© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Ophun1|4834 |
| Gene name | |
| Location | Contig_456:1089..4080 |
| Strand | + |
| Gene length (bp) | 2991 |
| Transcript length (bp) | 2415 |
| Coding sequence length (bp) | 2415 |
| Protein length (aa) | 805 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00884 | Sulfatase | Sulfatase | 2.4E-55 | 25 | 368 |
| PF10232 | Med8 | Mediator of RNA polymerase II transcription complex subunit 8 | 3.1E-35 | 557 | 741 |
| PF12411 | Choline_sulf_C | Choline sulfatase enzyme C terminal | 1.9E-25 | 480 | 531 |
| PF01663 | Phosphodiest | Type I phosphodiesterase / nucleotide pyrophosphatase | 5.9E-07 | 29 | 313 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|O69787|BETC_RHIME | Choline-sulfatase OS=Rhizobium meliloti (strain 1021) GN=betC PE=1 SV=2 | 24 | 532 | 6.0E-146 |
| sp|Q7SGQ0|MED8_NEUCR | Mediator of RNA polymerase II transcription subunit 8 OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=med-8 PE=3 SV=1 | 553 | 777 | 5.0E-37 |
| sp|Q2HDD6|MED8_CHAGB | Mediator of RNA polymerase II transcription subunit 8 OS=Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) GN=MED8 PE=3 SV=1 | 556 | 723 | 4.0E-35 |
| sp|Q148F3|ARSK_BOVIN | Arylsulfatase K OS=Bos taurus GN=ARSK PE=2 SV=1 | 20 | 492 | 1.0E-33 |
| sp|Q5ZK90|ARSK_CHICK | Arylsulfatase K OS=Gallus gallus GN=ARSK PE=2 SV=1 | 22 | 442 | 4.0E-33 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|O69787|BETC_RHIME | Choline-sulfatase OS=Rhizobium meliloti (strain 1021) GN=betC PE=1 SV=2 | 24 | 532 | 6.0E-146 |
| sp|Q7SGQ0|MED8_NEUCR | Mediator of RNA polymerase II transcription subunit 8 OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=med-8 PE=3 SV=1 | 553 | 777 | 5.0E-37 |
| sp|Q2HDD6|MED8_CHAGB | Mediator of RNA polymerase II transcription subunit 8 OS=Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) GN=MED8 PE=3 SV=1 | 556 | 723 | 4.0E-35 |
| sp|Q148F3|ARSK_BOVIN | Arylsulfatase K OS=Bos taurus GN=ARSK PE=2 SV=1 | 20 | 492 | 1.0E-33 |
| sp|Q5ZK90|ARSK_CHICK | Arylsulfatase K OS=Gallus gallus GN=ARSK PE=2 SV=1 | 22 | 442 | 4.0E-33 |
| sp|P31447|YIDJ_ECOLI | Uncharacterized sulfatase YidJ OS=Escherichia coli (strain K12) GN=yidJ PE=3 SV=1 | 24 | 441 | 4.0E-33 |
| sp|Q0TUK6|SULF_CLOP1 | Arylsulfatase OS=Clostridium perfringens (strain ATCC 13124 / DSM 756 / JCM 1290 / NCIMB 6125 / NCTC 8237 / Type A) GN=CPF_0221 PE=1 SV=1 | 24 | 441 | 6.0E-33 |
| sp|Q8XNV1|SULF_CLOPE | Arylsulfatase OS=Clostridium perfringens (strain 13 / Type A) GN=CPE0231 PE=3 SV=1 | 24 | 441 | 2.0E-32 |
| sp|Q08CJ7|ARSK_DANRE | Arylsulfatase K OS=Danio rerio GN=arsk PE=2 SV=1 | 24 | 442 | 4.0E-32 |
