© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | OphauG2|6284 |
| Gene name | |
| Location | Contig_633:6678..8445 |
| Strand | + |
| Gene length (bp) | 1767 |
| Transcript length (bp) | 1584 |
| Coding sequence length (bp) | 1584 |
| Protein length (aa) | 528 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF13649 | Methyltransf_25 | Methyltransferase domain | 6.7E-12 | 229 | 326 |
| PF08241 | Methyltransf_11 | Methyltransferase domain | 2.0E-10 | 230 | 329 |
| PF06325 | PrmA | Ribosomal protein L11 methyltransferase (PrmA) | 1.3E-10 | 225 | 300 |
| PF13847 | Methyltransf_31 | Methyltransferase domain | 1.2E-08 | 225 | 334 |
| PF13489 | Methyltransf_23 | Methyltransferase domain | 9.2E-07 | 223 | 329 |
| PF05175 | MTS | Methyltransferase small domain | 7.0E-06 | 225 | 298 |
| 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 | 6 | 517 | 1.0E-114 |
| sp|O60678|ANM3_HUMAN | Protein arginine N-methyltransferase 3 OS=Homo sapiens GN=PRMT3 PE=1 SV=3 | 2 | 507 | 8.0E-89 |
| sp|O70467|ANM3_RAT | Protein arginine N-methyltransferase 3 OS=Rattus norvegicus GN=Prmt3 PE=1 SV=1 | 13 | 507 | 7.0E-86 |
| sp|Q9URX7|ANM1_SCHPO | Protein arginine N-methyltransferase 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=rmt1 PE=1 SV=2 | 189 | 515 | 4.0E-83 |
| sp|Q922H1|ANM3_MOUSE | Protein arginine N-methyltransferase 3 OS=Mus musculus GN=Prmt3 PE=1 SV=2 | 13 | 507 | 7.0E-82 |
| 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 | 6 | 517 | 1.0E-114 |
| sp|O60678|ANM3_HUMAN | Protein arginine N-methyltransferase 3 OS=Homo sapiens GN=PRMT3 PE=1 SV=3 | 2 | 507 | 8.0E-89 |
| sp|O70467|ANM3_RAT | Protein arginine N-methyltransferase 3 OS=Rattus norvegicus GN=Prmt3 PE=1 SV=1 | 13 | 507 | 7.0E-86 |
| sp|Q9URX7|ANM1_SCHPO | Protein arginine N-methyltransferase 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=rmt1 PE=1 SV=2 | 189 | 515 | 4.0E-83 |
| sp|Q922H1|ANM3_MOUSE | Protein arginine N-methyltransferase 3 OS=Mus musculus GN=Prmt3 PE=1 SV=2 | 13 | 507 | 7.0E-82 |
| sp|O82210|ANM12_ARATH | Probable protein arginine N-methyltransferase 1.2 OS=Arabidopsis thaliana GN=PRMT12 PE=1 SV=1 | 186 | 526 | 3.0E-77 |
| sp|Q9SU94|ANM11_ARATH | Protein arginine N-methyltransferase 1.1 OS=Arabidopsis thaliana GN=PRMT11 PE=1 SV=1 | 172 | 517 | 2.0E-74 |
| sp|P38074|HMT1_YEAST | Protein arginine N-methyltransferase 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HMT1 PE=1 SV=1 | 177 | 515 | 3.0E-74 |
| sp|Q6VRB0|ANM1B_XENLA | Protein arginine N-methyltransferase 1-B OS=Xenopus laevis GN=prmt1-b PE=2 SV=1 | 185 | 517 | 4.0E-74 |
