Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acap3 |
G |
A |
4: 155,986,676 (GRCm39) |
V335M |
probably damaging |
Het |
Apex1 |
C |
T |
14: 51,163,711 (GRCm39) |
L113F |
possibly damaging |
Het |
Bltp1 |
T |
A |
3: 37,100,429 (GRCm39) |
H1218Q |
possibly damaging |
Het |
Cd33 |
C |
T |
7: 43,182,329 (GRCm39) |
V39M |
probably damaging |
Het |
Chek2 |
A |
G |
5: 110,996,536 (GRCm39) |
D166G |
probably damaging |
Het |
Col2a1 |
T |
C |
15: 97,874,054 (GRCm39) |
K1376R |
unknown |
Het |
Cpd |
C |
T |
11: 76,686,439 (GRCm39) |
R963H |
probably damaging |
Het |
Cracd |
A |
G |
5: 76,805,921 (GRCm39) |
|
probably benign |
Het |
Cyp2c67 |
A |
C |
19: 39,628,376 (GRCm39) |
Y189* |
probably null |
Het |
Dusp4 |
A |
T |
8: 35,285,666 (GRCm39) |
E309V |
probably benign |
Het |
Dync2h1 |
A |
G |
9: 7,162,789 (GRCm39) |
I600T |
probably damaging |
Het |
Fer1l4 |
A |
G |
2: 155,894,105 (GRCm39) |
V66A |
probably benign |
Het |
Fktn |
T |
C |
4: 53,737,568 (GRCm39) |
L269P |
possibly damaging |
Het |
Ftsj3 |
A |
G |
11: 106,141,185 (GRCm39) |
I645T |
probably damaging |
Het |
Fxr2 |
A |
G |
11: 69,534,713 (GRCm39) |
H198R |
probably damaging |
Het |
Fzd7 |
T |
C |
1: 59,523,539 (GRCm39) |
V474A |
probably damaging |
Het |
Gm10295 |
T |
A |
7: 71,000,406 (GRCm39) |
D58V |
unknown |
Het |
Hdlbp |
T |
C |
1: 93,357,891 (GRCm39) |
I337V |
probably benign |
Het |
Hydin |
T |
C |
8: 111,053,033 (GRCm39) |
V235A |
probably benign |
Het |
Igfbp4 |
C |
T |
11: 98,939,069 (GRCm39) |
H30Y |
probably damaging |
Het |
Kcna4 |
T |
C |
2: 107,126,736 (GRCm39) |
V490A |
probably damaging |
Het |
Kcnj13 |
T |
G |
1: 87,314,700 (GRCm39) |
D174A |
probably benign |
Het |
Krt7 |
T |
A |
15: 101,321,302 (GRCm39) |
L373Q |
probably benign |
Het |
Lama3 |
G |
A |
18: 12,614,094 (GRCm39) |
V1288I |
probably benign |
Het |
Mroh9 |
T |
C |
1: 162,875,435 (GRCm39) |
D488G |
possibly damaging |
Het |
Myh7 |
T |
C |
14: 55,216,994 (GRCm39) |
E1121G |
probably damaging |
Het |
Myom1 |
A |
G |
17: 71,384,912 (GRCm39) |
N768D |
probably damaging |
Het |
Naa16 |
T |
C |
14: 79,622,196 (GRCm39) |
T48A |
probably damaging |
Het |
Naglu |
C |
T |
11: 100,964,773 (GRCm39) |
P287S |
probably benign |
Het |
Nipbl |
A |
G |
15: 8,379,939 (GRCm39) |
V951A |
possibly damaging |
Het |
Nlrp3 |
T |
A |
11: 59,442,713 (GRCm39) |
M755K |
probably benign |
Het |
Nlrp4e |
T |
C |
7: 23,052,586 (GRCm39) |
|
probably benign |
Het |
Nt5dc1 |
C |
T |
10: 34,283,553 (GRCm39) |
A79T |
possibly damaging |
Het |
Or10aa3 |
T |
C |
1: 173,878,251 (GRCm39) |
F104S |
probably damaging |
Het |
Or6c205 |
A |
T |
10: 129,086,609 (GRCm39) |
I69F |
possibly damaging |
Het |
Or8b47 |
A |
G |
9: 38,435,029 (GRCm39) |
|
probably benign |
Het |
Otof |
A |
G |
5: 30,541,597 (GRCm39) |
L774P |
possibly damaging |
Het |
Phf20l1 |
C |
T |
15: 66,484,981 (GRCm39) |
R322C |
probably damaging |
Het |
Pkhd1 |
C |
T |
1: 20,279,400 (GRCm39) |
G2973R |
probably benign |
Het |
Plekhg5 |
G |
T |
4: 152,192,983 (GRCm39) |
D613Y |
probably damaging |
Het |
Ppm1h |
T |
A |
10: 122,714,534 (GRCm39) |
|
