Incidental Mutation 'R4604:Dock9'
ID |
345926 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dock9
|
Ensembl Gene |
ENSMUSG00000025558 |
Gene Name |
dedicator of cytokinesis 9 |
Synonyms |
D14Wsu89e, B230309H04Rik, Zizimin1 |
MMRRC Submission |
041816-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4604 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
14 |
Chromosomal Location |
121779458-122035249 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 121905871 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Lysine
at position 93
(T93K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000047881
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000040700]
[ENSMUST00000100299]
[ENSMUST00000212181]
[ENSMUST00000212376]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000040700
AA Change: T93K
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000047881 Gene: ENSMUSG00000025558 AA Change: T93K
Domain | Start | End | E-Value | Type |
Pfam:DUF3398
|
58 |
151 |
5.6e-36 |
PFAM |
PH
|
172 |
280 |
1.38e-16 |
SMART |
Blast:PH
|
297 |
372 |
4e-25 |
BLAST |
Pfam:DOCK-C2
|
631 |
822 |
5.3e-51 |
PFAM |
Pfam:DHR-2
|
1523 |
2068 |
2.1e-212 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000100299
AA Change: T95K
PolyPhen 2
Score 0.939 (Sensitivity: 0.80; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000097872 Gene: ENSMUSG00000025558 AA Change: T95K
Domain | Start | End | E-Value | Type |
Pfam:DUF3398
|
58 |
153 |
1.5e-32 |
PFAM |
PH
|
174 |
282 |
1.38e-16 |
SMART |
Blast:PH
|
299 |
374 |
4e-25 |
BLAST |
Pfam:DOCK-C2
|
632 |
825 |
1.3e-59 |
PFAM |
low complexity region
|
1752 |
1763 |
N/A |
INTRINSIC |
Pfam:Ded_cyto
|
1836 |
2013 |
2.4e-69 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000212181
AA Change: T93K
PolyPhen 2
Score 0.924 (Sensitivity: 0.81; Specificity: 0.94)
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000212376
AA Change: T107K
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.2%
- 20x: 95.1%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930518I15Rik |
C |
T |
2: 156,699,074 (GRCm39) |
|
probably benign |
Het |
Abcb6 |
G |
A |
1: 75,156,521 (GRCm39) |
T81I |
probably benign |
Het |
Acp6 |
A |
G |
3: 97,083,075 (GRCm39) |
K362R |
probably benign |
Het |
Adam26a |
A |
G |
8: 44,023,088 (GRCm39) |
M134T |
probably benign |
Het |
Ankrd27 |
C |
T |
7: 35,327,915 (GRCm39) |
P812S |
probably damaging |
Het |
Arl6ip1 |
AAAATAAATAAATAAATAAATAAATA |
AAAATAAATAAATAAATAAATAAATAAATA |
7: 117,721,122 (GRCm39) |
|
probably benign |
Het |
Atp2a1 |
G |
A |
7: 126,047,795 (GRCm39) |
R672C |
probably damaging |
Het |
Atxn2 |
G |
T |
5: 121,919,406 (GRCm39) |
W371C |
probably damaging |
Het |
B3gnt2 |
T |
TTCACAAA |
11: 22,786,426 (GRCm39) |
|
probably null |
Het |
Btnl6 |
T |
A |
17: 34,727,435 (GRCm39) |
D365V |
possibly damaging |
Het |
Ccdc80 |
T |
A |
16: 44,915,928 (GRCm39) |
L228Q |
probably damaging |
Het |
Cdc42bpa |
A |
G |
1: 179,936,759 (GRCm39) |
H718R |
probably benign |
Het |
Cdh18 |
A |
G |
15: 23,474,454 (GRCm39) |
K775E |
probably benign |
Het |
Cdh23 |
T |
G |
10: 60,173,445 (GRCm39) |
N1679T |
possibly damaging |
Het |
Cep192 |
T |
A |
18: 67,948,993 (GRCm39) |
D271E |
possibly damaging |
Het |
Cfap70 |
G |
