© 2022 - Robin Ohm - Utrecht University - The Netherlands
Built with Python Django and Wagtail
| Protein ID | Hirsu2|1645 |
| Gene name | |
| Location | Contig_1370:3203..5489 |
| Strand | + |
| Gene length (bp) | 2286 |
| Transcript length (bp) | 2121 |
| Coding sequence length (bp) | 2121 |
| Protein length (aa) | 707 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF13641 | Glyco_tranf_2_3 | Glycosyltransferase like family 2 | 1.5E-20 | 185 | 418 |
| PF13632 | Glyco_trans_2_3 | Glycosyl transferase family group 2 | 4.8E-17 | 285 | 469 |
| PF00535 | Glycos_transf_2 | Glycosyl transferase family 2 | 2.1E-16 | 187 | 365 |
| PF03552 | Cellulose_synt | Cellulose synthase | 8.6E-11 | 355 | 497 |
| PF13506 | Glyco_transf_21 | Glycosyl transferase family 21 | 7.0E-12 | 281 | 417 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q9RBJ2|BCSA4_KOMXY | Putative cellulose synthase 2 OS=Komagataeibacter xylinus GN=bcsABII-A PE=3 SV=1 | 184 | 473 | 3.0E-31 |
| sp|Q9WX75|BCSA5_KOMXY | Putative cellulose synthase 3 OS=Komagataeibacter xylinus GN=bcsABII-B PE=3 SV=1 | 184 | 473 | 3.0E-31 |
| sp|O82859|BCSA2_KOMXY | Cellulose synthase catalytic subunit [UDP-forming] OS=Komagataeibacter xylinus GN=bcsA PE=3 SV=1 | 182 | 478 | 2.0E-30 |
| sp|P58931|BCSA_PSEFS | Cellulose synthase catalytic subunit [UDP-forming] OS=Pseudomonas fluorescens (strain SBW25) GN=bcsA PE=3 SV=2 | 119 | 480 | 6.0E-30 |
| sp|P0CW87|ACSA1_KOMXY | Cellulose synthase 1 OS=Komagataeibacter xylinus GN=acsAB PE=1 SV=1 | 184 | 481 | 7.0E-30 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q9RBJ2|BCSA4_KOMXY | Putative cellulose synthase 2 OS=Komagataeibacter xylinus GN=bcsABII-A PE=3 SV=1 | 184 | 473 | 3.0E-31 |
| sp|Q9WX75|BCSA5_KOMXY | Putative cellulose synthase 3 OS=Komagataeibacter xylinus GN=bcsABII-B PE=3 SV=1 | 184 | 473 | 3.0E-31 |
| sp|O82859|BCSA2_KOMXY | Cellulose synthase catalytic subunit [UDP-forming] OS=Komagataeibacter xylinus GN=bcsA PE=3 SV=1 | 182 | 478 | 2.0E-30 |
| sp|P58931|BCSA_PSEFS | Cellulose synthase catalytic subunit [UDP-forming] OS=Pseudomonas fluorescens (strain SBW25) GN=bcsA PE=3 SV=2 | 119 | 480 | 6.0E-30 |
| sp|P0CW87|ACSA1_KOMXY | Cellulose synthase 1 OS=Komagataeibacter xylinus GN=acsAB PE=1 SV=1 | 184 | 481 | 7.0E-30 |
| sp|Q76KJ8|ACSA1_KOMHA | Cellulose synthase 1 OS=Komagataeibacter hansenii GN=acsAB PE=1 SV=1 | 184 | 481 | 9.0E-30 |
| sp|P19449|BCSA1_KOMXY | Cellulose synthase catalytic subunit [UDP-forming] OS=Komagataeibacter xylinus GN=bcsA PE=1 SV=1 | 182 | 540 | 1.0E-29 |