| sp|Q0IHJ2|ARSK_XENLA | Arylsulfatase K OS=Xenopus laevis GN=arsk PE=2 SV=1 | 19 | 502 | 2.0E-31 |
| sp|Q32KJ2|ARSK_RAT | Arylsulfatase K OS=Rattus norvegicus GN=Arsk PE=2 SV=1 | 7 | 492 | 8.0E-31 |
| sp|Q9D2L1|ARSK_MOUSE | Arylsulfatase K OS=Mus musculus GN=Arsk PE=2 SV=2 | 25 | 492 | 8.0E-31 |
| sp|Q32KH0|ARSK_CANLF | Arylsulfatase K OS=Canis lupus familiaris GN=ARSK PE=2 SV=1 | 25 | 492 | 2.0E-29 |
| sp|Q08890|IDS_MOUSE | Iduronate 2-sulfatase OS=Mus musculus GN=Ids PE=2 SV=3 | 26 | 390 | 6.0E-26 |
| sp|P22304|IDS_HUMAN | Iduronate 2-sulfatase OS=Homo sapiens GN=IDS PE=1 SV=1 | 26 | 396 | 5.0E-25 |
| sp|Q4WP83|MED8_ASPFU | Mediator of RNA polymerase II transcription subunit 8 OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=med8 PE=3 SV=1 | 556 | 723 | 5.0E-25 |
| sp|A1CXD6|MED8_NEOFI | Mediator of RNA polymerase II transcription subunit 8 OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=med8 PE=3 SV=1 | 556 | 723 | 8.0E-25 |
| sp|Q2UGT1|MED8_ASPOR | Mediator of RNA polymerase II transcription subunit 8 OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=med8 PE=3 SV=1 | 559 | 723 | 1.0E-24 |
| sp|A1CHE9|MED8_ASPCL | Mediator of RNA polymerase II transcription subunit 8 OS=Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1) GN=med8 PE=3 SV=1 | 559 | 723 | 2.0E-23 |
| sp|Q1DLG1|MED8_COCIM | Mediator of RNA polymerase II transcription subunit 8 OS=Coccidioides immitis (strain RS) GN=MED8 PE=3 SV=1 | 556 | 723 | 5.0E-23 |
| sp|Q1LZH9|GNS_BOVIN | N-acetylglucosamine-6-sulfatase OS=Bos taurus GN=GNS PE=2 SV=1 | 24 | 403 | 2.0E-21 |
| sp|Q8BFR4|GNS_MOUSE | N-acetylglucosamine-6-sulfatase OS=Mus musculus GN=Gns PE=1 SV=1 | 24 | 403 | 2.0E-21 |
| sp|Q571E4|GALNS_MOUSE | N-acetylgalactosamine-6-sulfatase OS=Mus musculus GN=Galns PE=1 SV=2 | 25 | 386 | 3.0E-21 |
| sp|Q32KJ6|GALNS_RAT | N-acetylgalactosamine-6-sulfatase OS=Rattus norvegicus GN=Galns PE=1 SV=1 | 25 | 386 | 6.0E-21 |
| sp|P50426|GNS_CAPHI | N-acetylglucosamine-6-sulfatase OS=Capra hircus GN=GNS PE=2 SV=1 | 24 | 403 | 9.0E-21 |
| sp|P34059|GALNS_HUMAN | N-acetylgalactosamine-6-sulfatase OS=Homo sapiens GN=GALNS PE=1 SV=1 | 25 | 386 | 1.0E-20 |
| sp|Q9VEX0|SULF1_DROME | Extracellular sulfatase SULF-1 homolog OS=Drosophila melanogaster GN=Sulf1 PE=1 SV=1 | 24 | 388 | 3.0E-20 |
| sp|P51691|ARS_PSEAE | Arylsulfatase OS=Pseudomonas aeruginosa (strain ATCC 15692 / PAO1 / 1C / PRS 101 / LMG 12228) GN=atsA PE=1 SV=3 | 24 | 442 | 3.0E-20 |
| sp|Q32KH5|GALNS_CANLF | N-acetylgalactosamine-6-sulfatase OS=Canis lupus familiaris GN=GALNS PE=2 SV=1 | 25 | 412 | 4.0E-20 |
| sp|Q8WNQ7|GALNS_PIG | N-acetylgalactosamine-6-sulfatase OS=Sus scrofa GN=GALNS PE=2 SV=1 | 25 | 386 | 5.0E-20 |
