Fungal Genomics

at Utrecht University

General Properties

Protein IDOphauG2|1135
Gene name
LocationContig_1317:1603..4439
Strand+
Gene length (bp)2836
Transcript length (bp)2718
Coding sequence length (bp)2718
Protein length (aa) 906

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF00613 PI3Ka Phosphoinositide 3-kinase family, accessory domain (PIK domain) 2.8E-58 355 524
PF00454 PI3_PI4_kinase Phosphatidylinositol 3- and 4-kinase 3.3E-43 647 850
PF00792 PI3K_C2 Phosphoinositide 3-kinase C2 7.7E-31 57 216

Swissprot hits

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Swissprot ID Swissprot Description Start End E-value
sp|Q6AZN6|PK3C3_XENLA Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Xenopus laevis GN=pik3c3 PE=2 SV=1 5 904 0.0E+00
sp|Q6PF93|PK3C3_MOUSE Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Mus musculus GN=Pik3c3 PE=1 SV=1 5 904 0.0E+00
sp|P54676|PI3K4_DICDI Phosphatidylinositol 3-kinase VPS34-like OS=Dictyostelium discoideum GN=pikE PE=3 SV=2 10 905 0.0E+00
sp|P50520|VPS34_SCHPO Phosphatidylinositol 3-kinase vps34 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=vps34 PE=2 SV=2 91 905 0.0E+00
sp|P42339|PI3K_ARATH Phosphatidylinositol 3-kinase VPS34 OS=Arabidopsis thaliana GN=At1g60490 PE=2 SV=2 8 904 0.0E+00
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Swissprot ID Swissprot Description Start End E-value
sp|Q6AZN6|PK3C3_XENLA Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Xenopus laevis GN=pik3c3 PE=2 SV=1 5 904 0.0E+00
sp|Q6PF93|PK3C3_MOUSE Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Mus musculus GN=Pik3c3 PE=1 SV=1 5 904 0.0E+00
sp|P54676|PI3K4_DICDI Phosphatidylinositol 3-kinase VPS34-like OS=Dictyostelium discoideum GN=pikE PE=3 SV=2 10 905 0.0E+00
sp|P50520|VPS34_SCHPO Phosphatidylinositol 3-kinase vps34 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=vps34 PE=2 SV=2 91 905 0.0E+00
sp|P42339|PI3K_ARATH Phosphatidylinositol 3-kinase VPS34 OS=Arabidopsis thaliana GN=At1g60490 PE=2 SV=2 8 904 0.0E+00
sp|P42347|PI3K1_SOYBN Phosphatidylinositol 3-kinase, root isoform OS=Glycine max PE=2 SV=1 8 904 0.0E+00
sp|P22543|VPS34_YEAST Phosphatidylinositol 3-kinase VPS34 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=VPS34 PE=1 SV=1 7 905 0.0E+00
sp|Q8NEB9|PK3C3_HUMAN Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Homo sapiens GN=PIK3C3 PE=1 SV=1 5 904 0.0E+00
sp|O88763|PK3C3_RAT Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Rattus norvegicus GN=Pik3c3 PE=1 SV=1 5 904 0.0E+00
sp|Q5D891|PK3C3_PIG Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Sus scrofa GN=PIK3C3 PE=2 SV=1 5 904 0.0E+00
