Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
C |
T |
12: 71,211,180 (GRCm39) |
T638M |
possibly damaging |
Het |
4930546C10Rik |
A |
G |
18: 69,083,067 (GRCm39) |
|
probably null |
Het |
Abi3 |
A |
T |
11: 95,723,619 (GRCm39) |
Y342N |
unknown |
Het |
Adk |
G |
A |
14: 21,368,111 (GRCm39) |
V195I |
probably benign |
Het |
Ago2 |
C |
T |
15: 72,998,375 (GRCm39) |
V268M |
possibly damaging |
Het |
Apaf1 |
T |
C |
10: 90,835,615 (GRCm39) |
I1077V |
probably benign |
Het |
Arap1 |
A |
T |
7: 101,053,621 (GRCm39) |
K1317* |
probably null |
Het |
Auts2 |
T |
A |
5: 131,469,211 (GRCm39) |
D493V |
|
Het |
Baz1b |
A |
T |
5: 135,260,533 (GRCm39) |
Q1110L |
probably damaging |
Het |
Brsk2 |
T |
A |
7: 141,546,957 (GRCm39) |
S467T |
possibly damaging |
Het |
Btbd9 |
A |
T |
17: 30,493,858 (GRCm39) |
M511K |
probably benign |
Het |
Cdh23 |
T |
A |
10: 60,218,485 (GRCm39) |
Y1385F |
probably benign |
Het |
Cfap100 |
A |
C |
6: 90,380,962 (GRCm39) |
L427V |
unknown |
Het |
Cnga1 |
A |
G |
5: 72,762,225 (GRCm39) |
F430L |
possibly damaging |
Het |
Csnk2a1-ps3 |
A |
T |
1: 156,352,562 (GRCm39) |
L254F |
probably damaging |
Het |
Dnhd1 |
A |
T |
7: 105,317,721 (GRCm39) |
D472V |
probably damaging |
Het |
Eif3a |
A |
T |
19: 60,764,280 (GRCm39) |
V379E |
probably damaging |
Het |
Erich4 |
T |
A |
7: 25,315,168 (GRCm39) |
N36Y |
probably damaging |
Het |
Frem2 |
T |
C |
3: 53,560,725 (GRCm39) |
T1261A |
probably damaging |
Het |
Fzd6 |
A |
T |
15: 38,894,503 (GRCm39) |
D223V |
probably damaging |
Het |
Gabra2 |
A |
T |
5: 71,165,315 (GRCm39) |
Y218* |
probably null |
Het |
Gcn1 |
G |
T |
5: 115,752,527 (GRCm39) |
M2177I |
probably benign |
Het |
Ghr |
G |
A |
15: 3,370,556 (GRCm39) |
T103I |
possibly damaging |
Het |
Gipc1 |
T |
C |
8: 84,387,857 (GRCm39) |
V79A |
probably benign |
Het |
Gm13272 |
T |
A |
4: 88,698,577 (GRCm39) |
V164D |
probably damaging |
Het |
Gramd4 |
C |
A |
15: 86,016,159 (GRCm39) |
H503Q |
probably benign |
Het |
Gstm4 |
A |
T |
3: 107,951,987 (GRCm39) |
M1K |
probably null |
Het |
Heatr5b |
T |
A |
17: 79,067,988 (GRCm39) |
Q1800L |
probably benign |
Het |
Hectd1 |
T |
A |
12: 51,836,978 (GRCm39) |
K826* |
probably null |
Het |
Hoxa9 |
T |
C |
6: 52,201,289 (GRCm39) |
I251V |
possibly damaging |
Het |
Il2ra |
A |
T |
2: 11,679,177 (GRCm39) |
I46F |
possibly damaging |
Het |
Ints2 |
T |
A |
11: 86,135,453 (GRCm39) |
R320S |
probably benign |
Het |
Iscu |
A |
T |
5: 113,912,343 (GRCm39) |
N46I |
probably damaging |
Het |
Iscu |
G |
A |
5: 113,912,410 (GRCm39) |
R60Q |
unknown |
Het |
Kcnk3 |
A |
T |
5: 30,745,875 (GRCm39) |
H72L |
probably damaging |
Het |
Kmt2a |
T |
G |
9: 44,754,157 (GRCm39) |
S1228R |
unknown |
Het |
Mbl2 |
T |
A |
19: 30,216,638 (GRCm39) |
L150Q |
probably damaging |
Het |
Med13 |
A |
T |
11: 86,161,831 (GRCm39) |
F2166Y |
probably damaging |
Het |
Mterf4 |
A |
C |
1: 93,229,275 (GRCm39) |
L246* |
probably null |
Het |
Muc16 |
T |
C |
9: 18,496,121 (GRCm39) |
Q6690R |
probably benign |
Het |
Myh10 |
T |
A |
11: 68,699,719 (GRCm39) |
L1722Q |
possibly damaging |
Het |
Neurod2 |
T |
C |
11: 98,218,454 (GRCm39) |
M237V |
probably benign |
Het |
Olfml1 |
A |
G |