| sp|P15586|GNS_HUMAN | N-acetylglucosamine-6-sulfatase OS=Homo sapiens GN=GNS PE=1 SV=3 | 57 | 403 | 8.0E-20 |
| sp|Q6UWY0|ARSK_HUMAN | Arylsulfatase K OS=Homo sapiens GN=ARSK PE=1 SV=1 | 265 | 492 | 1.0E-19 |
| sp|P50428|ARSA_MOUSE | Arylsulfatase A OS=Mus musculus GN=Arsa PE=1 SV=2 | 23 | 466 | 2.0E-19 |
| sp|Q08DD1|ARSA_BOVIN | Arylsulfatase A OS=Bos taurus GN=ARSA PE=2 SV=1 | 23 | 466 | 6.0E-19 |
| sp|A2QID5|MED8_ASPNC | Mediator of RNA polymerase II transcription subunit 8 OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=med8 PE=3 SV=1 | 556 | 723 | 7.0E-19 |
| sp|Q5BCL0|MED8_EMENI | Mediator of RNA polymerase II transcription subunit 8 OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=med8 PE=3 SV=1 | 556 | 664 | 5.0E-17 |
| sp|Q9C0V7|YHJ2_SCHPO | Uncharacterized sulfatase PB10D8.02c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBPB10D8.02c PE=3 SV=1 | 17 | 445 | 1.0E-16 |
| sp|Q90XB6|SULF1_COTCO | Extracellular sulfatase Sulf-1 OS=Coturnix coturnix GN=SULF1 PE=1 SV=1 | 24 | 385 | 4.0E-16 |
| sp|Q8K007|SULF1_MOUSE | Extracellular sulfatase Sulf-1 OS=Mus musculus GN=Sulf1 PE=2 SV=1 | 24 | 382 | 3.0E-15 |
| sp|Q8IWU6|SULF1_HUMAN | Extracellular sulfatase Sulf-1 OS=Homo sapiens GN=SULF1 PE=1 SV=1 | 24 | 382 | 4.0E-15 |
| sp|P50473|ARS_STRPU | Arylsulfatase OS=Strongylocentrotus purpuratus PE=2 SV=1 | 15 | 417 | 5.0E-15 |
| sp|Q32KJ9|ARSG_RAT | Arylsulfatase G OS=Rattus norvegicus GN=Arsg PE=2 SV=1 | 24 | 443 | 2.0E-14 |
| sp|P50429|ARSB_MOUSE | Arylsulfatase B OS=Mus musculus GN=Arsb PE=1 SV=3 | 25 | 381 | 5.0E-14 |
| sp|P77318|YDEN_ECOLI | Uncharacterized sulfatase YdeN OS=Escherichia coli (strain K12) GN=ydeN PE=3 SV=2 | 47 | 391 | 6.0E-14 |
| sp|Q9X759|ATSA_KLEPN | Arylsulfatase OS=Klebsiella pneumoniae GN=atsA PE=1 SV=1 | 24 | 442 | 1.0E-13 |
| sp|P14000|ARS_HEMPU | Arylsulfatase OS=Hemicentrotus pulcherrimus PE=1 SV=1 | 24 | 417 | 2.0E-13 |
| sp|P51688|SPHM_HUMAN | N-sulphoglucosamine sulphohydrolase OS=Homo sapiens GN=SGSH PE=1 SV=1 | 23 | 389 | 3.0E-13 |
| sp|Q21376|SULF1_CAEEL | Putative extracellular sulfatase Sulf-1 homolog OS=Caenorhabditis elegans GN=sul-1 PE=3 SV=1 | 57 | 398 | 9.0E-13 |
| sp|P50430|ARSB_RAT | Arylsulfatase B OS=Rattus norvegicus GN=Arsb PE=2 SV=2 | 25 | 381 | 1.0E-12 |
| sp|P15289|ARSA_HUMAN | Arylsulfatase A OS=Homo sapiens GN=ARSA PE=1 SV=3 | 25 | 125 | 2.0E-12 |
| sp|Q96EG1|ARSG_HUMAN | Arylsulfatase G OS=Homo sapiens GN=ARSG PE=1 SV=1 | 22 | 443 | 6.0E-12 |
| sp|P08842|STS_HUMAN | Steryl-sulfatase OS=Homo sapiens GN=STS PE=1 SV=2 | 23 | 131 | 8.0E-12 |
