Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700061I17Rik |
G |
T |
3: 116,861,385 (GRCm39) |
|
noncoding transcript |
Het |
2300003K06Rik |
G |
T |
11: 99,728,793 (GRCm39) |
Q17K |
probably benign |
Het |
Abca16 |
T |
C |
7: 120,119,256 (GRCm39) |
V999A |
probably benign |
Het |
Actn3 |
C |
T |
19: 4,915,483 (GRCm39) |
|
probably benign |
Het |
Agap2 |
T |
A |
10: 126,926,981 (GRCm39) |
|
probably benign |
Het |
Ago3 |
C |
A |
4: 126,265,580 (GRCm39) |
R278L |
probably benign |
Het |
Aldh1a2 |
T |
C |
9: 71,192,492 (GRCm39) |
V449A |
possibly damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Aplnr |
A |
G |
2: 84,967,353 (GRCm39) |
Y126C |
probably damaging |
Het |
Apob |
T |
C |
12: 8,066,084 (GRCm39) |
I4351T |
possibly damaging |
Het |
Ash1l |
T |
C |
3: 88,914,659 (GRCm39) |
L1763P |
probably benign |
Het |
Aspn |
T |
C |
13: 49,710,849 (GRCm39) |
S165P |
possibly damaging |
Het |
Atg13 |
A |
T |
2: 91,510,335 (GRCm39) |
V349E |
probably damaging |
Het |
Atp1b2 |
T |
A |
11: 69,493,309 (GRCm39) |
|
probably null |
Het |
B3glct |
A |
T |
5: 149,677,604 (GRCm39) |
D411V |
probably damaging |
Het |
Bcar3 |
A |
T |
3: 122,316,840 (GRCm39) |
I255F |
probably damaging |
Het |
Cacna1b |
G |
A |
2: 24,608,148 (GRCm39) |
|
probably benign |
Het |
Cep164 |
T |
G |
9: 45,690,198 (GRCm39) |
E675A |
possibly damaging |
Het |
Chd1l |
C |
T |
3: 97,490,047 (GRCm39) |
E503K |
probably benign |
Het |
Chst8 |
C |
A |
7: 34,447,593 (GRCm39) |
M8I |
possibly damaging |
Het |
Clec4n |
A |
G |
6: 123,212,475 (GRCm39) |
E67G |
probably benign |
Het |
Cobll1 |
A |
T |
2: 64,929,480 (GRCm39) |
D653E |
probably damaging |
Het |
Col9a1 |
T |
C |
1: 24,276,579 (GRCm39) |
|
probably null |
Het |
Crip2 |
T |
C |
12: 113,107,124 (GRCm39) |
L30P |
probably damaging |
Het |
Ctbp1 |
C |
T |
5: 33,418,407 (GRCm39) |
V22I |
probably benign |
Het |
Cwc22 |
T |
C |
2: 77,747,521 (GRCm39) |
|
probably benign |
Het |
Cyp4a32 |
C |
A |
4: 115,460,147 (GRCm39) |
Y119* |
probably null |
Het |
Dido1 |
G |
T |
2: 180,313,263 (GRCm39) |
A463E |
possibly damaging |
Het |
Dnah7a |
G |
A |
1: 53,567,956 (GRCm39) |
P1880L |
probably benign |
Het |
Dsp |
A |
G |
13: 38,375,907 (GRCm39) |
T1231A |
probably damaging |
Het |
Eif2ak1 |
G |
T |
5: 143,810,717 (GRCm39) |
|
probably benign |
Het |
Entrep1 |
G |
A |
19: 23,998,998 (GRCm39) |
T140M |
probably damaging |
Het |
Epc1 |
A |
T |
18: 6,452,360 (GRCm39) |
M233K |
probably damaging |
Het |
Gigyf2 |
A |
G |
1: 87,371,360 (GRCm39) |
|
probably benign |
Het |
Greb1 |
T |
G |
12: 16,757,852 (GRCm39) |
H58P |
probably damaging |
Het |
Gtpbp1 |
T |
C |
15: 79,597,649 (GRCm39) |
I348T |
possibly damaging |
Het |
Hck |
A |
T |
2: 152,970,192 (GRCm39) |
N64Y |
probably benign |
Het |
Herc2 |
T |
C |
7: 55,818,744 (GRCm39) |
S2812P |
probably damaging |
Het |
Inpp4b |
T |
A |
8: 82,679,463 (GRCm39) |
|
probably null |
Het |
Kcnq5 |
A |
C |
1: 21,475,248 (GRCm39) |
S473A |
probably benign |
Het |
Lrat |
T |
G |
3: 82,810,676 (GRCm39) |
