Fungal Genomics

at Utrecht University

General Properties

Protein IDHirsu2|725
Gene name
LocationContig_1149:2053..5717
Strand+
Gene length (bp)3664
Transcript length (bp)3606
Coding sequence length (bp)3606
Protein length (aa) 1202

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF18601 EZH2_N EZH2 N-terminal domain 3.2E-35 234 313
PF18600 Ezh2_MCSS MCSS domain 1.3E-25 460 510
PF00856 SET SET domain 1.4E-15 759 875
PF18264 preSET_CXC CXC domain 4.8E-06 678 716

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|P70351|EZH1_MOUSE Histone-lysine N-methyltransferase EZH1 OS=Mus musculus GN=Ezh1 PE=1 SV=1 542 874 9.0E-42
sp|Q92800|EZH1_HUMAN Histone-lysine N-methyltransferase EZH1 OS=Homo sapiens GN=EZH1 PE=1 SV=2 542 874 3.0E-41
sp|A7E2Z2|EZH1_BOVIN Histone-lysine N-methyltransferase EZH1 OS=Bos taurus GN=EZH1 PE=2 SV=2 542 874 3.0E-41
sp|Q08BS4|EZH2_DANRE Histone-lysine N-methyltransferase EZH2 OS=Danio rerio GN=ezh2 PE=2 SV=1 545 874 7.0E-41
sp|Q4R381|EZH2_MACFA Histone-lysine N-methyltransferase EZH2 OS=Macaca fascicularis GN=EZH2 PE=2 SV=1 545 874 1.0E-40
[Show all]
[Show less]
Swissprot ID Swissprot Description Start End E-value
sp|P70351|EZH1_MOUSE Histone-lysine N-methyltransferase EZH1 OS=Mus musculus GN=Ezh1 PE=1 SV=1 542 874 9.0E-42
sp|Q92800|EZH1_HUMAN Histone-lysine N-methyltransferase EZH1 OS=Homo sapiens GN=EZH1 PE=1 SV=2 542 874 3.0E-41
sp|A7E2Z2|EZH1_BOVIN Histone-lysine N-methyltransferase EZH1 OS=Bos taurus GN=EZH1 PE=2 SV=2 542 874 3.0E-41
sp|Q08BS4|EZH2_DANRE Histone-lysine N-methyltransferase EZH2 OS=Danio rerio GN=ezh2 PE=2 SV=1 545 874 7.0E-41
sp|Q4R381|EZH2_MACFA Histone-lysine N-methyltransferase EZH2 OS=Macaca fascicularis GN=EZH2 PE=2 SV=1 545 874 1.0E-40
sp|Q15910|EZH2_HUMAN Histone-lysine N-methyltransferase EZH2 OS=Homo sapiens GN=EZH2 PE=1 SV=2 545 874 1.0E-40
sp|Q5RDS6|EZH1_PONAB Histone-lysine N-methyltransferase EZH1 OS=Pongo abelii GN=EZH1 PE=2 SV=1 542 874 3.0E-40
sp|Q61188|EZH2_MOUSE Histone-lysine N-methyltransferase EZH2 OS=Mus musculus GN=Ezh2 PE=1 SV=2 545 874 4.0E-40
sp|Q98SM3|EZH2A_XENLA Histone-lysine N-methyltransferase EZH2 OS=Xenopus laevis GN=ezh2-a PE=2 SV=1 545 874 1.0E-39
sp|Q28D84|EZH2_XENTR Histone-lysine N-methyltransferase EZH2 OS=Xenopus tropicalis GN=ezh2 PE=2 SV=1 545 874 2.0E-39
sp|P42124|EZ_DROME Histone-lysine N-methyltransferase E(z) OS=Drosophila melanogaster GN=E(z) PE=1 SV=2 545 874 2.0E-39
sp|Q4V863|EZH2B_XENLA Histone-lysine N-methyltransferase EZH2 OS=Xenopus laevis GN=ezh2-b PE=2 SV=1 545 874 4.0E-39
sp|O65312|MEDEA_ARATH Histone-lysine N-methyltransferase MEDEA OS=Arabidopsis thaliana GN=MEA PE=1 SV=1 627 874 1.0E-29
sp|P93831|CLF_ARATH Histone-lysine N-methyltransferase CLF OS=Arabidopsis thaliana GN=CLF PE=1 SV=2 639 874 3.0E-27
sp|Q8S4P5|EZ2_MAIZE Histone-lysine N-methyltransferase EZ2 OS=Zea mays GN=EZ2 PE=2 SV=1 640 874 3.0E-26
sp|Q8S4P6|EZ1_MAIZE Histone-lysine N-methyltransferase EZ1 OS=Zea mays GN=EZ1 PE=2 SV=1 639 874 8.0E-26
sp|Q8S4P4|EZ3_MAIZE Histone-lysine N-methyltransferase EZ3 OS=Zea mays GN=EZ3 PE=2 SV=1 640 874 8.0E-26
sp|O17514|MES2_CAEEL Histone-lysine N-methyltransferase mes-2 OS=Caenorhabditis elegans GN=mes-2 PE=1 SV=2 622 874 1.0E-24
sp|Q9ZSM8|EZA1_ARATH Histone-lysine N-methyltransferase EZA1 OS=Arabidopsis thaliana GN=EZA1 PE=1 SV=1 639 874 6.0E-23
sp|Q5DW34|EHMT1_MOUSE Histone-lysine N-methyltransferase EHMT1 OS=Mus musculus GN=Ehmt1 PE=1 SV=2 735 891 8.0E-17
sp|Q9Z148|EHMT2_MOUSE Histone-lysine N-methyltransferase EHMT2 OS=Mus musculus GN=Ehmt2 PE=1 SV=2 682 896 1.0E-16
sp|Q96KQ7|EHMT2_HUMAN Histone-lysine N-methyltransferase EHMT2 OS=Homo sapiens GN=EHMT2 PE=1 SV=3 682 896 2.0E-16
sp|Q9H9B1|EHMT1_HUMAN Histone-lysine N-methyltransferase EHMT1 OS=Homo sapiens GN=EHMT1 PE=1 SV=4 735 891 6.0E-16
sp|O54864|SUV91_MOUSE Histone-lysine N-methyltransferase SUV39H1 OS=Mus musculus GN=Suv39h1 PE=1 SV=1 735 874 2.0E-14
sp|Q2NL30|SUV91_BOVIN Histone-lysine N-methyltransferase SUV39H1 OS=Bos taurus GN=SUV39H1 PE=2 SV=1 735 874 2.0E-14
sp|Q5RB81|SUV91_PONAB Histone-lysine N-methyltransferase SUV39H1 OS=Pongo abelii GN=SUV39H1 PE=2 SV=1 735 874 2.0E-14
sp|O43463|SUV91_HUMAN Histone-lysine N-methyltransferase SUV39H1 OS=Homo sapiens GN=SUV39H1 PE=1 SV=1 735 874 2.0E-14
sp|Q9VYD1|C1716_DROME Probable histone-lysine N-methyltransferase CG1716 OS=Drosophila melanogaster GN=Set2 PE=1 SV=2 697 874 1.0E-13
sp|Q6NRE8|SUV91_XENLA Histone-lysine N-methyltransferase SUV39H1 OS=Xenopus laevis GN=suv39h1 PE=2 SV=1 735 874 2.0E-13
sp|Q8MT36|MES4_DROME Probable histone-lysine N-methyltransferase Mes-4 OS=Drosophila melanogaster GN=Mes-4 PE=1 SV=2 697 884 2.0E-13
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=2 746 874 3.0E-13
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=1 746 874 5.0E-13
