Accession |
Clone |
Registered year |
Dir. |
Tissue |
Sequence |
Contig*1 |
Contig*2 |
Homology (BLAST) |
Swiss-Prot |
nr |
Top hit |
GO ID |
Term |
Top hit (Definition)
|
score
|
E-Value
|
BJ301304
|
whyd10a02
|
2002
|
5'
|
Spikelet at late flowering
|
453bp
|
|
Contig16195
Contig16195
|
Q9ZRR5
|
GO:0005525
|
GTP binding
|
unknown [Zea mays]
|
806
|
9.79572e-85
|
BJ301305
|
whyd10a04
|
2002
|
5'
|
Spikelet at late flowering
|
603bp
|
|
Contig8767
Contig8767
|
Q8Z187
|
GO:0006281
|
DNA repair
|
Os02g0828500 [Oryza sativa (japonica cultivar-group)]
|
654
|
7.55939e-67
|
BJ301306
|
whyd10a05
|
2002
|
5'
|
Spikelet at late flowering
|
428bp
|
|
Contig15691
Contig15691
|
Q9LEV3
|
GO:0005739
|
mitochondrion
|
hypothetical protein OsI_013021 [Oryza sativa (indica cultivar-group)]
|
493
|
1.94229e-48
|
BJ301307
|
whyd10a06
|
2002
|
5'
|
Spikelet at late flowering
|
413bp
|
|
|
Q9W5D0
|
GO:0005871
|
kinesin complex
|
hypothetical protein OsI_028719 [Oryza sativa (indica cultivar-group)]
|
202
|
1.06328e-14
|
BJ301308
|
whyd10a07
|
2002
|
5'
|
Spikelet at late flowering
|
462bp
|
|
Contig15665
Contig15665
|
Q43292
|
GO:0003735
|
structural constituent of ribosome
|
Os02g0815000 [Oryza sativa (japonica cultivar-group)]
|
481
|
4.69111e-47
|
BJ301309
|
whyd10a08
|
2002
|
5'
|
Spikelet at late flowering
|
560bp
|
|
Contig15086
Contig15086
|
P46290
|
GO:0003735
|
structural constituent of ribosome
|
unknown [Zea mays]
|
457
|
4.33964e-44
|
BJ301310
|
whyd10a09
|
2002
|
5'
|
Spikelet at late flowering
|
388bp
|
|
Contig5600
Contig5600
|
Q97I38
Q97I38
|
GO:0003723
GO:0016021
|
RNA binding
,
integral to membrane
|
unnamed protein product [Vitis vinifera]
|
384
|
8.36106e-36
|
BJ301311
|
whyd10a10
|
2002
|
5'
|
Spikelet at late flowering
|
165bp
|
|
Contig5600
Contig5600
|
Q9BV73
Q9BV73
|
GO:0005871
GO:0007049
|
kinesin complex
,
cell cycle
|
unknown [Zea mays]
|
121
|
2.64866e-05
|
BJ301312
|
whyd10a15
|
2002
|
5'
|
Spikelet at late flowering
|
314bp
|
|
Contig15932
Contig15932
|
Q9LZ17
|
GO:0003735
|
structural constituent of ribosome
|
unknown [Zea mays]
|
434
|
1.32089e-41
|
BJ301313
|
whyd10a16
|
2002
|
5'
|
Spikelet at late flowering
|
624bp
|
|
Contig14724
Contig14724
|
P08579
P08579
P08579
P08579
P08579
|
GO:0003723
GO:0005634
GO:0006371
GO:0006397
GO:0030529
|
RNA binding
,
nucleus
,
mRNA splicing
,
mRNA processing
,
ribonucleoprotein complex
|
unknown [Zea mays]
|
737
|
1.96962e-76
|
BJ301314
|
whyd10a17
|
2002
|
5'
|
Spikelet at late flowering
|
438bp
|
|
Contig14499
Contig14499
|
|
|
|
Putative apospory-associated protein C
|
374
|
1.20692e-34
|
BJ301315
|
whyd10a18
|
2002
|
5'
|
Spikelet at late flowering
|
461bp
|
|
Contig14520
Contig14520
|
Q63943
Q63943
Q63943
|
GO:0003677
GO:0005634
GO:0006355
|
DNA binding
,
nucleus
,
regulation of transcription, DNA-dependent
|
OSJNBa0068L06.9 [Oryza sativa (japonica cultivar-group)]
|
306
|
9.23808e-27
|
BJ301316
|
whyd10a20
|
2002
|
5'
|
Spikelet at late flowering
|
399bp
|
|
Contig5596
Contig5596
|
P02300
P02300
P02300
P02300
|
GO:0000786
GO:0003677
GO:0005634
GO:0005694
|
nucleosome
,
DNA binding
,
nucleus
,
chromosome
|
hypothetical protein BRAFLDRAFT_75126 [Branchiostoma floridae]
|
308
|
5.52487e-27
|
BJ301317
|
whyd10a21
|
2002
|
5'
|
Spikelet at late flowering
|
381bp
|
|
Contig14547
Contig14547
|
P45635
|
GO:0003735
|
structural constituent of ribosome
|
hypothetical protein OsI_034350 [Oryza sativa (indica cultivar-group)]
|
575
|
6.02164e-58
|
BJ301318
