Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts17 |
C |
A |
7: 66,908,601 (GRCm38) |
N264K |
probably damaging |
Het |
Adgrl3 |
C |
T |
5: 81,694,569 (GRCm38) |
T260I |
probably damaging |
Het |
Ambra1 |
G |
T |
2: 91,885,632 (GRCm38) |
K769N |
probably damaging |
Het |
Arel1 |
A |
G |
12: 84,934,162 (GRCm38) |
V357A |
possibly damaging |
Het |
Atp11b |
T |
A |
3: 35,849,502 (GRCm38) |
C76* |
probably null |
Het |
AW112010 |
C |
A |
19: 11,048,069 (GRCm38) |
|
noncoding transcript |
Het |
Bfar |
A |
T |
16: 13,687,387 (GRCm38) |
|
probably benign |
Het |
Ccdc70 |
T |
G |
8: 21,973,283 (GRCm38) |
L30V |
probably damaging |
Het |
Cep20 |
A |
G |
16: 14,304,511 (GRCm38) |
S130P |
probably benign |
Het |
Chrm5 |
C |
T |
2: 112,479,232 (GRCm38) |
R513Q |
probably benign |
Het |
Crem |
G |
A |
18: 3,276,732 (GRCm38) |
T7I |
probably benign |
Het |
Cyp4f39 |
C |
T |
17: 32,470,954 (GRCm38) |
|
probably benign |
Het |
Dlg5 |
T |
C |
14: 24,158,592 (GRCm38) |
T849A |
probably benign |
Het |
Eomes |
T |
C |
9: 118,482,249 (GRCm38) |
I380T |
probably damaging |
Het |
Fam13a |
T |
C |
6: 58,940,295 (GRCm38) |
D532G |
probably damaging |
Het |
Gm10061 |
G |
T |
16: 89,151,302 (GRCm38) |
*55L |
probably null |
Het |
Gm27438 |
T |
G |
2: 87,252,925 (GRCm38) |
|
probably benign |
Het |
Gpalpp1 |
T |
C |
14: 76,102,502 (GRCm38) |
K124E |
probably benign |
Het |
Hgs |
T |
A |
11: 120,477,509 (GRCm38) |
|
probably null |
Het |
Hpn |
T |
A |
7: 31,103,513 (GRCm38) |
M121L |
possibly damaging |
Het |
Il1r1 |
T |
C |
1: 40,294,928 (GRCm38) |
|
probably null |
Het |
Jag2 |
A |
T |
12: 112,914,363 (GRCm38) |
C583S |
probably damaging |
Het |
Katnal2 |
T |
C |
18: 77,012,000 (GRCm38) |
H146R |
probably benign |
Het |
Ldah |
T |
C |
12: 8,220,596 (GRCm38) |
|
probably benign |
Het |
Lvrn |
T |
A |
18: 46,900,484 (GRCm38) |
Y921N |
probably damaging |
Het |
Muc5b |
A |
G |
7: 141,870,006 (GRCm38) |
Y4572C |
possibly damaging |
Het |
Myo16 |
A |
G |
8: 10,400,551 (GRCm38) |
S518G |
probably benign |
Het |
Ncf1 |
T |
C |
5: 134,226,593 (GRCm38) |
N148S |
probably benign |
Het |
Nes |
T |
G |
3: 87,978,347 (GRCm38) |
D1260E |
possibly damaging |
Het |
Nup210 |
C |
A |
6: 91,085,999 (GRCm38) |
|
probably benign |
Het |
Olfr548-ps1 |
T |
C |
7: 102,542,656 (GRCm38) |
L240P |
probably damaging |
Het |
Rnf31 |
C |
A |
14: 55,602,623 (GRCm38) |
Q968K |
probably damaging |
Het |
Ros1 |
A |
G |
10: 52,090,938 (GRCm38) |
|
probably benign |
Het |
Ryk |
T |
C |
9: 102,897,266 (GRCm38) |
Y400H |
probably benign |
Het |
Slc4a5 |
T |
A |
6: 83,273,040 (GRCm38) |
|
probably null |
Het |
Sptssb |
A |
G |
3: 69,820,869 (GRCm38) |
|
probably benign |
Het |
Sstr5 |
T |
C |
17: 25,491,331 (GRCm38) |