sp|Q9EQQ0|SUV92_MOUSE Histone-lysine N-methyltransferase SUV39H2 OS=Mus musculus GN=Suv39h2 PE=1 SV=1 735 874 9.0E-13
sp|Q9NR48|ASH1L_HUMAN Histone-lysine N-methyltransferase ASH1L OS=Homo sapiens GN=ASH1L PE=1 SV=2 684 928 1.0E-12
sp|Q32PH7|SUV92_BOVIN Histone-lysine N-methyltransferase SUV39H2 OS=Bos taurus GN=SUV39H2 PE=2 SV=1 735 874 1.0E-12
sp|Q5F3W5|SUV92_CHICK Histone-lysine N-methyltransferase SUV39H2 OS=Gallus gallus GN=SUV39H2 PE=2 SV=1 735 874 1.0E-12
sp|Q1DU03|SET2_COCIM Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Coccidioides immitis (strain RS) GN=SET2 PE=3 SV=2 671 875 1.0E-12
sp|Q6DGD3|SV91A_DANRE Histone-lysine N-methyltransferase SUV39H1-A OS=Danio rerio GN=suv39h1a PE=2 SV=2 735 874 1.0E-12
sp|Q8BVE8|NSD2_MOUSE Histone-lysine N-methyltransferase NSD2 OS=Mus musculus GN=Whsc1 PE=1 SV=2 694 874 2.0E-12
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=1 733 874 2.0E-12
sp|Q6BM04|SET2_DEBHA Histone-lysine N-methyltransferase, H3 lysine-36 specific OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=SET2 PE=3 SV=2 669 875 2.0E-12
sp|Q96L73|NSD1_HUMAN Histone-lysine N-methyltransferase, H3 lysine-36 and H4 lysine-20 specific OS=Homo sapiens GN=NSD1 PE=1 SV=1 694 874 2.0E-12
sp|Q28CQ7|SUV92_XENTR Histone-lysine N-methyltransferase SUV39H2 OS=Xenopus tropicalis GN=suv39h2 PE=2 SV=2 735 874 2.0E-12
sp|Q8IE95|SETVS_PLAF7 Variant-silencing SET domain-containing protein OS=Plasmodium falciparum (isolate 3D7) GN=SETVS PE=2 SV=1 756 878 3.0E-12
sp|O96028|NSD2_HUMAN Histone-lysine N-methyltransferase NSD2 OS=Homo sapiens GN=WHSC1 PE=1 SV=1 694 874 4.0E-12
sp|Q99MY8|ASH1L_MOUSE Histone-lysine N-methyltransferase ASH1L OS=Mus musculus GN=Ash1l PE=1 SV=3 673 904 4.0E-12
sp|Q9H5I1|SUV92_HUMAN Histone-lysine N-methyltransferase SUV39H2 OS=Homo sapiens GN=SUV39H2 PE=1 SV=2 735 874 4.0E-12
sp|Q4R3E0|SUV92_MACFA Histone-lysine N-methyltransferase SUV39H2 OS=Macaca fascicularis GN=SUV39H2 PE=2 SV=2 735 874 4.0E-12
sp|E9Q5F9|SETD2_MOUSE Histone-lysine N-methyltransferase SETD2 OS=Mus musculus GN=Setd2 PE=1 SV=1 756 874 4.0E-12
sp|Q9BYW2|SETD2_HUMAN Histone-lysine N-methyltransferase SETD2 OS=Homo sapiens GN=SETD2 PE=1 SV=3 756 874 4.0E-12
sp|O88491|NSD1_MOUSE Histone-lysine N-methyltransferase, H3 lysine-36 and H4 lysine-20 specific OS=Mus musculus GN=Nsd1 PE=1 SV=1 694 874 5.0E-12
sp|Q9Y7R4|SET1_SCHPO Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=set1 PE=1 SV=1 698 885 6.0E-12
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=1 746 874 7.0E-12
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=1 668 875 9.0E-12
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=1 702 874 1.0E-11
sp|O64827|SUVR5_ARATH Histone-lysine N-methyltransferase SUVR5 OS=Arabidopsis thaliana GN=SUVR5 PE=1 SV=3 735 875 1.0E-11
sp|Q1DR06|SET1_COCIM Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Coccidioides immitis (strain RS) GN=SET1 PE=3 SV=1 746 874 1.0E-11
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=1 671 875 2.0E-11
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=1 669 874 3.0E-11
sp|Q8W595|SUVR4_ARATH Histone-lysine N-methyltransferase SUVR4 OS=Arabidopsis thaliana GN=SUVR4 PE=1 SV=2 735 878 3.0E-11
sp|P55200|KMT2A_MOUSE Histone-lysine N-methyltransferase 2A OS=Mus musculus GN=Kmt2a PE=1 SV=3 759 885 3.0E-11
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=1 746 874 4.0E-11
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=1 746 874 7.0E-11
sp|P38827|SET1_YEAST Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SET1 PE=1 SV=1 746 874 7.0E-11
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=1 702 874 7.0E-11
sp|Q9SRV2|SUVR3_ARATH Histone-lysine N-methyltransferase SUVR3 OS=Arabidopsis thaliana GN=SUVR3 PE=2 SV=4 735 876 1.0E-10
sp|Q2LAE1|ASHH2_ARATH Histone-lysine N-methyltransferase ASHH2 OS=Arabidopsis thaliana GN=ASHH2 PE=1 SV=1 697 874 1.0E-10
sp|Q8IRW8|TRR_DROME Histone-lysine N-methyltransferase trr OS=Drosophila melanogaster GN=trr PE=1 SV=2 730 874 1.0E-10
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=1 671 874 1.0E-10
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=2 732 874 2.0E-10
sp|Q9NH52|MES4_CAEEL Histone-lysine N-methyltransferase mes-4 OS=Caenorhabditis elegans GN=mes-4 PE=1 SV=1 759 904 2.0E-10
sp|F4K1J4|ATXR7_ARATH Histone-lysine N-methyltransferase ATXR7 OS=Arabidopsis thaliana GN=ATXR7 PE=2 SV=1 746 879 2.0E-10
sp|P45975|SUV39_DROME Histone-lysine N-methyltransferase Su(var)3-9 OS=Drosophila melanogaster GN=Su(var)3-9 PE=1 SV=2 740 874 2.0E-10
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=1 746 874 2.0E-10
sp|Q4PB36|SET1_USTMA Histone-lysine N-methyltransferase, H3 lysine-4 specific OS=Ustilago maydis (strain 521 / FGSC 9021) GN=SET1 PE=3 SV=1 760 874 3.0E-10