| sp|Q99873|ANM1_HUMAN | Protein arginine N-methyltransferase 1 OS=Homo sapiens GN=PRMT1 PE=1 SV=2 | 177 | 517 | 5.0E-74 |
| sp|Q28F07|ANM1_XENTR | Protein arginine N-methyltransferase 1 OS=Xenopus tropicalis GN=prmt1 PE=2 SV=1 | 185 | 517 | 6.0E-74 |
| sp|Q54EF2|ANM1_DICDI | Protein arginine N-methyltransferase 1 OS=Dictyostelium discoideum GN=prmt1 PE=3 SV=1 | 175 | 517 | 9.0E-74 |
| sp|Q6PAK3|ANM8_MOUSE | Protein arginine N-methyltransferase 8 OS=Mus musculus GN=Prmt8 PE=1 SV=2 | 185 | 517 | 2.0E-73 |
| sp|Q9NR22|ANM8_HUMAN | Protein arginine N-methyltransferase 8 OS=Homo sapiens GN=PRMT8 PE=1 SV=2 | 185 | 517 | 2.0E-73 |
| sp|Q0J2C6|ANM1_ORYSJ | Probable protein arginine N-methyltransferase 1 OS=Oryza sativa subsp. japonica GN=PRMT1 PE=2 SV=1 | 184 | 517 | 3.0E-73 |
| sp|Q8AV13|ANM1A_XENLA | Protein arginine N-methyltransferase 1-A OS=Xenopus laevis GN=prmt1-a PE=1 SV=1 | 185 | 507 | 3.0E-73 |
| sp|A2Z0C0|ANM1_ORYSI | Probable protein arginine N-methyltransferase 1 OS=Oryza sativa subsp. indica GN=PRMT1 PE=3 SV=1 | 184 | 517 | 3.0E-73 |
| sp|Q63009|ANM1_RAT | Protein arginine N-methyltransferase 1 OS=Rattus norvegicus GN=Prmt1 PE=1 SV=1 | 177 | 517 | 3.0E-73 |
| sp|Q9JIF0|ANM1_MOUSE | Protein arginine N-methyltransferase 1 OS=Mus musculus GN=Prmt1 PE=1 SV=1 | 177 | 517 | 4.0E-73 |
| sp|Q08A71|ANM6_ARATH | Probable protein arginine N-methyltransferase 6 OS=Arabidopsis thaliana GN=PRMT6 PE=2 SV=1 | 187 | 517 | 6.0E-73 |
| sp|Q5RGQ2|ANM8B_DANRE | Protein arginine N-methyltransferase 8-B OS=Danio rerio GN=prmt8b PE=2 SV=2 | 185 | 526 | 8.0E-72 |
| sp|A8IEF3|ANM1_CHLRE | Protein arginine N-methyltransferase 1 OS=Chlamydomonas reinhardtii GN=PRMT1 PE=1 SV=1 | 186 | 517 | 1.0E-71 |
| sp|Q75G68|ANM62_ORYSJ | Probable protein arginine N-methyltransferase 6.2 OS=Oryza sativa subsp. japonica GN=PRMT6.2 PE=2 SV=1 | 187 | 509 | 6.0E-70 |
| sp|A2Z8S0|ANM62_ORYSI | Probable protein arginine N-methyltransferase 6.2 OS=Oryza sativa subsp. indica GN=PRMT6.2 PE=3 SV=2 | 187 | 509 | 6.0E-70 |
| sp|Q7XKC0|ANM61_ORYSJ | Probable protein arginine N-methyltransferase 6.1 OS=Oryza sativa subsp. japonica GN=PRMT6.1 PE=3 SV=2 | 187 | 517 | 1.0E-69 |
| sp|Q0WVD6|ANM3_ARATH | Probable protein arginine N-methyltransferase 3 OS=Arabidopsis thaliana GN=PRMT3 PE=2 SV=1 | 16 | 488 | 2.0E-69 |
| sp|A2XYY8|ANM61_ORYSI | Probable protein arginine N-methyltransferase 6.1 OS=Oryza sativa subsp. indica GN=PRMT6.1 PE=3 SV=1 | 187 | 515 | 3.0E-68 |
| sp|A3BMN9|ANM3_ORYSJ | Probable protein arginine N-methyltransferase 3 OS=Oryza sativa subsp. japonica GN=PRMT3 PE=2 SV=1 | 33 | 506 | 1.0E-67 |