sp|P42348|PI3K2_SOYBN Phosphatidylinositol 3-kinase, nodule isoform OS=Glycine max PE=2 SV=1 8 904 0.0E+00
sp|Q92213|VPS34_CANAX Phosphatidylinositol 3-kinase VPS34 OS=Candida albicans GN=VPS34 PE=3 SV=1 11 905 4.0E-174
sp|P54675|PI3K3_DICDI Phosphatidylinositol 3-kinase 3 OS=Dictyostelium discoideum GN=pikC PE=2 SV=2 365 887 7.0E-74
sp|P54673|PI3K1_DICDI Phosphatidylinositol 3-kinase 1 OS=Dictyostelium discoideum GN=pikA PE=2 SV=2 362 902 2.0E-72
sp|O35904|PK3CD_MOUSE Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform OS=Mus musculus GN=Pik3cd PE=1 SV=2 324 877 1.0E-71
sp|O00329|PK3CD_HUMAN Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform OS=Homo sapiens GN=PIK3CD PE=1 SV=2 379 877 1.0E-70
sp|O02697|PK3CG_PIG Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform OS=Sus scrofa GN=PIK3CG PE=1 SV=2 359 882 2.0E-69
sp|Q9JHG7|PK3CG_MOUSE Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform OS=Mus musculus GN=Pik3cg PE=1 SV=2 359 882 2.0E-69
sp|P48736|PK3CG_HUMAN Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform OS=Homo sapiens GN=PIK3CG PE=1 SV=3 359 882 3.0E-69
sp|P54674|PI3K2_DICDI Phosphatidylinositol 3-kinase 2 OS=Dictyostelium discoideum GN=pikB PE=2 SV=2 367 900 2.0E-68
sp|Q8BTI9|PK3CB_MOUSE Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform OS=Mus musculus GN=Pik3cb PE=1 SV=2 367 885 1.0E-62
sp|O00443|P3C2A_HUMAN Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha OS=Homo sapiens GN=PIK3C2A PE=1 SV=2 379 901 2.0E-62
sp|Q9Z1L0|PK3CB_RAT Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform OS=Rattus norvegicus GN=Pik3cb PE=2 SV=1 367 885 2.0E-62
sp|Q5RAY1|P3C2A_PONAB Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha OS=Pongo abelii GN=PIK3C2A PE=2 SV=1 379 901 7.0E-62
sp|P42338|PK3CB_HUMAN Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform OS=Homo sapiens GN=PIK3CB PE=1 SV=1 367 885 1.0E-61
sp|P32871|PK3CA_BOVIN Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform OS=Bos taurus GN=PIK3CA PE=1 SV=1 354 877 2.0E-61
sp|P42337|PK3CA_MOUSE Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform OS=Mus musculus GN=Pik3ca PE=1 SV=2 354 877 2.0E-61
sp|P42336|PK3CA_HUMAN Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform OS=Homo sapiens GN=PIK3CA PE=1 SV=2 354 877 3.0E-61
sp|Q61194|P3C2A_MOUSE Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha OS=Mus musculus GN=Pik3c2a PE=1 SV=2 379 901 1.0E-60
sp|O00750|P3C2B_HUMAN Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit beta OS=Homo sapiens GN=PIK3C2B PE=1 SV=2 366 901 6.0E-56