sp|Q9BZ95|NSD3_HUMAN Histone-lysine N-methyltransferase NSD3 OS=Homo sapiens GN=WHSC1L1 PE=1 SV=1 697 874 3.0E-10
sp|Q6P2L6|NSD3_MOUSE Histone-lysine N-methyltransferase NSD3 OS=Mus musculus GN=Whsc1l1 PE=1 SV=2 759 874 3.0E-10
sp|Q294B9|SUV39_DROPS Histone-lysine N-methyltransferase Su(var)3-9 OS=Drosophila pseudoobscura pseudoobscura GN=Su(var)3-9 PE=3 SV=1 735 874 4.0E-10
sp|C6KTD2|SET1_PLAF7 Putative histone-lysine N-methyltransferase 1 OS=Plasmodium falciparum (isolate 3D7) GN=SET1 PE=2 SV=1 759 886 4.0E-10
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=2 733 874 7.0E-10
sp|Q0V9E9|SETD8_XENTR N-lysine methyltransferase SETD8 OS=Xenopus tropicalis GN=setd8 PE=2 SV=1 745 876 7.0E-10
sp|Q54HS3|SET1_DICDI Histone-lysine N-methyltransferase set1 OS=Dictyostelium discoideum GN=set1 PE=1 SV=1 760 874 8.0E-10
sp|O08550|KMT2B_MOUSE Histone-lysine N-methyltransferase 2B OS=Mus musculus GN=Kmt2b PE=1 SV=3 759 885 1.0E-09
sp|Q297V5|SETD8_DROPS Histone-lysine N-methyltransferase pr-set7 OS=Drosophila pseudoobscura pseudoobscura GN=pr-set7 PE=3 SV=2 757 876 1.0E-09
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=2 746 874 1.0E-09
sp|Q9UMN6|KMT2B_HUMAN Histone-lysine N-methyltransferase 2B OS=Homo sapiens GN=KMT2B PE=1 SV=1 759 885 2.0E-09
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=1 694 874 2.0E-09
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=1 746 874 2.0E-09
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=2 669 875 2.0E-09
sp|P20659|TRX_DROME Histone-lysine N-methyltransferase trithorax OS=Drosophila melanogaster GN=trx PE=1 SV=4 759 879 2.0E-09
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=1 746 874 2.0E-09
sp|Q8NEZ4|KMT2C_HUMAN Histone-lysine N-methyltransferase 2C OS=Homo sapiens GN=KMT2C PE=1 SV=3 723 888 3.0E-09
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=1 746 874 3.0E-09
sp|Q9VW15|ASH1_DROME Histone-lysine N-methyltransferase ash1 OS=Drosophila melanogaster GN=ash1 PE=1 SV=3 679 880 3.0E-09
sp|Q8BRH4|KMT2C_MOUSE Histone-lysine N-methyltransferase 2C OS=Mus musculus GN=Kmt2c PE=1 SV=2 723 888 4.0E-09
sp|Q949T8|ASHR3_ARATH Histone-lysine N-methyltransferase ASHR3 OS=Arabidopsis thaliana GN=ASHR3 PE=1 SV=1 756 874 5.0E-09
sp|A8XI75|SET23_CAEBR Probable histone-lysine N-methyltransferase set-23 OS=Caenorhabditis briggsae GN=set-23 PE=3 SV=1 666 875 7.0E-09
sp|Q9M1X9|ASHH4_ARATH Putative histone-lysine N-methyltransferase ASHH4 OS=Arabidopsis thaliana GN=ASHH4 PE=3 SV=1 754 874 8.0E-09
sp|Q9VFK6|SETD8_DROME Histone-lysine N-methyltransferase pr-set7 OS=Drosophila melanogaster GN=pr-set7 PE=1 SV=2 742 876 1.0E-08
sp|Q2YDW7|SETD8_MOUSE N-lysine methyltransferase SETD8 OS=Mus musculus GN=Setd8 PE=1 SV=1 755 876 2.0E-08
sp|O14686|KMT2D_HUMAN Histone-lysine N-methyltransferase 2D OS=Homo sapiens GN=KMT2D PE=1 SV=2 748 888 2.0E-08
sp|Q6PDK2|KMT2D_MOUSE Histone-lysine N-methyltransferase 2D OS=Mus musculus GN=Kmt2d PE=1 SV=2 748 888 2.0E-08
sp|Q9NQR1|SETD8_HUMAN N-lysine methyltransferase SETD8 OS=Homo sapiens GN=SETD8 PE=1 SV=3 755 876 3.0E-08
sp|Q95Y12|SET23_CAEEL Probable histone-lysine N-methyltransferase set-23 OS=Caenorhabditis elegans GN=set-23 PE=3 SV=1 666 877 3.0E-08
sp|Q08AY6|SET8A_XENLA N-lysine methyltransferase SETD8-A OS=Xenopus laevis GN=setd8-a PE=2 SV=1 745 876 3.0E-08
sp|Q18221|SET2_CAEEL Probable histone-lysine N-methyltransferase set-2 OS=Caenorhabditis elegans GN=set-2 PE=2 SV=2 759 879 3.0E-08
sp|Q84WW6|ASHH1_ARATH Histone-lysine N-methyltransferase ASHH1 OS=Arabidopsis thaliana GN=ASHH1 PE=1 SV=1 697 878 5.0E-08
sp|Q9SUE7|ATX4_ARATH Histone-lysine N-methyltransferase ATX4 OS=Arabidopsis thaliana GN=ATX4 PE=2 SV=3 740 874 6.0E-08
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=1 735 874 7.0E-08
sp|Q946J2|SUVR1_ARATH Probable inactive histone-lysine N-methyltransferase SUVR1 OS=Arabidopsis thaliana GN=SUVR1 PE=1 SV=2 735 878 1.0E-07
sp|O15047|SET1A_HUMAN Histone-lysine N-methyltransferase SETD1A OS=Homo sapiens GN=SETD1A PE=1 SV=3 746 879 1.0E-07
sp|Q945S8|ASHH3_ARATH Histone-lysine N-methyltransferase ASHH3 OS=Arabidopsis thaliana GN=ASHH3 PE=2 SV=2 754 874 2.0E-07
sp|Q498E6|SET8B_XENLA N-lysine methyltransferase SETD8-B OS=Xenopus laevis GN=setd8-b PE=1 SV=1 743 876 2.0E-07
sp|Q80UJ9|SETMR_MOUSE Histone-lysine N-methyltransferase SETMAR OS=Mus musculus GN=Setmar PE=2 SV=2 676 880 3.0E-07
sp|Q5I0M0|SETMR_RAT Histone-lysine N-methyltransferase SETMAR OS=Rattus norvegicus GN=Setmar PE=2 SV=1 735 880 8.0E-07
sp|Q53H47|SETMR_HUMAN Histone-lysine N-methyltransferase SETMAR OS=Homo sapiens GN=SETMAR PE=1 SV=2 697 894 2.0E-06
sp|P0CB22|ATX2_ARATH Histone-lysine N-methyltransferase ATX2 OS=Arabidopsis thaliana GN=ATX2 PE=2 SV=1 746 874 6.0E-06
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GO