|
whyd10a22
|
2002
|
5'
|
Spikelet at late flowering
|
619bp
|
|
Contig12412
Contig12412
|
Q9JI44
Q9JI44
Q9JI44
|
GO:0005634
GO:0005871
GO:0006355
|
nucleus
,
kinesin complex
,
regulation of transcription, DNA-dependent
|
Os05g0540800 [Oryza sativa (japonica cultivar-group)]
|
502
|
8.88452e-94
|
BJ301319
|
whyd10a24
|
2002
|
5'
|
Spikelet at late flowering
|
431bp
|
|
Contig16250
Contig16250
|
P82279
P82279
|
GO:0007601
GO:0007601
|
vision
,
vision
|
|
|
|
BJ301320
|
whyd10b01
|
2002
|
5'
|
Spikelet at late flowering
|
468bp
|
|
Contig5592
Contig5592
|
Q09277
|
GO:0016021
|
integral to membrane
|
hypothetical protein OsJ_012444 [Oryza sativa (japonica cultivar-group)]
|
76
|
4.41867
|
BJ301321
|
whyd10b02
|
2002
|
5'
|
Spikelet at late flowering
|
439bp
|
|
Contig11974
Contig11974
|
P02845
|
GO:0045735
|
nutrient reservoir activity
|
hypothetical protein LELG_00450 [Lodderomyces elongisporus NRRL YB-4239]
|
77
|
3.30336
|
BJ301322
|
whyd10b04
|
2002
|
5'
|
Spikelet at late flowering
|
177bp
|
|
Contig14802
Contig14802
|
|
|
|
|
|
|
BJ301323
|
whyd10b05
|
2002
|
5'
|
Spikelet at late flowering
|
515bp
|
|
Contig16094
Contig16094
|
P41098
|
GO:0003735
|
structural constituent of ribosome
|
unknown [Zea mays]
|
489
|
6.6482e-48
|
BJ301324
|
whyd10b06
|
2002
|
5'
|
Spikelet at late flowering
|
596bp
|
|
Contig16196
Contig16196
|
P02276
P02276
P02276
P02276
|
GO:0000786
GO:0003677
GO:0005634
GO:0005694
|
nucleosome
,
DNA binding
,
nucleus
,
chromosome
|
Histone H2A.2.1
|
466
|
4.63552e-45
|
BJ301325
|
whyd10b07
|
2002
|
5'
|
Spikelet at late flowering
|
486bp
|
|
Contig13500
Contig13500
|
P37829
P37829
|
GO:0016301
GO:0016740
|
kinase activity
,
transferase activity
|
hypothetical protein OsI_026607 [Oryza sativa (indica cultivar-group)]
|
607
|
1.18046e-61
|
BJ301326
|
whyd10b08
|
2002
|
5'
|
Spikelet at late flowering
|
421bp
|
|
Contig16151
Contig16151
|
P17073
|
GO:0003735
|
structural constituent of ribosome
|
unknown [Zea mays]
|
530
|
1.00353e-52
|
BJ301327
|
whyd10b10
|
2002
|
5'
|
Spikelet at late flowering
|
104bp
|
|
Contig15776
Contig15776
|
P08565
|
GO:0005634
|
nucleus
|
unknown [Zea mays]
|
174
|
1.9324e-11
|
BJ301328
|
whyd10b11
|
2002
|
5'
|
Spikelet at late flowering
|
361bp
|
|
Contig10650
Contig10650
|
Q8K3I4
|
GO:0003779
|
actin binding
|
hypothetical protein OsI_025975 [Oryza sativa (indica cultivar-group)]
|
265
|
5.2697e-22
|
BJ301329
|
whyd10b12
|
2002
|
5'
|
Spikelet at late flowering
|
499bp
|
|
Contig16105
Contig16105
|
P14344
P14344
P14344
P14344
|
GO:0005524
GO:0006259
GO:0016301
GO:0016740
|
ATP binding
,
DNA metabolism
,
kinase activity
,
transferase activity
|
hypothetical protein [Vitis vinifera]
|
201
|
1.51589e-14
|
BJ301330
|
whyd10b13
|
2002
|
5'
|
Spikelet at late flowering
|
500bp
|
|
|
P46681
|
GO:0016491
|
oxidoreductase activity
|
hypothetical protein OsI_024269 [Oryza sativa (indica cultivar-group)]
|
749
|
4.3295e-78
|
BJ301331
|
whyd10b14
|
2002
|
5'
|
Spikelet at late flowering
|
413bp
|
|
Contig13821
Contig13821
|
P35597
P35597
P35597
P35597
|
GO:0000287
GO:0005524
GO:0016021
GO:0016787
|
magnesium ion binding
,
ATP binding
,
integral to membrane
,
hydrolase activity
|
Os02g0708000 [Oryza sativa (japonica cultivar-group)]
|
423
|
2.51325e-40
|
BJ301332
|
whyd10b15
|
2002
|
5'
|
Spikelet at late flowering
|
217bp
|
|
|
O80988
O80988
|
GO:0005739
GO:0016491
|
mitochondrion
,
oxidoreductase activity
|
glycine decarboxylase P subunit [x Tritordeum sp.]
