Protein ID | Hirsu2|1019 |
Gene name | |
Location | Contig_121:24853..26880 |
Strand | - |
Gene length (bp) | 2027 |
Transcript length (bp) | 1743 |
Coding sequence length (bp) | 1743 |
Protein length (aa) | 581 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF00447 | HSF_DNA-bind | HSF-type DNA-binding | 4.4E-30 | 108 | 207 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q5A287|SFL1_CANAL | Transcription factor SFL1 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=SFL1 PE=1 SV=1 | 104 | 217 | 4.0E-31 |
sp|Q5AK51|SFL2_CANAL | Transcription factor SFL2 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=SFL2 PE=1 SV=2 | 101 | 209 | 1.0E-25 |
sp|P20134|SFL1_YEAST | Flocculation suppression protein OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SFL1 PE=1 SV=3 | 108 | 208 | 6.0E-25 |
sp|Q9SCW4|HFB2A_ARATH | Heat stress transcription factor B-2a OS=Arabidopsis thaliana GN=HSFB2A PE=2 SV=1 | 106 | 207 | 3.0E-18 |
sp|Q9R0L1|HSF4_MOUSE | Heat shock factor protein 4 OS=Mus musculus GN=Hsf4 PE=1 SV=2 | 107 | 268 | 6.0E-18 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q5A287|SFL1_CANAL | Transcription factor SFL1 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=SFL1 PE=1 SV=1 | 104 | 217 | 4.0E-31 |
sp|Q5AK51|SFL2_CANAL | Transcription factor SFL2 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=SFL2 PE=1 SV=2 | 101 | 209 | 1.0E-25 |
sp|P20134|SFL1_YEAST | Flocculation suppression protein OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SFL1 PE=1 SV=3 | 108 | 208 | 6.0E-25 |
sp|Q9SCW4|HFB2A_ARATH | Heat stress transcription factor B-2a OS=Arabidopsis thaliana GN=HSFB2A PE=2 SV=1 | 106 | 207 | 3.0E-18 |
sp|Q9R0L1|HSF4_MOUSE | Heat shock factor protein 4 OS=Mus musculus GN=Hsf4 PE=1 SV=2 | 107 | 268 | 6.0E-18 |
sp|Q02953|HSF_SCHPO | Heat shock factor protein OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=hsf1 PE=1 SV=2 | 106 | 210 | 9.0E-18 |
sp|P22121|HSF_KLULA | Heat shock factor protein OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=HSF PE=1 SV=1 | 107 | 219 | 3.0E-17 |
sp|Q9ULV5|HSF4_HUMAN | Heat shock factor protein 4 OS=Homo sapiens GN=HSF4 PE=1 SV=2 | 107 | 252 | 4.0E-17 |
sp|Q5A4X5|SKN7_CANAL | Transcription factor SKN7 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=SKN7 PE=3 SV=1 | 108 | 299 | 4.0E-17 |
sp|Q1HGE8|HSF4_CANLF | Heat shock factor protein 4 OS=Canis lupus familiaris GN=HSF4 PE=2 SV=1 | 107 | 208 | 2.0E-16 |