D115A |
probably damaging |
Het |
Lyst |
A |
G |
13: 13,814,639 (GRCm39) |
I1131M |
possibly damaging |
Het |
Man2a2 |
T |
C |
7: 80,018,310 (GRCm39) |
D160G |
probably benign |
Het |
Marf1 |
C |
T |
16: 13,933,688 (GRCm39) |
D1567N |
probably benign |
Het |
Mars1 |
T |
C |
10: 127,133,857 (GRCm39) |
D680G |
possibly damaging |
Het |
Mat1a |
T |
C |
14: 40,843,797 (GRCm39) |
S339P |
probably damaging |
Het |
Megf8 |
T |
C |
7: 25,042,081 (GRCm39) |
S1300P |
probably damaging |
Het |
Mga |
T |
C |
2: 119,733,179 (GRCm39) |
L9S |
probably damaging |
Het |
Mllt6 |
T |
C |
11: 97,563,277 (GRCm39) |
|
probably benign |
Het |
Mrpl37 |
A |
G |
4: 106,921,692 (GRCm39) |
L179P |
probably benign |
Het |
Mtnr1a |
G |
T |
8: 45,540,782 (GRCm39) |
V248L |
probably benign |
Het |
Mylk |
T |
C |
16: 34,635,835 (GRCm39) |
S19P |
possibly damaging |
Het |
Or11g1 |
A |
G |
14: 50,651,858 (GRCm39) |
T286A |
probably damaging |
Het |
Pacc1 |
A |
G |
1: 191,080,559 (GRCm39) |
|
probably benign |
Het |
Parp8 |
A |
T |
13: 117,161,886 (GRCm39) |
|
probably null |
Het |
Pcnx2 |
T |
C |
8: 126,479,023 (GRCm39) |
D2075G |
probably damaging |
Het |
Pigo |
A |
T |
4: 43,021,460 (GRCm39) |
I494K |
probably benign |
Het |
Pkd1l1 |
A |
T |
11: 8,820,313 (GRCm39) |
D1217E |
probably benign |
Het |
Pkhd1l1 |
T |
C |
15: 44,369,040 (GRCm39) |
V895A |
probably benign |
Het |
Plcb4 |
A |
T |
2: 135,842,109 (GRCm39) |
H1031L |
possibly damaging |
Het |
Plxnb1 |
A |
G |
9: 108,937,989 (GRCm39) |
K1245R |
probably null |
Het |
Pold1 |
C |
T |
7: 44,192,181 (GRCm39) |
|
probably benign |
Het |
Ptprq |
T |
C |
10: 107,498,423 (GRCm39) |
I885V |
probably damaging |
Het |
Ptprz1 |
A |
G |
6: 23,050,473 (GRCm39) |
D1398G |
probably damaging |
Het |
Pygm |
G |
A |
19: 6,439,917 (GRCm39) |
A364T |
probably benign |
Het |
Rbl1 |
T |
C |
2: 157,035,018 (GRCm39) |
N354S |
probably benign |
Het |
Scgb2b19 |
C |
T |
7: 32,979,037 (GRCm39) |
|
probably null |
Het |
Slc26a8 |
C |
T |
17: 28,867,187 (GRCm39) |
V545M |
possibly damaging |
Het |
Slc27a1 |
T |
A |
8: 72,036,757 (GRCm39) |
|
probably null |
Het |
Smpd1 |
A |
G |
7: 105,205,881 (GRCm39) |
D416G |
possibly damaging |
Het |
Sorbs3 |
A |
G |
14: 70,431,095 (GRCm39) |
V284A |
probably benign |
Het |
Stfa2l1 |
T |
C |
16: 35,982,154 (GRCm39) |
V75A |
probably damaging |
Het |
Syndig1 |
A |
G |
2: 149,772,841 (GRCm39) |
D166G |
probably damaging |
Het |
Tcp10a |
G |
A |
17: 7,593,406 (GRCm39) |
|
probably null |
Het |
Themis2 |
T |
A |
4: 132,510,212 (GRCm39) |
I663F |
possibly damaging |
Het |
Thrap3 |
T |
C |
4: 126,070,129 (GRCm39) |
Q586R |
probably damaging |
Het |
Tinag |
C |
A |
9: 76,952,798 (GRCm39) |
C62F |
probably damaging |
Het |
Tmod1 |
T |
C |
4: 46,090,884 (GRCm39) |
Y146H |
probably damaging |
Het |
Tmprss4 |
T |
A |
9: 45,095,683 (GRCm39) |
I54F |
possibly damaging |
Het |
Tnks |
A |
C |
8: 35,301,757 (GRCm39) |
|
probably benign |
Het |
Trim43a |
GATTTATTTATTTATTTATTTATTTATTTATTTATTTATT |
GATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATT |
