© 2022 - Robin Ohm - Utrecht University - The Netherlands
Built with Python Django and Wagtail
| Protein ID | OphauG2|7772 |
| Gene name | |
| Location | Contig_94:32708..34755 |
| Strand | - |
| Gene length (bp) | 2047 |
| Transcript length (bp) | 1728 |
| Coding sequence length (bp) | 1728 |
| Protein length (aa) | 576 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF07690 | MFS_1 | Major Facilitator Superfamily | 8.6E-28 | 83 | 517 |
| PF00083 | Sugar_tr | Sugar (and other) transporter | 2.1E-20 | 100 | 555 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q9C101|YKT8_SCHPO | Uncharacterized MFS-type transporter PB1E7.08c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAPB1E7.08c PE=1 SV=1 | 57 | 522 | 7.0E-77 |
| sp|Q5R5T8|SVOP_PONAB | Synaptic vesicle 2-related protein OS=Pongo abelii GN=SVOP PE=2 SV=1 | 60 | 554 | 4.0E-24 |
| sp|Q8N4V2|SVOP_HUMAN | Synaptic vesicle 2-related protein OS=Homo sapiens GN=SVOP PE=2 SV=1 | 60 | 554 | 5.0E-24 |
| sp|Q1JP63|SVOP_BOVIN | Synaptic vesicle 2-related protein OS=Bos taurus GN=SVOP PE=2 SV=1 | 60 | 554 | 7.0E-24 |
| sp|P30638|SVOP_CAEEL | Putative transporter svop-1 OS=Caenorhabditis elegans GN=svop-1 PE=3 SV=5 | 56 | 521 | 9.0E-24 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q9C101|YKT8_SCHPO | Uncharacterized MFS-type transporter PB1E7.08c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAPB1E7.08c PE=1 SV=1 | 57 | 522 | 7.0E-77 |
| sp|Q5R5T8|SVOP_PONAB | Synaptic vesicle 2-related protein OS=Pongo abelii GN=SVOP PE=2 SV=1 | 60 | 554 | 4.0E-24 |
| sp|Q8N4V2|SVOP_HUMAN | Synaptic vesicle 2-related protein OS=Homo sapiens GN=SVOP PE=2 SV=1 | 60 | 554 | 5.0E-24 |
| sp|Q1JP63|SVOP_BOVIN | Synaptic vesicle 2-related protein OS=Bos taurus GN=SVOP PE=2 SV=1 | 60 | 554 | 7.0E-24 |
| sp|P30638|SVOP_CAEEL | Putative transporter svop-1 OS=Caenorhabditis elegans GN=svop-1 PE=3 SV=5 | 56 | 521 | 9.0E-24 |
| sp|Q2XWK0|SVOP_XENLA | Synaptic vesicle 2-related protein OS=Xenopus laevis GN=svop PE=2 SV=1 | 60 | 554 | 1.0E-23 |
| sp|Q9Z2I7|SVOP_RAT | Synaptic vesicle 2-related protein OS=Rattus norvegicus GN=Svop PE=1 SV=1 | 60 | 554 | 5.0E-21 |
| sp|Q940M4|OCT7_ARATH | Organic cation/carnitine transporter 7 OS=Arabidopsis thaliana GN=OCT7 PE=2 SV=1 | 61 | 523 | 1.0E-20 |
| sp|Q8BFT9|SVOP_MOUSE | Synaptic vesicle 2-related protein OS=Mus musculus GN=Svop PE=1 SV=1 | 60 | 570 | 2.0E-20 |