GO Term Description Terminal node
GO:0005515 protein binding Yes
GO:0003674 molecular_function No
GO:0005488 binding No

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)
D score
(significance: > 0.45)
No 1 - 40 0.45

Transmembrane Domains

(None)

Transcription Factor Class

(None)

Expression data

No expression data available for this genome

Sequences

Type of sequenceSequence
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 >Hirsu2|725
MAASTTRRSSVSLGHDVDGDRGSETDGWPDDPDSLASRLEAFGSRKATSLVPTGATPVTPPPLRRSSVAVFRPTD
RPAPLFAREASPVAIADSASEGGRCSSVPRPDPAMSRPATPLPPRPASPSPSPSPSPSPPPSPSPSSFPGISDPP
AAPGPDPGPDPGTPPGQTDSHTDWTIPEIAEQLSHFRQDVRDGHAQLTAYIIESTKATERRVHHGPDLFAGIKLA
SVPAKKGATMRVKFKQHLKNNKRDTKEEHYPARGIKTNKDRVPRYRFHHVGIKKNVLTPNTMLTFVPHLRDLESS
EETKYNLWLKELEDIDLKSGFKPMNREEKQALTYQLERAATISLYLETWLDNLVIPGCNKSALISYMASREPDDA
ITPQQKTDILRSHRENDGAAPENNAAAQMFTEAFQLVFKESVPPEKQIDLRKVLLLDESVDSIMDSKPTAKDGAG
TQNDDEDELAESNLATYCILGCLICFSHSCDHGEYDNKNLKRTFSISSCSHLSDALKRRRRDAVNGHLMPPPPCA
RRCYRLGPWSPDLAACPRPWSDDEEVVLRSIFVTASHSVYRGDAICLAANFLNRTCNEAYEKFRSLRIVLPEPAP
REPIRVKNLTWYDRRRKVLLGDWQDHTVSHEHQRRETLEPCSHEGPCVPRVCSCVDAGLLCDKFCGCSVEDCAYK
FTGCACHSQGKTCQQKQKDRPCICVQLNRECDPELCGSCGALERADPLNADDTRLHATGCQNCDLQRGLGKPLIL
GQSQLEGVGYGLFTAEDIAQDDFIIEYVGELITHDEGVRREARRGDVFDEDSNISYVFTLLENEGIWVDAAIYGN
LSRYINHASENDKRGCNITPRILYVNGEYRIKFTAMRDIAAGEELFFNYGENFPNLTKKLLDHKAGEQPSKAKGG
RSRRAEAGGQVARKAPRSEQKRGPGRPKTKRELTAESDLYNFESSETPAKSRKRKRRSDDNPGEEDYQPSAVSAG
PSQATNAVVEPEDGEIGSMTRLRKRTRASAGMQPADADMKRVEPPKKKGKRGGARPGSGRPRKHPRPVPKPTQAS
KIKEEDEGRSQGAATAATEPAPAVATAPDPMPPLEPVTAPAVTPPAADVAEVVPVPEAAAAAAAPEAAPATSAPV
PAPEPEVKAEVIEIQDSDDGAARVVFNDQSLVELGSEDGEAHDEEDEDQDVVVRKRNDRARNRRPPAKFREDDIW
T*
Coding >Hirsu2|725
ATGGCTGCTAGCACGACCCGGCGCTCCAGCGTCAGCCTCGGCCACGACGTCGACGGTGATCGCGGGTCCGAGACC
GACGGCTGGCCAGACGATCCGGACAGCCTGGCCTCGCGCCTCGAGGCCTTCGGCAGCAGGAAAGCCACCAGCCTC
GTCCCCACCGGCGCCACCCCCGTCACCCCGCCGCCGCTCAGGAGGTCGTCCGTGGCCGTCTTCCGACCGACCGAC
CGCCCGGCTCCCTTGTTCGCCCGGGAGGCCTCGCCCGTCGCAATCGCCGACAGTGCCAGCGAGGGGGGCCGCTGC
TCCTCCGTCCCGAGGCCCGACCCGGCCATGTCGCGCCCGGCCACGCCCTTGCCGCCCCGGCCCGCCTCGCCGTCG
CCGTCGCCGTCGCCGTCGCCGTCGCCCCCGCCGTCGCCGTCGCCCTCGTCCTTCCCCGGCATCTCGGATCCCCCG
GCCGCCCCCGGCCCCGATCCCGGCCCCGACCCCGGCACCCCGCCCGGCCAGACGGACTCCCACACCGACTGGACC
ATCCCGGAGATCGCCGAGCAGCTGAGCCACTTCCGCCAGGATGTCAGGGACGGCCACGCTCAGCTGACGGCATAC
ATCATCGAGTCCACAAAGGCGACGGAGCGCCGAGTCCACCACGGCCCGGACCTCTTTGCCGGCATCAAGCTGGCA
TCGGTGCCCGCCAAGAAGGGGGCGACCATGAGGGTCAAGTTCAAGCAACATCTGAAAAATAATAAGAGAGATACA
AAAGAGGAGCATTACCCGGCCCGCGGCATCAAGACGAACAAGGACCGTGTCCCCCGCTACCGCTTTCATCATGTC
GGCATCAAGAAGAACGTCCTCACCCCAAACACCATGCTGACCTTTGTCCCCCACCTGCGAGATCTTGAGAGTTCG
