Incidental Mutation 'R5579:Dock9'
ID |
438321 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dock9
|
Ensembl Gene |
ENSMUSG00000025558 |
Gene Name |
dedicator of cytokinesis 9 |
Synonyms |
D14Wsu89e, B230309H04Rik, Zizimin1 |
MMRRC Submission |
043267-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R5579 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
14 |
Chromosomal Location |
121779458-122035249 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 121837107 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Leucine to Glutamine
at position 67
(L67Q)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000148303
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000040700]
[ENSMUST00000100299]
[ENSMUST00000212181]
[ENSMUST00000212376]
[ENSMUST00000212416]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000040700
AA Change: L1271Q
PolyPhen 2
Score 0.986 (Sensitivity: 0.74; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000047881 Gene: ENSMUSG00000025558 AA Change: L1271Q
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 |
probably damaging
Transcript: ENSMUST00000100299
AA Change: L1273Q
PolyPhen 2
Score 0.973 (Sensitivity: 0.76; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000097872 Gene: ENSMUSG00000025558 AA Change: L1273Q
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 |
noncoding transcript
Transcript: ENSMUST00000211993
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000212181
AA Change: L1271Q
PolyPhen 2
Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
|
Predicted Effect |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000212376
AA Change: L1285Q
PolyPhen 2
Score 0.645 (Sensitivity: 0.87; Specificity: 0.91)
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000212416
AA Change: L67Q
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.8%
- 10x: 98.9%
- 20x: 97.0%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 114 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca3 |
G |
T |
17: 24,595,703 (GRCm39) |
C352F |
probably damaging |
Het |
Abce1 |
A |
T |
8: 80,427,215 (GRCm39) |
I237N |
possibly damaging |
Het |
Acrbp |
A |
G |
6: 125,038,062 (GRCm39) |
D421G |
probably benign |
Het |
Adam8 |
T |
A |
7: 139,568,897 (GRCm39) |
Y201F |
probably benign |
Het |
Adgrf1 |
T |
A |
17: 43,621,955 (GRCm39) |
C731S |
probably damaging |
Het |
Akap8l |
A |
T |
17: 32,540,916 (GRCm39) |
I529N |
probably damaging |
Het |
Akap9 |
G |
A |
5: 4,114,714 (GRCm39) |
G114D |
possibly damaging |
Het |
Alox12b |
T |
A |
11: 69,053,758 (GRCm39) |
D158E |
probably benign |
Het |
Ankrd11 |
A |
G |
8: 123,610,970 (GRCm39) |
S2639P |
probably damaging |
Het |
Ankrd42 |
T |
C |
7: 92,239,390 (GRCm39) |
Y466C |
