Protein ID | OphauG2|3817 |
Gene name | |
Location | Contig_3:47809..50697 |
Strand | - |
Gene length (bp) | 2888 |
Transcript length (bp) | 2721 |
Coding sequence length (bp) | 2721 |
Protein length (aa) | 907 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF08236 | SRI | SRI (Set2 Rpb1 interacting) domain | 1.3E-21 | 652 | 734 |
PF00856 | SET | SET domain | 8.6E-17 | 182 | 288 |
PF17907 | AWS | AWS domain | 3.4E-10 | 129 | 168 |
PF08711 | Med26 | TFIIS helical bundle-like domain | 1.0E-06 | 433 | 481 |
PF00397 | WW | WW domain | 2.4E-06 | 561 | 589 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q4IB50|SET2_GIBZE | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN=SET2 PE=3 SV=2 | 11 | 896 | 0.0E+00 |
sp|Q7RZU4|SET2_NEUCR | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=set-2 PE=3 SV=1 | 4 | 884 | 0.0E+00 |
sp|Q2H988|SET2_CHAGB | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) GN=SET2 PE=3 SV=1 | 52 | 886 | 0.0E+00 |
sp|Q1DU03|SET2_COCIM | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Coccidioides immitis (strain RS) GN=SET2 PE=3 SV=2 | 31 | 814 | 0.0E+00 |
sp|Q4WTT2|SET2_ASPFU | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=set2 PE=3 SV=1 | 5 | 819 | 0.0E+00 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q4IB50|SET2_GIBZE | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN=SET2 PE=3 SV=2 | 11 | 896 | 0.0E+00 |
sp|Q7RZU4|SET2_NEUCR | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=set-2 PE=3 SV=1 | 4 | 884 | 0.0E+00 |
sp|Q2H988|SET2_CHAGB | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) GN=SET2 PE=3 SV=1 | 52 | 886 | 0.0E+00 |
sp|Q1DU03|SET2_COCIM | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Coccidioides immitis (strain RS) GN=SET2 PE=3 SV=2 | 31 | 814 | 0.0E+00 |
sp|Q4WTT2|SET2_ASPFU | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=set2 PE=3 SV=1 | 5 | 819 | 0.0E+00 |
sp|Q2UTN6|SET2_ASPOR | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=set2 PE=3 SV=1 | 62 | 819 | 0.0E+00 |
sp|Q5ASA5|SET2_EMENI | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=set2 PE=3 SV=1 | 62 | 810 | 0.0E+00 |
sp|O14026|SET2_SCHPO | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=set2 PE=1 SV=1 | 80 | 498 | 1.0E-148 |
sp|Q6C5G5|SET2_YARLI | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=set-2 PE=3 SV=1 | 82 | 759 | 4.0E-133 |
sp|Q6CXP5|SET2_KLULA | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=SET2 PE=3 SV=1 | 78 | 730 | 5.0E-133 |
sp|Q6FX50|SET2_CANGA | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=SET2 PE=3 SV=1 | 90 | 739 | 4.0E-124 |
sp|P46995|SET2_YEAST | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SET2 PE=1 SV=2 | 77 | 727 | 1.0E-116 |
sp|Q59XV0|SET2_CANAL | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=SET2 PE=3 SV=1 | 80 | 589 | 3.0E-116 |
sp|Q757Y8|SET2_ASHGO | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=SET2 PE=3 SV=2 | 90 | 736 | 2.0E-112 |
sp|P0CO28|SET2_CRYNJ | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) GN=SET2 PE=3 SV=1 | 27 | 524 | 2.0E-111 |
sp|P0CO29|SET2_CRYNB | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) GN=SET2 PE=3 SV=1 | 46 | 524 | 2.0E-111 |
sp|Q4PBL3|SET2_USTMA | Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Ustilago maydis (strain 521 / FGSC 9021) GN=SET2 PE=3 SV=1 | 79 | 505 | 4.0E-100 |
sp|E9Q5F9|SETD2_MOUSE | Histone-lysine N-methyltransferase SETD2 OS=Mus musculus GN=Setd2 PE=1 SV=1 | 78 | 458 | 4.0E-57 |
sp|Q9BYW2|SETD2_HUMAN | Histone-lysine N-methyltransferase SETD2 OS=Homo sapiens GN=SETD2 PE=1 SV=3 | 78 | 458 | 7.0E-56 |
sp|Q9VYD1|C1716_DROME | Probable histone-lysine N-methyltransferase CG1716 OS=Drosophila melanogaster GN=Set2 PE=1 SV=2 | 97 | 322 | 4.0E-50 |
sp|Q2LAE1|ASHH2_ARATH | Histone-lysine N-methyltransferase ASHH2 OS=Arabidopsis thaliana GN=ASHH2 PE=1 SV=1 | 113 | 312 | 6.0E-48 |
sp|Q96L73|NSD1_HUMAN | Histone-lysine N-methyltransferase, H3 lysine-36 and H4 lysine-20 specific OS=Homo sapiens GN=NSD1 PE=1 SV=1 | 134 | 311 | 5.0E-46 |
sp|O88491|NSD1_MOUSE | Histone-lysine N-methyltransferase, H3 lysine-36 and H4 lysine-20 specific OS=Mus musculus GN=Nsd1 PE=1 SV=1 | 134 | 311 | 4.0E-45 |
sp|Q84WW6|ASHH1_ARATH | Histone-lysine N-methyltransferase ASHH1 OS=Arabidopsis thaliana GN=ASHH1 PE=1 SV=1 | 77 | 315 | 6.0E-43 |