9: 88,465,042 (GRCm39) |
|
probably benign |
Het |
Trpc6 |
A |
G |
9: 8,680,538 (GRCm39) |
E844G |
probably benign |
Het |
Ubtd2 |
C |
T |
11: 32,466,125 (GRCm39) |
R115W |
probably damaging |
Het |
Ubxn6 |
T |
C |
17: 56,376,042 (GRCm39) |
D373G |
probably benign |
Het |
Upf1 |
T |
A |
8: 70,794,174 (GRCm39) |
Q244L |
probably benign |
Het |
Usp33 |
A |
G |
3: 152,074,271 (GRCm39) |
I372M |
probably damaging |
Het |
Usp34 |
A |
G |
11: 23,301,629 (GRCm39) |
E351G |
probably damaging |
Het |
Utrn |
A |
G |
10: 12,554,318 (GRCm39) |
|
probably benign |
Het |
Vmn1r78 |
A |
G |
7: 11,886,508 (GRCm39) |
K40E |
possibly damaging |
Het |
Vmn2r7 |
T |
A |
3: 64,632,223 (GRCm39) |
M80L |
probably benign |
Het |
Vps13a |
G |
T |
19: 16,678,602 (GRCm39) |
Y1126* |
probably null |
Het |
Wfdc11 |
T |
C |
2: 164,506,366 (GRCm39) |
N60S |
probably benign |
Het |
Wnk2 |
C |
T |
13: 49,224,586 (GRCm39) |
D992N |
probably damaging |
Het |
Zpbp2 |
C |
A |
11: 98,444,670 (GRCm39) |
T66K |
probably damaging |
Het |
|
Other mutations in Dock2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00334:Dock2
|
APN |
11 |
34,595,488 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00469:Dock2
|
APN |
11 |
34,179,603 (GRCm39) |
splice site |
probably benign |
|
IGL01061:Dock2
|
APN |
11 |
34,596,653 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01319:Dock2
|
APN |
11 |
34,589,617 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL01451:Dock2
|
APN |
11 |
34,260,390 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01490:Dock2
|
APN |
11 |
34,596,608 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01601:Dock2
|
APN |
11 |
34,189,528 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01800:Dock2
|
APN |
11 |
34,647,100 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01804:Dock2
|
APN |
11 |
34,212,433 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01823:Dock2
|
APN |
11 |
34,212,391 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01829:Dock2
|
APN |
11 |
34,596,668 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01830:Dock2
|
APN |
11 |
34,582,744 (GRCm39) |
nonsense |
probably null |
|
IGL01835:Dock2
|
APN |
11 |
34,260,435 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL01845:Dock2
|
APN |
11 |
34,599,692 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01953:Dock2
|
APN |
11 |
34,623,183 (GRCm39) |
missense |
probably benign |
0.28 |
IGL01989:Dock2
|
APN |
11 |
34,218,053 (GRCm39) |
missense |
probably benign |
|
IGL02081:Dock2
|
APN |
11 |
34,204,355 (GRCm39) |
missense |
probably benign |
|
IGL02105:Dock2
|
APN |
11 |
34,605,352 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02153:Dock2
|
APN |
11 |
34,180,670 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02170:Dock2
|
APN |
11 |
34,217,949 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02344:Dock2
|
APN |
11 |
34,622,337 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02389:Dock2
|
APN |
11 |
34,589,567 (GRCm39) |