sp|O70167|P3C2G_MOUSE Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma OS=Mus musculus GN=Pik3c2g PE=2 SV=1 378 901 6.0E-55
sp|O70173|P3C2G_RAT Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma OS=Rattus norvegicus GN=Pik3c2g PE=2 SV=1 375 901 1.0E-54
sp|O75747|P3C2G_HUMAN Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma OS=Homo sapiens GN=PIK3C2G PE=1 SV=3 378 901 6.0E-52
sp|Q94125|AGE1_CAEEL Phosphatidylinositol 3-kinase age-1 OS=Caenorhabditis elegans GN=age-1 PE=1 SV=6 378 882 1.0E-47
sp|P0C5E7|AGE1_CAEBR Phosphatidylinositol 3-kinase age-1 OS=Caenorhabditis briggsae GN=age-1 PE=3 SV=1 368 827 9.0E-43
sp|Q8SQY7|STT4_ENCCU Probable phosphatidylinositol 4-kinase STT4 homolog OS=Encephalitozoon cuniculi (strain GB-M1) GN=STT4 PE=3 SV=2 429 873 2.0E-34
sp|P54677|PI4K_DICDI Phosphatidylinositol 4-kinase OS=Dictyostelium discoideum GN=pikD PE=3 SV=3 647 903 3.0E-34
sp|A4IID4|PI4KB_XENTR Phosphatidylinositol 4-kinase beta OS=Xenopus tropicalis GN=pi4kb PE=2 SV=1 649 894 5.0E-32
sp|Q49GP3|PI4KB_DANRE Phosphatidylinositol 4-kinase beta OS=Danio rerio GN=pi4kb PE=2 SV=2 649 894 7.0E-32
sp|Q8BKC8|PI4KB_MOUSE Phosphatidylinositol 4-kinase beta OS=Mus musculus GN=Pi4kb PE=1 SV=2 649 894 1.0E-31
sp|O08561|PI4KB_RAT Phosphatidylinositol 4-kinase beta OS=Rattus norvegicus GN=Pi4kb PE=1 SV=1 649 894 2.0E-31
sp|B3EX61|PI4KB_SORAR Phosphatidylinositol 4-kinase beta OS=Sorex araneus GN=PI4KB PE=3 SV=1 649 894 6.0E-31
sp|Q9UBF8|PI4KB_HUMAN Phosphatidylinositol 4-kinase beta OS=Homo sapiens GN=PI4KB PE=1 SV=1 649 894 6.0E-31
sp|B4UT09|PI4KB_OTOGA Phosphatidylinositol 4-kinase beta OS=Otolemur garnettii GN=PI4KB PE=3 SV=1 649 894 6.0E-31
sp|B0KWC1|PI4KB_CALJA Phosphatidylinositol 4-kinase beta OS=Callithrix jacchus GN=PI4KB PE=3 SV=1 649 894 6.0E-31
sp|B2KI64|PI4KB_RHIFE Phosphatidylinositol 4-kinase beta OS=Rhinolophus ferrumequinum GN=PI4KB PE=3 SV=1 649 894 6.0E-31
sp|A9X1A0|PI4KB_PAPAN Phosphatidylinositol 4-kinase beta OS=Papio anubis GN=PI4KB PE=3 SV=2 649 894 6.0E-31
sp|B1MTG7|PI4KB_CALMO Phosphatidylinositol 4-kinase beta OS=Callicebus moloch GN=PI4KB PE=3 SV=1 649 894 6.0E-31
sp|Q6GN16|PI4KB_XENLA Phosphatidylinositol 4-kinase beta OS=Xenopus laevis GN=pi4kb PE=2 SV=1 649 894 1.0E-30
sp|O02810|PI4KB_BOVIN Phosphatidylinositol 4-kinase beta OS=Bos taurus GN=PI4KB PE=1 SV=2 649 894 3.0E-30
sp|Q5UR69|YL615_MIMIV Putative phosphatidylinositol kinase L615 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_L615 PE=3 SV=1 510 839 3.0E-29