sp|Q8BVE8|NSD2_MOUSE | Histone-lysine N-methyltransferase NSD2 OS=Mus musculus GN=Whsc1 PE=1 SV=2 | 134 | 316 | 1.0E-42 |
sp|Q6P2L6|NSD3_MOUSE | Histone-lysine N-methyltransferase NSD3 OS=Mus musculus GN=Whsc1l1 PE=1 SV=2 | 120 | 311 | 2.0E-42 |
sp|Q9BZ95|NSD3_HUMAN | Histone-lysine N-methyltransferase NSD3 OS=Homo sapiens GN=WHSC1L1 PE=1 SV=1 | 134 | 311 | 2.0E-42 |
sp|O96028|NSD2_HUMAN | Histone-lysine N-methyltransferase NSD2 OS=Homo sapiens GN=WHSC1 PE=1 SV=1 | 134 | 316 | 7.0E-42 |
sp|Q99MY8|ASH1L_MOUSE | Histone-lysine N-methyltransferase ASH1L OS=Mus musculus GN=Ash1l PE=1 SV=3 | 116 | 324 | 8.0E-41 |
sp|Q9NR48|ASH1L_HUMAN | Histone-lysine N-methyltransferase ASH1L OS=Homo sapiens GN=ASH1L PE=1 SV=2 | 116 | 315 | 2.0E-39 |
sp|Q8MT36|MES4_DROME | Probable histone-lysine N-methyltransferase Mes-4 OS=Drosophila melanogaster GN=Mes-4 PE=1 SV=2 | 134 | 315 | 3.0E-37 |
sp|Q9VW15|ASH1_DROME | Histone-lysine N-methyltransferase ash1 OS=Drosophila melanogaster GN=ash1 PE=1 SV=3 | 116 | 329 | 2.0E-35 |
sp|Q949T8|ASHR3_ARATH | Histone-lysine N-methyltransferase ASHR3 OS=Arabidopsis thaliana GN=ASHR3 PE=1 SV=1 | 134 | 348 | 1.0E-34 |
sp|Q9M1X9|ASHH4_ARATH | Putative histone-lysine N-methyltransferase ASHH4 OS=Arabidopsis thaliana GN=ASHH4 PE=3 SV=1 | 162 | 327 | 2.0E-31 |
sp|Q945S8|ASHH3_ARATH | Histone-lysine N-methyltransferase ASHH3 OS=Arabidopsis thaliana GN=ASHH3 PE=2 SV=2 | 162 | 306 | 5.0E-30 |
sp|Q8IE95|SETVS_PLAF7 | Variant-silencing SET domain-containing protein OS=Plasmodium falciparum (isolate 3D7) GN=SETVS PE=2 SV=1 | 97 | 327 | 9.0E-26 |
sp|Q75D88|SET1_ASHGO | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=SET1 PE=3 SV=2 | 105 | 310 | 5.0E-23 |
sp|P38827|SET1_YEAST | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SET1 PE=1 SV=1 | 130 | 311 | 8.0E-23 |
sp|Q8IRW8|TRR_DROME | Histone-lysine N-methyltransferase trr OS=Drosophila melanogaster GN=trr PE=1 SV=2 | 167 | 306 | 3.0E-21 |
sp|Q6FKB1|SET1_CANGA | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=SET1 PE=3 SV=1 | 162 | 311 | 8.0E-21 |
sp|Q9Y7R4|SET1_SCHPO | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=set1 PE=1 SV=1 | 183 | 310 | 1.0E-20 |
sp|F4K1J4|ATXR7_ARATH | Histone-lysine N-methyltransferase ATXR7 OS=Arabidopsis thaliana GN=ATXR7 PE=2 SV=1 | 177 | 309 | 2.0E-20 |
sp|Q2UMH3|SET1_ASPOR | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=set1 PE=3 SV=1 | 162 | 310 | 3.0E-20 |
sp|Q4WNH8|SET1_ASPFU | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=set1 PE=3 SV=1 | 157 | 310 | 4.0E-20 |
sp|Q28CQ7|SUV92_XENTR | Histone-lysine N-methyltransferase SUV39H2 OS=Xenopus tropicalis GN=suv39h2 PE=2 SV=2 | 148 | 310 | 5.0E-20 |
sp|Q5B0Y5|SET1_EMENI | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=set1 PE=3 SV=1 | 157 | 310 | 7.0E-20 |
sp|Q1DR06|SET1_COCIM | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Coccidioides immitis (strain RS) GN=SET1 PE=3 SV=1 | 162 | 310 | 1.0E-19 |
sp|Q4PB36|SET1_USTMA | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Ustilago maydis (strain 521 / FGSC 9021) GN=SET1 PE=3 SV=1 | 190 | 310 | 2.0E-19 |
sp|Q6CEK8|SET1_YARLI | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=SET1 PE=3 SV=1 | 167 | 310 | 2.0E-19 |
sp|Q9H5I1|SUV92_HUMAN | Histone-lysine N-methyltransferase SUV39H2 OS=Homo sapiens GN=SUV39H2 PE=1 SV=2 | 148 | 310 | 3.0E-19 |
sp|Q8X0S9|SET1_NEUCR | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=set-1 PE=3 SV=1 | 142 | 310 | 3.0E-19 |
sp|Q4R3E0|SUV92_MACFA | Histone-lysine N-methyltransferase SUV39H2 OS=Macaca fascicularis GN=SUV39H2 PE=2 SV=2 | 148 | 310 | 3.0E-19 |
sp|Q4I5R3|SET1_GIBZE | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN=SET1 PE=3 SV=2 | 162 | 310 | 4.0E-19 |
sp|Q6BKL7|SET1_DEBHA | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=SET1 PE=3 SV=2 | 173 | 311 | 4.0E-19 |
sp|Q24742|TRX_DROVI | Histone-lysine N-methyltransferase trithorax OS=Drosophila virilis GN=trx PE=3 SV=1 | 173 | 310 | 7.0E-19 |
sp|Q9EQQ0|SUV92_MOUSE | Histone-lysine N-methyltransferase SUV39H2 OS=Mus musculus GN=Suv39h2 PE=1 SV=1 | 147 | 310 | 7.0E-19 |
sp|Q6CIT4|SET1_KLULA | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=SET1 PE=3 SV=1 | 162 | 310 | 8.0E-19 |
sp|Q32PH7|SUV92_BOVIN | Histone-lysine N-methyltransferase SUV39H2 OS=Bos taurus GN=SUV39H2 PE=2 SV=1 | 148 | 310 | 1.0E-18 |
