Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
G |
A |
6: 128,522,030 (GRCm39) |
T1264I |
probably damaging |
Het |
Aadac |
T |
A |
3: 59,946,986 (GRCm39) |
V228E |
probably benign |
Het |
Abca4 |
A |
T |
3: 121,931,274 (GRCm39) |
R1436W |
probably benign |
Het |
Abo |
A |
G |
2: 26,738,287 (GRCm39) |
L39S |
probably benign |
Het |
Acnat1 |
T |
A |
4: 49,447,773 (GRCm39) |
R269S |
probably benign |
Het |
Adap2 |
T |
C |
11: 80,045,942 (GRCm39) |
V74A |
probably damaging |
Het |
Ahctf1 |
C |
A |
1: 179,603,638 (GRCm39) |
A803S |
possibly damaging |
Het |
Ak6 |
A |
G |
13: 100,792,003 (GRCm39) |
S149G |
probably benign |
Het |
Ank |
T |
C |
15: 27,591,588 (GRCm39) |
V444A |
probably damaging |
Het |
Armt1 |
AC |
A |
10: 4,400,848 (GRCm39) |
|
probably null |
Het |
Atf7 |
A |
C |
15: 102,462,286 (GRCm39) |
V112G |
probably damaging |
Het |
Brca2 |
A |
G |
5: 150,464,982 (GRCm39) |
Y1582C |
probably damaging |
Het |
Bricd5 |
G |
T |
17: 24,693,083 (GRCm39) |
|
probably benign |
Het |
Bsn |
C |
A |
9: 108,016,652 (GRCm39) |
E120* |
probably null |
Het |
Cacna1g |
T |
G |
11: 94,321,050 (GRCm39) |
N1348T |
probably damaging |
Het |
Ccnc |
T |
G |
4: 21,746,776 (GRCm39) |
|
probably null |
Het |
Cd163 |
A |
G |
6: 124,297,497 (GRCm39) |
D881G |
probably benign |
Het |
Cep295 |
G |
A |
9: 15,244,619 (GRCm39) |
P1279L |
probably benign |
Het |
Cic |
G |
A |
7: 24,971,414 (GRCm39) |
V382I |
possibly damaging |
Het |
Cyp21a1 |
G |
A |
17: 35,020,860 (GRCm39) |
S453F |
probably damaging |
Het |
D16Ertd472e |
A |
T |
16: 78,344,646 (GRCm39) |
I154N |
probably benign |
Het |
Dbf4 |
A |
G |
5: 8,447,764 (GRCm39) |
V482A |
possibly damaging |
Het |
Dchs2 |
G |
A |
3: 83,192,573 (GRCm39) |
V1673M |
probably benign |
Het |
Dctd |
T |
A |
8: 48,590,385 (GRCm39) |
C119S |
probably damaging |
Het |
Efcab3 |
T |
A |
11: 104,621,255 (GRCm39) |
|
probably null |
Het |
Eya4 |
A |
T |
10: 22,999,805 (GRCm39) |
M386K |
|
Het |
Fbxw19 |
T |
A |
9: 109,315,101 (GRCm39) |
M154L |
probably benign |
Het |
Frmpd1 |
T |
A |
4: 45,279,182 (GRCm39) |
S636T |
probably benign |
Het |
Glb1l |
A |
T |
1: 75,177,683 (GRCm39) |
Y412N |
probably damaging |
Het |
Gnb5 |
T |
A |
9: 75,218,696 (GRCm39) |
L7Q |
probably damaging |
Het |
Gpr19 |
C |
T |
6: 134,864,704 (GRCm39) |
V3M |
unknown |
Het |
Hivep2 |
A |
G |
10: 14,007,505 (GRCm39) |
T1368A |
probably damaging |
Het |
Hmx3 |
A |
T |
7: 131,146,102 (GRCm39) |
Q270L |
probably damaging |
Het |
Il1rap |
A |
T |
16: 26,533,675 (GRCm39) |
I524F |
possibly damaging |
Het |
Mettl17 |
G |
A |
14: 52,125,491 (GRCm39) |
G198D |
probably damaging |
Het |
Mga |
T |
A |
2: 119,765,999 (GRCm39) |
I1421N |
possibly damaging |
Het |
Myb |
T |
A |
10: 21,026,275 (GRCm39) |
Q231L |
probably benign |
Het |
Myef2l |
T |
A |
3: 10,154,407 (GRCm39) |
M392K |
probably benign |