sp|Q9T0D3|HFB2B_ARATH | Heat stress transcription factor B-2b OS=Arabidopsis thaliana GN=HSFB2B PE=2 SV=1 | 106 | 207 | 2.0E-16 |
sp|P10961|HSF_YEAST | Heat shock factor protein OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HSF1 PE=1 SV=1 | 107 | 207 | 3.0E-16 |
sp|O14283|PRR1_SCHPO | Transcription factor prr1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=prr1 PE=1 SV=2 | 108 | 208 | 4.0E-16 |
sp|Q1PDN3|HFA6A_ARATH | Heat stress transcription factor A-6a OS=Arabidopsis thaliana GN=HSFA6A PE=2 SV=1 | 106 | 209 | 5.0E-16 |
sp|P22335|HSF24_SOLPE | Heat shock factor protein HSF24 OS=Solanum peruvianum GN=HSF24 PE=2 SV=1 | 108 | 209 | 5.0E-16 |
sp|Q6Z9C8|HFB2B_ORYSJ | Heat stress transcription factor B-2b OS=Oryza sativa subsp. japonica GN=HSFB2B PE=2 SV=1 | 99 | 207 | 5.0E-16 |
sp|O81821|HFA1B_ARATH | Heat stress transcription factor A-1b OS=Arabidopsis thaliana GN=HSFA1B PE=2 SV=2 | 108 | 297 | 1.0E-15 |
sp|Q9LQM7|HFA1D_ARATH | Heat stress transcription factor A-1d OS=Arabidopsis thaliana GN=HSFA1D PE=1 SV=2 | 88 | 297 | 2.0E-15 |
sp|Q03933|HSF2_HUMAN | Heat shock factor protein 2 OS=Homo sapiens GN=HSF2 PE=1 SV=1 | 107 | 250 | 2.0E-15 |
sp|Q6F388|HFA2E_ORYSJ | Heat stress transcription factor A-2e OS=Oryza sativa subsp. japonica GN=HSFA2E PE=2 SV=1 | 108 | 297 | 2.0E-15 |
sp|Q96320|HSFB1_ARATH | Heat stress transcription factor B-1 OS=Arabidopsis thaliana GN=HSFB1 PE=2 SV=2 | 108 | 209 | 2.0E-15 |
sp|P38533|HSF2_MOUSE | Heat shock factor protein 2 OS=Mus musculus GN=Hsf2 PE=2 SV=2 | 107 | 250 | 3.0E-15 |
sp|Q93VB5|HFA4D_ORYSJ | Heat stress transcription factor A-4d OS=Oryza sativa subsp. japonica GN=HSFA4D PE=1 SV=1 | 108 | 212 | 3.0E-15 |
sp|Q94BZ5|HSFA5_ARATH | Heat stress transcription factor A-5 OS=Arabidopsis thaliana GN=HSFA5 PE=2 SV=1 | 108 | 215 | 3.0E-15 |
sp|Q08DJ8|HSF1_BOVIN | Heat shock factor protein 1 OS=Bos taurus GN=HSF1 PE=2 SV=1 | 107 | 252 | 4.0E-15 |
sp|P38529|HSF1_CHICK | Heat shock factor protein 1 OS=Gallus gallus GN=HSF1 PE=2 SV=1 | 106 | 251 | 5.0E-15 |
sp|P38530|HSF2_CHICK | Heat shock factor protein 2 OS=Gallus gallus GN=HSF2 PE=2 SV=1 | 107 | 250 | 1.0E-14 |
sp|Q6VBB2|HFA2B_ORYSJ | Heat stress transcription factor A-2b OS=Oryza sativa subsp. japonica GN=HSFA2B PE=2 SV=1 | 108 | 207 | 1.0E-14 |
sp|Q652B0|HFB2C_ORYSJ | Heat stress transcription factor B-2c OS=Oryza sativa subsp. japonica GN=HSFB2C PE=2 SV=1 | 106 | 207 | 1.0E-14 |