| sp|Q59167|ACSA2_KOMHA | Cellulose synthase 2 OS=Komagataeibacter hansenii GN=acsAII PE=3 SV=1 | 182 | 451 | 2.0E-29 |
| sp|Q9WX61|BCSA3_KOMXY | Cellulose synthase 1 catalytic subunit [UDP-forming] OS=Komagataeibacter xylinus GN=bcsAI PE=3 SV=1 | 184 | 540 | 5.0E-29 |
| sp|Q8Z291|BCSA_SALTI | Cellulose synthase catalytic subunit [UDP-forming] OS=Salmonella typhi GN=bcsA PE=3 SV=1 | 184 | 468 | 7.0E-28 |
| sp|Q93IN2|BCSA_SALTY | Cellulose synthase catalytic subunit [UDP-forming] OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=bcsA PE=3 SV=1 | 184 | 468 | 1.0E-27 |
| sp|P58932|BCSA_XANAC | Cellulose synthase catalytic subunit [UDP-forming] OS=Xanthomonas axonopodis pv. citri (strain 306) GN=bcsA PE=3 SV=1 | 184 | 481 | 7.0E-27 |
| sp|P37653|BCSA_ECOLI | Cellulose synthase catalytic subunit [UDP-forming] OS=Escherichia coli (strain K12) GN=bcsA PE=1 SV=3 | 184 | 445 | 3.0E-26 |
| sp|Q8X5L7|BCSA_ECO57 | Cellulose synthase catalytic subunit [UDP-forming] OS=Escherichia coli O157:H7 GN=bcsA PE=3 SV=2 | 184 | 445 | 4.0E-26 |
| sp|Q9U720|DCSA_DICDI | Cellulose synthase catalytic subunit A [UDP-forming] OS=Dictyostelium discoideum GN=dcsA PE=1 SV=1 | 242 | 422 | 9.0E-19 |
| sp|Q9SB75|CSLC5_ARATH | Probable xyloglucan glycosyltransferase 5 OS=Arabidopsis thaliana GN=CSLC5 PE=1 SV=1 | 180 | 419 | 4.0E-16 |
| sp|Q7PC70|CSLC2_ORYSI | Probable xyloglucan glycosyltransferase 2 OS=Oryza sativa subsp. indica GN=CSLC2 PE=2 SV=1 | 180 | 419 | 5.0E-16 |
| sp|Q69L19|CSLC2_ORYSJ | Probable xyloglucan glycosyltransferase 2 OS=Oryza sativa subsp. japonica GN=CSLC2 PE=2 SV=2 | 180 | 419 | 6.0E-16 |
| sp|Q9SJA2|CSLC8_ARATH | Probable xyloglucan glycosyltransferase 8 OS=Arabidopsis thaliana GN=CSLC8 PE=2 SV=1 | 180 | 466 | 1.0E-15 |
| sp|Q6UDF0|CSLA1_CYATE | Mannan synthase 1 OS=Cyamopsis tetragonoloba GN=ManS PE=1 SV=1 | 126 | 427 | 2.0E-15 |
| sp|Q9LZR3|CSLA9_ARATH | Glucomannan 4-beta-mannosyltransferase 9 OS=Arabidopsis thaliana GN=CSLA9 PE=2 SV=1 | 203 | 435 | 3.0E-15 |
| sp|Q6YWK8|CSLAB_ORYSJ | Probable mannan synthase 11 OS=Oryza sativa subsp. japonica GN=CSLA11 PE=2 SV=1 | 203 | 469 | 9.0E-15 |
| sp|Q6Z2T9|CSLA6_ORYSJ | Probable mannan synthase 6 OS=Oryza sativa subsp. japonica GN=CSLA6 PE=2 SV=2 | 184 | 419 | 9.0E-14 |
| sp|Q7XIF5|CSLA7_ORYSJ | Probable mannan synthase 7 OS=Oryza sativa subsp. japonica GN=CSLA7 PE=2 SV=1 | 203 | 422 | 1.0E-13 |
| sp|Q9SRT3|CSLC6_ARATH | Probable xyloglucan glycosyltransferase 6 OS=Arabidopsis thaliana GN=CSLC6 PE=1 SV=1 | 178 | 429 | 1.0E-13 |
| sp|Q9FNI7|CSLA2_ARATH | Glucomannan 4-beta-mannosyltransferase 2 OS=Arabidopsis thaliana GN=CSLA2 PE=2 SV=1 | 182 | 427 | 2.0E-13 |