GAAGAGACAAAGTACAACCTCTGGCTTAAGGAGCTCGAGGACATCGATCTCAAGTCTGGCTTCAAGCCCATGAAC
CGCGAGGAGAAACAGGCTCTGACCTATCAGCTGGAGCGGGCGGCCACCATCTCGCTCTACCTCGAGACCTGGCTC
GACAACCTGGTCATTCCCGGCTGCAACAAGTCGGCCCTGATCAGCTACATGGCCAGCCGCGAGCCCGACGACGCC
ATCACGCCGCAGCAGAAGACAGACATTCTGCGGTCCCACCGCGAGAACGACGGCGCCGCGCCGGAAAACAATGCT
GCGGCCCAGATGTTCACCGAGGCCTTTCAGCTCGTCTTCAAAGAGAGCGTGCCGCCCGAGAAGCAGATTGACCTC
CGCAAGGTCCTACTGCTCGACGAGTCTGTCGACAGCATCATGGACTCGAAGCCCACGGCCAAGGACGGCGCCGGC
ACGCAAAACGACGACGAGGATGAGCTGGCCGAGTCGAACCTGGCCACGTACTGCATCCTGGGATGCCTCATCTGC
TTCAGCCACTCTTGCGACCATGGCGAATACGACAACAAGAACCTCAAACGCACCTTCTCCATATCCTCCTGCTCT
CACCTCTCCGACGCCCTCAAGCGGCGGCGGCGAGACGCCGTCAACGGCCATCTCATGCCTCCGCCTCCCTGCGCG
CGGCGGTGTTACCGCCTCGGCCCCTGGTCTCCGGACCTGGCCGCGTGCCCTCGCCCCTGGTCCGACGACGAGGAG
GTTGTGCTCCGATCCATCTTCGTCACGGCCTCGCACAGTGTGTACCGAGGCGATGCGATATGCCTGGCAGCCAAT
TTCCTGAATCGGACCTGCAACGAGGCCTACGAAAAGTTCCGGTCGCTGCGCATCGTTCTGCCCGAGCCGGCCCCG
CGGGAGCCGATCAGGGTCAAGAATCTGACGTGGTACGACCGCCGGAGGAAGGTTCTCCTGGGGGACTGGCAGGAC
CACACCGTCAGCCACGAGCACCAAAGACGGGAGACGCTGGAGCCGTGCTCGCACGAGGGGCCCTGCGTCCCGAGG
GTCTGCTCCTGCGTCGACGCGGGCCTGCTGTGCGACAAGTTTTGCGGCTGTTCCGTGGAGGACTGCGCCTACAAG
TTCACGGGGTGTGCGTGCCATTCCCAGGGCAAGACGTGCCAGCAGAAGCAGAAGGACAGGCCGTGCATCTGCGTG
CAGCTGAACCGAGAGTGCGACCCGGAGCTGTGCGGCTCGTGCGGCGCCCTGGAGCGTGCGGACCCGCTGAACGCC
GACGACACACGGCTCCACGCGACGGGCTGCCAAAACTGCGACCTGCAGCGCGGCCTGGGCAAGCCTCTGATCCTG
GGTCAGAGCCAGCTCGAGGGCGTCGGGTACGGCCTCTTCACGGCCGAAGACATCGCGCAGGACGACTTCATCATC
GAATACGTCGGAGAGCTGATCACGCACGACGAGGGCGTGCGCCGAGAGGCGCGGCGCGGCGACGTCTTCGACGAG
GACTCCAACATCTCGTATGTCTTCACGCTACTCGAGAACGAGGGCATCTGGGTGGACGCGGCGATATACGGCAAC
CTCAGCCGGTACATCAACCACGCGTCCGAGAACGACAAGCGCGGATGCAACATCACGCCGCGGATCCTGTACGTC
AACGGGGAGTATCGCATCAAGTTCACGGCGATGCGGGACATTGCAGCCGGCGAGGAGCTCTTCTTCAACTACGGC
GAGAACTTCCCCAACCTGACGAAGAAACTGCTGGACCACAAGGCGGGTGAACAGCCCAGCAAGGCCAAGGGGGGG
CGGTCACGGCGAGCGGAAGCCGGGGGCCAGGTGGCGCGGAAGGCGCCCCGGTCGGAGCAGAAGAGGGGCCCGGGC
CGGCCCAAGACGAAGAGGGAGCTCACGGCAGAGAGCGACCTATATAATTTTGAGTCCTCGGAGACGCCGGCGAAG
TCGCGAAAGCGCAAGCGACGGTCCGACGACAACCCCGGAGAGGAGGACTACCAGCCGTCCGCCGTGAGCGCCGGG
CCGTCGCAGGCGACGAACGCGGTCGTCGAACCGGAGGATGGCGAAATCGGGTCGATGACGCGACTGCGCAAGCGA
ACGCGGGCCTCGGCCGGTATGCAGCCAGCCGACGCGGACATGAAACGCGTCGAGCCGCCCAAGAAGAAAGGCAAG
CGGGGCGGCGCGCGACCAGGAAGCGGCCGGCCTAGAAAGCATCCTCGACCAGTCCCCAAGCCAACGCAAGCTTCA
AAAATCAAAGAGGAGGACGAGGGGAGGTCCCAGGGGGCAGCAACGGCGGCGACGGAGCCTGCGCCCGCAGTGGCG
ACGGCGCCCGACCCCATGCCACCGCTCGAGCCCGTGACTGCGCCCGCGGTTACGCCTCCGGCCGCGGACGTGGCC
GAGGTTGTCCCCGTGCCCGAAGCTGCGGCCGCCGCAGCTGCGCCCGAGGCTGCACCTGCGACAAGCGCGCCGGTC