sp|Q9SXA1|P4KA1_ARATH Phosphatidylinositol 4-kinase alpha 1 OS=Arabidopsis thaliana GN=PI4KA1 PE=1 SV=2 364 873 1.0E-28
sp|O08662|PI4KA_RAT Phosphatidylinositol 4-kinase alpha OS=Rattus norvegicus GN=Pi4ka PE=1 SV=1 414 885 1.0E-27
sp|P42356|PI4KA_HUMAN Phosphatidylinositol 4-kinase alpha OS=Homo sapiens GN=PI4KA PE=1 SV=3 414 885 4.0E-27
sp|O02811|PI4KA_BOVIN Phosphatidylinositol 4-kinase alpha OS=Bos taurus GN=PI4KA PE=2 SV=1 414 885 1.0E-26
sp|Q9FMJ0|P4KB1_ARATH Phosphatidylinositol 4-kinase beta 1 OS=Arabidopsis thaliana GN=PI4KB1 PE=1 SV=1 649 873 6.0E-26
sp|Q9USR3|STT4_SCHPO Phosphatidylinositol 4-kinase stt4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=stt4 PE=3 SV=1 640 882 9.0E-26
sp|Q0WPX9|P4KB2_ARATH Phosphatidylinositol 4-kinase beta 2 OS=Arabidopsis thaliana GN=PI4KB2 PE=2 SV=1 649 873 4.0E-25
sp|P39104|PIK1_YEAST Phosphatidylinositol 4-kinase PIK1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PIK1 PE=1 SV=1 649 903 2.0E-24
sp|Q8SR56|VPS34_ENCCU Probable phosphatidylinositol 3-kinase VPS34 homolog OS=Encephalitozoon cuniculi (strain GB-M1) GN=VPS34 PE=3 SV=2 611 904 2.0E-23
sp|P37297|STT4_YEAST Phosphatidylinositol 4-kinase STT4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=STT4 PE=1 SV=1 650 881 2.0E-23
sp|Q9C680|P4KA2_ARATH Phosphatidylinositol 4-kinase alpha 2 OS=Arabidopsis thaliana GN=PI4KA2 PE=1 SV=1 581 880 2.0E-21
sp|A4QPH2|PI4P2_HUMAN Putative phosphatidylinositol 4-kinase alpha-like protein P2 OS=Homo sapiens GN=PI4KAP2 PE=5 SV=3 650 885 3.0E-19
sp|Q9UW20|PIK1_CANAL Phosphatidylinositol 4-kinase PIK1alpha OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=PIKALPHA PE=3 SV=1 649 841 3.0E-19
sp|Q9UW24|PIK1A_CANAL Phosphatidylinositol 4-kinase PIK1a OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=PIKA PE=3 SV=1 649 841 2.0E-18
sp|P38110|ATM_YEAST Serine/threonine-protein kinase TEL1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=TEL1 PE=1 SV=3 634 880 2.0E-14
sp|Q5BHE2|ATM_EMENI Serine/threonine-protein kinase tel1 OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=tel1 PE=3 SV=1 644 843 3.0E-11
sp|Q4WVM7|ATM_ASPFU Serine/threonine-protein kinase tel1 OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=tel1 PE=3 SV=2 642 853 8.0E-11
sp|Q59LR2|ATR_CANAL Serine/threonine-protein kinase MEC1 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=MEC1 PE=3 SV=1 623 874 1.0E-10
sp|Q6CAD2|ATM_YARLI Serine/threonine-protein kinase TEL1 OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=TEL1 PE=3 SV=1 605 855 6.0E-10
sp|Q10366|PIK1_SCHPO Phosphatidylinositol 4-kinase pik1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=pik1 PE=1 SV=1 649 850 7.0E-09