7: 107,170,356 (GRCm39) |
Y81C |
probably damaging |
Het |
Or4q3 |
A |
G |
14: 50,583,872 (GRCm39) |
V9A |
probably benign |
Het |
Pcdhga7 |
A |
T |
18: 37,849,226 (GRCm39) |
N411I |
probably benign |
Het |
Pcdhgb8 |
T |
C |
18: 37,897,002 (GRCm39) |
F691L |
probably benign |
Het |
Pik3c2a |
A |
G |
7: 115,990,517 (GRCm39) |
V481A |
probably damaging |
Het |
Pik3r6 |
A |
T |
11: 68,424,701 (GRCm39) |
R435S |
probably benign |
Het |
Pkd1l1 |
G |
A |
11: 8,799,013 (GRCm39) |
H2250Y |
|
Het |
Pkd1l1 |
A |
G |
11: 8,859,857 (GRCm39) |
S1034P |
|
Het |
Plcd1 |
C |
A |
9: 118,903,720 (GRCm39) |
R400L |
possibly damaging |
Het |
Ppp2r1a |
A |
G |
17: 21,174,879 (GRCm39) |
T58A |
probably benign |
Het |
Ppp5c |
T |
C |
7: 16,761,725 (GRCm39) |
E5G |
possibly damaging |
Het |
Pradc1 |
A |
C |
6: 85,424,950 (GRCm39) |
F82L |
probably benign |
Het |
Prkag3 |
A |
T |
1: 74,780,416 (GRCm39) |
S416R |
probably benign |
Het |
Rab3gap2 |
T |
C |
1: 184,982,117 (GRCm39) |
C390R |
probably benign |
Het |
Rhot1 |
A |
G |
11: 80,156,629 (GRCm39) |
T655A |
probably benign |
Het |
Rorc |
A |
G |
3: 94,298,495 (GRCm39) |
I348V |
probably damaging |
Het |
Ryr1 |
A |
T |
7: 28,796,649 (GRCm39) |
V1051E |
probably benign |
Het |
Sema5b |
GCAC |
GC |
16: 35,478,626 (GRCm39) |
|
probably null |
Het |
Serpinb3c |
G |
A |
1: 107,199,744 (GRCm39) |
T259I |
probably damaging |
Het |
Sh3gl1 |
A |
T |
17: 56,326,438 (GRCm39) |
M70K |
probably damaging |
Het |
Sinhcaf |
T |
A |
6: 148,827,644 (GRCm39) |
T125S |
probably benign |
Het |
Slc7a4 |
C |
T |
16: 17,391,230 (GRCm39) |
V607I |
probably benign |
Het |
Spop |
A |
T |
11: 95,362,154 (GRCm39) |
N62Y |
probably damaging |
Het |
Spout1 |
A |
G |
2: 30,066,823 (GRCm39) |
F130S |
probably benign |
Het |
Tab1 |
A |
G |
15: 80,043,066 (GRCm39) |
H420R |
possibly damaging |
Het |
Tecpr2 |
CA |
C |
12: 110,899,076 (GRCm39) |
|
probably null |
Het |
Tnxb |
G |
C |
17: 34,933,577 (GRCm39) |
K2332N |
probably damaging |
Het |
Togaram1 |
T |
C |
12: 65,014,512 (GRCm39) |
Y588H |
probably damaging |
Het |
Trim71 |
G |
A |
9: 114,342,153 (GRCm39) |
R710C |
probably damaging |
Het |
Tsen54 |
C |
T |
11: 115,711,608 (GRCm39) |
Q342* |
probably null |
Het |
Ube2r2 |
T |
A |
4: 41,190,812 (GRCm39) |
N235K |
unknown |
Het |
Utrn |
C |
A |
10: 12,543,271 (GRCm39) |
K1792N |
possibly damaging |
Het |
Vmn1r122 |
A |
G |
7: 20,867,587 (GRCm39) |
I156T |
possibly damaging |
Het |
Vmn1r94 |
T |
C |
7: 19,901,636 (GRCm39) |
T223A |
possibly damaging |
Het |
Vmn2r120 |
G |
A |
17: 57,831,683 (GRCm39) |
R369W |
probably damaging |
Het |
Vwa7 |
G |
T |
17: 35,243,409 (GRCm39) |
A717S |
possibly damaging |
Het |
Zc3h4 |
T |
A |
7: 16,159,647 (GRCm39) |
C398S |
unknown |
Het |
Zc3hc1 |
T |
A |
6: 30,390,874 (GRCm39) |
E43V |
possibly damaging |
Het |
Zfp101 |
A |
T |
17: 33,600,511 (GRCm39) |
V415D |
possibly damaging |
Het |
Zfp553 |
A |
G |
7: 126,835,768 (GRCm39) |
H441R |
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 |
|
R1445:Dock2
|
UTSW |
11 |
34,189,705 (GRCm39) |
missense |
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 |
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 |
|