Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts20 |
T |
A |
15: 94,226,726 (GRCm39) |
D1109V |
possibly damaging |
Het |
Apc2 |
G |
C |
10: 80,150,922 (GRCm39) |
R1992P |
possibly damaging |
Het |
Atmin |
A |
G |
8: 117,683,036 (GRCm39) |
N232S |
probably benign |
Het |
Brat1 |
A |
C |
5: 140,703,751 (GRCm39) |
D668A |
possibly damaging |
Het |
Casp16 |
A |
T |
17: 23,771,922 (GRCm39) |
V101E |
probably damaging |
Het |
Cass4 |
C |
T |
2: 172,274,478 (GRCm39) |
P753L |
probably damaging |
Het |
Cimip3 |
AC |
A |
17: 47,744,348 (GRCm39) |
|
probably benign |
Het |
Clec7a |
A |
G |
6: 129,445,877 (GRCm39) |
S98P |
possibly damaging |
Het |
Cpne5 |
G |
A |
17: 29,378,082 (GRCm39) |
R566C |
unknown |
Het |
Csrnp1 |
C |
T |
9: 119,801,707 (GRCm39) |
E451K |
probably damaging |
Het |
Dlst |
A |
G |
12: 85,179,465 (GRCm39) |
T435A |
possibly damaging |
Het |
Dync2li1 |
A |
G |
17: 84,939,070 (GRCm39) |
T45A |
probably damaging |
Het |
Efcab3 |
A |
G |
11: 104,974,713 (GRCm39) |
N5307S |
possibly damaging |
Het |
Epha4 |
A |
G |
1: 77,357,539 (GRCm39) |
Y820H |
probably damaging |
Het |
F5 |
A |
G |
1: 164,003,798 (GRCm39) |
T198A |
probably benign |
Het |
Fbn2 |
T |
A |
18: 58,199,083 (GRCm39) |
N1395I |
probably damaging |
Het |
Fcnb |
T |
A |
2: 27,969,208 (GRCm39) |
Y163F |
probably damaging |
Het |
Gm5444 |
T |
C |
13: 4,884,278 (GRCm39) |
|
noncoding transcript |
Het |
Jph3 |
G |
T |
8: 122,480,158 (GRCm39) |
D279Y |
possibly damaging |
Het |
Kcnj3 |
A |
G |
2: 55,327,360 (GRCm39) |
N50D |
possibly damaging |
Het |
Kcnma1 |
A |
G |
14: 23,555,323 (GRCm39) |
I416T |
probably damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Kmt2e |
A |
G |
5: 23,706,640 (GRCm39) |
N1401S |
probably benign |
Het |
Lama5 |
C |
T |
2: 179,824,144 (GRCm39) |
|
probably benign |
Het |
Lrp1b |
A |
G |
2: 40,712,707 (GRCm39) |
V3095A |
probably damaging |
Het |
Mmp1a |
A |
G |
9: 7,475,346 (GRCm39) |
*372W |
probably null |
Het |
Or7d11 |
C |
T |
9: 19,966,169 (GRCm39) |
V197I |
probably benign |
Het |
Pdgfra |
T |
A |
5: 75,353,169 (GRCm39) |
N986K |
probably benign |
Het |
Pgap1 |
C |
T |
1: 54,532,507 (GRCm39) |
V671I |
probably benign |
Het |
Pla2g4e |
T |
C |
2: 119,999,085 (GRCm39) |
S760G |
probably benign |
Het |
Plk3 |
T |
C |
4: 116,990,633 (GRCm39) |
I94V |
probably benign |
Het |
Pogk |
C |
T |
1: 166,231,193 (GRCm39) |
V45I |
probably damaging |
Het |
Pou2f1 |
G |
C |
1: 165,722,538 (GRCm39) |
P349R |
probably damaging |
Het |
Rims1 |
T |
A |
1: 22,572,578 (GRCm39) |
Q541L |
probably benign |
Het |
Rptn |
A |
G |
3: 93,305,664 (GRCm39) |
Q999R |
probably benign |
Het |
Stxbp5 |
A |
G |
10: 9,645,163 (GRCm39) |
L911P |
probably damaging |
Het |
Tgfbr3 |
A |
G |
5: 107,362,753 (GRCm39) |
|
probably benign |
Het |
Trim7 |
A |
T |
11: 48,728,435 (GRCm39) |
T28S |
probably damaging |
Het |
Zfp595 |
T |
C |
13: 67,465,379 (GRCm39) |
I295V |
probably benign |
Het |
|
Other mutations in Dock8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
captain_morgan
|
APN |
19 |
25,105,076 (GRCm39) |
critical splice donor site |
probably benign |
|
primurus
|
APN |
19 |
25,160,973 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00737:Dock8
|
APN |
19 |
25,160,340 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00755:Dock8
|
APN |
19 |
25,028,873 (GRCm39) |
missense |
probably benign |
0.09 |
IGL00822:Dock8