splice site |
probably benign |
|
IGL02409:Dock2
|
APN |
11 |
34,451,204 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02472:Dock2
|
APN |
11 |
34,199,801 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02625:Dock2
|
APN |
11 |
34,451,168 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02929:Dock2
|
APN |
11 |
34,218,048 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02951:Dock2
|
APN |
11 |
34,260,448 (GRCm39) |
unclassified |
probably benign |
|
IGL02999:Dock2
|
APN |
11 |
34,583,086 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03165:Dock2
|
APN |
11 |
34,578,360 (GRCm39) |
missense |
probably damaging |
0.99 |
Arches
|
UTSW |
11 |
34,580,587 (GRCm39) |
missense |
probably damaging |
1.00 |
capitol_reef
|
UTSW |
11 |
34,244,170 (GRCm39) |
critical splice acceptor site |
probably null |
|
Croesus
|
UTSW |
11 |
34,611,854 (GRCm39) |
missense |
probably damaging |
1.00 |
denali
|
UTSW |
11 |
34,179,472 (GRCm39) |
critical splice donor site |
probably null |
|
dew
|
UTSW |
11 |
34,198,636 (GRCm39) |
nonsense |
probably null |
|
Dinghy
|
UTSW |
11 |
34,212,460 (GRCm39) |
missense |
possibly damaging |
0.70 |
Dry
|
UTSW |
11 |
34,181,652 (GRCm39) |
missense |
possibly damaging |
0.79 |
frazz
|
UTSW |
11 |
34,198,572 (GRCm39) |
critical splice donor site |
probably benign |
|
frizz
|
UTSW |
11 |
34,208,184 (GRCm39) |
splice site |
probably benign |
|
gildenstern
|
UTSW |
11 |
34,623,166 (GRCm39) |
critical splice donor site |
probably null |
|
godsgrace
|
UTSW |
11 |
34,586,280 (GRCm39) |
missense |
probably damaging |
1.00 |
Harborside
|
UTSW |
11 |
34,212,445 (GRCm39) |
missense |
probably benign |
|
Landing
|
UTSW |
11 |
34,605,328 (GRCm39) |
missense |
possibly damaging |
0.83 |
latest
|
UTSW |
11 |
34,647,049 (GRCm39) |
missense |
probably damaging |
1.00 |
Launch
|
UTSW |
11 |
34,206,562 (GRCm39) |
missense |
probably damaging |
1.00 |
liaoning
|
UTSW |
11 |
34,599,620 (GRCm39) |
missense |
probably damaging |
1.00 |
lucre
|
UTSW |
11 |
34,595,436 (GRCm39) |
frame shift |
probably null |
|
midas
|
UTSW |
11 |
34,244,323 (GRCm39) |
missense |
probably damaging |
0.99 |
muelle
|
UTSW |
11 |
34,578,365 (GRCm39) |
missense |
probably damaging |
1.00 |
narrowest
|
UTSW |
11 |
34,232,652 (GRCm39) |
missense |
probably damaging |
0.98 |
pier
|
UTSW |
11 |
34,580,593 (GRCm39) |
missense |
probably damaging |
1.00 |
Plank
|
UTSW |
11 |
34,674,622 (GRCm39) |
missense |
possibly damaging |
0.51 |
resplendent
|
UTSW |
11 |
34,618,287 (GRCm39) |
nonsense |
probably null |
|
riches
|
UTSW |
11 |
34,579,279 (GRCm39) |
critical splice donor site |
probably null |
|
skiff
|
UTSW |
11 |
34,212,388 (GRCm39) |
missense |
probably null |
0.80 |
Slip
|
UTSW |
11 |
34,244,286 (GRCm39) |
missense |
probably benign |
0.25 |
toothskin
|
UTSW |
11 |
34,414,922 (GRCm39) |
missense |
probably damaging |
1.00 |
Touch
|
UTSW |
11 |
34,223,750 (GRCm39) |
missense |
possibly damaging |
0.95 |
wassup
|
UTSW |
11 |
34,453,413 (GRCm39) |
missense |