| sp|Q8S7W0|CSLA4_ORYSJ | Probable mannan synthase 4 OS=Oryza sativa subsp. japonica GN=CSLA4 PE=2 SV=1 | 184 | 427 | 2.0E-13 |
| sp|Q7PC67|CSLA2_ORYSJ | Probable mannan synthase 2 OS=Oryza sativa subsp. japonica GN=CSLA2 PE=2 SV=2 | 195 | 427 | 2.0E-13 |
| sp|Q9T0L2|CSLAF_ARATH | Probable mannan synthase 15 OS=Arabidopsis thaliana GN=CSLA15 PE=3 SV=2 | 173 | 419 | 4.0E-13 |
| sp|Q67X45|CSLA3_ORYSJ | Probable mannan synthase 3 OS=Oryza sativa subsp. japonica GN=CSLA3 PE=2 SV=1 | 195 | 422 | 4.0E-13 |
| sp|Q7PC69|CSLC3_ORYSJ | Probable xyloglucan glycosyltransferase 3 OS=Oryza sativa subsp. japonica GN=CSLC3 PE=2 SV=1 | 180 | 465 | 5.0E-13 |
| sp|Q7PC76|CSLA1_ORYSJ | Glucomannan 4-beta-mannosyltransferase 1 OS=Oryza sativa subsp. japonica GN=CSLA1 PE=3 SV=1 | 195 | 427 | 8.0E-13 |
| sp|Q9LJP4|CSLC4_ARATH | Xyloglucan glycosyltransferase 4 OS=Arabidopsis thaliana GN=CSLC4 PE=1 SV=1 | 166 | 419 | 1.0E-12 |
| sp|Q6AU53|CSLC9_ORYSJ | Probable xyloglucan glycosyltransferase 9 OS=Oryza sativa subsp. japonica GN=CSLC9 PE=2 SV=2 | 184 | 419 | 3.0E-12 |
| sp|Q8LIY0|CSLC1_ORYSJ | Probable xyloglucan glycosyltransferase 1 OS=Oryza sativa subsp. japonica GN=CSLC1 PE=3 SV=1 | 182 | 429 | 4.0E-12 |
| sp|Q8NUI7|ICAA_STAAW | Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus aureus (strain MW2) GN=icaA PE=3 SV=1 | 156 | 419 | 1.0E-11 |
| sp|Q6G608|ICAA_STAAS | Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus aureus (strain MSSA476) GN=icaA PE=3 SV=1 | 156 | 419 | 1.0E-11 |
| sp|Q7PC73|CSLA5_ORYSJ | Probable mannan synthase 5 OS=Oryza sativa subsp. japonica GN=CSLA5 PE=2 SV=1 | 203 | 427 | 2.0E-11 |
| sp|Q9LQC9|CSLA3_ARATH | Probable mannan synthase 3 OS=Arabidopsis thaliana GN=CSLA3 PE=2 SV=1 | 79 | 419 | 2.0E-11 |
| sp|Q6GDD8|ICAA_STAAR | Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus aureus (strain MRSA252) GN=icaA PE=3 SV=1 | 156 | 419 | 3.0E-11 |
| sp|Q7A351|ICAA_STAAN | Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus aureus (strain N315) GN=icaA PE=3 SV=1 | 156 | 419 | 3.0E-11 |
| sp|Q99QX3|ICAA_STAAM | Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=icaA PE=3 SV=1 | 156 | 419 | 3.0E-11 |
| sp|Q5HCN1|ICAA_STAAC | Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus aureus (strain COL) GN=icaA PE=3 SV=1 | 156 | 419 | 3.0E-11 |
| sp|Q9RQP9|ICAA_STAA8 | Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus aureus (strain NCTC 8325) GN=icaA PE=3 SV=2 | 156 | 419 | 3.0E-11 |
| sp|Q9LF09|CSLAB_ARATH | Probable mannan synthase 11 OS=Arabidopsis thaliana GN=CSLA11 PE=2 SV=2 | 173 | 419 | 3.0E-11 |
