Protein ID | OphauB2|8172 |
Gene name | |
Location | Contig_99:65794..67595 |
Strand | - |
Gene length (bp) | 1801 |
Transcript length (bp) | 1611 |
Coding sequence length (bp) | 1611 |
Protein length (aa) | 537 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF13649 | Methyltransf_25 | Methyltransferase domain | 1.1E-11 | 238 | 335 |
PF06325 | PrmA | Ribosomal protein L11 methyltransferase (PrmA) | 1.2E-10 | 234 | 309 |
PF13847 | Methyltransf_31 | Methyltransferase domain | 1.5E-09 | 234 | 343 |
PF08241 | Methyltransf_11 | Methyltransferase domain | 4.0E-09 | 239 | 338 |
PF13489 | Methyltransf_23 | Methyltransferase domain | 2.2E-06 | 232 | 338 |
PF05175 | MTS | Methyltransferase small domain | 8.2E-06 | 234 | 307 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|O13648|ANM3_SCHPO | Ribosomal protein arginine N-methyltransferase rmt3 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=rmt3 PE=1 SV=3 | 15 | 536 | 3.0E-114 |
sp|O60678|ANM3_HUMAN | Protein arginine N-methyltransferase 3 OS=Homo sapiens GN=PRMT3 PE=1 SV=3 | 2 | 516 | 8.0E-89 |
sp|O70467|ANM3_RAT | Protein arginine N-methyltransferase 3 OS=Rattus norvegicus GN=Prmt3 PE=1 SV=1 | 23 | 516 | 6.0E-86 |
sp|Q922H1|ANM3_MOUSE | Protein arginine N-methyltransferase 3 OS=Mus musculus GN=Prmt3 PE=1 SV=2 | 23 | 516 | 3.0E-84 |
sp|Q9URX7|ANM1_SCHPO | Protein arginine N-methyltransferase 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=rmt1 PE=1 SV=2 | 198 | 524 | 1.0E-79 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|O13648|ANM3_SCHPO | Ribosomal protein arginine N-methyltransferase rmt3 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=rmt3 PE=1 SV=3 | 15 | 536 | 3.0E-114 |
sp|O60678|ANM3_HUMAN | Protein arginine N-methyltransferase 3 OS=Homo sapiens GN=PRMT3 PE=1 SV=3 | 2 | 516 | 8.0E-89 |
sp|O70467|ANM3_RAT | Protein arginine N-methyltransferase 3 OS=Rattus norvegicus GN=Prmt3 PE=1 SV=1 | 23 | 516 | 6.0E-86 |
sp|Q922H1|ANM3_MOUSE | Protein arginine N-methyltransferase 3 OS=Mus musculus GN=Prmt3 PE=1 SV=2 | 23 | 516 | 3.0E-84 |
sp|Q9URX7|ANM1_SCHPO | Protein arginine N-methyltransferase 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=rmt1 PE=1 SV=2 | 198 | 524 | 1.0E-79 |
sp|O82210|ANM12_ARATH | Probable protein arginine N-methyltransferase 1.2 OS=Arabidopsis thaliana GN=PRMT12 PE=1 SV=1 | 194 | 526 | 4.0E-76 |