| sp|Q3TYD4|ARSG_MOUSE | Arylsulfatase G OS=Mus musculus GN=Arsg PE=2 SV=1 | 24 | 433 | 1.0E-11 |
| sp|P51690|ARSE_HUMAN | Arylsulfatase E OS=Homo sapiens GN=ARSE PE=1 SV=2 | 3 | 125 | 4.0E-11 |
| sp|Q60HH5|ARSE_MACFA | Arylsulfatase E OS=Macaca fascicularis GN=ARSE PE=2 SV=1 | 14 | 125 | 1.0E-10 |
| sp|P15589|STS_RAT | Steryl-sulfatase OS=Rattus norvegicus GN=Sts PE=1 SV=2 | 22 | 159 | 1.0E-10 |
| sp|P15848|ARSB_HUMAN | Arylsulfatase B OS=Homo sapiens GN=ARSB PE=1 SV=1 | 12 | 313 | 1.0E-10 |
| sp|Q32KJ8|ARSI_RAT | Arylsulfatase I OS=Rattus norvegicus GN=Arsi PE=2 SV=1 | 26 | 383 | 1.0E-10 |
| sp|Q5FYA8|ARSH_HUMAN | Arylsulfatase H OS=Homo sapiens GN=ARSH PE=2 SV=1 | 23 | 124 | 3.0E-10 |
| sp|Q5FYB1|ARSI_HUMAN | Arylsulfatase I OS=Homo sapiens GN=ARSI PE=1 SV=1 | 26 | 383 | 4.0E-10 |
| sp|P20713|ATSA_ENTAE | Arylsulfatase OS=Enterobacter aerogenes GN=atsA PE=1 SV=1 | 24 | 381 | 7.0E-10 |
| sp|Q32KH8|ARSH_CANLF | Arylsulfatase H OS=Canis lupus familiaris GN=ARSH PE=2 SV=1 | 23 | 124 | 8.0E-10 |
| sp|P15289|ARSA_HUMAN | Arylsulfatase A OS=Homo sapiens GN=ARSA PE=1 SV=3 | 271 | 441 | 2.0E-09 |
| sp|P50427|STS_MOUSE | Steryl-sulfatase OS=Mus musculus GN=Sts PE=1 SV=1 | 26 | 125 | 2.0E-09 |
| sp|P50427|STS_MOUSE | Steryl-sulfatase OS=Mus musculus GN=Sts PE=1 SV=1 | 276 | 387 | 6.0E-09 |
| sp|P51689|ARSD_HUMAN | Arylsulfatase D OS=Homo sapiens GN=ARSD PE=1 SV=2 | 18 | 124 | 2.0E-08 |
| sp|P54793|ARSF_HUMAN | Arylsulfatase F OS=Homo sapiens GN=ARSF PE=1 SV=4 | 24 | 160 | 3.0E-08 |
| sp|Q32KH9|ARSG_CANLF | Arylsulfatase G OS=Canis lupus familiaris GN=ARSG PE=2 SV=1 | 22 | 125 | 5.0E-08 |
| sp|Q6BM45|MED8_DEBHA | Mediator of RNA polymerase II transcription subunit 8 OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=MED8 PE=3 SV=2 | 542 | 658 | 1.0E-07 |
| sp|Q59TD3|MED8_CANAL | Mediator of RNA polymerase II transcription subunit 8 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=MED8 PE=3 SV=1 | 542 | 698 | 8.0E-07 |
| sp|P15589|STS_RAT | Steryl-sulfatase OS=Rattus norvegicus GN=Sts PE=1 SV=2 | 276 | 388 | 2.0E-06 |
| sp|Q6CG02|MED8_YARLI | Mediator of RNA polymerase II transcription subunit 8 OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=MED8 PE=3 SV=1 | 562 | 665 | 3.0E-06 |
| sp|P25549|ASLA_ECOLI | Arylsulfatase OS=Escherichia coli (strain K12) GN=aslA PE=3 SV=2 | 273 | 410 | 3.0E-06 |
| sp|P54793|ARSF_HUMAN | Arylsulfatase F OS=Homo sapiens GN=ARSF PE=1 SV=4 | 266 | 402 | 9.0E-06 |
| sp|P51689|ARSD_HUMAN | Arylsulfatase D OS=Homo sapiens GN=ARSD PE=1 SV=2 | 266 | 402 | 1.0E-05 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0016592 | mediator complex | Yes |
| GO:0003712 | transcription coregulator activity | Yes |