D308G |
probably damaging |
Het |
Taf2 |
A |
G |
15: 55,049,486 (GRCm38) |
W493R |
possibly damaging |
Het |
Vmn2r28 |
T |
A |
7: 5,486,464 (GRCm38) |
I459L |
probably benign |
Het |
Vti1b |
A |
C |
12: 79,165,138 (GRCm38) |
L1W |
probably null |
Het |
Wdr1 |
T |
C |
5: 38,535,187 (GRCm38) |
Y125C |
probably damaging |
Het |
|
Other mutations in Dock8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
captain_morgan
|
APN |
19 |
25,127,712 (GRCm38) |
critical splice donor site |
probably benign |
|
primurus
|
APN |
19 |
25,183,609 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00737:Dock8
|
APN |
19 |
25,182,976 (GRCm38) |
missense |
probably benign |
0.00 |
IGL00755:Dock8
|
APN |
19 |
25,051,509 (GRCm38) |
missense |
probably benign |
0.09 |
IGL00822:Dock8
|
APN |
19 |
25,188,409 (GRCm38) |
nonsense |
probably null |
|
IGL00838:Dock8
|
APN |
19 |
25,175,459 (GRCm38) |
nonsense |
probably null |
|
IGL01419:Dock8
|
APN |
19 |
25,119,452 (GRCm38) |
missense |
probably benign |
0.08 |
IGL01456:Dock8
|
APN |
19 |
25,119,499 (GRCm38) |
missense |
possibly damaging |
0.95 |
IGL01602:Dock8
|
APN |
19 |
25,089,888 (GRCm38) |
splice site |
probably benign |
|
IGL01605:Dock8
|
APN |
19 |
25,089,888 (GRCm38) |
splice site |
probably benign |
|
IGL01753:Dock8
|
APN |
19 |
25,061,292 (GRCm38) |
splice site |
probably benign |
|
IGL01843:Dock8
|
APN |
19 |
25,089,928 (GRCm38) |
missense |
probably benign |
0.02 |
IGL02032:Dock8
|
APN |
19 |
25,130,405 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02073:Dock8
|
APN |
19 |
25,200,986 (GRCm38) |
critical splice acceptor site |
probably null |
|
IGL02192:Dock8
|
APN |
19 |
25,078,205 (GRCm38) |
critical splice donor site |
probably null |
|
IGL02402:Dock8
|
APN |
19 |
25,078,145 (GRCm38) |
missense |
probably benign |
0.25 |
IGL02529:Dock8
|
APN |
19 |
25,100,926 (GRCm38) |
nonsense |
probably null |
|
IGL02728:Dock8
|
APN |
19 |
25,132,220 (GRCm38) |
missense |
probably benign |
|
IGL02739:Dock8
|
APN |
19 |
25,188,488 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03037:Dock8
|
APN |
19 |
25,086,181 (GRCm38) |
missense |
probably benign |
0.02 |
IGL03104:Dock8
|
APN |
19 |
25,201,020 (GRCm38) |
nonsense |
probably null |
|
IGL03137:Dock8
|
APN |
19 |
25,155,948 (GRCm38) |
missense |
probably benign |
0.19 |
IGL03365:Dock8
|
APN |
19 |
25,099,684 (GRCm38) |
missense |
possibly damaging |
0.70 |
Defenseless
|
UTSW |
19 |
25,051,563 (GRCm38) |
missense |
probably benign |
0.00 |
Guardate
|
UTSW |
19 |
25,149,831 (GRCm38) |
missense |
probably benign |
|
hillock
|
UTSW |
19 |
25,174,333 (GRCm38) |
critical splice donor site |
probably null |
|
Molehill
|
UTSW |
19 |
25,130,461 (GRCm38) |
missense |