sp|Q9SU94|ANM11_ARATH | Protein arginine N-methyltransferase 1.1 OS=Arabidopsis thaliana GN=PRMT11 PE=1 SV=1 | 194 | 535 | 5.0E-75 |
sp|P38074|HMT1_YEAST | Protein arginine N-methyltransferase 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HMT1 PE=1 SV=1 | 186 | 524 | 1.0E-74 |
sp|Q0J2C6|ANM1_ORYSJ | Probable protein arginine N-methyltransferase 1 OS=Oryza sativa subsp. japonica GN=PRMT1 PE=2 SV=1 | 193 | 535 | 6.0E-73 |
sp|A2Z0C0|ANM1_ORYSI | Probable protein arginine N-methyltransferase 1 OS=Oryza sativa subsp. indica GN=PRMT1 PE=3 SV=1 | 193 | 535 | 6.0E-73 |
sp|Q54EF2|ANM1_DICDI | Protein arginine N-methyltransferase 1 OS=Dictyostelium discoideum GN=prmt1 PE=3 SV=1 | 194 | 526 | 6.0E-73 |
sp|Q7XKC0|ANM61_ORYSJ | Probable protein arginine N-methyltransferase 6.1 OS=Oryza sativa subsp. japonica GN=PRMT6.1 PE=3 SV=2 | 196 | 526 | 5.0E-71 |
sp|Q6VRB0|ANM1B_XENLA | Protein arginine N-methyltransferase 1-B OS=Xenopus laevis GN=prmt1-b PE=2 SV=1 | 194 | 528 | 8.0E-71 |
sp|Q28F07|ANM1_XENTR | Protein arginine N-methyltransferase 1 OS=Xenopus tropicalis GN=prmt1 PE=2 SV=1 | 194 | 528 | 9.0E-71 |
sp|Q5RGQ2|ANM8B_DANRE | Protein arginine N-methyltransferase 8-B OS=Danio rerio GN=prmt8b PE=2 SV=2 | 194 | 526 | 9.0E-71 |
sp|Q9NR22|ANM8_HUMAN | Protein arginine N-methyltransferase 8 OS=Homo sapiens GN=PRMT8 PE=1 SV=2 | 194 | 528 | 1.0E-70 |
sp|Q6PAK3|ANM8_MOUSE | Protein arginine N-methyltransferase 8 OS=Mus musculus GN=Prmt8 PE=1 SV=2 | 194 | 528 | 1.0E-70 |
sp|Q99873|ANM1_HUMAN | Protein arginine N-methyltransferase 1 OS=Homo sapiens GN=PRMT1 PE=1 SV=2 | 194 | 528 | 1.0E-70 |
sp|A8IEF3|ANM1_CHLRE | Protein arginine N-methyltransferase 1 OS=Chlamydomonas reinhardtii GN=PRMT1 PE=1 SV=1 | 176 | 532 | 2.0E-70 |
sp|Q8AV13|ANM1A_XENLA | Protein arginine N-methyltransferase 1-A OS=Xenopus laevis GN=prmt1-a PE=1 SV=1 | 185 | 528 | 2.0E-70 |
sp|Q08A71|ANM6_ARATH | Probable protein arginine N-methyltransferase 6 OS=Arabidopsis thaliana GN=PRMT6 PE=2 SV=1 | 196 | 526 | 3.0E-70 |
sp|A2XYY8|ANM61_ORYSI | Probable protein arginine N-methyltransferase 6.1 OS=Oryza sativa subsp. indica GN=PRMT6.1 PE=3 SV=1 | 196 | 524 | 7.0E-70 |
sp|Q63009|ANM1_RAT | Protein arginine N-methyltransferase 1 OS=Rattus norvegicus GN=Prmt1 PE=1 SV=1 | 194 | 528 | 9.0E-70 |
sp|Q9JIF0|ANM1_MOUSE | Protein arginine N-methyltransferase 1 OS=Mus musculus GN=Prmt1 PE=1 SV=1 | 194 | 528 | 1.0E-69 |