sp|P41152|HSF30_SOLPE | Heat shock factor protein HSF30 OS=Solanum peruvianum GN=HSF30 PE=2 SV=1 | 108 | 207 | 1.0E-14 |
sp|Q9S7U5|HSFA8_ARATH | Heat stress transcription factor A-8 OS=Arabidopsis thaliana GN=HSFA8 PE=2 SV=1 | 108 | 207 | 1.0E-14 |
sp|P41154|HSF_XENLA | Heat shock factor protein OS=Xenopus laevis GN=hsf1 PE=2 SV=1 | 107 | 251 | 2.0E-14 |
sp|Q67TP9|HSFB1_ORYSJ | Heat stress transcription factor B-1 OS=Oryza sativa subsp. japonica GN=HSFB1 PE=2 SV=1 | 108 | 209 | 2.0E-14 |
sp|P38532|HSF1_MOUSE | Heat shock factor protein 1 OS=Mus musculus GN=Hsf1 PE=1 SV=2 | 107 | 251 | 3.0E-14 |
sp|Q00613|HSF1_HUMAN | Heat shock factor protein 1 OS=Homo sapiens GN=HSF1 PE=1 SV=1 | 107 | 251 | 3.0E-14 |
sp|P38889|SKN7_YEAST | Transcription factor SKN7 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SKN7 PE=1 SV=1 | 40 | 275 | 3.0E-14 |
sp|Q9C635|HSFB4_ARATH | Heat stress transcription factor B-4 OS=Arabidopsis thaliana GN=HSFB4 PE=2 SV=1 | 100 | 220 | 3.0E-14 |
sp|P22813|HSF_DROME | Heat shock factor protein OS=Drosophila melanogaster GN=Hsf PE=1 SV=1 | 107 | 211 | 4.0E-14 |
sp|Q10PR4|HSFA9_ORYSJ | Heat stress transcription factor A-9 OS=Oryza sativa subsp. japonica GN=HSFA9 PE=2 SV=1 | 108 | 299 | 4.0E-14 |
sp|P38531|HSF3_CHICK | Heat shock factor protein 3 OS=Gallus gallus GN=HSF3 PE=2 SV=1 | 107 | 209 | 4.0E-14 |
sp|Q9LUH8|HFA6B_ARATH | Heat stress transcription factor A-6b OS=Arabidopsis thaliana GN=HSFA6b PE=2 SV=1 | 108 | 209 | 4.0E-14 |
sp|O80982|HSFA2_ARATH | Heat stress transcription factor A-2 OS=Arabidopsis thaliana GN=HSFA2 PE=1 SV=1 | 108 | 285 | 5.0E-14 |
sp|Q84T61|HSFA1_ORYSJ | Heat stress transcription factor A-1 OS=Oryza sativa subsp. japonica GN=HSFA1 PE=2 SV=1 | 90 | 290 | 6.0E-14 |
sp|Q40152|HSF8_SOLLC | Heat shock factor protein HSF8 OS=Solanum lycopersicum GN=HSF8 PE=3 SV=1 | 108 | 212 | 7.0E-14 |
sp|P41151|HFA1A_ARATH | Heat stress transcription factor A-1a OS=Arabidopsis thaliana GN=HSFA1A PE=1 SV=2 | 108 | 209 | 8.0E-14 |
sp|Q84MN7|HFA2A_ORYSJ | Heat stress transcription factor A-2a OS=Oryza sativa subsp. japonica GN=HSFA2A PE=2 SV=1 | 73 | 207 | 1.0E-13 |
sp|Q8GYY1|HSFA3_ARATH | Heat stress transcription factor A-3 OS=Arabidopsis thaliana GN=HSFA3 PE=2 SV=2 | 108 | 291 | 1.0E-13 |
sp|Q9LVW2|HSFA9_ARATH | Heat stress transcription factor A-9 OS=Arabidopsis thaliana GN=HSFA9 PE=2 SV=1 | 98 | 270 | 1.0E-13 |