T |
14: 20,493,729 (GRCm39) |
T124K |
probably benign |
Het |
Ckap5 |
A |
T |
2: 91,408,476 (GRCm39) |
E890D |
probably benign |
Het |
Col22a1 |
G |
T |
15: 71,824,188 (GRCm39) |
P569T |
probably benign |
Het |
Colq |
A |
T |
14: 31,267,060 (GRCm39) |
L150Q |
possibly damaging |
Het |
Csf1 |
T |
C |
3: 107,664,278 (GRCm39) |
|
probably null |
Het |
Csmd3 |
A |
T |
15: 47,868,211 (GRCm39) |
S770T |
possibly damaging |
Het |
Cul9 |
C |
A |
17: 46,841,072 (GRCm39) |
V733L |
probably damaging |
Het |
Cyp2c55 |
A |
G |
19: 39,019,830 (GRCm39) |
D256G |
possibly damaging |
Het |
Dclk3 |
A |
T |
9: 111,298,253 (GRCm39) |
D599V |
probably damaging |
Het |
Defb26 |
T |
A |
2: 152,350,104 (GRCm39) |
I59F |
possibly damaging |
Het |
Dnah6 |
A |
G |
6: 73,106,643 (GRCm39) |
V1646A |
possibly damaging |
Het |
Dnm2 |
T |
C |
9: 21,415,960 (GRCm39) |
|
probably null |
Het |
Dock6 |
A |
G |
9: 21,713,836 (GRCm39) |
L1867P |
probably damaging |
Het |
Dync2h1 |
T |
C |
9: 7,140,995 (GRCm39) |
H1344R |
probably benign |
Het |
Enam |
A |
C |
5: 88,652,142 (GRCm39) |
Q1217P |
possibly damaging |
Het |
Fbf1 |
A |
T |
11: 116,049,748 (GRCm39) |
D91E |
possibly damaging |
Het |
Fbxo7 |
T |
G |
10: 85,882,666 (GRCm39) |
W393G |
probably damaging |
Het |
Gab2 |
A |
G |
7: 96,953,420 (GRCm39) |
T599A |
probably damaging |
Het |
Gfy |
T |
A |
7: 44,826,612 (GRCm39) |
I409F |
possibly damaging |
Het |
Gm19345 |
T |
A |
7: 19,591,433 (GRCm39) |
|
probably null |
Het |
Gm4787 |
A |
G |
12: 81,425,987 (GRCm39) |
M57T |
probably benign |
Het |
Gper1 |
A |
G |
5: 139,412,480 (GRCm39) |
E275G |
probably damaging |
Het |
Grik4 |
T |
C |
9: 42,435,882 (GRCm39) |
E803G |
probably damaging |
Het |
Gstm3 |
G |
A |
3: 107,875,513 (GRCm39) |
P39L |
possibly damaging |
Het |
Hax1 |
A |
T |
3: 89,904,767 (GRCm39) |
V142D |
probably damaging |
Het |
Hcn3 |
A |
T |
3: 89,057,747 (GRCm39) |
I383N |
probably damaging |
Het |
Hdac10 |
C |
A |
15: 89,009,600 (GRCm39) |
|
probably null |
Het |
Hipk3 |
A |
C |
2: 104,269,674 (GRCm39) |
M505R |
probably damaging |
Het |
Hivep1 |
C |
T |
13: 42,313,225 (GRCm39) |
P1822S |
probably benign |
Het |
Hsd17b13 |
G |
T |
5: 104,104,124 (GRCm39) |
H281N |
unknown |
Het |
Ilrun |
T |
C |
17: 28,039,289 (GRCm39) |
D7G |
probably damaging |
Het |
Irak2 |
T |
A |
6: 113,649,848 (GRCm39) |
I222N |
probably damaging |
Het |
Kalrn |
G |
A |
16: 34,334,296 (GRCm39) |
L7F |
possibly damaging |
Het |
Kcnma1 |
A |
G |
14: 23,359,106 (GRCm39) |
|
probably null |
Het |
Kcnn3 |
G |
T |
3: 89,427,727 (GRCm39) |
|
probably benign |
Het |
Lamb1 |
A |
C |
12: 31,328,775 (GRCm39) |
D218A |
probably damaging |
Het |
Lrrtm1 |
A |
T |
6: 77,221,127 (GRCm39) |
N195Y |
probably damaging |
Het |
Ltf |
A |
T |
9: 110,851,409 (GRCm39) |
N72I |
probably damaging |
Het |
Mcm4 |
A |
G |
16: 15,447,527 (GRCm39) |
I479T |
probably damaging |
Het |
Mfhas1 |
T |
C |
8: 36,055,764 (GRCm39) |
S80P |
probably benign |
Het |
Mknk1 |
A |
G |
4: 115,735,224 (GRCm39) |
E364G |
probably damaging |
Het |
Msh4 |
C |
T |
3: 153,577,920 (GRCm39) |
C458Y |
probably damaging |
Het |
Mtrr |
A |
T |
13: 68,712,631 (GRCm39) |
|
probably null |
Het |
Myo1a |
T |
C |
10: 127,547,007 (GRCm39) |
W356R |
probably damaging |
Het |
Nbea |