sp|Q75G68|ANM62_ORYSJ | Probable protein arginine N-methyltransferase 6.2 OS=Oryza sativa subsp. japonica GN=PRMT6.2 PE=2 SV=1 | 196 | 518 | 9.0E-69 |
sp|A2Z8S0|ANM62_ORYSI | Probable protein arginine N-methyltransferase 6.2 OS=Oryza sativa subsp. indica GN=PRMT6.2 PE=3 SV=2 | 196 | 518 | 9.0E-69 |
sp|Q0WVD6|ANM3_ARATH | Probable protein arginine N-methyltransferase 3 OS=Arabidopsis thaliana GN=PRMT3 PE=2 SV=1 | 33 | 497 | 2.0E-66 |
sp|A2YP56|ANM3_ORYSI | Probable protein arginine N-methyltransferase 3 OS=Oryza sativa subsp. indica GN=PRMT3 PE=3 SV=1 | 33 | 486 | 9.0E-63 |
sp|A3BMN9|ANM3_ORYSJ | Probable protein arginine N-methyltransferase 3 OS=Oryza sativa subsp. japonica GN=PRMT3 PE=2 SV=1 | 33 | 513 | 1.0E-62 |
sp|Q68EZ3|ANM6_XENLA | Protein arginine N-methyltransferase 6 OS=Xenopus laevis GN=prmt6 PE=2 SV=1 | 190 | 530 | 6.0E-57 |
sp|B0JYW5|ANM6_XENTR | Protein arginine N-methyltransferase 6 OS=Xenopus tropicalis GN=prmt6 PE=2 SV=1 | 190 | 530 | 1.0E-55 |
sp|Q96LA8|ANM6_HUMAN | Protein arginine N-methyltransferase 6 OS=Homo sapiens GN=PRMT6 PE=1 SV=1 | 196 | 516 | 2.0E-55 |
sp|Q6NWG4|ANM6_DANRE | Protein arginine N-methyltransferase 6 OS=Danio rerio GN=prmt6 PE=2 SV=2 | 184 | 525 | 4.0E-55 |
sp|Q6NZB1|ANM6_MOUSE | Protein arginine N-methyltransferase 6 OS=Mus musculus GN=Prmt6 PE=1 SV=2 | 196 | 516 | 5.0E-54 |
sp|Q5E9L5|ANM6_BOVIN | Protein arginine N-methyltransferase 6 OS=Bos taurus GN=PRMT6 PE=2 SV=1 | 196 | 516 | 2.0E-53 |
sp|Q54HI0|ANM2_DICDI | Protein arginine N-methyltransferase 2 OS=Dictyostelium discoideum GN=prmt2 PE=3 SV=1 | 196 | 439 | 7.0E-48 |
sp|Q9R144|ANM2_MOUSE | Protein arginine N-methyltransferase 2 OS=Mus musculus GN=Prmt2 PE=1 SV=1 | 173 | 489 | 1.0E-47 |
sp|P55345|ANM2_HUMAN | Protein arginine N-methyltransferase 2 OS=Homo sapiens GN=PRMT2 PE=1 SV=1 | 173 | 503 | 2.0E-47 |
sp|B3DLB3|ANM2_XENTR | Protein arginine N-methyltransferase 2 OS=Xenopus tropicalis GN=prmt2 PE=2 SV=1 | 124 | 526 | 2.0E-42 |
sp|Q9SNQ2|ANM10_ORYSJ | Protein arginine N-methyltransferase PRMT10 OS=Oryza sativa subsp. japonica GN=PRMT10 PE=2 SV=1 | 199 | 532 | 1.0E-40 |
sp|A2Y953|ANM10_ORYSI | Protein arginine N-methyltransferase PRMT10 OS=Oryza sativa subsp. indica GN=PRMT10 PE=3 SV=1 | 199 | 532 | 1.0E-40 |
sp|Q9MAT5|ANM10_ARATH | Protein arginine N-methyltransferase PRMT10 OS=Arabidopsis thaliana GN=PRMT10 PE=1 SV=1 | 199 | 485 | 1.0E-39 |