sp|Q18221|SET2_CAEEL | Probable histone-lysine N-methyltransferase set-2 OS=Caenorhabditis elegans GN=set-2 PE=2 SV=2 | 182 | 311 | 2.0E-18 |
sp|P55200|KMT2A_MOUSE | Histone-lysine N-methyltransferase 2A OS=Mus musculus GN=Kmt2a PE=1 SV=3 | 172 | 310 | 2.0E-18 |
sp|Q98SM3|EZH2A_XENLA | Histone-lysine N-methyltransferase EZH2 OS=Xenopus laevis GN=ezh2-a PE=2 SV=1 | 160 | 287 | 2.0E-18 |
sp|P20659|TRX_DROME | Histone-lysine N-methyltransferase trithorax OS=Drosophila melanogaster GN=trx PE=1 SV=4 | 173 | 310 | 2.0E-18 |
sp|Q03164|KMT2A_HUMAN | Histone-lysine N-methyltransferase 2A OS=Homo sapiens GN=KMT2A PE=1 SV=5 | 172 | 310 | 2.0E-18 |
sp|Q80UJ9|SETMR_MOUSE | Histone-lysine N-methyltransferase SETMAR OS=Mus musculus GN=Setmar PE=2 SV=2 | 147 | 310 | 2.0E-18 |
sp|P42124|EZ_DROME | Histone-lysine N-methyltransferase E(z) OS=Drosophila melanogaster GN=E(z) PE=1 SV=2 | 94 | 302 | 3.0E-18 |
sp|Q54HS3|SET1_DICDI | Histone-lysine N-methyltransferase set1 OS=Dictyostelium discoideum GN=set1 PE=1 SV=1 | 152 | 306 | 3.0E-18 |
sp|Q5ABG1|SET1_CANAL | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=SET1 PE=3 SV=1 | 173 | 311 | 4.0E-18 |
sp|Q2GWF3|SET1_CHAGB | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) GN=SET1 PE=3 SV=1 | 162 | 310 | 4.0E-18 |
sp|Q4R381|EZH2_MACFA | Histone-lysine N-methyltransferase EZH2 OS=Macaca fascicularis GN=EZH2 PE=2 SV=1 | 159 | 287 | 5.0E-18 |
sp|Q5I0M0|SETMR_RAT | Histone-lysine N-methyltransferase SETMAR OS=Rattus norvegicus GN=Setmar PE=2 SV=1 | 147 | 310 | 5.0E-18 |
sp|Q15910|EZH2_HUMAN | Histone-lysine N-methyltransferase EZH2 OS=Homo sapiens GN=EZH2 PE=1 SV=2 | 159 | 287 | 5.0E-18 |
sp|Q4V863|EZH2B_XENLA | Histone-lysine N-methyltransferase EZH2 OS=Xenopus laevis GN=ezh2-b PE=2 SV=1 | 134 | 287 | 5.0E-18 |
sp|Q28D84|EZH2_XENTR | Histone-lysine N-methyltransferase EZH2 OS=Xenopus tropicalis GN=ezh2 PE=2 SV=1 | 160 | 287 | 5.0E-18 |
sp|Q61188|EZH2_MOUSE | Histone-lysine N-methyltransferase EZH2 OS=Mus musculus GN=Ezh2 PE=1 SV=2 | 159 | 287 | 6.0E-18 |
sp|Q08BS4|EZH2_DANRE | Histone-lysine N-methyltransferase EZH2 OS=Danio rerio GN=ezh2 PE=2 SV=1 | 160 | 287 | 7.0E-18 |
sp|A7E2Z2|EZH1_BOVIN | Histone-lysine N-methyltransferase EZH1 OS=Bos taurus GN=EZH1 PE=2 SV=2 | 159 | 287 | 7.0E-18 |
sp|Q5F3W5|SUV92_CHICK | Histone-lysine N-methyltransferase SUV39H2 OS=Gallus gallus GN=SUV39H2 PE=2 SV=1 | 148 | 289 | 8.0E-18 |
sp|P70351|EZH1_MOUSE | Histone-lysine N-methyltransferase EZH1 OS=Mus musculus GN=Ezh1 PE=1 SV=1 | 159 | 287 | 9.0E-18 |
sp|Q92800|EZH1_HUMAN | Histone-lysine N-methyltransferase EZH1 OS=Homo sapiens GN=EZH1 PE=1 SV=2 | 159 | 287 | 1.0E-17 |
sp|O64827|SUVR5_ARATH | Histone-lysine N-methyltransferase SUVR5 OS=Arabidopsis thaliana GN=SUVR5 PE=1 SV=3 | 148 | 310 | 1.0E-17 |
sp|Q2NL30|SUV91_BOVIN | Histone-lysine N-methyltransferase SUV39H1 OS=Bos taurus GN=SUV39H1 PE=2 SV=1 | 148 | 289 | 2.0E-17 |
sp|Q6NRE8|SUV91_XENLA | Histone-lysine N-methyltransferase SUV39H1 OS=Xenopus laevis GN=suv39h1 PE=2 SV=1 | 148 | 289 | 2.0E-17 |
sp|Q5RB81|SUV91_PONAB | Histone-lysine N-methyltransferase SUV39H1 OS=Pongo abelii GN=SUV39H1 PE=2 SV=1 | 148 | 289 | 3.0E-17 |
sp|O43463|SUV91_HUMAN | Histone-lysine N-methyltransferase SUV39H1 OS=Homo sapiens GN=SUV39H1 PE=1 SV=1 | 148 | 289 | 3.0E-17 |
sp|Q66J90|SET1B_XENLA | Histone-lysine N-methyltransferase SETD1B OS=Xenopus laevis GN=setd1b PE=2 SV=1 | 149 | 310 | 4.0E-17 |
sp|Q5RDS6|EZH1_PONAB | Histone-lysine N-methyltransferase EZH1 OS=Pongo abelii GN=EZH1 PE=2 SV=1 | 159 | 287 | 5.0E-17 |
sp|Q08D57|SET1B_XENTR | Histone-lysine N-methyltransferase SETD1B OS=Xenopus tropicalis GN=setd1b PE=2 SV=1 | 183 | 310 | 7.0E-17 |
sp|Q5F3P8|SET1B_CHICK | Histone-lysine N-methyltransferase SETD1B OS=Gallus gallus GN=SETD1B PE=2 SV=1 | 183 | 310 | 7.0E-17 |
sp|Q9UPS6|SET1B_HUMAN | Histone-lysine N-methyltransferase SETD1B OS=Homo sapiens GN=SETD1B PE=1 SV=3 | 183 | 310 | 1.0E-16 |
sp|Q6DGD3|SV91A_DANRE | Histone-lysine N-methyltransferase SUV39H1-A OS=Danio rerio GN=suv39h1a PE=2 SV=2 | 148 | 310 | 2.0E-16 |
sp|Q1LY77|SE1BA_DANRE | Histone-lysine N-methyltransferase SETD1B-A OS=Danio rerio GN=setd1ba PE=1 SV=2 | 164 | 310 | 2.0E-16 |
sp|P93831|CLF_ARATH | Histone-lysine N-methyltransferase CLF OS=Arabidopsis thaliana GN=CLF PE=1 SV=2 | 160 | 308 | 2.0E-16 |
