Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810021J22Rik |
T |
A |
11: 58,770,940 (GRCm39) |
S141T |
probably benign |
Het |
Afap1l2 |
A |
G |
19: 56,906,408 (GRCm39) |
|
probably null |
Het |
Aox1 |
C |
T |
1: 58,346,566 (GRCm39) |
Q567* |
probably null |
Het |
Aqp4 |
T |
A |
18: 15,526,648 (GRCm39) |
M278L |
probably benign |
Het |
Atp23 |
A |
C |
10: 126,723,538 (GRCm39) |
L188R |
probably benign |
Het |
Catsperg1 |
C |
T |
7: 28,905,782 (GRCm39) |
G215D |
probably benign |
Het |
Cavin4 |
T |
C |
4: 48,663,824 (GRCm39) |
V68A |
possibly damaging |
Het |
Ccl4 |
T |
C |
11: 83,553,504 (GRCm39) |
S6P |
unknown |
Het |
Cfap46 |
T |
C |
7: 139,260,747 (GRCm39) |
E117G |
probably damaging |
Het |
Cfhr4 |
A |
G |
1: 139,701,662 (GRCm39) |
|
probably null |
Het |
Chek1 |
A |
G |
9: 36,625,788 (GRCm39) |
S286P |
possibly damaging |
Het |
Cntn4 |
G |
A |
6: 106,321,747 (GRCm39) |
V35I |
probably benign |
Het |
Cntn4 |
C |
A |
6: 106,483,153 (GRCm39) |
P236Q |
probably benign |
Het |
Cyp2d40 |
C |
A |
15: 82,645,753 (GRCm39) |
G84V |
probably benign |
Het |
Dnah12 |
A |
T |
14: 26,427,989 (GRCm39) |
H205L |
possibly damaging |
Het |
Drg1 |
T |
C |
11: 3,216,292 (GRCm39) |
K7E |
possibly damaging |
Het |
Eloa |
G |
A |
4: 135,737,133 (GRCm39) |
P488S |
probably damaging |
Het |
Evi5 |
G |
A |
5: 107,968,387 (GRCm39) |
R187* |
probably null |
Het |
Fam53a |
T |
A |
5: 33,758,219 (GRCm39) |
L301F |
probably damaging |
Het |
Fmnl3 |
T |
C |
15: 99,235,534 (GRCm39) |
K63E |
probably damaging |
Het |
Gast |
C |
A |
11: 100,227,438 (GRCm39) |
Q44K |
probably benign |
Het |
Gng10 |
T |
A |
4: 59,035,257 (GRCm39) |
V7E |
probably benign |
Het |
Gtf3c5 |
G |
A |
2: 28,460,474 (GRCm39) |
T375I |
probably benign |
Het |
Haus5 |
C |
T |
7: 30,358,401 (GRCm39) |
W298* |
probably null |
Het |
Hspa14 |
A |
T |
2: 3,490,109 (GRCm39) |
|
probably null |
Het |
Kcna3 |
T |
C |
3: 106,943,740 (GRCm39) |
M1T |
probably null |
Het |
Kcnj15 |
T |
G |
16: 95,097,095 (GRCm39) |
L239R |
probably damaging |
Het |
Klhl2 |
G |
T |
8: 65,212,842 (GRCm39) |
D232E |
probably benign |
Het |
Lamb3 |
A |
T |
1: 193,017,782 (GRCm39) |
I888F |
probably damaging |
Het |
Lars1 |
C |
A |
18: 42,350,551 (GRCm39) |
M919I |
probably benign |
Het |
Lfng |
T |
C |
5: 140,598,522 (GRCm39) |
V247A |
possibly damaging |
Het |
Lrp1b |
C |
T |
2: 41,679,045 (GRCm39) |
A16T |
probably benign |
Het |
Mamdc2 |
A |
T |
19: 23,341,270 (GRCm39) |
I235N |
probably damaging |
Het |
Map9 |
T |
A |
3: 82,290,612 (GRCm39) |
L492Q |
probably damaging |
Het |
Mcpt8 |
A |
G |
14: 56,322,604 (GRCm39) |
V14A |
possibly damaging |
Het |
Myo1b |
T |
C |
1: 51,807,810 (GRCm39) |
K823R |
probably null |
Het |
Nbea |
G |
T |
3: 55,944,570 (GRCm39) |
T598K |
probably damaging |
Het |
Nrcam |
C |
A |
12: 44,619,083 (GRCm39) |
H877N |
probably benign |
Het |
Nrxn2 |
T |
C |
19: 6,581,322 (GRCm39) |
|
probably null |
Het |
Nwd2 |
A |
T |
5: 63,957,596 (GRCm39) |
I309F |
possibly damaging |
Het |
Phyhd1 |
G |
A |
2: 30,164,736 (GRCm39) |
|
probably null |
Het |
Pkp2 |
C |
T |
16: 16,043,933 (GRCm39) |
T229I |
probably damaging |
Het |
Plagl2 |
G |
A |