probably damaging |
1.00 |
Pap
|
UTSW |
19 |
25,122,441 (GRCm38) |
missense |
probably benign |
0.31 |
Papilla
|
UTSW |
19 |
25,078,084 (GRCm38) |
nonsense |
probably null |
|
snowdrop
|
UTSW |
19 |
25,184,941 (GRCm38) |
critical splice donor site |
probably null |
|
warts_and_all
|
UTSW |
19 |
25,169,501 (GRCm38) |
critical splice donor site |
probably null |
|
R0021:Dock8
|
UTSW |
19 |
25,163,047 (GRCm38) |
missense |
probably benign |
0.01 |
R0147:Dock8
|
UTSW |
19 |
25,119,459 (GRCm38) |
missense |
probably benign |
0.00 |
R0148:Dock8
|
UTSW |
19 |
25,119,459 (GRCm38) |
missense |
probably benign |
0.00 |
R0294:Dock8
|
UTSW |
19 |
25,188,350 (GRCm38) |
missense |
probably damaging |
1.00 |
R0537:Dock8
|
UTSW |
19 |
25,171,577 (GRCm38) |
missense |
probably benign |
0.08 |
R0630:Dock8
|
UTSW |
19 |
25,061,160 (GRCm38) |
missense |
probably benign |
0.10 |
R1163:Dock8
|
UTSW |
19 |
25,051,503 (GRCm38) |
missense |
probably benign |
|
R1164:Dock8
|
UTSW |
19 |
25,090,027 (GRCm38) |
missense |
probably benign |
0.44 |
R1471:Dock8
|
UTSW |
19 |
25,201,036 (GRCm38) |
missense |
possibly damaging |
0.74 |
R1477:Dock8
|
UTSW |
19 |
25,095,550 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1633:Dock8
|
UTSW |
19 |
25,051,563 (GRCm38) |
missense |
probably benign |
0.00 |
R1803:Dock8
|
UTSW |
19 |
25,132,235 (GRCm38) |
missense |
probably benign |
0.00 |
R1822:Dock8
|
UTSW |
19 |
25,161,058 (GRCm38) |
missense |
probably benign |
0.31 |
R1852:Dock8
|
UTSW |
19 |
25,127,128 (GRCm38) |
missense |
probably benign |
0.45 |
R1916:Dock8
|
UTSW |
19 |
25,061,157 (GRCm38) |
missense |
probably benign |
0.02 |
R1984:Dock8
|
UTSW |
19 |
25,121,181 (GRCm38) |
missense |
probably null |
|
R2311:Dock8
|
UTSW |
19 |
25,183,004 (GRCm38) |
missense |
possibly damaging |
0.93 |
R2341:Dock8
|
UTSW |
19 |
25,200,393 (GRCm38) |
missense |
probably damaging |
0.99 |
R2483:Dock8
|
UTSW |
19 |
25,079,877 (GRCm38) |
missense |
probably benign |
|
R3116:Dock8
|
UTSW |
19 |
25,188,494 (GRCm38) |
missense |
probably benign |
0.00 |
R3157:Dock8
|
UTSW |
19 |
25,149,831 (GRCm38) |
missense |
probably benign |
|
R3623:Dock8
|
UTSW |
19 |
25,079,877 (GRCm38) |
missense |
probably benign |
|
R3624:Dock8
|
UTSW |
19 |
25,079,877 (GRCm38) |
missense |
probably benign |
|
R3800:Dock8
|
UTSW |
19 |
25,164,352 (GRCm38) |
missense |
probably benign |
0.08 |
R3844:Dock8
|
UTSW |
19 |
25,065,430 (GRCm38) |
nonsense |
probably null |
|
R3895:Dock8
|
UTSW |
19 |
25,051,501 (GRCm38) |
missense |
probably benign |
0.31 |
R3901:Dock8
|
UTSW |
19 |
25,100,905 (GRCm38) |
missense |
possibly damaging |
0.69 |
R3959:Dock8
|
UTSW |
19 |
25,184,941 (GRCm38) |
critical splice donor site |
probably null |
|