probably null |
Het |
Pramel31 |
T |
A |
4: 144,089,947 (GRCm39) |
L329Q |
probably damaging |
Het |
Prpf39 |
T |
C |
12: 65,089,255 (GRCm39) |
|
probably benign |
Het |
Rtn3 |
A |
G |
19: 7,460,406 (GRCm39) |
S15P |
unknown |
Het |
Slc22a28 |
G |
T |
19: 8,094,272 (GRCm39) |
|
probably benign |
Het |
Slc4a5 |
T |
A |
6: 83,239,515 (GRCm39) |
L143Q |
probably damaging |
Het |
Sox17 |
T |
C |
1: 4,562,426 (GRCm39) |
D130G |
possibly damaging |
Het |
Stag1 |
A |
G |
9: 100,833,710 (GRCm39) |
T1108A |
possibly damaging |
Het |
Sugp2 |
G |
A |
8: 70,695,185 (GRCm39) |
D53N |
probably damaging |
Het |
Trim33 |
G |
A |
3: 103,261,234 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
G |
2: 76,629,568 (GRCm39) |
I14291T |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,619,869 (GRCm39) |
V15933A |
probably damaging |
Het |
Tulp3 |
A |
C |
6: 128,302,847 (GRCm39) |
I324S |
probably damaging |
Het |
Zfhx2 |
T |
C |
14: 55,301,717 (GRCm39) |
E2089G |
probably damaging |
Het |
Zhx1 |
T |
C |
15: 57,918,075 (GRCm39) |
D57G |
probably benign |
Het |
|
Other mutations in Dock6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00944:Dock6
|
APN |
9 |
21,757,930 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01390:Dock6
|
APN |
9 |
21,714,341 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02025:Dock6
|
APN |
9 |
21,720,885 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02028:Dock6
|
APN |
9 |
21,750,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02311:Dock6
|
APN |
9 |
21,755,624 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02441:Dock6
|
APN |
9 |
21,753,222 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02504:Dock6
|
APN |
9 |
21,757,951 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02516:Dock6
|
APN |
9 |
21,713,881 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02836:Dock6
|
APN |
9 |
21,713,160 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02894:Dock6
|
APN |
9 |
21,723,111 (GRCm39) |
missense |
probably damaging |
1.00 |
backwater
|
UTSW |
9 |
21,735,712 (GRCm39) |
missense |
probably benign |
0.29 |
bayfront
|
UTSW |
9 |
21,733,041 (GRCm39) |
missense |
probably benign |
0.29 |
marshland
|
UTSW |
9 |
21,752,899 (GRCm39) |
missense |
probably benign |
0.00 |
Shallows
|
UTSW |
9 |
21,731,918 (GRCm39) |
missense |
probably benign |
|
IGL03048:Dock6
|
UTSW |
9 |
21,720,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R0370:Dock6
|
UTSW |
9 |
21,725,861 (GRCm39) |
missense |
probably benign |
0.29 |
R0504:Dock6
|
UTSW |
9 |
21,713,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R0633:Dock6
|
UTSW |
9 |
21,755,713 (GRCm39) |
missense |
probably benign |
0.00 |
R0634:Dock6
|
UTSW |
9 |
21,752,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R0671:Dock6
|
UTSW |
9 |
21,715,923 (GRCm39) |
splice site |
probably benign |
|
R0839:Dock6
|
UTSW |
9 |
21,729,188 (GRCm39) |
missense |
probably benign |
0.01 |
R0948:Dock6
|
UTSW |
9 |
21,712,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R1022:Dock6
|
UTSW |
9 |
21,744,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R1024:Dock6