| sp|A2YP56|ANM3_ORYSI | Probable protein arginine N-methyltransferase 3 OS=Oryza sativa subsp. indica GN=PRMT3 PE=3 SV=1 | 33 | 506 | 2.0E-67 |
| sp|Q68EZ3|ANM6_XENLA | Protein arginine N-methyltransferase 6 OS=Xenopus laevis GN=prmt6 PE=2 SV=1 | 181 | 523 | 9.0E-60 |
| sp|B0JYW5|ANM6_XENTR | Protein arginine N-methyltransferase 6 OS=Xenopus tropicalis GN=prmt6 PE=2 SV=1 | 181 | 523 | 6.0E-58 |
| sp|Q6NWG4|ANM6_DANRE | Protein arginine N-methyltransferase 6 OS=Danio rerio GN=prmt6 PE=2 SV=2 | 187 | 527 | 2.0E-57 |
| sp|Q96LA8|ANM6_HUMAN | Protein arginine N-methyltransferase 6 OS=Homo sapiens GN=PRMT6 PE=1 SV=1 | 187 | 507 | 6.0E-56 |
| sp|Q6NZB1|ANM6_MOUSE | Protein arginine N-methyltransferase 6 OS=Mus musculus GN=Prmt6 PE=1 SV=2 | 187 | 507 | 2.0E-54 |
| sp|Q5E9L5|ANM6_BOVIN | Protein arginine N-methyltransferase 6 OS=Bos taurus GN=PRMT6 PE=2 SV=1 | 187 | 507 | 3.0E-54 |
| sp|P55345|ANM2_HUMAN | Protein arginine N-methyltransferase 2 OS=Homo sapiens GN=PRMT2 PE=1 SV=1 | 164 | 515 | 6.0E-50 |
| sp|Q9R144|ANM2_MOUSE | Protein arginine N-methyltransferase 2 OS=Mus musculus GN=Prmt2 PE=1 SV=1 | 130 | 477 | 1.0E-49 |
| sp|Q54HI0|ANM2_DICDI | Protein arginine N-methyltransferase 2 OS=Dictyostelium discoideum GN=prmt2 PE=3 SV=1 | 187 | 430 | 3.0E-49 |
| sp|B3DLB3|ANM2_XENTR | Protein arginine N-methyltransferase 2 OS=Xenopus tropicalis GN=prmt2 PE=2 SV=1 | 187 | 517 | 9.0E-45 |
| sp|Q9SNQ2|ANM10_ORYSJ | Protein arginine N-methyltransferase PRMT10 OS=Oryza sativa subsp. japonica GN=PRMT10 PE=2 SV=1 | 190 | 515 | 1.0E-40 |
| sp|A2Y953|ANM10_ORYSI | Protein arginine N-methyltransferase PRMT10 OS=Oryza sativa subsp. indica GN=PRMT10 PE=3 SV=1 | 190 | 515 | 1.0E-40 |
| sp|Q9MAT5|ANM10_ARATH | Protein arginine N-methyltransferase PRMT10 OS=Arabidopsis thaliana GN=PRMT10 PE=1 SV=1 | 190 | 485 | 4.0E-40 |
| sp|D9IVE5|ANM2_XENLA | Protein arginine N-methyltransferase 2 OS=Xenopus laevis GN=prmt2 PE=1 SV=2 | 187 | 516 | 5.0E-40 |
| sp|A3KPF2|ANM14_ARATH | Probable histone-arginine methyltransferase 1.4 OS=Arabidopsis thaliana GN=PRMT14 PE=1 SV=1 | 181 | 517 | 2.0E-37 |
| sp|Q84W92|ANM13_ARATH | Probable histone-arginine methyltransferase 1.3 OS=Arabidopsis thaliana GN=PRMT13 PE=2 SV=3 | 181 | 517 | 4.0E-37 |
| sp|Q7XI75|CARM1_ORYSJ | Probable histone-arginine methyltransferase CARM1 OS=Oryza sativa subsp. japonica GN=CARM1 PE=2 SV=1 | 182 | 517 | 2.0E-36 |
| sp|A2YPT7|CARM1_ORYSI | Probable histone-arginine methyltransferase CARM1 OS=Oryza sativa subsp. indica GN=CARM1 PE=3 SV=2 | 182 | 517 | 2.0E-36 |
| sp|B4GZ20|CARM1_DROPE | Histone-arginine methyltransferase CARMER OS=Drosophila persimilis GN=Art4 PE=3 SV=1 | 179 | 471 | 1.0E-35 |
