KEGG   Homo sapiens (human): 100170841
Entry
100170841         CDS       T01001                                 
Symbol
EPOP, C17orf96, PRR28
Name
(RefSeq) elongin BC and polycomb repressive complex 2 associated protein
  KO
K26259  elongin BC and Polycomb repressive complex 2-associated protein
Organism
hsa  Homo sapiens (human)
Pathway
hsa03083  Polycomb repressive complex
Network
nt06523  Epigenetic regulation by Polycomb complexes
  Element
N01577  Gene silencing by methylation of H3K27 and ubiquitination of H2AK119
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09126 Chromosome
   03083 Polycomb repressive complex
    100170841 (EPOP)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    100170841 (EPOP)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Histone modification proteins
   Polycomb repressive complex (PRC) and associated proteins
    PRC2.1
     100170841 (EPOP)
SSDB
Motif
Pfam: EPOP
Other DBs
NCBI-GeneID: 100170841
NCBI-ProteinID: NP_001124149
OMIM: 617795
HGNC: 34493
Ensembl: ENSG00000273604
UniProt: A6NHQ4
LinkDB
Position
17:complement(38671703..38674957)
AA seq 379 aa
METLCPAPRLAVPASPRGSPCSPTPRKPCRGTQEFSPLCLRALAFCALAKPRASSLGPGP
GELAARSPVLRGPQAPLRPGGWAPDGLKHLWAPTGRPGVPNTAAGEDADVAACPRRGEEE
EGGGGFPHFGVRSCAPPGRCPAPPHPRESTTSFASAPPRPAPGLEPQRGPAASPPQEPSS
RPPSPPAGLSTEPAGPGTAPRPFLPGQPAEVDGNPPPAAPEAPAASPSTASPAPAAPGDL
RQEHFDRLIRRSKLWCYAKGFALDTPSLRRGPERPPAKGPARGAAKKRRLPAPPPRTAQP
RRPAPTLPTTSTFSLLNCFPCPPALVVGEDGDLKPASSLRLQGDSKPPPAHPLWRWQMGG
PAVPEPPGLKFWGINMDES
NT seq 1140 nt   +upstreamnt  +downstreamnt
atggagaccctgtgccctgcgccccgcctggcagtgccggcgtccccgcgagggtcgccc
tgctcccccacgccccggaagccgtgtcgggggacccaggaattctctccgctgtgcctg
cgtgccctcgccttctgcgcccttgccaagccccgggcgtcctctctgggcccggggcct
ggggagctggcggcgcggtccccagtgctgcggggccctcaggcccccctgcgccctggc
ggctgggccccggatggcctgaagcacctctgggcaccgaccgggcggcccggcgttcct
aacaccgccgccggcgaggatgcggacgtcgcagcgtgcccccgccgcggagaggaggaa
gagggcggaggcggtttcccgcacttcggcgttcgctcctgtgcacctccgggccgctgc
cctgcgcccccgcaccctcgggaatctacgaccagcttcgcctcggccccgcctcgcccg
gccccgggtctcgagcctcagcgtggcccagccgccagcccgcctcaggaacccagttcc
cggcctccgtcgccacctgcgggcctctccaccgagcccgcgggtcccgggacggcgccg
cggccgttcctgcccggccagcctgccgaagtcgatggaaaccccccgccggccgccccc
gaggctccagcggccagcccctcgacggccagcccggctccggccgcacccggagatctc
cgccaggaacatttcgatcgtctgatccgccggtcgaaactttggtgttacgcgaagggc
ttcgccttggacactccgagtttgcgccgggggccagagcggccgcctgcgaaagggccg
gctcggggagccgccaagaaacgccggctgccggcgccccctccgcgcaccgcgcagccc
cgccgccctgcaccgacgctccccaccacgagcaccttcagcctcctcaactgcttcccc
tgccccccggccctggtggtgggggaagacggagacctaaagccggcatcctcgcttcgc
ctccagggagactctaagcccccgcccgcccacccgctgtggaggtggcagatggggggt
cccgctgtccctgagccccctggcctcaaattctgggggatcaacatggatgaaagctga

KEGG   Homo sapiens (human): 6923
Entry
6923              CDS       T01001                                 
Symbol
ELOB, SIII, TCEB2
Name
(RefSeq) elongin B
  KO
K03873  elongin-B
Organism
hsa  Homo sapiens (human)
Pathway
hsa04066  HIF-1 signaling pathway
hsa04120  Ubiquitin mediated proteolysis
hsa05170  Human immunodeficiency virus 1 infection
hsa05200  Pathways in cancer
hsa05211  Renal cell carcinoma
Network
