Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ache |
T |
G |
5: 137,289,104 (GRCm39) |
V270G |
probably damaging |
Het |
Acss1 |
A |
T |
2: 150,470,459 (GRCm39) |
W394R |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,330,791 (GRCm39) |
V6088A |
possibly damaging |
Het |
Ankrd36 |
A |
G |
11: 5,580,691 (GRCm39) |
|
probably benign |
Het |
Anxa1 |
A |
T |
19: 20,361,141 (GRCm39) |
Y84N |
probably damaging |
Het |
Arnt2 |
G |
A |
7: 83,996,738 (GRCm39) |
R63C |
probably damaging |
Het |
Avpr1b |
A |
G |
1: 131,527,524 (GRCm39) |
T16A |
probably benign |
Het |
Bpifb1 |
G |
A |
2: 154,048,460 (GRCm39) |
R165H |
possibly damaging |
Het |
Cables1 |
A |
G |
18: 12,056,470 (GRCm39) |
E316G |
possibly damaging |
Het |
Cadm1 |
A |
T |
9: 47,761,629 (GRCm39) |
I427L |
probably damaging |
Het |
Ccdc97 |
T |
C |
7: 25,415,405 (GRCm39) |
D86G |
probably benign |
Het |
Cgnl1 |
C |
A |
9: 71,548,679 (GRCm39) |
D1081Y |
probably damaging |
Het |
Cgnl1 |
T |
A |
9: 71,632,122 (GRCm39) |
R410W |
probably damaging |
Het |
Cntnap4 |
G |
A |
8: 113,512,416 (GRCm39) |
E593K |
probably damaging |
Het |
Dazap1 |
T |
C |
10: 80,097,415 (GRCm39) |
|
probably benign |
Het |
Dip2b |
A |
G |
15: 100,113,121 (GRCm39) |
E1512G |
probably benign |
Het |
Dock5 |
A |
T |
14: 68,018,485 (GRCm39) |
F1230Y |
probably benign |
Het |
Dym |
G |
A |
18: 75,176,243 (GRCm39) |
E15K |
possibly damaging |
Het |
Ednra |
C |
A |
8: 78,393,951 (GRCm39) |
|
probably null |
Het |
Faf1 |
A |
G |
4: 109,593,821 (GRCm39) |
Q133R |
probably benign |
Het |
Fbxw28 |
A |
G |
9: 109,157,279 (GRCm39) |
I323T |
probably benign |
Het |
Fcer2a |
T |
C |
8: 3,738,111 (GRCm39) |
|
probably benign |
Het |
Fmo2 |
A |
T |
1: 162,713,893 (GRCm39) |
S204R |
probably benign |
Het |
Frmd4b |
A |
G |
6: 97,400,460 (GRCm39) |
V63A |
probably damaging |
Het |
Fzd8 |
G |
A |
18: 9,213,985 (GRCm39) |
A356T |
possibly damaging |
Het |
Ghitm |
A |
G |
14: 36,853,549 (GRCm39) |
L97P |
probably damaging |
Het |
Gins4 |
A |
G |
8: 23,719,526 (GRCm39) |
|
probably benign |
Het |
Golga3 |
T |
A |
5: 110,350,643 (GRCm39) |
F766Y |
possibly damaging |
Het |
Hapln1 |
T |
C |
13: 89,755,997 (GRCm39) |
I267T |
probably benign |
Het |
Helz |
A |
T |
11: 107,563,384 (GRCm39) |
|
probably benign |
Het |
Herc2 |
T |
C |
7: 55,820,231 (GRCm39) |
V2851A |
possibly damaging |
Het |
Igkv8-18 |
G |
A |
6: 70,333,105 (GRCm39) |
|
probably benign |
Het |
Igll1 |
A |
T |
16: 16,681,740 (GRCm39) |
V5E |
probably benign |
Het |
Irx3 |
T |
C |
8: 92,527,168 (GRCm39) |
T179A |
possibly damaging |
Het |
Kif16b |
A |
G |
2: 142,699,225 (GRCm39) |
|
probably null |
Het |
Limk1 |
A |
T |
5: 134,688,725 (GRCm39) |
W507R |
probably damaging |
Het |
Marf1 |