possibly damaging |
Het |
Apobr |
T |
C |
7: 126,186,847 (GRCm39) |
I786T |
probably benign |
Het |
Arhgef12 |
C |
T |
9: 42,921,489 (GRCm39) |
G329R |
probably benign |
Het |
Btnl1 |
T |
C |
17: 34,600,526 (GRCm39) |
|
probably null |
Het |
Ccdc174 |
A |
G |
6: 91,858,331 (GRCm39) |
|
probably null |
Het |
Ccdc183 |
T |
C |
2: 25,505,434 (GRCm39) |
D177G |
possibly damaging |
Het |
Cd14 |
A |
G |
18: 36,859,288 (GRCm39) |
Y56H |
probably benign |
Het |
Cep162 |
G |
A |
9: 87,085,724 (GRCm39) |
A1200V |
probably benign |
Het |
Clic3 |
T |
C |
2: 25,348,319 (GRCm39) |
L128P |
probably damaging |
Het |
Cntnap5b |
A |
T |
1: 100,311,120 (GRCm39) |
R538* |
probably null |
Het |
Cntnap5b |
A |
T |
1: 100,311,124 (GRCm39) |
Q539L |
probably benign |
Het |
Coq7 |
A |
T |
7: 118,116,558 (GRCm39) |
N214K |
unknown |
Het |
Cramp1 |
G |
A |
17: 25,192,087 (GRCm39) |
H1018Y |
possibly damaging |
Het |
Crtac1 |
T |
A |
19: 42,293,245 (GRCm39) |
D288V |
probably damaging |
Het |
Dab2ip |
C |
T |
2: 35,605,339 (GRCm39) |
R132* |
probably null |
Het |
Dis3l |
C |
A |
9: 64,238,117 (GRCm39) |
C125F |
probably benign |
Het |
Dnmt1 |
A |
T |
9: 20,831,501 (GRCm39) |
V543D |
probably damaging |
Het |
Ehbp1 |
A |
T |
11: 22,087,846 (GRCm39) |
S413T |
probably damaging |
Het |
Endov |
A |
G |
11: 119,395,923 (GRCm39) |
I158V |
probably benign |
Het |
Epb41l4b |
A |
G |
4: 57,064,802 (GRCm39) |
V469A |
possibly damaging |
Het |
Etf1 |
G |
A |
18: 35,046,654 (GRCm39) |
P119S |
probably damaging |
Het |
Fam135a |
A |
G |
1: 24,068,808 (GRCm39) |
L491P |
possibly damaging |
Het |
Fancd2 |
A |
T |
6: 113,537,012 (GRCm39) |
|
probably null |
Het |
Fank1 |
T |
A |
7: 133,471,058 (GRCm39) |
|
probably null |
Het |
Fbh1 |
A |
G |
2: 11,753,804 (GRCm39) |
I846T |
probably damaging |
Het |
Gas2l3 |
T |
C |
10: 89,249,928 (GRCm39) |
T397A |
probably benign |
Het |
Gga1 |
T |
C |
15: 78,777,388 (GRCm39) |
V513A |
probably damaging |
Het |
Ggt1 |
T |
C |
10: 75,421,782 (GRCm39) |
V543A |
probably damaging |
Het |
Gm11596 |
A |
T |
11: 99,683,717 (GRCm39) |
C134* |
probably null |
Het |
Gnal |
C |
T |
18: 67,221,842 (GRCm39) |
R82C |
unknown |
Het |
Hat1 |
T |
C |
2: 71,240,582 (GRCm39) |
V92A |
possibly damaging |
Het |
Icosl |
C |
T |
10: 77,909,597 (GRCm39) |
R181C |
probably damaging |
Het |
Ift46 |
A |
G |
9: 44,698,160 (GRCm39) |
M208V |
possibly damaging |
Het |
Ighv1-26 |
T |
C |
12: 114,752,219 (GRCm39) |
K42E |
possibly damaging |
Het |
Ipo5 |
A |
G |
14: 121,176,025 (GRCm39) |
K617E |
probably benign |
Het |
Irx5 |
A |
G |
8: 93,086,541 (GRCm39) |
D208G |
probably benign |
Het |
Itgal |
T |
G |
7: 126,906,101 (GRCm39) |
V397G |
probably benign |
Het |
Itpr2 |
G |
A |
6: 146,074,864 (GRCm39) |
