Homo sapiens (human): 8678
Help
Entry
8678 CDS
T01001
Symbol
BECN1, ATG6, VPS30, beclin1
Name
(RefSeq) beclin 1
KO
K08334
beclin
Organism
hsa
Homo sapiens (human)
Pathway
hsa04136
Autophagy - other
hsa04137
Mitophagy - animal
hsa04140
Autophagy - animal
hsa04215
Apoptosis - multiple species
hsa04371
Apelin signaling pathway
hsa05010
Alzheimer disease
hsa05014
Amyotrophic lateral sclerosis
hsa05016
Huntington disease
hsa05017
Spinocerebellar ataxia
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05131
Shigellosis
hsa05167
Kaposi sarcoma-associated herpesvirus infection
Network
nt06164
Kaposi sarcoma-associated herpesvirus (KSHV)
nt06461
Huntington disease
nt06462
Spinocerebellar ataxia
nt06466
Pathways of neurodegeneration
nt06532
Autophagy
Element
N00155
Autophagy-vesicle nucleation/elongation/maturation, mTORC1-PI3KC3-C1
N00177
KSHV vBCL2 to autophagy-vesicle nucleation
N00962
Mutation-inactivated ATXN3 to autophagy-vesicle nucleation
N00993
Mutation-caused aberrant Htt to autophagy-vesicle nucleation
N01715
Autophagy-vesicle nucleation/elongation/maturation, PI3P synthesis by PI3KC3-C1
N01717
Regulation of autophagy-vesicle nucleation/elongation/maturation, ATXN3
N01718
Autophagy-vesicle nucleation/elongation/maturation, PACER-RUBCN-PI3KC3-C2
N01719
Autophagy-vesicle nucleation/elongation/maturation, E3 ubiquitin-ligase Malin
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04371 Apelin signaling pathway
8678 (BECN1)
09140 Cellular Processes
09141 Transport and catabolism
04140 Autophagy - animal
8678 (BECN1)
04136 Autophagy - other
8678 (BECN1)
04137 Mitophagy - animal
8678 (BECN1)
09143 Cell growth and death
04215 Apoptosis - multiple species
8678 (BECN1)
09160 Human Diseases
09172 Infectious disease: viral
05167 Kaposi sarcoma-associated herpesvirus infection
8678 (BECN1)
09171 Infectious disease: bacterial
05131 Shigellosis
8678 (BECN1)
09164 Neurodegenerative disease
05010 Alzheimer disease
8678 (BECN1)
05014 Amyotrophic lateral sclerosis
8678 (BECN1)
05016 Huntington disease
8678 (BECN1)
05017 Spinocerebellar ataxia
8678 (BECN1)
05022 Pathways of neurodegeneration - multiple diseases
8678 (BECN1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
8678 (BECN1)
03029 Mitochondrial biogenesis [BR:
hsa03029
]
8678 (BECN1)
Membrane trafficking [BR:
hsa04131
]
Autophagy
Autophagosome formation proteins
PI3K complex
8678 (BECN1)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial quality control factors
Mitophagy factors
Autophagy-related proteins
8678 (BECN1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
APG6
APG6_N
BH3
MT
HAUS-augmin3
FPP
V_ATPase_I
Exonuc_VII_L
FapA
DUF4200
GAS
Motif
Other DBs
NCBI-GeneID:
8678
NCBI-ProteinID:
NP_001300927
OMIM:
604378
HGNC:
1034
Ensembl:
ENSG00000126581
UniProt:
Q14457
A0A024R1X5
Structure
PDB
LinkDB
All DBs
Position
17:complement(42810132..42824282)
Genome browser
AA seq
450 aa
AA seq
DB search
MEGSKTSNNSTMQVSFVCQRCSQPLKLDTSFKILDRVTIQELTAPLLTTAQAKPGETQEE
ETNSGEEPFIETPRQDGVSRRFIPPARMMSTESANSFTLIGEASDGGTMENLSRRLKVTG
DLFDIMSGQTDVDHPLCEECTDTLLDQLDTQLNVTENECQNYKRCLEILEQMNEDDSEQL
QMELKELALEEERLIQELEDVEKNRKIVAENLEKVQAEAERLDQEEAQYQREYSEFKRQQ
LELDDELKSVENQMRYAQTQLDKLKKTNVFNATFHIWHSGQFGTINNFRLGRLPSVPVEW
NEINAAWGQTVLLLHALANKMGLKFQRYRLVPYGNHSYLESLTDKSKELPLYCSGGLRFF
WDNKFDHAMVAFLDCVQQFKEEVEKGETRFCLPYRMDVEKGKIEDTGGSGGSYSIKTQFN
SEEQWTKALKFMLTNLKWGLAWVSSQFYNK
NT seq
1353 nt
NT seq
+upstream
nt +downstream
nt
atggaagggtctaagacgtccaacaacagcaccatgcaggtgagcttcgtgtgccagcgc
tgcagccagcccctgaaactggacacgagtttcaagatcctggaccgtgtcaccatccag
gaactcacagctccattacttaccacagcccaggcgaaaccaggagagacccaggaggaa
gagactaactcaggagaggagccatttattgaaactcctcgccaggatggtgtctctcgc
agattcatccccccagccaggatgatgtccacagaaagtgccaacagcttcactctgatt
ggggaggcatctgatggcggcaccatggagaacctcagccgaagactgaaggtcactggg
gacctttttgacatcatgtcgggccagacagatgtggatcacccactctgtgaggaatgc
acagatactcttttagaccagctggacactcagctcaacgtcactgaaaatgagtgtcag
aactacaaacgctgtttggagatcttagagcaaatgaatgaggatgacagtgaacagtta
cagatggagctaaaggagctggcactagaggaggagaggctgatccaggagctggaagac
gtggaaaagaaccgcaagatagtggcagaaaatctcgagaaggtccaggctgaggctgag
agactggatcaggaggaagctcagtatcagagagaatacagtgaatttaaacgacagcag
ctggagctggatgatgagctgaagagtgttgaaaaccagatgcgttatgcccagacgcag
ctggataagctgaagaaaaccaacgtctttaatgcaaccttccacatctggcacagtgga
cagtttggcacaatcaataacttcaggctgggtcgcctgcccagtgttcccgtggaatgg
aatgagattaatgctgcttggggccagactgtgttgctgctccatgctctggccaataag
atgggtctgaaatttcagagataccgacttgttccttacggaaaccattcatatctggag
tctctgacagacaaatctaaggagctgccgttatactgttctggggggttgcggtttttc
tgggacaacaagtttgaccatgcaatggtggctttcctggactgtgtgcagcagttcaaa
gaagaggttgagaaaggcgagacacgtttttgtcttccctacaggatggatgtggagaaa
ggcaagattgaagacacaggaggcagtggcggctcctattccatcaaaacccagtttaac
tctgaggagcagtggacaaaagctctcaagttcatgctgacgaatcttaagtggggtctt
gcttgggtgtcctcacaattttataacaaatga
Homo sapiens (human): 5289
Help
Entry
5289 CDS
T01001
Symbol
PIK3C3, VPS34, hVps34
Name
(RefSeq) phosphatidylinositol 3-kinase catalytic subunit type 3
KO
K00914
phosphatidylinositol 3-kinase [EC:
2.7.1.137
]
Organism
hsa
Homo sapiens (human)
Pathway
hsa00562
Inositol phosphate metabolism
hsa01100
Metabolic pathways
hsa04070
Phosphatidylinositol signaling system
hsa04136
Autophagy - other
hsa04140
Autophagy - animal
hsa04145
Phagosome
hsa04371
Apelin signaling pathway
hsa05010
Alzheimer disease
hsa05014
Amyotrophic lateral sclerosis
hsa05016
Huntington disease
hsa05017
Spinocerebellar ataxia
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05131
Shigellosis
hsa05132
Salmonella infection