sp|D9IVE5|ANM2_XENLA | Protein arginine N-methyltransferase 2 OS=Xenopus laevis GN=prmt2 PE=1 SV=2 | 196 | 534 | 5.0E-39 |
sp|A3KPF2|ANM14_ARATH | Probable histone-arginine methyltransferase 1.4 OS=Arabidopsis thaliana GN=PRMT14 PE=1 SV=1 | 190 | 526 | 4.0E-36 |
sp|Q84W92|ANM13_ARATH | Probable histone-arginine methyltransferase 1.3 OS=Arabidopsis thaliana GN=PRMT13 PE=2 SV=3 | 184 | 526 | 5.0E-36 |
sp|B4LVS8|CARM1_DROVI | Histone-arginine methyltransferase CARMER OS=Drosophila virilis GN=Art4 PE=3 SV=1 | 184 | 491 | 1.0E-35 |
sp|B4KA23|CARM1_DROMO | Histone-arginine methyltransferase CARMER OS=Drosophila mojavensis GN=Art4 PE=3 SV=1 | 184 | 491 | 1.0E-35 |
sp|B4PVH6|CARM1_DROYA | Histone-arginine methyltransferase CARMER OS=Drosophila yakuba GN=Art4 PE=3 SV=1 | 184 | 491 | 2.0E-35 |
sp|B3P4N5|CARM1_DROER | Histone-arginine methyltransferase CARMER OS=Drosophila erecta GN=Art4 PE=3 SV=1 | 184 | 491 | 2.0E-35 |
sp|B4JXV2|CARM1_DROGR | Histone-arginine methyltransferase CARMER OS=Drosophila grimshawi GN=Art4 PE=3 SV=1 | 184 | 491 | 2.0E-35 |
sp|Q29B63|CARM1_DROPS | Histone-arginine methyltransferase CARMER OS=Drosophila pseudoobscura pseudoobscura GN=Art4 PE=3 SV=1 | 184 | 491 | 3.0E-35 |
sp|B4GZ20|CARM1_DROPE | Histone-arginine methyltransferase CARMER OS=Drosophila persimilis GN=Art4 PE=3 SV=1 | 184 | 491 | 3.0E-35 |
sp|B4HJC0|CARM1_DROSE | Histone-arginine methyltransferase CARMER OS=Drosophila sechellia GN=Art4 PE=3 SV=1 | 184 | 491 | 3.0E-35 |
sp|B4QVW6|CARM1_DROSI | Histone-arginine methyltransferase CARMER OS=Drosophila simulans GN=Art4 PE=3 SV=1 | 184 | 491 | 3.0E-35 |
sp|Q9VH48|CARM1_DROME | Probable histone-arginine methyltransferase CARMER OS=Drosophila melanogaster GN=Art4 PE=1 SV=1 | 184 | 491 | 3.0E-35 |
sp|Q7XI75|CARM1_ORYSJ | Probable histone-arginine methyltransferase CARM1 OS=Oryza sativa subsp. japonica GN=CARM1 PE=2 SV=1 | 155 | 526 | 4.0E-35 |
sp|A2YPT7|CARM1_ORYSI | Probable histone-arginine methyltransferase CARM1 OS=Oryza sativa subsp. indica GN=CARM1 PE=3 SV=2 | 155 | 526 | 4.0E-35 |
sp|B4NKI9|CARM1_DROWI | Histone-arginine methyltransferase CARMER OS=Drosophila willistoni GN=Art4 PE=3 SV=1 | 184 | 491 | 5.0E-35 |
sp|B3M1E1|CARM1_DROAN | Histone-arginine methyltransferase CARMER OS=Drosophila ananassae GN=Art4 PE=3 SV=1 | 184 | 491 | 2.0E-34 |