| sp|Q6L538|CSLC7_ORYSJ | Probable xyloglucan glycosyltransferase 7 OS=Oryza sativa subsp. japonica GN=CSLC7 PE=2 SV=1 | 182 | 429 | 5.0E-11 |
| sp|Q84W54|CSLA1_ARATH | Probable mannan synthase 1 OS=Arabidopsis thaliana GN=CSLA1 PE=2 SV=1 | 182 | 465 | 7.0E-11 |
| sp|Q9ZQB9|CSLCC_ARATH | Probable xyloglucan glycosyltransferase 12 OS=Arabidopsis thaliana GN=CSLC12 PE=1 SV=1 | 179 | 419 | 7.0E-11 |
| sp|Q67VS7|CSLA9_ORYSJ | Probable mannan synthase 9 OS=Oryza sativa subsp. japonica GN=CSLA9 PE=2 SV=1 | 203 | 427 | 9.0E-11 |
| sp|Q9ZQN8|CSLA7_ARATH | Probable mannan synthase 7 OS=Arabidopsis thaliana GN=CSLA7 PE=2 SV=2 | 195 | 419 | 1.0E-10 |
| sp|Q84W06|CSLAE_ARATH | Probable mannan synthase 14 OS=Arabidopsis thaliana GN=CSLA14 PE=2 SV=2 | 196 | 419 | 2.0E-10 |
| sp|P75905|PGAC_ECOLI | Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Escherichia coli (strain K12) GN=pgaC PE=1 SV=1 | 182 | 469 | 2.0E-10 |
| sp|Q8GLC5|ICAA_STAEP | Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus epidermidis GN=icaA PE=3 SV=1 | 189 | 419 | 3.0E-10 |
| sp|Q8XAR5|PGAC_ECO57 | Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Escherichia coli O157:H7 GN=pgaC PE=3 SV=1 | 182 | 469 | 3.0E-10 |
| sp|Q84Z01|CSLCA_ORYSJ | Putative xyloglucan glycosyltransferase 10 OS=Oryza sativa subsp. japonica GN=CSLC10 PE=3 SV=1 | 184 | 419 | 5.0E-10 |
| sp|A2YHR9|CSLCA_ORYSI | Putative xyloglucan glycosyltransferase 10 OS=Oryza sativa subsp. indica GN=CSLC10 PE=3 SV=1 | 184 | 419 | 5.0E-10 |
| sp|Q5HKQ0|ICAA_STAEQ | Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus epidermidis (strain ATCC 35984 / RP62A) GN=icaA PE=1 SV=1 | 189 | 419 | 5.0E-10 |
| sp|Q9LR87|CSLAA_ARATH | Probable mannan synthase 10 OS=Arabidopsis thaliana GN=CSLA10 PE=2 SV=2 | 173 | 419 | 4.0E-09 |
| sp|P96587|YDAM_BACSU | Uncharacterized glycosyltransferase YdaM OS=Bacillus subtilis (strain 168) GN=ydaM PE=3 SV=1 | 170 | 420 | 7.0E-09 |
| sp|P74165|BMGDS_SYNY3 | Beta-monoglucosyldiacylglycerol synthase OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=sll1377 PE=1 SV=1 | 189 | 419 | 3.0E-07 |
| sp|O49323|CSLD1_ARATH | Cellulose synthase-like protein D1 OS=Arabidopsis thaliana GN=CSLD1 PE=2 SV=1 | 371 | 499 | 7.0E-07 |
| sp|Q84ZN6|CESA8_ORYSJ | Probable cellulose synthase A catalytic subunit 8 [UDP-forming] OS=Oryza sativa subsp. japonica GN=CESA8 PE=2 SV=1 | 341 | 492 | 9.0E-07 |
| sp|Q84M43|CESA2_ORYSJ | Probable cellulose synthase A catalytic subunit 2 [UDP-forming] OS=Oryza sativa subsp. japonica GN=CESA2 PE=2 SV=1 | 341 | 492 | 2.0E-06 |