|
312
|
1.85049e-27
|
BJ301333
|
whyd10b16
|
2002
|
5'
|
Spikelet at late flowering
|
222bp
|
|
Contig15981
Contig15981
|
Q9NDR5
Q9NDR5
Q9NDR5
Q9NDR5
|
GO:0006754
GO:0015078
GO:0015992
GO:0016787
|
ATP biosynthesis
,
hydrogen ion transporter activity
,
proton transport
,
hydrolase activity
|
|
|
|
BJ301334
|
whyd10b17
|
2002
|
5'
|
Spikelet at late flowering
|
320bp
|
|
Contig15976
Contig15976
|
O22518
|
GO:0003735
|
structural constituent of ribosome
|
hypothetical protein OsI_010032 [Oryza sativa (indica cultivar-group)]
|
374
|
1.23156e-34
|
BJ301335
|
whyd10b19
|
2002
|
5'
|
Spikelet at late flowering
|
419bp
|
|
Contig13438
Contig13438
|
Q40082
Q40082
Q40082
Q40082
|
GO:0000287
GO:0005996
GO:0006098
GO:0016853
|
magnesium ion binding
,
monosaccharide metabolism
,
pentose-phosphate shunt
,
isomerase activity
|
Xylose isomerase
|
423
|
2.49261e-40
|
BJ301336
|
whyd10b20
|
2002
|
5'
|
Spikelet at late flowering
|
405bp
|
|
Contig14806
Contig14806
|
Q96321
Q96321
Q96321
Q96321
|
GO:0006810
GO:0006886
GO:0008565
GO:0015031
|
transport
,
intracellular protein transport
,
protein transporter activity
,
protein transport
|
hypothetical protein OsI_001178 [Oryza sativa (indica cultivar-group)]
|
382
|
1.44469e-35
|
BJ301337
|
whyd10b22
|
2002
|
5'
|
Spikelet at late flowering
|
188bp
|
|
Contig16291
Contig16291
|
|
|
|
hypothetical protein Bm1_17870 [Brugia malayi]
|
174
|
1.92074e-11
|
BJ301338
|
whyd10b23
|
2002
|
5'
|
Spikelet at late flowering
|
568bp
|
|
Contig15674
Contig15674
|
P05690
|
GO:0045735
|
nutrient reservoir activity
|
histone deacetylase HDAC2 [Triticum aestivum]
|
614
|
2.79731e-62
|
BJ301339
|
whyd10b24
|
2002
|
5'
|
Spikelet at late flowering
|
217bp
|
|
Contig12654
Contig12654
|
Q06441
Q06441
Q06441
|
GO:0005194
GO:0005509
GO:0007155
|
cell adhesion molecule activity
,
calcium ion binding
,
cell adhesion
|
|
|
|
BJ301340
|
whyd10c01
|
2002
|
5'
|
Spikelet at late flowering
|
480bp
|
|
Contig12715
Contig12715
|
Q63413
Q63413
Q63413
Q63413
|
GO:0003723
GO:0004386
GO:0005524
GO:0005634
|
RNA binding
,
helicase activity
,
ATP binding
,
nucleus
|
hypothetical protein OsJ_002111 [Oryza sativa (japonica cultivar-group)]
|
746
|
8.8447e-78
|
BJ301341
|
whyd10c02
|
2002
|
5'
|
Spikelet at late flowering
|
456bp
|
|
Contig13199
Contig13199
|
Q9CFG0
Q9CFG0
Q9CFG0
Q9CFG0
|
GO:0003824
GO:0006164
GO:0016740
GO:0016787
|
catalytic activity
,
purine nucleotide biosynthesis
,
transferase activity
,
hydrolase activity
|
hypothetical protein CPCC7001_942 [Cyanobium sp. PCC 7001]
|
79
|
1.94816
|
BJ301342
|
whyd10c03
|
2002
|
5'
|
Spikelet at late flowering
|
462bp
|
|
Contig8502
Contig8502
|
|
|
|
unknown [Oryza sativa (indica cultivar-group)]
|
374
|
1.20374e-34
|
BJ301343
|
whyd10c05
|
2002
|
5'
|
Spikelet at late flowering
|
587bp
|
|
Contig13874
Contig13874
|
P25325
|
GO:0016740
|
transferase activity
|
Os12g0608600 [Oryza sativa (japonica cultivar-group)]
|
922
|
6.01561e-98
|
BJ301344
|
whyd10c07
|
2002
|
5'
|
Spikelet at late flowering
|
399bp
|
|
Contig12984
Contig12984
|
P29435
P29435
P29435
|
GO:0003916
GO:0005524
GO:0016853
|
DNA topoisomerase activity
,
ATP binding
,
