Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb5 |
T |
A |
12: 118,865,089 (GRCm39) |
|
probably null |
Het |
Acot4 |
A |
C |
12: 84,088,783 (GRCm39) |
E210D |
probably damaging |
Het |
Adamts9 |
A |
C |
6: 92,882,172 (GRCm39) |
S476A |
probably damaging |
Het |
Ajm1 |
C |
CTCTA |
2: 25,469,733 (GRCm39) |
|
probably null |
Het |
Ak1 |
T |
A |
2: 32,520,385 (GRCm39) |
M61K |
probably damaging |
Het |
Ambp |
G |
T |
4: 63,072,243 (GRCm39) |
S17* |
probably null |
Het |
Anxa6 |
T |
A |
11: 54,870,326 (GRCm39) |
M662L |
probably benign |
Het |
Atp11b |
T |
C |
3: 35,868,329 (GRCm39) |
I467T |
possibly damaging |
Het |
B3gat1 |
G |
T |
9: 26,662,998 (GRCm39) |
|
probably benign |
Het |
Bccip |
T |
G |
7: 133,319,488 (GRCm39) |
I193S |
probably damaging |
Het |
Ccdc170 |
A |
G |
10: 4,491,782 (GRCm39) |
E401G |
probably damaging |
Het |
Cldn16 |
A |
G |
16: 26,296,257 (GRCm39) |
T78A |
probably damaging |
Het |
Cldn24 |
G |
T |
8: 48,275,757 (GRCm39) |
A194S |
probably benign |
Het |
Cltc |
A |
G |
11: 86,595,054 (GRCm39) |
V1348A |
possibly damaging |
Het |
Clvs1 |
T |
C |
4: 9,282,014 (GRCm39) |
|
probably null |
Het |
Csmd1 |
C |
T |
8: 16,235,341 (GRCm39) |
D1161N |
probably damaging |
Het |
Cuzd1 |
A |
G |
7: 130,918,394 (GRCm39) |
V181A |
probably damaging |
Het |
Dhx30 |
A |
G |
9: 109,917,099 (GRCm39) |
I435T |
probably damaging |
Het |
Dip2b |
T |
C |
15: 100,091,835 (GRCm39) |
V858A |
probably benign |
Het |
Dnmt3b |
C |
T |
2: 153,528,204 (GRCm39) |
T822M |
probably damaging |
Het |
Dock10 |
A |
T |
1: 80,593,082 (GRCm39) |
F97I |
possibly damaging |
Het |
Dvl2 |
T |
C |
11: 69,900,099 (GRCm39) |
L631P |
probably damaging |
Het |
Faf2 |
T |
A |
13: 54,789,419 (GRCm39) |
|
probably null |
Het |
Fat2 |
T |
A |
11: 55,200,167 (GRCm39) |
H969L |
probably benign |
Het |
Fsip2 |
T |
A |
2: 82,815,544 (GRCm39) |
V3759E |
probably benign |
Het |
Gm10985 |
A |
C |
3: 53,752,674 (GRCm39) |
Y19S |
probably damaging |
Het |
Gm973 |
T |
C |
1: 59,669,328 (GRCm39) |
L793P |
probably damaging |
Het |
H2-M1 |
A |
G |
17: 36,981,327 (GRCm39) |
I236T |
probably damaging |
Het |
Hif1a |
A |
T |
12: 73,992,337 (GRCm39) |
R765* |
probably null |
Het |
Htt |
A |
G |
5: 34,940,111 (GRCm39) |
K77E |
probably damaging |
Het |
Ift172 |
G |
T |
5: 31,423,304 (GRCm39) |
Q826K |
probably benign |
Het |
Inafm1 |
C |
T |
7: 16,007,086 (GRCm39) |
A44T |
probably damaging |
Het |
Kctd4 |
A |
G |
14: 76,200,748 (GRCm39) |
T240A |
probably damaging |
Het |
Klk1 |
A |
T |
7: 43,878,883 (GRCm39) |
I124F |
probably damaging |
Het |
Krbox5 |
A |
G |
13: 67,981,986 (GRCm39) |
Q66R |
possibly damaging |
Het |
Kremen1 |
T |
C |
11: 5,145,051 (GRCm39) |
T442A |
probably benign |
Het |
Mei4 |
T |
A |
9: 81,907,574 (GRCm39) |
D202E |
probably benign |
Het |
Mest |
T |
A |
6: 30,746,286 (GRCm39) |
D284E |
probably damaging |
Het |
Nsfl1c |
T |
A |
2: 151,344,940 (GRCm39) |
Y95* |
probably null |
Het |
Or10al5 |
T |
A |
17: 38,063,315 (GRCm39) |
V190D |
possibly damaging |
Het |
Or10am5 |
T |
C |
7: 6,517,550 (GRCm39) |
M293V |
probably damaging |
Het |
Or2ak4 |
T |
A |
11: 58,648,783 (GRCm39) |
C97* |
probably null |
Het |
Or4k38 |
T |
G |
2: 111,165,659 (GRCm39) |
I255L |
probably benign |
Het |
Pgm1 |
T |
A |
4: 99,820,763 (GRCm39) |
I220N |
probably damaging |
Het |
Pirt |
T |
A |
11: 66,816,719 (GRCm39) |
V10E |
possibly damaging |
Het |
Prl7d1 |
C |
A |
13: 27,898,454 (GRCm39) |
M19I |
probably benign |
Het |
Samhd1 |
T |
C |
2: 156,949,417 (GRCm39) |
N490D |
probably benign |
Het |
Scn2a |
C |
A |
2: 65,519,013 (GRCm39) |
S413* |
probably null |
Het |
Serpinb6e |
A |
T |
13: 34,016,337 (GRCm39) |
|
probably null |
Het |
Slitrk5 |
A |
G |
14: 111,917,726 (GRCm39) |
D450G |
probably benign |
Het |
Tchh |
A |
G |
3: 93,350,718 (GRCm39) |
T53A |
probably damaging |
Het |
Tmem44 |
A |
T |
16: 30,362,039 (GRCm39) |
|
probably null |
Het |
Tpm3-rs7 |
A |
G |
14: 113,552,448 (GRCm39) |
E114G |
possibly damaging |
Het |
Treml2 |
A |
G |
17: 48,609,925 (GRCm39) |
Y119C |
probably damaging |
Het |
Ubxn1 |
T |
A |
19: 8,851,245 (GRCm39) |
|
probably null |
Het |
Vmn2r84 |
A |
T |
10: 130,222,147 (GRCm39) |
M691K |
probably benign |
Het |
Vmn2r97 |
A |
T |
17: 19,168,193 (GRCm39) |
I816F |
possibly damaging |
Het |
Was |
GCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTC |
GCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTC |
X: 7,952,450 (GRCm39) |
|
probably benign |
Het |
Wfdc2 |
T |
C |
2: 164,405,070 (GRCm39) |
|
probably null |
Het |
Zscan4-ps3 |
T |
C |
7: 11,346,986 (GRCm39) |
S341P |
probably 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 |
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 |
|