (GRCm39) |
missense |
probably benign |
0.40 |
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 |
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 |
|