sp|Q6EUG4|HFC2A_ORYSJ | Heat stress transcription factor C-2a OS=Oryza sativa subsp. japonica GN=HSFC2A PE=2 SV=1 | 108 | 209 | 2.0E-13 |
sp|Q7XRX3|HFB2A_ORYSJ | Heat stress transcription factor B-2a OS=Oryza sativa subsp. japonica GN=HSFB2A PE=2 SV=2 | 108 | 207 | 2.0E-13 |
sp|Q5AQ33|HSF_CANAL | Heat shock transcription factor OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=CTA8 PE=1 SV=1 | 107 | 287 | 2.0E-13 |
sp|P41153|HSF8_SOLPE | Heat shock factor protein HSF8 OS=Solanum peruvianum GN=HSF8 PE=2 SV=1 | 108 | 207 | 2.0E-13 |
sp|Q9FK72|HFA4C_ARATH | Heat stress transcription factor A-4c OS=Arabidopsis thaliana GN=HSFA4C PE=2 SV=1 | 108 | 289 | 6.0E-13 |
sp|Q9SCW5|HFA1E_ARATH | Heat stress transcription factor A-1e OS=Arabidopsis thaliana GN=HSFA1E PE=2 SV=2 | 108 | 207 | 6.0E-13 |
sp|Q9LV52|HSFC1_ARATH | Heat stress transcription factor C-1 OS=Arabidopsis thaliana GN=HSFC1 PE=2 SV=1 | 108 | 212 | 6.0E-13 |
sp|Q94J16|HFA4B_ORYSJ | Heat stress transcription factor A-4b OS=Oryza sativa subsp. japonica GN=HSFA4B PE=2 SV=1 | 108 | 207 | 9.0E-13 |
sp|O22230|HSFB3_ARATH | Heat stress transcription factor B-3 OS=Arabidopsis thaliana GN=HSFB3 PE=2 SV=1 | 108 | 219 | 2.0E-12 |
sp|Q9SV12|HFA7A_ARATH | Heat stress transcription factor A-7a OS=Arabidopsis thaliana GN=HSFA7A PE=2 SV=1 | 108 | 207 | 3.0E-12 |
sp|Q6Z9R8|HFB4A_ORYSJ | Putative heat stress transcription factor B-4a OS=Oryza sativa subsp. japonica GN=HSFB4A PE=3 SV=1 | 108 | 209 | 4.0E-12 |
sp|Q0DBL6|HFC2B_ORYSJ | Heat stress transcription factor C-2b OS=Oryza sativa subsp. japonica GN=HSFC2B PE=3 SV=1 | 108 | 207 | 4.0E-12 |
sp|Q338B0|HFA2C_ORYSJ | Heat stress transcription factor A-2c OS=Oryza sativa subsp. japonica GN=HSFA2C PE=1 SV=2 | 108 | 207 | 6.0E-12 |
sp|Q6VBA4|HFC1A_ORYSJ | Heat stress transcription factor C-1a OS=Oryza sativa subsp. japonica GN=HSFC1A PE=2 SV=2 | 105 | 210 | 7.0E-12 |
sp|Q67U94|HFB4C_ORYSJ | Heat stress transcription factor B-4c OS=Oryza sativa subsp. japonica GN=HSFB4C PE=3 SV=1 | 108 | 207 | 8.0E-12 |
sp|Q657C0|HFA6B_ORYSJ | Heat stress transcription factor A-6a OS=Oryza sativa subsp. japonica GN=HSFA6B PE=2 SV=1 | 108 | 285 | 1.0E-11 |
sp|Q9M1V5|HFA7B_ARATH | Heat stress transcription factor A-7b OS=Arabidopsis thaliana GN=HSFA7B PE=2 SV=1 | 86 | 208 | 1.0E-11 |
sp|D0VYS2|HSF3_MOUSE | Heat shock factor protein 3 OS=Mus musculus GN=Hsf3 PE=2 SV=1 | 108 | 208 | 1.0E-11 |
sp|Q7XHZ0|HFB4B_ORYSJ | Heat stress transcription factor B-4b OS=Oryza sativa subsp. japonica GN=HSFB4B PE=1 SV=1 | 108 | 209 | 1.0E-11 |
