Incidental Mutation 'R4865:Dock9'
| ID |
374862 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Dock9
|
| Ensembl Gene |
ENSMUSG00000025558 |
| Gene Name |
dedicator of cytokinesis 9 |
| Synonyms |
D14Wsu89e, Zizimin1, B230309H04Rik |
| 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 |
121542046-121797837 bp(-) (GRCm38) |
| Type of Mutation |
makesense |
| DNA Base Change (assembly) |
A to T
at 121543505 bp (GRCm38)
|
| 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: 61,805,086 (GRCm38) |
V639M |
probably damaging |
Het |
| Adgrf4 |
A |
G |
17: 42,667,265 (GRCm38) |
S396P |
probably damaging |
Het |
| Aldh3b2 |
T |
A |
19: 3,978,469 (GRCm38) |
I123N |
probably damaging |
Het |
| Aldh5a1 |
A |
G |
13: 24,911,584 (GRCm38) |
Y517H |
probably damaging |
Het |
| Aph1c |
A |
C |
9: 66,827,838 (GRCm38) |
I77S |
probably damaging |
Het |
| Armc8 |
A |
G |
9: 99,526,889 (GRCm38) |
|
probably null |
Het |
| Atp13a5 |
G |
A |
16: 29,248,160 (GRCm38) |
P1020L |
probably damaging |
Het |
| BC024139 |
A |
T |
15: 76,126,066 (GRCm38) |
M80K |
possibly damaging |
Het |
| Cdk5rap1 |
C |
T |
2: 154,370,956 (GRCm38) |
|
probably null |
Het |
| Cenpn |
A |
G |
8: 116,934,773 (GRCm38) |
I204V |
probably damaging |
Het |
| Ces4a |
A |
T |
8: 105,147,158 (GRCm38) |
M420L |
probably benign |
Het |
| Chdh |
T |
A |
14: 30,033,724 (GRCm38) |
D322E |
probably benign |
Het |
| Clcn6 |
A |
T |
4: 148,019,766 (GRCm38) |
I223N |
probably damaging |
Het |
| Clec4b1 |
A |
G |
6: 123,068,469 (GRCm38) |
K50E |
possibly damaging |
Het |
| Creg1 |
T |
A |
1: 165,769,863 (GRCm38) |
C135* |
probably null |
Het |
| Cyp4f13 |
C |
T |
17: 32,925,704 (GRCm38) |
R411Q |
probably damaging |
Het |
| Dnah7b |
T |
C |
1: 46,195,074 (GRCm38) |
F1426L |
probably damaging |
Het |
| Dync1h1 |
T |
G |
12: 110,639,801 (GRCm38) |
L2435R |
possibly damaging |
Het |
| Eif3l |
C |
A |
15: 79,081,649 (GRCm38) |
Y166* |
probably null |
Het |
| Emilin1 |
T |
A |
5: 30,917,784 (GRCm38) |
N456K |
possibly damaging |
Het |
| Fam83f |
C |
T |
15: 80,692,449 (GRCm38) |
R434C |
probably damaging |
Het |
| Fbxw9 |
A |
G |
8: 85,060,156 (GRCm38) |
D10G |
possibly damaging |
Het |
| Flt1 |
C |
A |
5: 147,683,939 (GRCm38) |
A132S |
probably benign |
Het |
| Fsip2 |
T |
G |
2: 82,990,951 (GRCm38) |
V5676G |
possibly damaging |
Het |
| Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,430,958 (GRCm38) |
|
probably benign |
Het |
| Gm11596 |
A |
G |
11: 99,793,238 (GRCm38) |
|
probably benign |
Het |
| Gm6522 |
T |
C |
3: 106,275,970 (GRCm38) |
|
noncoding transcript |
Het |
| Gm6728 |
A |
G |
6: 136,487,074 (GRCm38) |
|
noncoding transcript |
Het |
| Gria4 |
T |
A |
9: 4,464,295 (GRCm38) |
I556F |
possibly damaging |
Het |
| Grp |
A |
T |
18: 65,879,970 (GRCm38) |
D69V |
probably damaging |
Het |
| Gucy1a1 |
G |
T |
3: 82,119,162 (GRCm38) |
|
probably benign |
Het |
| Haus5 |
A |
T |
7: 30,658,555 (GRCm38) |
L376Q |
probably damaging |
Het |
| Ifne |
A |
T |
4: 88,879,705 (GRCm38) |
Y159N |
probably damaging |
Het |
| Ift80 |
A |
G |
3: 68,990,759 (GRCm38) |
V81A |
probably benign |
Het |
| Inpp5b |
T |
C |
4: 124,751,495 (GRCm38) |
V192A |
probably benign |
Het |
| Kcnh4 |
A |
G |