CCCGCGCCGGAACCTGAGGTCAAGGCCGAGGTAATCGAAATCCAGGACAGCGACGACGGGGCAGCGAGGGTGGTG
TTCAACGACCAGTCGCTGGTCGAGCTGGGGAGCGAGGACGGGGAAGCGCATGACGAGGAGGACGAGGACCAGGAC
GTGGTGGTGCGCAAGAGGAACGACCGGGCGCGAAACCGACGGCCGCCAGCCAAGTTTCGAGAGGACGACATCTGG
ACTTGA
Transcript >Hirsu2|725
ATGGCTGCTAGCACGACCCGGCGCTCCAGCGTCAGCCTCGGCCACGACGTCGACGGTGATCGCGGGTCCGAGACC
GACGGCTGGCCAGACGATCCGGACAGCCTGGCCTCGCGCCTCGAGGCCTTCGGCAGCAGGAAAGCCACCAGCCTC
GTCCCCACCGGCGCCACCCCCGTCACCCCGCCGCCGCTCAGGAGGTCGTCCGTGGCCGTCTTCCGACCGACCGAC
CGCCCGGCTCCCTTGTTCGCCCGGGAGGCCTCGCCCGTCGCAATCGCCGACAGTGCCAGCGAGGGGGGCCGCTGC
TCCTCCGTCCCGAGGCCCGACCCGGCCATGTCGCGCCCGGCCACGCCCTTGCCGCCCCGGCCCGCCTCGCCGTCG
CCGTCGCCGTCGCCGTCGCCGTCGCCCCCGCCGTCGCCGTCGCCCTCGTCCTTCCCCGGCATCTCGGATCCCCCG
GCCGCCCCCGGCCCCGATCCCGGCCCCGACCCCGGCACCCCGCCCGGCCAGACGGACTCCCACACCGACTGGACC
ATCCCGGAGATCGCCGAGCAGCTGAGCCACTTCCGCCAGGATGTCAGGGACGGCCACGCTCAGCTGACGGCATAC
ATCATCGAGTCCACAAAGGCGACGGAGCGCCGAGTCCACCACGGCCCGGACCTCTTTGCCGGCATCAAGCTGGCA
TCGGTGCCCGCCAAGAAGGGGGCGACCATGAGGGTCAAGTTCAAGCAACATCTGAAAAATAATAAGAGAGATACA
AAAGAGGAGCATTACCCGGCCCGCGGCATCAAGACGAACAAGGACCGTGTCCCCCGCTACCGCTTTCATCATGTC
GGCATCAAGAAGAACGTCCTCACCCCAAACACCATGCTGACCTTTGTCCCCCACCTGCGAGATCTTGAGAGTTCG
GAAGAGACAAAGTACAACCTCTGGCTTAAGGAGCTCGAGGACATCGATCTCAAGTCTGGCTTCAAGCCCATGAAC
CGCGAGGAGAAACAGGCTCTGACCTATCAGCTGGAGCGGGCGGCCACCATCTCGCTCTACCTCGAGACCTGGCTC
GACAACCTGGTCATTCCCGGCTGCAACAAGTCGGCCCTGATCAGCTACATGGCCAGCCGCGAGCCCGACGACGCC
ATCACGCCGCAGCAGAAGACAGACATTCTGCGGTCCCACCGCGAGAACGACGGCGCCGCGCCGGAAAACAATGCT
GCGGCCCAGATGTTCACCGAGGCCTTTCAGCTCGTCTTCAAAGAGAGCGTGCCGCCCGAGAAGCAGATTGACCTC
CGCAAGGTCCTACTGCTCGACGAGTCTGTCGACAGCATCATGGACTCGAAGCCCACGGCCAAGGACGGCGCCGGC
ACGCAAAACGACGACGAGGATGAGCTGGCCGAGTCGAACCTGGCCACGTACTGCATCCTGGGATGCCTCATCTGC
TTCAGCCACTCTTGCGACCATGGCGAATACGACAACAAGAACCTCAAACGCACCTTCTCCATATCCTCCTGCTCT
CACCTCTCCGACGCCCTCAAGCGGCGGCGGCGAGACGCCGTCAACGGCCATCTCATGCCTCCGCCTCCCTGCGCG
CGGCGGTGTTACCGCCTCGGCCCCTGGTCTCCGGACCTGGCCGCGTGCCCTCGCCCCTGGTCCGACGACGAGGAG
GTTGTGCTCCGATCCATCTTCGTCACGGCCTCGCACAGTGTGTACCGAGGCGATGCGATATGCCTGGCAGCCAAT
TTCCTGAATCGGACCTGCAACGAGGCCTACGAAAAGTTCCGGTCGCTGCGCATCGTTCTGCCCGAGCCGGCCCCG
CGGGAGCCGATCAGGGTCAAGAATCTGACGTGGTACGACCGCCGGAGGAAGGTTCTCCTGGGGGACTGGCAGGAC
CACACCGTCAGCCACGAGCACCAAAGACGGGAGACGCTGGAGCCGTGCTCGCACGAGGGGCCCTGCGTCCCGAGG
GTCTGCTCCTGCGTCGACGCGGGCCTGCTGTGCGACAAGTTTTGCGGCTGTTCCGTGGAGGACTGCGCCTACAAG
TTCACGGGGTGTGCGTGCCATTCCCAGGGCAAGACGTGCCAGCAGAAGCAGAAGGACAGGCCGTGCATCTGCGTG
CAGCTGAACCGAGAGTGCGACCCGGAGCTGTGCGGCTCGTGCGGCGCCCTGGAGCGTGCGGACCCGCTGAACGCC
GACGACACACGGCTCCACGCGACGGGCTGCCAAAACTGCGACCTGCAGCGCGGCCTGGGCAAGCCTCTGATCCTG
GGTCAGAGCCAGCTCGAGGGCGTCGGGTACGGCCTCTTCACGGCCGAAGACATCGCGCAGGACGACTTCATCATC