sp|Q62388|ATM_MOUSE Serine-protein kinase ATM OS=Mus musculus GN=Atm PE=1 SV=2 605 857 1.0E-08
sp|Q75DB8|ATR_ASHGO Serine/threonine-protein kinase MEC1 OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=MEC1 PE=3 SV=3 627 863 3.0E-08
sp|Q13315|ATM_HUMAN Serine-protein kinase ATM OS=Homo sapiens GN=ATM PE=1 SV=4 655 857 4.0E-08
sp|Q6CT34|ATR_KLULA Serine/threonine-protein kinase MEC1 OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=MEC1 PE=3 SV=1 624 863 2.0E-07
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GO

(None)

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)		 D score
(significance: > 0.45)
No 1 - 39 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 >OphauG2|1135
MADYGRMDPFSFAGSKDLDLPVSVRIINLEGHEPPVKASTLVDRPDLRHIGSNTSASSDVFVTVQVWAGSKPLTV
PVQTAYKPFRLERRWNEWLELPISYKQLPANARLAMTIWDLSPSGARDTLAHAIPFGGTTLPLFDADNQVHKGRQ
KCLVHRHCRADGTDASRTPALVSASMGRAKLSLDQDAEELDRMEKLFKKHEMGEIPRVDWLDQLVFRTFEKRGLQ
AAKSSLKLLHAAGHDADHDADHDADHDASHQAVFLLNVQLVRFDFPIVFADHEYEPPPISPLHPLSASQANLPPR
QPQVHLGPGINAVAHGAHGSLIKVYDPEVGQRDNPAEAKHRRLFRSSHRRGILDKDLKPNAKVRDELNMVMSYPP
THVLSPEEADLVWKFRYHLTRDKRALTKFVKSVNWADQSEAKQAIQVLGRWTEIDVDDALELLGPSFDNPAVRSY
AVDRLRKSGDEELLLYLLQLVQALKYEHISADSGHESIRDSSLASFLVQRAAANFMLGNYFYWYLMVECDDHSPE
QGQENRNIYRKVAYDFVSELVKQPGGSQDRKTLLRQAEMVAILSKLAADVKASSESIAKKVDRVKSFLADAKNEL
VAFDPPLPMPLDPSIKVTGVMRDQVVVFKSSLNPIKLCFKTTAGTAYPVIFKLGDDMRQDQLVIQIITLMDQLLQ
KENLDLRLTPYKILATSTTAGASQFVQSQSLSSIVNKFKTNPALAYLRHHNPDDRQPLGVRQETLDTYVRSCAGY
CVITYILGVGDRHLDNLLLAPDGHFFHADFGFILGRDPKPFAPVMKLSKEMVDCMGGVNSDHYQRFRQYCFLAYA
ALRKSSNLILNLFSLMMHANIPDIRLEPDKAVLKVRERFHLELSEEEAIVYFGNVIDGTLTAFAPVVIDKLHEWA
QALRA*
Coding >OphauG2|1135
ATGGCCGACTACGGCCGCATGGATCCCTTTTCCTTTGCCGGCTCCAAGGACCTTGATCTGCCCGTCAGCGTCCGC
ATAATCAACTTGGAAGGCCATGAGCCTCCTGTAAAGGCGTCGACGCTGGTTGACCGGCCCGACCTCAGACATATA
GGATCCAACACGAGTGCCTCTTCGGATGTTTTTGTCACTGTCCAGGTCTGGGCTGGCTCCAAGCCGCTGACGGTT
CCTGTGCAGACGGCATACAAGCCATTTCGACTGGAGCGCAGATGGAACGAGTGGCTCGAGCTGCCCATCAGCTAC
AAGCAGCTGCCTGCCAACGCCCGCCTTGCCATGACGATATGGGACTTGTCGCCCTCGGGAGCCCGCGACACGCTG
GCCCACGCCATCCCCTTTGGCGGCACCACACTGCCCCTGTTTGACGCCGACAACCAGGTGCACAAGGGCCGCCAG
AAATGCCTTGTCCACAGACACTGCCGCGCCGACGGAACAGACGCCTCGCGCACCCCGGCGCTCGTCTCGGCCAGC
ATGGGCCGCGCCAAGCTGAGCCTGGACCAAGATGCCGAGGAGCTGGACCGCATGGAGAAGCTGTTCAAAAAGCAC
GAAATGGGCGAGATTCCCCGTGTCGACTGGCTCGACCAGCTCGTGTTTCGCACCTTTGAGAAGCGCGGCCTGCAG
GCGGCAAAGTCGTCGTTGAAGCTGCTGCACGCCGCTGGCCACGACGCAGACCACGACGCAGACCACGACGCAGAC
CACGACGCCAGCCACCAGGCCGTCTTTTTGCTCAACGTCCAACTCGTGCGCTTCGACTTTCCCATCGTCTTTGCC