sp|Q8CFT2|SET1B_MOUSE | Histone-lysine N-methyltransferase SETD1B OS=Mus musculus GN=Setd1b PE=1 SV=2 | 183 | 310 | 2.0E-16 |
sp|O54864|SUV91_MOUSE | Histone-lysine N-methyltransferase SUV39H1 OS=Mus musculus GN=Suv39h1 PE=1 SV=1 | 148 | 289 | 3.0E-16 |
sp|A8XI75|SET23_CAEBR | Probable histone-lysine N-methyltransferase set-23 OS=Caenorhabditis briggsae GN=set-23 PE=3 SV=1 | 120 | 310 | 3.0E-16 |
sp|Q0VD24|SETMR_BOVIN | Histone-lysine N-methyltransferase SETMAR OS=Bos taurus GN=SETMAR PE=2 SV=1 | 136 | 329 | 3.0E-16 |
sp|O08550|KMT2B_MOUSE | Histone-lysine N-methyltransferase 2B OS=Mus musculus GN=Kmt2b PE=1 SV=3 | 172 | 310 | 3.0E-16 |
sp|Q9UMN6|KMT2B_HUMAN | Histone-lysine N-methyltransferase 2B OS=Homo sapiens GN=KMT2B PE=1 SV=1 | 172 | 310 | 4.0E-16 |
sp|O60016|CLR4_SCHPO | Histone-lysine N-methyltransferase, H3 lysine-9 specific OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=clr4 PE=1 SV=2 | 144 | 312 | 7.0E-16 |
sp|Q8NEZ4|KMT2C_HUMAN | Histone-lysine N-methyltransferase 2C OS=Homo sapiens GN=KMT2C PE=1 SV=3 | 164 | 306 | 9.0E-16 |
sp|Q53H47|SETMR_HUMAN | Histone-lysine N-methyltransferase SETMAR OS=Homo sapiens GN=SETMAR PE=1 SV=2 | 120 | 310 | 9.0E-16 |
sp|Q9NH52|MES4_CAEEL | Histone-lysine N-methyltransferase mes-4 OS=Caenorhabditis elegans GN=mes-4 PE=1 SV=1 | 124 | 311 | 9.0E-16 |
sp|O44757|LIN59_CAEEL | Probable histone-lysine N-methyltransferase lin-59 OS=Caenorhabditis elegans GN=lin-59 PE=2 SV=1 | 117 | 312 | 1.0E-15 |
sp|Q8BRH4|KMT2C_MOUSE | Histone-lysine N-methyltransferase 2C OS=Mus musculus GN=Kmt2c PE=1 SV=2 | 164 | 306 | 1.0E-15 |
sp|Q8S4P6|EZ1_MAIZE | Histone-lysine N-methyltransferase EZ1 OS=Zea mays GN=EZ1 PE=2 SV=1 | 160 | 308 | 1.0E-15 |
sp|Q9ZSM8|EZA1_ARATH | Histone-lysine N-methyltransferase EZA1 OS=Arabidopsis thaliana GN=EZA1 PE=1 SV=1 | 119 | 304 | 2.0E-15 |
sp|Q8S4P5|EZ2_MAIZE | Histone-lysine N-methyltransferase EZ2 OS=Zea mays GN=EZ2 PE=2 SV=1 | 157 | 304 | 8.0E-15 |
sp|Q8S4P4|EZ3_MAIZE | Histone-lysine N-methyltransferase EZ3 OS=Zea mays GN=EZ3 PE=2 SV=1 | 157 | 304 | 8.0E-15 |
sp|Q5LJZ2|SET1_DROME | Histone-lysine N-methyltransferase SETD1 OS=Drosophila melanogaster GN=Set1 PE=1 SV=1 | 164 | 311 | 2.0E-14 |
sp|P0CB22|ATX2_ARATH | Histone-lysine N-methyltransferase ATX2 OS=Arabidopsis thaliana GN=ATX2 PE=2 SV=1 | 182 | 328 | 2.0E-14 |
sp|O65312|MEDEA_ARATH | Histone-lysine N-methyltransferase MEDEA OS=Arabidopsis thaliana GN=MEA PE=1 SV=1 | 71 | 287 | 2.0E-14 |
sp|O15047|SET1A_HUMAN | Histone-lysine N-methyltransferase SETD1A OS=Homo sapiens GN=SETD1A PE=1 SV=3 | 183 | 310 | 3.0E-14 |
sp|Q9SUE7|ATX4_ARATH | Histone-lysine N-methyltransferase ATX4 OS=Arabidopsis thaliana GN=ATX4 PE=2 SV=3 | 163 | 310 | 3.0E-14 |
sp|Q8GZ42|ATX5_ARATH | Histone-lysine N-methyltransferase ATX5 OS=Arabidopsis thaliana GN=ATX5 PE=2 SV=1 | 163 | 310 | 5.0E-14 |
sp|Q95Y12|SET23_CAEEL | Probable histone-lysine N-methyltransferase set-23 OS=Caenorhabditis elegans GN=set-23 PE=3 SV=1 | 132 | 310 | 6.0E-14 |
sp|O14686|KMT2D_HUMAN | Histone-lysine N-methyltransferase 2D OS=Homo sapiens GN=KMT2D PE=1 SV=2 | 164 | 306 | 2.0E-13 |
sp|Q6PDK2|KMT2D_MOUSE | Histone-lysine N-methyltransferase 2D OS=Mus musculus GN=Kmt2d PE=1 SV=2 | 164 | 306 | 2.0E-13 |
sp|Q93YF5|SUVH1_TOBAC | Histone-lysine N-methyltransferase, H3 lysine-9 specific SUVH1 OS=Nicotiana tabacum GN=SUVH1 PE=1 SV=1 | 119 | 310 | 3.0E-13 |
sp|P0CO26|SET1_CRYNJ | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) GN=SET1 PE=3 SV=1 | 164 | 310 | 8.0E-13 |
sp|P0CO27|SET1_CRYNB | Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) GN=SET1 PE=3 SV=1 | 164 | 310 | 8.0E-13 |
sp|P45975|SUV39_DROME | Histone-lysine N-methyltransferase Su(var)3-9 OS=Drosophila melanogaster GN=Su(var)3-9 PE=1 SV=2 | 182 | 306 | 3.0E-12 |
sp|Q294B9|SUV39_DROPS | Histone-lysine N-methyltransferase Su(var)3-9 OS=Drosophila pseudoobscura pseudoobscura GN=Su(var)3-9 PE=3 SV=1 | 148 | 306 | 3.0E-12 |
sp|Q9H9B1|EHMT1_HUMAN | Histone-lysine N-methyltransferase EHMT1 OS=Homo sapiens GN=EHMT1 PE=1 SV=4 | 147 | 306 | 4.0E-12 |
sp|Q9C5X4|ATX1_ARATH | Histone-lysine N-methyltransferase ATX1 OS=Arabidopsis thaliana GN=ATX1 PE=1 SV=2 | 161 | 322 | 8.0E-12 |
sp|Q9M364|ATX3_ARATH | Histone-lysine N-methyltransferase ATX3 OS=Arabidopsis thaliana GN=ATX3 PE=2 SV=2 | 163 | 310 | 1.0E-11 |
