Incidental Mutation 'R4865:Dock9'
ID |
374862 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dock9
|
Ensembl Gene |
ENSMUSG00000025558 |
Gene Name |
dedicator of cytokinesis 9 |
Synonyms |
D14Wsu89e, B230309H04Rik, Zizimin1 |
MMRRC Submission |
042475-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4865 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
14 |
Chromosomal Location |
121779458-122035249 bp(-) (GRCm39) |
Type of Mutation |
makesense |
DNA Base Change (assembly) |
A to T
at 121780917 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Stop codon to Arginine
at position 1917
(*1917R)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000040700]
[ENSMUST00000100299]
[ENSMUST00000212181]
[ENSMUST00000212376]
[ENSMUST00000212416]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably null
Transcript: ENSMUST00000040700
AA Change: *2114R
|
SMART Domains |
Protein: ENSMUSP00000047881 Gene: ENSMUSG00000025558 AA Change: *2114R
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 null
Transcript: ENSMUST00000100299
AA Change: *2059R
|
SMART Domains |
Protein: ENSMUSP00000097872 Gene: ENSMUSG00000025558 AA Change: *2059R
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: ENSMUST00000211803
|
Predicted Effect |
probably null
Transcript: ENSMUST00000212181
AA Change: *2089R
|
Predicted Effect |
probably null
Transcript: ENSMUST00000212283
AA Change: *1917R
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000212376
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000212416
|
Meta Mutation Damage Score |
0.8787 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.4%
|
Validation Efficiency |
98% (86/88) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim3 |
C |
T |
18: 61,938,157 (GRCm39) |
V639M |
probably damaging |
Het |
Adgrf4 |
A |
G |
17: 42,978,156 (GRCm39) |
S396P |
probably damaging |
Het |
Aldh3b2 |
T |
A |
19: 4,028,469 (GRCm39) |
I123N |
probably damaging |
Het |
Aldh5a1 |
A |
G |
13: 25,095,567 (GRCm39) |
Y517H |
probably damaging |
Het |
Aph1c |
A |
C |
9: 66,735,120 (GRCm39) |
I77S |
probably damaging |
Het |
Armc8 |
A |
G |
9: 99,408,942 (GRCm39) |
|
probably null |
Het |
Atp13a5 |
G |
A |
16: 29,066,912 (GRCm39) |
P1020L |
probably damaging |
Het |
BC024139 |
A |
T |
15: 76,010,266 (GRCm39) |
M80K |
possibly damaging |
Het |
Cdk5rap1 |
C |
T |
2: 154,212,876 (GRCm39) |
|
probably null |
Het |
Cenpn |
A |
G |
8: 117,661,512 (GRCm39) |
I204V |
probably damaging |
Het |
Ces4a |
A |
T |
8: 105,873,790 (GRCm39) |
M420L |
probably benign |
Het |
Chdh |
T |
A |
14: 29,755,681 (GRCm39) |
D322E |
probably benign |
Het |
Clcn6 |
A |
T |
4: 148,104,223 (GRCm39) |
I223N |
probably damaging |
Het |
Clec4b1 |
A |
G |
6: 123,045,428 (GRCm39) |
K50E |
possibly damaging |
Het |
Creg1 |
T |
A |
1: 165,597,432 (GRCm39) |
C135* |
probably null |
Het |
Cyp4f13 |
C |
T |
17: 33,144,678 (GRCm39) |
R411Q |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,234,234 (GRCm39) |
F1426L |
probably damaging |
Het |
Dync1h1 |
T |
G |
12: 110,606,235 (GRCm39) |
L2435R |
possibly damaging |
Het |
Eif3l |
C |
A |
15: 78,965,849 (GRCm39) |
Y166* |
probably null |
Het |
Emilin1 |
T |
A |
5: 31,075,128 (GRCm39) |
N456K |
possibly damaging |
Het |
Fam83f |
C |
T |
15: 80,576,650 (GRCm39) |
R434C |
probably damaging |
Het |
Fbxw9 |
A |
G |
8: 85,786,785 (GRCm39) |
D10G |
possibly damaging |
Het |
Flt1 |
C |
A |
5: 147,620,749 (GRCm39) |
A132S |
probably benign |
Het |
Fsip2 |
T |
G |
2: 82,821,295 (GRCm39) |
V5676G |
possibly damaging |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
Gm11596 |
A |
G |
11: 99,684,064 (GRCm39) |
|
probably benign |
Het |
Gm6522 |
T |
C |
3: 106,183,286 (GRCm39) |
|
noncoding transcript |
Het |
Gm6728 |
A |
G |
6: 136,464,072 (GRCm39) |
|
noncoding transcript |
Het |
Gria4 |
T |
A |
9: 4,464,295 (GRCm39) |
I556F |
possibly damaging |
Het |
Grp |
A |
T |
18: 66,013,041 (GRCm39) |
D69V |
