Incidental Mutation 'R1772:Dock9'
ID |
196745 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dock9
|
Ensembl Gene |
ENSMUSG00000025558 |
Gene Name |
dedicator of cytokinesis 9 |
Synonyms |
D14Wsu89e, B230309H04Rik, Zizimin1 |
MMRRC Submission |
039803-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1772 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
14 |
Chromosomal Location |
121779458-122035249 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 121847210 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Asparagine to Lysine
at position 1042
(N1042K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000148834
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000040700]
[ENSMUST00000100299]
[ENSMUST00000212181]
[ENSMUST00000212376]
[ENSMUST00000212416]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000040700
AA Change: N1042K
PolyPhen 2
Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)
|
SMART Domains |
Protein: ENSMUSP00000047881 Gene: ENSMUSG00000025558 AA Change: N1042K
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 benign
Transcript: ENSMUST00000100299
AA Change: N1044K
PolyPhen 2
Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)
|
SMART Domains |
Protein: ENSMUSP00000097872 Gene: ENSMUSG00000025558 AA Change: N1044K
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 |
probably benign
Transcript: ENSMUST00000212181
AA Change: N1042K
PolyPhen 2
Score 0.067 (Sensitivity: 0.94; Specificity: 0.84)
|
Predicted Effect |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000212376
AA Change: N1056K
PolyPhen 2
Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000212416
|
Meta Mutation Damage Score |
0.0876 |
Coding Region Coverage |
- 1x: 97.5%
- 3x: 97.0%
- 10x: 95.6%
- 20x: 93.5%
|
Validation Efficiency |
97% (107/110) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgb |
G |
T |
10: 10,258,465 (GRCm39) |
|
probably benign |
Het |
Aldh1a7 |
T |
C |
19: 20,693,383 (GRCm39) |
K179E |
probably damaging |
Het |
Angptl7 |
G |
A |
4: 148,581,883 (GRCm39) |
R168C |
probably damaging |
Het |
Atp8b1 |
T |
A |
18: 64,706,563 (GRCm39) |
I208F |
possibly damaging |
Het |
Bco1 |
A |
G |
8: 117,857,347 (GRCm39) |
Y438C |
probably benign |
Het |
Bltp1 |
T |
C |
3: 37,013,581 (GRCm39) |
S1937P |
probably damaging |
Het |
Btrc |
A |
C |
19: 45,501,100 (GRCm39) |
K218Q |
probably damaging |
Het |
Cct8l1 |
G |
A |
5: 25,722,697 (GRCm39) |
V471M |
probably damaging |
Het |
Cd180 |
C |
T |
13: 102,842,750 (GRCm39) |
L599F |
probably benign |
Het |
Cd300e |
T |
C |
11: 114,945,344 (GRCm39) |
N150S |
probably benign |
Het |
Clcn1 |
C |
A |
6: 42,271,079 (GRCm39) |
T281K |
probably damaging |
Het |
Cnnm3 |
T |
C |
1: 36,558,038 (GRCm39) |
S417P |
probably damaging |
Het |
Cspg4 |
T |
A |
9: 56,804,776 (GRCm39) |
S1862R |
probably benign |
Het |
Cspg5 |
A |
T |
9: 110,091,206 (GRCm39) |
N432Y |
probably damaging |
Het |
Cyp2r1 |
T |
A |
7: 114,152,451 (GRCm39) |
I169F |
probably damaging |
Het |
D130043K22Rik |
T |
A |
13: 25,059,982 (GRCm39) |
S618T |
probably damaging |
Het |
Diaph3 |
G |
A |
14: 87,202,985 (GRCm39) |
P635L |
probably damaging |
Het |
Dlg1 |
A |
G |
16: 31,484,485 (GRCm39) |
I38V |
possibly damaging |
Het |
Dlk1 |
T |
G |
12: 109,425,685 (GRCm39) |
V186G |
probably damaging |
Het |
Dmxl2 |
T |
C |
9: 54,330,508 (GRCm39) |