|
APN |
19 |
25,165,773 (GRCm39) |
nonsense |
probably null |
|
IGL00838:Dock8
|
APN |
19 |
25,152,823 (GRCm39) |
nonsense |
probably null |
|
IGL01419:Dock8
|
APN |
19 |
25,096,816 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01456:Dock8
|
APN |
19 |
25,096,863 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01532:Dock8
|
APN |
19 |
25,146,805 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01602:Dock8
|
APN |
19 |
25,067,252 (GRCm39) |
splice site |
probably benign |
|
IGL01605:Dock8
|
APN |
19 |
25,067,252 (GRCm39) |
splice site |
probably benign |
|
IGL01753:Dock8
|
APN |
19 |
25,038,656 (GRCm39) |
splice site |
probably benign |
|
IGL01843:Dock8
|
APN |
19 |
25,067,292 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02032:Dock8
|
APN |
19 |
25,107,769 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02073:Dock8
|
APN |
19 |
25,178,350 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02192:Dock8
|
APN |
19 |
25,055,569 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02402:Dock8
|
APN |
19 |
25,055,509 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02529:Dock8
|
APN |
19 |
25,078,290 (GRCm39) |
nonsense |
probably null |
|
IGL02728:Dock8
|
APN |
19 |
25,109,584 (GRCm39) |
missense |
probably benign |
|
IGL02739:Dock8
|
APN |
19 |
25,165,852 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03037:Dock8
|
APN |
19 |
25,063,545 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03104:Dock8
|
APN |
19 |
25,178,384 (GRCm39) |
nonsense |
probably null |
|
IGL03137:Dock8
|
APN |
19 |
25,133,312 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03365:Dock8
|
APN |
19 |
25,077,048 (GRCm39) |
missense |
possibly damaging |
0.70 |
Defenseless
|
UTSW |
19 |
25,028,927 (GRCm39) |
missense |
probably benign |
0.00 |
Guardate
|
UTSW |
19 |
25,127,195 (GRCm39) |
missense |
probably benign |
|
hillock
|
UTSW |
19 |
25,151,697 (GRCm39) |
critical splice donor site |
probably null |
|
Molehill
|
UTSW |
19 |
25,107,825 (GRCm39) |
missense |
probably damaging |
1.00 |
Pap
|
UTSW |
19 |
25,099,805 (GRCm39) |
missense |
probably benign |
0.31 |
Papilla
|
UTSW |
19 |
25,055,448 (GRCm39) |
nonsense |
probably null |
|
snowdrop
|
UTSW |
19 |
25,162,305 (GRCm39) |
critical splice donor site |
probably null |
|
warts_and_all
|
UTSW |
19 |
25,146,865 (GRCm39) |
critical splice donor site |
probably null |
|
R0021:Dock8
|
UTSW |
19 |
25,140,411 (GRCm39) |
missense |
probably benign |
0.01 |
R0147:Dock8
|
UTSW |
19 |
25,096,823 (GRCm39) |
missense |
probably benign |
0.00 |
R0148:Dock8
|
UTSW |
19 |
25,096,823 (GRCm39) |
missense |
probably benign |
0.00 |
R0294:Dock8
|
UTSW |
19 |
25,165,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R0537:Dock8
|
UTSW |
19 |
25,148,941 (GRCm39) |
missense |
probably benign |
0.08 |
R0630:Dock8
|
UTSW |
19 |
25,038,524 (GRCm39) |
missense |
probably benign |
0.10 |
R1163:Dock8
|
UTSW |
19 |
25,028,867 (GRCm39) |
missense |
probably benign |
|
R1164:Dock8
|
UTSW |
19 |
25,067,391 (GRCm39) |
missense |
probably benign |
0.44 |
R1471:Dock8
|
UTSW |
19 |
25,178,400 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1477:Dock8
|
UTSW |
19 |
25,072,914 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1633:Dock8
|
UTSW |
19 |
25,028,927 (GRCm39) |
missense |
probably benign |
0.00 |
R1803:Dock8
|
UTSW |
19 |
25,109,599 (GRCm39) |