sp|Q6H6Q7|HSFA3_ORYSJ | Heat stress transcription factor A-3 OS=Oryza sativa subsp. japonica GN=HSFA3 PE=2 SV=1 | 34 | 209 | 2.0E-11 |
sp|Q6K6S5|HSFA5_ORYSJ | Heat stress transcription factor A-5 OS=Oryza sativa subsp. japonica GN=HSFA5 PE=2 SV=1 | 108 | 271 | 2.0E-11 |
sp|Q942D6|HFC1B_ORYSJ | Heat stress transcription factor C-1b OS=Oryza sativa subsp. japonica GN=HSFC1B PE=2 SV=1 | 108 | 264 | 2.0E-11 |
sp|P53050|MGA1_YEAST | Protein MGA1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=MGA1 PE=3 SV=1 | 100 | 209 | 5.0E-11 |
sp|Q8H7Y6|HFA2D_ORYSJ | Heat stress transcription factor A-2d OS=Oryza sativa subsp. japonica GN=HSFA2D PE=2 SV=2 | 108 | 295 | 2.0E-10 |
sp|Q10KX8|HFB4D_ORYSJ | Heat stress transcription factor B-4d OS=Oryza sativa subsp. japonica GN=HSFB4D PE=3 SV=1 | 108 | 207 | 4.0E-10 |
sp|O49403|HFA4A_ARATH | Heat stress transcription factor A-4a OS=Arabidopsis thaliana GN=HSFA4A PE=2 SV=1 | 108 | 285 | 3.0E-09 |
sp|Q5Z6A4|HFA6A_ORYSJ | Putative heat stress transcription factor A-6a OS=Oryza sativa subsp. japonica GN=HSFA6A PE=3 SV=1 | 108 | 169 | 3.0E-07 |
GO Term | Description | Terminal node |
---|---|---|
GO:0006355 | regulation of transcription, DNA-templated | Yes |
GO:0003700 | DNA-binding transcription factor activity | Yes |
GO:0043565 | sequence-specific DNA binding | Yes |
GO:0097159 | organic cyclic compound binding | No |
GO:0003677 | DNA binding | No |
GO:0009889 | regulation of biosynthetic process | No |
GO:0008150 | biological_process | No |
GO:0010468 | regulation of gene expression | No |
GO:0005488 | binding | No |
GO:2001141 | regulation of RNA biosynthetic process | No |
GO:0050794 | regulation of cellular process | No |
GO:0003676 | nucleic acid binding | No |
GO:0031323 | regulation of cellular metabolic process | No |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | No |
GO:0051252 | regulation of RNA metabolic process | No |
GO:0140110 | transcription regulator activity | No |
GO:1901363 | heterocyclic compound binding | No |
GO:0050789 | regulation of biological process | No |
GO:0010556 | regulation of macromolecule biosynthetic process | No |
GO:1903506 | regulation of nucleic acid-templated transcription | No |
GO:0019222 | regulation of metabolic process | No |
GO:0031326 | regulation of cellular biosynthetic process | No |
GO:0065007 | biological regulation | No |