nt06225  HIF-1 signaling (cancer)
nt06264  Renal cell carcinoma
nt06509  DNA replication
nt06523  Epigenetic regulation by Polycomb complexes
nt06542  HIF signaling
  Element
N00080  Loss of VHL to HIF-1 signaling pathway
N00081  Mutation-inactivated VHL to HIF-1 signaling pathway
N01473  DNA replication termination
N01577  Gene silencing by methylation of H3K27 and ubiquitination of H2AK119
N01872  Proteasomal degradation of HIF by VHL complex
N01873  VHL mutation to HIF-2 signaling pathway
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09123 Folding, sorting and degradation
   04120 Ubiquitin mediated proteolysis
    6923 (ELOB)
 09130 Environmental Information Processing
  09132 Signal transduction
   04066 HIF-1 signaling pathway
    6923 (ELOB)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    6923 (ELOB)
  09162 Cancer: specific types
   05211 Renal cell carcinoma
    6923 (ELOB)
  09172 Infectious disease: viral
   05170 Human immunodeficiency virus 1 infection
    6923 (ELOB)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04121 Ubiquitin system [BR:hsa04121]
    6923 (ELOB)
   03400 DNA repair and recombination proteins [BR:hsa03400]
    6923 (ELOB)
Ubiquitin system [BR:hsa04121]
 Ubiquitin ligases (E3)
  Multi subunit type E3
   Cul2 complex
    Adoptor protein
     6923 (ELOB)
   Cul5 complex
     6923 (ELOB)
DNA repair and recombination proteins [BR:hsa03400]
 Eukaryotic type
  SSBR (single strand breaks repair)
   NER (nucleotide excision repair)
    Other NER factors
     6923 (ELOB)
SSDB
Motif
Pfam: ubiquitin Rad60-SLD
Other DBs
NCBI-GeneID: 6923
NCBI-ProteinID: NP_009039
OMIM: 600787
HGNC: 11619
Ensembl: ENSG00000103363
UniProt: Q15370
Structure
LinkDB
Position
16:complement(2771414..2777280)
AA seq 118 aa
MDVFLMIRRHKTTIFTDAKESSTVFELKRIVEGILKRPPDEQRLYKDDQLLDDGKTLGEC
GFTSQTARPQAPATVGLAFRADDTFEALCIEPFSSPPELPDVMKPQDSGSSANEQAVQ
NT seq 357 nt   +upstreamnt  +downstreamnt
atggacgtgttcctcatgatccggcgccacaagaccaccatcttcacggacgccaaggag
tccagcacggtgttcgaactgaagcgcatcgtcgagggcatcctcaagcggcctcctgac
gagcagcggctgtacaaggatgaccaactcttggatgatggcaagacactgggcgagtgt
ggcttcaccagtcaaacagcacggccacaggccccagccacagtggggctggccttccgg
gcagatgacacctttgaggccctgtgcatcgagccgttttccagcccgccagagctgccc
gatgtgatgaagccccaggactcgggaagcagtgccaatgaacaagccgtgcagtga

KEGG   Homo sapiens (human): 6921
Entry
6921              CDS       T01001                                 
Symbol
ELOC, SIII, TCEB1
Name
(RefSeq) elongin C
  KO
K03872  elongin-C
Organism
hsa  Homo sapiens (human)
Pathway
hsa04066  HIF-1 signaling pathway
hsa04120  Ubiquitin mediated proteolysis
hsa05170  Human immunodeficiency virus 1 infection
hsa05200  Pathways in cancer
hsa05211  Renal cell carcinoma
Network
nt06225  HIF-1 signaling (cancer)
nt06264  Renal cell carcinoma
nt06509  DNA replication
nt06523  Epigenetic regulation by Polycomb complexes
nt06542  HIF signaling
  Element
N00080  Loss of VHL to HIF-1 signaling pathway
N00081  Mutation-inactivated VHL to HIF-1 signaling pathway
N01473  DNA replication termination
N01577  Gene silencing by methylation of H3K27 and ubiquitination of H2AK119