sp|C6KTD2|SET1_PLAF7 | Putative histone-lysine N-methyltransferase 1 OS=Plasmodium falciparum (isolate 3D7) GN=SET1 PE=2 SV=1 | 175 | 308 | 2.0E-11 |
sp|Q9SRV2|SUVR3_ARATH | Histone-lysine N-methyltransferase SUVR3 OS=Arabidopsis thaliana GN=SUVR3 PE=2 SV=4 | 148 | 308 | 2.0E-11 |
sp|Q0V9E9|SETD8_XENTR | N-lysine methyltransferase SETD8 OS=Xenopus tropicalis GN=setd8 PE=2 SV=1 | 181 | 287 | 5.0E-11 |
sp|Q498E6|SET8B_XENLA | N-lysine methyltransferase SETD8-B OS=Xenopus laevis GN=setd8-b PE=1 SV=1 | 181 | 287 | 7.0E-11 |
sp|O17514|MES2_CAEEL | Histone-lysine N-methyltransferase mes-2 OS=Caenorhabditis elegans GN=mes-2 PE=1 SV=2 | 104 | 288 | 1.0E-10 |
sp|Q08AY6|SET8A_XENLA | N-lysine methyltransferase SETD8-A OS=Xenopus laevis GN=setd8-a PE=2 SV=1 | 181 | 287 | 1.0E-10 |
sp|Q5DW34|EHMT1_MOUSE | Histone-lysine N-methyltransferase EHMT1 OS=Mus musculus GN=Ehmt1 PE=1 SV=2 | 147 | 306 | 3.0E-10 |
sp|Q8W595|SUVR4_ARATH | Histone-lysine N-methyltransferase SUVR4 OS=Arabidopsis thaliana GN=SUVR4 PE=1 SV=2 | 148 | 306 | 4.0E-10 |
sp|Q9Z148|EHMT2_MOUSE | Histone-lysine N-methyltransferase EHMT2 OS=Mus musculus GN=Ehmt2 PE=1 SV=2 | 147 | 306 | 6.0E-10 |
sp|Q96KQ7|EHMT2_HUMAN | Histone-lysine N-methyltransferase EHMT2 OS=Homo sapiens GN=EHMT2 PE=1 SV=3 | 147 | 306 | 7.0E-10 |
sp|O82175|SUVH5_ARATH | Histone-lysine N-methyltransferase, H3 lysine-9 specific SUVH5 OS=Arabidopsis thaliana GN=SUVH5 PE=1 SV=1 | 108 | 308 | 3.0E-09 |
sp|Q1L8U8|STB1A_DANRE | Histone-lysine N-methyltransferase SETDB1-A OS=Danio rerio GN=setdb1a PE=3 SV=1 | 235 | 308 | 4.0E-09 |
sp|Q2YDW7|SETD8_MOUSE | N-lysine methyltransferase SETD8 OS=Mus musculus GN=Setd8 PE=1 SV=1 | 161 | 287 | 4.0E-09 |
sp|Q28Z18|SETB1_DROPS | Histone-lysine N-methyltransferase eggless OS=Drosophila pseudoobscura pseudoobscura GN=egg PE=3 SV=2 | 227 | 306 | 5.0E-09 |
sp|P34544|MET2_CAEEL | Histone-lysine N-methyltransferase met-2 OS=Caenorhabditis elegans GN=met-2 PE=3 SV=5 | 236 | 308 | 5.0E-09 |
sp|Q9NQR1|SETD8_HUMAN | N-lysine methyltransferase SETD8 OS=Homo sapiens GN=SETD8 PE=1 SV=3 | 179 | 288 | 5.0E-09 |
sp|Q08BR4|STB1B_DANRE | Histone-lysine N-methyltransferase SETDB1-B OS=Danio rerio GN=setdb1b PE=2 SV=2 | 225 | 317 | 7.0E-09 |
sp|Q6INA9|SETB1_XENLA | Histone-lysine N-methyltransferase SETDB1 OS=Xenopus laevis GN=setdb1 PE=2 SV=1 | 226 | 308 | 7.0E-09 |
sp|Q2YDJ8|SETD8_BOVIN | N-lysine methyltransferase SETD8 OS=Bos taurus GN=SETD8 PE=2 SV=1 | 179 | 288 | 8.0E-09 |
sp|Q946J2|SUVR1_ARATH | Probable inactive histone-lysine N-methyltransferase SUVR1 OS=Arabidopsis thaliana GN=SUVR1 PE=1 SV=2 | 141 | 306 | 9.0E-09 |
sp|Q32KD2|SETB1_DROME | Histone-lysine N-methyltransferase eggless OS=Drosophila melanogaster GN=egg PE=1 SV=1 | 235 | 306 | 2.0E-08 |
sp|O88974|SETB1_MOUSE | Histone-lysine N-methyltransferase SETDB1 OS=Mus musculus GN=Setdb1 PE=1 SV=1 | 235 | 308 | 2.0E-08 |
sp|Q15047|SETB1_HUMAN | Histone-lysine N-methyltransferase SETDB1 OS=Homo sapiens GN=SETDB1 PE=1 SV=1 | 235 | 308 | 3.0E-08 |
sp|Q8VZ17|SUVH6_ARATH | Histone-lysine N-methyltransferase, H3 lysine-9 specific SUVH6 OS=Arabidopsis thaliana GN=SUVH6 PE=2 SV=2 | 112 | 306 | 3.0E-08 |
sp|Q9C5P4|SUVH3_ARATH | Histone-lysine N-methyltransferase, H3 lysine-9 specific SUVH3 OS=Arabidopsis thaliana GN=SUVH3 PE=2 SV=2 | 143 | 311 | 3.0E-08 |
sp|Q071E0|SET8A_DANRE | N-lysine methyltransferase SETD8-A OS=Danio rerio GN=setd8a PE=2 SV=1 | 181 | 287 | 4.0E-08 |
sp|Q8X225|DIM5_NEUCR | Histone-lysine N-methyltransferase, H3 lysine-9 specific dim-5 OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=dim-5 PE=1 SV=2 | 148 | 310 | 2.0E-07 |
sp|Q6YI93|SETB2_XENLA | Histone-lysine N-methyltransferase SETDB2 OS=Xenopus laevis GN=setdb2 PE=2 SV=2 | 234 | 306 | 2.0E-07 |
sp|Q9C5P1|SUVH7_ARATH | Histone-lysine N-methyltransferase, H3 lysine-9 specific SUVH7 OS=Arabidopsis thaliana GN=SUVH7 PE=2 SV=1 | 119 | 308 | 2.0E-07 |
sp|A4IGY9|SETB2_XENTR | Histone-lysine N-methyltransferase SETDB2 OS=Xenopus tropicalis GN=setdb2 PE=2 SV=1 | 234 | 306 | 4.0E-07 |
sp|O23372|ATXR3_ARATH | Histone-lysine N-methyltransferase ATXR3 OS=Arabidopsis thaliana GN=ATXR3 PE=2 SV=2 | 173 | 308 | 8.0E-07 |
GO Term | Description | Terminal node |
---|---|---|
GO:0005515 | protein binding | Yes |