isomerase activity
|
Os04g0441900 [Oryza sativa (japonica cultivar-group)]
|
142
|
9.83724e-08
|
BJ301345
|
whyd10c08
|
2002
|
5'
|
Spikelet at late flowering
|
411bp
|
|
Contig15126
Contig15126
|
Q9ZFK1
Q9ZFK1
Q9ZFK1
|
GO:0003916
GO:0005524
GO:0016853
|
DNA topoisomerase activity
,
ATP binding
,
isomerase activity
|
hypothetical protein OsJ_002018 [Oryza sativa (japonica cultivar-group)]
|
672
|
3.37921e-69
|
BJ301346
|
whyd10c09
|
2002
|
5'
|
Spikelet at late flowering
|
520bp
|
|
|
P26323
P26323
P26323
P26323
|
GO:0003677
GO:0005634
GO:0006355
GO:0008151
|
DNA binding
,
nucleus
,
regulation of transcription, DNA-dependent
,
cell growth and/or maintenance
|
hypothetical protein CHGG_00844 [Chaetomium globosum CBS 148.51]
|
82
|
1.08526
|
BJ301347
|
whyd10c11
|
2002
|
5'
|
Spikelet at late flowering
|
421bp
|
|
Contig14602
Contig14602
|
O23290
|
GO:0003735
|
structural constituent of ribosome
|
unknown [Zea mays]
|
422
|
3.25545e-40
|
BJ301348
|
whyd10c12
|
2002
|
5'
|
Spikelet at late flowering
|
604bp
|
|
Contig15126
Contig15126
|
P08392
P08392
P08392
|
GO:0003677
GO:0005634
GO:0006355
|
DNA binding
,
nucleus
,
regulation of transcription, DNA-dependent
|
hypothetical protein OsJ_002018 [Oryza sativa (japonica cultivar-group)]
|
826
|
8.58909e-87
|
BJ301349
|
whyd10c13
|
2002
|
5'
|
Spikelet at late flowering
|
379bp
|
|
Contig12031
Contig12031
|
Q9LST7
Q9LST7
Q9LST7
|
GO:0005829
GO:0008233
GO:0016787
|
cytosol
,
peptidase activity
,
hydrolase activity
|
hypothetical protein OsI_005977 [Oryza sativa (indica cultivar-group)]
|
255
|
9.04917e-22
|
BJ301350
|
whyd10c16
|
2002
|
5'
|
Spikelet at late flowering
|
334bp
|
|
Contig5591
Contig5591
|
Q52716
Q52716
Q52716
|
GO:0006118
GO:0009399
GO:0019866
|
electron transport
,
nitrogen fixation
,
inner membrane
|
|
|
|
BJ301351
|
whyd10c17
|
2002
|
5'
|
Spikelet at late flowering
|
344bp
|
|
Contig5589
Contig5589
|
|
|
|
unknown [Zea mays]
|
294
|
2.25943e-25
|
BJ301352
|
whyd10c18
|
2002
|
5'
|
Spikelet at late flowering
|
620bp
|
|
Contig12412
Contig12412
|
Q9JI44
Q9JI44
Q9JI44
|
GO:0005634
GO:0005871
GO:0006355
|
nucleus
,
kinesin complex
,
regulation of transcription, DNA-dependent
|
Os05g0540800 [Oryza sativa (japonica cultivar-group)]
|
502
|
2.35115e-94
|
BJ301353
|
whyd10c19
|
2002
|
5'
|
Spikelet at late flowering
|
394bp
|
|
Contig16126
Contig16126
|
P29546
P29546
|
GO:0003746
GO:0006412
|
translation elongation factor activity
,
protein biosynthesis
|
Elongation factor 1-beta (EF-1-beta) (Elongation factor 1B-alpha 2) (eEF-1B alpha 2) (Elongation factor 1-beta') (EF-1-beta')
|
287
|
1.47339e-24
|
BJ301354
|
whyd10c20
|
2002
|
5'
|
Spikelet at late flowering
|
404bp
|
|
Contig16137
Contig16137
|
Q9LUQ6
|
GO:0003735
|
structural constituent of ribosome
|
ribosomal protein L19 [Triticum aestivum]
|
499
|
3.91605e-49
|
BJ301355
|
whyd10c22
|
2002
|
5'
|
Spikelet at late flowering
|
472bp
|
|
Contig13023
Contig13023
|
P59268
|
GO:0016021
|
integral to membrane
|
hypothetical protein OsI_004892 [Oryza sativa (indica cultivar-group)]
|
803
|
2.20252e-84
|
BJ301356
|
whyd10c24
|
2002
|
5'
|
Spikelet at late flowering
|
660bp
|
|
|
Q05859