GO:0051171 | regulation of nitrogen compound metabolic process | No |
GO:0060255 | regulation of macromolecule metabolic process | No |
GO:0003674 | molecular_function | No |
GO:0080090 | regulation of primary metabolic process | No |
Localizations | Signals | Cytoplasm | Nucleus | Extracellular | Cell membrane | Mitochondrion | Plastid | Endoplasmic reticulum | Lysosome vacuole | Golgi apparatus | Peroxisome |
---|---|---|---|---|---|---|---|---|---|---|---|
Nucleus | Nuclear localization signal | 0.2459 | 0.9602 | 0.1298 | 0.0132 | 0.1071 | 0.0002 | 0.0453 | 0.0374 | 0.0157 | 0.0119 |
Orthofinder run ID | 4 |
Orthogroup | 1130 |
Change Orthofinder run |
Type of sequence | Sequence |
---|---|
Locus | Download genbank file of locus
Download genbank file of locus (reverse complement)
The gene with 5 kb flanks (if sufficient flanking sequence is available). For use in cloning design programs. NOTE: features (genes or exons) that are only partially contained within the sequence are completely excluded. |
Protein | >Hirsu2|1019 MVTRTERFQRPTTADPFPSARKSMGARVVPISAPPVIVMSASAHGVDAMDIAPSAPSQAPDHETNGKPSHRSNHS SPPDQGHGNMTMPAPPPAAAAAVHQPKIVQTAFIHKLYNMLEDSSIQHLISWSANAESFVMSPSADFSKVLSQYF KHTNISSFVRQLNMYGFHKERDVFHTGNPDTTLWEFKHGNGNFKRGDLMGLREIKRRASRHALVHRESNFNKPNP SQQGTPTEPAQMATESSEARLANLEHNLYEMGARLQRSEENAHYMSIKNQAAMDTVSRLLHFNQELSRAVLSLVP ADSPVHRDVLALQGEVQRQADVARTYDDTHEASLGGRQQFLGTVDHAPVSPRQLPQDDSRRAGNLAVPQARGQPL YRPAVPSSVLASSRRPYGSIGGSSTTQSSPLRNANPAPPPGPHPLSNVEPPPGSLARRHTAADIRAHGWQPTPSA FSAPNAPSAPWPSSPSRVAPEDQRIRDSLSTYSLQAASHPHSRPATPPPPLPPPCHSTNGGNNGVEPFGSWSWNT AASRDVKGLALRDSSAPPTRRGSMAHILNPSDTVERSDEDEDPRGDEDRKRKRMQ* |
Coding | >Hirsu2|1019 ATGGTCACGAGAACTGAGCGCTTCCAGAGACCGACAACGGCCGACCCGTTCCCCTCGGCCCGCAAGTCAATGGGT GCCCGAGTCGTCCCCATCTCCGCGCCGCCCGTCATCGTCATGTCTGCCTCTGCACACGGCGTTGATGCCATGGAC ATTGCCCCGTCTGCCCCCAGCCAGGCGCCCGACCACGAAACCAACGGCAAGCCGTCCCACCGATCCAACCACTCG TCGCCCCCGGATCAAGGCCACGGCAACATGACCATGCCCGCGCCTCCGCCCGCCGCGGCCGCCGCCGTCCACCAG CCCAAGATCGTCCAGACGGCCTTCATCCACAAGCTCTATAACATGCTCGAGGACTCCAGCATTCAGCACTTGATA TCGTGGTCTGCCAACGCCGAGAGCTTCGTCATGTCGCCTTCAGCCGACTTCTCCAAAGTCCTGTCGCAATACTTC AAGCATACAAACATCTCCTCCTTCGTACGGCAGCTCAACATGTATGGCTTTCACAAGGAGCGCGACGTTTTCCAC ACCGGAAACCCAGACACCACTCTCTGGGAGTTCAAGCACGGTAATGGCAACTTCAAGCGCGGCGACCTCATGGGC CTTCGAGAAATCAAACGCCGCGCGAGCAGACACGCCCTAGTCCACCGCGAAAGCAACTTCAACAAGCCGAACCCG TCGCAGCAGGGCACGCCCACTGAGCCGGCGCAGATGGCCACCGAGAGCTCCGAGGCCAGGCTGGCCAACCTCGAA