GO:0005634 | nucleus | Yes |
GO:0018024 | histone-lysine N-methyltransferase activity | Yes |
GO:0005694 | chromosome | Yes |
GO:0034968 | histone lysine methylation | Yes |
GO:0006355 | regulation of transcription, DNA-templated | Yes |
GO:0016570 | histone modification | No |
GO:0043227 | membrane-bounded organelle | No |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | No |
GO:0043412 | macromolecule modification | No |
GO:0018193 | peptidyl-amino acid modification | No |
GO:0008152 | metabolic process | No |
GO:0031323 | regulation of cellular metabolic process | No |
GO:0005575 | cellular_component | No |
GO:0008170 | N-methyltransferase activity | No |
GO:0008150 | biological_process | No |
GO:0080090 | regulation of primary metabolic process | No |
GO:0060255 | regulation of macromolecule metabolic process | No |
GO:0018205 | peptidyl-lysine modification | No |
GO:0010468 | regulation of gene expression | No |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | No |
GO:0050789 | regulation of biological process | No |
GO:0043231 | intracellular membrane-bounded organelle | No |
GO:0016279 | protein-lysine N-methyltransferase activity | No |
GO:0016741 | transferase activity, transferring one-carbon groups | No |
GO:0044238 | primary metabolic process | No |
GO:0043226 | organelle | No |
GO:0019538 | protein metabolic process | No |
GO:0016278 | lysine N-methyltransferase activity | No |
GO:0019222 | regulation of metabolic process | No |
GO:2001141 | regulation of RNA biosynthetic process | No |
GO:1903506 | regulation of nucleic acid-templated transcription | No |
GO:0140096 | catalytic activity, acting on a protein | No |
GO:0050794 | regulation of cellular process | No |
GO:0031326 | regulation of cellular biosynthetic process | No |
GO:0016740 | transferase activity | No |
GO:0008213 | protein alkylation | No |
GO:0003824 | catalytic activity | No |
GO:0051252 | regulation of RNA metabolic process | No |
GO:0044237 | cellular metabolic process | No |
GO:1901564 | organonitrogen compound metabolic process | No |
GO:0044260 | cellular macromolecule metabolic process | No |
GO:0010556 | regulation of macromolecule biosynthetic process | No |
GO:0006479 | protein methylation | No |
GO:0051171 | regulation of nitrogen compound metabolic process | No |
GO:0110165 | cellular anatomical entity | No |
GO:0003674 | molecular_function | No |
GO:0032259 | methylation | No |
GO:0016571 | histone methylation | No |
GO:0043414 | macromolecule methylation | No |
GO:0043229 | intracellular organelle | No |
GO:0043232 | intracellular non-membrane-bounded organelle | No |
GO:0036211 | protein modification process | No |
GO:0071704 | organic substance metabolic process | No |
GO:0042054 | histone methyltransferase activity | No |
GO:0006807 | nitrogen compound metabolic process | No |
GO:0005488 | binding | No |
GO:0008276 | protein methyltransferase activity | No |
GO:0065007 | biological regulation | No |
GO:0043170 | macromolecule metabolic process | No |
GO:0008168 | methyltransferase activity | No |
GO:0009889 | regulation of biosynthetic process | No |
GO:0009987 | cellular process | No |
GO:0018022 | peptidyl-lysine methylation | No |
GO:0043228 | non-membrane-bounded organelle | No |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 11 | 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|3817 MEDEEHAMSRMSRIKLDDGTASAAALDESSSMPGPDSRNGASTSVAPSPNGSSNGPGTPASARPARLSRKASQKT AGREPPLFNHLAQVTAQSCQGFQLIRDCLYGSKHLGATDNDALDCDCREEWRDGQNLACGDDSDCINRATKMECS ASAGNCGGGCQNQRFQRKQWASVSVIQTDKKGFGLRTDADLLPHDFVYEYIGEVINEPTFRRRMLQYDHEGIKHF YFMSLNKSEFVDATKKGNLGRFCNHSCNPNCYVDKWVVGDKLRMGIFALRRIRAGEELVFNYNVDRYGADPQPCY CGEPNCVGFIGGKTQTERATKLPASTVEALGIDYADGWDTAVAKKPRKKRPDEDDEDYVNSIQPRSLTEDGARKV MAALMQCKEKWIAVKLLQRIQSCQEERVIHCVMRMHAYQILKTTLNTFIDDDNVVLQVLDILDKFPRLTRNKIQD SNIEATIQGLTDKRNPQVESKSKSLLDEWSKLQMAYRIQRRKVDAATPAQNIYEDRRGAQARDKETVQSTPKAPS PRPVDAPKGPRNNAPQRNNSYFANIQRQRRQFNAPLPDGWFSAKDARGNTYFYNKTGQTTWKRPAQPAEPVQIKP SRALQEQLAIQSIIDKVTKEGTPKQPPPQPSEVVEPPLEDAKREKWRSLPVDKQMKIYENTLFPSVKYVLDKFKH KLPKDELKRLGKEIAKKLVASDYKNNRVQDPTVELSDKQAAKIKKFVTDFLNRAVEKFNTRQSRKAARKSGPNGQ QANGEQSQDDKPPPSTDASRDGSVATPGVKDELKLDDAGADIAMSDADADSPASQERKRKREADLADSACATPTE GPGIKRLKDDETSSPTPPPPPPPLDSGLDDDISAEQRALQQQEEDLMRENEEAQRLEDEAQNSKMMEEGVDKMRK DIALAA* |
