Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Albfm1 |
A |
G |
5: 90,725,652 (GRCm39) |
N288S |
probably benign |
Het |
Ap4b1 |
T |
A |
3: 103,719,530 (GRCm39) |
D81E |
probably benign |
Het |
Atg16l1 |
A |
T |
1: 87,702,078 (GRCm39) |
|
probably null |
Het |
Atp11a |
A |
G |
8: 12,906,949 (GRCm39) |
T459A |
probably damaging |
Het |
Bloc1s5 |
T |
A |
13: 38,815,040 (GRCm39) |
I40F |
probably damaging |
Het |
Bltp2 |
T |
A |
11: 78,165,452 (GRCm39) |
S1323T |
possibly damaging |
Het |
Capn5 |
T |
A |
7: 97,778,461 (GRCm39) |
Q386L |
probably damaging |
Het |
Cbfa2t2 |
C |
T |
2: 154,376,903 (GRCm39) |
H529Y |
probably damaging |
Het |
Cd3d |
T |
C |
9: 44,897,157 (GRCm39) |
|
probably benign |
Het |
Cenpa |
A |
G |
5: 30,829,806 (GRCm39) |
|
probably null |
Het |
Chit1 |
A |
T |
1: 134,077,163 (GRCm39) |
Y322F |
probably null |
Het |
Cntnap5c |
T |
A |
17: 58,399,345 (GRCm39) |
N399K |
possibly damaging |
Het |
Firrm |
A |
G |
1: 163,814,454 (GRCm39) |
|
probably null |
Het |
Fkbp2 |
A |
G |
19: 6,956,537 (GRCm39) |
|
|
Het |
Fsip1 |
G |
A |
2: 118,080,394 (GRCm39) |
R121C |
probably benign |
Het |
Gbp2b |
T |
C |
3: 142,306,320 (GRCm39) |
I131T |
probably benign |
Het |
Gm12695 |
T |
C |
4: 96,658,053 (GRCm39) |
N39D |
probably benign |
Het |
Gm4922 |
T |
C |
10: 18,659,616 (GRCm39) |
R369G |
probably damaging |
Het |
Gpatch3 |
C |
T |
4: 133,309,836 (GRCm39) |
L390F |
probably damaging |
Het |
Gpd2 |
G |
A |
2: 57,245,800 (GRCm39) |
M443I |
probably damaging |
Het |
Gpt2 |
G |
A |
8: 86,244,681 (GRCm39) |
E325K |
probably benign |
Het |
Hdac1-ps |
A |
G |
17: 78,800,343 (GRCm39) |
T445A |
possibly damaging |
Het |
Jph3 |
A |
G |
8: 122,480,110 (GRCm39) |
T263A |
possibly damaging |
Het |
Me3 |
C |
A |
7: 89,495,093 (GRCm39) |
A337E |
probably damaging |
Het |
Mndal |
A |
C |
1: 173,712,264 (GRCm39) |
|
probably null |
Het |
Msantd5l |
C |
T |
11: 51,144,808 (GRCm39) |
D158N |
probably damaging |
Het |
Muc6 |
C |
T |
7: 141,217,453 (GRCm39) |
E2342K |
possibly damaging |
Het |
Neb |
A |
G |
2: 52,076,076 (GRCm39) |
V5659A |
probably damaging |
Het |
Nkapd1 |
T |
A |
9: 50,521,610 (GRCm39) |
I104L |
probably benign |
Het |
Nrxn1 |
G |
A |
17: 91,395,661 (GRCm39) |
A165V |
probably benign |
Het |
Or5b94 |
T |
A |
19: 12,652,409 (GRCm39) |
I280N |
possibly damaging |
Het |
Or5b97 |
T |
C |
19: 12,878,676 (GRCm39) |
N156S |
probably benign |
Het |
Orc2 |
A |
G |
1: 58,539,534 (GRCm39) |
L35S |
probably benign |
Het |
Pax4 |
A |
G |
6: 28,447,118 (GRCm39) |
|
probably null |
Het |
Pcdhb7 |
C |
T |
18: 37,475,522 (GRCm39) |
|
probably null |
Het |
Pla2r1 |
C |
T |
2: 60,345,310 (GRCm39) |
E349K |
probably benign |
Het |
Polr2a |
C |
T |
11: 69,626,787 (GRCm39) |
A1516T |
probably benign |
Het |
Pramel23 |
A |
T |
4: 143,425,676 (GRCm39) |
I89N |
probably benign |
Het |
Prpf38a |
G |
T |
4: 108,427,401 (GRCm39) |
D187E |
possibly damaging |
Het |
Rdh16f1 |
T |
A |
10: 127,624,737 (GRCm39) |
|
probably null |
Het |
S100z |
T |
A |
13: 95,615,090 (GRCm39) |
D25V |
probably damaging |
Het |
Scamp2 |
T |
G |
9: 57,488,895 (GRCm39) |
F199V |
probably damaging |
Het |
Semp2l2b |
C |
A |
10: 21,943,654 (GRCm39) |
G109C |
probably damaging |
Het |
Senp2 |
T |
G |
16: 21,830,326 (GRCm39) |
|
probably benign |
Het |
Sltm |
T |
A |
9: 70,481,892 (GRCm39) |
S365T |
probably damaging |
Het |
Smg6 |
C |
G |
11: 74,820,169 (GRCm39) |
P147A |
possibly damaging |
Het |
Spem2 |
T |
A |
11: 69,708,603 (GRCm39) |
R121W |
probably damaging |
Het |
Sufu |
A |
G |
19: 46,439,405 (GRCm39) |
|
probably null |
Het |
Syt2 |
T |
C |
1: 134,674,501 (GRCm39) |
V313A |
possibly damaging |
Het |
Tet2 |
C |
T |
3: 133,185,102 (GRCm39) |
|
probably null |
Het |
Tfeb |
T |
A |
17: 48,097,908 (GRCm39) |
I232N |
probably benign |
Het |
Ticrr |
T |
G |
7: 79,341,601 (GRCm39) |
I1062M |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Vrk2 |
G |
A |
11: 26,439,893 (GRCm39) |
A226V |
probably damaging |
Het |
Wnk1 |
A |
T |
6: 119,942,639 (GRCm39) |
|
probably benign |
Het |
Xpo4 |
G |
T |
14: 57,841,168 (GRCm39) |
T505K |
probably benign |
Het |
Yy1 |
A |
T |
12: 108,759,594 (GRCm39) |
I86F |
probably benign |
Het |
Zc3h15 |
A |
G |
2: 83,487,400 (GRCm39) |
D73G |
possibly damaging |
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 |
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 |
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 |
|