Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad11 |
A |
G |
9: 104,003,864 (GRCm39) |
D770G |
possibly damaging |
Het |
Amph |
G |
A |
13: 19,284,071 (GRCm39) |
G200D |
probably benign |
Het |
Asap2 |
T |
A |
12: 21,253,999 (GRCm39) |
L170H |
possibly damaging |
Het |
Asap3 |
T |
C |
4: 135,966,299 (GRCm39) |
|
probably null |
Het |
Bltp1 |
T |
A |
3: 37,052,493 (GRCm39) |
D3064E |
probably benign |
Het |
Ccnf |
A |
T |
17: 24,445,679 (GRCm39) |
Y522* |
probably null |
Het |
Ceacam5 |
A |
T |
7: 17,448,877 (GRCm39) |
Y81F |
possibly damaging |
Het |
Chd2 |
A |
T |
7: 73,091,393 (GRCm39) |
M1616K |
probably benign |
Het |
Clint1 |
T |
A |
11: 45,797,042 (GRCm39) |
S374R |
probably benign |
Het |
Col6a6 |
A |
T |
9: 105,586,745 (GRCm39) |
F1759I |
possibly damaging |
Het |
Crocc |
T |
A |
4: 140,749,674 (GRCm39) |
I1487F |
probably benign |
Het |
Dll4 |
TC |
T |
2: 119,163,054 (GRCm39) |
|
probably null |
Het |
Dop1a |
T |
C |
9: 86,402,490 (GRCm39) |
I1230T |
probably benign |
Het |
Dsp |
A |
T |
13: 38,380,808 (GRCm39) |
I2518L |
possibly damaging |
Het |
Eps8l2 |
G |
T |
7: 140,936,117 (GRCm39) |
V224L |
possibly damaging |
Het |
Etv1 |
T |
C |
12: 38,830,971 (GRCm39) |
V13A |
probably benign |
Het |
Fam78a |
T |
C |
2: 31,959,313 (GRCm39) |
M266V |
probably benign |
Het |
Fam81a |
A |
G |
9: 70,017,538 (GRCm39) |
|
probably null |
Het |
Fhad1 |
T |
C |
4: 141,709,620 (GRCm39) |
I245V |
probably damaging |
Het |
Flot2 |
T |
C |
11: 77,949,805 (GRCm39) |
V378A |
probably benign |
Het |
Fras1 |
T |
A |
5: 96,888,609 (GRCm39) |
S2718R |
probably damaging |
Het |
Gata3os |
T |
A |
2: 9,887,345 (GRCm39) |
|
probably benign |
Het |
Gm14305 |
A |
G |
2: 176,413,167 (GRCm39) |
K353R |
possibly damaging |
Het |
Inppl1 |
A |
C |
7: 101,480,915 (GRCm39) |
V315G |
probably damaging |
Het |
Kbtbd6 |
A |
T |
14: 79,690,822 (GRCm39) |
I506F |
probably damaging |
Het |
Klf6 |
G |
C |
13: 5,915,160 (GRCm39) |
G200R |
probably benign |
Het |
Lrp6 |
A |
G |
6: 134,518,930 (GRCm39) |
I45T |
probably benign |
Het |
Lrriq4 |
T |
G |
3: 30,704,401 (GRCm39) |
V143G |
probably benign |
Het |
Map2k2 |
G |
T |
10: 80,955,159 (GRCm39) |
G217C |
probably damaging |
Het |
Mcm10 |
T |
C |
2: 4,997,782 (GRCm39) |
N813S |
probably benign |
Het |
Mfng |
T |
A |
15: 78,657,348 (GRCm39) |
N42I |
probably benign |
Het |
Mical1 |
A |
G |
10: 41,361,141 (GRCm39) |
D808G |
probably benign |
Het |
Mmp14 |
T |
C |
14: 54,673,632 (GRCm39) |
F99L |
probably benign |
Het |
Mroh8 |
A |
T |
2: 157,064,787 (GRCm39) |
V763E |
probably benign |
Het |
Mycbp2 |
G |
T |
14: 103,551,752 (GRCm39) |
P193T |
probably benign |
Het |
Myo1b |
T |
C |
1: 51,821,142 (GRCm39) |
D447G |
possibly damaging |
Het |
Myoz2 |
T |
A |
3: 122,807,284 (GRCm39) |
|
probably benign |
Het |
Narf |
C |
A |
11: 121,136,209 (GRCm39) |
P195Q |
probably damaging |
Het |
Nfatc3 |
T |
A |
8: 106,818,745 (GRCm39) |
F496I |
probably damaging |
Het |
Nudt13 |