| GO:0006357 | regulation of transcription by RNA polymerase II | Yes |
| GO:0008484 | sulfuric ester hydrolase activity | Yes |
| GO:0031323 | regulation of cellular metabolic process | No |
| GO:1903506 | regulation of nucleic acid-templated transcription | No |
| GO:0016788 | hydrolase activity, acting on ester bonds | No |
| GO:0003824 | catalytic activity | No |
| GO:0140110 | transcription regulator activity | No |
| GO:0009889 | regulation of biosynthetic process | No |
| GO:0060255 | regulation of macromolecule metabolic process | No |
| GO:0032991 | protein-containing complex | No |
| GO:0010468 | regulation of gene expression | No |
| GO:0140513 | nuclear protein-containing complex | No |
| GO:2001141 | regulation of RNA biosynthetic process | No |
| GO:0019222 | regulation of metabolic process | No |
| GO:0051252 | regulation of RNA metabolic process | No |
| GO:0006355 | regulation of transcription, DNA-templated | No |
| GO:0019219 | regulation of nucleobase-containing compound metabolic process | No |
| GO:0005575 | cellular_component | No |
| GO:0003674 | molecular_function | No |
| GO:0008150 | biological_process | No |
| GO:0050794 | regulation of cellular process | No |
| GO:0016787 | hydrolase activity | No |
| GO:0051171 | regulation of nitrogen compound metabolic process | No |
| GO:0080090 | regulation of primary metabolic process | No |
| GO:0065007 | biological regulation | No |
| GO:0010556 | regulation of macromolecule biosynthetic process | No |
| GO:0050789 | regulation of biological process | No |
| GO:0031326 | regulation of cellular biosynthetic process | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 57 | 0.45 |
| 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 | >Ophun1|4834 MSPDLNSLPVSAPPTGKKGPDGSRPNMLYIMADQLAAPQLAMYNAESQIKTPNLDRLAAASVQFDSAYCPSPLCA PSRMSMITGLLPMKIGAFDNAAQISSEIPTYAHYLRSRGYHTALAGKMHFVGDQLHGYEQRLTSDIYPADFGWAV NWDEPETRLEWYHNASSILQAGPCGRSNQLDYDEEVMFRSTQYLWDHVRQGPGKRPFALTVSLTHPHDPYTITRK YWDLYEDVDIALPKARVPKDELDAHSQRLMRVCDLWDHDLTDDQIKRAKRAYYGSVSYVDDCIGRLLETLRDAGL ADDTIVIFSGDHGDMLGERGLWYKMSYFESSVRVPLLVHYPRWFSPRRVSQNVSTLDLLPTICDFIGVKPAPLLP MDGISMLPHLLGREGGHDTVLAEYTGEGTVRPIMMIRRGPWKYITCPADEPQLYNLDDDPLELDNLARLRNQAPQ NTAQAKAKAIFAEYDAEAKERWDFDAITAQVLQSQRSRRLVWDALKQGAFTSWDFDPVDDGRTKYIRSTIPLDEL ERRARYPFVDSKAYSFSKTVDSTRRMATLGLDDDELKSVEQLVARLAQLSSSIQSLKMDILKSNPLPHASSLQAS AQILQRNLQTVLDSLAENADLFGRMALHPATNYPGRTQEGVLTQLLRKKLEPDVEELVVEGREAARLATAEGVAA LQAIWDELRQWTHDRIATYVRDEAGQVFTAEERAAGTETVRTGLRRALDEESDDEDEEGGDEEDEDAAAAVRARL ERGPEPETLLWFAARGDFELPRNVEYERKVGVNRGLEGVNIPPEEVVPDATAAA* |