hsa05152
Tuberculosis
hsa05167
Kaposi sarcoma-associated herpesvirus infection
Network
nt06164
Kaposi sarcoma-associated herpesvirus (KSHV)
nt06181
Salmonella
nt06461
Huntington disease
nt06462
Spinocerebellar ataxia
nt06466
Pathways of neurodegeneration
nt06532
Autophagy
Element
N00155
Autophagy-vesicle nucleation/elongation/maturation, mTORC1-PI3KC3-C1
N00177
KSHV vBCL2 to autophagy-vesicle nucleation
N00962
Mutation-inactivated ATXN3 to autophagy-vesicle nucleation
N00993
Mutation-caused aberrant Htt to autophagy-vesicle nucleation
N01302
Early endosomal fusion
N01303
Salmonella SopB to Early endosomal fusion
N01715
Autophagy-vesicle nucleation/elongation/maturation, PI3P synthesis by PI3KC3-C1
N01718
Autophagy-vesicle nucleation/elongation/maturation, PACER-RUBCN-PI3KC3-C2
N01719
Autophagy-vesicle nucleation/elongation/maturation, E3 ubiquitin-ligase Malin
Drug target
Fimepinostat:
D11319
Safingol:
D05784
Safingol hydrochloride:
D05785
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09100 Metabolism
09101 Carbohydrate metabolism
00562 Inositol phosphate metabolism
5289 (PIK3C3)
09130 Environmental Information Processing
09132 Signal transduction
04371 Apelin signaling pathway
5289 (PIK3C3)
04070 Phosphatidylinositol signaling system
5289 (PIK3C3)
09140 Cellular Processes
09141 Transport and catabolism
04145 Phagosome
5289 (PIK3C3)
04140 Autophagy - animal
5289 (PIK3C3)
04136 Autophagy - other
5289 (PIK3C3)
09160 Human Diseases
09172 Infectious disease: viral
05167 Kaposi sarcoma-associated herpesvirus infection
5289 (PIK3C3)
09171 Infectious disease: bacterial
05132 Salmonella infection
5289 (PIK3C3)
05131 Shigellosis
5289 (PIK3C3)
05152 Tuberculosis
5289 (PIK3C3)
09164 Neurodegenerative disease
05010 Alzheimer disease
5289 (PIK3C3)
05014 Amyotrophic lateral sclerosis
5289 (PIK3C3)
05016 Huntington disease
5289 (PIK3C3)
05017 Spinocerebellar ataxia
5289 (PIK3C3)
05022 Pathways of neurodegeneration - multiple diseases
5289 (PIK3C3)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
5289 (PIK3C3)
Enzymes [BR:
hsa01000
]
2. Transferases
2.7 Transferring phosphorus-containing groups
2.7.1 Phosphotransferases with an alcohol group as acceptor
2.7.1.137 phosphatidylinositol 3-kinase
5289 (PIK3C3)
Membrane trafficking [BR:
hsa04131
]
Endocytosis
Macropinocytosis
Kinases
5289 (PIK3C3)
Rab GTPases and associated proteins
Rab associated proteins
5289 (PIK3C3)
Endosome - Lysosome transport
5289 (PIK3C3)
Autophagy
Autophagosome formation proteins
PI3K complex
5289 (PIK3C3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PI3_PI4_kinase
PI3Ka
PI3K_C2
HEAT_2
Motif
Other DBs
NCBI-GeneID:
5289
NCBI-ProteinID:
NP_002638
OMIM:
602609
HGNC:
8974
Ensembl:
ENSG00000078142
UniProt:
Q8NEB9
Structure
PDB
LinkDB
