Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadat |
A |
T |
8: 60,960,126 (GRCm39) |
D31V |
probably damaging |
Het |
Acaca |
A |
T |
11: 84,211,368 (GRCm39) |
Y1560F |
probably benign |
Het |
Actl7a |
A |
G |
4: 56,743,980 (GRCm39) |
E169G |
probably damaging |
Het |
Adgrb3 |
A |
G |
1: 25,598,895 (GRCm39) |
V270A |
probably benign |
Het |
Adgre4 |
G |
A |
17: 56,104,740 (GRCm39) |
V269I |
probably benign |
Het |
Ankhd1 |
A |
G |
18: 36,781,427 (GRCm39) |
T2160A |
probably damaging |
Het |
Bltp1 |
T |
C |
3: 37,095,512 (GRCm39) |
V4505A |
probably benign |
Het |
Bnip2 |
T |
A |
9: 69,909,398 (GRCm39) |
|
probably benign |
Het |
Casp16 |
A |
G |
17: 23,771,027 (GRCm39) |
V126A |
probably damaging |
Het |
Ccser1 |
C |
A |
6: 61,695,136 (GRCm39) |
T157K |
probably benign |
Het |
Cdh23 |
A |
G |
10: 60,151,503 (GRCm39) |
S2459P |
probably damaging |
Het |
Cdk5rap3 |
A |
T |
11: 96,804,291 (GRCm39) |
C21S |
probably damaging |
Het |
Chmp6 |
G |
A |
11: 119,807,812 (GRCm39) |
E72K |
probably benign |
Het |
Cldn23 |
T |
C |
8: 36,292,816 (GRCm39) |
Y224C |
probably damaging |
Het |
Cry1 |
C |
T |
10: 84,982,338 (GRCm39) |
G336D |
probably damaging |
Het |
Cyp4f17 |
T |
A |
17: 32,725,956 (GRCm39) |
F30I |
probably benign |
Het |
Dgcr8 |
T |
A |
16: 18,096,200 (GRCm39) |
D496V |
probably damaging |
Het |
Dhx9 |
A |
G |
1: 153,344,614 (GRCm39) |
|
probably benign |
Het |
Dnah10 |
C |
T |
5: 124,820,801 (GRCm39) |
|
probably benign |
Het |
Dscam |
A |
G |
16: 96,456,136 (GRCm39) |
V1264A |
probably damaging |
Het |
Eno1 |
T |
C |
4: 150,331,167 (GRCm39) |
Y270H |
probably benign |
Het |
Eprs1 |
A |
G |
1: 185,117,112 (GRCm39) |
D385G |
probably damaging |
Het |
Ercc2 |
A |
G |
7: 19,124,346 (GRCm39) |
Y215C |
probably damaging |
Het |
Fscn2 |
A |
G |
11: 120,258,576 (GRCm39) |
N400S |
possibly damaging |
Het |
Fuca1 |
C |
T |
4: 135,666,512 (GRCm39) |
T449I |
probably benign |
Het |
Gm43638 |
T |
C |
5: 87,613,290 (GRCm39) |
K492E |
probably damaging |
Het |
Gm5263 |
T |
G |
1: 146,296,302 (GRCm39) |
|
noncoding transcript |
Het |
Gm8122 |
T |
C |
14: 43,090,158 (GRCm39) |
T111A |
unknown |
Het |
Gtf3c2 |
T |
A |
5: 31,314,979 (GRCm39) |
N923Y |
probably benign |
Het |
Il17a |
T |
A |
1: 20,803,864 (GRCm39) |
D86E |
probably benign |
Het |
Itgb2l |
G |
T |
16: 96,231,775 (GRCm39) |
N330K |
probably benign |
Het |
Kcnj11 |
T |
C |
7: 45,748,489 (GRCm39) |
H278R |
probably benign |
Het |
Khdrbs2 |
T |
A |
1: 32,658,257 (GRCm39) |
Y272* |
probably null |
Het |
Kndc1 |
A |
T |
7: 139,509,959 (GRCm39) |
Q1267L |
probably damaging |
Het |
Loxhd1 |
T |
A |
18: 77,374,120 (GRCm39) |
F64I |
possibly damaging |
Het |
Lrig2 |
T |
A |
3: 104,398,861 (GRCm39) |
K222N |
probably benign |
Het |
Lrrcc1 |
T |
A |
3: 14,612,332 (GRCm39) |
Y378N |
probably damaging |
Het |
Mblac2 |
T |
C |
13: 81,898,434 (GRCm39) |
L270P |
probably damaging |
Het |
Med13 |
A |
T |
11: 86,210,609 (GRCm39) |
I511N |
probably benign |
Het |
Myo3a |
A |
T |
2: 22,428,033 (GRCm39) |
E763D |
probably damaging |
Het |
Or1e25 |
T |
A |
11: 73,493,858 (GRCm39) |
F151I |
probably benign |
Het |
Or2n1 |
G |
T |
17: 38,486,577 (GRCm39) |
V201L |
probably benign |
Het |
Or4a68 |
C |
T |
2: 89,270,144 (GRCm39) |
V160I |
probably benign |
Het |
Or5b97 |
T |
A |
19: 12,879,112 (GRCm39) |
T11S |
probably benign |
Het |
Or7g27 |
G |
A |
9: 19,250,598 (GRCm39) |
V281I |
possibly damaging |
Het |
Plxna4 |
T |
A |
6: 32,214,613 (GRCm39) |
I623F |
possibly damaging |
Het |
Ppp2ca |
T |
A |
11: 52,008,882 (GRCm39) |
Y127* |
probably null |