GACCACGAGTACGAGCCGCCGCCTATATCGCCCCTTCACCCGCTGTCGGCATCCCAGGCAAATCTGCCGCCGCGA
CAGCCCCAAGTCCACCTGGGCCCTGGCATCAACGCTGTGGCGCATGGCGCCCATGGCTCGCTCATCAAGGTCTAC
GACCCCGAGGTGGGACAGAGGGACAATCCTGCAGAGGCCAAGCACCGCCGCCTGTTTCGCAGCTCGCACCGCCGC
GGCATCTTGGACAAGGACCTCAAGCCCAATGCCAAGGTGCGCGACGAGCTCAACATGGTCATGTCGTACCCGCCC
ACCCACGTCCTCTCGCCCGAGGAGGCCGACCTGGTGTGGAAGTTTCGCTATCACTTGACGCGCGACAAGAGGGCC
CTGACCAAGTTTGTCAAGTCGGTCAACTGGGCCGACCAGAGCGAGGCCAAGCAGGCAATCCAGGTGCTTGGCCGC
TGGACCGAGATTGACGTCGACGATGCCCTCGAGCTGCTTGGCCCCTCGTTCGACAACCCGGCTGTTCGCTCCTAT
GCCGTCGACCGCCTGCGCAAGTCGGGCGACGAGGAGCTTTTGCTCTACCTGCTGCAGCTGGTGCAGGCTCTCAAG
TACGAGCACATATCGGCCGACTCGGGCCACGAGAGCATCCGTGACTCGTCGCTGGCCAGCTTCCTCGTCCAACGT
GCCGCCGCCAACTTTATGCTGGGCAACTATTTCTACTGGTATCTCATGGTTGAGTGCGACGACCACAGCCCGGAG
CAGGGCCAGGAAAACCGCAACATCTACCGCAAGGTGGCCTACGACTTTGTCTCGGAGCTTGTCAAGCAGCCGGGC
GGCAGCCAAGACAGGAAGACGCTGCTGCGCCAGGCAGAAATGGTTGCCATTCTCTCCAAATTGGCCGCCGACGTC
AAGGCCTCGAGCGAGTCCATTGCCAAAAAGGTGGACCGTGTCAAGAGCTTCTTGGCAGACGCCAAGAATGAACTT
GTCGCCTTTGATCCACCCCTGCCCATGCCTCTGGATCCGTCCATCAAGGTGACTGGCGTCATGCGCGACCAGGTG
GTGGTGTTCAAGTCGTCGCTCAATCCCATCAAGCTGTGCTTCAAGACCACGGCAGGCACCGCGTACCCCGTCATC
TTCAAACTCGGCGACGACATGAGGCAGGATCAGCTCGTCATCCAGATCATCACCCTCATGGACCAGCTGCTGCAA
AAGGAGAATCTGGACCTGCGGCTGACGCCCTACAAGATTTTGGCCACGAGCACTACAGCAGGCGCATCGCAGTTT
GTCCAGTCCCAGAGCCTCTCGAGCATTGTCAACAAGTTCAAGACCAATCCGGCCCTGGCCTATCTGCGACATCAC
AACCCCGACGACCGCCAGCCGCTGGGAGTGCGGCAGGAGACGCTTGACACATATGTGCGCTCCTGCGCCGGGTAC
TGCGTCATCACGTACATTCTGGGGGTCGGGGATCGCCACCTGGACAATCTGCTGCTGGCCCCCGACGGGCATTTT
TTCCACGCCGACTTTGGCTTTATTCTGGGCCGCGATCCCAAGCCCTTTGCGCCCGTCATGAAGCTTTCCAAAGAA
ATGGTGGACTGCATGGGGGGCGTCAATTCGGACCACTACCAGCGCTTCAGGCAGTACTGTTTTCTTGCCTATGCT
GCCCTGCGCAAGTCGTCCAACCTCATCCTCAATCTCTTTAGCCTCATGATGCACGCAAACATTCCCGACATTCGC
CTGGAGCCGGACAAGGCGGTGCTCAAGGTGCGCGAGCGGTTTCATCTTGAGCTCAGCGAGGAAGAAGCCATTGTA
TACTTTGGCAATGTTATAGACGGAACTTTGACAGCCTTTGCGCCTGTGGTTATTGACAAGCTGCACGAGTGGGCG
CAGGCACTGCGGGCGTAG
Transcript >OphauG2|1135
ATGGCCGACTACGGCCGCATGGATCCCTTTTCCTTTGCCGGCTCCAAGGACCTTGATCTGCCCGTCAGCGTCCGC
ATAATCAACTTGGAAGGCCATGAGCCTCCTGTAAAGGCGTCGACGCTGGTTGACCGGCCCGACCTCAGACATATA
GGATCCAACACGAGTGCCTCTTCGGATGTTTTTGTCACTGTCCAGGTCTGGGCTGGCTCCAAGCCGCTGACGGTT
CCTGTGCAGACGGCATACAAGCCATTTCGACTGGAGCGCAGATGGAACGAGTGGCTCGAGCTGCCCATCAGCTAC
AAGCAGCTGCCTGCCAACGCCCGCCTTGCCATGACGATATGGGACTTGTCGCCCTCGGGAGCCCGCGACACGCTG
GCCCACGCCATCCCCTTTGGCGGCACCACACTGCCCCTGTTTGACGCCGACAACCAGGTGCACAAGGGCCGCCAG
AAATGCCTTGTCCACAGACACTGCCGCGCCGACGGAACAGACGCCTCGCGCACCCCGGCGCTCGTCTCGGCCAGC
ATGGGCCGCGCCAAGCTGAGCCTGGACCAAGATGCCGAGGAGCTGGACCGCATGGAGAAGCTGTTCAAAAAGCAC