| sp|Q29B63|CARM1_DROPS | Histone-arginine methyltransferase CARMER OS=Drosophila pseudoobscura pseudoobscura GN=Art4 PE=3 SV=1 | 179 | 471 | 1.0E-35 |
| sp|B4JXV2|CARM1_DROGR | Histone-arginine methyltransferase CARMER OS=Drosophila grimshawi GN=Art4 PE=3 SV=1 | 179 | 471 | 2.0E-35 |
| sp|B4PVH6|CARM1_DROYA | Histone-arginine methyltransferase CARMER OS=Drosophila yakuba GN=Art4 PE=3 SV=1 | 179 | 471 | 5.0E-35 |
| sp|B4NKI9|CARM1_DROWI | Histone-arginine methyltransferase CARMER OS=Drosophila willistoni GN=Art4 PE=3 SV=1 | 179 | 471 | 7.0E-35 |
| sp|Q6DC04|CARM1_DANRE | Histone-arginine methyltransferase CARM1 OS=Danio rerio GN=carm1 PE=2 SV=1 | 181 | 478 | 7.0E-35 |
| sp|B3P4N5|CARM1_DROER | Histone-arginine methyltransferase CARMER OS=Drosophila erecta GN=Art4 PE=3 SV=1 | 179 | 471 | 8.0E-35 |
| sp|B4HJC0|CARM1_DROSE | Histone-arginine methyltransferase CARMER OS=Drosophila sechellia GN=Art4 PE=3 SV=1 | 179 | 471 | 8.0E-35 |
| sp|Q9VH48|CARM1_DROME | Probable histone-arginine methyltransferase CARMER OS=Drosophila melanogaster GN=Art4 PE=1 SV=1 | 179 | 471 | 8.0E-35 |
| sp|B4QVW6|CARM1_DROSI | Histone-arginine methyltransferase CARMER OS=Drosophila simulans GN=Art4 PE=3 SV=1 | 179 | 471 | 8.0E-35 |
| sp|B4KA23|CARM1_DROMO | Histone-arginine methyltransferase CARMER OS=Drosophila mojavensis GN=Art4 PE=3 SV=1 | 179 | 471 | 9.0E-35 |
| sp|Q9WVG6|CARM1_MOUSE | Histone-arginine methyltransferase CARM1 OS=Mus musculus GN=Carm1 PE=1 SV=2 | 160 | 471 | 1.0E-34 |
| sp|B3M1E1|CARM1_DROAN | Histone-arginine methyltransferase CARMER OS=Drosophila ananassae GN=Art4 PE=3 SV=1 | 179 | 471 | 1.0E-34 |
| sp|Q86X55|CARM1_HUMAN | Histone-arginine methyltransferase CARM1 OS=Homo sapiens GN=CARM1 PE=1 SV=3 | 160 | 471 | 1.0E-34 |
| sp|B4LVS8|CARM1_DROVI | Histone-arginine methyltransferase CARMER OS=Drosophila virilis GN=Art4 PE=3 SV=1 | 179 | 471 | 1.0E-34 |
| sp|Q4AE70|CARM1_RAT | Histone-arginine methyltransferase CARM1 OS=Rattus norvegicus GN=Carm1 PE=1 SV=1 | 160 | 471 | 2.0E-34 |
| sp|Q5XK84|CARM1_XENLA | Histone-arginine methyltransferase CARM1 OS=Xenopus laevis GN=carm1 PE=2 SV=1 | 174 | 485 | 3.0E-34 |
| sp|B0W3L6|CARM1_CULQU | Histone-arginine methyltransferase CARMER OS=Culex quinquefasciatus GN=Art4 PE=3 SV=1 | 150 | 505 | 6.0E-34 |
| sp|Q174R2|CARM1_AEDAE | Histone-arginine methyltransferase CARMER OS=Aedes aegypti GN=CARM1 PE=3 SV=1 | 181 | 505 | 3.0E-33 |
| sp|Q7Q2B7|CARM1_ANOGA | Histone-arginine methyltransferase CARMER OS=Anopheles gambiae GN=CARM1 PE=1 SV=5 | 181 | 505 | 4.0E-33 |