2: 153,074,611 (GRCm39) |
P97S |
probably benign |
Het |
Plekhh2 |
C |
A |
17: 84,874,294 (GRCm39) |
N526K |
probably benign |
Het |
Plin4 |
A |
G |
17: 56,410,261 (GRCm39) |
L1217P |
probably benign |
Het |
Polr3e |
T |
C |
7: 120,527,222 (GRCm39) |
S67P |
possibly damaging |
Het |
Postn |
A |
G |
3: 54,292,703 (GRCm39) |
K757E |
probably benign |
Het |
Prpf39 |
T |
A |
12: 65,089,587 (GRCm39) |
|
probably null |
Het |
Ptprg |
C |
T |
14: 12,166,832 (GRCm38) |
T745I |
probably damaging |
Het |
Pxylp1 |
C |
G |
9: 96,707,307 (GRCm39) |
A292P |
probably damaging |
Het |
Rpl35 |
G |
T |
2: 38,891,754 (GRCm39) |
D82E |
possibly damaging |
Het |
Slc9a1 |
G |
A |
4: 133,149,519 (GRCm39) |
V782I |
possibly damaging |
Het |
Syn2 |
T |
A |
6: 115,240,875 (GRCm39) |
M415K |
possibly damaging |
Het |
Tmem117 |
A |
C |
15: 94,909,324 (GRCm39) |
I246L |
probably benign |
Het |
Tmem221 |
A |
T |
8: 72,011,428 (GRCm39) |
V9E |
probably damaging |
Het |
Trav13-5 |
A |
G |
14: 54,033,399 (GRCm39) |
T103A |
probably damaging |
Het |
Ubxn7 |
T |
A |
16: 32,191,007 (GRCm39) |
|
probably null |
Het |
Vmn2r101 |
G |
T |
17: 19,810,112 (GRCm39) |
M299I |
possibly damaging |
Het |
Vmn2r103 |
T |
A |
17: 20,014,344 (GRCm39) |
S379T |
probably damaging |
Het |
Vmn2r109 |
T |
C |
17: 20,761,440 (GRCm39) |
N639S |
probably benign |
Het |
Wdr26 |
T |
C |
1: 181,030,771 (GRCm39) |
|
|
Het |
Zfp109 |
T |
A |
7: 23,928,308 (GRCm39) |
Y367F |
probably damaging |
Het |
Zfp143 |
G |
A |
7: 109,685,338 (GRCm39) |
C389Y |
probably damaging |
Het |
Zfp553 |
G |
T |
7: 126,836,064 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Dock1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00484:Dock1
|
APN |
7 |
134,748,260 (GRCm39) |
splice site |
probably benign |
|
IGL01319:Dock1
|
APN |
7 |
134,391,007 (GRCm39) |
missense |
probably benign |
|
IGL01390:Dock1
|
APN |
7 |
134,346,776 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01394:Dock1
|
APN |
7 |
134,367,945 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01489:Dock1
|
APN |
7 |
134,601,050 (GRCm39) |
splice site |
probably benign |
|
IGL01505:Dock1
|
APN |
7 |
134,760,239 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01586:Dock1
|
APN |
7 |
134,355,106 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01637:Dock1
|
APN |
7 |
134,739,542 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01649:Dock1
|
APN |
7 |
134,379,139 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01652:Dock1
|
APN |
7 |
134,379,226 (GRCm39) |
splice site |
probably benign |
|
IGL01859:Dock1
|
APN |
7 |
134,678,890 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02068:Dock1
|
APN |
7 |
134,373,277 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02168:Dock1
|
APN |
7 |
134,678,860 (GRCm39) |
splice site |
probably benign |
|
IGL02200:Dock1
|
APN |
7 |
134,346,000 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02244:Dock1
|
APN |
7 |
134,379,174 (GRCm39) |
nonsense |
probably null |
|
IGL02285:Dock1
|
APN |
7 |
134,683,649 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02319:Dock1
|
APN |
7 |
134,374,178 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02334:Dock1
