Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
A |
G |
13: 81,707,543 (GRCm39) |
F568L |
probably benign |
Het |
AW112010 |
T |
A |
19: 11,025,741 (GRCm39) |
|
noncoding transcript |
Het |
Bbs4 |
A |
T |
9: 59,237,729 (GRCm39) |
L205H |
probably benign |
Het |
Bmal2 |
T |
C |
6: 146,711,266 (GRCm39) |
V90A |
possibly damaging |
Het |
C2cd2l |
T |
C |
9: 44,227,878 (GRCm39) |
K121R |
probably benign |
Het |
Car14 |
A |
G |
3: 95,806,870 (GRCm39) |
V198A |
possibly damaging |
Het |
Cd22 |
G |
T |
7: 30,576,955 (GRCm39) |
H117Q |
possibly damaging |
Het |
Celf1 |
T |
A |
2: 90,829,068 (GRCm39) |
I45N |
probably damaging |
Het |
Cluh |
T |
C |
11: 74,547,997 (GRCm39) |
S103P |
probably damaging |
Het |
Cyp39a1 |
T |
A |
17: 44,002,613 (GRCm39) |
L276Q |
probably benign |
Het |
Ddx27 |
T |
G |
2: 166,857,245 (GRCm39) |
|
probably benign |
Het |
Defb4 |
A |
T |
8: 19,251,279 (GRCm39) |
I49F |
possibly damaging |
Het |
Dpp6 |
T |
C |
5: 27,839,541 (GRCm39) |
V352A |
probably damaging |
Het |
Elmo2 |
C |
T |
2: 165,139,312 (GRCm39) |
E412K |
probably damaging |
Het |
Eme1 |
G |
A |
11: 94,541,733 (GRCm39) |
P30S |
possibly damaging |
Het |
Espnl |
G |
T |
1: 91,272,535 (GRCm39) |
A632S |
probably benign |
Het |
Gfod1 |
C |
A |
13: 43,354,211 (GRCm39) |
A255S |
probably benign |
Het |
Helz2 |
T |
A |
2: 180,872,704 (GRCm39) |
K2432M |
probably damaging |
Het |
Idua |
T |
C |
5: 108,827,657 (GRCm39) |
L157P |
probably damaging |
Het |
Ifi207 |
T |
A |
1: 173,555,159 (GRCm39) |
D848V |
probably damaging |
Het |
Jag1 |
C |
T |
2: 136,927,858 (GRCm39) |
S851N |
possibly damaging |
Het |
Kat6b |
T |
A |
14: 21,681,415 (GRCm39) |
F571I |
probably damaging |
Het |
Lrrc74b |
G |
A |
16: 17,376,028 (GRCm39) |
|
probably benign |
Het |
Mst1r |
A |
G |
9: 107,794,026 (GRCm39) |
K1160E |
probably damaging |
Het |
Muc19 |
C |
A |
15: 91,778,192 (GRCm39) |
|
noncoding transcript |
Het |
Nrg4 |
G |
A |
9: 55,135,198 (GRCm39) |
|
probably benign |
Het |
Ociad1 |
T |
C |
5: 73,458,037 (GRCm39) |
I12T |
possibly damaging |
Het |
Or1o3 |
A |
G |
17: 37,574,111 (GRCm39) |
V148A |
possibly damaging |
Het |
Pold3 |
A |
G |
7: 99,749,618 (GRCm39) |
|
probably benign |
Het |
Psmd5 |
T |
C |
2: 34,747,784 (GRCm39) |
E291G |
probably damaging |
Het |
Ptpn23 |
A |
G |
9: 110,222,781 (GRCm39) |
V92A |
possibly damaging |
Het |
Rab44 |
T |
A |
17: 29,359,490 (GRCm39) |
H559Q |
probably benign |
Het |
Rbm6 |
T |
C |
9: 107,730,051 (GRCm39) |
D199G |
probably damaging |
Het |
Rps18-ps3 |
C |
T |
8: 107,989,754 (GRCm39) |
|
noncoding transcript |
Het |
Septin10 |
T |
C |
10: 59,006,758 (GRCm39) |
T93A |
probably benign |
Het |
Slmap |
T |
C |
14: 26,184,865 (GRCm39) |
T111A |
probably damaging |
Het |
Spata25 |
C |
T |
2: 164,670,377 (GRCm39) |
M1I |
probably null |
Het |
Spink5 |
T |
A |
18: 44,100,171 (GRCm39) |
C63S |
probably damaging |
Het |
Sycp3 |
T |
C |
10: 88,302,425 (GRCm39) |
|
probably benign |
Het |
Tarbp1 |
A |
G |
8: 127,177,567 (GRCm39) |
|
probably benign |
Het |
Thbs2 |
A |
T |
17: 14,891,716 (GRCm39) |
N940K |
probably benign |
Het |
Tmem106b |
A |
T |
6: 13,081,600 (GRCm39) |
Q169L |
possibly damaging |
Het |
Trpm6 |
G |
T |
19: 18,764,120 (GRCm39) |
C242F |
probably benign |
Het |
Ush2a |
T |
A |
1: 187,999,305 (GRCm39) |
M205K |
probably benign |
Het |
Utp18 |
A |
C |
11: 93,774,617 (GRCm39) |
|
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 |
|
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 |
R3901:Dock8
|
UTSW |
19 |
25,078,269 (GRCm39) |
missense |
possibly damaging |
0.69 |
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 |
|