| sp|A2XN66|CESA2_ORYSI | Probable cellulose synthase A catalytic subunit 2 [UDP-forming] OS=Oryza sativa subsp. indica GN=CESA2 PE=3 SV=1 | 341 | 492 | 2.0E-06 |
| sp|Q84JA6|CESA4_ARATH | Cellulose synthase A catalytic subunit 4 [UDP-forming] OS=Arabidopsis thaliana GN=CESA4 PE=1 SV=1 | 341 | 505 | 9.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0030244 | cellulose biosynthetic process | Yes |
| GO:0016020 | membrane | Yes |
| GO:0016757 | glycosyltransferase activity | Yes |
| GO:0016760 | cellulose synthase (UDP-forming) activity | Yes |
| GO:0071704 | organic substance metabolic process | No |
| GO:0044260 | cellular macromolecule metabolic process | No |
| GO:0033692 | cellular polysaccharide biosynthetic process | No |
| GO:0044264 | cellular polysaccharide metabolic process | No |
| GO:0051273 | beta-glucan metabolic process | No |
| GO:0044262 | cellular carbohydrate metabolic process | No |
| GO:0009059 | macromolecule biosynthetic process | No |
| GO:0006073 | cellular glucan metabolic process | No |
| GO:0009987 | cellular process | No |
| GO:0003824 | catalytic activity | No |
| GO:0030243 | cellulose metabolic process | No |
| GO:0044249 | cellular biosynthetic process | No |
| GO:0046527 | glucosyltransferase activity | No |
| GO:0009058 | biosynthetic process | No |
| GO:0008150 | biological_process | No |
| GO:0034645 | cellular macromolecule biosynthetic process | No |
| GO:0008194 | UDP-glycosyltransferase activity | No |
| GO:0000271 | polysaccharide biosynthetic process | No |
| GO:0003674 | molecular_function | No |
| GO:0044042 | glucan metabolic process | No |
| GO:0016740 | transferase activity | No |
| GO:0016758 | hexosyltransferase activity | No |
| GO:0016051 | carbohydrate biosynthetic process | No |
| GO:0051274 | beta-glucan biosynthetic process | No |
| GO:0043170 | macromolecule metabolic process | No |
| GO:0044237 | cellular metabolic process | No |
| GO:0005575 | cellular_component | No |
| GO:1901576 | organic substance biosynthetic process | No |
| GO:0016759 | cellulose synthase activity | No |
| GO:0110165 | cellular anatomical entity | No |
| GO:0005976 | polysaccharide metabolic process | No |
| GO:0044238 | primary metabolic process | No |
| GO:0034637 | cellular carbohydrate biosynthetic process | No |
| GO:0009250 | glucan biosynthetic process | No |
| GO:0005975 | carbohydrate metabolic process | No |
| GO:0035251 | UDP-glucosyltransferase activity | No |
| GO:0008152 | metabolic process | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 11 | 0.45 |
| Domain # | Start | End | Length |
|---|---|---|---|