All DBs
Position
18:41955234..42087830
Genome browser
AA seq
887 aa
AA seq
DB search
MGEAEKFHYIYSCDLDINVQLKIGSLEGKREQKSYKAVLEDPMLKFSGLYQETCSDLYVT
CQVFAEGKPLALPVRTSYKAFSTRWNWNEWLKLPVKYPDLPRNAQVALTIWDVYGPGKAV
PVGGTTVSLFGKYGMFRQGMHDLKVWPNVEADGSEPTKTPGRTSSTLSEDQMSRLAKLTK
AHRQGHMVKVDWLDRLTFREIEMINESEKRSSNFMYLMVEFRCVKCDDKEYGIVYYEKDG
DESSPILTSFELVKVPDPQMSMENLVESKHHKLARSLRSGPSDHDLKPNAATRDQLNIIV
SYPPTKQLTYEEQDLVWKFRYYLTNQEKALTKFLKCVNWDLPQEAKQALELLGKWKPMDV
EDSLELLSSHYTNPTVRRYAVARLRQADDEDLLMYLLQLVQALKYENFDDIKNGLEPTKK
DSQSSVSENVSNSGINSAEIDSSQIITSPLPSVSSPPPASKTKEVPDGENLEQDLCTFLI
SRACKNSTLANYLYWYVIVECEDQDTQQRDPKTHEMYLNVMRRFSQALLKGDKSVRVMRS
LLAAQQTFVDRLVHLMKAVQRESGNRKKKNERLQALLGDNEKMNLSDVELIPLPLEPQVK
IRGIIPETATLFKSALMPAQLFFKTEDGGKYPVIFKHGDDLRQDQLILQIISLMDKLLRK
ENLDLKLTPYKVLATSTKHGFMQFIQSVPVAEVLDTEGSIQNFFRKYAPSENGPNGISAE
VMDTYVKSCAGYCVITYILGVGDRHLDNLLLTKTGKLFHIDFGYILGRDPKPLPPPMKLN
KEMVEGMGGTQSEQYQEFRKQCYTAFLHLRRYSNLILNLFSLMVDANIPDIALEPDKTVK
KVQDKFRLDLSDEEAVHYMQSLIDESVHALFAAVVEQIHKFAQYWRK
NT seq
2664 nt
NT seq
+upstream
nt +downstream
nt
atgggggaagcagagaagtttcactacatctatagttgtgacctggatatcaacgtccag
cttaagataggaagcttggaagggaagagagaacaaaagagttataaagctgtcctggaa
gacccaatgttgaagttctcaggactatatcaagagacatgctctgatctttatgttact
tgtcaagtttttgcagaagggaagcctttggccttgccagtgagaacatcctacaaagca
tttagtacaagatggaactggaatgaatggctgaaactaccagtaaaataccctgacctg
cccaggaatgcccaagtggccctcaccatatgggatgtgtatggtcccggaaaagcagtg
cctgtaggaggaacaacggtttcgctctttggaaaatacggcatgtttcgccaagggatg
catgacttgaaagtctggcctaatgtagaagcagatggatcagaacccacaaaaactcct
ggcagaacaagtagcactctctcagaagatcagatgagccgtcttgccaagctcaccaaa
gctcatcgacaaggacacatggtgaaagtagattggctggatagattgacatttagagaa
atagaaatgataaatgagagtgaaaaacgaagttctaatttcatgtacctgatggttgaa
tttcgatgtgtcaagtgtgatgataaggaatatggtattgtttattatgaaaaggacggt
gatgaatcatctccaattttaacaagttttgaattagtgaaagttcctgacccccagatg
tctatggagaatttagttgagagcaaacaccacaagcttgcccggagtttaagaagtgga
ccttctgaccacgatctgaaacccaatgctgccacgagagatcagttaaatattattgtg
agttatccaccaaccaagcaacttacatatgaagaacaagatcttgtttggaagtttaga
tattatcttacgaatcaagaaaaagccttgacaaaattcttgaaatgtgttaattgggat
ctacctcaagaggccaaacaggccttggaacttctgggaaaatggaagccgatggatgta
gaggactccttggagctgttatcctctcattacaccaacccaactgtgaggcgttatgct
gttgcccggttgcgacaggccgatgatgaggatttgttgatgtacctattacaattggtc
caggctctcaaatatgaaaattttgatgatataaagaatggattggaacctaccaagaag
gatagtcagagttcagtgtcagaaaatgtgtcaaattctggaataaattctgcagaaata
gatagctcccaaattataaccagcccccttccttcagtctcttcacctcctcctgcatca
aaaacaaaagaagttccagatggcgaaaatctggaacaagatctctgtaccttcttgata
tcgagagcctgcaaaaactcaacactggctaattatttatactggtatgtgatagtggaa
tgtgaagatcaagatactcagcagagagatccaaagacccatgagatgtacttgaacgta
atgagaagattcagccaagcattgttgaagggtgataagtctgtcagagttatgcgttct
ttgctggctgcacaacagacatttgtagatcggttggtgcatctaatgaaggcagtacaa