probably damaging |
1.00 |
Wharf
|
UTSW |
11 |
34,623,198 (GRCm39) |
missense |
possibly damaging |
0.81 |
BB009:Dock2
|
UTSW |
11 |
34,217,998 (GRCm39) |
missense |
probably benign |
0.00 |
BB019:Dock2
|
UTSW |
11 |
34,217,998 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03052:Dock2
|
UTSW |
11 |
34,182,853 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4377001:Dock2
|
UTSW |
11 |
34,611,835 (GRCm39) |
missense |
probably benign |
0.02 |
R0006:Dock2
|
UTSW |
11 |
34,262,453 (GRCm39) |
unclassified |
probably benign |
|
R0012:Dock2
|
UTSW |
11 |
34,674,622 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0063:Dock2
|
UTSW |
11 |
34,647,111 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0063:Dock2
|
UTSW |
11 |
34,647,111 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0116:Dock2
|
UTSW |
11 |
34,579,392 (GRCm39) |
intron |
probably benign |
|
R0149:Dock2
|
UTSW |
11 |
34,388,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R0361:Dock2
|
UTSW |
11 |
34,388,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R0462:Dock2
|
UTSW |
11 |
34,218,052 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0471:Dock2
|
UTSW |
11 |
34,579,380 (GRCm39) |
missense |
probably benign |
0.30 |
R0538:Dock2
|
UTSW |
11 |
34,595,545 (GRCm39) |
splice site |
probably benign |
|
R0543:Dock2
|
UTSW |
11 |
34,244,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R0660:Dock2
|
UTSW |
11 |
34,198,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R0676:Dock2
|
UTSW |
11 |
34,586,063 (GRCm39) |
missense |
probably damaging |
0.99 |
R0722:Dock2
|
UTSW |
11 |
34,414,970 (GRCm39) |
splice site |
probably benign |
|
R0801:Dock2
|
UTSW |
11 |
34,599,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1110:Dock2
|
UTSW |
11 |
34,206,535 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1171:Dock2
|
UTSW |
11 |
34,586,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R1387:Dock2
|
UTSW |
11 |
34,223,309 (GRCm39) |
splice site |
probably benign |
|
R1494:Dock2
|
UTSW |
11 |
34,232,761 (GRCm39) |
nonsense |
probably null |
|
R1589:Dock2
|
UTSW |
11 |
34,597,288 (GRCm39) |
missense |
probably damaging |
0.99 |
R1597:Dock2
|
UTSW |
11 |
34,595,474 (GRCm39) |
missense |
probably benign |
0.00 |
R1629:Dock2
|
UTSW |
11 |
34,212,480 (GRCm39) |
splice site |
probably null |
|
R1749:Dock2
|
UTSW |
11 |
34,182,767 (GRCm39) |
critical splice donor site |
probably null |
|
R1888:Dock2
|
UTSW |
11 |
34,598,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R1888:Dock2
|
UTSW |
11 |
34,598,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R1899:Dock2
|
UTSW |
11 |
34,244,286 (GRCm39) |
missense |
probably benign |
0.25 |
R1924:Dock2
|
UTSW |
11 |
34,414,934 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2031:Dock2
|
UTSW |
11 |
34,618,297 (GRCm39) |
splice site |
probably benign |
|
R2045:Dock2
|
UTSW |
11 |
34,244,106 (GRCm39) |
splice site |
probably null |
|
R2098:Dock2
|
UTSW |
11 |
34,609,832 (GRCm39) |
missense |
probably damaging |