R2297* |
probably null |
Het |
Itpr3 |
A |
G |
17: 27,332,493 (GRCm39) |
D1779G |
probably damaging |
Het |
Khdc4 |
T |
C |
3: 88,607,582 (GRCm39) |
S345P |
probably benign |
Het |
Krt4 |
T |
A |
15: 101,829,669 (GRCm39) |
E286D |
probably benign |
Het |
Loxl4 |
C |
T |
19: 42,592,729 (GRCm39) |
G317E |
probably damaging |
Het |
Mapk6 |
T |
G |
9: 75,295,344 (GRCm39) |
H718P |
possibly damaging |
Het |
Mark2 |
A |
C |
19: 7,260,181 (GRCm39) |
V14G |
probably damaging |
Het |
Mbd5 |
A |
G |
2: 49,162,826 (GRCm39) |
T1103A |
possibly damaging |
Het |
Mcph1 |
A |
G |
8: 18,682,309 (GRCm39) |
E482G |
probably benign |
Het |
Mme |
G |
A |
3: 63,256,066 (GRCm39) |
E509K |
probably damaging |
Het |
Mrgbp |
A |
G |
2: 180,227,276 (GRCm39) |
T204A |
probably damaging |
Het |
Mycbp2 |
A |
T |
14: 103,528,769 (GRCm39) |
F430I |
probably damaging |
Het |
Myo6 |
A |
G |
9: 80,125,002 (GRCm39) |
D27G |
probably damaging |
Het |
Ncoa6 |
A |
G |
2: 155,248,597 (GRCm39) |
L1569S |
probably damaging |
Het |
Ndc1 |
T |
A |
4: 107,237,901 (GRCm39) |
F235Y |
possibly damaging |
Het |
Nmur2 |
A |
T |
11: 55,923,835 (GRCm39) |
S240T |
probably benign |
Het |
Or14c44 |
T |
A |
7: 86,061,934 (GRCm39) |
Y121* |
probably null |
Het |
Or52ae7 |
G |
A |
7: 103,120,121 (GRCm39) |
V292M |
probably damaging |
Het |
Or5d46 |
A |
T |
2: 88,170,757 (GRCm39) |
I283F |
possibly damaging |
Het |
Osbpl1a |
G |
T |
18: 12,974,249 (GRCm39) |
A62E |
probably damaging |
Het |
Osbpl1a |
A |
C |
18: 13,025,319 (GRCm39) |
S333A |
probably benign |
Het |
Otud4 |
C |
T |
8: 80,390,737 (GRCm39) |
T417I |
probably benign |
Het |
Pagr1a |
T |
C |
7: 126,614,614 (GRCm39) |
E197G |
probably damaging |
Het |
Pcdh18 |
T |
C |
3: 49,699,426 (GRCm39) |
Q1012R |
probably damaging |
Het |
Pcdhgb5 |
A |
C |
18: 37,864,690 (GRCm39) |
I162L |
probably benign |
Het |
Pdpr |
T |
A |
8: 111,850,448 (GRCm39) |
Y462N |
probably damaging |
Het |
Pkhd1 |
A |
T |
1: 20,593,366 (GRCm39) |
H1582Q |
probably damaging |
Het |
Polr1b |
A |
G |
2: 128,952,028 (GRCm39) |
K352R |
probably damaging |
Het |
Poteg |
G |
A |
8: 27,938,065 (GRCm39) |
V12M |
probably damaging |
Het |
Pou2f1 |
A |
C |
1: 165,742,731 (GRCm39) |
V54G |
probably damaging |
Het |
Ppme1 |
A |
G |
7: 99,994,182 (GRCm39) |
L177P |
probably damaging |
Het |
Prkce |
A |
G |
17: 86,927,376 (GRCm39) |
D550G |
probably damaging |
Het |
Prrc2c |
A |
G |
1: 162,508,327 (GRCm39) |
|
probably null |
Het |
Ptpn22 |
A |
G |
3: 103,789,455 (GRCm39) |
|
probably null |
Het |
Rabif |
G |
A |
1: 134,433,943 (GRCm39) |
V86M |
probably damaging |
Het |
Rbm25 |
T |
A |
12: 83,715,281 (GRCm39) |
M484K |
probably benign |
Het |
Rcn2 |
G |
A |
9: 55,964,713 (GRCm39) |
A224T |
probably benign |