| 1 | 102 | 124 | 22 |
| 2 | 139 | 161 | 22 |
| 3 | 445 | 467 | 22 |
| 4 | 524 | 546 | 22 |
| 5 | 579 | 601 | 22 |
| 6 | 624 | 646 | 22 |
| 7 | 682 | 704 | 22 |
| Type of sequence | Sequence |
|---|---|
| Locus | Download genbank file of locus
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|1645 MAARSDAQTLVDSPNASRASLRSFQTGQQTPADSSASTKFSPFADSGPSTPMNQSNISLAALLQNAASQQSGKNS PEHDATDSISVLHSRDDADIWHGWRRHLFRLVPFMTFANTGIYLAYLVLRILCVLSAQKYHQEIYAAAWVFIAVE IAVAIPSLLHNSWTMWSMKKRARQKLRLRGYDVPTVDVFITCCGEEDDLVLDTVRAACDLDYPYDRFRVVVLDDG KSTGLEAAVARLAFNYPNVCYMAREKIPGKPHHFKAGNLNYGLEQVHRLPGGAGQFMAALDADMIPERDWLRAVL PHLLADPKMALACPPQLFYNTPSCDPLAQSLDFFVHVIEPIKDTLGVAWCTGSGYVVRREALDDIGNFPLGSLAE DVATSTLMLGKGWKTAYVHEPLQFGTVPEDYGSHLKQRTRWAIGTVDTSFKLNFCLWGEKVRQMTFAQRFSGFLY ATLSLYTILLTISLFAIPIILVSGKSLVAYADDDQLRWLIRLCFAATISNRLCEFVLSIPAGYHTGQRSARYQLW MSPYIALCIIRSFILPTWLGGTTQAFKPTGSLSSALNERDPVRKKNMVRRLWAILVNYMGVFHLAFVYLTLVGVV LTSFRCFVLQKSTKDLLLGLVTHAFWPPLTFIFICSSLWVPIAYAIDPPMMPDREELLERDPKTMVAHPTAKSKK IAFGGQAAWFELELTTTTLYTAFIFVLSFVF* |
| Coding | >Hirsu2|1645 ATGGCGGCCAGGTCCGACGCCCAGACTCTGGTCGACAGCCCCAACGCCTCCCGCGCCAGCCTTCGCTCCTTTCAG ACTGGACAGCAGACGCCCGCCGACTCGTCGGCCTCGACCAAGTTCTCCCCCTTTGCCGATTCCGGCCCTTCCACG CCCATGAATCAAAGCAACATCAGTCTCGCCGCCCTCCTCCAGAATGCCGCCTCGCAACAGAGCGGCAAGAACTCG CCTGAACACGACGCTACCGACTCCATTTCTGTCCTGCACAGCCGCGACGATGCCGATATCTGGCATGGCTGGAGG CGCCACCTCTTTCGACTCGTGCCGTTCATGACCTTTGCCAACACGGGCATCTACCTGGCTTACCTCGTCCTGCGC ATCTTGTGCGTCCTCTCGGCACAGAAGTATCACCAGGAAATCTATGCCGCCGCCTGGGTCTTCATCGCCGTCGAG ATTGCTGTTGCCATTCCGTCGCTCCTGCACAACTCATGGACCATGTGGTCCATGAAGAAGCGCGCCCGCCAAAAG CTGCGCCTTCGCGGCTACGATGTCCCCACTGTTGATGTCTTCATCACCTGCTGCGGCGAGGAGGACGATCTTGTC CTCGACACCGTCCGGGCCGCCTGCGACCTCGACTACCCATACGACCGCTTCCGCGTCGTCGTCCTCGACGACGGC AAGTCGACTGGCCTTGAGGCCGCTGTCGCCCGCCTGGCCTTCAACTACCCCAACGTCTGCTACATGGCTCGCGAG AAGATTCCTGGCAAGCCCCATCACTTCAAGGCTGGCAACCTCAACTATGGCCTCGAGCAGGTCCACCGCCTGCCC GGCGGCGCCGGCCAGTTCATGGCTGCCTTGGACGCCGACATGATTCCCGAGCGAGACTGGCTCCGCGCCGTGCTT CCTCACTTGTTGGCCGATCCCAAGATGGCCCTCGCCTGCCCGCCGCAGTTGTTCTACAACACCCCGTCCTGCGAC CCACTCGCCCAGAGCCTCGACTTTTTCGTCCATGTCATCGAGCCCATCAAGGACACGCTCGGCGTGGCCTGGTGT ACCGGGTCCGGATACGTTGTCCGCCGCGAAGCCCTCGACGACATTGGCAACTTCCCCCTGGGCTCGCTCGCCGAG GACGTGGCGACCTCGACGCTTATGCTGGGCAAGGGTTGGAAGACGGCCTACGTCCACGAGCCCCTGCAGTTCGGC ACGGTCCCCGAGGACTACGGTAGCCATCTGAAGCAGCGGACGCGCTGGGCCATCGGCACCGTCGACACGTCCTTC AAGCTCAACTTTTGCCTGTGGGGAGAAAAGGTCCGGCAGATGACGTTCGCCCAGCGCTTCTCCGGCTTCCTCTAC GCGACGCTCAGCCTGTACACGATCCTGCTCACCATTTCGCTCTTCGCCATTCCCATCATCCTCGTCTCGGGCAAG TCGCTGGTTGCCTACGCCGACGACGACCAGCTGCGTTGGCTCATCCGCCTGTGCTTCGCCGCGACCATCAGCAAC