A |
G |
3: 55,631,069 (GRCm39) |
V2186A |
probably benign |
Het |
Nfe2l3 |
T |
C |
6: 51,427,992 (GRCm39) |
S185P |
probably damaging |
Het |
Nhsl1 |
A |
C |
10: 18,407,158 (GRCm39) |
K1397Q |
probably damaging |
Het |
Nmbr |
C |
T |
10: 14,645,908 (GRCm39) |
R261W |
probably damaging |
Het |
Npy2r |
A |
G |
3: 82,448,365 (GRCm39) |
S137P |
probably damaging |
Het |
Obscn |
C |
T |
11: 58,971,031 (GRCm39) |
G2494D |
probably damaging |
Het |
Obscn |
T |
C |
11: 59,013,572 (GRCm39) |
K1092E |
probably damaging |
Het |
Oosp2 |
A |
C |
19: 11,627,047 (GRCm39) |
I92S |
probably benign |
Het |
Or5ar1 |
C |
T |
2: 85,671,526 (GRCm39) |
C203Y |
probably damaging |
Het |
Pcdh9 |
T |
C |
14: 94,124,616 (GRCm39) |
D518G |
probably damaging |
Het |
Pde11a |
G |
T |
2: 76,168,137 (GRCm39) |
T272K |
possibly damaging |
Het |
Plekha2 |
T |
A |
8: 25,549,851 (GRCm39) |
Q162L |
probably null |
Het |
Prkag2 |
T |
A |
5: 25,083,732 (GRCm39) |
I84F |
probably damaging |
Het |
Prm2 |
G |
T |
16: 10,609,613 (GRCm39) |
|
probably benign |
Het |
Prpf40a |
A |
T |
2: 53,032,035 (GRCm39) |
C800S |
probably damaging |
Het |
Prr5l |
A |
T |
2: 101,559,793 (GRCm39) |
C158S |
probably benign |
Het |
Prrt3 |
C |
A |
6: 113,475,198 (GRCm39) |
C8F |
possibly damaging |
Het |
Psg25 |
T |
C |
7: 18,263,728 (GRCm39) |
T32A |
probably benign |
Het |
Ruvbl1 |
T |
C |
6: 88,462,887 (GRCm39) |
V337A |
probably benign |
Het |
Sall1 |
T |
A |
8: 89,756,969 (GRCm39) |
Q1045L |
probably damaging |
Het |
Sec22c |
T |
C |
9: 121,524,708 (GRCm39) |
Y25C |
probably damaging |
Het |
Serpina3i |
A |
T |
12: 104,234,036 (GRCm39) |
T335S |
possibly damaging |
Het |
Setd1b |
TCCACCACCACCACCACCACCACCA |
TCCACCACCACCACCACCACCA |
5: 123,290,137 (GRCm39) |
|
probably benign |
Het |
Slc12a8 |
T |
A |
16: 33,428,529 (GRCm39) |
I279N |
probably damaging |
Het |
Slc15a1 |
G |
A |
14: 121,727,319 (GRCm39) |
T83I |
probably damaging |
Het |
Slc22a3 |
A |
G |
17: 12,678,658 (GRCm39) |
F222S |
probably benign |
Het |
Sorcs3 |
A |
T |
19: 48,682,353 (GRCm39) |
T463S |
probably benign |
Het |
Spsb4 |
C |
A |
9: 96,877,931 (GRCm39) |
A131S |
probably benign |
Het |
Sting1 |
T |
A |
18: 35,871,743 (GRCm39) |
I170F |
probably damaging |
Het |
Syne2 |
A |
G |
12: 76,014,484 (GRCm39) |
E3225G |
probably damaging |
Het |
Tchp |
G |
A |
5: 114,857,634 (GRCm39) |
|
probably null |
Het |
Tekt4 |
T |
A |
17: 25,690,749 (GRCm39) |
D18E |
probably benign |
Het |
Timm50 |
A |
G |
7: 28,010,443 (GRCm39) |
V37A |
probably benign |
Het |
Tlx2 |
A |
C |
6: 83,045,741 (GRCm39) |
*285G |
probably null |
Het |
Tshz1 |
C |
A |
18: 84,031,499 (GRCm39) |
D970Y |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,700,805 (GRCm39) |
V50E |
probably damaging |
Het |
Txndc17 |
T |
A |
11: 72,100,274 (GRCm39) |
S113T |
probably benign |
Het |
Tyk2 |
T |
C |
9: 21,019,305 (GRCm39) |
Y1039C |
probably damaging |
Het |
Ubqln3 |
A |
G |
7: 103,791,698 (GRCm39) |
S131P |
probably benign |
Het |
Uncx |
A |
T |
5: 139,529,837 (GRCm39) |
H30L |
possibly damaging |
Het |
Usp25 |
T |
A |
16: 76,912,303 (GRCm39) |
D1007E |
probably damaging |
Het |
Usp47 |
T |
C |
7: 111,701,038 (GRCm39) |
V1083A |
probably damaging |
Het |
Wdr24 |
T |
A |
17: 26,047,479 (GRCm39) |
H765Q |