GAATACGTCGGAGAGCTGATCACGCACGACGAGGGCGTGCGCCGAGAGGCGCGGCGCGGCGACGTCTTCGACGAG
GACTCCAACATCTCGTATGTCTTCACGCTACTCGAGAACGAGGGCATCTGGGTGGACGCGGCGATATACGGCAAC
CTCAGCCGGTACATCAACCACGCGTCCGAGAACGACAAGCGCGGATGCAACATCACGCCGCGGATCCTGTACGTC
AACGGGGAGTATCGCATCAAGTTCACGGCGATGCGGGACATTGCAGCCGGCGAGGAGCTCTTCTTCAACTACGGC
GAGAACTTCCCCAACCTGACGAAGAAACTGCTGGACCACAAGGCGGGTGAACAGCCCAGCAAGGCCAAGGGGGGG
CGGTCACGGCGAGCGGAAGCCGGGGGCCAGGTGGCGCGGAAGGCGCCCCGGTCGGAGCAGAAGAGGGGCCCGGGC
CGGCCCAAGACGAAGAGGGAGCTCACGGCAGAGAGCGACCTATATAATTTTGAGTCCTCGGAGACGCCGGCGAAG
TCGCGAAAGCGCAAGCGACGGTCCGACGACAACCCCGGAGAGGAGGACTACCAGCCGTCCGCCGTGAGCGCCGGG
CCGTCGCAGGCGACGAACGCGGTCGTCGAACCGGAGGATGGCGAAATCGGGTCGATGACGCGACTGCGCAAGCGA
ACGCGGGCCTCGGCCGGTATGCAGCCAGCCGACGCGGACATGAAACGCGTCGAGCCGCCCAAGAAGAAAGGCAAG
CGGGGCGGCGCGCGACCAGGAAGCGGCCGGCCTAGAAAGCATCCTCGACCAGTCCCCAAGCCAACGCAAGCTTCA
AAAATCAAAGAGGAGGACGAGGGGAGGTCCCAGGGGGCAGCAACGGCGGCGACGGAGCCTGCGCCCGCAGTGGCG
ACGGCGCCCGACCCCATGCCACCGCTCGAGCCCGTGACTGCGCCCGCGGTTACGCCTCCGGCCGCGGACGTGGCC
GAGGTTGTCCCCGTGCCCGAAGCTGCGGCCGCCGCAGCTGCGCCCGAGGCTGCACCTGCGACAAGCGCGCCGGTC
CCCGCGCCGGAACCTGAGGTCAAGGCCGAGGTAATCGAAATCCAGGACAGCGACGACGGGGCAGCGAGGGTGGTG
TTCAACGACCAGTCGCTGGTCGAGCTGGGGAGCGAGGACGGGGAAGCGCATGACGAGGAGGACGAGGACCAGGAC
GTGGTGGTGCGCAAGAGGAACGACCGGGCGCGAAACCGACGGCCGCCAGCCAAGTTTCGAGAGGACGACATCTGG
ACTTGA
Gene >Hirsu2|725
ATGGCTGCTAGCACGACCCGGCGCTCCAGCGTCAGCCTCGGCCACGACGTCGACGGTGATCGCGGGTCCGAGACC
GACGGCTGGCCAGACGATCCGGACAGCCTGGCCTCGCGCCTCGAGGCCTTCGGCAGCAGGAAAGCCACCAGCCTC
GTCCCCACCGGCGCCACCCCCGTCACCCCGCCGCCGCTCAGGAGGTCGTCCGTGGCCGTCTTCCGACCGACCGAC
CGCCCGGCTCCCTTGTTCGCCCGGGAGGCCTCGCCCGTCGCAATCGCCGACAGTGCCAGCGAGGGGGGCCGCTGC
TCCTCCGTCCCGAGGCCCGACCCGGCCATGTCGCGCCCGGCCACGCCCTTGCCGCCCCGGCCCGCCTCGCCGTCG
CCGTCGCCGTCGCCGTCGCCGTCGCCCCCGCCGTCGCCGTCGCCCTCGTCCTTCCCCGGCATCTCGGATCCCCCG
GCCGCCCCCGGCCCCGATCCCGGCCCCGACCCCGGCACCCCGCCCGGCCAGACGGACTCCCACACCGACTGGACC
ATCCCGGAGATCGCCGAGCAGCTGAGCCACTTCCGCCAGGATGTCAGGGACGGCCACGCTCAGCTGACGGCATAC
ATCATCGAGTCCACAAAGGCGACGGAGCGCCGAGTCCACCACGGCCCGGACCTCTTTGCCGGCATCAAGCTGGCA
TCGGTGCCCGCCAAGAAGGGGGCGACCATGAGGGTCAAGTTCAAGGCAAGCCCCTCTCTCCGGAACGCAGCCGAG
GAAACCGTCCGCTGATGCCCCGTAACAGCAACATCTGAAAAATAATAAGAGAGATACAAAAGAGGAGCATTACCC
GGCCCGCGGCATCAAGACGAACAAGGACCGTGTCCCCCGCTACCGCTTTCATCATGTCGGCATCAAGAAGAACGT
CCTCACCCCAAACACCATGCTGACCTTTGTCCCCCACCTGCGAGATCTTGAGAGTTCGGAAGAGACAAAGTACAA
CCTCTGGCTTAAGGAGCTCGAGGACATCGATCTCAAGTCTGGCTTCAAGCCCATGAACCGCGAGGAGAAACAGGC
TCTGACCTATCAGCTGGAGCGGGCGGCCACCATCTCGCTCTACCTCGAGACCTGGCTCGACAACCTGGTCATTCC
CGGCTGCAACAAGTCGGCCCTGATCAGCTACATGGCCAGCCGCGAGCCCGACGACGCCATCACGCCGCAGCAGAA