cgcgaaagtggaaatcgtaagaaaaagaatgagagactacaggcattgcttggagataat
gaaaagatgaatttgtcagatgtggaacttatcccgttgcctttagaaccccaagtgaaa
attagaggaataattccggaaacagctacactgtttaaaagtgcccttatgcctgcacag
ttgttttttaagacggaagatggaggcaaatatccagttatatttaagcatggagatgat
ttacgtcaagatcaacttattcttcaaatcatttcactcatggacaagctgttacggaaa
gaaaatctggacttgaaattgacaccttataaggtgttagccaccagtacaaaacatggc
ttcatgcagtttatccagtcagttcctgtggctgaagttcttgatacagagggaagcatt
cagaacttttttagaaaatatgcaccaagtgagaatgggccaaatgggattagtgctgag
gtcatggacacttacgttaaaagctgtgctggatattgcgtgatcacctatatacttgga
gttggagacaggcacctggataaccttttgctaacaaaaacaggcaaactcttccacata
gactttggatatattttgggtcgggatccaaagcctcttcctccaccaatgaagctgaat
aaagaaatggtagaaggaatggggggcacacagagtgagcagtaccaagagttccgtaaa
cagtgttacacggctttcctccacctgcgaaggtattctaatctgattttgaacttgttt
tccttgatggttgatgcaaacattccagatattgcacttgaaccagataaaactgtgaaa
aaggttcaggataaattccgcttagacctgtcggatgaagaggctgtgcattacatgcag
agtctgattgatgagagtgtccatgctctttttgctgcagtggtggaacagattcacaag
tttgcccagtactggagaaaatga
Homo sapiens (human): 22863
Help
Entry
22863 CDS
T01001
Symbol
ATG14, ATG14L, BARKOR, KIAA0831
Name
(RefSeq) autophagy related 14
KO
K17889
beclin 1-associated autophagy-related key regulator
Organism
hsa
Homo sapiens (human)
Pathway
hsa04140
Autophagy - animal
hsa05010
Alzheimer disease
hsa05014
Amyotrophic lateral sclerosis
hsa05016
Huntington disease
hsa05017
Spinocerebellar ataxia
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05131
Shigellosis
hsa05167
Kaposi sarcoma-associated herpesvirus infection
Network
nt06164
Kaposi sarcoma-associated herpesvirus (KSHV)
nt06461
Huntington disease
nt06462
Spinocerebellar ataxia
nt06466
Pathways of neurodegeneration
nt06532
Autophagy
Element
N00155
Autophagy-vesicle nucleation/elongation/maturation, mTORC1-PI3KC3-C1
N00177
KSHV vBCL2 to autophagy-vesicle nucleation
N00962
Mutation-inactivated ATXN3 to autophagy-vesicle nucleation
N00993
Mutation-caused aberrant Htt to autophagy-vesicle nucleation
N01715
Autophagy-vesicle nucleation/elongation/maturation, PI3P synthesis by PI3KC3-C1
N01719
Autophagy-vesicle nucleation/elongation/maturation, E3 ubiquitin-ligase Malin
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04140 Autophagy - animal
22863 (ATG14)
09160 Human Diseases
09172 Infectious disease: viral
05167 Kaposi sarcoma-associated herpesvirus infection
22863 (ATG14)
09171 Infectious disease: bacterial
05131 Shigellosis
22863 (ATG14)
09164 Neurodegenerative disease
05010 Alzheimer disease
22863 (ATG14)
05014 Amyotrophic lateral sclerosis
22863 (ATG14)
05016 Huntington disease
22863 (ATG14)
05017 Spinocerebellar ataxia
22863 (ATG14)
05022 Pathways of neurodegeneration - multiple diseases
22863 (ATG14)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
22863 (ATG14)