probably damaging |
Het |
Wrnip1 |
A |
G |
13: 32,986,330 (GRCm39) |
D37G |
probably damaging |
Het |
Xpo6 |
T |
C |
7: 125,712,924 (GRCm39) |
T686A |
possibly damaging |
Het |
Zfp941 |
G |
A |
7: 140,392,124 (GRCm39) |
R412C |
probably damaging |
Het |
Znrf2 |
T |
A |
6: 54,855,425 (GRCm39) |
C71* |
probably null |
Het |
|
Other mutations in Dock9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00236:Dock9
|
APN |
14 |
121,905,880 (GRCm39) |
missense |
probably benign |
0.12 |
IGL00817:Dock9
|
APN |
14 |
121,935,703 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00923:Dock9
|
APN |
14 |
121,844,504 (GRCm39) |
unclassified |
probably benign |
|
IGL01385:Dock9
|
APN |
14 |
121,817,995 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01567:Dock9
|
APN |
14 |
121,890,496 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01767:Dock9
|
APN |
14 |
121,860,282 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01811:Dock9
|
APN |
14 |
121,796,440 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02512:Dock9
|
APN |
14 |
121,856,950 (GRCm39) |
splice site |
probably benign |
|
IGL02525:Dock9
|
APN |
14 |
121,877,538 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02550:Dock9
|
APN |
14 |
121,935,724 (GRCm39) |
start codon destroyed |
probably null |
0.07 |
IGL02559:Dock9
|
APN |
14 |
121,862,559 (GRCm39) |
splice site |
probably benign |
|
IGL02666:Dock9
|
APN |
14 |
121,818,111 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02674:Dock9
|
APN |
14 |
121,833,023 (GRCm39) |
splice site |
probably null |
|
IGL02795:Dock9
|
APN |
14 |
121,877,390 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03074:Dock9
|
APN |
14 |
121,844,682 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03095:Dock9
|
APN |
14 |
121,876,940 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03294:Dock9
|
APN |
14 |
121,879,035 (GRCm39) |
splice site |
probably benign |
|
R0036:Dock9
|
UTSW |
14 |
121,860,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0050:Dock9
|
UTSW |
14 |
121,844,637 (GRCm39) |
missense |
probably benign |
0.43 |
R0050:Dock9
|
UTSW |
14 |
121,844,637 (GRCm39) |
missense |
probably benign |
0.43 |
R0164:Dock9
|
UTSW |
14 |
121,835,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R0164:Dock9
|
UTSW |
14 |
121,835,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R0270:Dock9
|
UTSW |
14 |
121,813,411 (GRCm39) |
missense |
probably benign |
0.02 |
R0494:Dock9
|
UTSW |
14 |
121,899,996 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0726:Dock9
|
UTSW |
14 |
121,889,180 (GRCm39) |
nonsense |
probably null |
|
R1029:Dock9
|
UTSW |
14 |
121,837,096 (GRCm39) |
splice site |
probably null |
|
R1214:Dock9
|
UTSW |
14 |
121,823,728 (GRCm39) |
missense |
probably benign |
0.02 |
R1231:Dock9
|
UTSW |
14 |
121,813,362 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1535:Dock9
|
UTSW |
14 |
121,783,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R1629:Dock9
|
UTSW |
14 |
121,780,986 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1637:Dock9
|
UTSW |
14 |
121,889,187 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1733:Dock9
|
UTSW |
14 |
121,864,292 (GRCm39) |
missense |
probably benign |
0.01 |
R1772:Dock9
|
UTSW |
14 |