Het |
Psg18 |
A |
G |
7: 18,087,322 (GRCm39) |
V112A |
possibly damaging |
Het |
Ptprj |
A |
T |
2: 90,299,918 (GRCm39) |
N108K |
probably benign |
Het |
Rictor |
A |
G |
15: 6,806,865 (GRCm39) |
Y707C |
probably damaging |
Het |
Rptn |
T |
C |
3: 93,302,946 (GRCm39) |
F93S |
probably benign |
Het |
Rxrg |
T |
A |
1: 167,454,884 (GRCm39) |
C156S |
probably damaging |
Het |
Slc24a4 |
T |
C |
12: 102,189,946 (GRCm39) |
|
probably benign |
Het |
Slc25a27 |
C |
T |
17: 43,974,964 (GRCm39) |
|
probably null |
Het |
Slx4 |
T |
C |
16: 3,808,112 (GRCm39) |
K481E |
probably benign |
Het |
Snx19 |
T |
C |
9: 30,374,560 (GRCm39) |
W940R |
possibly damaging |
Het |
Spopfm1 |
T |
A |
3: 94,173,791 (GRCm39) |
D262E |
probably benign |
Het |
Tasor2 |
G |
A |
13: 3,626,633 (GRCm39) |
P1106S |
probably benign |
Het |
Tcf20 |
G |
A |
15: 82,740,209 (GRCm39) |
P414L |
probably damaging |
Het |
Treml2 |
T |
C |
17: 48,609,838 (GRCm39) |
V90A |
probably benign |
Het |
Uckl1 |
C |
T |
2: 181,211,327 (GRCm39) |
V501M |
probably damaging |
Het |
Unc79 |
C |
T |
12: 103,108,256 (GRCm39) |
T1937I |
probably damaging |
Het |
Vmn2r17 |
A |
T |
5: 109,567,903 (GRCm39) |
I9F |
probably benign |
Het |
Vmn2r44 |
T |
C |
7: 8,383,237 (GRCm39) |
H119R |
probably benign |
Het |
Vmn2r78 |
A |
G |
7: 86,603,643 (GRCm39) |
D607G |
probably benign |
Het |
Vps13a |
C |
T |
19: 16,641,258 (GRCm39) |
G2288D |
probably damaging |
Het |
Znfx1 |
G |
T |
2: 166,897,643 (GRCm39) |
T427N |
probably damaging |
Het |
|
Other mutations in Dock9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00236:Dock9
|
APN |
14 |
121,905,880 (GRCm39) |
missense |
probably benign |
0.12 |
IGL00817:Dock9
|
APN |
14 |
121,935,703 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00923:Dock9
|
APN |
14 |
121,844,504 (GRCm39) |
unclassified |
probably benign |
|
IGL01385:Dock9
|
APN |
14 |
121,817,995 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01567:Dock9
|
APN |
14 |
121,890,496 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01811:Dock9
|
APN |
14 |
121,796,440 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02512:Dock9
|
APN |
14 |
121,856,950 (GRCm39) |
splice site |
probably benign |
|
IGL02525:Dock9
|
APN |
14 |
121,877,538 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02550:Dock9
|
APN |
14 |
121,935,724 (GRCm39) |
start codon destroyed |
probably null |
0.07 |
IGL02559:Dock9
|
APN |
14 |
121,862,559 (GRCm39) |
splice site |
probably benign |
|
IGL02666:Dock9
|
APN |
14 |
121,818,111 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02674:Dock9
|
APN |
14 |
121,833,023 (GRCm39) |
splice site |
probably null |
|
IGL02795:Dock9
|
APN |
14 |
121,877,390 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03074:Dock9
|
APN |
14 |
121,844,682 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03095:Dock9
|
APN |
14 |
121,876,940 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03294:Dock9
|
APN |
14 |
121,879,035 (GRCm39) |
splice site |
probably benign |
|
R0036:Dock9
|
UTSW |
14 |
121,860,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0050:Dock9
|
UTSW |
14 |
121,844,637 (GRCm39) |
missense |
probably benign |
0.43 |
R0050:Dock9
|
UTSW |
14 |
121,844,637 (GRCm39) |
missense |
probably benign |
0.43 |
R0164:Dock9
|
UTSW |
14 |
121,835,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R0164:Dock9
|
UTSW |
14 |
121,835,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R0270:Dock9
|
UTSW |
14 |
121,813,411 (GRCm39) |
missense |
probably benign |
0.02 |
R0494:Dock9
|
UTSW |
14 |