11: 100,749,743 (GRCm38) |
S486P |
probably damaging |
Het |
| Kif5b |
A |
G |
18: 6,222,912 (GRCm38) |
|
probably benign |
Het |
| Macf1 |
T |
A |
4: 123,433,303 (GRCm38) |
E4800D |
probably damaging |
Het |
| Mblac2 |
C |
T |
13: 81,711,976 (GRCm38) |
Q150* |
probably null |
Het |
| Mc1r |
A |
T |
8: 123,407,516 (GRCm38) |
T3S |
probably benign |
Het |
| Med17 |
G |
A |
9: 15,265,372 (GRCm38) |
Q70* |
probably null |
Het |
| Myocd |
A |
T |
11: 65,179,030 (GRCm38) |
|
probably null |
Het |
| Nphp3 |
T |
C |
9: 104,031,970 (GRCm38) |
L793P |
probably benign |
Het |
| Olfr1020 |
T |
A |
2: 85,849,716 (GRCm38) |
M88K |
probably damaging |
Het |
| Olfr1240 |
T |
G |
2: 89,439,659 (GRCm38) |
T207P |
possibly damaging |
Het |
| Olfr1377 |
A |
G |
11: 50,985,543 (GRCm38) |
T281A |
probably damaging |
Het |
| Olfr1436 |
T |
C |
19: 12,298,580 (GRCm38) |
D184G |
probably damaging |
Het |
| Olfr165 |
A |
T |
16: 19,407,301 (GRCm38) |
F238L |
probably damaging |
Het |
| Olfr891 |
T |
A |
9: 38,179,900 (GRCm38) |
T308S |
possibly damaging |
Het |
| Piezo1 |
A |
T |
8: 122,486,921 (GRCm38) |
L1745Q |
probably damaging |
Het |
| Prdm10 |
T |
A |
9: 31,347,080 (GRCm38) |
H600Q |
probably damaging |
Het |
| Psapl1 |
C |
A |
5: 36,204,867 (GRCm38) |
L268M |
probably damaging |
Het |
| Psg23 |
T |
C |
7: 18,612,114 (GRCm38) |
I219V |
probably benign |
Het |
| Rexo5 |
A |
T |
7: 119,801,330 (GRCm38) |
R113* |
probably null |
Het |
| Rgs22 |
A |
T |
15: 36,100,212 (GRCm38) |
I243N |
probably damaging |
Het |
| Rhbdf1 |
G |
A |
11: 32,214,517 (GRCm38) |
T183I |
probably damaging |
Het |
| Rhobtb1 |
T |
C |
10: 69,270,724 (GRCm38) |
M373T |
probably benign |
Het |
| Ros1 |
G |
T |
10: 52,172,870 (GRCm38) |
A88E |
probably damaging |
Het |
| Sdr16c6 |
A |
G |
4: 4,058,834 (GRCm38) |
F251L |
probably benign |
Het |
| Skil |
A |
G |
3: 31,113,413 (GRCm38) |
Y398C |
probably damaging |
Het |
| Slc22a3 |
A |
T |
17: 12,464,532 (GRCm38) |
M148K |
probably benign |
Het |
| Slco4c1 |
G |
A |
1: 96,841,228 (GRCm38) |
P303L |
probably damaging |
Het |
| Sntn |
A |
T |
14: 13,679,103 (GRCm38) |
K92N |
probably benign |
Het |
| Spry4 |
A |
T |
18: 38,589,823 (GRCm38) |
S296T |
probably benign |
Het |
| St8sia1 |
A |
G |
6: 142,829,070 (GRCm38) |
F261S |
probably damaging |
Het |
| Stab2 |
C |
T |
10: 86,843,500 (GRCm38) |
|
probably null |
Het |
| Stk24 |
A |
T |
14: 121,293,454 (GRCm38) |
C363* |
probably null |
Het |
| Tank |
G |
A |
2: 61,578,635 (GRCm38) |
|
probably benign |
Het |
| Tmem67 |
T |
C |
4: 12,070,262 (GRCm38) |
N387S |
probably benign |
Het |
| Treml1 |
A |
T |
17: 48,366,857 (GRCm38) |
I304L |
probably benign |
Het |
| Trim13 |
A |
G |
14: 61,605,517 (GRCm38) |
I328V |
probably benign |
Het |
| Upk2 |
A |
G |
9: 44,454,085 (GRCm38) |
V62A |
probably damaging |
Het |
| Urb2 |
A |
T |
8: 124,029,635 (GRCm38) |
K694* |
probably null |
Het |
| Vmn2r17 |
C |
A |
5: 109,427,119 (GRCm38) |
N97K |
probably damaging |
Het |
| Vmn2r57 |
A |
T |
7: 41,400,468 (GRCm38) |
V619D |
probably damaging |
Het |
| Vmn2r92 |
G |
A |
17: 18,167,372 (GRCm38) |
R213Q |
probably benign |
Het |
| Wnt6 |
G |
A |
1: 74,782,629 (GRCm38) |
C123Y |
probably damaging |
Het |
| Zfp292 |