Het |
Myf5 |
G |
A |
10: 107,321,527 (GRCm39) |
T89I |
probably damaging |
Het |
Nup214 |
T |
A |
2: 31,937,523 (GRCm39) |
L1999Q |
probably damaging |
Het |
Or10aa3 |
T |
C |
1: 173,878,329 (GRCm39) |
L130P |
|
Het |
Or1ad6 |
T |
A |
11: 50,860,613 (GRCm39) |
L256Q |
probably damaging |
Het |
Or4a76 |
A |
G |
2: 89,460,388 (GRCm39) |
Y285H |
probably damaging |
Het |
Or51t4 |
A |
T |
7: 102,598,443 (GRCm39) |
H257L |
probably damaging |
Het |
Or5w19 |
G |
A |
2: 87,698,379 (GRCm39) |
G15R |
probably damaging |
Het |
Or7a36 |
A |
G |
10: 78,820,220 (GRCm39) |
M199V |
probably benign |
Het |
Otog |
A |
T |
7: 45,916,721 (GRCm39) |
D886V |
possibly damaging |
Het |
Pde7a |
A |
C |
3: 19,287,958 (GRCm39) |
V237G |
possibly damaging |
Het |
Pigs |
T |
C |
11: 78,230,213 (GRCm39) |
Y327H |
probably damaging |
Het |
Pkd2l2 |
T |
C |
18: 34,563,383 (GRCm39) |
V478A |
probably damaging |
Het |
Pnrc1 |
C |
A |
4: 33,246,488 (GRCm39) |
G157V |
probably damaging |
Het |
Poglut1 |
G |
T |
16: 38,347,137 (GRCm39) |
S343R |
probably benign |
Het |
Ppwd1 |
A |
G |
13: 104,346,155 (GRCm39) |
M500T |
possibly damaging |
Het |
Pyy |
C |
T |
11: 101,998,111 (GRCm39) |
G23E |
probably damaging |
Het |
Ripor3 |
T |
A |
2: 167,831,238 (GRCm39) |
D521V |
probably benign |
Het |
Rnpepl1 |
T |
C |
1: 92,845,424 (GRCm39) |
S448P |
probably benign |
Het |
Sash1 |
G |
A |
10: 8,637,994 (GRCm39) |
|
probably benign |
Het |
Sbf2 |
T |
C |
7: 110,040,702 (GRCm39) |
Q375R |
possibly damaging |
Het |
Synj1 |
C |
T |
16: 90,741,740 (GRCm39) |
C1252Y |
probably benign |
Het |
Tenm2 |
A |
T |
11: 35,960,246 (GRCm39) |
L1027Q |
probably damaging |
Het |
Tep1 |
A |
G |
14: 51,074,637 (GRCm39) |
V1796A |
possibly damaging |
Het |
Timp3 |
A |
T |
10: 86,136,782 (GRCm39) |
E22V |
possibly damaging |
Het |
Tlk1 |
A |
C |
2: 70,617,219 (GRCm39) |
|
probably null |
Het |
Tmco1 |
C |
A |
1: 167,141,700 (GRCm39) |
T69K |
|
Het |
Topaz1 |
T |
A |
9: 122,626,728 (GRCm39) |
M1452K |
probably benign |
Het |
Tsc22d2 |
T |
C |
3: 58,367,453 (GRCm39) |
Y668H |
unknown |
Het |
Uri1 |
A |
T |
7: 37,669,031 (GRCm39) |
D153E |
probably benign |
Het |
Vmn1r169 |
A |
T |
7: 23,277,342 (GRCm39) |
T245S |
probably damaging |
Het |
Vmn1r60 |
A |
G |
7: 5,547,918 (GRCm39) |
Y61H |
|
Het |
Zfp541 |
A |
T |
7: 15,806,139 (GRCm39) |
E91D |
probably damaging |
Het |
Zfp946 |
A |
G |
17: 22,673,569 (GRCm39) |
N108D |
possibly damaging |
Het |
Zpr1 |
T |
C |
9: 46,186,747 (GRCm39) |
L194P |
probably damaging |
Het |
Zzef1 |
T |
A |
11: 72,755,653 (GRCm39) |
N1027K |
possibly damaging |
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 |
R6334:Dock1
|
UTSW |
7 |
134,453,305 (GRCm39) |
missense |
probably benign |
0.01 |
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 |
|
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 |
|
|