Het |
Rexo5 |
T |
A |
7: 119,433,626 (GRCm39) |
|
probably null |
Het |
Rnase1 |
A |
T |
14: 51,383,219 (GRCm39) |
I45N |
probably benign |
Het |
Rnmt |
T |
A |
18: 68,439,186 (GRCm39) |
D98E |
possibly damaging |
Het |
Rprd2 |
A |
G |
3: 95,692,371 (GRCm39) |
F188L |
probably damaging |
Het |
Scube2 |
G |
A |
7: 109,409,944 (GRCm39) |
T643M |
probably damaging |
Het |
Skic3 |
T |
C |
13: 76,333,319 (GRCm39) |
W25R |
probably damaging |
Het |
Slc7a15 |
T |
C |
12: 8,589,344 (GRCm39) |
I68V |
probably benign |
Het |
Slco1a5 |
A |
T |
6: 142,187,851 (GRCm39) |
V496D |
possibly damaging |
Het |
Slitrk6 |
T |
G |
14: 110,988,649 (GRCm39) |
S353R |
possibly damaging |
Het |
Smpd5 |
T |
A |
15: 76,179,325 (GRCm39) |
I53K |
possibly damaging |
Het |
Tas2r108 |
T |
C |
6: 40,471,021 (GRCm39) |
S166P |
probably benign |
Het |
Tcstv7a |
T |
A |
13: 120,289,951 (GRCm39) |
M82L |
probably benign |
Het |
Tecpr1 |
C |
A |
5: 144,151,162 (GRCm39) |
V245L |
possibly damaging |
Het |
Tenm3 |
G |
T |
8: 48,689,799 (GRCm39) |
N1929K |
probably damaging |
Het |
Tigd5 |
T |
G |
15: 75,782,874 (GRCm39) |
F412C |
probably damaging |
Het |
Timm17a |
A |
T |
1: 135,233,926 (GRCm39) |
S74T |
possibly damaging |
Het |
Tle1 |
A |
T |
4: 72,058,045 (GRCm39) |
L60Q |
probably damaging |
Het |
Tmem132d |
T |
C |
5: 127,873,064 (GRCm39) |
E515G |
possibly damaging |
Het |
Tmem65 |
T |
C |
15: 58,666,246 (GRCm39) |
N115S |
probably benign |
Het |
Trmt5 |
C |
A |
12: 73,328,426 (GRCm39) |
R259L |
possibly damaging |
Het |
Trmt9b |
T |
C |
8: 36,979,195 (GRCm39) |
V266A |
probably benign |
Het |
Vmn2r50 |
A |
T |
7: 9,784,016 (GRCm39) |
W153R |
probably benign |
Het |
Vwa3a |
T |
G |
7: 120,367,396 (GRCm39) |
S184A |
probably benign |
Het |
Zbtb25 |
A |
G |
12: 76,395,938 (GRCm39) |
L428P |
possibly damaging |
Het |
Zbtb49 |
C |
T |
5: 38,358,160 (GRCm39) |
D698N |
probably damaging |
Het |
Zbtb8os |
T |
G |
4: 129,234,528 (GRCm39) |
D35E |
probably damaging |
Het |
Zfp316 |
T |
C |
5: 143,250,246 (GRCm39) |
T56A |
unknown |
Het |
Zfp334 |
A |
T |
2: 165,222,407 (GRCm39) |
C545* |
probably null |
Het |
Zmiz1 |
C |
A |
14: 25,645,280 (GRCm39) |
S247R |
probably damaging |
Het |
Zscan18 |
A |
G |
7: 12,509,308 (GRCm39) |
|
probably benign |
Het |
Zzef1 |
T |
C |
11: 72,791,463 (GRCm39) |
V2189A |
probably damaging |
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 |
R4604:Dock9
|
UTSW |
14 |
121,905,871 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
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'- TGTCATTACCAGCAGCGACC -3'
(R):5'- GTACAACTCTCGAGCCATATGAC -3'
Sequencing Primer
(F):5'- GAGACAATGACTGAGTCACAATC -3'
(R):5'- TTAATGGCCACAAAAACACTTCCTC -3'
|
Posted On |
2016-10-26 |