Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts19 |
A |
G |
18: 59,185,726 (GRCm39) |
D1200G |
probably damaging |
Het |
Adnp2 |
A |
G |
18: 80,172,537 (GRCm39) |
L624P |
probably damaging |
Het |
Akap9 |
A |
G |
5: 4,114,949 (GRCm39) |
|
probably null |
Het |
Ap2a2 |
A |
G |
7: 141,189,760 (GRCm39) |
Y249C |
probably damaging |
Het |
Asxl2 |
A |
T |
12: 3,534,531 (GRCm39) |
N243Y |
probably damaging |
Het |
Btnl4 |
A |
G |
17: 34,693,257 (GRCm39) |
S53P |
probably damaging |
Het |
Caly |
T |
C |
7: 139,651,513 (GRCm39) |
D116G |
possibly damaging |
Het |
Ccdc121rt2 |
G |
A |
5: 112,598,791 (GRCm39) |
R446H |
probably benign |
Het |
Ccdc168 |
T |
A |
1: 44,098,869 (GRCm39) |
H743L |
probably benign |
Het |
Ccdc81 |
G |
A |
7: 89,539,609 (GRCm39) |
A209V |
probably benign |
Het |
Cdc14a |
A |
G |
3: 116,101,887 (GRCm39) |
S347P |
probably benign |
Het |
Cdh9 |
G |
T |
15: 16,828,489 (GRCm39) |
A194S |
probably damaging |
Het |
Clca3a2 |
A |
G |
3: 144,519,756 (GRCm39) |
V206A |
probably benign |
Het |
Clca4a |
A |
T |
3: 144,658,500 (GRCm39) |
V905E |
possibly damaging |
Het |
Cluap1 |
A |
G |
16: 3,746,485 (GRCm39) |
E282G |
probably damaging |
Het |
Cmtm2b |
T |
A |
8: 105,056,419 (GRCm39) |
C109* |
probably null |
Het |
Crtac1 |
T |
C |
19: 42,322,399 (GRCm39) |
N114D |
probably benign |
Het |
Dennd1b |
T |
C |
1: 139,013,634 (GRCm39) |
Y168H |
|
Het |
Eps8 |
C |
T |
6: 137,505,569 (GRCm39) |
R53Q |
possibly damaging |
Het |
Erfl |
G |
A |
7: 24,627,975 (GRCm39) |
P185S |
possibly damaging |
Het |
Fh1 |
T |
C |
1: 175,437,337 (GRCm39) |
Y254C |
probably damaging |
Het |
H2-Q1 |
T |
A |
17: 35,540,356 (GRCm39) |
L147Q |
probably damaging |
Het |
H3c8 |
T |
A |
13: 23,719,887 (GRCm39) |
M91K |
probably benign |
Het |
Hnrnpu |
A |
T |
1: 178,159,871 (GRCm39) |
D403E |
unknown |
Het |
Il34 |
T |
C |
8: 111,476,122 (GRCm39) |
K33E |
probably benign |
Het |
Klhl20 |
A |
G |
1: 160,934,434 (GRCm39) |
V195A |
possibly damaging |
Het |
Lair1 |
G |
T |
7: 4,031,969 (GRCm39) |
T46N |
probably damaging |
Het |
Lama4 |
A |
G |
10: 38,921,805 (GRCm39) |
E442G |
possibly damaging |
Het |
Lifr |
A |
T |
15: 7,202,963 (GRCm39) |
I400F |
possibly damaging |
Het |
Man2a1 |
T |
C |
17: 64,908,771 (GRCm39) |
I14T |
probably benign |
Het |
Or13p10 |
T |
A |
4: 118,523,489 (GRCm39) |
C258* |
probably null |
Het |
Or1ad8 |
T |
G |
11: 50,898,071 (GRCm39) |
S91A |
possibly damaging |
Het |
Or4z4 |
A |
C |
19: 12,076,190 (GRCm39) |
V271G |
possibly damaging |
Het |
Or51h7 |
A |
G |
7: 102,591,760 (GRCm39) |
L8P |
probably benign |
Het |
Or5an10 |
T |
A |
19: 12,275,639 (GRCm39) |
I286F |
probably damaging |
Het |
Or8s10 |
T |
C |
15: 98,335,419 (GRCm39) |
I23T |