0.99 |
R2098:Dock2
|
UTSW |
11 |
34,216,279 (GRCm39) |
missense |
probably benign |
0.16 |
R2129:Dock2
|
UTSW |
11 |
34,618,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R2147:Dock2
|
UTSW |
11 |
34,179,472 (GRCm39) |
critical splice donor site |
probably null |
|
R2149:Dock2
|
UTSW |
11 |
34,179,472 (GRCm39) |
critical splice donor site |
probably null |
|
R2150:Dock2
|
UTSW |
11 |
34,179,472 (GRCm39) |
critical splice donor site |
probably null |
|
R2176:Dock2
|
UTSW |
11 |
34,586,044 (GRCm39) |
missense |
probably benign |
0.00 |
R2230:Dock2
|
UTSW |
11 |
34,244,323 (GRCm39) |
missense |
probably damaging |
0.99 |
R2508:Dock2
|
UTSW |
11 |
34,262,485 (GRCm39) |
missense |
probably benign |
0.04 |
R2875:Dock2
|
UTSW |
11 |
34,609,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R2885:Dock2
|
UTSW |
11 |
34,580,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R2910:Dock2
|
UTSW |
11 |
34,182,910 (GRCm39) |
splice site |
probably benign |
|
R3081:Dock2
|
UTSW |
11 |
34,181,610 (GRCm39) |
missense |
probably benign |
|
R3418:Dock2
|
UTSW |
11 |
34,580,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R3552:Dock2
|
UTSW |
11 |
34,611,787 (GRCm39) |
missense |
probably benign |
0.22 |
R3731:Dock2
|
UTSW |
11 |
34,599,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R3846:Dock2
|
UTSW |
11 |
34,623,198 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4135:Dock2
|
UTSW |
11 |
34,605,328 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4598:Dock2
|
UTSW |
11 |
34,189,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R4599:Dock2
|
UTSW |
11 |
34,189,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R4715:Dock2
|
UTSW |
11 |
34,244,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R4722:Dock2
|
UTSW |
11 |
34,586,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R4742:Dock2
|
UTSW |
11 |
34,244,170 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4830:Dock2
|
UTSW |
11 |
34,223,767 (GRCm39) |
splice site |
probably null |
|
R4884:Dock2
|
UTSW |
11 |
34,216,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R4990:Dock2
|
UTSW |
11 |
34,586,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R5334:Dock2
|
UTSW |
11 |
34,178,643 (GRCm39) |
missense |
probably benign |
0.00 |
R5570:Dock2
|
UTSW |
11 |
34,618,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R5602:Dock2
|
UTSW |
11 |
34,204,391 (GRCm39) |
missense |
probably benign |
0.16 |
R5681:Dock2
|
UTSW |
11 |
34,199,836 (GRCm39) |
missense |
probably benign |
0.06 |
R5809:Dock2
|
UTSW |
11 |
34,212,445 (GRCm39) |
missense |
probably benign |
|
R5860:Dock2
|
UTSW |
11 |
34,206,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R6111:Dock2
|
UTSW |
11 |
34,599,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R6155:Dock2
|
UTSW |
11 |
34,244,123 (GRCm39) |
missense |
probably benign |
0.06 |
R6156:Dock2
|
UTSW |
11 |
34,197,789 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6173:Dock2
|
UTSW |
11 |
34,212,388 (GRCm39) |
missense |
probably null |