| sp|Q29397|SV2A_BOVIN | Synaptic vesicle glycoprotein 2A OS=Bos taurus GN=SV2A PE=2 SV=1 | 69 | 308 | 5.0E-17 |
| sp|Q7L0J3|SV2A_HUMAN | Synaptic vesicle glycoprotein 2A OS=Homo sapiens GN=SV2A PE=1 SV=1 | 69 | 308 | 6.0E-17 |
| sp|Q02563|SV2A_RAT | Synaptic vesicle glycoprotein 2A OS=Rattus norvegicus GN=Sv2a PE=1 SV=2 | 69 | 308 | 6.0E-17 |
| sp|Q4R4X3|SV2A_MACFA | Synaptic vesicle glycoprotein 2A OS=Macaca fascicularis GN=SV2A PE=2 SV=1 | 69 | 308 | 6.0E-17 |
| sp|Q9JIS5|SV2A_MOUSE | Synaptic vesicle glycoprotein 2A OS=Mus musculus GN=Sv2a PE=1 SV=1 | 69 | 308 | 7.0E-17 |
| sp|Q5R4L9|SV2A_PONAB | Synaptic vesicle glycoprotein 2A OS=Pongo abelii GN=SV2A PE=2 SV=1 | 71 | 308 | 2.0E-16 |
| sp|Q8BG39|SV2B_MOUSE | Synaptic vesicle glycoprotein 2B OS=Mus musculus GN=Sv2b PE=1 SV=1 | 65 | 388 | 3.0E-14 |
| sp|Q7L1I2|SV2B_HUMAN | Synaptic vesicle glycoprotein 2B OS=Homo sapiens GN=SV2B PE=1 SV=1 | 7 | 308 | 9.0E-14 |
| sp|Q63564|SV2B_RAT | Synaptic vesicle glycoprotein 2B OS=Rattus norvegicus GN=Sv2b PE=1 SV=1 | 7 | 388 | 1.0E-13 |
| sp|Q69ZS6|SV2C_MOUSE | Synaptic vesicle glycoprotein 2C OS=Mus musculus GN=Sv2c PE=1 SV=2 | 69 | 226 | 3.0E-13 |
| sp|Q9Z2I6|SV2C_RAT | Synaptic vesicle glycoprotein 2C OS=Rattus norvegicus GN=Sv2c PE=1 SV=1 | 69 | 226 | 4.0E-13 |
| sp|Q496J9|SV2C_HUMAN | Synaptic vesicle glycoprotein 2C OS=Homo sapiens GN=SV2C PE=1 SV=1 | 69 | 226 | 7.0E-13 |
| sp|O34691|NAIP_BACSU | Putative niacin/nicotinamide transporter NaiP OS=Bacillus subtilis (strain 168) GN=naiP PE=1 SV=1 | 80 | 225 | 4.0E-11 |
| sp|Q43975|PCAK_ACIAD | 4-hydroxybenzoate transporter PcaK OS=Acinetobacter baylyi (strain ATCC 33305 / BD413 / ADP1) GN=pcaK PE=1 SV=3 | 52 | 397 | 6.0E-11 |
| sp|Q09852|YAEC_SCHPO | Putative inorganic phosphate transporter C23D3.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC23D3.12 PE=1 SV=1 | 69 | 565 | 1.0E-10 |
| sp|O70577|S22A2_MOUSE | Solute carrier family 22 member 2 OS=Mus musculus GN=Slc22a2 PE=1 SV=1 | 121 | 523 | 3.0E-10 |
| sp|Q8GSD9|PHT12_ORYSJ | Inorganic phosphate transporter 1-2 OS=Oryza sativa subsp. japonica GN=PTH1-2 PE=2 SV=1 | 55 | 575 | 8.0E-10 |
| sp|Q8H074|PT112_ORYSJ | Probable inorganic phosphate transporter 1-12 OS=Oryza sativa subsp. japonica GN=PHT1-12 PE=2 SV=1 | 54 | 574 | 1.0E-09 |
| sp|Q8H6G8|PHT18_ORYSJ | Probable inorganic phosphate transporter 1-8 OS=Oryza sativa subsp. japonica GN=PHT1-8 PE=2 SV=1 | 54 | 335 | 1.0E-08 |