R4428:Dock8
|
UTSW |
19 |
25,065,390 (GRCm38) |
missense |
probably benign |
0.00 |
R4428:Dock8
|
UTSW |
19 |
25,200,499 (GRCm38) |
missense |
probably damaging |
0.98 |
R4429:Dock8
|
UTSW |
19 |
25,065,390 (GRCm38) |
missense |
probably benign |
0.00 |
R4431:Dock8
|
UTSW |
19 |
25,065,390 (GRCm38) |
missense |
probably benign |
0.00 |
R4545:Dock8
|
UTSW |
19 |
25,188,358 (GRCm38) |
missense |
probably damaging |
1.00 |
R4839:Dock8
|
UTSW |
19 |
25,169,494 (GRCm38) |
missense |
probably benign |
0.00 |
R4897:Dock8
|
UTSW |
19 |
25,181,637 (GRCm38) |
missense |
probably benign |
0.00 |
R4939:Dock8
|
UTSW |
19 |
25,122,400 (GRCm38) |
missense |
probably damaging |
1.00 |
R4995:Dock8
|
UTSW |
19 |
25,158,383 (GRCm38) |
missense |
probably benign |
0.02 |
R5035:Dock8
|
UTSW |
19 |
25,086,207 (GRCm38) |
missense |
probably damaging |
0.99 |
R5294:Dock8
|
UTSW |
19 |
25,061,153 (GRCm38) |
missense |
probably benign |
0.01 |
R5324:Dock8
|
UTSW |
19 |
25,163,094 (GRCm38) |
missense |
probably benign |
0.17 |
R5478:Dock8
|
UTSW |
19 |
25,079,822 (GRCm38) |
missense |
probably benign |
|
R5704:Dock8
|
UTSW |
19 |
25,174,222 (GRCm38) |
missense |
probably damaging |
1.00 |
R5724:Dock8
|
UTSW |
19 |
25,122,421 (GRCm38) |
missense |
probably damaging |
1.00 |
R5745:Dock8
|
UTSW |
19 |
25,130,397 (GRCm38) |
missense |
probably benign |
0.02 |
R5864:Dock8
|
UTSW |
19 |
25,061,220 (GRCm38) |
missense |
probably damaging |
0.99 |
R5870:Dock8
|
UTSW |
19 |
25,132,126 (GRCm38) |
missense |
probably benign |
|
R5893:Dock8
|
UTSW |
19 |
25,122,447 (GRCm38) |
missense |
probably damaging |
1.00 |
R5954:Dock8
|
UTSW |
19 |
25,171,619 (GRCm38) |
missense |
probably damaging |
1.00 |
R6087:Dock8
|
UTSW |
19 |
25,161,074 (GRCm38) |
missense |
probably benign |
0.00 |
R6223:Dock8
|
UTSW |
19 |
25,161,052 (GRCm38) |
missense |
probably benign |
0.00 |
R6391:Dock8
|
UTSW |
19 |
25,095,550 (GRCm38) |
missense |
possibly damaging |
0.95 |
R6759:Dock8
|
UTSW |
19 |
25,127,484 (GRCm38) |
missense |
probably damaging |
0.99 |
R6786:Dock8
|
UTSW |
19 |
25,183,022 (GRCm38) |
missense |
possibly damaging |
0.49 |
R6794:Dock8
|
UTSW |
19 |
25,122,441 (GRCm38) |
missense |
probably benign |
0.31 |
R6818:Dock8
|
UTSW |
19 |
25,169,501 (GRCm38) |
critical splice donor site |
probably null |
|
R6885:Dock8
|
UTSW |
19 |
25,147,378 (GRCm38) |
missense |
possibly damaging |
0.95 |
R6908:Dock8
|
UTSW |
19 |
25,188,382 (GRCm38) |
missense |
probably damaging |
1.00 |
R6923:Dock8
|
UTSW |
19 |
25,095,606 (GRCm38) |
missense |
probably benign |
|
R7001:Dock8
|
UTSW |
19 |
25,099,677 (GRCm38) |
missense |
probably benign |
|
R7141:Dock8
|
UTSW |
19 |
25,181,620 (GRCm38) |
missense |
probably null |
0.75 |