121,899,996 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0726:Dock9
|
UTSW |
14 |
121,889,180 (GRCm39) |
nonsense |
probably null |
|
R1029:Dock9
|
UTSW |
14 |
121,837,096 (GRCm39) |
splice site |
probably null |
|
R1214:Dock9
|
UTSW |
14 |
121,823,728 (GRCm39) |
missense |
probably benign |
0.02 |
R1231:Dock9
|
UTSW |
14 |
121,813,362 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1535:Dock9
|
UTSW |
14 |
121,783,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R1629:Dock9
|
UTSW |
14 |
121,780,986 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1637:Dock9
|
UTSW |
14 |
121,889,187 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1733:Dock9
|
UTSW |
14 |
121,864,292 (GRCm39) |
missense |
probably benign |
0.01 |
R1772:Dock9
|
UTSW |
14 |
121,847,210 (GRCm39) |
missense |
probably benign |
0.07 |
R1855:Dock9
|
UTSW |
14 |
121,877,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R1888:Dock9
|
UTSW |
14 |
121,862,617 (GRCm39) |
missense |
probably benign |
0.18 |
R1888:Dock9
|
UTSW |
14 |
121,862,617 (GRCm39) |
missense |
probably benign |
0.18 |
R1901:Dock9
|
UTSW |
14 |
121,862,565 (GRCm39) |
splice site |
probably null |
|
R1920:Dock9
|
UTSW |
14 |
121,820,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R1987:Dock9
|
UTSW |
14 |
121,829,242 (GRCm39) |
missense |
probably benign |
0.00 |
R3035:Dock9
|
UTSW |
14 |
121,844,249 (GRCm39) |
missense |
possibly damaging |
0.60 |
R3851:Dock9
|
UTSW |
14 |
121,866,498 (GRCm39) |
splice site |
probably null |
|
R4020:Dock9
|
UTSW |
14 |
121,844,267 (GRCm39) |
missense |
probably benign |
0.00 |
R4021:Dock9
|
UTSW |
14 |
121,864,324 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4089:Dock9
|
UTSW |
14 |
121,820,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R4258:Dock9
|
UTSW |
14 |
121,818,854 (GRCm39) |
missense |
probably benign |
0.00 |
R4423:Dock9
|
UTSW |
14 |
121,799,465 (GRCm39) |
critical splice donor site |
probably null |
|
R4561:Dock9
|
UTSW |
14 |
121,796,419 (GRCm39) |
missense |
probably benign |
0.01 |
R4604:Dock9
|
UTSW |
14 |
121,905,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R4646:Dock9
|
UTSW |
14 |
121,823,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R4647:Dock9
|
UTSW |
14 |
121,823,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R4776:Dock9
|
UTSW |
14 |
121,847,509 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4809:Dock9
|
UTSW |
14 |
121,784,008 (GRCm39) |
missense |
probably benign |
0.37 |
R4865:Dock9
|
UTSW |
14 |
121,780,917 (GRCm39) |
makesense |
probably null |
|
R4951:Dock9
|
UTSW |
14 |
121,890,547 (GRCm39) |
missense |
probably benign |
0.35 |
R5151:Dock9
|
UTSW |
14 |
121,815,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R5359:Dock9
|
UTSW |
14 |
121,890,472 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5366:Dock9
|
UTSW |
14 |
121,815,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R5502:Dock9
|
UTSW |
14 |
121,847,594 (GRCm39) |
splice site |
probably null |
|
R5579:Dock9
|
UTSW |
14 |
121,837,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R5753:Dock9
|
UTSW |
14 |
121,872,037 (GRCm39) |
missense |
probably benign |
0.05 |
R5836:Dock9
|
UTSW |
14 |
121,918,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R5858:Dock9
|
UTSW |
14 |
121,866,204 (GRCm39) |
missense |
probably benign |
0.00 |
R5890:Dock9
|
UTSW |
14 |
121,905,820 (GRCm39) |
critical splice donor site |
probably null |
|
R6075:Dock9
|
UTSW |
14 |
121,783,385 (GRCm39) |
missense |
probably benign |
|
R6298:Dock9
|
UTSW |
14 |