| Coding | >Ophun1|4834 ATGTCTCCCGACCTCAACTCACTGCCAGTCTCAGCGCCCCCAACCGGCAAAAAGGGCCCGGACGGCTCACGCCCC AACATGCTCTACATCATGGCCGATCAGTTGGCGGCGCCGCAGCTGGCCATGTACAACGCCGAGTCGCAGATCAAG ACGCCCAACCTCGATCGATTGGCGGCCGCATCCGTGCAGTTCGACTCGGCTTACTGTCCCTCGCCGCTGTGCGCG CCCTCGCGGATGAGCATGATTACGGGATTGCTGCCCATGAAGATTGGCGCTTTTGATAATGCGGCCCAGATTAGC TCTGAGATCCCGACGTATGCGCATTACTTGCGCTCGCGTGGCTACCATACCGCTCTTGCTGGGAAGATGCACTTT GTGGGCGATCAGTTGCATGGTTACGAGCAGCGCCTTACCAGCGACATCTATCCGGCTGACTTTGGATGGGCTGTC AATTGGGATGAGCCGGAGACTCGGCTTGAGTGGTATCATAATGCCAGCTCTATCCTGCAGGCTGGACCGTGTGGC CGCAGCAATCAGCTTGACTATGACGAGGAGGTCATGTTCCGCAGCACGCAGTATCTGTGGGATCATGTTCGGCAG GGGCCTGGGAAGAGGCCTTTTGCTCTGACGGTCTCTCTCACCCACCCGCACGACCCTTATACCATCACGAGAAAG TACTGGGATCTCTACGAAGATGTCGACATTGCGCTACCCAAGGCTCGCGTCCCCAAGGACGAGCTCGACGCTCAT AGCCAGCGCCTCATGCGCGTCTGCGACCTGTGGGATCACGACCTTACCGACGACCAGATCAAGAGGGCCAAGCGC GCATACTACGGCTCCGTCAGCTACGTCGATGACTGCATCGGCCGTCTGCTCGAGACGTTGCGCGACGCCGGTCTG GCTGACGACACCATTGTCATCTTCAGCGGCGACCATGGCGATATGCTGGGCGAGCGCGGACTCTGGTACAAGATG AGCTACTTCGAGTCGTCGGTTCGTGTGCCGCTGCTCGTTCACTACCCGCGCTGGTTCTCGCCTCGTCGCGTGTCG CAGAATGTGTCGACGCTGGACCTGCTGCCGACCATCTGCGACTTCATCGGCGTCAAGCCTGCGCCTCTTTTGCCA ATGGATGGCATCAGCATGCTGCCTCATCTTCTGGGCCGCGAGGGCGGGCACGACACCGTCCTGGCCGAGTACACG GGCGAGGGCACCGTCCGGCCCATCATGATGATCCGCCGTGGGCCTTGGAAGTACATCACCTGTCCGGCCGACGAG CCGCAGCTGTACAACCTCGACGATGACCCGCTCGAGCTGGATAACCTGGCTCGTCTGCGCAACCAGGCGCCCCAG AACACCGCGCAGGCCAAGGCAAAGGCCATCTTTGCAGAGTATGATGCTGAGGCCAAGGAGCGGTGGGACTTTGAC GCCATTACCGCTCAGGTGCTGCAGTCGCAGCGTAGCCGTCGGCTGGTGTGGGATGCGCTGAAGCAGGGTGCCTTT ACGAGTTGGGACTTTGACCCTGTCGACGATGGCCGGACAAAATACATTCGCTCCACTATACCTCTTGACGAACTC GAGCGTCGCGCGCGCTACCCGTTTGTCGACTCCAAGGCGTACTCGTTCTCCAAGACGGTCGACTCGACCCGCCGT ATGGCGACGCTGGGTCTCGACGATGACGAGCTCAAGTCGGTGGAGCAGCTCGTCGCCCGTCTGGCGCAGCTCTCC AGCAGCATCCAGAGCCTGAAGATGGACATACTCAAAAGCAACCCGCTGCCTCACGCCTCATCCCTCCAAGCGTCT GCGCAAATCCTCCAGCGCAACCTTCAGACCGTGCTAGACAGCCTCGCCGAAAACGCCGACCTCTTTGGCCGCATG GCCCTCCACCCGGCGACCAACTATCCCGGCCGCACGCAGGAAGGTGTGCTAACGCAGCTGCTGCGCAAGAAGCTC GAGCCGGATGTCGAGGAGCTGGTCGTCGAGGGGCGGGAGGCGGCACGGCTTGCTACGGCCGAGGGTGTCGCTGCG CTGCAGGCTATATGGGATGAGCTGCGGCAGTGGACGCATGATAGGATTGCTACGTATGTTCGTGACGAGGCGGGG CAGGTGTTTACGGCCGAGGAGCGGGCTGCGGGGACGGAAACGGTGCGCACCGGCTTGAGGCGGGCGCTTGATGAG GAGAGTGATGATGAGGATGAGGAGGGGGGGGACGAGGAGGATGAGGATGCTGCTGCTGCGGTGAGGGCGCGGCTC GAGAGGGGACCCGAGCCTGAGACGTTGCTTTGGTTCGCTGCTCGTGGCGACTTTGAACTGCCGAGGAACGTCGAG TACGAGAGAAAGGTGGGCGTCAACAGGGGCCTTGAGGGTGTCAACATCCCACCTGAGGAGGTGGTGCCCGATGCA ACAGCCGCGGCTTAG |