A |
G |
14: 20,360,772 (GRCm39) |
Y225C |
probably damaging |
Het |
Or10ab5 |
A |
T |
7: 108,245,428 (GRCm39) |
Y118* |
probably null |
Het |
Or11h4 |
T |
G |
14: 50,974,554 (GRCm39) |
I22L |
probably benign |
Het |
Or2i1 |
G |
T |
17: 37,508,380 (GRCm39) |
R85S |
possibly damaging |
Het |
Or56b1 |
C |
T |
7: 104,285,291 (GRCm39) |
R137C |
probably benign |
Het |
Osbpl10 |
C |
T |
9: 114,807,939 (GRCm39) |
A65V |
unknown |
Het |
Pdcd2l |
A |
G |
7: 33,885,760 (GRCm39) |
L308P |
probably damaging |
Het |
Pitx2 |
T |
A |
3: 129,008,432 (GRCm39) |
|
probably null |
Het |
Pms2 |
T |
A |
5: 143,862,744 (GRCm39) |
F617Y |
probably damaging |
Het |
Poc1b |
A |
G |
10: 98,980,183 (GRCm39) |
N180S |
possibly damaging |
Het |
Poln |
T |
A |
5: 34,286,485 (GRCm39) |
M228L |
probably benign |
Het |
Prex1 |
C |
A |
2: 166,432,429 (GRCm39) |
V707F |
possibly damaging |
Het |
Rasal2 |
A |
T |
1: 157,058,514 (GRCm39) |
V12D |
unknown |
Het |
Ripk1 |
A |
G |
13: 34,205,373 (GRCm39) |
E284G |
probably benign |
Het |
Rpa2 |
T |
C |
4: 132,499,251 (GRCm39) |
W107R |
probably damaging |
Het |
Selp |
A |
G |
1: 163,954,177 (GRCm39) |
Y159C |
probably damaging |
Het |
Serpina1a |
A |
T |
12: 103,824,293 (GRCm39) |
W30R |
probably benign |
Het |
Skic2 |
A |
G |
17: 35,065,579 (GRCm39) |
V325A |
probably damaging |
Het |
Slco6d1 |
A |
G |
1: 98,371,396 (GRCm39) |
R294G |
probably benign |
Het |
Supt5 |
A |
T |
7: 28,016,671 (GRCm39) |
I737N |
probably damaging |
Het |
Thap11 |
T |
C |
8: 106,582,660 (GRCm39) |
V223A |
probably damaging |
Het |
Trabd |
T |
A |
15: 88,968,913 (GRCm39) |
S144T |
possibly damaging |
Het |
Trim24 |
T |
A |
6: 37,933,949 (GRCm39) |
S701T |
probably damaging |
Het |
Trim52 |
C |
T |
14: 106,344,986 (GRCm39) |
P215S |
possibly damaging |
Het |
Vmn1r172 |
G |
T |
7: 23,359,749 (GRCm39) |
L211F |
probably damaging |
Het |
Vmn2r86 |
A |
C |
10: 130,282,934 (GRCm39) |
Y561D |
probably damaging |
Het |
Zfp384 |
C |
A |
6: 125,013,336 (GRCm39) |
A468E |
|
Het |
Zfp658 |
A |
G |
7: 43,223,381 (GRCm39) |
H552R |
possibly damaging |
Het |
Zranb2 |
T |
C |
3: 157,250,720 (GRCm39) |
V297A |
unknown |
Het |
|
Other mutations in Atxn2l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00325:Atxn2l
|
APN |
7 |
126,097,460 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00507:Atxn2l
|
APN |
7 |
126,095,756 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL00846:Atxn2l
|
APN |
7 |
126,098,350 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01813:Atxn2l
|
APN |
7 |
126,099,425 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4378001:Atxn2l
|
UTSW |
7 |
126,096,443 (GRCm39) |
missense |
probably benign |
0.11 |
R0005:Atxn2l
|
UTSW |
7 |
126,097,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R0267:Atxn2l
|
UTSW |
7 |
126,092,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R0608:Atxn2l
|
UTSW |
7 |
126,100,588 (GRCm39) |
splice site |
probably null |
|
R0749:Atxn2l
|
UTSW |