| sp|Q582G4|ANM7_TRYB2 | Protein arginine N-methyltransferase 7 OS=Trypanosoma brucei brucei (strain 927/4 GUTat10.1) GN=PRMT7 PE=1 SV=1 | 195 | 364 | 1.0E-16 |
| 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 | 220 | 332 | 7.0E-09 |
| sp|A0JMU5|ANM9_XENLA | Putative protein arginine N-methyltransferase 9 OS=Xenopus laevis GN=prmt9 PE=2 SV=1 | 184 | 335 | 2.0E-08 |
| sp|C3L3G5|PRMA_CLOB6 | Ribosomal protein L11 methyltransferase OS=Clostridium botulinum (strain 657 / Type Ba4) GN=prmA PE=3 SV=1 | 221 | 350 | 3.0E-08 |
| sp|Q9XW42|ANM7_CAEEL | Protein arginine N-methyltransferase 7 OS=Caenorhabditis elegans GN=prmt-7 PE=1 SV=2 | 164 | 340 | 5.0E-08 |
| sp|B4JWL5|ANM7_DROGR | Protein arginine N-methyltransferase 7 OS=Drosophila grimshawi GN=Art7 PE=3 SV=1 | 183 | 334 | 2.0E-07 |
| sp|Q5U4E8|ANM7_RAT | Protein arginine N-methyltransferase 7 OS=Rattus norvegicus GN=Prmt7 PE=2 SV=1 | 184 | 402 | 3.0E-07 |
| sp|Q665E3|PRMA_YERPS | Ribosomal protein L11 methyltransferase OS=Yersinia pseudotuberculosis serotype I (strain IP32953) GN=prmA PE=3 SV=2 | 224 | 350 | 5.0E-07 |
| sp|B2K467|PRMA_YERPB | Ribosomal protein L11 methyltransferase OS=Yersinia pseudotuberculosis serotype IB (strain PB1/+) GN=prmA PE=3 SV=1 | 224 | 350 | 5.0E-07 |
| sp|A6TSL8|PRMA_ALKMQ | Ribosomal protein L11 methyltransferase OS=Alkaliphilus metalliredigens (strain QYMF) GN=prmA PE=3 SV=1 | 229 | 335 | 6.0E-07 |
| sp|B4GA28|ANM7_DROPE | Protein arginine N-methyltransferase 7 OS=Drosophila persimilis GN=Art7 PE=3 SV=1 | 183 | 333 | 6.0E-07 |
| sp|B5DZN7|ANM7_DROPS | Protein arginine N-methyltransferase 7 OS=Drosophila pseudoobscura pseudoobscura GN=Art7 PE=3 SV=1 | 183 | 333 | 6.0E-07 |
| sp|B3MF31|ANM7_DROAN | Protein arginine N-methyltransferase 7 OS=Drosophila ananassae GN=Art7 PE=3 SV=1 | 183 | 333 | 7.0E-07 |
| sp|Q0AWM5|PRMA_SYNWW | Ribosomal protein L11 methyltransferase OS=Syntrophomonas wolfei subsp. wolfei (strain DSM 2245B / Goettingen) GN=prmA PE=3 SV=1 | 229 | 287 | 9.0E-07 |
| sp|B1KZN5|PRMA_CLOBM | Ribosomal protein L11 methyltransferase OS=Clostridium botulinum (strain Loch Maree / Type A3) GN=prmA PE=3 SV=1 | 221 | 350 | 1.0E-06 |
| sp|B1JKF2|PRMA_YERPY | Ribosomal protein L11 methyltransferase OS=Yersinia pseudotuberculosis serotype O:3 (strain YPIII) GN=prmA PE=3 SV=1 | 224 | 350 | 2.0E-06 |
| sp|A2AV36|ANM7_DANRE | Protein arginine N-methyltransferase 7 OS=Danio rerio GN=prmt7 PE=2 SV=1 | 184 | 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 | 229 | 332 | 2.0E-06 |
| sp|A7FXL3|PRMA_CLOB1 | Ribosomal protein L11 methyltransferase OS=Clostridium botulinum (strain ATCC 19397 / Type A) GN=prmA PE=3 SV=1 | 221 | 350 | 2.0E-06 |