Coding | >OphauG2|3817 ATGGAGGATGAAGAGCATGCAATGAGCAGGATGAGCAGGATCAAACTCGACGACGGCACAGCCAGCGCTGCTGCC CTGGACGAGAGCAGCTCCATGCCTGGCCCTGATAGTCGCAATGGCGCGTCCACCTCTGTGGCGCCCTCGCCCAAC GGAAGCAGCAACGGCCCTGGCACTCCAGCCTCGGCCAGGCCTGCTCGTCTCTCGCGCAAGGCCTCGCAAAAGACA GCAGGCCGCGAGCCGCCCTTGTTCAACCACCTTGCTCAGGTCACTGCCCAGTCGTGCCAGGGCTTCCAGCTTATT CGGGACTGTCTCTACGGATCCAAGCACCTGGGCGCTACCGACAACGATGCCCTCGACTGCGACTGCAGAGAAGAA TGGCGCGATGGCCAAAACCTGGCCTGCGGCGACGACTCTGACTGCATCAACCGCGCCACCAAGATGGAGTGCAGT GCCAGTGCTGGCAACTGTGGCGGAGGTTGCCAGAACCAGCGCTTCCAGCGCAAGCAGTGGGCCAGCGTCTCCGTC ATCCAAACGGACAAGAAGGGCTTCGGCCTGCGCACCGACGCCGACTTGCTCCCCCATGACTTTGTCTACGAGTAC ATTGGCGAGGTCATCAATGAGCCCACTTTTCGCCGTCGCATGCTGCAGTACGACCATGAGGGAATCAAGCACTTT TACTTCATGTCTCTCAACAAGAGCGAGTTTGTCGATGCTACCAAAAAGGGCAATCTGGGTCGTTTCTGCAACCAC TCGTGCAATCCCAACTGCTATGTCGACAAGTGGGTGGTTGGAGACAAGTTGCGCATGGGCATTTTTGCTTTGCGC CGCATTCGTGCTGGCGAAGAGCTCGTCTTCAACTACAACGTTGATCGCTATGGAGCCGACCCACAGCCCTGCTAC TGCGGAGAGCCCAACTGCGTCGGCTTTATTGGCGGCAAAACGCAGACTGAGCGCGCCACCAAGCTCCCGGCCTCT ACTGTTGAGGCTCTGGGCATTGACTATGCTGATGGCTGGGATACCGCCGTGGCCAAGAAGCCGCGCAAGAAGCGT CCCGACGAGGACGACGAGGACTACGTCAACAGCATCCAGCCTCGCAGCCTCACCGAGGATGGCGCGCGCAAAGTC ATGGCCGCTCTGATGCAGTGCAAGGAGAAGTGGATTGCTGTAAAGCTGCTCCAGCGCATCCAGAGCTGCCAAGAG GAGCGCGTCATTCACTGCGTCATGCGCATGCACGCCTACCAAATCCTCAAGACCACCCTCAACACTTTTATAGAC GACGACAATGTCGTGCTGCAGGTCCTTGACATTCTCGACAAGTTTCCTCGCCTGACAAGAAACAAGATCCAAGAC TCCAACATCGAGGCCACCATACAAGGCCTGACAGATAAGCGCAATCCCCAGGTGGAATCCAAGTCCAAGAGTCTT CTTGATGAATGGAGCAAGCTGCAGATGGCCTATCGCATCCAGCGCAGAAAGGTAGACGCTGCTACTCCTGCCCAA AACATCTATGAAGATCGCCGAGGTGCCCAGGCCCGCGACAAGGAAACAGTACAGTCCACCCCCAAGGCGCCCTCT CCCCGCCCTGTGGATGCACCCAAAGGCCCACGGAATAACGCCCCCCAGCGAAACAATAGCTATTTTGCCAACATA CAGCGACAGCGCCGCCAGTTCAATGCTCCGTTGCCAGACGGTTGGTTTTCGGCAAAGGACGCCAGGGGTAACACT TATTTTTACAACAAGACAGGACAAACCACCTGGAAGCGACCGGCTCAGCCAGCCGAACCCGTTCAGATCAAACCA TCGAGGGCTCTTCAGGAGCAGCTGGCCATTCAAAGCATCATTGACAAGGTCACCAAGGAGGGAACCCCCAAGCAA CCGCCACCTCAGCCCAGCGAGGTGGTGGAGCCGCCGCTGGAAGATGCCAAAAGGGAGAAGTGGCGGTCGTTGCCA GTTGACAAGCAAATGAAGATTTACGAGAATACTCTCTTCCCTTCGGTCAAGTACGTGTTGGACAAGTTTAAGCAC AAACTTCCCAAGGATGAGCTTAAGCGCCTTGGTAAAGAAATTGCCAAGAAACTTGTTGCGTCAGACTACAAGAAC AACAGAGTACAGGATCCTACGGTTGAGCTCTCTGACAAGCAGGCTGCCAAAATCAAGAAGTTTGTGACAGACTTC TTGAACCGTGCAGTCGAAAAGTTTAATACGCGCCAGAGTCGAAAGGCCGCAAGGAAATCTGGGCCCAATGGACAG CAGGCAAATGGAGAGCAGAGTCAAGACGATAAGCCACCTCCCAGTACAGATGCCTCACGAGACGGCTCTGTTGCC ACACCCGGTGTCAAAGACGAGCTCAAGCTGGATGACGCCGGCGCCGATATTGCTATGAGTGACGCCGACGCCGAT TCGCCCGCCAGCCAGGAGCGCAAACGGAAGCGTGAAGCGGACCTTGCAGACTCGGCTTGCGCTACACCAACTGAG GGCCCTGGCATCAAGAGGCTTAAAGACGACGAAACCAGCTCGCCAACGCCGCCACCGCCGCCGCCACCTCTGGAT TCAGGTCTCGACGATGACATTTCGGCTGAACAACGGGCGCTCCAGCAGCAGGAAGAGGACCTGATGCGAGAAAAC GAGGAAGCACAAAGGCTGGAAGACGAGGCCCAAAACTCCAAGATGATGGAAGAAGGTGTAGACAAGATGCGAAAA GATATTGCTCTTGCAGCATGA |
Transcript | >OphauG2|3817 ATGGAGGATGAAGAGCATGCAATGAGCAGGATGAGCAGGATCAAACTCGACGACGGCACAGCCAGCGCTGCTGCC CTGGACGAGAGCAGCTCCATGCCTGGCCCTGATAGTCGCAATGGCGCGTCCACCTCTGTGGCGCCCTCGCCCAAC GGAAGCAGCAACGGCCCTGGCACTCCAGCCTCGGCCAGGCCTGCTCGTCTCTCGCGCAAGGCCTCGCAAAAGACA GCAGGCCGCGAGCCGCCCTTGTTCAACCACCTTGCTCAGGTCACTGCCCAGTCGTGCCAGGGCTTCCAGCTTATT CGGGACTGTCTCTACGGATCCAAGCACCTGGGCGCTACCGACAACGATGCCCTCGACTGCGACTGCAGAGAAGAA TGGCGCGATGGCCAAAACCTGGCCTGCGGCGACGACTCTGACTGCATCAACCGCGCCACCAAGATGGAGTGCAGT GCCAGTGCTGGCAACTGTGGCGGAGGTTGCCAGAACCAGCGCTTCCAGCGCAAGCAGTGGGCCAGCGTCTCCGTC ATCCAAACGGACAAGAAGGGCTTCGGCCTGCGCACCGACGCCGACTTGCTCCCCCATGACTTTGTCTACGAGTAC ATTGGCGAGGTCATCAATGAGCCCACTTTTCGCCGTCGCATGCTGCAGTACGACCATGAGGGAATCAAGCACTTT TACTTCATGTCTCTCAACAAGAGCGAGTTTGTCGATGCTACCAAAAAGGGCAATCTGGGTCGTTTCTGCAACCAC TCGTGCAATCCCAACTGCTATGTCGACAAGTGGGTGGTTGGAGACAAGTTGCGCATGGGCATTTTTGCTTTGCGC CGCATTCGTGCTGGCGAAGAGCTCGTCTTCAACTACAACGTTGATCGCTATGGAGCCGACCCACAGCCCTGCTAC TGCGGAGAGCCCAACTGCGTCGGCTTTATTGGCGGCAAAACGCAGACTGAGCGCGCCACCAAGCTCCCGGCCTCT ACTGTTGAGGCTCTGGGCATTGACTATGCTGATGGCTGGGATACCGCCGTGGCCAAGAAGCCGCGCAAGAAGCGT CCCGACGAGGACGACGAGGACTACGTCAACAGCATCCAGCCTCGCAGCCTCACCGAGGATGGCGCGCGCAAAGTC ATGGCCGCTCTGATGCAGTGCAAGGAGAAGTGGATTGCTGTAAAGCTGCTCCAGCGCATCCAGAGCTGCCAAGAG GAGCGCGTCATTCACTGCGTCATGCGCATGCACGCCTACCAAATCCTCAAGACCACCCTCAACACTTTTATAGAC GACGACAATGTCGTGCTGCAGGTCCTTGACATTCTCGACAAGTTTCCTCGCCTGACAAGAAACAAGATCCAAGAC TCCAACATCGAGGCCACCATACAAGGCCTGACAGATAAGCGCAATCCCCAGGTGGAATCCAAGTCCAAGAGTCTT