| Transcript | >Ophun1|4834 ATGTCTCCCGACCTCAACTCACTGCCAGTCTCAGCGCCCCCAACCGGCAAAAAGGGCCCGGACGGCTCACGCCCC AACATGCTCTACATCATGGCCGATCAGTTGGCGGCGCCGCAGCTGGCCATGTACAACGCCGAGTCGCAGATCAAG ACGCCCAACCTCGATCGATTGGCGGCCGCATCCGTGCAGTTCGACTCGGCTTACTGTCCCTCGCCGCTGTGCGCG CCCTCGCGGATGAGCATGATTACGGGATTGCTGCCCATGAAGATTGGCGCTTTTGATAATGCGGCCCAGATTAGC TCTGAGATCCCGACGTATGCGCATTACTTGCGCTCGCGTGGCTACCATACCGCTCTTGCTGGGAAGATGCACTTT GTGGGCGATCAGTTGCATGGTTACGAGCAGCGCCTTACCAGCGACATCTATCCGGCTGACTTTGGATGGGCTGTC AATTGGGATGAGCCGGAGACTCGGCTTGAGTGGTATCATAATGCCAGCTCTATCCTGCAGGCTGGACCGTGTGGC CGCAGCAATCAGCTTGACTATGACGAGGAGGTCATGTTCCGCAGCACGCAGTATCTGTGGGATCATGTTCGGCAG GGGCCTGGGAAGAGGCCTTTTGCTCTGACGGTCTCTCTCACCCACCCGCACGACCCTTATACCATCACGAGAAAG TACTGGGATCTCTACGAAGATGTCGACATTGCGCTACCCAAGGCTCGCGTCCCCAAGGACGAGCTCGACGCTCAT AGCCAGCGCCTCATGCGCGTCTGCGACCTGTGGGATCACGACCTTACCGACGACCAGATCAAGAGGGCCAAGCGC GCATACTACGGCTCCGTCAGCTACGTCGATGACTGCATCGGCCGTCTGCTCGAGACGTTGCGCGACGCCGGTCTG GCTGACGACACCATTGTCATCTTCAGCGGCGACCATGGCGATATGCTGGGCGAGCGCGGACTCTGGTACAAGATG AGCTACTTCGAGTCGTCGGTTCGTGTGCCGCTGCTCGTTCACTACCCGCGCTGGTTCTCGCCTCGTCGCGTGTCG CAGAATGTGTCGACGCTGGACCTGCTGCCGACCATCTGCGACTTCATCGGCGTCAAGCCTGCGCCTCTTTTGCCA ATGGATGGCATCAGCATGCTGCCTCATCTTCTGGGCCGCGAGGGCGGGCACGACACCGTCCTGGCCGAGTACACG GGCGAGGGCACCGTCCGGCCCATCATGATGATCCGCCGTGGGCCTTGGAAGTACATCACCTGTCCGGCCGACGAG CCGCAGCTGTACAACCTCGACGATGACCCGCTCGAGCTGGATAACCTGGCTCGTCTGCGCAACCAGGCGCCCCAG AACACCGCGCAGGCCAAGGCAAAGGCCATCTTTGCAGAGTATGATGCTGAGGCCAAGGAGCGGTGGGACTTTGAC GCCATTACCGCTCAGGTGCTGCAGTCGCAGCGTAGCCGTCGGCTGGTGTGGGATGCGCTGAAGCAGGGTGCCTTT ACGAGTTGGGACTTTGACCCTGTCGACGATGGCCGGACAAAATACATTCGCTCCACTATACCTCTTGACGAACTC GAGCGTCGCGCGCGCTACCCGTTTGTCGACTCCAAGGCGTACTCGTTCTCCAAGACGGTCGACTCGACCCGCCGT ATGGCGACGCTGGGTCTCGACGATGACGAGCTCAAGTCGGTGGAGCAGCTCGTCGCCCGTCTGGCGCAGCTCTCC AGCAGCATCCAGAGCCTGAAGATGGACATACTCAAAAGCAACCCGCTGCCTCACGCCTCATCCCTCCAAGCGTCT GCGCAAATCCTCCAGCGCAACCTTCAGACCGTGCTAGACAGCCTCGCCGAAAACGCCGACCTCTTTGGCCGCATG GCCCTCCACCCGGCGACCAACTATCCCGGCCGCACGCAGGAAGGTGTGCTAACGCAGCTGCTGCGCAAGAAGCTC GAGCCGGATGTCGAGGAGCTGGTCGTCGAGGGGCGGGAGGCGGCACGGCTTGCTACGGCCGAGGGTGTCGCTGCG CTGCAGGCTATATGGGATGAGCTGCGGCAGTGGACGCATGATAGGATTGCTACGTATGTTCGTGACGAGGCGGGG CAGGTGTTTACGGCCGAGGAGCGGGCTGCGGGGACGGAAACGGTGCGCACCGGCTTGAGGCGGGCGCTTGATGAG GAGAGTGATGATGAGGATGAGGAGGGGGGGGACGAGGAGGATGAGGATGCTGCTGCTGCGGTGAGGGCGCGGCTC GAGAGGGGACCCGAGCCTGAGACGTTGCTTTGGTTCGCTGCTCGTGGCGACTTTGAACTGCCGAGGAACGTCGAG TACGAGAGAAAGGTGGGCGTCAACAGGGGCCTTGAGGGTGTCAACATCCCACCTGAGGAGGTGGTGCCCGATGCA ACAGCCGCGGCTTAG |
| Gene | >Ophun1|4834 ATGTCTCCCGACCTCAACTCACTGCCAGTCTCAGCGCCCCCAACCGGCAAAAAGGGCCCGGACGGCTCACGCCCC AACATGCTCTACATCATGGCCGATCAGTTGGCGGCGCCGCAGCTGGCCATGTACAACGCCGAGTCGCAGATCAAG ACGCCCAACCTCGATCGATTGGCGGCCGCATCCGTGCAGTTCGACTCGGCTTACTGTCCCTCGCCGCTGTGCGCG CCCTCGCGGATGAGCATGATTACGGGATTGCTGCCCATGAAGATTGGCGCTTTTGATAATGCGGCCCAGATTAGC TCTGAGATCCCGACGTATGCGCATTACTTGCGCTCGCGTGGCTACCATACCGCTCTTGCTGGGAAGATGCACTTT