Q05859
Q05859
|
GO:0005634
GO:0005871
GO:0007275
|
nucleus
,
kinesin complex
,
development
|
PREDICTED: similar to proline rich 8 [Ornithorhynchus anatinus]
|
94
|
0.0811161
|
BJ301357
|
whyd10d01
|
2002
|
5'
|
Spikelet at late flowering
|
391bp
|
|
Contig15943
Contig15943
|
|
|
|
Os01g0918300 [Oryza sativa (japonica cultivar-group)]
|
414
|
2.76583e-39
|
BJ301358
|
whyd10d02
|
2002
|
5'
|
Spikelet at late flowering
|
487bp
|
|
Contig16266
Contig16266
|
Q91661
Q91661
Q91661
|
GO:0003677
GO:0005634
GO:0006355
|
DNA binding
,
nucleus
,
regulation of transcription, DNA-dependent
|
hypothetical protein [Oryza sativa Japonica Group]
|
222
|
1.34378e-23
|
BJ301359
|
whyd10d04
|
2002
|
5'
|
Spikelet at late flowering
|
431bp
|
|
|
P04087
P04087
|
GO:0005179
GO:0008083
|
hormone activity
,
growth factor activity
|
hypothetical protein OsJ_015883 [Oryza sativa (japonica cultivar-group)]
|
503
|
2.51863e-52
|
BJ301360
|
whyd10d05
|
2002
|
5'
|
Spikelet at late flowering
|
682bp
|
|
Contig16245
Contig16245
|
P33126
P33126
P33126
|
GO:0003754
GO:0003773
GO:0005524
|
chaperone activity
,
heat shock protein activity
,
ATP binding
|
heat shock protein 90 [Triticum aestivum]
|
993
|
4.89912e-106
|
BJ301361
|
whyd10d06
|
2002
|
5'
|
Spikelet at late flowering
|
580bp
|
|
Contig16255
Contig16255
|
O81361
|
GO:0003735
|
structural constituent of ribosome
|
ribosomal subunit 8E protein [Brachypodium sylvaticum]
|
617
|
1.35858e-62
|
BJ301362
|
whyd10d09
|
2002
|
5'
|
Spikelet at late flowering
|
424bp
|
|
Contig15102
Contig15102
|
P02275
P02275
P02275
P02275
|
GO:0000786
GO:0003677
GO:0005634
GO:0005694
|
nucleosome
,
DNA binding
,
nucleus
,
chromosome
|
Protein H2A.5 (wcH2A-2)
|
480
|
6.27421e-47
|
BJ301363
|
whyd10d11
|
2002
|
5'
|
Spikelet at late flowering
|
616bp
|
|
Contig15889
Contig15889
|
P12778
P12778
P12778
P12778
|
GO:0005739
GO:0005746
GO:0006118
GO:0016021
|
mitochondrion
,
mitochondrial electron transport chain
,
electron transport
,
integral to membrane
|
|
|
|
BJ301364
|
whyd10d14
|
2002
|
5'
|
Spikelet at late flowering
|
409bp
|
|
Contig9249
Contig9249
|
|
|
|
hypothetical protein OsJ_004606 [Oryza sativa (japonica cultivar-group)]
|
213
|
5.68432e-16
|
BJ301365
|
whyd10d16
|
2002
|
5'
|
Spikelet at late flowering
|
135bp
|
|
Contig15694
Contig15694
|
O62732
O62732
|
GO:0003779
GO:0045202
|
actin binding
,
synaptic junction
|
putative secreted protein [Streptomyces ambofaciens ATCC 23877]
|
78
|
2.53247
|
BJ301366
|
whyd10d17
|
2002
|
5'
|
Spikelet at late flowering
|
401bp
|
|
Contig7427
Contig7427
|
|
|
|
putative ABC transporter [Oryza sativa Japonica Group]
|
644
|
6.03804e-66
|
BJ301367
|
whyd10d19
|
2002
|
5'
|
Spikelet at late flowering
|
480bp
|
|
Contig12319
Contig12319
|
P49299
P49299
P49299
P49299
|
GO:0006097
GO:0006099
GO:0009514
GO:0016740
|
glyoxylate cycle
,
tricarboxylic acid cycle
,
glyoxysome
,
transferase activity
|
hypothetical protein OsJ_005821 [Oryza sativa (japonica cultivar-group)]
|
667
|
1.28014e-68
|
BJ301368
|
whyd10d20
|
2002
|
5'
|
Spikelet at late flowering
|
458bp
|
|
Contig16144
Contig16144
|
Q9ZRI7
Q9ZRI7
|
GO:0003746
GO:0006412
|