sp|Q6DC04|CARM1_DANRE | Histone-arginine methyltransferase CARM1 OS=Danio rerio GN=carm1 PE=2 SV=1 | 183 | 486 | 2.0E-32 |
sp|B0W3L6|CARM1_CULQU | Histone-arginine methyltransferase CARMER OS=Culex quinquefasciatus GN=Art4 PE=3 SV=1 | 181 | 486 | 7.0E-32 |
sp|Q9WVG6|CARM1_MOUSE | Histone-arginine methyltransferase CARM1 OS=Mus musculus GN=Carm1 PE=1 SV=2 | 183 | 480 | 1.0E-31 |
sp|Q86X55|CARM1_HUMAN | Histone-arginine methyltransferase CARM1 OS=Homo sapiens GN=CARM1 PE=1 SV=3 | 183 | 480 | 1.0E-31 |
sp|Q5XK84|CARM1_XENLA | Histone-arginine methyltransferase CARM1 OS=Xenopus laevis GN=carm1 PE=2 SV=1 | 183 | 486 | 1.0E-31 |
sp|Q174R2|CARM1_AEDAE | Histone-arginine methyltransferase CARMER OS=Aedes aegypti GN=CARM1 PE=3 SV=1 | 181 | 486 | 2.0E-31 |
sp|Q4AE70|CARM1_RAT | Histone-arginine methyltransferase CARM1 OS=Rattus norvegicus GN=Carm1 PE=1 SV=1 | 183 | 480 | 2.0E-31 |
sp|Q7Q2B7|CARM1_ANOGA | Histone-arginine methyltransferase CARMER OS=Anopheles gambiae GN=CARM1 PE=1 SV=5 | 181 | 486 | 5.0E-31 |
sp|Q582G4|ANM7_TRYB2 | Protein arginine N-methyltransferase 7 OS=Trypanosoma brucei brucei (strain 927/4 GUTat10.1) GN=PRMT7 PE=1 SV=1 | 204 | 373 | 4.0E-15 |
sp|A0JMU5|ANM9_XENLA | Putative protein arginine N-methyltransferase 9 OS=Xenopus laevis GN=prmt9 PE=2 SV=1 | 193 | 344 | 1.0E-08 |
sp|B8I303|PRMA_CLOCE | Ribosomal protein L11 methyltransferase OS=Clostridium cellulolyticum (strain ATCC 35319 / DSM 5812 / JCM 6584 / H10) GN=prmA PE=3 SV=1 | 229 | 341 | 3.0E-08 |
sp|C3L3G5|PRMA_CLOB6 | Ribosomal protein L11 methyltransferase OS=Clostridium botulinum (strain 657 / Type Ba4) GN=prmA PE=3 SV=1 | 230 | 337 | 2.0E-07 |
sp|Q6P2P2|ANM9_HUMAN | Putative protein arginine N-methyltransferase 9 OS=Homo sapiens GN=PRMT9 PE=2 SV=1 | 193 | 345 | 6.0E-07 |
sp|A6TSL8|PRMA_ALKMQ | Ribosomal protein L11 methyltransferase OS=Alkaliphilus metalliredigens (strain QYMF) GN=prmA PE=3 SV=1 | 238 | 344 | 8.0E-07 |
sp|Q9XW42|ANM7_CAEEL | Protein arginine N-methyltransferase 7 OS=Caenorhabditis elegans GN=prmt-7 PE=1 SV=2 | 238 | 349 | 2.0E-06 |
sp|Q944R7|ANM16_ARATH | Protein arginine N-methyltransferase 1.6 OS=Arabidopsis thaliana GN=PRMT16 PE=2 SV=2 | 212 | 343 | 2.0E-06 |
sp|A3DF23|PRMA_CLOTH | Ribosomal protein L11 methyltransferase OS=Clostridium thermocellum (strain ATCC 27405 / DSM 1237 / NBRC 103400 / NCIMB 10682 / NRRL B-4536 / VPI 7372) GN=prmA PE=3 SV=1 | 238 | 341 | 3.0E-06 |