|
APN |
7 |
134,747,294 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02338:Dock1
|
APN |
7 |
134,734,804 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02351:Dock1
|
APN |
7 |
134,710,548 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02358:Dock1
|
APN |
7 |
134,710,548 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02607:Dock1
|
APN |
7 |
134,453,242 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02638:Dock1
|
APN |
7 |
134,748,209 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02724:Dock1
|
APN |
7 |
134,765,082 (GRCm39) |
missense |
probably benign |
|
IGL02820:Dock1
|
APN |
7 |
134,768,944 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02950:Dock1
|
APN |
7 |
134,331,753 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02993:Dock1
|
APN |
7 |
134,346,027 (GRCm39) |
missense |
probably benign |
|
IGL03000:Dock1
|
APN |
7 |
134,390,969 (GRCm39) |
missense |
probably benign |
0.17 |
IGL03092:Dock1
|
APN |
7 |
134,366,945 (GRCm39) |
splice site |
probably benign |
|
IGL03131:Dock1
|
APN |
7 |
134,475,912 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03136:Dock1
|
APN |
7 |
134,770,118 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03210:Dock1
|
APN |
7 |
134,358,668 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL03220:Dock1
|
APN |
7 |
134,710,251 (GRCm39) |
critical splice donor site |
probably null |
|
P0028:Dock1
|
UTSW |
7 |
134,601,053 (GRCm39) |
splice site |
probably benign |
|
PIT4453001:Dock1
|
UTSW |
7 |
134,754,029 (GRCm39) |
missense |
probably benign |
|
R0003:Dock1
|
UTSW |
7 |
134,331,793 (GRCm39) |
splice site |
probably benign |
|
R0058:Dock1
|
UTSW |
7 |
134,710,490 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0058:Dock1
|
UTSW |
7 |
134,710,490 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0062:Dock1
|
UTSW |
7 |
134,379,224 (GRCm39) |
splice site |
probably null |
|
R0062:Dock1
|
UTSW |
7 |
134,379,224 (GRCm39) |
splice site |
probably null |
|
R0179:Dock1
|
UTSW |
7 |
134,700,566 (GRCm39) |
missense |
probably damaging |
0.99 |
R0180:Dock1
|
UTSW |
7 |
134,700,566 (GRCm39) |
missense |
probably damaging |
0.99 |
R0347:Dock1
|
UTSW |
7 |
134,365,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R0399:Dock1
|
UTSW |
7 |
134,765,171 (GRCm39) |
missense |
probably benign |
0.00 |
R0457:Dock1
|
UTSW |
7 |
134,739,874 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0480:Dock1
|
UTSW |
7 |
134,339,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R0521:Dock1
|
UTSW |
7 |
134,745,507 (GRCm39) |
missense |
probably benign |
0.21 |
R0792:Dock1
|
UTSW |
7 |
134,475,879 (GRCm39) |
missense |
probably benign |
0.02 |
R1136:Dock1
|
UTSW |
7 |
134,449,902 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1224:Dock1
|
UTSW |
7 |
134,710,548 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1267:Dock1
|
UTSW |
7 |
134,348,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R1373:Dock1
|
UTSW |
7 |
134,768,904 (GRCm39) |
missense |
probably benign |
0.01 |
R1401:Dock1
|
UTSW |
7 |
134,735,665 (GRCm39) |
nonsense |
probably null |
|
R1454:Dock1
|
UTSW |
7 |