121,847,210 (GRCm39) |
missense |
probably benign |
0.07 |
R1855:Dock9
|
UTSW |
14 |
121,877,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R1888:Dock9
|
UTSW |
14 |
121,862,617 (GRCm39) |
missense |
probably benign |
0.18 |
R1888:Dock9
|
UTSW |
14 |
121,862,617 (GRCm39) |
missense |
probably benign |
0.18 |
R1901:Dock9
|
UTSW |
14 |
121,862,565 (GRCm39) |
splice site |
probably null |
|
R1920:Dock9
|
UTSW |
14 |
121,820,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R1987:Dock9
|
UTSW |
14 |
121,829,242 (GRCm39) |
missense |
probably benign |
0.00 |
R3035:Dock9
|
UTSW |
14 |
121,844,249 (GRCm39) |
missense |
possibly damaging |
0.60 |
R3851:Dock9
|
UTSW |
14 |
121,866,498 (GRCm39) |
splice site |
probably null |
|
R4020:Dock9
|
UTSW |
14 |
121,844,267 (GRCm39) |
missense |
probably benign |
0.00 |
R4021:Dock9
|
UTSW |
14 |
121,864,324 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4089:Dock9
|
UTSW |
14 |
121,820,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R4258:Dock9
|
UTSW |
14 |
121,818,854 (GRCm39) |
missense |
probably benign |
0.00 |
R4423:Dock9
|
UTSW |
14 |
121,799,465 (GRCm39) |
critical splice donor site |
probably null |
|
R4561:Dock9
|
UTSW |
14 |
121,796,419 (GRCm39) |
missense |
probably benign |
0.01 |
R4646:Dock9
|
UTSW |
14 |
121,823,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R4647:Dock9
|
UTSW |
14 |
121,823,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R4776:Dock9
|
UTSW |
14 |
121,847,509 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4809:Dock9
|
UTSW |
14 |
121,784,008 (GRCm39) |
missense |
probably benign |
0.37 |
R4865:Dock9
|
UTSW |
14 |
121,780,917 (GRCm39) |
makesense |
probably null |
|
R4951:Dock9
|
UTSW |
14 |
121,890,547 (GRCm39) |
missense |
probably benign |
0.35 |
R5151:Dock9
|
UTSW |
14 |
121,815,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R5359:Dock9
|
UTSW |
14 |
121,890,472 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5366:Dock9
|
UTSW |
14 |
121,815,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R5502:Dock9
|
UTSW |
14 |
121,847,594 (GRCm39) |
splice site |
probably null |
|
R5579:Dock9
|
UTSW |
14 |
121,837,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R5753:Dock9
|
UTSW |
14 |
121,872,037 (GRCm39) |
missense |
probably benign |
0.05 |
R5836:Dock9
|
UTSW |
14 |
121,918,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R5858:Dock9
|
UTSW |
14 |
121,866,204 (GRCm39) |
missense |
probably benign |
0.00 |
R5890:Dock9
|
UTSW |
14 |
121,905,820 (GRCm39) |
critical splice donor site |
probably null |
|
R6075:Dock9
|
UTSW |
14 |
121,783,385 (GRCm39) |
missense |
probably benign |
|
R6298:Dock9
|
UTSW |
14 |
121,872,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R6306:Dock9
|
UTSW |
14 |
121,799,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R6321:Dock9
|
UTSW |
14 |
121,783,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R6330:Dock9
|
UTSW |
14 |
121,842,655 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R6719:Dock9
|
UTSW |
14 |
121,847,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R6784:Dock9
|
UTSW |
14 |
121,780,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R6826:Dock9
|
UTSW |
14 |
121,860,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R6830:Dock9