A |
G |
4: 34,819,563 (GRCm38) |
I253T |
probably damaging |
Het |
| Zfp52 |
C |
T |
17: 21,561,243 (GRCm38) |
S451L |
probably damaging |
Het |
|
| Other mutations in Dock9 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00236:Dock9
|
APN |
14 |
121,668,468 (GRCm38) |
missense |
probably benign |
0.12 |
|
IGL00817:Dock9
|
APN |
14 |
121,698,291 (GRCm38) |
missense |
probably damaging |
0.96 |
|
IGL00923:Dock9
|
APN |
14 |
121,607,092 (GRCm38) |
unclassified |
probably benign |
|
|
IGL01385:Dock9
|
APN |
14 |
121,580,583 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
IGL01567:Dock9
|
APN |
14 |
121,653,084 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01767:Dock9
|
APN |
14 |
121,622,870 (GRCm38) |
missense |
possibly damaging |
0.91 |
|
IGL01811:Dock9
|
APN |
14 |
121,559,028 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02512:Dock9
|
APN |
14 |
121,619,538 (GRCm38) |
splice site |
probably benign |
|
|
IGL02525:Dock9
|
APN |
14 |
121,640,126 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02550:Dock9
|
APN |
14 |
121,698,312 (GRCm38) |
start codon destroyed |
probably null |
0.07 |
|
IGL02559:Dock9
|
APN |
14 |
121,625,147 (GRCm38) |
splice site |
probably benign |
|
|
IGL02666:Dock9
|
APN |
14 |
121,580,699 (GRCm38) |
missense |
probably benign |
0.42 |
|
IGL02674:Dock9
|
APN |
14 |
121,595,611 (GRCm38) |
splice site |
probably null |
|
|
IGL02795:Dock9
|
APN |
14 |
121,639,978 (GRCm38) |
missense |
probably benign |
0.04 |
|
IGL03074:Dock9
|
APN |
14 |
121,607,270 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
IGL03095:Dock9
|
APN |
14 |
121,639,528 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL03294:Dock9
|
APN |
14 |
121,641,623 (GRCm38) |
splice site |
probably benign |
|
|
R0036:Dock9
|
UTSW |
14 |
121,622,853 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0050:Dock9
|
UTSW |
14 |
121,607,225 (GRCm38) |
missense |
probably benign |
0.43 |
|
R0050:Dock9
|
UTSW |
14 |
121,607,225 (GRCm38) |
missense |
probably benign |
0.43 |
|
R0164:Dock9
|
UTSW |
14 |
121,597,665 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0164:Dock9
|
UTSW |
14 |
121,597,665 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0270:Dock9
|
UTSW |
14 |
121,575,999 (GRCm38) |
missense |
probably benign |
0.02 |
|
R0494:Dock9
|
UTSW |
14 |
121,662,584 (GRCm38) |
missense |
possibly damaging |
0.64 |
|
R0726:Dock9
|
UTSW |
14 |
121,651,768 (GRCm38) |
nonsense |
probably null |
|
|
R1029:Dock9
|
UTSW |
14 |
121,599,684 (GRCm38) |
splice site |
probably null |
|
|
R1214:Dock9
|
UTSW |
14 |
121,586,316 (GRCm38) |
missense |
probably benign |
0.02 |
|
R1231:Dock9
|
UTSW |
14 |
121,575,950 (GRCm38) |
missense |
possibly damaging |
0.61 |
|
R1535:Dock9
|
UTSW |
14 |
121,546,064 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1629:Dock9
|
UTSW |
14 |
121,543,574 (GRCm38) |
missense |
possibly damaging |
0.88 |
|
R1637:Dock9
|
UTSW |
14 |
121,651,775 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R1733:Dock9
|
UTSW |
14 |
121,626,880 (GRCm38) |
missense |
probably benign |
0.01 |
|
R1772:Dock9
|
UTSW |
14 |
121,609,798 (GRCm38) |
missense |
probably benign |
0.07 |
|
R1855:Dock9
|
UTSW |
14 |