7 |
126,100,009 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0831:Atxn2l
|
UTSW |
7 |
126,098,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R0881:Atxn2l
|
UTSW |
7 |
126,095,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R1022:Atxn2l
|
UTSW |
7 |
126,096,466 (GRCm39) |
missense |
probably benign |
0.01 |
R1024:Atxn2l
|
UTSW |
7 |
126,096,466 (GRCm39) |
missense |
probably benign |
0.01 |
R1081:Atxn2l
|
UTSW |
7 |
126,093,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R1132:Atxn2l
|
UTSW |
7 |
126,093,420 (GRCm39) |
small deletion |
probably benign |
|
R1489:Atxn2l
|
UTSW |
7 |
126,095,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:Atxn2l
|
UTSW |
7 |
126,092,340 (GRCm39) |
missense |
probably damaging |
0.99 |
R2062:Atxn2l
|
UTSW |
7 |
126,095,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R2170:Atxn2l
|
UTSW |
7 |
126,102,411 (GRCm39) |
start gained |
probably benign |
|
R3719:Atxn2l
|
UTSW |
7 |
126,097,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R3861:Atxn2l
|
UTSW |
7 |
126,101,123 (GRCm39) |
critical splice donor site |
probably null |
|
R5061:Atxn2l
|
UTSW |
7 |
126,099,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R6022:Atxn2l
|
UTSW |
7 |
126,095,607 (GRCm39) |
critical splice donor site |
probably null |
|
R6075:Atxn2l
|
UTSW |
7 |
126,091,689 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6131:Atxn2l
|
UTSW |
7 |
126,102,337 (GRCm39) |
unclassified |
probably benign |
|
R6460:Atxn2l
|
UTSW |
7 |
126,093,420 (GRCm39) |
small deletion |
probably benign |
|
R6552:Atxn2l
|
UTSW |
7 |
126,092,993 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7167:Atxn2l
|
UTSW |
7 |
126,098,394 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7234:Atxn2l
|
UTSW |
7 |
126,092,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R7301:Atxn2l
|
UTSW |
7 |
126,093,383 (GRCm39) |
nonsense |
probably null |
|
R7432:Atxn2l
|
UTSW |
7 |
126,093,046 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7691:Atxn2l
|
UTSW |
7 |
126,091,782 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7711:Atxn2l
|
UTSW |
7 |
126,100,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R7849:Atxn2l
|
UTSW |
7 |
126,092,345 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7870:Atxn2l
|
UTSW |
7 |
126,091,924 (GRCm39) |
missense |
probably benign |
|
R8907:Atxn2l
|
UTSW |
7 |
126,099,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R8929:Atxn2l
|
UTSW |
7 |
126,092,928 (GRCm39) |
splice site |
probably benign |
|
R8949:Atxn2l
|
UTSW |
7 |
126,091,377 (GRCm39) |
missense |
probably damaging |
0.99 |
R8982:Atxn2l
|
UTSW |
7 |
126,093,420 (GRCm39) |
small deletion |
probably benign |
|
R9127:Atxn2l
|
UTSW |
7 |
126,097,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R9769:Atxn2l
|
UTSW |
7 |
126,095,692 (GRCm39) |
missense |
probably benign |
0.00 |
RF006:Atxn2l
|
UTSW |
7 |
126,095,063 (GRCm39) |
missense |
probably benign |
0.00 |
|