C |
T |
16: 13,960,398 (GRCm39) |
A549T |
probably damaging |
Het |
Mtif3 |
C |
A |
5: 146,893,731 (GRCm39) |
V159F |
probably benign |
Het |
Myh6 |
C |
T |
14: 55,200,861 (GRCm39) |
R169Q |
probably damaging |
Het |
Ncoa7 |
T |
A |
10: 30,523,537 (GRCm39) |
D887V |
probably damaging |
Het |
Obox7 |
C |
T |
7: 14,398,313 (GRCm39) |
P76S |
probably benign |
Het |
Or10ak12 |
A |
G |
4: 118,666,677 (GRCm39) |
M128T |
probably benign |
Het |
Or11l3 |
A |
T |
11: 58,516,494 (GRCm39) |
I126N |
probably damaging |
Het |
Pitpnm2 |
G |
A |
5: 124,262,093 (GRCm39) |
A862V |
probably damaging |
Het |
Pkd1 |
G |
C |
17: 24,783,677 (GRCm39) |
A162P |
probably benign |
Het |
Plce1 |
A |
G |
19: 38,513,628 (GRCm39) |
D309G |
possibly damaging |
Het |
Plk4 |
T |
C |
3: 40,760,307 (GRCm39) |
V401A |
probably benign |
Het |
Prdx3 |
T |
C |
19: 60,862,950 (GRCm39) |
|
probably benign |
Het |
Prrc2c |
C |
T |
1: 162,526,453 (GRCm39) |
V253I |
unknown |
Het |
Ranbp2 |
T |
A |
10: 58,316,353 (GRCm39) |
S2358T |
probably damaging |
Het |
Setd2 |
T |
A |
9: 110,423,494 (GRCm39) |
V2183E |
probably damaging |
Het |
Sgsm1 |
T |
A |
5: 113,432,953 (GRCm39) |
S232C |
probably damaging |
Het |
Skint6 |
A |
T |
4: 112,904,012 (GRCm39) |
|
probably benign |
Het |
Slc15a2 |
A |
G |
16: 36,574,909 (GRCm39) |
I531T |
probably benign |
Het |
Slc36a1 |
C |
T |
11: 55,112,820 (GRCm39) |
|
probably benign |
Het |
Sorbs2 |
C |
A |
8: 46,249,300 (GRCm39) |
D831E |
probably damaging |
Het |
Sorbs2 |
T |
A |
8: 46,238,291 (GRCm39) |
|
probably null |
Het |
Sptan1 |
T |
C |
2: 29,883,708 (GRCm39) |
|
probably null |
Het |
Stam |
T |
C |
2: 14,142,952 (GRCm39) |
C336R |
probably damaging |
Het |
Stil |
G |
T |
4: 114,898,495 (GRCm39) |
A1042S |
probably damaging |
Het |
Stxbp5l |
T |
A |
16: 36,962,736 (GRCm39) |
D773V |
possibly damaging |
Het |
Sugct |
A |
T |
13: 17,847,166 (GRCm39) |
L39Q |
probably damaging |
Het |
Tep1 |
A |
G |
14: 51,071,522 (GRCm39) |
V2041A |
possibly damaging |
Het |
Tex15 |
C |
T |
8: 34,071,530 (GRCm39) |
|
probably benign |
Het |
Tlr9 |
T |
G |
9: 106,102,164 (GRCm39) |
L485R |
possibly damaging |
Het |
Tmem207 |
A |
G |
16: 26,343,579 (GRCm39) |
|
probably benign |
Het |
Triml2 |
T |
C |
8: 43,638,306 (GRCm39) |
|
probably benign |
Het |
Trip6 |
A |
G |
5: 137,309,107 (GRCm39) |
|
probably benign |
Het |
Tspear |
T |
C |
10: 77,705,465 (GRCm39) |
F288L |
probably benign |
Het |
Vmn1r179 |
C |
T |
7: 23,628,592 (GRCm39) |
T261I |
possibly damaging |
Het |
Zfp644 |
A |
T |
5: 106,784,869 (GRCm39) |
S559R |
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 |
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 |
|
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 |
|
|