121,640,159 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1888:Dock9
|
UTSW |
14 |
121,625,205 (GRCm38) |
missense |
probably benign |
0.18 |
|
R1888:Dock9
|
UTSW |
14 |
121,625,205 (GRCm38) |
missense |
probably benign |
0.18 |
|
R1901:Dock9
|
UTSW |
14 |
121,625,153 (GRCm38) |
splice site |
probably null |
|
|
R1920:Dock9
|
UTSW |
14 |
121,583,380 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1987:Dock9
|
UTSW |
14 |
121,591,830 (GRCm38) |
missense |
probably benign |
0.00 |
|
R3035:Dock9
|
UTSW |
14 |
121,606,837 (GRCm38) |
missense |
possibly damaging |
0.60 |
|
R3851:Dock9
|
UTSW |
14 |
121,629,086 (GRCm38) |
splice site |
probably null |
|
|
R4020:Dock9
|
UTSW |
14 |
121,606,855 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4021:Dock9
|
UTSW |
14 |
121,626,912 (GRCm38) |
missense |
possibly damaging |
0.80 |
|
R4089:Dock9
|
UTSW |
14 |
121,583,471 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4258:Dock9
|
UTSW |
14 |
121,581,442 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4423:Dock9
|
UTSW |
14 |
121,562,053 (GRCm38) |
critical splice donor site |
probably null |
|
|
R4561:Dock9
|
UTSW |
14 |
121,559,007 (GRCm38) |
missense |
probably benign |
0.01 |
|
R4604:Dock9
|
UTSW |
14 |
121,668,459 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4646:Dock9
|
UTSW |
14 |
121,586,246 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4647:Dock9
|
UTSW |
14 |
121,586,246 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4776:Dock9
|
UTSW |
14 |
121,610,097 (GRCm38) |
missense |
possibly damaging |
0.81 |
|
R4809:Dock9
|
UTSW |
14 |
121,546,596 (GRCm38) |
missense |
probably benign |
0.37 |
|
R4951:Dock9
|
UTSW |
14 |
121,653,135 (GRCm38) |
missense |
probably benign |
0.35 |
|
R5151:Dock9
|
UTSW |
14 |
121,578,170 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5359:Dock9
|
UTSW |
14 |
121,653,060 (GRCm38) |
missense |
possibly damaging |
0.69 |
|
R5366:Dock9
|
UTSW |
14 |
121,578,203 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5502:Dock9
|
UTSW |
14 |
121,610,182 (GRCm38) |
splice site |
probably null |
|
|
R5579:Dock9
|
UTSW |
14 |
121,599,695 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5753:Dock9
|
UTSW |
14 |
121,634,625 (GRCm38) |
missense |
probably benign |
0.05 |
|
R5836:Dock9
|
UTSW |
14 |
121,681,351 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5858:Dock9
|
UTSW |
14 |
121,628,792 (GRCm38) |
missense |
probably benign |
0.00 |
|
R5890:Dock9
|
UTSW |
14 |
121,668,408 (GRCm38) |
critical splice donor site |
probably null |
|
|
R6075:Dock9
|
UTSW |
14 |
121,545,973 (GRCm38) |
missense |
probably benign |
|
|
R6298:Dock9
|
UTSW |
14 |
121,634,594 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6306:Dock9
|
UTSW |
14 |
121,562,080 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6321:Dock9
|
UTSW |
14 |
121,546,021 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6330:Dock9
|
UTSW |
14 |
121,605,243 (GRCm38) |
start codon destroyed |
probably null |
0.00 |
|
R6719:Dock9
|
UTSW |
14 |
121,610,027 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6784:Dock9
|
UTSW |
14 |
121,543,514 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6826:Dock9