| sp|Q51955|PCAK_PSEPU | 4-hydroxybenzoate transporter PcaK OS=Pseudomonas putida GN=pcaK PE=1 SV=1 | 57 | 201 | 8.0E-08 |
| sp|Q7XDZ7|PHT13_ORYSJ | Probable inorganic phosphate transporter 1-3 OS=Oryza sativa subsp. japonica GN=PHT1-3 PE=2 SV=1 | 72 | 574 | 1.0E-07 |
| sp|Q494P0|PHT17_ARATH | Probable inorganic phosphate transporter 1-7 OS=Arabidopsis thaliana GN=PHT1-7 PE=2 SV=2 | 65 | 574 | 3.0E-07 |
| sp|Q9I6Q3|PCAK_PSEAE | 4-hydroxybenzoate transporter PcaK OS=Pseudomonas aeruginosa (strain ATCC 15692 / PAO1 / 1C / PRS 101 / LMG 12228) GN=pcaK PE=3 SV=1 | 61 | 201 | 5.0E-07 |
| sp|O48639|PHT13_ARATH | Probable inorganic phosphate transporter 1-3 OS=Arabidopsis thaliana GN=PHT1-3 PE=2 SV=1 | 61 | 574 | 6.0E-07 |
| sp|Q7X7V2|PHT15_ORYSJ | Probable inorganic phosphate transporter 1-5 OS=Oryza sativa subsp. japonica GN=PHT1-5 PE=2 SV=2 | 62 | 325 | 8.0E-07 |
| sp|A9MNY7|NANT_SALAR | Putative sialic acid transporter OS=Salmonella arizonae (strain ATCC BAA-731 / CDC346-86 / RSK2980) GN=nanT PE=3 SV=1 | 70 | 206 | 1.0E-06 |
| sp|Q9LHQ6|OCT4_ARATH | Organic cation/carnitine transporter 4 OS=Arabidopsis thaliana GN=OCT4 PE=2 SV=1 | 112 | 519 | 1.0E-06 |
| sp|A9N832|NANT_SALPB | Putative sialic acid transporter OS=Salmonella paratyphi B (strain ATCC BAA-1250 / SPB7) GN=nanT PE=3 SV=1 | 70 | 206 | 2.0E-06 |
| sp|A7MJD1|NANT_CROS8 | Putative sialic acid transporter OS=Cronobacter sakazakii (strain ATCC BAA-894) GN=nanT PE=3 SV=1 | 70 | 206 | 2.0E-06 |
| sp|B4TWI9|NANT_SALSV | Putative sialic acid transporter OS=Salmonella schwarzengrund (strain CVM19633) GN=nanT PE=3 SV=1 | 70 | 206 | 2.0E-06 |
| sp|B5FIR7|NANT_SALDC | Putative sialic acid transporter OS=Salmonella dublin (strain CT_02021853) GN=nanT PE=3 SV=1 | 70 | 206 | 2.0E-06 |
| sp|B5R0L1|NANT_SALEP | Putative sialic acid transporter OS=Salmonella enteritidis PT4 (strain P125109) GN=nanT PE=3 SV=1 | 70 | 206 | 2.0E-06 |
| sp|B5RET6|NANT_SALG2 | Putative sialic acid transporter OS=Salmonella gallinarum (strain 287/91 / NCTC 13346) GN=nanT PE=3 SV=1 | 70 | 206 | 2.0E-06 |
| sp|B4T749|NANT_SALNS | Putative sialic acid transporter OS=Salmonella newport (strain SL254) GN=nanT PE=3 SV=1 | 70 | 206 | 2.0E-06 |
| sp|P0A2G6|NANT_SALTI | Putative sialic acid transporter OS=Salmonella typhi GN=nanT PE=3 SV=1 | 70 | 206 | 2.0E-06 |