R7203:Dock8
|
UTSW |
19 |
25,181,563 (GRCm38) |
missense |
probably damaging |
1.00 |
R7257:Dock8
|
UTSW |
19 |
25,127,085 (GRCm38) |
missense |
probably benign |
0.08 |
R7296:Dock8
|
UTSW |
19 |
25,184,881 (GRCm38) |
missense |
probably benign |
0.00 |
R7538:Dock8
|
UTSW |
19 |
25,158,418 (GRCm38) |
missense |
probably damaging |
1.00 |
R7555:Dock8
|
UTSW |
19 |
25,175,400 (GRCm38) |
missense |
probably damaging |
0.99 |
R7641:Dock8
|
UTSW |
19 |
25,174,333 (GRCm38) |
critical splice donor site |
probably null |
|
R7764:Dock8
|
UTSW |
19 |
25,097,535 (GRCm38) |
missense |
probably benign |
|
R7859:Dock8
|
UTSW |
19 |
25,183,570 (GRCm38) |
missense |
probably damaging |
1.00 |
R7864:Dock8
|
UTSW |
19 |
25,163,500 (GRCm38) |
missense |
possibly damaging |
0.95 |
R8090:Dock8
|
UTSW |
19 |
25,154,242 (GRCm38) |
missense |
probably damaging |
1.00 |
R8160:Dock8
|
UTSW |
19 |
25,147,347 (GRCm38) |
missense |
probably damaging |
1.00 |
R8287:Dock8
|
UTSW |
19 |
25,130,461 (GRCm38) |
missense |
probably damaging |
1.00 |
R8295:Dock8
|
UTSW |
19 |
25,123,236 (GRCm38) |
missense |
probably benign |
0.04 |
R8443:Dock8
|
UTSW |
19 |
25,155,917 (GRCm38) |
missense |
probably benign |
0.04 |
R8537:Dock8
|
UTSW |
19 |
25,130,506 (GRCm38) |
missense |
probably benign |
0.00 |
R8673:Dock8
|
UTSW |
19 |
25,183,503 (GRCm38) |
missense |
probably damaging |
0.96 |
R8709:Dock8
|
UTSW |
19 |
25,078,084 (GRCm38) |
nonsense |
probably null |
|
R8834:Dock8
|
UTSW |
19 |
25,163,470 (GRCm38) |
missense |
probably benign |
0.16 |
R8991:Dock8
|
UTSW |
19 |
25,188,367 (GRCm38) |
missense |
possibly damaging |
0.82 |
R9292:Dock8
|
UTSW |
19 |
25,183,631 (GRCm38) |
splice site |
probably benign |
|
R9509:Dock8
|
UTSW |
19 |
25,095,621 (GRCm38) |
missense |
probably benign |
0.00 |
R9526:Dock8
|
UTSW |
19 |
25,188,375 (GRCm38) |
missense |
probably benign |
0.10 |
R9622:Dock8
|
UTSW |
19 |
25,121,181 (GRCm38) |
missense |
probably null |
|
R9634:Dock8
|
UTSW |
19 |
25,192,221 (GRCm38) |
missense |
probably damaging |
1.00 |
R9654:Dock8
|
UTSW |
19 |
25,147,346 (GRCm38) |
missense |
probably damaging |
1.00 |
R9670:Dock8
|
UTSW |
19 |
25,171,562 (GRCm38) |
missense |
probably null |
0.01 |
R9699:Dock8
|
UTSW |
19 |
25,156,024 (GRCm38) |
critical splice donor site |
probably null |
|
R9726:Dock8
|
UTSW |
19 |
25,177,010 (GRCm38) |
missense |
probably damaging |
0.97 |
R9765:Dock8
|
UTSW |
19 |
25,169,468 (GRCm38) |
missense |
possibly damaging |
0.94 |
X0027:Dock8
|
UTSW |
19 |
25,161,129 (GRCm38) |
missense |
probably benign |
|
Z1177:Dock8
|
UTSW |
19 |
25,155,972 (GRCm38) |
missense |
probably benign |
0.16 |
Z1177:Dock8
|
UTSW |
19 |
25,132,123 (GRCm38) |
missense |
probably benign |
0.05 |
|