translation elongation factor activity
,
protein biosynthesis
|
unknown [Zea mays]
|
502
|
1.73768e-49
|
BJ301369
|
whyd10d21
|
2002
|
5'
|
Spikelet at late flowering
|
502bp
|
|
|
P87117
|
GO:0005871
|
kinesin complex
|
unknown [Zea mays]
|
684
|
1.52699e-70
|
BJ301370
|
whyd10d22
|
2002
|
5'
|
Spikelet at late flowering
|
178bp
|
|
Contig16169
Contig16169
|
P19950
|
GO:0003735
|
structural constituent of ribosome
|
unknown [Zea mays]
|
128
|
4.02216e-06
|
BJ301371
|
whyd10d23
|
2002
|
5'
|
Spikelet at late flowering
|
403bp
|
|
Contig9324
Contig9324
|
P02300
P02300
P02300
P02300
|
GO:0000786
GO:0003677
GO:0005634
GO:0005694
|
nucleosome
,
DNA binding
,
nucleus
,
chromosome
|
histone H3 (AA 1-123) [Medicago sativa]
|
373
|
1.60377e-34
|
BJ301372
|
whyd10d24
|
2002
|
5'
|
Spikelet at late flowering
|
582bp
|
|
Contig5586
Contig5586
|
|
|
|
hypothetical protein OsJ_015803 [Oryza sativa (japonica cultivar-group)]
|
678
|
1.16483e-69
|
BJ301373
|
whyd10e01
|
2002
|
5'
|
Spikelet at late flowering
|
428bp
|
|
Contig7819
Contig7819
|
Q00313
Q00313
Q00313
|
GO:0003677
GO:0003916
GO:0016853
|
DNA binding
,
DNA topoisomerase activity
,
isomerase activity
|
hypothetical protein OsI_011098 [Oryza sativa (indica cultivar-group)]
|
336
|
3.11533e-30
|
BJ301374
|
whyd10e02
|
2002
|
5'
|
Spikelet at late flowering
|
119bp
|
|
|
|
|
|
|
|
|
BJ301375
|
whyd10e03
|
2002
|
5'
|
Spikelet at late flowering
|
470bp
|
|
|
Q92339
Q92339
Q92339
|
GO:0005351
GO:0006810
GO:0016021
|
sugar porter activity
,
transport
,
integral to membrane
|
GG18694 [Drosophila erecta]
|
83
|
0.67872
|
BJ301376
|
whyd10e05
|
2002
|
5'
|
Spikelet at late flowering
|
380bp
|
|
|
P55876
P55876
P55876
|
GO:0003743
GO:0005525
GO:0006412
|
translation initiation factor activity
,
GTP binding
,
protein biosynthesis
|
unknown [Zea mays]
|
301
|
3.56312e-26
|
BJ301377
|
whyd10e06
|
2002
|
5'
|
Spikelet at late flowering
|
386bp
|
|
Contig9033
Contig9033
|
P43903
|
GO:0016491
|
oxidoreductase activity
|
oxidoreductase, zinc-binding dehydrogenase family protein, expressed [Oryza sativa (japonica cultivar-group)]
|
325
|
1.16008e-32
|
BJ301378
|
whyd10e09
|
2002
|
5'
|
Spikelet at late flowering
|
585bp
|
|
Contig5585
Contig5585
|
Q9V1H0
Q9V1H0
|
GO:0009073
GO:0016829
|
aromatic amino acid family biosynthesis
,
lyase activity
|
Os03g0385900 [Oryza sativa (japonica cultivar-group)]
|
191
|
3.49602e-13
|
BJ301379
|
whyd10e11
|
2002
|
5'
|
Spikelet at late flowering
|
354bp
|
|
Contig11569
Contig11569
|
P52746
P52746
P52746
|
GO:0003677
GO:0005634
GO:0006355
|
DNA binding
,
nucleus
,
regulation of transcription, DNA-dependent
|
hypothetical protein OsI_011687 [Oryza sativa (indica cultivar-group)]
|
93
|
0.0467382
|
BJ301380
|
whyd10e13
|
2002
|
5'
|
Spikelet at late flowering
|
406bp
|
|
Contig13467
Contig13467
|
P37395
P37395
|
GO:0006118
GO:0009507
|
electron transport
,
chloroplast
|
NADP-thioredoxin reductase C precursor [Hordeum vulgare]
|
623
|
1.63767e-63
|
BJ301381
|
whyd10e14
|
2002
|
5'
|
Spikelet at late flowering
|
466bp
|
|
Contig15866
Contig15866
|
P59258
P59258
P59258
P59258
|
GO:0000786
GO:0003677
GO:0005634
GO:0005694
|
nucleosome
,
DNA binding