| sp|P0A2G5|NANT_SALTY | Putative sialic acid transporter OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=nanT PE=3 SV=1 | 70 | 206 | 2.0E-06 |
| sp|Q57JD0|NANT_SALCH | Putative sialic acid transporter OS=Salmonella choleraesuis (strain SC-B67) GN=nanT PE=3 SV=1 | 70 | 206 | 2.0E-06 |
| sp|C0PZN3|NANT_SALPC | Putative sialic acid transporter OS=Salmonella paratyphi C (strain RKS4594) GN=nanT PE=3 SV=1 | 70 | 206 | 2.0E-06 |
| sp|B5F7J8|NANT_SALA4 | Putative sialic acid transporter OS=Salmonella agona (strain SL483) GN=nanT PE=3 SV=1 | 70 | 206 | 2.0E-06 |
| sp|Q5PLF0|NANT_SALPA | Putative sialic acid transporter OS=Salmonella paratyphi A (strain ATCC 9150 / SARB42) GN=nanT PE=3 SV=1 | 70 | 206 | 2.0E-06 |
| sp|B5BGP4|NANT_SALPK | Putative sialic acid transporter OS=Salmonella paratyphi A (strain AKU_12601) GN=nanT PE=3 SV=1 | 70 | 206 | 2.0E-06 |
| sp|B4TJR2|NANT_SALHS | Putative sialic acid transporter OS=Salmonella heidelberg (strain SL476) GN=nanT PE=3 SV=1 | 70 | 206 | 2.0E-06 |
| sp|Q9SYQ1|PHT18_ARATH | Probable inorganic phosphate transporter 1-8 OS=Arabidopsis thaliana GN=PHT1-8 PE=2 SV=2 | 63 | 574 | 2.0E-06 |
| sp|Q96303|PHT14_ARATH | Inorganic phosphate transporter 1-4 OS=Arabidopsis thaliana GN=PHT1-4 PE=1 SV=1 | 65 | 326 | 3.0E-06 |
| sp|Q01MW8|PHT14_ORYSI | Probable inorganic phosphate transporter 1-4 OS=Oryza sativa subsp. indica GN=PHT1-4 PE=2 SV=2 | 63 | 325 | 3.0E-06 |
| sp|Q8VYM2|PHT11_ARATH | Inorganic phosphate transporter 1-1 OS=Arabidopsis thaliana GN=PHT1-1 PE=1 SV=2 | 61 | 221 | 3.0E-06 |
| sp|A8AQB4|NANT_CITK8 | Putative sialic acid transporter OS=Citrobacter koseri (strain ATCC BAA-895 / CDC 4225-83 / SGSC4696) GN=nanT PE=3 SV=1 | 70 | 206 | 4.0E-06 |
| sp|Q96243|PHT12_ARATH | Probable inorganic phosphate transporter 1-2 OS=Arabidopsis thaliana GN=PHT1-2 PE=2 SV=2 | 61 | 221 | 5.0E-06 |
| sp|Q8H6H4|PHT11_ORYSJ | Inorganic phosphate transporter 1-1 OS=Oryza sativa subsp. japonica GN=PHT1-1 PE=2 SV=1 | 72 | 261 | 5.0E-06 |
| sp|Q9ZWT3|PHT16_ARATH | Probable inorganic phosphate transporter 1-6 OS=Arabidopsis thaliana GN=PHT1-6 PE=1 SV=1 | 65 | 574 | 6.0E-06 |
| sp|B7LRJ2|NANT_ESCF3 | Putative sialic acid transporter OS=Escherichia fergusonii (strain ATCC 35469 / DSM 13698 / CDC 0568-73) GN=nanT PE=3 SV=1 | 70 | 206 | 8.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0022857 | transmembrane transporter activity | Yes |
| GO:0016021 | integral component of membrane | Yes |