|
UTSW |
9 |
21,744,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R1073:Dock6
|
UTSW |
9 |
21,757,814 (GRCm39) |
missense |
probably benign |
|
R1463:Dock6
|
UTSW |
9 |
21,743,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R1481:Dock6
|
UTSW |
9 |
21,731,918 (GRCm39) |
missense |
probably benign |
|
R1494:Dock6
|
UTSW |
9 |
21,726,038 (GRCm39) |
missense |
probably benign |
0.34 |
R1547:Dock6
|
UTSW |
9 |
21,725,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R1654:Dock6
|
UTSW |
9 |
21,716,139 (GRCm39) |
missense |
probably damaging |
0.98 |
R1782:Dock6
|
UTSW |
9 |
21,723,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R1905:Dock6
|
UTSW |
9 |
21,740,870 (GRCm39) |
missense |
probably benign |
0.37 |
R1908:Dock6
|
UTSW |
9 |
21,752,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R1916:Dock6
|
UTSW |
9 |
21,724,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Dock6
|
UTSW |
9 |
21,757,814 (GRCm39) |
missense |
probably benign |
|
R2197:Dock6
|
UTSW |
9 |
21,744,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R2316:Dock6
|
UTSW |
9 |
21,750,973 (GRCm39) |
missense |
probably damaging |
0.98 |
R2341:Dock6
|
UTSW |
9 |
21,750,782 (GRCm39) |
splice site |
probably benign |
|
R2519:Dock6
|
UTSW |
9 |
21,727,629 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2924:Dock6
|
UTSW |
9 |
21,720,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R2939:Dock6
|
UTSW |
9 |
21,750,496 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2940:Dock6
|
UTSW |
9 |
21,750,496 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3078:Dock6
|
UTSW |
9 |
21,757,050 (GRCm39) |
splice site |
probably benign |
|
R3081:Dock6
|
UTSW |
9 |
21,750,496 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3810:Dock6
|
UTSW |
9 |
21,712,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R4246:Dock6
|
UTSW |
9 |
21,750,786 (GRCm39) |
splice site |
probably null |
|
R4604:Dock6
|
UTSW |
9 |
21,713,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R4833:Dock6
|
UTSW |
9 |
21,755,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R4849:Dock6
|
UTSW |
9 |
21,723,068 (GRCm39) |
critical splice donor site |
probably null |
|
R4896:Dock6
|
UTSW |
9 |
21,735,733 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4926:Dock6
|
UTSW |
9 |
21,757,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R5183:Dock6
|
UTSW |
9 |
21,752,899 (GRCm39) |
missense |
probably benign |
0.00 |
R5211:Dock6
|
UTSW |
9 |
21,731,648 (GRCm39) |
missense |
probably benign |
0.36 |
R5337:Dock6
|
UTSW |
9 |
21,740,844 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5353:Dock6
|
UTSW |
9 |
21,726,082 (GRCm39) |
missense |
probably benign |
0.00 |
R5429:Dock6
|
UTSW |
9 |
21,744,177 (GRCm39) |
missense |
probably damaging |
0.99 |
R5463:Dock6
|
UTSW |
9 |
21,721,254 (GRCm39) |
splice site |
probably null |
|
R5476:Dock6
|
UTSW |
9 |
21,720,885 (GRCm39) |
missense |
probably damaging |
0.98 |
R5511:Dock6
|
UTSW |
9 |
21,728,703 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5534:Dock6
|
UTSW |