GAAATGGGCGAGATTCCCCGTGTCGACTGGCTCGACCAGCTCGTGTTTCGCACCTTTGAGAAGCGCGGCCTGCAG
GCGGCAAAGTCGTCGTTGAAGCTGCTGCACGCCGCTGGCCACGACGCAGACCACGACGCAGACCACGACGCAGAC
CACGACGCCAGCCACCAGGCCGTCTTTTTGCTCAACGTCCAACTCGTGCGCTTCGACTTTCCCATCGTCTTTGCC
GACCACGAGTACGAGCCGCCGCCTATATCGCCCCTTCACCCGCTGTCGGCATCCCAGGCAAATCTGCCGCCGCGA
CAGCCCCAAGTCCACCTGGGCCCTGGCATCAACGCTGTGGCGCATGGCGCCCATGGCTCGCTCATCAAGGTCTAC
GACCCCGAGGTGGGACAGAGGGACAATCCTGCAGAGGCCAAGCACCGCCGCCTGTTTCGCAGCTCGCACCGCCGC
GGCATCTTGGACAAGGACCTCAAGCCCAATGCCAAGGTGCGCGACGAGCTCAACATGGTCATGTCGTACCCGCCC
ACCCACGTCCTCTCGCCCGAGGAGGCCGACCTGGTGTGGAAGTTTCGCTATCACTTGACGCGCGACAAGAGGGCC
CTGACCAAGTTTGTCAAGTCGGTCAACTGGGCCGACCAGAGCGAGGCCAAGCAGGCAATCCAGGTGCTTGGCCGC
TGGACCGAGATTGACGTCGACGATGCCCTCGAGCTGCTTGGCCCCTCGTTCGACAACCCGGCTGTTCGCTCCTAT
GCCGTCGACCGCCTGCGCAAGTCGGGCGACGAGGAGCTTTTGCTCTACCTGCTGCAGCTGGTGCAGGCTCTCAAG
TACGAGCACATATCGGCCGACTCGGGCCACGAGAGCATCCGTGACTCGTCGCTGGCCAGCTTCCTCGTCCAACGT
GCCGCCGCCAACTTTATGCTGGGCAACTATTTCTACTGGTATCTCATGGTTGAGTGCGACGACCACAGCCCGGAG
CAGGGCCAGGAAAACCGCAACATCTACCGCAAGGTGGCCTACGACTTTGTCTCGGAGCTTGTCAAGCAGCCGGGC
GGCAGCCAAGACAGGAAGACGCTGCTGCGCCAGGCAGAAATGGTTGCCATTCTCTCCAAATTGGCCGCCGACGTC
AAGGCCTCGAGCGAGTCCATTGCCAAAAAGGTGGACCGTGTCAAGAGCTTCTTGGCAGACGCCAAGAATGAACTT
GTCGCCTTTGATCCACCCCTGCCCATGCCTCTGGATCCGTCCATCAAGGTGACTGGCGTCATGCGCGACCAGGTG
GTGGTGTTCAAGTCGTCGCTCAATCCCATCAAGCTGTGCTTCAAGACCACGGCAGGCACCGCGTACCCCGTCATC
TTCAAACTCGGCGACGACATGAGGCAGGATCAGCTCGTCATCCAGATCATCACCCTCATGGACCAGCTGCTGCAA
AAGGAGAATCTGGACCTGCGGCTGACGCCCTACAAGATTTTGGCCACGAGCACTACAGCAGGCGCATCGCAGTTT
GTCCAGTCCCAGAGCCTCTCGAGCATTGTCAACAAGTTCAAGACCAATCCGGCCCTGGCCTATCTGCGACATCAC
AACCCCGACGACCGCCAGCCGCTGGGAGTGCGGCAGGAGACGCTTGACACATATGTGCGCTCCTGCGCCGGGTAC
TGCGTCATCACGTACATTCTGGGGGTCGGGGATCGCCACCTGGACAATCTGCTGCTGGCCCCCGACGGGCATTTT
TTCCACGCCGACTTTGGCTTTATTCTGGGCCGCGATCCCAAGCCCTTTGCGCCCGTCATGAAGCTTTCCAAAGAA
ATGGTGGACTGCATGGGGGGCGTCAATTCGGACCACTACCAGCGCTTCAGGCAGTACTGTTTTCTTGCCTATGCT
GCCCTGCGCAAGTCGTCCAACCTCATCCTCAATCTCTTTAGCCTCATGATGCACGCAAACATTCCCGACATTCGC
CTGGAGCCGGACAAGGCGGTGCTCAAGGTGCGCGAGCGGTTTCATCTTGAGCTCAGCGAGGAAGAAGCCATTGTA
TACTTTGGCAATGTTATAGACGGAACTTTGACAGCCTTTGCGCCTGTGGTTATTGACAAGCTGCACGAGTGGGCG
CAGGCACTGCGGGCGTAG
Gene >OphauG2|1135
ATGGCCGACTACGGCCGCATGGATCCCTTTTCCTTTGCCGGCTCCAAGGACCTTGATCTGCCCGTCAGCGTCCGC
ATGTGCGTCTCGGTCCGTGCCGCCAAAGACGCAATGGCTTGGCTGACGTGCGCCCTGCAGAATCAACTTGGAAGG
CCATGAGCCTCCTGTAAAGGCGTCGACGCTGGTTGACCGGCCCGACCTCAGACATATAGGATCCAACACGAGTGC
CTCTTCGGATGTTTTTGTCACTGTCCAGGTCTGGGCTGGCTCCAAGCCGCTGACGGTTCCTGTGCAGACGGCATA
CAAGCCATTTCGACTGGAGCGCAGGTATGTGTGTCTGGCCGCCGACAAGAGATGAAAGGCTAAGCAAGCCATGCC
CGTGTCCAGATGGAACGAGTGGCTCGAGCTGCCCATCAGCTACAAGCAGCTGCCTGCCAACGCCCGCCTTGCCAT