CGGCTCTGCGAGTTCGTCTTGTCCATCCCCGCCGGCTACCACACCGGGCAGCGCAGCGCCCGCTACCAGCTGTGG ATGTCTCCCTACATCGCCCTGTGCATCATCCGCTCCTTCATCCTGCCCACCTGGCTCGGCGGCACGACGCAGGCC TTCAAGCCGACGGGCTCCCTCTCCTCGGCCCTCAACGAGCGCGACCCGGTCAGGAAGAAGAACATGGTCCGCCGG CTCTGGGCCATCCTGGTCAACTACATGGGTGTCTTCCACCTGGCCTTTGTCTACCTGACGCTGGTTGGCGTTGTC CTGACGTCGTTCCGCTGCTTCGTGCTGCAGAAGAGCACCAAGGACCTGCTGCTCGGCCTTGTGACGCACGCCTTC TGGCCACCCTTGACGTTCATCTTCATCTGCAGCTCCCTCTGGGTCCCGATTGCGTACGCCATCGACCCCCCGATG ATGCCGGATCGCGAGGAGCTGCTGGAGCGCGACCCAAAGACGATGGTCGCCCACCCCACGGCTAAGAGCAAGAAG ATTGCGTTCGGCGGCCAGGCGGCCTGGTTCGAGCTCGAGCTCACCACGACGACTCTCTACACCGCATTCATTTTC GTTTTATCATTCGTCTTCTGA |
| Transcript | >Hirsu2|1645 ATGGCGGCCAGGTCCGACGCCCAGACTCTGGTCGACAGCCCCAACGCCTCCCGCGCCAGCCTTCGCTCCTTTCAG ACTGGACAGCAGACGCCCGCCGACTCGTCGGCCTCGACCAAGTTCTCCCCCTTTGCCGATTCCGGCCCTTCCACG CCCATGAATCAAAGCAACATCAGTCTCGCCGCCCTCCTCCAGAATGCCGCCTCGCAACAGAGCGGCAAGAACTCG CCTGAACACGACGCTACCGACTCCATTTCTGTCCTGCACAGCCGCGACGATGCCGATATCTGGCATGGCTGGAGG CGCCACCTCTTTCGACTCGTGCCGTTCATGACCTTTGCCAACACGGGCATCTACCTGGCTTACCTCGTCCTGCGC ATCTTGTGCGTCCTCTCGGCACAGAAGTATCACCAGGAAATCTATGCCGCCGCCTGGGTCTTCATCGCCGTCGAG ATTGCTGTTGCCATTCCGTCGCTCCTGCACAACTCATGGACCATGTGGTCCATGAAGAAGCGCGCCCGCCAAAAG CTGCGCCTTCGCGGCTACGATGTCCCCACTGTTGATGTCTTCATCACCTGCTGCGGCGAGGAGGACGATCTTGTC CTCGACACCGTCCGGGCCGCCTGCGACCTCGACTACCCATACGACCGCTTCCGCGTCGTCGTCCTCGACGACGGC AAGTCGACTGGCCTTGAGGCCGCTGTCGCCCGCCTGGCCTTCAACTACCCCAACGTCTGCTACATGGCTCGCGAG AAGATTCCTGGCAAGCCCCATCACTTCAAGGCTGGCAACCTCAACTATGGCCTCGAGCAGGTCCACCGCCTGCCC GGCGGCGCCGGCCAGTTCATGGCTGCCTTGGACGCCGACATGATTCCCGAGCGAGACTGGCTCCGCGCCGTGCTT CCTCACTTGTTGGCCGATCCCAAGATGGCCCTCGCCTGCCCGCCGCAGTTGTTCTACAACACCCCGTCCTGCGAC CCACTCGCCCAGAGCCTCGACTTTTTCGTCCATGTCATCGAGCCCATCAAGGACACGCTCGGCGTGGCCTGGTGT ACCGGGTCCGGATACGTTGTCCGCCGCGAAGCCCTCGACGACATTGGCAACTTCCCCCTGGGCTCGCTCGCCGAG GACGTGGCGACCTCGACGCTTATGCTGGGCAAGGGTTGGAAGACGGCCTACGTCCACGAGCCCCTGCAGTTCGGC ACGGTCCCCGAGGACTACGGTAGCCATCTGAAGCAGCGGACGCGCTGGGCCATCGGCACCGTCGACACGTCCTTC AAGCTCAACTTTTGCCTGTGGGGAGAAAAGGTCCGGCAGATGACGTTCGCCCAGCGCTTCTCCGGCTTCCTCTAC GCGACGCTCAGCCTGTACACGATCCTGCTCACCATTTCGCTCTTCGCCATTCCCATCATCCTCGTCTCGGGCAAG TCGCTGGTTGCCTACGCCGACGACGACCAGCTGCGTTGGCTCATCCGCCTGTGCTTCGCCGCGACCATCAGCAAC CGGCTCTGCGAGTTCGTCTTGTCCATCCCCGCCGGCTACCACACCGGGCAGCGCAGCGCCCGCTACCAGCTGTGG ATGTCTCCCTACATCGCCCTGTGCATCATCCGCTCCTTCATCCTGCCCACCTGGCTCGGCGGCACGACGCAGGCC TTCAAGCCGACGGGCTCCCTCTCCTCGGCCCTCAACGAGCGCGACCCGGTCAGGAAGAAGAACATGGTCCGCCGG CTCTGGGCCATCCTGGTCAACTACATGGGTGTCTTCCACCTGGCCTTTGTCTACCTGACGCTGGTTGGCGTTGTC CTGACGTCGTTCCGCTGCTTCGTGCTGCAGAAGAGCACCAAGGACCTGCTGCTCGGCCTTGTGACGCACGCCTTC TGGCCACCCTTGACGTTCATCTTCATCTGCAGCTCCCTCTGGGTCCCGATTGCGTACGCCATCGACCCCCCGATG ATGCCGGATCGCGAGGAGCTGCTGGAGCGCGACCCAAAGACGATGGTCGCCCACCCCACGGCTAAGAGCAAGAAG ATTGCGTTCGGCGGCCAGGCGGCCTGGTTCGAGCTCGAGCTCACCACGACGACTCTCTACACCGCATTCATTTTC GTTTTATCATTCGTCTTCTGA |