| GO:0055085 | transmembrane transport | Yes |
| GO:0051234 | establishment of localization | No |
| GO:0003674 | molecular_function | No |
| GO:0005215 | transporter activity | No |
| GO:0051179 | localization | No |
| GO:0006810 | transport | No |
| GO:0009987 | cellular process | No |
| GO:0031224 | intrinsic component of membrane | No |
| GO:0008150 | biological_process | No |
| GO:0005575 | cellular_component | No |
| GO:0110165 | cellular anatomical entity | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 34 | 0.45 |
| Domain # | Start | End | Length |
|---|---|---|---|
| 1 | 75 | 97 | 22 |
| 2 | 112 | 134 | 22 |
| 3 | 141 | 163 | 22 |
| 4 | 167 | 189 | 22 |
| 5 | 201 | 223 | 22 |
| 6 | 257 | 279 | 22 |
| 7 | 371 | 393 | 22 |
| 8 | 413 | 435 | 22 |
| 9 | 442 | 464 | 22 |
| 10 | 537 | 559 | 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 | >OphauG2|7772 MSVDFTRDIDSDVASRPSTSLSAPSDTCAYVATDVELAPALPLDVSGLQGLSLHEQKCVLVNRELDAQGMGRYQW YVWCLCGFGYFLDLMWAQAFSLCLSPLQQELGFSNSQSGRISTCFNAGLTAGALFWGFMSDIVGRRWAFNLTCLL SSVFGLALGFSNSYTTFLILTAFVGFGVGGNIPVDGAIFLEFVPQSRRFLLACLSVFQPLGVVACSSLAFAFIPS HSCAPNFSQPDALPSCRNSEAPCCSRSDNMGWRYLLFTLGGITLFVFAARFLVFTCRETPKFLIYQGQDEKAIET MRHVSRVNKNHCRLSLQIFEALDREHQHLCHPASNDRNPPAMPAVSKPKWKLSQHLDRYKMLFCSWQMTRLTLLT WLTYILDFSGFTVAGFYLPRILALKNGSAHVSLKFTYASYIYTYAPGIIGVLVGAWTCRIPRIGRKWTMVLASGL MGTSIFLLSQVDTVAKREGLFTLEYFFQSMFNAVLYGWTPEAFPAPVRGTACGMASFWGRLFGIVSPLIAQHLYG RSSSGNGDVNSVLYLAGGVTLGCVVSTALLPTAMMETQDERSQNAQADST* |
| Coding | >OphauG2|7772 ATGAGCGTGGATTTCACGCGCGACATTGACTCTGATGTCGCTTCTAGACCGTCGACTTCGCTCTCGGCGCCCAGC GACACTTGTGCATACGTCGCCACCGATGTGGAACTGGCGCCCGCGCTGCCTCTCGACGTGTCGGGCCTGCAGGGC CTGTCGCTGCATGAGCAAAAGTGCGTCTTGGTGAACCGCGAGCTGGACGCGCAGGGCATGGGGCGCTACCAGTGG TATGTGTGGTGCCTGTGCGGGTTTGGATACTTTCTCGATCTCATGTGGGCGCAGGCGTTTAGTCTGTGCTTGAGT CCGCTGCAGCAGGAGCTGGGGTTTTCGAATTCGCAGTCGGGCAGGATATCGACGTGCTTCAATGCGGGCTTGACG GCCGGCGCGCTGTTTTGGGGCTTCATGTCGGATATTGTCGGCCGGCGCTGGGCATTCAACCTCACCTGTCTGCTC TCCTCCGTCTTTGGCCTGGCCCTCGGCTTTTCCAACAGCTACACCACCTTTCTCATCCTCACCGCCTTTGTCGGC TTCGGCGTCGGCGGCAACATCCCCGTCGACGGCGCCATCTTTCTCGAATTCGTGCCCCAGTCGCGGCGTTTCCTA CTCGCCTGTCTTTCCGTCTTCCAGCCGCTGGGCGTCGTGGCCTGTTCGTCGCTGGCCTTTGCCTTTATACCTAGC CACTCGTGCGCGCCAAACTTTTCGCAACCTGATGCGCTGCCGTCGTGCCGGAACAGCGAGGCGCCTTGCTGTTCG CGCTCTGATAACATGGGCTGGCGATATCTGCTCTTTACGCTTGGCGGCATCACGCTCTTTGTCTTTGCTGCGCGG