| sp|A5I638|PRMA_CLOBH | Ribosomal protein L11 methyltransferase OS=Clostridium botulinum (strain Hall / ATCC 3502 / NCTC 13319 / Type A) GN=prmA PE=3 SV=1 | 221 | 350 | 2.0E-06 |
| sp|C1FVT8|PRMA_CLOBJ | Ribosomal protein L11 methyltransferase OS=Clostridium botulinum (strain Kyoto / Type A2) GN=prmA PE=3 SV=1 | 221 | 350 | 2.0E-06 |
| sp|A6LRN8|PRMA_CLOB8 | Ribosomal protein L11 methyltransferase OS=Clostridium beijerinckii (strain ATCC 51743 / NCIMB 8052) GN=prmA PE=3 SV=1 | 220 | 366 | 2.0E-06 |
| sp|A7FDQ3|PRMA_YERP3 | Ribosomal protein L11 methyltransferase OS=Yersinia pseudotuberculosis serotype O:1b (strain IP 31758) GN=prmA PE=3 SV=1 | 224 | 350 | 2.0E-06 |
| sp|Q8ZAX6|PRMA_YERPE | Ribosomal protein L11 methyltransferase OS=Yersinia pestis GN=prmA PE=3 SV=1 | 224 | 350 | 2.0E-06 |
| sp|Q6P2P2|ANM9_HUMAN | Putative protein arginine N-methyltransferase 9 OS=Homo sapiens GN=PRMT9 PE=2 SV=1 | 184 | 322 | 2.0E-06 |
| sp|B1ILM1|PRMA_CLOBK | Ribosomal protein L11 methyltransferase OS=Clostridium botulinum (strain Okra / Type B1) GN=prmA PE=3 SV=1 | 221 | 350 | 2.0E-06 |
| sp|A7GHH4|PRMA_CLOBL | Ribosomal protein L11 methyltransferase OS=Clostridium botulinum (strain Langeland / NCTC 10281 / Type F) GN=prmA PE=3 SV=1 | 221 | 350 | 2.0E-06 |
| sp|A9B5V4|PRMA_HERA2 | Ribosomal protein L11 methyltransferase OS=Herpetosiphon aurantiacus (strain ATCC 23779 / DSM 785) GN=prmA PE=3 SV=1 | 224 | 303 | 3.0E-06 |
| sp|B4KSL6|ANM7_DROMO | Protein arginine N-methyltransferase 7 OS=Drosophila mojavensis GN=Art7 PE=3 SV=1 | 184 | 334 | 4.0E-06 |
| sp|Q6PCI6|ANM7_XENLA | Protein arginine N-methyltransferase 7 OS=Xenopus laevis GN=prmt7 PE=2 SV=1 | 184 | 335 | 6.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0008168 | methyltransferase activity | Yes |
| GO:0003674 | molecular_function | No |
| GO:0016740 | transferase activity | No |
| GO:0016741 | transferase activity, transferring one-carbon groups | No |
| GO:0003824 | catalytic activity | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 39 | 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 | >OphauG2|6284 MAIDSSDTDPSCSSDSDQSEWLDMEPDDEPTTFISLLDSRAFTTLDSMLAYCKQRHGFDLVGEIERLRLDYIGGI KLVNFIRRRVKQGEALPREIAQTDLDSTELLQPVLENDTVLFSLEDAVDFERHAENDPEDGGAQTRNRQLEAELE RLETAFADYRVCVQKTLDRKWGDEQDADAAKKHEASDSYYFESYAAHEIHETMLKDRVRTDAYRDFIYGNKHLFK DKVVLDIGCGTGILSMFCAKAGASRVIAVDKSDIIDKARENIFNNGLSSTITCLRGAIEDVQLPVAKVDIIVSEW MGYCLLYEAMLPSVLFARDKYLKPDGLLVPSAATLVLAPVHDDDYVVDTVTYWRDVYGFDMKAMQQGIYDDARIH AMSSDSVCGSAAVFKTLNLHHVQPQDLVFTAKWESSLDRPVDQIHGFLIWFDCFFSTSRDDATPDASQTPVAWRA QKPGRVVMTTSPYATETHWKQGLLLVEAQPTVSQAPASSRIVGQITLSVPASNARSLGLEASWSMAGCDRRHKWK LS* |