134,453,338 (GRCm39) |
splice site |
probably benign |
|
R1465:Dock1
|
UTSW |
7 |
134,384,138 (GRCm39) |
missense |
probably benign |
0.00 |
R1465:Dock1
|
UTSW |
7 |
134,384,138 (GRCm39) |
missense |
probably benign |
0.00 |
R1523:Dock1
|
UTSW |
7 |
134,345,976 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1643:Dock1
|
UTSW |
7 |
134,700,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R1659:Dock1
|
UTSW |
7 |
134,390,972 (GRCm39) |
missense |
probably damaging |
0.98 |
R1793:Dock1
|
UTSW |
7 |
134,700,456 (GRCm39) |
splice site |
probably null |
|
R1864:Dock1
|
UTSW |
7 |
134,748,236 (GRCm39) |
missense |
probably benign |
0.07 |
R1911:Dock1
|
UTSW |
7 |
134,601,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R2567:Dock1
|
UTSW |
7 |
134,747,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R3816:Dock1
|
UTSW |
7 |
134,346,015 (GRCm39) |
nonsense |
probably null |
|
R3971:Dock1
|
UTSW |
7 |
134,348,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R4063:Dock1
|
UTSW |
7 |
134,717,021 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4163:Dock1
|
UTSW |
7 |
134,346,051 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4271:Dock1
|
UTSW |
7 |
134,335,783 (GRCm39) |
missense |
probably damaging |
0.99 |
R4684:Dock1
|
UTSW |
7 |
134,326,138 (GRCm39) |
nonsense |
probably null |
|
R4717:Dock1
|
UTSW |
7 |
134,449,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R4725:Dock1
|
UTSW |
7 |
134,346,743 (GRCm39) |
nonsense |
probably null |
|
R4788:Dock1
|
UTSW |
7 |
134,747,213 (GRCm39) |
missense |
probably damaging |
0.98 |
R4869:Dock1
|
UTSW |
7 |
134,335,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R4889:Dock1
|
UTSW |
7 |
134,346,705 (GRCm39) |
missense |
probably benign |
0.02 |
R4953:Dock1
|
UTSW |
7 |
134,754,017 (GRCm39) |
missense |
probably benign |
0.34 |
R5031:Dock1
|
UTSW |
7 |
134,753,975 (GRCm39) |
missense |
probably benign |
0.02 |
R5161:Dock1
|
UTSW |
7 |
134,335,791 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5168:Dock1
|
UTSW |
7 |
134,720,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R5212:Dock1
|
UTSW |
7 |
134,390,923 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5648:Dock1
|
UTSW |
7 |
134,348,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R5685:Dock1
|
UTSW |
7 |
134,374,091 (GRCm39) |
missense |
probably benign |
0.19 |
R5834:Dock1
|
UTSW |
7 |
134,365,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R6181:Dock1
|
UTSW |
7 |
134,760,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R6406:Dock1
|
UTSW |
7 |
134,747,215 (GRCm39) |
missense |
probably benign |
0.26 |
R6425:Dock1
|
UTSW |
7 |
134,765,110 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6489:Dock1
|
UTSW |
7 |
134,592,270 (GRCm39) |
missense |
probably damaging |
0.99 |
R6616:Dock1
|
UTSW |
7 |
134,710,221 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6706:Dock1
|
UTSW |
7 |
134,735,615 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6766:Dock1
|
UTSW |
7 |
134,358,522 (GRCm39) |
splice site |
probably null |
|
R6861:Dock1
|
UTSW |
7 |
134,373,207 (GRCm39) |
missense |
probably benign |
0.00 |
R6985:Dock1
|