CTTGATGAATGGAGCAAGCTGCAGATGGCCTATCGCATCCAGCGCAGAAAGGTAGACGCTGCTACTCCTGCCCAA AACATCTATGAAGATCGCCGAGGTGCCCAGGCCCGCGACAAGGAAACAGTACAGTCCACCCCCAAGGCGCCCTCT CCCCGCCCTGTGGATGCACCCAAAGGCCCACGGAATAACGCCCCCCAGCGAAACAATAGCTATTTTGCCAACATA CAGCGACAGCGCCGCCAGTTCAATGCTCCGTTGCCAGACGGTTGGTTTTCGGCAAAGGACGCCAGGGGTAACACT TATTTTTACAACAAGACAGGACAAACCACCTGGAAGCGACCGGCTCAGCCAGCCGAACCCGTTCAGATCAAACCA TCGAGGGCTCTTCAGGAGCAGCTGGCCATTCAAAGCATCATTGACAAGGTCACCAAGGAGGGAACCCCCAAGCAA CCGCCACCTCAGCCCAGCGAGGTGGTGGAGCCGCCGCTGGAAGATGCCAAAAGGGAGAAGTGGCGGTCGTTGCCA GTTGACAAGCAAATGAAGATTTACGAGAATACTCTCTTCCCTTCGGTCAAGTACGTGTTGGACAAGTTTAAGCAC AAACTTCCCAAGGATGAGCTTAAGCGCCTTGGTAAAGAAATTGCCAAGAAACTTGTTGCGTCAGACTACAAGAAC AACAGAGTACAGGATCCTACGGTTGAGCTCTCTGACAAGCAGGCTGCCAAAATCAAGAAGTTTGTGACAGACTTC TTGAACCGTGCAGTCGAAAAGTTTAATACGCGCCAGAGTCGAAAGGCCGCAAGGAAATCTGGGCCCAATGGACAG CAGGCAAATGGAGAGCAGAGTCAAGACGATAAGCCACCTCCCAGTACAGATGCCTCACGAGACGGCTCTGTTGCC ACACCCGGTGTCAAAGACGAGCTCAAGCTGGATGACGCCGGCGCCGATATTGCTATGAGTGACGCCGACGCCGAT TCGCCCGCCAGCCAGGAGCGCAAACGGAAGCGTGAAGCGGACCTTGCAGACTCGGCTTGCGCTACACCAACTGAG GGCCCTGGCATCAAGAGGCTTAAAGACGACGAAACCAGCTCGCCAACGCCGCCACCGCCGCCGCCACCTCTGGAT TCAGGTCTCGACGATGACATTTCGGCTGAACAACGGGCGCTCCAGCAGCAGGAAGAGGACCTGATGCGAGAAAAC GAGGAAGCACAAAGGCTGGAAGACGAGGCCCAAAACTCCAAGATGATGGAAGAAGGTGTAGACAAGATGCGAAAA GATATTGCTCTTGCAGCATGA |
Gene | >OphauG2|3817 ATGGAGGATGAAGAGCATGCAATGAGCAGGATGAGCAGGATCAAACTCGACGACGGCACAGCCAGCGCTGCTGCC CTGGACGAGAGCAGCTCCATGCCTGGCCCTGATAGTCGCAATGGCGCGTCCACCTCTGTGGCGCCCTCGCCCAAC GGAAGCAGCAACGGCCCTGGCACTCCAGCCTCGGCCAGGCCTGCTCGTCTCTCGCGCAAGGCCTCGCAAAAGACA GCAGGCCGCGAGCCGCCCTTGTTCAACCACCTTGCTCAGGTCACTGCCCAGTCGTGCCAGGGCTTCCAGCTTATT CGGGACTGTCTCTACGGATCCAAGCACCTGGGCGCTACCGACAACGATGCCCTCGACTGCGACTGCAGAGAAGAA TGGCGTACGTCTACACTGTCCTCATTTCCTCCCCCGCGCTCAAGCTGCCATGGTGCTGGCTGTGCGAGGCGTTGT GGCACTGACCTCATGTCCCCAAAGGCGATGGCCAAAACCTGGCCTGCGGCGACGACTCTGACTGCATCAACCGCG CCACCAAGATGGAGTGCAGTGCCAGTGCTGGCAACTGTGGCGGAGGTTGCCAGAACCAGCGCTTCCAGCGCAAGC AGTGGGCCAGCGTCTCCGTCATCCAAACGGACAAGAAGGGCTTCGGCCTGCGCACCGACGCCGACTTGCTCCCCC ATGACTTTGTCTACGAGTACATTGGCGAGGTCATCAATGAGCCCACTTTTCGCCGTCGCATGCTGCAGTACGACC ATGAGGGAATCAAGCACTTTTACTTCATGTCTCTCAACAAGAGCGAGTTTGTCGATGCTACCAAAAAGGGCAATC TGGGTCGTTTCTGCAACCACTCGTGCAATCCCAACTGCTATGTCGACAAGTGGGTGGTTGGAGACAAGTTGCGCA TGGGCATTTTTGCTTTGCGCCGCATTCGTGCTGGCGAAGAGCTCGTCTTCAACTACAACGTTGATCGCTATGGAG CCGACCCACAGCCCTGCTACTGCGGAGAGCCCAACTGCGTCGGCTTTATTGGCGGCAAAACGCAGACTGAGCGCG CCACCAAGCTCCCGGCCTCTACTGTTGAGGCTCTGGGCATTGACTATGCTGATGGCTGGGATACCGCCGTGGCCA AGAAGCCGCGCAAGAAGCGTCCCGACGAGGACGACGAGGACTACGTCAACAGCATCCAGCCTCGCAGCCTCACCG AGGATGGCGCGCGCAAAGTCATGGCCGCTCTGATGCAGTGCAAGGAGAAGTGGATTGCTGTAAAGCTGCTCCAGC GCATCCAGAGCTGCCAAGAGGAGCGCGTCATTCACTGCGTCATGCGCATGCACGCCTACCAAATCCTCAAGACCA CCCTCAACACTTTTATAGACGACGACAATGTCGTGCTGCAGGTCCTTGACATTCTCGACAAGTTTCCTCGCCTGA CAAGAAACAAGATCCAAGACTCCAACATCGAGGCCACCATACAAGGCCTGACAGATAAGCGCAATCCCCAGGTGG AATCCAAGTCCAAGAGTCTTCTTGATGAATGGAGCAAGCTGCAGATGGCCTATCGCATCCAGCGCAGAAAGGTAG ACGCTGCTACTCCTGCCCAAAACATCTATGAAGATCGCCGAGGTGCCCAGGCCCGCGACAAGGAAACAGTACAGT CCACCCCCAAGGCGCCCTCTCCCCGCCCTGTGGATGCACCCAAAGGCCCACGGAATAACGCCCCCCAGCGAAACA ATAGCTATTTTGCCAACATACAGCGACAGCGCCGCCAGTTCAATGCTCCGTTGCCAGACGGTTGGTTTTCGGCAA AGGACGCCAGGGGTAACACTTATTTTTACAACAAGACAGGACAAACCACCTGGAAGCGACCGGCTCAGCCAGCCG AACCCGTTCAGATCAAACCATCGAGGGCTCTTCAGGAGCAGCTGGCCATTCAAAGCATCATTGACAAGGTCACCA AGGAGGGAACCCCCAAGCAACCGCCACCTCAGCCCAGCGAGGTGGTGGAGCCGCCGCTGGAAGATGCCAAAAGGG AGAAGTGGCGGTCGTTGCCAGTTGACAAGCAAATGAAGATTTACGAGAATACTGTGAGTCAACTTGGGCCTCGCG CAGAAACCACGGCGCAGAAAATGCATAGTCCCGGGCTAACTCGACGGCAGCTCTTCCCTTCGGTCAAGTACGTGT TGGACAAGTTTAAGCACAAACTTCCCAAGGATGAGCTTAAGCGCCTTGGTAAAGAAATTGCCAAGAAACTTGTTG CGTCAGACTACAAGAACAACAGAGTACAGGATCCTACGGTTGAGCTCTCTGACAAGCAGGCTGCCAAAATCAAGA AGTTTGTGACAGACTTCTTGAACCGTGCAGTCGAAAAGTTTAATACGCGCCAGAGTCGAAAGGCCGCAAGGAAAT CTGGGCCCAATGGACAGCAGGCAAATGGAGAGCAGAGTCAAGACGATAAGCCACCTCCCAGTACAGATGCCTCAC GAGACGGCTCTGTTGCCACACCCGGTGTCAAAGACGAGCTCAAGCTGGATGACGCCGGCGCCGATATTGCTATGA GTGACGCCGACGCCGATTCGCCCGCCAGCCAGGAGCGCAAACGGAAGCGTGAAGCGGACCTTGCAGACTCGGCTT GCGCTACACCAACTGAGGGCCCTGGCATCAAGAGGCTTAAAGACGACGAAACCAGCTCGCCAACGCCGCCACCGC CGCCGCCACCTCTGGATTCAGGTCTCGACGATGACATTTCGGCTGAACAACGGGCGCTCCAGCAGCAGGAAGAGG ACCTGATGCGAGAAAACGAGGAAGCACAAAGGCTGGAAGACGAGGCCCAAAACTCCAAGATGATGGAAGAAGGTG TAGACAAGATGCGAAAAGATATTGCTCTTGCAGCATGA |