sp|Q6PCI6|ANM7_XENLA | Protein arginine N-methyltransferase 7 OS=Xenopus laevis GN=prmt7 PE=2 SV=1 | 193 | 411 | 3.0E-06 |
sp|A6LRN8|PRMA_CLOB8 | Ribosomal protein L11 methyltransferase OS=Clostridium beijerinckii (strain ATCC 51743 / NCIMB 8052) GN=prmA PE=3 SV=1 | 229 | 341 | 3.0E-06 |
sp|Q665E3|PRMA_YERPS | Ribosomal protein L11 methyltransferase OS=Yersinia pseudotuberculosis serotype I (strain IP32953) GN=prmA PE=3 SV=2 | 233 | 359 | 3.0E-06 |
sp|B2K467|PRMA_YERPB | Ribosomal protein L11 methyltransferase OS=Yersinia pseudotuberculosis serotype IB (strain PB1/+) GN=prmA PE=3 SV=1 | 233 | 359 | 3.0E-06 |
sp|Q0AWM5|PRMA_SYNWW | Ribosomal protein L11 methyltransferase OS=Syntrophomonas wolfei subsp. wolfei (strain DSM 2245B / Goettingen) GN=prmA PE=3 SV=1 | 238 | 296 | 4.0E-06 |
sp|B3MF31|ANM7_DROAN | Protein arginine N-methyltransferase 7 OS=Drosophila ananassae GN=Art7 PE=3 SV=1 | 192 | 342 | 6.0E-06 |
GO Term | Description | Terminal node |
---|---|---|
GO:0008168 | methyltransferase activity | Yes |
GO:0003824 | catalytic activity | No |
GO:0003674 | molecular_function | No |
GO:0016740 | transferase activity | No |
GO:0016741 | transferase activity, transferring one-carbon groups | No |
Orthofinder run ID | 4 |
Orthogroup | 6076 |
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 | >OphauB2|8172 MAMDSSDTEPSCSSDSEQGEWLDVEPDHEATTFISLLDSRAFSTLDSMLADCKQRHGFDLVAEVERLRLDYIGGV KLVNFIRRRVKQAEPLPSVIARADLDSAELLQPVLENDAVLFSLEDAVDFEREEEEEEEEEREPEGQEAGDAQTR NRQLEAELKRLGAAFADYRVCVQKTLDAKWGDDQGAVTAKKHEASDSYYFESYAAHEIHETMLKDRVRTDAYRDF IYGNKHLFKDKVVLDIGCGTGILSMFCAKAGAASVIAVDKSDIIDKARENMFHNGLSSTITCLRGAIEDVQLPVA KVDVIVSEWMGYCLLYEAMLPSILFARDKYLKPHGLLVPSAATLLLAPVHDDDYVADTVTYWRDVYGFDMKAMQQ GIYDDVRIHAMPSDSVCGSAAVFKTLHLHHVQPQDLVFTAKWQSSLNRPVDQIHGFLIWFDCFFSTSSDDAPPDA SQTPEAWRAQKPGRVVMTTSPHATETHWKQGLLLVEPQPTLSQTPASSDIVGQLTVSVPESNARSLGLEASWSMA GCERRQVWKLS* |
Coding | >OphauB2|8172 ATGGCCATGGACAGCAGCGACACAGAGCCGTCTTGTAGCTCCGACTCGGAGCAGGGCGAGTGGCTAGATGTGGAG CCAGATCATGAAGCAACGACATTTATATCGCTGCTCGACTCGCGCGCCTTTTCGACGCTCGACTCGATGCTGGCA GATTGTAAGCAGCGCCACGGCTTCGACTTGGTAGCCGAAGTTGAGCGCCTGCGCCTCGACTACATTGGCGGCGTC AAGCTAGTCAATTTCATCCGCAGGCGCGTCAAGCAAGCCGAGCCGCTTCCAAGCGTGATTGCGCGCGCCGACCTA GACTCGGCCGAGCTGCTACAGCCGGTGCTAGAAAACGACGCCGTCTTATTTTCACTAGAAGACGCCGTCGACTTT GAGCGCGAGGAGGAGGAGGAGGAGGAGGAGGAGCGGGAGCCAGAGGGCCAAGAAGCTGGAGATGCGCAGACGCGT