GACAGACATTCTGCGGTCCCACCGCGAGAACGACGGCGCCGCGCCGGAAAACAATGCTGCGGCCCAGATGTTCAC
CGAGGCCTTTCAGCTCGTCTTCAAAGAGAGCGTGCCGCCCGAGAAGCAGATTGACCTCCGCAAGGTCCTACTGCT
CGACGAGTCTGTCGACAGCATCATGGACTCGAAGCCCACGGCCAAGGACGGCGCCGGCACGCAAAACGACGACGA
GGATGAGCTGGCCGAGTCGAACCTGGCCACGTACTGCATCCTGGGATGCCTCATCTGCTTCAGCCACTCTTGCGA
CCATGGCGAATACGACAACAAGAACCTCAAACGCACCTTCTCCATATCCTCCTGCTCTCACCTCTCCGACGCCCT
CAAGCGGCGGCGGCGAGACGCCGTCAACGGCCATCTCATGCCTCCGCCTCCCTGCGCGCGGCGGTGTTACCGCCT
CGGCCCCTGGTCTCCGGACCTGGCCGCGTGCCCTCGCCCCTGGTCCGACGACGAGGAGGTTGTGCTCCGATCCAT
CTTCGTCACGGCCTCGCACAGTGTGTACCGAGGCGATGCGATATGCCTGGCAGCCAATTTCCTGAATCGGACCTG
CAACGAGGCCTACGAAAAGTTCCGGTCGCTGCGCATCGTTCTGCCCGAGCCGGCCCCGCGGGAGCCGATCAGGGT
CAAGAATCTGACGTGGTACGACCGCCGGAGGAAGGTTCTCCTGGGGGACTGGCAGGACCACACCGTCAGCCACGA
GCACCAAAGACGGGAGACGCTGGAGCCGTGCTCGCACGAGGGGCCCTGCGTCCCGAGGGTCTGCTCCTGCGTCGA
CGCGGGCCTGCTGTGCGACAAGTTTTGCGGCTGTTCCGTGGAGGACTGCGCCTACAAGTTCACGGGGTGTGCGTG
CCATTCCCAGGGCAAGACGTGCCAGCAGAAGCAGAAGGACAGGCCGTGCATCTGCGTGCAGCTGAACCGAGAGTG
CGACCCGGAGCTGTGCGGCTCGTGCGGCGCCCTGGAGCGTGCGGACCCGCTGAACGCCGACGACACACGGCTCCA
CGCGACGGGCTGCCAAAACTGCGACCTGCAGCGCGGCCTGGGCAAGCCTCTGATCCTGGGTCAGAGCCAGCTCGA
GGGCGTCGGGTACGGCCTCTTCACGGCCGAAGACATCGCGCAGGACGACTTCATCATCGAATACGTCGGAGAGCT
GATCACGCACGACGAGGGCGTGCGCCGAGAGGCGCGGCGCGGCGACGTCTTCGACGAGGACTCCAACATCTCGTA
TGTCTTCACGCTACTCGAGAACGAGGGCATCTGGGTGGACGCGGCGATATACGGCAACCTCAGCCGGTACATCAA
CCACGCGTCCGAGAACGACAAGCGCGGATGCAACATCACGCCGCGGATCCTGTACGTCAACGGGGAGTATCGCAT
CAAGTTCACGGCGATGCGGGACATTGCAGCCGGCGAGGAGCTCTTCTTCAACTACGGCGAGAACTTCCCCAACCT
GACGAAGAAACTGCTGGACCACAAGGCGGGTGAACAGCCCAGCAAGGCCAAGGGGGGGCGGTCACGGCGAGCGGA
AGCCGGGGGCCAGGTGGCGCGGAAGGCGCCCCGGTCGGAGCAGAAGAGGGGCCCGGGCCGGCCCAAGACGAAGAG
GGAGCTCACGGCAGAGAGCGACCTATATAATTTTGAGTCCTCGGAGACGCCGGCGAAGTCGCGAAAGCGCAAGCG
ACGGTCCGACGACAACCCCGGAGAGGAGGACTACCAGCCGTCCGCCGTGAGCGCCGGGCCGTCGCAGGCGACGAA
CGCGGTCGTCGAACCGGAGGATGGCGAAATCGGGTCGATGACGCGACTGCGCAAGCGAACGCGGGCCTCGGCCGG
TATGCAGCCAGCCGACGCGGACATGAAACGCGTCGAGCCGCCCAAGAAGAAAGGCAAGCGGGGCGGCGCGCGACC
AGGAAGCGGCCGGCCTAGAAAGCATCCTCGACCAGTCCCCAAGCCAACGCAAGCTTCAAAAATCAAAGAGGAGGA
CGAGGGGAGGTCCCAGGGGGCAGCAACGGCGGCGACGGAGCCTGCGCCCGCAGTGGCGACGGCGCCCGACCCCAT
GCCACCGCTCGAGCCCGTGACTGCGCCCGCGGTTACGCCTCCGGCCGCGGACGTGGCCGAGGTTGTCCCCGTGCC
CGAAGCTGCGGCCGCCGCAGCTGCGCCCGAGGCTGCACCTGCGACAAGCGCGCCGGTCCCCGCGCCGGAACCTGA
GGTCAAGGCCGAGGTAATCGAAATCCAGGACAGCGACGACGGGGCAGCGAGGGTGGTGTTCAACGACCAGTCGCT
GGTCGAGCTGGGGAGCGAGGACGGGGAAGCGCATGACGAGGAGGACGAGGACCAGGACGTGGTGGTGCGCAAGAG
GAACGACCGGGCGCGAAACCGACGGCCGCCAGCCAAGTTTCGAGAGGACGACATCTGGACTTGA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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