0.80 |
R6182:Dock2
|
UTSW |
11 |
34,179,476 (GRCm39) |
missense |
probably damaging |
0.97 |
R6188:Dock2
|
UTSW |
11 |
34,453,396 (GRCm39) |
missense |
probably damaging |
0.98 |
R6191:Dock2
|
UTSW |
11 |
34,181,652 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6283:Dock2
|
UTSW |
11 |
34,598,152 (GRCm39) |
missense |
probably damaging |
0.99 |
R6395:Dock2
|
UTSW |
11 |
34,182,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R6465:Dock2
|
UTSW |
11 |
34,453,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R6500:Dock2
|
UTSW |
11 |
34,312,822 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6561:Dock2
|
UTSW |
11 |
34,578,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R6745:Dock2
|
UTSW |
11 |
34,596,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R6745:Dock2
|
UTSW |
11 |
34,596,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R6880:Dock2
|
UTSW |
11 |
34,579,279 (GRCm39) |
critical splice donor site |
probably null |
|
R6913:Dock2
|
UTSW |
11 |
34,647,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R6997:Dock2
|
UTSW |
11 |
34,414,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R7057:Dock2
|
UTSW |
11 |
34,586,044 (GRCm39) |
missense |
probably benign |
0.00 |
R7057:Dock2
|
UTSW |
11 |
34,177,684 (GRCm39) |
missense |
probably benign |
0.10 |
R7134:Dock2
|
UTSW |
11 |
34,260,363 (GRCm39) |
missense |
probably benign |
0.03 |
R7188:Dock2
|
UTSW |
11 |
34,189,675 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7239:Dock2
|
UTSW |
11 |
34,181,677 (GRCm39) |
missense |
probably benign |
0.00 |
R7247:Dock2
|
UTSW |
11 |
34,605,340 (GRCm39) |
nonsense |
probably null |
|
R7250:Dock2
|
UTSW |
11 |
34,586,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R7250:Dock2
|
UTSW |
11 |
34,586,032 (GRCm39) |
missense |
probably benign |
0.01 |
R7271:Dock2
|
UTSW |
11 |
34,223,750 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7284:Dock2
|
UTSW |
11 |
34,180,672 (GRCm39) |
missense |
probably benign |
0.01 |
R7397:Dock2
|
UTSW |
11 |
34,609,816 (GRCm39) |
missense |
probably benign |
0.00 |
R7464:Dock2
|
UTSW |
11 |
34,586,105 (GRCm39) |
missense |
probably damaging |
0.99 |
R7512:Dock2
|
UTSW |
11 |
34,262,542 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7556:Dock2
|
UTSW |
11 |
34,611,778 (GRCm39) |
missense |
probably benign |
0.43 |
R7663:Dock2
|
UTSW |
11 |
34,611,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R7779:Dock2
|
UTSW |
11 |
34,605,282 (GRCm39) |
missense |
probably benign |
0.38 |
R7797:Dock2
|
UTSW |
11 |
34,232,652 (GRCm39) |
missense |
probably damaging |
0.98 |
R7855:Dock2
|
UTSW |
11 |
34,223,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R7922:Dock2
|
UTSW |
11 |
34,598,154 (GRCm39) |
missense |
probably benign |
0.29 |
R7932:Dock2
|
UTSW |
11 |
34,217,998 (GRCm39) |
missense |
probably benign |
0.00 |
R8013:Dock2
|
UTSW |
11 |
34,596,677 (GRCm39) |
missense |
probably damaging |
0.96 |
R8192:Dock2
|
UTSW |
11 |
34,623,166 (GRCm39) |
critical splice donor site |