probably damaging |
Het |
Gucy1a1 |
G |
T |
3: 82,026,469 (GRCm39) |
|
probably benign |
Het |
Haus5 |
A |
T |
7: 30,357,980 (GRCm39) |
L376Q |
probably damaging |
Het |
Ifne |
A |
T |
4: 88,797,942 (GRCm39) |
Y159N |
probably damaging |
Het |
Ift80 |
A |
G |
3: 68,898,092 (GRCm39) |
V81A |
probably benign |
Het |
Inpp5b |
T |
C |
4: 124,645,288 (GRCm39) |
V192A |
probably benign |
Het |
Kcnh4 |
A |
G |
11: 100,640,569 (GRCm39) |
S486P |
probably damaging |
Het |
Kif5b |
A |
G |
18: 6,222,912 (GRCm39) |
|
probably benign |
Het |
Macf1 |
T |
A |
4: 123,327,096 (GRCm39) |
E4800D |
probably damaging |
Het |
Mblac2 |
C |
T |
13: 81,860,095 (GRCm39) |
Q150* |
probably null |
Het |
Mc1r |
A |
T |
8: 124,134,255 (GRCm39) |
T3S |
probably benign |
Het |
Med17 |
G |
A |
9: 15,176,668 (GRCm39) |
Q70* |
probably null |
Het |
Myocd |
A |
T |
11: 65,069,856 (GRCm39) |
|
probably null |
Het |
Nphp3 |
T |
C |
9: 103,909,169 (GRCm39) |
L793P |
probably benign |
Het |
Or1ad1 |
A |
G |
11: 50,876,370 (GRCm39) |
T281A |
probably damaging |
Het |
Or2m13 |
A |
T |
16: 19,226,051 (GRCm39) |
F238L |
probably damaging |
Het |
Or4a68 |
T |
G |
2: 89,270,003 (GRCm39) |
T207P |
possibly damaging |
Het |
Or5an10 |
T |
C |
19: 12,275,944 (GRCm39) |
D184G |
probably damaging |
Het |
Or5ap2 |
T |
A |
2: 85,680,060 (GRCm39) |
M88K |
probably damaging |
Het |
Or8c13 |
T |
A |
9: 38,091,196 (GRCm39) |
T308S |
possibly damaging |
Het |
Piezo1 |
A |
T |
8: 123,213,660 (GRCm39) |
L1745Q |
probably damaging |
Het |
Prdm10 |
T |
A |
9: 31,258,376 (GRCm39) |
H600Q |
probably damaging |
Het |
Psapl1 |
C |
A |
5: 36,362,211 (GRCm39) |
L268M |
probably damaging |
Het |
Psg23 |
T |
C |
7: 18,346,039 (GRCm39) |
I219V |
probably benign |
Het |
Rexo5 |
A |
T |
7: 119,400,553 (GRCm39) |
R113* |
probably null |
Het |
Rgs22 |
A |
T |
15: 36,100,358 (GRCm39) |
I243N |
probably damaging |
Het |
Rhbdf1 |
G |
A |
11: 32,164,517 (GRCm39) |
T183I |
probably damaging |
Het |
Rhobtb1 |
T |
C |
10: 69,106,554 (GRCm39) |
M373T |
probably benign |
Het |
Ros1 |
G |
T |
10: 52,048,966 (GRCm39) |
A88E |
probably damaging |
Het |
Sdr16c6 |
A |
G |
4: 4,058,834 (GRCm39) |
F251L |
probably benign |
Het |
Skil |
A |
G |
3: 31,167,562 (GRCm39) |
Y398C |
probably damaging |
Het |
Slc22a3 |
A |
T |
17: 12,683,419 (GRCm39) |
M148K |
probably benign |
Het |
Slco4c1 |
G |
A |
1: 96,768,953 (GRCm39) |
P303L |
probably damaging |
Het |
Sntn |
A |
T |
14: 13,679,103 (GRCm38) |
K92N |
probably benign |
Het |
Spry4 |
A |
T |
18: 38,722,876 (GRCm39) |
S296T |
probably benign |
Het |
St8sia1 |
A |
G |
6: 142,774,796 (GRCm39) |
F261S |
probably damaging |
Het |
Stab2 |
C |
T |
10: 86,679,364 (GRCm39) |
|
probably null |
Het |
Stk24 |
A |
T |
14: 121,530,866 (GRCm39) |
C363* |
probably null |
Het |
Tank |
G |
A |
2: 61,408,979 (GRCm39) |
|
probably benign |
Het |
Tmem67 |
T |
C |
4: 12,070,262 (GRCm39) |
N387S |
probably benign |
Het |
Treml1 |
A |
T |
17: 48,673,885 (GRCm39) |
I304L |
probably benign |
Het |
Trim13 |
A |
G |
14: 61,842,966 (GRCm39) |
I328V |
probably benign |
Het |
Upk2 |
A |
G |
9: 44,365,382 (GRCm39) |
V62A |
probably damaging |
Het |
Urb2 |
A |
T |
8: 124,756,374 (GRCm39) |
K694* |
probably null |
Het |
Vmn2r17 |
C |
A |
5: 109,574,985 (GRCm39) |
N97K |
probably damaging |
Het |
Vmn2r57 |
A |
T |
7: 41,049,892 (GRCm39) |
V619D |
probably damaging |
Het |
Vmn2r92 |
G |
A |
17: 18,387,634 (GRCm39) |
R213Q |
probably benign |
Het |
Wnt6 |
G |
A |
1: 74,821,788 (GRCm39) |
C123Y |
probably damaging |
Het |
Zfp292 |
A |
G |
4: 34,819,563 (GRCm39) |
I253T |
probably damaging |
Het |
Zfp52 |
C |
T |
17: 21,781,505 (GRCm39) |
S451L |
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 |
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'- AAACTATGTGCACCTTCCCC -3'
(R):5'- CCTTTCTGCAGAACGACAGC -3'
Sequencing Primer
(F):5'- TCCCCCGACTCCTATAAAATCTG -3'
(R):5'- AGGGGAATTGTGATGTCACC -3'
|
Posted On |
2016-03-17 |