UTSW |
7 |
134,765,132 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7259:Dock1
|
UTSW |
7 |
134,384,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R7285:Dock1
|
UTSW |
7 |
134,346,737 (GRCm39) |
missense |
probably benign |
0.01 |
R7471:Dock1
|
UTSW |
7 |
134,765,072 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7497:Dock1
|
UTSW |
7 |
134,367,003 (GRCm39) |
missense |
probably benign |
|
R7691:Dock1
|
UTSW |
7 |
134,739,886 (GRCm39) |
critical splice donor site |
probably null |
|
R7732:Dock1
|
UTSW |
7 |
134,346,699 (GRCm39) |
missense |
probably benign |
0.01 |
R7818:Dock1
|
UTSW |
7 |
134,365,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R7918:Dock1
|
UTSW |
7 |
134,747,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R7960:Dock1
|
UTSW |
7 |
134,678,917 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7961:Dock1
|
UTSW |
7 |
134,346,786 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7985:Dock1
|
UTSW |
7 |
134,348,683 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8009:Dock1
|
UTSW |
7 |
134,346,786 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8060:Dock1
|
UTSW |
7 |
134,592,358 (GRCm39) |
splice site |
probably benign |
|
R8060:Dock1
|
UTSW |
7 |
134,770,132 (GRCm39) |
missense |
probably benign |
|
R8061:Dock1
|
UTSW |
7 |
134,374,052 (GRCm39) |
missense |
probably benign |
0.00 |
R8101:Dock1
|
UTSW |
7 |
134,601,017 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8405:Dock1
|
UTSW |
7 |
134,379,192 (GRCm39) |
missense |
probably benign |
0.04 |
R8508:Dock1
|
UTSW |
7 |
134,384,138 (GRCm39) |
missense |
probably benign |
0.00 |
R8803:Dock1
|
UTSW |
7 |
134,475,816 (GRCm39) |
missense |
probably benign |
0.28 |
R9007:Dock1
|
UTSW |
7 |
134,500,825 (GRCm39) |
intron |
probably benign |
|
R9026:Dock1
|
UTSW |
7 |
134,720,746 (GRCm39) |
missense |
probably damaging |
0.97 |
R9111:Dock1
|
UTSW |
7 |
134,601,017 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9359:Dock1
|
UTSW |
7 |
134,770,125 (GRCm39) |
missense |
probably benign |
|
R9398:Dock1
|
UTSW |
7 |
134,774,228 (GRCm39) |
missense |
probably damaging |
0.99 |
R9403:Dock1
|
UTSW |
7 |
134,770,125 (GRCm39) |
missense |
probably benign |
|
R9408:Dock1
|
UTSW |
7 |
134,717,065 (GRCm39) |
missense |
probably damaging |
0.99 |
R9476:Dock1
|
UTSW |
7 |
134,592,279 (GRCm39) |
missense |
probably benign |
0.10 |
R9478:Dock1
|
UTSW |
7 |
134,367,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R9510:Dock1
|
UTSW |
7 |
134,592,279 (GRCm39) |
missense |
probably benign |
0.10 |
R9544:Dock1
|
UTSW |
7 |
134,348,186 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9605:Dock1
|
UTSW |
7 |
134,384,141 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9657:Dock1
|
UTSW |
7 |
134,339,429 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9767:Dock1
|
UTSW |
7 |
134,342,796 (GRCm39) |
missense |
possibly damaging |
0.68 |
X0062:Dock1
|
UTSW |
7 |
134,710,180 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dock1
|
UTSW |
7 |
134,406,276 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Dock1
|
UTSW |
7 |
134,384,129 (GRCm39) |
nonsense |
probably null |
|
|