|
UTSW |
14 |
121,860,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R6838:Dock9
|
UTSW |
14 |
121,784,008 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6868:Dock9
|
UTSW |
14 |
121,823,676 (GRCm39) |
missense |
probably benign |
0.37 |
R6919:Dock9
|
UTSW |
14 |
121,880,564 (GRCm39) |
missense |
probably benign |
0.42 |
R6989:Dock9
|
UTSW |
14 |
121,864,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R7539:Dock9
|
UTSW |
14 |
121,818,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R7645:Dock9
|
UTSW |
14 |
121,835,075 (GRCm39) |
missense |
probably benign |
0.44 |
R7875:Dock9
|
UTSW |
14 |
121,863,396 (GRCm39) |
nonsense |
probably null |
|
R7900:Dock9
|
UTSW |
14 |
121,783,491 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8040:Dock9
|
UTSW |
14 |
121,889,206 (GRCm39) |
missense |
probably benign |
0.06 |
R8420:Dock9
|
UTSW |
14 |
121,783,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R8511:Dock9
|
UTSW |
14 |
121,918,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R8511:Dock9
|
UTSW |
14 |
121,864,801 (GRCm39) |
missense |
probably benign |
0.40 |
R8514:Dock9
|
UTSW |
14 |
121,896,199 (GRCm39) |
missense |
probably benign |
0.25 |
R8691:Dock9
|
UTSW |
14 |
121,877,517 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8804:Dock9
|
UTSW |
14 |
121,842,595 (GRCm39) |
missense |
probably damaging |
0.98 |
R8894:Dock9
|
UTSW |
14 |
121,860,373 (GRCm39) |
missense |
probably benign |
0.10 |
R8900:Dock9
|
UTSW |
14 |
121,817,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R9069:Dock9
|
UTSW |
14 |
121,866,324 (GRCm39) |
missense |
probably damaging |
0.98 |
R9218:Dock9
|
UTSW |
14 |
121,905,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R9233:Dock9
|
UTSW |
14 |
121,820,781 (GRCm39) |
missense |
probably benign |
0.09 |
R9236:Dock9
|
UTSW |
14 |
121,876,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R9285:Dock9
|
UTSW |
14 |
121,833,012 (GRCm39) |
missense |
probably benign |
|
R9451:Dock9
|
UTSW |
14 |
121,787,601 (GRCm39) |
splice site |
probably benign |
|
R9461:Dock9
|
UTSW |
14 |
121,842,601 (GRCm39) |
missense |
probably benign |
0.05 |
R9484:Dock9
|
UTSW |
14 |
121,818,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R9517:Dock9
|
UTSW |
14 |
121,829,236 (GRCm39) |
missense |
probably benign |
0.07 |
R9542:Dock9
|
UTSW |
14 |
121,864,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R9694:Dock9
|
UTSW |
14 |
121,818,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R9701:Dock9
|
UTSW |
14 |
121,876,983 (GRCm39) |
missense |
probably benign |
0.01 |
R9703:Dock9
|
UTSW |
14 |
121,781,989 (GRCm39) |
makesense |
probably null |
|
R9726:Dock9
|
UTSW |
14 |
121,835,149 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9741:Dock9
|
UTSW |
14 |
121,877,516 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dock9
|
UTSW |
14 |
121,792,687 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dock9
|
UTSW |
14 |
121,889,194 (GRCm39) |
missense |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- TATGCTCTGACAACGTCTCATC -3'
(R):5'- TGCTACCTCGTCTGGAATGG -3'
Sequencing Primer
(F):5'- CATAAAACCCGCCATTACTTCTTTG -3'
(R):5'- CTACCTCGTCTGGAATGGGAACTTAG -3'
|
Posted On |
2015-09-25 |