probably null |
|
R8244:Dock2
|
UTSW |
11 |
34,586,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R8307:Dock2
|
UTSW |
11 |
34,260,362 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8418:Dock2
|
UTSW |
11 |
34,609,795 (GRCm39) |
missense |
probably benign |
0.01 |
R8460:Dock2
|
UTSW |
11 |
34,180,825 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8495:Dock2
|
UTSW |
11 |
34,181,622 (GRCm39) |
missense |
probably benign |
0.14 |
R8556:Dock2
|
UTSW |
11 |
34,212,457 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8690:Dock2
|
UTSW |
11 |
34,618,287 (GRCm39) |
nonsense |
probably null |
|
R8743:Dock2
|
UTSW |
11 |
34,223,252 (GRCm39) |
nonsense |
probably null |
|
R8757:Dock2
|
UTSW |
11 |
34,586,067 (GRCm39) |
missense |
probably benign |
0.13 |
R8759:Dock2
|
UTSW |
11 |
34,586,067 (GRCm39) |
missense |
probably benign |
0.13 |
R8793:Dock2
|
UTSW |
11 |
34,451,215 (GRCm39) |
missense |
probably benign |
0.00 |
R8882:Dock2
|
UTSW |
11 |
34,595,436 (GRCm39) |
frame shift |
probably null |
|
R8885:Dock2
|
UTSW |
11 |
34,260,396 (GRCm39) |
missense |
probably benign |
0.01 |
R8943:Dock2
|
UTSW |
11 |
34,599,646 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9171:Dock2
|
UTSW |
11 |
34,589,670 (GRCm39) |
missense |
probably benign |
0.12 |
R9182:Dock2
|
UTSW |
11 |
34,260,398 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9203:Dock2
|
UTSW |
11 |
34,622,366 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9310:Dock2
|
UTSW |
11 |
34,244,139 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9388:Dock2
|
UTSW |
11 |
34,212,460 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9490:Dock2
|
UTSW |
11 |
34,589,582 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9568:Dock2
|
UTSW |
11 |
34,599,638 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9593:Dock2
|
UTSW |
11 |
34,178,607 (GRCm39) |
missense |
probably benign |
0.34 |
R9694:Dock2
|
UTSW |
11 |
34,218,054 (GRCm39) |
missense |
probably benign |
|
R9697:Dock2
|
UTSW |
11 |
34,204,417 (GRCm39) |
missense |
probably benign |
|
R9753:Dock2
|
UTSW |
11 |
34,223,673 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9783:Dock2
|
UTSW |
11 |
34,208,128 (GRCm39) |
missense |
possibly damaging |
0.83 |
X0017:Dock2
|
UTSW |
11 |
34,216,271 (GRCm39) |
missense |
probably benign |
0.08 |
X0018:Dock2
|
UTSW |
11 |
34,182,833 (GRCm39) |
missense |
possibly damaging |
0.65 |
X0058:Dock2
|
UTSW |
11 |
34,206,564 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Dock2
|
UTSW |
11 |
34,260,357 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1088:Dock2
|
UTSW |
11 |
34,583,209 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dock2
|
UTSW |
11 |
34,388,300 (GRCm39) |
missense |
probably benign |
0.14 |
Z1088:Dock2
|
UTSW |
11 |
34,586,039 (GRCm39) |
nonsense |
probably null |
|
Z1176:Dock2
|
UTSW |
11 |
34,609,751 (GRCm39) |
missense |
probably benign |
0.04 |
Z1177:Dock2
|
UTSW |
11 |
34,262,553 (GRCm39) |
missense |
possibly damaging |
0.68 |
|