|
probably benign |
Het |
Dnajc17 |
G |
A |
2: 119,014,164 (GRCm39) |
R132* |
probably null |
Het |
Dok7 |
A |
T |
5: 35,243,994 (GRCm39) |
Q511L |
probably damaging |
Het |
Espnl |
G |
A |
1: 91,272,325 (GRCm39) |
E562K |
possibly damaging |
Het |
Evi5 |
G |
A |
5: 107,943,707 (GRCm39) |
T562I |
probably benign |
Het |
Exd2 |
T |
A |
12: 80,536,253 (GRCm39) |
D294E |
probably benign |
Het |
Fbn1 |
A |
T |
2: 125,245,148 (GRCm39) |
D246E |
possibly damaging |
Het |
Fbxw16 |
A |
T |
9: 109,268,650 (GRCm39) |
W247R |
possibly damaging |
Het |
Fcer1a |
A |
G |
1: 173,053,004 (GRCm39) |
I64T |
probably benign |
Het |
Fcgbp |
C |
A |
7: 27,804,600 (GRCm39) |
Q1903K |
possibly damaging |
Het |
Fmn1 |
A |
G |
2: 113,195,700 (GRCm39) |
S467G |
unknown |
Het |
Fndc7 |
T |
A |
3: 108,777,850 (GRCm39) |
T369S |
probably damaging |
Het |
Fnta |
T |
C |
8: 26,490,994 (GRCm39) |
|
probably benign |
Het |
Gak |
A |
T |
5: 108,754,758 (GRCm39) |
H289Q |
probably damaging |
Het |
Gas2l3 |
A |
G |
10: 89,252,876 (GRCm39) |
|
probably benign |
Het |
Gbp8 |
T |
C |
5: 105,163,987 (GRCm39) |
N437S |
probably benign |
Het |
Gk5 |
G |
A |
9: 96,032,850 (GRCm39) |
|
probably null |
Het |
Hid1 |
A |
T |
11: 115,239,299 (GRCm39) |
V788E |
probably damaging |
Het |
Hmcn1 |
T |
C |
1: 150,439,319 (GRCm39) |
T5505A |
probably damaging |
Het |
Igf1r |
T |
A |
7: 67,844,822 (GRCm39) |
M865K |
probably benign |
Het |
Katnal2 |
G |
A |
18: 77,090,233 (GRCm39) |
T258I |
probably damaging |
Het |
Kdm3b |
A |
T |
18: 34,936,557 (GRCm39) |
I280L |
probably benign |
Het |
Kif24 |
A |
G |
4: 41,409,787 (GRCm39) |
V382A |
probably damaging |
Het |
Kif2a |
A |
T |
13: 107,114,640 (GRCm39) |
|
probably benign |
Het |
Klhl10 |
A |
G |
11: 100,333,022 (GRCm39) |
I56V |
probably benign |
Het |
Klk6 |
C |
T |
7: 43,478,695 (GRCm39) |
Q201* |
probably null |
Het |
Klra3 |
A |
T |
6: 130,300,671 (GRCm39) |
S233T |
probably benign |
Het |
Krt9 |
A |
T |
11: 100,082,131 (GRCm39) |
M223K |
probably damaging |
Het |
Lama4 |
G |
A |
10: 38,936,220 (GRCm39) |
E632K |
probably benign |
Het |
Lamb1 |
T |
C |
12: 31,328,524 (GRCm39) |
Y163H |
probably damaging |
Het |
Lipo3 |
A |
G |
19: 33,764,821 (GRCm39) |
I11T |
probably benign |
Het |
Lix1l |
T |
A |
3: 96,531,207 (GRCm39) |
H333Q |
possibly damaging |
Het |
Mal2 |
T |
A |
15: 54,451,783 (GRCm39) |
M68K |
probably damaging |
Het |
Map2k2 |
T |
C |
10: 80,956,934 (GRCm39) |
I104T |
probably damaging |
Het |
Matn2 |
T |
C |
15: 34,428,931 (GRCm39) |
V765A |
probably damaging |
Het |
Mptx2 |
T |
A |
1: 173,102,040 (GRCm39) |
K216N |
probably damaging |
Het |
Mup5 |
C |
T |
4: 61,750,578 (GRCm39) |
|
probably null |
Het |
Mycbp2 |
A |
G |
14: 103,419,855 (GRCm39) |
Y2494H |
probably damaging |
Het |
Myh3 |
G |
A |
11: 66,990,220 (GRCm39) |
D1622N |
probably benign |
Het |
Myo6 |
T |
C |
9: 80,177,331 (GRCm39) |
I609T |
possibly damaging |
Het |
Ndst1 |
G |
A |
18: 60,835,909 (GRCm39) |
T458I |
probably damaging |
Het |
Neb |
A |
T |
2: 52,125,689 (GRCm39) |
Y3622N |
probably damaging |
Het |
Ntm |
A |
G |
9: 29,090,396 (GRCm39) |
Y108H |
probably benign |
Het |
Or13c3 |
T |
G |
4: 52,855,730 (GRCm39) |
K261T |
probably benign |
Het |
Or1a1b |
T |
C |
11: 74,097,398 (GRCm39) |
I215V |
probably benign |
Het |
Or52e19 |
T |
C |
7: 102,959,449 (GRCm39) |
Y174H |
possibly damaging |