| Coding | >OphauG2|6284 ATGGCCATTGACAGCAGCGACACAGACCCGTCTTGTAGCTCCGACTCGGACCAGAGCGAGTGGCTAGACATGGAG CCAGATGACGAACCAACGACATTTATATCGCTGCTCGACTCGCGGGCCTTTACTACGCTTGACTCGATGCTGGCA TATTGCAAGCAGCGCCACGGCTTCGACTTGGTAGGCGAGATTGAGCGCCTGCGCCTCGACTACATTGGCGGCATC AAGCTAGTCAACTTTATTCGCAGGCGCGTCAAGCAAGGCGAGGCGCTTCCAAGGGAGATTGCACAGACGGACCTC GACTCGACGGAGCTGCTGCAGCCGGTGCTGGAAAACGACACCGTCTTGTTTTCGCTAGAAGACGCCGTCGACTTT GAGCGCCACGCAGAGAATGACCCAGAGGATGGGGGTGCGCAGACGCGTAATCGCCAGCTCGAGGCTGAGCTGGAG CGTCTCGAGACTGCGTTTGCAGACTATCGCGTCTGCGTGCAAAAGACGCTTGATAGGAAATGGGGCGACGAGCAA GACGCAGACGCGGCCAAGAAGCACGAGGCGTCGGATTCATATTACTTTGAATCATATGCCGCTCATGAGATTCAC GAGACGATGCTCAAGGACCGTGTGCGGACAGATGCCTACCGAGACTTTATTTACGGAAACAAGCACCTCTTCAAA GACAAGGTAGTCCTTGATATTGGCTGTGGCACAGGCATTCTCAGCATGTTTTGCGCAAAGGCTGGCGCGTCAAGA GTAATTGCAGTCGACAAGTCTGACATTATCGACAAGGCGCGAGAAAACATCTTCAACAACGGCCTGTCAAGCACC ATTACCTGTCTCCGGGGTGCCATTGAAGACGTCCAGCTGCCCGTGGCCAAGGTTGATATCATTGTCAGCGAGTGG ATGGGTTACTGCCTTCTCTACGAGGCAATGCTTCCCAGTGTCCTTTTTGCCCGCGACAAGTATCTCAAGCCCGAC GGCTTGCTTGTGCCCAGTGCCGCGACGCTTGTCTTGGCCCCCGTCCACGACGACGACTACGTAGTTGACACCGTC ACCTACTGGCGAGACGTCTATGGCTTCGACATGAAGGCCATGCAGCAGGGCATCTACGACGATGCGCGCATCCAC GCTATGTCCTCTGACTCAGTTTGCGGCTCAGCCGCCGTCTTCAAAACTCTCAACCTGCATCACGTGCAGCCTCAA GACTTGGTCTTTACAGCAAAGTGGGAATCGAGCCTCGATAGGCCCGTCGACCAAATCCACGGTTTCCTCATTTGG TTCGACTGCTTCTTCTCCACGTCACGCGATGATGCAACACCCGACGCGTCTCAGACGCCAGTGGCATGGCGTGCG CAAAAACCGGGCCGTGTGGTCATGACGACGAGCCCATATGCCACCGAGACACACTGGAAGCAGGGCCTCTTGCTT GTAGAGGCACAGCCCACAGTGTCTCAGGCGCCCGCGTCGAGCCGCATCGTTGGGCAAATCACACTGTCAGTCCCC GCGTCCAATGCGCGGTCCCTTGGCCTTGAGGCCTCGTGGTCCATGGCGGGCTGTGACAGACGCCATAAGTGGAAG CTTAGTTGA |
| Transcript | >OphauG2|6284 ATGGCCATTGACAGCAGCGACACAGACCCGTCTTGTAGCTCCGACTCGGACCAGAGCGAGTGGCTAGACATGGAG CCAGATGACGAACCAACGACATTTATATCGCTGCTCGACTCGCGGGCCTTTACTACGCTTGACTCGATGCTGGCA TATTGCAAGCAGCGCCACGGCTTCGACTTGGTAGGCGAGATTGAGCGCCTGCGCCTCGACTACATTGGCGGCATC AAGCTAGTCAACTTTATTCGCAGGCGCGTCAAGCAAGGCGAGGCGCTTCCAAGGGAGATTGCACAGACGGACCTC GACTCGACGGAGCTGCTGCAGCCGGTGCTGGAAAACGACACCGTCTTGTTTTCGCTAGAAGACGCCGTCGACTTT GAGCGCCACGCAGAGAATGACCCAGAGGATGGGGGTGCGCAGACGCGTAATCGCCAGCTCGAGGCTGAGCTGGAG CGTCTCGAGACTGCGTTTGCAGACTATCGCGTCTGCGTGCAAAAGACGCTTGATAGGAAATGGGGCGACGAGCAA GACGCAGACGCGGCCAAGAAGCACGAGGCGTCGGATTCATATTACTTTGAATCATATGCCGCTCATGAGATTCAC GAGACGATGCTCAAGGACCGTGTGCGGACAGATGCCTACCGAGACTTTATTTACGGAAACAAGCACCTCTTCAAA GACAAGGTAGTCCTTGATATTGGCTGTGGCACAGGCATTCTCAGCATGTTTTGCGCAAAGGCTGGCGCGTCAAGA GTAATTGCAGTCGACAAGTCTGACATTATCGACAAGGCGCGAGAAAACATCTTCAACAACGGCCTGTCAAGCACC