GTGGGCGATCAGTTGCATGGTTACGAGCAGCGCCTTACCAGCGACATCTATCCGGCTGACTTTGGATGGGCTGTC AATTGGGATGAGCCGGAGACTCGGCTTGAGTGGTATCATAATGCCAGCTCTATCCTGCAGGCTGGACCGTGTGGC CGCAGCAATCAGCTTGACTATGACGAGGAGGTCATGTTCCGCAGCACGCAGTATCTGTGGGATCATGTTCGGCAG GGGCCTGGGAAGAGGCCTTTTGCTCTGACGGTATGTTGCAGTTGATCAAGGCTGGGGGTTTTGAGGCTGATGGTC GGGATAGGTCTCTCTCACCCACCCGCACGACCCTTATACCATCACGAGAAAGTACTGGGATCTCTACGAAGATGT CGACATTGCGCTACCCAAGGCTCGCGTCCCCAAGGACGAGCTCGACGCTCATAGCCAGCGCCTCATGCGCGTCTG CGACCTGTGGGATCACGACCTTACCGACGACCAGATCAAGAGGGCCAAGCGCGCATACTACGGCTCCGTCAGCTA CGTCGATGACTGCATCGGCCGTCTGCTCGAGACGTTGCGCGACGCCGGTCTGGCTGACGACACCATTGTCATCTT CAGCGGCGACCATGGCGATATGCTGGGCGAGCGCGGACTCTGGTACAAGATGAGCTACTTCGAGTCGTCGGTTCG TGTGCCGCTGCTCGTTCACTACCCGCGCTGGTTCTCGCCTCGTCGCGTGTCGCAGAATGTGTCGACGCTGGACCT GCTGCCGACCATCTGCGACTTCATCGGCGTCAAGCCTGCGCCTCTTTTGCCAATGGATGGCATCAGCATGCTGCC TCATCTTCTGGGCCGCGAGGGCGGGCACGACACCGTCCTGGCCGAGTACACGGGCGAGGGCACCGTCCGGCCCAT CATGATGATCCGCCGTGGGCCTTGGAAGTACATCACCTGTCCGGCCGACGAGCCGCAGCTGTACAACCTCGACGA TGACCCGCTCGAGCTGGATAACCTGGCTCGTCTGCGCAACCAGGCGCCCCAGAACACCGCGCAGGCCAAGGCAAA GGCCATCTTTGCAGAGTATGATGCTGAGGCCAAGGAGCGGTGGGACTTTGACGCCATTACCGCTCAGGTGCTGCA GTCGCAGCGTAGCCGTCGGCTGGTGTGGGATGCGCTGAAGCAGGGTGCCTTTACGAGTTGGGACTTTGACCCTGT CGACGATGGCCGGACAAAGTGAGCAGCTCCCCCATGCCGACTCTTTCGTGATGCAGTGCTGACCAGGACGATTTC AAGATACATTCGCTCCACTATACCTCTTGACGAACTCGAGCGTCGCGCGCGCTACCCGTTTGTCGACTCCAAGGC GTACTCGTTCTCCAAGACGGTCGACTCGACCCGCCGGTAAGGGAAGGCGTGTATCGACAGGTTGAACGAGGCAGC ATCAGGCGAAGCTGCTGCTGCTGCGCATTAGGAGGCGTGACTCCGAAGAGGATGAAAGGGGGAAAAGAGTGGGAC ATGAGGATCGGTGTTTGGTTGCTTTTTTTCCGCTTGGCTGTCGTTGGGTTGAGGCTCTGCGCATGAAGTCGCTGG TGGAGCCTGTGGAGTTGTGGAGTCGGGACGGGGCTTAGGGCTGTGGATACTTGGATTGACGCACAGAATGTATGG CTGCGTTTGTACCTGTTATGTACCGTTTCTTATCACGCACCATCGTCATCATCCTCTTTCTGCGCCCATTTCTCA GACTTCCAAGTGCCTCGGCCTCTACGACTCTCGCATAGCATCGACCTACGAGTTTAGTTCACTAGTATGGCGACG CTGGGTCTCGACGATGACGAGCTCAAGTCGGTGGAGCAGCTCGTCGCCCGTCTGGCGCAGCTCTCCAGCAGCATC CAGAGCCTGAAGATGGACATACTCAAAAGCAACCCGCTGCCTCACGCGTTTGTTTCCCAATCATGCTGTGACGAG TATCAACTGACACCTCAAACGCATCCTTGCAGCTCATCCCTCCAAGCGTCTGCGCAAATCCTCCAGCGCAACCTT CAGACCGTGCTAGACAGCCTCGCCGAAAACGCCGACCTCTTTGGCCGCATGGCCCTCCACCCGGCGACCAACTAT CCCGGCCGCACGCAGGAAGGTGTGCTAACGCAGCTGCTGCGCAAGAAGCTCGAGCCGGATGTCGAGGAGCTGGTC GTCGAGGGGCGGGAGGCGGCACGGCTTGCTACGGCCGAGGGTGTCGCTGCGCTGCAGGCTATATGGGATGAGCTG CGGCAGTGGACGCATGATAGGATTGCTACGTATGTTCGTGACGAGGCGGGGCAGGTGTTTACGGCCGAGGAGCGG GCTGCGGGGACGGAAACGGTGCGCACCGGCTTGAGGCGGGCGCTTGATGAGGAGAGTGATGATGAGGATGAGGAG GGGGGGGACGAGGAGGATGAGGATGCTGCTGCTGCGGTGAGGGCGCGGCTCGAGAGGGGACCCGAGCCTGAGACG TTGCTTTGGTTCGCTGCTCGTGGCGACTTTGAACTGCCGAGGAACGTCGAGTACGAGAGAAAGGTGGGCGTCAAC AGGGGCCTTGAGGGTGTCAACATCCCACCTGAGGAGGTGGTGCCCGATGCAACAGCCGCGGCTTAG |