|
UTSW |
14 |
121,622,918 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6830:Dock9
|
UTSW |
14 |
121,622,918 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6838:Dock9
|
UTSW |
14 |
121,546,596 (GRCm38) |
missense |
possibly damaging |
0.71 |
|
R6868:Dock9
|
UTSW |
14 |
121,586,264 (GRCm38) |
missense |
probably benign |
0.37 |
|
R6919:Dock9
|
UTSW |
14 |
121,643,152 (GRCm38) |
missense |
probably benign |
0.42 |
|
R6989:Dock9
|
UTSW |
14 |
121,627,379 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7539:Dock9
|
UTSW |
14 |
121,581,436 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7645:Dock9
|
UTSW |
14 |
121,597,663 (GRCm38) |
missense |
probably benign |
0.44 |
|
R7875:Dock9
|
UTSW |
14 |
121,625,984 (GRCm38) |
nonsense |
probably null |
|
|
R7900:Dock9
|
UTSW |
14 |
121,546,079 (GRCm38) |
missense |
possibly damaging |
0.84 |
|
R8040:Dock9
|
UTSW |
14 |
121,651,794 (GRCm38) |
missense |
probably benign |
0.06 |
|
R8420:Dock9
|
UTSW |
14 |
121,546,042 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8511:Dock9
|
UTSW |
14 |
121,681,435 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8511:Dock9
|
UTSW |
14 |
121,627,389 (GRCm38) |
missense |
probably benign |
0.40 |
|
R8514:Dock9
|
UTSW |
14 |
121,658,787 (GRCm38) |
missense |
probably benign |
0.25 |
|
R8691:Dock9
|
UTSW |
14 |
121,640,105 (GRCm38) |
missense |
possibly damaging |
0.49 |
|
R8804:Dock9
|
UTSW |
14 |
121,605,183 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R8894:Dock9
|
UTSW |
14 |
121,622,961 (GRCm38) |
missense |
probably benign |
0.10 |
|
R8900:Dock9
|
UTSW |
14 |
121,580,528 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9069:Dock9
|
UTSW |
14 |
121,628,912 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R9218:Dock9
|
UTSW |
14 |
121,668,459 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9233:Dock9
|
UTSW |
14 |
121,583,369 (GRCm38) |
missense |
probably benign |
0.09 |
|
R9236:Dock9
|
UTSW |
14 |
121,639,558 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9285:Dock9
|
UTSW |
14 |
121,595,600 (GRCm38) |
missense |
probably benign |
|
|
R9451:Dock9
|
UTSW |
14 |
121,550,189 (GRCm38) |
splice site |
probably benign |
|
|
R9461:Dock9
|
UTSW |
14 |
121,605,189 (GRCm38) |
missense |
probably benign |
0.05 |
|
R9484:Dock9
|
UTSW |
14 |
121,581,432 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9517:Dock9
|
UTSW |
14 |
121,591,824 (GRCm38) |
missense |
probably benign |
0.07 |
|
R9542:Dock9
|
UTSW |
14 |
121,627,363 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9694:Dock9
|
UTSW |
14 |
121,581,379 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9701:Dock9
|
UTSW |
14 |
121,639,571 (GRCm38) |
missense |
probably benign |
0.01 |
|
R9703:Dock9
|
UTSW |
14 |
121,544,577 (GRCm38) |
makesense |
probably null |
|
|
R9726:Dock9
|
UTSW |
14 |
121,597,737 (GRCm38) |
missense |
possibly damaging |
0.61 |
|
R9741:Dock9
|
UTSW |
14 |
121,640,104 (GRCm38) |
missense |
probably damaging |
1.00 |
|
Z1088:Dock9
|
UTSW |
14 |
121,555,275 (GRCm38) |
missense |
probably damaging |
1.00 |
|
Z1176:Dock9
|
UTSW |
14 |
121,651,782 (GRCm38) |
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 |
Incidental Mutation