ATTACCTGTCTCCGGGGTGCCATTGAAGACGTCCAGCTGCCCGTGGCCAAGGTTGATATCATTGTCAGCGAGTGG ATGGGTTACTGCCTTCTCTACGAGGCAATGCTTCCCAGTGTCCTTTTTGCCCGCGACAAGTATCTCAAGCCCGAC GGCTTGCTTGTGCCCAGTGCCGCGACGCTTGTCTTGGCCCCCGTCCACGACGACGACTACGTAGTTGACACCGTC ACCTACTGGCGAGACGTCTATGGCTTCGACATGAAGGCCATGCAGCAGGGCATCTACGACGATGCGCGCATCCAC GCTATGTCCTCTGACTCAGTTTGCGGCTCAGCCGCCGTCTTCAAAACTCTCAACCTGCATCACGTGCAGCCTCAA GACTTGGTCTTTACAGCAAAGTGGGAATCGAGCCTCGATAGGCCCGTCGACCAAATCCACGGTTTCCTCATTTGG TTCGACTGCTTCTTCTCCACGTCACGCGATGATGCAACACCCGACGCGTCTCAGACGCCAGTGGCATGGCGTGCG CAAAAACCGGGCCGTGTGGTCATGACGACGAGCCCATATGCCACCGAGACACACTGGAAGCAGGGCCTCTTGCTT GTAGAGGCACAGCCCACAGTGTCTCAGGCGCCCGCGTCGAGCCGCATCGTTGGGCAAATCACACTGTCAGTCCCC GCGTCCAATGCGCGGTCCCTTGGCCTTGAGGCCTCGTGGTCCATGGCGGGCTGTGACAGACGCCATAAGTGGAAG CTTAGTTGA |
| Gene | >OphauG2|6284 ATGGCCATTGACAGCAGCGACACAGACCCGTCTTGTAGCTCCGACTCGGACCAGAGCGAGTGGCTAGACATGGAG CCAGATGACGAACCAACGACATTTATATCGCTGCTCGACTCGCGGGCCTTTACTACGCTTGACTCGATGCTGGCA TATTGCAAGCAGCGCCACGGCTTCGACTTGGTAGGCGAGATTGAGCGCCTGCGCCTCGACTACATTGGCGGCATC AAGCTAGTCAACTTTATTCGCAGGCGCGTCAAGCAAGGCGAGGCGCTTCCAAGGGAGATTGCACAGACGGACCTC GACTCGACGGAGCTGCTGCAGCCGGTGCTGGAAAACGACACCGTCTTGTTTTCGCTAGAAGACGCCGTCGACTTT GAGCGCCACGCAGAGAATGACCCAGAGGATGGGGGTGCGCAGACGCGTAATCGCCAGCTCGAGGCTGAGCTGGAG CGTCTCGAGACTGCGTTTGCAGACTATCGCGTCTGCGTGCAAAAGACGCTTGATAGGAAATGGGGCGACGAGCAA GACGCAGACGCGGCCAAGAAGCACGAGGCGTCGGATTCATATTACTTTGAATCATATGCCGCTCATGGTATGCTG CGCCGCTTTGCATTACATGGCTGCCCGACTCGCGGAAAGAAGAGAAAAAAAAATAATGCTAGACAACTGACACGG GCGTGCTAGAGATTCACGAGACGATGCTCAAGGACCGTGTGCGGACAGATGCCTACCGAGACTTTATTTACGGAA ACAAGCACCTCTTCAAAGACAAGGTAGTCCTTGATATTGGCTGTGGCACAGGTGAGAGGAACAAGAGGAACAAGA AACATCAAGCCCCTTTCTCCATCTGTCTCCTGCTACACAAGCCAAGCTAAGACTGTGCCACCAACAGGCATTCTC AGCATGTTTTGCGCAAAGGCTGGCGCGTCAAGAGTAATTGCAGTCGACAAGTCTGACATTATCGACAAGGCGCGA GAAAACATCTTCAACAACGGCCTGTCAAGCACCATTACCTGTCTCCGGGGTGCCATTGAAGACGTCCAGCTGCCC GTGGCCAAGGTTGATATCATTGTCAGCGAGTGGATGGGTTACTGCCTTCTCTACGAGGCAATGCTTCCCAGTGTC CTTTTTGCCCGCGACAAGTATCTCAAGCCCGACGGCTTGCTTGTGCCCAGTGCCGCGACGCTTGTCTTGGCCCCC GTCCACGACGACGACTACGTAGTTGACACCGTCACCTACTGGCGAGACGTCTATGGCTTCGACATGAAGGCCATG CAGCAGGGCATCTACGACGATGCGCGCATCCACGCTATGTCCTCTGACTCAGTTTGCGGCTCAGCCGCCGTCTTC AAAACTCTCAACCTGCATCACGTGCAGCCTCAAGACTTGGTCTTTACAGCAAAGTGGGAATCGAGCCTCGATAGG CCCGTCGACCAAATCCACGGTTTCCTCATTTGGTTCGACTGCTTCTTCTCCACGTCACGCGATGATGCAACACCC GACGCGTCTCAGACGCCAGTGGCATGGCGTGCGCAAAAACCGGGCCGTGTGGTCATGACGACGAGCCCATATGCC ACCGAGACACACTGGAAGCAGGGCCTCTTGCTTGTAGAGGCACAGCCCACAGTGTCTCAGGCGCCCGCGTCGAGC CGCATCGTTGGGCAAATCACACTGTCAGTCCCCGCGTCCAATGCGCGGTCCCTTGGCCTTGAGGCCTCGTGGTCC ATGGCGGGCTGTGACAGACGCCATAAGTGGAAGCTTAGTTGA |