,
nucleus
,
chromosome
|
unknown [Zea mays]
|
412
|
4.70201e-39
|
BJ301382
|
whyd10e17
|
2002
|
5'
|
Spikelet at late flowering
|
368bp
|
|
Contig16291
Contig16291
|
P22739
P22739
P22739
P22739
P22739
P22739
|
GO:0005216
GO:0005244
GO:0006810
GO:0006811
GO:0006813
GO:0016021
|
ion channel activity
,
voltage-gated ion channel activity
,
transport
,
ion transport
,
potassium ion transport
,
integral to membrane
|
hypothetical protein Bm1_17870 [Brugia malayi]
|
174
|
1.86409e-11
|
BJ301383
|
whyd10e19
|
2002
|
5'
|
Spikelet at late flowering
|
254bp
|
|
Contig15407
Contig15407
|
P42766
|
GO:0003735
|
structural constituent of ribosome
|
unknown [Zea mays]
|
134
|
8.37302e-07
|
BJ301384
|
whyd10e20
|
2002
|
5'
|
Spikelet at late flowering
|
507bp
|
|
Contig10884
Contig10884
|
P56693
P56693
P56693
P56693
|
GO:0003677
GO:0005634
GO:0006355
GO:0007605
|
DNA binding
,
nucleus
,
regulation of transcription, DNA-dependent
,
hearing
|
Inorganic pyrophosphatase [Methylobacterium chloromethanicum CM4]
|
94
|
0.0405725
|
BJ301385
|
whyd10e22
|
2002
|
5'
|
Spikelet at late flowering
|
363bp
|
|
Contig8059
Contig8059
|
O30279
|
GO:0005871
|
kinesin complex
|
PREDICTED: similar to ankyrin repeat domain 53 [Equus caballus]
|
81
|
1.13795
|
BJ301386
|
whyd10e24
|
2002
|
5'
|
Spikelet at late flowering
|
362bp
|
|
|
P24152
P24152
|
GO:0005198
GO:0005618
|
structural molecule activity
,
cell wall
|
extensin [Hordeum vulgare]
|
155
|
2.84262e-10
|
BJ301387
|
whyd10f01
|
2002
|
5'
|
Spikelet at late flowering
|
386bp
|
|
Contig11606
Contig11606
|
P04819
P04819
P04819
P04819
P04819
P04819
P04819
P04819
|
GO:0000910
GO:0005524
GO:0005634
GO:0005739
GO:0006260
GO:0006281
GO:0006310
GO:0016874
|
cytokinesis
,
ATP binding
,
nucleus
,
mitochondrion
,
DNA replication
,
DNA repair
,
DNA recombination
,
ligase activity
|
hypothetical protein LOC_Os03g60950 [Oryza sativa (japonica cultivar-group)]
|
166
|
1.59417e-10
|
BJ301388
|
whyd10f04
|
2002
|
5'
|
Spikelet at late flowering
|
446bp
|
|
Contig11796
Contig11796
|
|
|
|
hypothetical protein OsJ_026567 [Oryza sativa (japonica cultivar-group)]
|
87
|
0.234122
|
BJ301389
|
whyd10f05
|
2002
|
5'
|
Spikelet at late flowering
|
562bp
|
|
Contig13970
Contig13970
|
P17317
P17317
P17317
P17317
|
GO:0000786
GO:0003677
GO:0005634
GO:0005694
|
nucleosome
,
DNA binding
,
nucleus
,
chromosome
|
unknown [Zea mays]
|
538
|
1.75779e-53
|
BJ301390
|
whyd10f08
|
2002
|
5'
|
Spikelet at late flowering
|
591bp
|
|
Contig12035
Contig12035
|
P29193
P29193
P29193
P29193
P29193
|
GO:0003824
GO:0006099
GO:0015977
GO:0015979
GO:0016829
|
catalytic activity
,
tricarboxylic acid cycle
,
carbon utilization by fixation of carbon dioxide
,
photosynthesis
,
lyase activity
|
hypothetical protein OsJ_003425 [Oryza sativa (japonica cultivar-group)]
|
929
|
9.23828e-99
|
BJ301391
|
whyd10f10
|
2002
|
5'
|
Spikelet at late flowering
|
269bp
|
|
Contig14989
Contig14989
|
P59258
P59258
P59258
P59258
|
GO:0000786
GO:0003677
GO:0005634
GO:0005694
|
nucleosome
,
DNA binding
,
nucleus
,
chromosome
|
unknown [Zea mays]
|
297
|
1.03381e-25
|
BJ301392
|
whyd10f12
|
2002
|
5'
|
Spikelet at late flowering