AATCGCCAGCTCGAGGCTGAGCTGAAGCGTCTTGGAGCTGCGTTTGCAGACTATCGCGTCTGCGTGCAAAAGACA CTTGATGCGAAATGGGGCGACGACCAGGGCGCAGTCACGGCCAAGAAGCATGAGGCGTCGGATTCGTATTATTTT GAATCATATGCCGCTCACGAGATTCACGAGACGATGCTCAAGGACCGTGTGCGGACAGATGCCTACCGAGACTTT ATTTACGGAAACAAGCACCTCTTCAAGGACAAGGTGGTGCTTGACATTGGCTGTGGCACAGGCATCCTCAGCATG TTTTGCGCAAAGGCTGGCGCGGCAAGCGTAATCGCAGTCGACAAGTCTGACATTATCGACAAGGCGCGAGAAAAC ATGTTTCACAACGGCCTGTCAAGCACCATTACCTGTCTGCGGGGCGCCATTGAAGACGTGCAGCTGCCCGTGGCA AAGGTGGACGTTATTGTCAGCGAGTGGATGGGCTACTGCCTTCTCTACGAGGCAATGCTTCCCAGCATCCTCTTT GCCCGCGACAAGTACCTCAAGCCCCATGGCTTGCTTGTGCCCAGCGCCGCGACTCTACTCTTGGCCCCCGTGCAC GACGACGACTACGTAGCCGATACCGTCACCTACTGGCGAGACGTCTATGGCTTCGACATGAAGGCCATGCAGCAG GGCATCTACGACGACGTGCGCATCCACGCCATGCCCTCAGACTCGGTCTGCGGCTCAGCCGCCGTCTTCAAAACT CTGCACCTGCATCACGTGCAGCCTCAAGACTTGGTCTTTACAGCAAAGTGGCAGTCAAGCCTCAATAGGCCCGTC GACCAAATCCACGGTTTCCTCATTTGGTTCGACTGCTTCTTCTCCACGTCAAGCGACGATGCACCCCCCGACGCG TCTCAGACGCCAGAGGCGTGGCGTGCCCAAAAGCCGGGCCGTGTCGTCATGACCACCAGCCCACATGCCACCGAG ACACACTGGAAGCAGGGTCTCTTGCTTGTAGAGCCGCAGCCCACCCTGTCTCAGACGCCTGCGTCGAGCGACATT GTTGGGCAATTAACAGTGTCAGTCCCCGAGTCCAATGCGCGGTCCCTTGGCCTTGAGGCCTCGTGGTCCATGGCT GGCTGTGAGAGACGACAAGTGTGGAAACTAAGTTGA |
Transcript | >OphauB2|8172 ATGGCCATGGACAGCAGCGACACAGAGCCGTCTTGTAGCTCCGACTCGGAGCAGGGCGAGTGGCTAGATGTGGAG CCAGATCATGAAGCAACGACATTTATATCGCTGCTCGACTCGCGCGCCTTTTCGACGCTCGACTCGATGCTGGCA GATTGTAAGCAGCGCCACGGCTTCGACTTGGTAGCCGAAGTTGAGCGCCTGCGCCTCGACTACATTGGCGGCGTC AAGCTAGTCAATTTCATCCGCAGGCGCGTCAAGCAAGCCGAGCCGCTTCCAAGCGTGATTGCGCGCGCCGACCTA GACTCGGCCGAGCTGCTACAGCCGGTGCTAGAAAACGACGCCGTCTTATTTTCACTAGAAGACGCCGTCGACTTT GAGCGCGAGGAGGAGGAGGAGGAGGAGGAGGAGCGGGAGCCAGAGGGCCAAGAAGCTGGAGATGCGCAGACGCGT AATCGCCAGCTCGAGGCTGAGCTGAAGCGTCTTGGAGCTGCGTTTGCAGACTATCGCGTCTGCGTGCAAAAGACA CTTGATGCGAAATGGGGCGACGACCAGGGCGCAGTCACGGCCAAGAAGCATGAGGCGTCGGATTCGTATTATTTT GAATCATATGCCGCTCACGAGATTCACGAGACGATGCTCAAGGACCGTGTGCGGACAGATGCCTACCGAGACTTT ATTTACGGAAACAAGCACCTCTTCAAGGACAAGGTGGTGCTTGACATTGGCTGTGGCACAGGCATCCTCAGCATG TTTTGCGCAAAGGCTGGCGCGGCAAGCGTAATCGCAGTCGACAAGTCTGACATTATCGACAAGGCGCGAGAAAAC ATGTTTCACAACGGCCTGTCAAGCACCATTACCTGTCTGCGGGGCGCCATTGAAGACGTGCAGCTGCCCGTGGCA AAGGTGGACGTTATTGTCAGCGAGTGGATGGGCTACTGCCTTCTCTACGAGGCAATGCTTCCCAGCATCCTCTTT GCCCGCGACAAGTACCTCAAGCCCCATGGCTTGCTTGTGCCCAGCGCCGCGACTCTACTCTTGGCCCCCGTGCAC GACGACGACTACGTAGCCGATACCGTCACCTACTGGCGAGACGTCTATGGCTTCGACATGAAGGCCATGCAGCAG