missense |
probably benign |
0.00 |
R1822:Dock8
|
UTSW |
19 |
25,138,422 (GRCm39) |
missense |
probably benign |
0.31 |
R1852:Dock8
|
UTSW |
19 |
25,104,492 (GRCm39) |
missense |
probably benign |
0.45 |
R1916:Dock8
|
UTSW |
19 |
25,038,521 (GRCm39) |
missense |
probably benign |
0.02 |
R1984:Dock8
|
UTSW |
19 |
25,098,545 (GRCm39) |
missense |
probably null |
|
R2311:Dock8
|
UTSW |
19 |
25,160,368 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2341:Dock8
|
UTSW |
19 |
25,177,757 (GRCm39) |
missense |
probably damaging |
0.99 |
R2483:Dock8
|
UTSW |
19 |
25,057,241 (GRCm39) |
missense |
probably benign |
|
R3116:Dock8
|
UTSW |
19 |
25,165,858 (GRCm39) |
missense |
probably benign |
0.00 |
R3157:Dock8
|
UTSW |
19 |
25,127,195 (GRCm39) |
missense |
probably benign |
|
R3623:Dock8
|
UTSW |
19 |
25,057,241 (GRCm39) |
missense |
probably benign |
|
R3624:Dock8
|
UTSW |
19 |
25,057,241 (GRCm39) |
missense |
probably benign |
|
R3800:Dock8
|
UTSW |
19 |
25,141,716 (GRCm39) |
missense |
probably benign |
0.08 |
R3844:Dock8
|
UTSW |
19 |
25,042,794 (GRCm39) |
nonsense |
probably null |
|
R3895:Dock8
|
UTSW |
19 |
25,028,865 (GRCm39) |
missense |
probably benign |
0.31 |
R3959:Dock8
|
UTSW |
19 |
25,162,305 (GRCm39) |
critical splice donor site |
probably null |
|
R4428:Dock8
|
UTSW |
19 |
25,042,754 (GRCm39) |
missense |
probably benign |
0.00 |
R4428:Dock8
|
UTSW |
19 |
25,177,863 (GRCm39) |
missense |
probably damaging |
0.98 |
R4429:Dock8
|
UTSW |
19 |
25,042,754 (GRCm39) |
missense |
probably benign |
0.00 |
R4431:Dock8
|
UTSW |
19 |
25,042,754 (GRCm39) |
missense |
probably benign |
0.00 |
R4545:Dock8
|
UTSW |
19 |
25,165,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R4839:Dock8
|
UTSW |
19 |
25,146,858 (GRCm39) |
missense |
probably benign |
0.00 |
R4897:Dock8
|
UTSW |
19 |
25,159,001 (GRCm39) |
missense |
probably benign |
0.00 |
R4939:Dock8
|
UTSW |
19 |
25,099,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R4995:Dock8
|
UTSW |
19 |
25,135,747 (GRCm39) |
missense |
probably benign |
0.02 |
R5035:Dock8
|
UTSW |
19 |
25,063,571 (GRCm39) |
missense |
probably damaging |
0.99 |
R5294:Dock8
|
UTSW |
19 |
25,038,517 (GRCm39) |
missense |
probably benign |
0.01 |
R5324:Dock8
|
UTSW |
19 |
25,140,458 (GRCm39) |
missense |
probably benign |
0.17 |
R5478:Dock8
|
UTSW |
19 |
25,057,186 (GRCm39) |
missense |
probably benign |
|
R5704:Dock8
|
UTSW |
19 |
25,151,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R5724:Dock8
|
UTSW |
19 |
25,099,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R5745:Dock8
|
UTSW |
19 |
25,107,761 (GRCm39) |
missense |
probably benign |
0.02 |
R5864:Dock8
|
UTSW |
19 |
25,038,584 (GRCm39) |
missense |
probably damaging |
0.99 |
R5870:Dock8
|
UTSW |
19 |
25,109,490 (GRCm39) |
missense |
probably benign |
|
R5893:Dock8
|
UTSW |
19 |
25,099,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R5954:Dock8
|
UTSW |
19 |
25,148,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R6087:Dock8
|
UTSW |
19 |
25,138,438 (GRCm39) |
missense |
probably benign |
0.00 |
R6223:Dock8
|
UTSW |
19 |
25,138,416 (GRCm39) |
missense |
probably benign |
0.00 |
R6391:Dock8
|
UTSW |
19 |
25,072,914 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6759:Dock8
|
UTSW |
19 |
25,104,848 (GRCm39) |
missense |
probably damaging |
0.99 |
R6786:Dock8
|
UTSW |
19 |