03029 Mitochondrial biogenesis [BR:
hsa03029
]
22863 (ATG14)
Membrane trafficking [BR:
hsa04131
]
Autophagy
Autophagosome formation proteins
PI3K complex
22863 (ATG14)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial quality control factors
Mitophagy factors
Autophagy-related proteins
22863 (ATG14)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
ATG14
SHPRH_helical-1st
Exonuc_VII_L
Motif
Other DBs
NCBI-GeneID:
22863
NCBI-ProteinID:
NP_055739
OMIM:
613515
HGNC:
19962
Ensembl:
ENSG00000126775
UniProt:
Q6ZNE5
Structure
PDB
LinkDB
All DBs
Position
14:complement(55366391..55411830)
Genome browser
AA seq
492 aa
AA seq
DB search
MASPSGKGARALEAPGCGPRPLARDLVDSVDDAEGLYVAVERCPLCNTTRRRLTCAKCVQ
SGDFVYFDGRDRERFIDKKERLSRLKSKQEEFQKEVLKAMEGKWITDQLRWKIMSCKMRI
EQLKQTICKGNEEMEKNSEGLLKTKEKNQKLYSRAQRHQEKKEKIQRHNRKLGDLVEKKT
IDLRSHYERLANLRRSHILELTSVIFPIEEVKTGVRDPADVSSESDSAMTSSTVSKLAEA
RRTTYLSGRWVCDDHNGDTSISITGPWISLPNNGDYSAYYSWVEEKKTTQGPDMEQSNPA
YTISAALCYATQLVNILSHILDVNLPKKLCNSEFCGENLSKQKFTRAVKKLNANILYLCF
SQHVNLDQLQPLHTLRNLMYLVSPSSEHLGRSGPFEVRADLEESMEFVDPGVAGESDESG
DERVSDEETDLGTDWENLPSPRFCDIPSQSVEVSQSQSTQASPPIASSSAGGMISSAAAS
VTSWFKAYTGHR
NT seq
1479 nt
NT seq
+upstream
nt +downstream
nt
atggcgtctcccagtgggaagggagcccgggcgctggaggctcctggctgcgggccccgg
ccgctcgcccgggacctggtggactccgtggacgatgcggaggggctgtacgtggctgtg
gagcgctgcccgctgtgcaacactacccgccggcggctgacctgcgccaaatgcgttcag
agcggcgatttcgtctacttcgacggccgcgaccgggagaggtttatcgacaagaaggaa
aggttaagccgacttaagagcaagcaagaagaatttcagaaagaagtgttaaaagctatg
gaaggaaaatggataacagatcagttgagatggaaaataatgtcctgcaagatgaggatt
gaacagttaaaacaaacaatatgtaaaggaaatgaagaaatggagaaaaattctgaaggc
cttctcaaaaccaaggaaaagaatcagaagctttacagtcgagcacaacggcaccaagag
aaaaaggagaagattcagaggcataatcgcaaacttggtgacctggtagaaaaaaagacc
attgacttaagaagtcattatgagcgtctggcaaatcttcgacgatcccatatattagag
ctcacctctgtcatttttccaatcgaggaagtaaagacgggtgtgagagaccccgcagat
gtgtcttcagagagtgacagtgccatgacctccagcactgtgagcaagcttgctgaagcc
cggaggacaacttacctctcaggacgatgggtctgtgacgatcacaacggagacaccagc
attagcattacagggccttggattagcctccctaacaatggggactactctgcctactac
agctgggtggaggagaagaaaacaacccaggggcctgacatggagcagagtaaccctgcc
tacaccatcagtgctgcgctgtgctatgcaactcagctggtcaacattctgtctcatata
cttgatgtaaatcttcccaaaaagctctgcaacagtgaattttgtggcgaaaatctaagc
aagcagaaatttactcgagcagtgaagaaactgaatgcaaatattctttacctttgtttt
tctcagcatgtaaatttagatcaattacaaccactgcataccctcaggaatctaatgtac
ctggtcagtccaagctctgaacacctaggcaggtcagggccctttgaagtacgagcagac
cttgaggagtccatggaatttgtggatcccggagttgctggagaatcagatgagagcgga
gatgagcgcgtcagcgatgaagaaaccgacctgggcacagactgggagaacttgcctagt
ccccggttttgtgatatcccttcccagtctgtggaagtctcccagagtcagagcacccag
gcgtccccacccatcgcgagcagcagtgcaggtgggatgatctcctctgcagcagcctcg
gtgacctcctggtttaaagcttacactggacaccgttaa
DBGET
integrated database retrieval system