121,872,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R6306:Dock9
|
UTSW |
14 |
121,799,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R6321:Dock9
|
UTSW |
14 |
121,783,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R6330:Dock9
|
UTSW |
14 |
121,842,655 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R6719:Dock9
|
UTSW |
14 |
121,847,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R6784:Dock9
|
UTSW |
14 |
121,780,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R6826:Dock9
|
UTSW |
14 |
121,860,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R6830:Dock9
|
UTSW |
14 |
121,860,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R6838:Dock9
|
UTSW |
14 |
121,784,008 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6868:Dock9
|
UTSW |
14 |
121,823,676 (GRCm39) |
missense |
probably benign |
0.37 |
R6919:Dock9
|
UTSW |
14 |
121,880,564 (GRCm39) |
missense |
probably benign |
0.42 |
R6989:Dock9
|
UTSW |
14 |
121,864,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R7539:Dock9
|
UTSW |
14 |
121,818,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R7645:Dock9
|
UTSW |
14 |
121,835,075 (GRCm39) |
missense |
probably benign |
0.44 |
R7875:Dock9
|
UTSW |
14 |
121,863,396 (GRCm39) |
nonsense |
probably null |
|
R7900:Dock9
|
UTSW |
14 |
121,783,491 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8040:Dock9
|
UTSW |
14 |
121,889,206 (GRCm39) |
missense |
probably benign |
0.06 |
R8420:Dock9
|
UTSW |
14 |
121,783,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R8511:Dock9
|
UTSW |
14 |
121,918,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R8511:Dock9
|
UTSW |
14 |
121,864,801 (GRCm39) |
missense |
probably benign |
0.40 |
R8514:Dock9
|
UTSW |
14 |
121,896,199 (GRCm39) |
missense |
probably benign |
0.25 |
R8691:Dock9
|
UTSW |
14 |
121,877,517 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8804:Dock9
|
UTSW |
14 |
121,842,595 (GRCm39) |
missense |
probably damaging |
0.98 |
R8894:Dock9
|
UTSW |
14 |
121,860,373 (GRCm39) |
missense |
probably benign |
0.10 |
R8900:Dock9
|
UTSW |
14 |
121,817,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R9069:Dock9
|
UTSW |
14 |
121,866,324 (GRCm39) |
missense |
probably damaging |
0.98 |
R9218:Dock9
|
UTSW |
14 |
121,905,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R9233:Dock9
|
UTSW |
14 |
121,820,781 (GRCm39) |
missense |
probably benign |
0.09 |
R9236:Dock9
|
UTSW |
14 |
121,876,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R9285:Dock9
|
UTSW |
14 |
121,833,012 (GRCm39) |
missense |
probably benign |
|
R9451:Dock9
|
UTSW |
14 |
121,787,601 (GRCm39) |
splice site |
probably benign |
|
R9461:Dock9
|
UTSW |
14 |
121,842,601 (GRCm39) |
missense |
probably benign |
0.05 |
R9484:Dock9
|
UTSW |
14 |
121,818,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R9517:Dock9
|
UTSW |
14 |
121,829,236 (GRCm39) |
missense |
probably benign |
0.07 |
R9542:Dock9
|
UTSW |
14 |
121,864,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R9694:Dock9
|
UTSW |
14 |
121,818,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R9701:Dock9
|
UTSW |
14 |
121,876,983 (GRCm39) |
missense |
probably benign |
0.01 |
R9703:Dock9
|
UTSW |
14 |
121,781,989 (GRCm39) |
makesense |
probably null |
|
R9726:Dock9
|
UTSW |
14 |
121,835,149 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9741:Dock9
|
UTSW |
14 |
121,877,516 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dock9
|
UTSW |
14 |
121,792,687 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dock9
|
UTSW |
14 |
121,889,194 (GRCm39) |
missense |
probably benign |
|
|