CACAACCTGTACGAAATGGGCGCTCGCCTGCAGCGCAGCGAAGAGAACGCCCACTACATGAGCATCAAGAACCAG GCAGCCATGGACACCGTCAGCCGGCTCCTTCACTTCAACCAGGAGTTGTCGAGGGCCGTTCTGTCGCTTGTTCCG GCCGACAGTCCCGTCCACCGCGATGTACTCGCCCTGCAAGGAGAGGTACAGCGACAAGCCGACGTGGCGCGGACG TACGACGATACCCACGAGGCGTCTTTGGGGGGCAGGCAGCAGTTTCTCGGCACCGTCGACCACGCCCCCGTATCC CCGAGACAGCTGCCGCAGGACGATTCCAGACGGGCGGGCAACCTGGCCGTCCCGCAGGCCAGGGGCCAGCCCCTC TACCGGCCGGCGGTGCCCTCGAGCGTACTGGCGAGCTCAAGGCGACCGTACGGGTCGATTGGGGGGAGCAGTACC ACGCAGTCGTCGCCCTTGCGCAACGCCAATCCGGCGCCGCCCCCAGGACCCCACCCCCTCTCCAATGTCGAGCCG CCGCCCGGGAGTCTGGCCCGACGACACACGGCAGCCGACATCCGCGCGCACGGATGGCAGCCCACGCCCTCGGCG TTTTCGGCGCCGAACGCCCCATCCGCGCCGTGGCCCTCGTCGCCGAGCCGCGTGGCGCCGGAAGATCAACGGATC CGCGACTCGCTGTCCACATATTCCCTTCAGGCGGCGTCGCATCCGCACTCGCGGCCGGCCACGCCGCCGCCCCCA TTGCCGCCGCCTTGTCACAGCACGAATGGGGGAAACAATGGGGTCGAGCCGTTTGGCAGCTGGTCATGGAACACG GCGGCCAGCAGAGACGTCAAGGGCCTCGCGCTAAGAGACTCGTCGGCACCACCCACCCGGCGGGGAAGTATGGCC CACATTCTCAACCCCAGCGATACGGTCGAGCGATCCGACGAGGACGAAGATCCCCGAGGCGACGAGGACAGAAAA CGCAAGCGAATGCAGTAG |
Transcript | >Hirsu2|1019 ATGGTCACGAGAACTGAGCGCTTCCAGAGACCGACAACGGCCGACCCGTTCCCCTCGGCCCGCAAGTCAATGGGT GCCCGAGTCGTCCCCATCTCCGCGCCGCCCGTCATCGTCATGTCTGCCTCTGCACACGGCGTTGATGCCATGGAC ATTGCCCCGTCTGCCCCCAGCCAGGCGCCCGACCACGAAACCAACGGCAAGCCGTCCCACCGATCCAACCACTCG TCGCCCCCGGATCAAGGCCACGGCAACATGACCATGCCCGCGCCTCCGCCCGCCGCGGCCGCCGCCGTCCACCAG CCCAAGATCGTCCAGACGGCCTTCATCCACAAGCTCTATAACATGCTCGAGGACTCCAGCATTCAGCACTTGATA TCGTGGTCTGCCAACGCCGAGAGCTTCGTCATGTCGCCTTCAGCCGACTTCTCCAAAGTCCTGTCGCAATACTTC AAGCATACAAACATCTCCTCCTTCGTACGGCAGCTCAACATGTATGGCTTTCACAAGGAGCGCGACGTTTTCCAC ACCGGAAACCCAGACACCACTCTCTGGGAGTTCAAGCACGGTAATGGCAACTTCAAGCGCGGCGACCTCATGGGC CTTCGAGAAATCAAACGCCGCGCGAGCAGACACGCCCTAGTCCACCGCGAAAGCAACTTCAACAAGCCGAACCCG TCGCAGCAGGGCACGCCCACTGAGCCGGCGCAGATGGCCACCGAGAGCTCCGAGGCCAGGCTGGCCAACCTCGAA CACAACCTGTACGAAATGGGCGCTCGCCTGCAGCGCAGCGAAGAGAACGCCCACTACATGAGCATCAAGAACCAG GCAGCCATGGACACCGTCAGCCGGCTCCTTCACTTCAACCAGGAGTTGTCGAGGGCCGTTCTGTCGCTTGTTCCG GCCGACAGTCCCGTCCACCGCGATGTACTCGCCCTGCAAGGAGAGGTACAGCGACAAGCCGACGTGGCGCGGACG TACGACGATACCCACGAGGCGTCTTTGGGGGGCAGGCAGCAGTTTCTCGGCACCGTCGACCACGCCCCCGTATCC CCGAGACAGCTGCCGCAGGACGATTCCAGACGGGCGGGCAACCTGGCCGTCCCGCAGGCCAGGGGCCAGCCCCTC TACCGGCCGGCGGTGCCCTCGAGCGTACTGGCGAGCTCAAGGCGACCGTACGGGTCGATTGGGGGGAGCAGTACC ACGCAGTCGTCGCCCTTGCGCAACGCCAATCCGGCGCCGCCCCCAGGACCCCACCCCCTCTCCAATGTCGAGCCG CCGCCCGGGAGTCTGGCCCGACGACACACGGCAGCCGACATCCGCGCGCACGGATGGCAGCCCACGCCCTCGGCG TTTTCGGCGCCGAACGCCCCATCCGCGCCGTGGCCCTCGTCGCCGAGCCGCGTGGCGCCGGAAGATCAACGGATC CGCGACTCGCTGTCCACATATTCCCTTCAGGCGGCGTCGCATCCGCACTCGCGGCCGGCCACGCCGCCGCCCCCA TTGCCGCCGCCTTGTCACAGCACGAATGGGGGAAACAATGGGGTCGAGCCGTTTGGCAGCTGGTCATGGAACACG GCGGCCAGCAGAGACGTCAAGGGCCTCGCGCTAAGAGACTCGTCGGCACCACCCACCCGGCGGGGAAGTATGGCC CACATTCTCAACCCCAGCGATACGGTCGAGCGATCCGACGAGGACGAAGATCCCCGAGGCGACGAGGACAGAAAA CGCAAGCGAATGCAGTAG |