probably benign |
Het |
Papss2 |
G |
T |
19: 32,629,403 (GRCm39) |
V331F |
possibly damaging |
Het |
Pcdha11 |
T |
C |
18: 37,145,909 (GRCm39) |
S667P |
probably damaging |
Het |
Pcolce |
A |
T |
5: 137,607,390 (GRCm39) |
S75T |
probably benign |
Het |
Phf20l1 |
A |
C |
15: 66,502,768 (GRCm39) |
D716A |
possibly damaging |
Het |
Pkd1 |
A |
G |
17: 24,791,595 (GRCm39) |
E1094G |
possibly damaging |
Het |
Ppm1h |
A |
G |
10: 122,618,152 (GRCm39) |
K104E |
probably benign |
Het |
Ppp6r3 |
T |
C |
19: 3,509,750 (GRCm39) |
Y195C |
probably benign |
Het |
Pramel6 |
T |
A |
2: 87,340,031 (GRCm39) |
L265Q |
probably benign |
Het |
Prc1 |
A |
T |
7: 79,961,969 (GRCm39) |
N489I |
possibly damaging |
Het |
Prss59 |
A |
C |
6: 40,905,444 (GRCm39) |
|
probably null |
Het |
Psg22 |
A |
C |
7: 18,460,861 (GRCm39) |
N497H |
probably damaging |
Het |
Pum3 |
T |
A |
19: 27,389,620 (GRCm39) |
I411F |
possibly damaging |
Het |
Repin1 |
G |
T |
6: 48,574,279 (GRCm39) |
E403* |
probably null |
Het |
Rev3l |
A |
T |
10: 39,739,734 (GRCm39) |
I2861L |
possibly damaging |
Het |
Rsf1 |
A |
C |
7: 97,310,540 (GRCm39) |
K423N |
|
Het |
Samd4b |
A |
G |
7: 28,103,458 (GRCm39) |
I553T |
probably benign |
Het |
Septin3 |
A |
G |
15: 82,170,654 (GRCm39) |
E216G |
probably benign |
Het |
Sppl2c |
T |
C |
11: 104,078,640 (GRCm39) |
V480A |
possibly damaging |
Het |
Sppl2c |
A |
G |
11: 104,078,189 (GRCm39) |
T330A |
probably benign |
Het |
Srebf2 |
A |
G |
15: 82,088,253 (GRCm39) |
D1073G |
probably damaging |
Het |
Sv2c |
C |
T |
13: 96,224,797 (GRCm39) |
V171M |
probably damaging |
Het |
Tbc1d4 |
T |
A |
14: 101,845,715 (GRCm39) |
E61V |
probably damaging |
Het |
Tnc |
T |
A |
4: 63,926,983 (GRCm39) |
T848S |
probably benign |
Het |
Trmt5 |
A |
G |
12: 73,329,439 (GRCm39) |
Y240H |
probably damaging |
Het |
Trpv1 |
T |
C |
11: 73,132,583 (GRCm39) |
V399A |
possibly damaging |
Het |
Tstd2 |
T |
C |
4: 46,133,646 (GRCm39) |
T59A |
unknown |
Het |
Ubash3a |
T |
A |
17: 31,456,869 (GRCm39) |
L510M |
probably benign |
Het |
Ubr3 |
T |
A |
2: 69,783,200 (GRCm39) |
I713N |
probably damaging |
Het |
Upf3a |
A |
G |
8: 13,842,166 (GRCm39) |
E194G |
probably damaging |
Het |
Usp22 |
A |
T |
11: 61,065,588 (GRCm39) |
Y42N |
probably benign |
Het |
Vav3 |
T |
A |
3: 109,470,478 (GRCm39) |
C555S |
probably damaging |
Het |
Vmn1r210 |
T |
A |
13: 23,011,684 (GRCm39) |
M201L |
probably benign |
Het |
Wdr64 |
C |
A |
1: 175,554,051 (GRCm39) |
Q194K |
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 |
IGL01025:Dock6
|
APN |
9 |
21,723,103 (GRCm39) |
missense |
possibly damaging |
0.89 |
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 |
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 |
|