GACGATATGGGACTTGTCGCCCTCGGGAGCCCGCGACACGCTGGCCCACGCCATCCCCTTTGGCGGCACCACACT
GCCCCTGTTTGACGCCGACAACCAGGTGCACAAGGGCCGCCAGAAATGCCTTGTCCACAGACACTGCCGCGCCGA
CGGAACAGACGCCTCGCGCACCCCGGCGCTCGTCTCGGCCAGCATGGGCCGCGCCAAGCTGAGCCTGGACCAAGA
TGCCGAGGAGCTGGACCGCATGGAGAAGCTGTTCAAAAAGCACGAAATGGGCGAGATTCCCCGTGTCGACTGGCT
CGACCAGCTCGTGTTTCGCACCTTTGAGAAGCGCGGCCTGCAGGCGGCAAAGTCGTCGTTGAAGCTGCTGCACGC
CGCTGGCCACGACGCAGACCACGACGCAGACCACGACGCAGACCACGACGCCAGCCACCAGGCCGTCTTTTTGCT
CAACGTCCAACTCGTGCGCTTCGACTTTCCCATCGTCTTTGCCGACCACGAGTACGAGCCGCCGCCTATATCGCC
CCTTCACCCGCTGTCGGCATCCCAGGCAAATCTGCCGCCGCGACAGCCCCAAGTCCACCTGGGCCCTGGCATCAA
CGCTGTGGCGCATGGCGCCCATGGCTCGCTCATCAAGGTCTACGACCCCGAGGTGGGACAGAGGGACAATCCTGC
AGAGGCCAAGCACCGCCGCCTGTTTCGCAGCTCGCACCGCCGCGGCATCTTGGACAAGGACCTCAAGCCCAATGC
CAAGGTGCGCGACGAGCTCAACATGGTCATGTCGTACCCGCCCACCCACGTCCTCTCGCCCGAGGAGGCCGACCT
GGTGTGGAAGTTTCGCTATCACTTGACGCGCGACAAGAGGGCCCTGACCAAGTTTGTCAAGTCGGTCAACTGGGC
CGACCAGAGCGAGGCCAAGCAGGCAATCCAGGTGCTTGGCCGCTGGACCGAGATTGACGTCGACGATGCCCTCGA
GCTGCTTGGCCCCTCGTTCGACAACCCGGCTGTTCGCTCCTATGCCGTCGACCGCCTGCGCAAGTCGGGCGACGA
GGAGCTTTTGCTCTACCTGCTGCAGCTGGTGCAGGCTCTCAAGTACGAGCACATATCGGCCGACTCGGGCCACGA
GAGCATCCGTGACTCGTCGCTGGCCAGCTTCCTCGTCCAACGTGCCGCCGCCAACTTTATGCTGGGCAACTATTT
CTACTGGTATCTCATGGTTGAGTGCGACGACCACAGCCCGGAGCAGGGCCAGGAAAACCGCAACATCTACCGCAA
GGTGGCCTACGACTTTGTCTCGGAGCTTGTCAAGCAGCCGGGCGGCAGCCAAGACAGGAAGACGCTGCTGCGCCA
GGCAGAAATGGTTGCCATTCTCTCCAAATTGGCCGCCGACGTCAAGGCCTCGAGCGAGTCCATTGCCAAAAAGGT
GGACCGTGTCAAGAGCTTCTTGGCAGACGCCAAGAATGAACTTGTCGCCTTTGATCCACCCCTGCCCATGCCTCT
GGATCCGTCCATCAAGGTGACTGGCGTCATGCGCGACCAGGTGGTGGTGTTCAAGTCGTCGCTCAATCCCATCAA
GCTGTGCTTCAAGACCACGGCAGGCACCGCGTACCCCGTCATCTTCAAACTCGGCGACGACATGAGGCAGGATCA
GCTCGTCATCCAGATCATCACCCTCATGGACCAGCTGCTGCAAAAGGAGAATCTGGACCTGCGGCTGACGCCCTA
CAAGATTTTGGCCACGAGCACTACAGCAGGCGCATCGCAGTTTGTCCAGTCCCAGAGCCTCTCGAGCATTGTCAA
CAAGTTCAAGACCAATCCGGCCCTGGCCTATCTGCGACATCACAACCCCGACGACCGCCAGCCGCTGGGAGTGCG
GCAGGAGACGCTTGACACATATGTGCGCTCCTGCGCCGGGTACTGCGTCATCACGTACATTCTGGGGGTCGGGGA
TCGCCACCTGGACAATCTGCTGCTGGCCCCCGACGGGCATTTTTTCCACGCCGACTTTGGCTTTATTCTGGGCCG
CGATCCCAAGCCCTTTGCGCCCGTCATGAAGCTTTCCAAAGAAATGGTGGACTGCATGGGGGGCGTCAATTCGGA
CCACTACCAGCGCTTCAGGCAGTACTGTTTTCTTGCCTATGCTGCCCTGCGCAAGTCGTCCAACCTCATCCTCAA
TCTCTTTAGCCTCATGATGCACGCAAACATTCCCGACATTCGCCTGGAGCCGGACAAGGCGGTGCTCAAGGTGCG
CGAGCGGTTTCATCTTGAGCTCAGCGAGGAAGAAGCCATTGTATACTTTGGCAATGTTATAGACGGAACTTTGAC
AGCCTTTGCGCCTGTGGTTATTGACAAGCTGCACGAGTGGGCGCAGGCACTGCGGGCGTAG

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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