| Gene | >Hirsu2|1645 ATGGCGGCCAGGTCCGACGCCCAGACTCTGGTCGACAGCCCCAACGCCTCCCGCGCCAGCCTTCGCTCCTTTCAG ACTGGACAGCAGACGCCCGCCGACTCGTCGGCCTCGACCAAGTTCTCCCCCTTTGCCGATTCCGGCCCTTCCACG CCCATGGTGAGCGCGGCCCCCGGCTGGCCCTCCTTGGCTCGAGCCCGTGCCCGAGCCCTCGGCCGTGCCGCCTCG TCGCTAACCCGTTCGCCTGTAGAATCAAAGCAACATCAGTCTCGCCGCCCTCCTCCAGAATGCCGCCTCGCAACA GAGCGGCAAGAACTCGCCTGAACACGACGCTACCGACTCCATTTCTGTCCTGCACAGCCGCGACGATGCCGATAT CTGGCATGGCTGGAGGCGCCACCTCTTTCGACTCGTGCCGTTCATGACCTTTGCCAACACGGGCATCTACCTGGC TTACCTCGTCCTGCGCATCTTGTGCGTCCTCTCGGCACAGAAGTATCACCAGGAAATCTATGCCGCCGCCTGGGT CTTCATCGCCGTCGAGATTGCTGTTGCCATTCCGTCGCTCCTGCACAACTCATGGACCATGTGGTCCATGAAGAA GCGCGCCCGCCAAAAGCTGCGCCTTCGCGGCTACGATGTCCCCACTGTTGATGTCTTCATCACCTGCTGCGGCGA GGAGGACGATCTTGTCCTCGACACCGTCCGGGCCGCCTGCGACCTCGACTACCCATACGACCGCTTCCGCGTCGT CGTCCTCGACGACGGCAAGTCGACTGGCCTTGAGGCCGCTGTCGCCCGCCTGGCCTTCAACTACCCCAACGTCTG CTACATGGCTCGCGAGAAGATTCCTGGCAAGCCCCATCACTTCAAGGCTGGCAACCTCAACTATGGCCTCGAGCA GGTCCACCGCCTGCCCGGCGGCGCCGGCCAGTTCATGGCTGCCTTGGACGCCGACATGGTAAGGCCCCCCTCCCT AGCACTTGCCCCTCCCCTCTTAACCCTCGGCCTCTTCTGACGACTGGACTCCAACAGATTCCCGAGCGAGACTGG CTCCGCGCCGTGCTTCCTCACTTGTTGGCCGATCCCAAGATGGCCCTCGCCTGCCCGCCGCAGTTGTTCTACAAC ACCCCGTCCTGCGACCCACTCGCCCAGAGCCTCGACTTTTTCGTCCATGTCATCGAGCCCATCAAGGACACGCTC GGCGTGGCCTGGTGTACCGGGTCCGGATACGTTGTCCGCCGCGAAGCCCTCGACGACATTGGCAACTTCCCCCTG GGCTCGCTCGCCGAGGACGTGGCGACCTCGACGCTTATGCTGGGCAAGGGTTGGAAGACGGCCTACGTCCACGAG CCCCTGCAGTTCGGCACGGTCCCCGAGGACTACGGTAGCCATCTGAAGCAGCGGACGCGCTGGGCCATCGGCACC GTCGACACGTCCTTCAAGCTCAACTTTTGCCTGTGGGGAGAAAAGGTCCGGCAGATGACGTTCGCCCAGCGCTTC TCCGGCTTCCTCTACGCGACGCTCAGCCTGTACACGATCCTGCTCACCATTTCGCTCTTCGCCATTCCCATCATC CTCGTCTCGGGCAAGTCGCTGGTTGCCTACGCCGACGACGACCAGCTGCGTTGGCTCATCCGCCTGTGCTTCGCC GCGACCATCAGCAACCGGCTCTGCGAGTTCGTCTTGTCCATCCCCGCCGGCTACCACACCGGGCAGCGCAGCGCC CGCTACCAGCTGTGGATGTCTCCCTACATCGCCCTGTGCATCATCCGCTCCTTCATCCTGCCCACCTGGCTCGGC GGCACGACGCAGGCCTTCAAGCCGACGGGCTCCCTCTCCTCGGCCCTCAACGAGCGCGACCCGGTCAGGAAGAAG AACATGGTCCGCCGGCTCTGGGCCATCCTGGTCAACTACATGGGTGTCTTCCACCTGGCCTTTGTCTACCTGACG CTGGTTGGCGTTGTCCTGACGTCGTTCCGCTGCTTCGTGCTGCAGAAGAGCACCAAGGACCTGCTGCTCGGCCTT GTGACGCACGCCTTCTGGCCACCCTTGACGTTCATCTTCATCTGCAGCTCCCTCTGGGTCCCGATTGCGTACGCC ATCGACCCCCCGATGATGCCGGATCGCGAGGAGCTGCTGGAGCGCGACCCAAAGACGATGGTCGCCCACCCCACG GCTAAGAGCAAGAAGATTGCGTTCGGCGGCCAGGCGGCCTGGTTCGAGCTCGAGCTCACCACGACGACTCTCTAC ACCGCATTCATTTTCGTTTTATCATTCGTCTTCTGA |