TTCCTCGTTTTCACGTGTCGCGAGACACCAAAGTTTCTCATCTATCAAGGACAGGACGAAAAGGCTATAGAGACG ATGCGCCATGTTTCTCGCGTCAATAAGAATCACTGTCGTCTGAGTCTACAAATCTTTGAGGCGCTGGATCGCGAG CATCAGCATCTTTGCCATCCAGCAAGCAACGACAGAAACCCCCCAGCGATGCCTGCCGTGTCCAAGCCCAAGTGG AAACTGAGCCAGCATCTCGATAGATACAAGATGCTCTTCTGTAGCTGGCAAATGACGCGCCTGACGCTGCTCACT TGGCTGACGTATATTCTCGACTTTTCCGGCTTCACCGTCGCCGGCTTCTACCTACCGCGGATTCTGGCGCTTAAA AATGGCAGCGCCCACGTCAGCCTCAAGTTCACCTACGCCTCGTACATTTACACCTATGCTCCGGGAATCATTGGC GTCCTCGTCGGCGCCTGGACATGTCGTATTCCTCGAATAGGCCGCAAGTGGACCATGGTGCTCGCTTCAGGCCTC ATGGGCACTTCCATCTTCTTGCTGTCCCAGGTAGATACTGTGGCCAAGCGCGAGGGCCTCTTTACGCTCGAGTAC TTTTTCCAGTCCATGTTCAACGCTGTTCTTTACGGCTGGACGCCAGAGGCCTTTCCAGCGCCGGTTCGAGGCACG GCTTGCGGCATGGCGAGTTTCTGGGGCCGCCTGTTTGGCATTGTGAGCCCGCTCATTGCTCAGCATCTTTATGGC CGTAGCTCCAGCGGCAACGGCGATGTTAATAGCGTCCTCTATCTCGCTGGCGGGGTGACTTTGGGCTGCGTTGTT AGCACGGCTCTGCTGCCCACAGCCATGATGGAGACGCAGGATGAACGCTCGCAAAATGCTCAGGCTGACAGCACT TGA |
| Transcript | >OphauG2|7772 ATGAGCGTGGATTTCACGCGCGACATTGACTCTGATGTCGCTTCTAGACCGTCGACTTCGCTCTCGGCGCCCAGC GACACTTGTGCATACGTCGCCACCGATGTGGAACTGGCGCCCGCGCTGCCTCTCGACGTGTCGGGCCTGCAGGGC CTGTCGCTGCATGAGCAAAAGTGCGTCTTGGTGAACCGCGAGCTGGACGCGCAGGGCATGGGGCGCTACCAGTGG TATGTGTGGTGCCTGTGCGGGTTTGGATACTTTCTCGATCTCATGTGGGCGCAGGCGTTTAGTCTGTGCTTGAGT CCGCTGCAGCAGGAGCTGGGGTTTTCGAATTCGCAGTCGGGCAGGATATCGACGTGCTTCAATGCGGGCTTGACG GCCGGCGCGCTGTTTTGGGGCTTCATGTCGGATATTGTCGGCCGGCGCTGGGCATTCAACCTCACCTGTCTGCTC TCCTCCGTCTTTGGCCTGGCCCTCGGCTTTTCCAACAGCTACACCACCTTTCTCATCCTCACCGCCTTTGTCGGC TTCGGCGTCGGCGGCAACATCCCCGTCGACGGCGCCATCTTTCTCGAATTCGTGCCCCAGTCGCGGCGTTTCCTA CTCGCCTGTCTTTCCGTCTTCCAGCCGCTGGGCGTCGTGGCCTGTTCGTCGCTGGCCTTTGCCTTTATACCTAGC CACTCGTGCGCGCCAAACTTTTCGCAACCTGATGCGCTGCCGTCGTGCCGGAACAGCGAGGCGCCTTGCTGTTCG CGCTCTGATAACATGGGCTGGCGATATCTGCTCTTTACGCTTGGCGGCATCACGCTCTTTGTCTTTGCTGCGCGG TTCCTCGTTTTCACGTGTCGCGAGACACCAAAGTTTCTCATCTATCAAGGACAGGACGAAAAGGCTATAGAGACG ATGCGCCATGTTTCTCGCGTCAATAAGAATCACTGTCGTCTGAGTCTACAAATCTTTGAGGCGCTGGATCGCGAG CATCAGCATCTTTGCCATCCAGCAAGCAACGACAGAAACCCCCCAGCGATGCCTGCCGTGTCCAAGCCCAAGTGG AAACTGAGCCAGCATCTCGATAGATACAAGATGCTCTTCTGTAGCTGGCAAATGACGCGCCTGACGCTGCTCACT TGGCTGACGTATATTCTCGACTTTTCCGGCTTCACCGTCGCCGGCTTCTACCTACCGCGGATTCTGGCGCTTAAA AATGGCAGCGCCCACGTCAGCCTCAAGTTCACCTACGCCTCGTACATTTACACCTATGCTCCGGGAATCATTGGC GTCCTCGTCGGCGCCTGGACATGTCGTATTCCTCGAATAGGCCGCAAGTGGACCATGGTGCTCGCTTCAGGCCTC ATGGGCACTTCCATCTTCTTGCTGTCCCAGGTAGATACTGTGGCCAAGCGCGAGGGCCTCTTTACGCTCGAGTAC TTTTTCCAGTCCATGTTCAACGCTGTTCTTTACGGCTGGACGCCAGAGGCCTTTCCAGCGCCGGTTCGAGGCACG GCTTGCGGCATGGCGAGTTTCTGGGGCCGCCTGTTTGGCATTGTGAGCCCGCTCATTGCTCAGCATCTTTATGGC CGTAGCTCCAGCGGCAACGGCGATGTTAATAGCGTCCTCTATCTCGCTGGCGGGGTGACTTTGGGCTGCGTTGTT AGCACGGCTCTGCTGCCCACAGCCATGATGGAGACGCAGGATGAACGCTCGCAAAATGCTCAGGCTGACAGCACT TGA |