Het |
Pappa2 |
T |
A |
1: 158,641,938 (GRCm39) |
I1373F |
possibly damaging |
Het |
Pear1 |
A |
G |
3: 87,661,799 (GRCm39) |
|
probably benign |
Het |
Phc3 |
C |
T |
3: 31,015,969 (GRCm39) |
A81T |
probably damaging |
Het |
Pmepa1 |
A |
G |
2: 173,076,153 (GRCm39) |
S105P |
probably damaging |
Het |
Ppp6r1 |
T |
C |
7: 4,645,030 (GRCm39) |
I248V |
probably benign |
Het |
Prdm4 |
G |
A |
10: 85,729,256 (GRCm39) |
T717I |
probably damaging |
Het |
Prom1 |
T |
C |
5: 44,168,566 (GRCm39) |
T669A |
probably benign |
Het |
Ptpn5 |
T |
A |
7: 46,740,516 (GRCm39) |
I96F |
probably benign |
Het |
Ptpro |
T |
C |
6: 137,407,741 (GRCm39) |
L922P |
probably damaging |
Het |
Reck |
A |
T |
4: 43,890,982 (GRCm39) |
H40L |
probably benign |
Het |
Rreb1 |
T |
A |
13: 38,114,899 (GRCm39) |
C753S |
probably benign |
Het |
Sacs |
T |
C |
14: 61,448,346 (GRCm39) |
L3464P |
probably damaging |
Het |
Samsn1 |
A |
T |
16: 75,667,663 (GRCm39) |
D304E |
probably benign |
Het |
Scgb2b3 |
T |
C |
7: 31,059,621 (GRCm39) |
N51S |
possibly damaging |
Het |
Shroom3 |
T |
C |
5: 93,088,515 (GRCm39) |
S341P |
probably damaging |
Het |
Siglece |
T |
C |
7: 43,308,717 (GRCm39) |
D212G |
probably damaging |
Het |
Sirpa |
A |
G |
2: 129,458,376 (GRCm39) |
T331A |
probably damaging |
Het |
Spata21 |
T |
C |
4: 140,838,607 (GRCm39) |
S553P |
possibly damaging |
Het |
Speer4b |
T |
A |
5: 27,705,236 (GRCm39) |
|
probably benign |
Het |
Srgap2 |
T |
C |
1: 131,247,376 (GRCm39) |
D552G |
probably damaging |
Het |
Stab2 |
A |
G |
10: 86,790,098 (GRCm39) |
I556T |
probably benign |
Het |
Strip1 |
C |
T |
3: 107,534,047 (GRCm39) |
|
probably null |
Het |
Stxbp6 |
T |
A |
12: 44,949,653 (GRCm39) |
D92V |
probably damaging |
Het |
Styx |
A |
G |
14: 45,594,215 (GRCm39) |
K46E |
probably damaging |
Het |
Supt20 |
T |
A |
3: 54,617,841 (GRCm39) |
V314E |
probably damaging |
Het |
Syne2 |
T |
A |
12: 75,985,503 (GRCm39) |
D1650E |
probably benign |
Het |
Szt2 |
T |
A |
4: 118,262,714 (GRCm39) |
K21M |
probably damaging |
Het |
Tbx4 |
A |
T |
11: 85,802,033 (GRCm39) |
H222L |
probably damaging |
Het |
Tcstv1b |
T |
A |
13: 120,634,725 (GRCm39) |
D2E |
probably benign |
Het |
Tmx3 |
A |
T |
18: 90,551,121 (GRCm39) |
I254L |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trpv2 |
A |
T |
11: 62,485,052 (GRCm39) |
|
probably benign |
Het |
Ubap2 |
A |
G |
4: 41,202,380 (GRCm39) |
S683P |
probably benign |
Het |
Ube2d3 |
C |
T |
3: 135,170,972 (GRCm39) |
R139W |
probably benign |
Het |
Ubox5 |
G |
T |
2: 130,433,794 (GRCm39) |
Q518K |
probably benign |
Het |
Usp42 |
T |
C |
5: 143,702,857 (GRCm39) |
N588S |
probably damaging |
Het |
Vars2 |
G |
A |
17: 35,970,976 (GRCm39) |
T618M |
probably damaging |
Het |
Wfdc17 |
A |
T |
11: 83,595,730 (GRCm39) |
N65Y |
probably damaging |
Het |
Zbtb38 |
G |
A |
9: 96,570,094 (GRCm39) |
P330L |
probably damaging |
Het |
Zfp385a |
C |
T |
15: 103,224,308 (GRCm39) |
|
probably null |
Het |
Zfp637 |
T |
A |
6: 117,822,373 (GRCm39) |
L167H |
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 |
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 |
|
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'- TGCTTAGACGTGAAAACCTCACCG -3'
(R):5'- AGCACAGTGATGCCCTCAGTACTC -3'
Sequencing Primer
(F):5'- gctcctctatgtctaaaaaggatttc -3'
(R):5'- GTACTCAGTACTCAGTACTCTGACAG -3'
|
Posted On |
2014-05-23 |