|
367bp
|
|
Contig16291
Contig16291
|
P22739
P22739
P22739
P22739
P22739
P22739
|
GO:0005216
GO:0005244
GO:0006810
GO:0006811
GO:0006813
GO:0016021
|
ion channel activity
,
voltage-gated ion channel activity
,
transport
,
ion transport
,
potassium ion transport
,
integral to membrane
|
hypothetical protein Bm1_17870 [Brugia malayi]
|
174
|
1.86409e-11
|
BJ301393
|
whyd10f19
|
2002
|
5'
|
Spikelet at late flowering
|
467bp
|
|
Contig16272
Contig16272
|
Q9ZRB7
|
GO:0005525
|
GTP binding
|
alpha tubulin-2A [Triticum aestivum]
|
700
|
6.01847e-73
|
BJ301394
|
whyd10f21
|
2002
|
5'
|
Spikelet at late flowering
|
129bp
|
|
|
|
|
|
|
|
|
BJ301395
|
whyd10f23
|
2002
|
5'
|
Spikelet at late flowering
|
178bp
|
|
Contig16269
Contig16269
|
P49398
P49398
|
GO:0003723
GO:0003735
|
RNA binding
,
structural constituent of ribosome
|
Os05g0368300 [Oryza sativa (japonica cultivar-group)]
|
216
|
2.51348e-16
|
BJ301396
|
whyd10f24
|
2002
|
5'
|
Spikelet at late flowering
|
342bp
|
|
Contig16291
Contig16291
|
O95755
O95755
O95755
O95755
O95755
|
GO:0005525
GO:0005794
GO:0006886
GO:0008565
GO:0015031
|
GTP binding
,
Golgi apparatus
,
intracellular protein transport
,
protein transporter activity
,
protein transport
|
hypothetical protein CHLREDRAFT_155068 [Chlamydomonas reinhardtii]
|
197
|
4.01269e-14
|
BJ301397
|
whyd10g02
|
2002
|
5'
|
Spikelet at late flowering
|
423bp
|
|
Contig10880
Contig10880
|
Q9PU36
|
GO:0005544
|
calcium-dependent phospholipid binding
|
hypothetical protein OsI_010595 [Oryza sativa (indica cultivar-group)]
|
82
|
0.891452
|
BJ301398
|
whyd10g03
|
2002
|
5'
|
Spikelet at late flowering
|
252bp
|
|
|
O54828
|
GO:0007165
|
signal transduction
|
regulator of G-protein signaling 9 [Mus musculus]
|
79
|
1.93096
|
BJ301399
|
whyd10g04
|
2002
|
5'
|
Spikelet at late flowering
|
545bp
|
|
Contig16291
Contig16291
|
|
|
|
hypothetical protein OsJ_023714 [Oryza sativa (japonica cultivar-group)]
|
127
|
1.21433e-13
|
BJ301400
|
whyd10g07
|
2002
|
5'
|
Spikelet at late flowering
|
421bp
|
|
|
P42450
P42450
P42450
|
GO:0006097
GO:0006099
GO:0016740
|
glyoxylate cycle
,
tricarboxylic acid cycle
,
transferase activity
|
PREDICTED: similar to hairy/enhancer-of-split related with YRPW motif-like [Canis familiaris]
|
75
|
5.61772
|
BJ301401
|
whyd10g08
|
2002
|
5'
|
Spikelet at late flowering
|
520bp
|
|
Contig15409
Contig15409
|
P59258
P59258
P59258
P59258
|
GO:0000786
GO:0003677
GO:0005634
GO:0005694
|
nucleosome
,
DNA binding
,
nucleus
,
chromosome
|
unknown [Zea mays]
|
410
|
1.00406e-38
|
BJ301402
|
whyd10g09
|
2002
|
5'
|
Spikelet at late flowering
|
323bp
|
|
|
P02562
P02562
P02562
P02562
P02562
P02562
P02562
|
GO:0003779
GO:0005524
GO:0005863
GO:0005871
GO:0006941
GO:0007517
GO:0016459
|
actin binding
,
ATP binding
,
striated muscle thick filament
,
kinesin complex
,
striated muscle contraction
,
muscle development
,
myosin
|
hypothetical protein OsJ_010342 [Oryza sativa (japonica cultivar-group)]
|
340
|
1.07493e-30
|
BJ301403
|
whyd10g10
|
2002
|
5'
|
Spikelet at late flowering
|
293bp
|
|
Contig8649
Contig8649
|
|
|
|
predicted protein [Laccaria bicolor S238N-H82]
|
85
|
0.398789
|