Gene | >Hirsu2|1019 ATGGTCACGAGAACTGAGCGCTTCCAGAGACCGACAACGGCCGACCCGTTCCCCTCGGCCCGCAAGTCAATGGGT GCCCGAGTCGTCCCCATCTCCGCGCCGCCCGTCATCGTCATGTCTGCCTCTGCACACGGCGTTGATGCCATGGAC ATTGCCCCGTCTGCCCCCAGCCAGGCGCCCGACCACGAAACCAACGGCAAGCCGTCCCACCGATCCAACCACTCG TCGCCCCCGGATCAAGGCCACGGCAACATGACCATGCCCGCGCCTCCGCCCGCCGCGGCCGCCGCCGTCCACCAG CCCAAGATCGTCCAGACGGCCTTCATCCACAAGCTCTATAAGTGAGATCAGCCTGTGCGGCCGTTGCTCGCCGAC GGCTTCCTTTTGCTGACAAACGGGTCTTTGTGCCGCAGCATGCTCGAGGACTCCAGCATTCAGCACTTGATATCG TGGTCTGCCAACGCCGAGAGCTTCGTCATGTCGCCTTCAGCCGACTTCTCCAAAGTCCTGTCGTACGTTCGCCTT GTACTGCCCCGACAAGCCTCGGTACAATCGTCTCACGCCCTTCTCTTTCCCCCCTCCCTTACAGGCAATACTTCA AGCATACAAACATCTCCTCCTTCGTACGGCAGCTCAACATGTATGGCTTTCACAAGGGTAAGTGCTAGGTCGACA GCTCGCACGCGGCGGATCGGCTTCCTCTCATGCGTCCCATCACAGAGCGCGACGTTTTCCACACCGGAAACCCAG ACACCACTCTCTGGGAGTTCAAGCACGGTAATGGCAACTTCAAGCGCGGCGACCTCATGGGCCTTCGAGAAATCA AACGCCGCGCGAGCAGACACGCCCTAGTCCACCGCGAAAGCAACTTCAACAAGCCGAACCCGTCGCAGCAGGGCA CGCCCACTGAGCCGGCGCAGATGGCCACCGAGAGCTCCGAGGCCAGGCTGGCCAACCTCGAACACAACCTGTACG AAATGGGCGCTCGCCTGCAGCGCAGCGAAGAGAACGCCCACTACATGAGCATCAAGAACCAGGCAGCCATGGACA CCGTCAGCCGGCTCCTTCACTTCAACCAGGAGTTGTCGAGGGCCGTTCTGTCGCTTGTTCCGGCCGACAGTCCCG TCCACCGCGATGGTTCGTCGTGCTTGCCCTCCCCATTGTCTGGCGCAGAGGGCACAGTGCTAACGTCTACAACGC GGAAAACAGTACTCGCCCTGCAAGGAGAGGTACAGCGACAAGCCGACGTGGCGCGGACGTACGACGATACCCACG AGGCGTCTTTGGGGGGCAGGCAGCAGTTTCTCGGCACCGTCGACCACGCCCCCGTATCCCCGAGACAGCTGCCGC AGGACGATTCCAGACGGGCGGGCAACCTGGCCGTCCCGCAGGCCAGGGGCCAGCCCCTCTACCGGCCGGCGGTGC CCTCGAGCGTACTGGCGAGCTCAAGGCGACCGTACGGGTCGATTGGGGGGAGCAGTACCACGCAGTCGTCGCCCT TGCGCAACGCCAATCCGGCGCCGCCCCCAGGACCCCACCCCCTCTCCAATGTCGAGCCGCCGCCCGGGAGTCTGG CCCGACGACACACGGCAGCCGACATCCGCGCGCACGGATGGCAGCCCACGCCCTCGGCGTTTTCGGCGCCGAACG CCCCATCCGCGCCGTGGCCCTCGTCGCCGAGCCGCGTGGCGCCGGAAGATCAACGGATCCGCGACTCGCTGTCCA CATATTCCCTTCAGGCGGCGTCGCATCCGCACTCGCGGCCGGCCACGCCGCCGCCCCCATTGCCGCCGCCTTGTC ACAGCACGAATGGGGGAAACAATGGGGTCGAGCCGTTTGGCAGCTGGTCATGGAACACGGCGGCCAGCAGAGACG TCAAGGGCCTCGCGCTAAGAGACTCGTCGGCACCACCCACCCGGCGGGGAAGTATGGCCCACATTCTCAACCCCA GCGATACGGTCGAGCGATCCGACGAGGACGAAGATCCCCGAGGCGACGAGGACAGAAAACGCAAGCGAATGCAGT AG |