GGCATCTACGACGACGTGCGCATCCACGCCATGCCCTCAGACTCGGTCTGCGGCTCAGCCGCCGTCTTCAAAACT CTGCACCTGCATCACGTGCAGCCTCAAGACTTGGTCTTTACAGCAAAGTGGCAGTCAAGCCTCAATAGGCCCGTC GACCAAATCCACGGTTTCCTCATTTGGTTCGACTGCTTCTTCTCCACGTCAAGCGACGATGCACCCCCCGACGCG TCTCAGACGCCAGAGGCGTGGCGTGCCCAAAAGCCGGGCCGTGTCGTCATGACCACCAGCCCACATGCCACCGAG ACACACTGGAAGCAGGGTCTCTTGCTTGTAGAGCCGCAGCCCACCCTGTCTCAGACGCCTGCGTCGAGCGACATT GTTGGGCAATTAACAGTGTCAGTCCCCGAGTCCAATGCGCGGTCCCTTGGCCTTGAGGCCTCGTGGTCCATGGCT GGCTGTGAGAGACGACAAGTGTGGAAACTAAGTTGA |
Gene | >OphauB2|8172 ATGGCCATGGACAGCAGCGACACAGAGCCGTCTTGTAGCTCCGACTCGGAGCAGGGCGAGTGGCTAGATGTGGAG CCAGATCATGAAGCAACGACATTTATATCGCTGCTCGACTCGCGCGCCTTTTCGACGCTCGACTCGATGCTGGCA GATTGTAAGCAGCGCCACGGCTTCGACTTGGTAGCCGAAGTTGAGCGCCTGCGCCTCGACTACATTGGCGGCGTC AAGCTAGTCAATTTCATCCGCAGGCGCGTCAAGCAAGCCGAGCCGCTTCCAAGCGTGATTGCGCGCGCCGACCTA GACTCGGCCGAGCTGCTACAGCCGGTGCTAGAAAACGACGCCGTCTTATTTTCACTAGAAGACGCCGTCGACTTT GAGCGCGAGGAGGAGGAGGAGGAGGAGGAGGAGCGGGAGCCAGAGGGCCAAGAAGCTGGAGATGCGCAGACGCGT AATCGCCAGCTCGAGGCTGAGCTGAAGCGTCTTGGAGCTGCGTTTGCAGACTATCGCGTCTGCGTGCAAAAGACA CTTGATGCGAAATGGGGCGACGACCAGGGCGCAGTCACGGCCAAGAAGCATGAGGCGTCGGATTCGTATTATTTT GAATCATATGCCGCTCACGGTATGCGCACCGCTTTTACCTGGCTGCCAGCTTGGCAGAAACAAAGGAGAAAGAAA AAAAAAACCCTAGAGAAAAAAAAACTAAAAAACTGACACACTCGTGCTAGAGATTCACGAGACGATGCTCAAGGA CCGTGTGCGGACAGATGCCTACCGAGACTTTATTTACGGAAACAAGCACCTCTTCAAGGACAAGGTGGTGCTTGA CATTGGCTGTGGCACAGGTGAGGAGAAGAAGCAACAACAACATCAAGTCTTTTGCTACATGCCTCTCCTGTAGCA CGAGCCAAGCTAAAACTGTCCCCCAGGCATCCTCAGCATGTTTTGCGCAAAGGCTGGCGCGGCAAGCGTAATCGC AGTCGACAAGTCTGACATTATCGACAAGGCGCGAGAAAACATGTTTCACAACGGCCTGTCAAGCACCATTACCTG TCTGCGGGGCGCCATTGAAGACGTGCAGCTGCCCGTGGCAAAGGTGGACGTTATTGTCAGCGAGTGGATGGGCTA CTGCCTTCTCTACGAGGCAATGCTTCCCAGCATCCTCTTTGCCCGCGACAAGTACCTCAAGCCCCATGGCTTGCT TGTGCCCAGCGCCGCGACTCTACTCTTGGCCCCCGTGCACGACGACGACTACGTAGCCGATACCGTCACCTACTG GCGAGACGTCTATGGCTTCGACATGAAGGCCATGCAGCAGGGCATCTACGACGACGTGCGCATCCACGCCATGCC CTCAGACTCGGTCTGCGGCTCAGCCGCCGTCTTCAAAACTCTGCACCTGCATCACGTGCAGCCTCAAGACTTGGT CTTTACAGCAAAGTGGCAGTCAAGCCTCAATAGGCCCGTCGACCAAATCCACGGTTTCCTCATTTGGTTCGACTG CTTCTTCTCCACGTCAAGCGACGATGCACCCCCCGACGCGTCTCAGACGCCAGAGGCGTGGCGTGCCCAAAAGCC GGGCCGTGTCGTCATGACCACCAGCCCACATGCCACCGAGACACACTGGAAGCAGGGTCTCTTGCTTGTAGAGCC GCAGCCCACCCTGTCTCAGACGCCTGCGTCGAGCGACATTGTTGGGCAATTAACAGTGTCAGTCCCCGAGTCCAA TGCGCGGTCCCTTGGCCTTGAGGCCTCGTGGTCCATGGCTGGCTGTGAGAGACGACAAGTGTGGAAACTAAGTTG A |