| Gene | >OphauG2|7772 ATGAGCGTGGATTTCACGCGCGACATTGACTCTGATGTCGCTTCTAGAGTAAGTCCTCCACGCCTTTGTGCTTGT GTGGCTTTTTGTCACCTGTTTCTATTTGCTTTTTTTTTTGAAAGTCTTGCTGCCTGGTAAAAAGCACGGGTTTTT ATAAAAACCCGAGCTTGTACAGCGCAAAAGAGACCAAAAAAACATCAAGGCTTGAAAAACAGAAAAAAACAAAGC AGCATGAAGGAAAAATCTGCTGACGCGTCGTCGCTCAAGCCGTCGACTTCGCTCTCGGCGCCCAGCGACACTTGT GCATACGTCGCCACCGATGTGGAACTGGCGCCCGCGCTGCCTCTCGACGTGTCGGGCCTGCAGGGCCTGTCGCTG CATGAGCAAAAGTGCGTCTTGGTGAACCGCGAGCTGGACGCGCAGGGCATGGGGCGCTACCAGTGGTATGTGTGG TGCCTGTGCGGGTTTGGATACTTTCTCGATCTCATGTGGGCGCAGGCGTTTAGTCTGTGCTTGAGTCCGCTGCAG CAGGAGCTGGGGTTTTCGAATTCGCAGTCGGGCAGGATATCGACGTGCTTCAATGCGGGCTTGACGGCCGGCGCG CTGTTTTGGGGCTTCATGTCGGATATTGTCGGTGAGCAGACATGACGCTCAGCATTGTTTTTTTTCCCTCGCCTT GGCTTCACCGAGGAGTAGAAAAGAAGAGAAGCAAGACTTGGGCTGAAACTCTTTTCCAGGCCGGCGCTGGGCATT CAACCTCACCTGTCTGCTCTCCTCCGTCTTTGGCCTGGCCCTCGGCTTTTCCAACAGCTACACCACCTTTCTCAT CCTCACCGCCTTTGTCGGCTTCGGCGTCGGCGGCAACATCCCCGTCGACGGCGCCATCTTTCTCGAATTCGTGCC CCAGTCGCGGCGTTTCCTACTCGCCTGTCTTTCCGTCTTCCAGCCGCTGGGCGTCGTGGCCTGTTCGTCGCTGGC CTTTGCCTTTATACCTAGCCACTCGTGCGCGCCAAACTTTTCGCAACCTGATGCGCTGCCGTCGTGCCGGAACAG CGAGGCGCCTTGCTGTTCGCGCTCTGATAACATGGGCTGGCGATATCTGCTCTTTACGCTTGGCGGCATCACGCT CTTTGTCTTTGCTGCGCGGTTCCTCGTTTTCACGTGTCGCGAGACACCAAAGTTTCTCATCTATCAAGGACAGGA CGAAAAGGCTATAGAGACGATGCGCCATGTTTCTCGCGTCAATAAGAATCACTGTCGTCTGAGTCTACAAATCTT TGAGGCGCTGGATCGCGAGCATCAGCATCTTTGCCATCCAGCAAGCAACGACAGAAACCCCCCAGCGATGCCTGC CGTGTCCAAGCCCAAGTGGAAACTGAGCCAGCATCTCGATAGATACAAGATGCTCTTCTGTAGCTGGCAAATGAC GCGCCTGACGCTGCTCACTTGGCTGACGTATATTCTCGACTTTTCCGGCTTCACCGTCGCCGGCTTCTACCTACC GCGGATTCTGGCGCTTAAAAATGGCAGCGCCCACGTCAGCCTCAAGTTCACCTACGCCTCGTACATTTACACCTA TGCTCCGGGAATCATTGGCGTCCTCGTCGGCGCCTGGACATGTCGTATTCCTCGAATAGGCCGCAAGTGGACCAT GGTGCTCGCTTCAGGCCTCATGGGCACTTCCATCTTCTTGCTGTCCCAGGTAGATACTGTGGCCAAGCGCGAGGG CCTCTTTACGCTCGAGTACTTTTTCCAGTCCATGTTCAACGCTGTTCTTTACGGCTGGACGCCAGAGGCCTTTCC AGCGCCGGTTCGAGGCACGGCTTGCGGCATGGCGAGTTTCTGGGGCCGCCTGTTTGGCATTGTGAGCCCGCTCAT TGCTCAGCATCTTTATGGCCGTAGCTCCAGCGGCAACGGCGATGTTAATAGCGTCCTCTATCTCGCTGGCGGGGT GACTTTGGGCTGCGTTGTTAGCACGGCTCTGCTGCCCACAGCCATGATGGAGACGCAGGATGAACGCTCGCAAAA TGCTCAGGCTGACAGCACTTGA |