9 |
21,714,372 (GRCm39) |
nonsense |
probably null |
|
R5718:Dock6
|
UTSW |
9 |
21,735,789 (GRCm39) |
missense |
probably benign |
0.11 |
R5823:Dock6
|
UTSW |
9 |
21,716,124 (GRCm39) |
missense |
probably damaging |
0.99 |
R5831:Dock6
|
UTSW |
9 |
21,714,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R5887:Dock6
|
UTSW |
9 |
21,731,690 (GRCm39) |
missense |
probably damaging |
0.96 |
R5930:Dock6
|
UTSW |
9 |
21,735,712 (GRCm39) |
missense |
probably benign |
0.29 |
R6159:Dock6
|
UTSW |
9 |
21,733,041 (GRCm39) |
missense |
probably benign |
0.29 |
R6633:Dock6
|
UTSW |
9 |
21,732,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R6633:Dock6
|
UTSW |
9 |
21,731,627 (GRCm39) |
missense |
probably benign |
0.17 |
R6665:Dock6
|
UTSW |
9 |
21,751,208 (GRCm39) |
missense |
probably damaging |
0.99 |
R6744:Dock6
|
UTSW |
9 |
21,742,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R6903:Dock6
|
UTSW |
9 |
21,720,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R6981:Dock6
|
UTSW |
9 |
21,756,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R7024:Dock6
|
UTSW |
9 |
21,731,666 (GRCm39) |
missense |
probably benign |
|
R7030:Dock6
|
UTSW |
9 |
21,724,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R7045:Dock6
|
UTSW |
9 |
21,733,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R7139:Dock6
|
UTSW |
9 |
21,712,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R7356:Dock6
|
UTSW |
9 |
21,721,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R7400:Dock6
|
UTSW |
9 |
21,713,103 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7847:Dock6
|
UTSW |
9 |
21,712,503 (GRCm39) |
missense |
unknown |
|
R7863:Dock6
|
UTSW |
9 |
21,757,954 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7991:Dock6
|
UTSW |
9 |
21,757,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R7992:Dock6
|
UTSW |
9 |
21,744,135 (GRCm39) |
critical splice donor site |
probably null |
|
R8012:Dock6
|
UTSW |
9 |
21,757,807 (GRCm39) |
missense |
probably benign |
0.16 |
R8184:Dock6
|
UTSW |
9 |
21,741,596 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8213:Dock6
|
UTSW |
9 |
21,742,740 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8560:Dock6
|
UTSW |
9 |
21,714,132 (GRCm39) |
missense |
probably benign |
0.00 |
R8828:Dock6
|
UTSW |
9 |
21,757,797 (GRCm39) |
missense |
probably benign |
|
R9090:Dock6
|
UTSW |
9 |
21,752,796 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9221:Dock6
|
UTSW |
9 |
21,721,153 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9271:Dock6
|
UTSW |
9 |
21,752,796 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9301:Dock6
|
UTSW |
9 |
21,729,111 (GRCm39) |
missense |
probably benign |
|
R9308:Dock6
|
UTSW |
9 |
21,728,744 (GRCm39) |
nonsense |
probably null |
|
R9476:Dock6
|
UTSW |
9 |
21,724,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R9526:Dock6
|
UTSW |
9 |
21,713,802 (GRCm39) |
nonsense |
probably null |
|
R9544:Dock6
|
UTSW |
9 |
21,732,830 (GRCm39) |
nonsense |
probably null |
|
R9716:Dock6
|
UTSW |
9 |
21,742,418 (GRCm39) |
missense |
probably benign |
0.00 |
|