25,160,386 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6794:Dock8
|
UTSW |
19 |
25,099,805 (GRCm39) |
missense |
probably benign |
0.31 |
R6818:Dock8
|
UTSW |
19 |
25,146,865 (GRCm39) |
critical splice donor site |
probably null |
|
R6885:Dock8
|
UTSW |
19 |
25,124,742 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6908:Dock8
|
UTSW |
19 |
25,165,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R6923:Dock8
|
UTSW |
19 |
25,072,970 (GRCm39) |
missense |
probably benign |
|
R7001:Dock8
|
UTSW |
19 |
25,077,041 (GRCm39) |
missense |
probably benign |
|
R7141:Dock8
|
UTSW |
19 |
25,158,984 (GRCm39) |
missense |
probably null |
0.75 |
R7203:Dock8
|
UTSW |
19 |
25,158,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R7257:Dock8
|
UTSW |
19 |
25,104,449 (GRCm39) |
missense |
probably benign |
0.08 |
R7296:Dock8
|
UTSW |
19 |
25,162,245 (GRCm39) |
missense |
probably benign |
0.00 |
R7538:Dock8
|
UTSW |
19 |
25,135,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R7555:Dock8
|
UTSW |
19 |
25,152,764 (GRCm39) |
missense |
probably damaging |
0.99 |
R7641:Dock8
|
UTSW |
19 |
25,151,697 (GRCm39) |
critical splice donor site |
probably null |
|
R7764:Dock8
|
UTSW |
19 |
25,074,899 (GRCm39) |
missense |
probably benign |
|
R7859:Dock8
|
UTSW |
19 |
25,160,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R7864:Dock8
|
UTSW |
19 |
25,140,864 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8090:Dock8
|
UTSW |
19 |
25,131,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R8160:Dock8
|
UTSW |
19 |
25,124,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R8287:Dock8
|
UTSW |
19 |
25,107,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R8295:Dock8
|
UTSW |
19 |
25,100,600 (GRCm39) |
missense |
probably benign |
0.04 |
R8443:Dock8
|
UTSW |
19 |
25,133,281 (GRCm39) |
missense |
probably benign |
0.04 |
R8537:Dock8
|
UTSW |
19 |
25,107,870 (GRCm39) |
missense |
probably benign |
0.00 |
R8673:Dock8
|
UTSW |
19 |
25,160,867 (GRCm39) |
missense |
probably damaging |
0.96 |
R8709:Dock8
|
UTSW |
19 |
25,055,448 (GRCm39) |
nonsense |
probably null |
|
R8834:Dock8
|
UTSW |
19 |
25,140,834 (GRCm39) |
missense |
probably benign |
0.16 |
R8991:Dock8
|
UTSW |
19 |
25,165,731 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9292:Dock8
|
UTSW |
19 |
25,160,995 (GRCm39) |
splice site |
probably benign |
|
R9509:Dock8
|
UTSW |
19 |
25,072,985 (GRCm39) |
missense |
probably benign |
0.00 |
R9526:Dock8
|
UTSW |
19 |
25,165,739 (GRCm39) |
missense |
probably benign |
0.10 |
R9622:Dock8
|
UTSW |
19 |
25,098,545 (GRCm39) |
missense |
probably null |
|
R9634:Dock8
|
UTSW |
19 |
25,169,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R9654:Dock8
|
UTSW |
19 |
25,124,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R9670:Dock8
|
UTSW |
19 |
25,148,926 (GRCm39) |
missense |
probably null |
0.01 |
R9699:Dock8
|
UTSW |
19 |
25,133,388 (GRCm39) |
critical splice donor site |
probably null |
|
R9726:Dock8
|
UTSW |
19 |
25,154,374 (GRCm39) |
missense |
probably damaging |
0.97 |
R9765:Dock8
|
UTSW |
19 |
25,146,832 (GRCm39) |
missense |
possibly damaging |
0.94 |
X0027:Dock8
|
UTSW |
19 |
25,138,493 (GRCm39) |
missense |
probably benign |
|
Z1177:Dock8
|
UTSW |
19 |
25,133,336 (GRCm39) |
missense |
probably benign |
0.16 |
Z1177:Dock8
|
UTSW |
19 |
25,109,487 (GRCm39) |
missense |
probably benign |
0.05 |
|