N01872  Proteasomal degradation of HIF by VHL complex
N01873  VHL mutation to HIF-2 signaling pathway
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09123 Folding, sorting and degradation
   04120 Ubiquitin mediated proteolysis
    6921 (ELOC)
 09130 Environmental Information Processing
  09132 Signal transduction
   04066 HIF-1 signaling pathway
    6921 (ELOC)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    6921 (ELOC)
  09162 Cancer: specific types
   05211 Renal cell carcinoma
    6921 (ELOC)
  09172 Infectious disease: viral
   05170 Human immunodeficiency virus 1 infection
    6921 (ELOC)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04121 Ubiquitin system [BR:hsa04121]
    6921 (ELOC)
   03400 DNA repair and recombination proteins [BR:hsa03400]
    6921 (ELOC)
Ubiquitin system [BR:hsa04121]
 Ubiquitin ligases (E3)
  Multi subunit type E3
   Cul2 complex
    Adoptor protein
     6921 (ELOC)
   Cul5 complex
     6921 (ELOC)
DNA repair and recombination proteins [BR:hsa03400]
 Eukaryotic type
  SSBR (single strand breaks repair)
   NER (nucleotide excision repair)
    Other NER factors
     6921 (ELOC)
SSDB
Motif
Pfam: Skp1_POZ
Other DBs
NCBI-GeneID: 6921
NCBI-ProteinID: NP_001191786
OMIM: 600788
HGNC: 11617
Ensembl: ENSG00000154582
UniProt: Q15369
Structure
LinkDB
Position
8:complement(73945119..73972287)
AA seq 112 aa
MDGEEKTYGGCEGPDAMYVKLISSDGHEFIVKREHALTSGTIKAMLSGPGQFAENETNEV
NFREIPSHVLSKVCMYFTYKVRYTNSSTEIPEFPIAPEIALELLMAANFLDC
NT seq 339 nt   +upstreamnt  +downstreamnt
atggatggagaggagaaaacctatggtggctgtgaaggacctgatgccatgtatgtcaaa
ttgatatcatctgatggccatgaatttattgtaaaaagagaacatgcattaacatcaggc
acgataaaagccatgttgagtggcccaggtcagtttgctgagaacgaaaccaatgaggtc
aattttagagagataccttcacatgtgctatcgaaagtatgcatgtattttacgtacaag
gttcgctacactaacagctccaccgagattcctgaattcccaattgcacctgaaattgca
ctggaactgctgatggctgcgaacttcttagattgttaa

KEGG   Homo sapiens (human): 84458
Entry
84458             CDS       T01001                                 
Symbol
LCOR, C10orf12, MLR2
Name
(RefSeq) ligand dependent nuclear receptor corepressor
  KO
K26260  ligand-dependent corepressor
Organism
hsa  Homo sapiens (human)
Pathway
hsa03083  Polycomb repressive complex
Network
nt06523  Epigenetic regulation by Polycomb complexes
  Element
N01577  Gene silencing by methylation of H3K27 and ubiquitination of H2AK119
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09126 Chromosome
   03083 Polycomb repressive complex
    84458 (LCOR)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    84458 (LCOR)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Histone modification proteins
   Polycomb repressive complex (PRC) and associated proteins
    PRC2.1
     84458 (LCOR)
SSDB
Motif
Pfam: HTH_psq
Other DBs
NCBI-GeneID: 84458
NCBI-ProteinID: NP_001164236
OMIM: 607698
HGNC: 29503
Ensembl: ENSG00000196233
UniProt: Q96JN0
Structure
LinkDB
Position
10:96832298..96995956
AA seq 433 aa
MQRMIQQFAAEYTSKNSSTQDPSQPNSTKNQSLPKASPVTTSPTAATTQNPVLSKLLMAD
QDSPLDLTVRKSQSEPSEQDGVLDLSTKKSPCAGSTSLSHSPGCSSTQGNGRPGRPSQYR
PDGLRSGDGVPPRSLQDGTREGFGHSTSLKVPLARSLQISEELLSRNQLSTAASLGPSGL
QNHGQHLILSREASWAKPHYEFNLSRMKFRGNGALSNISDLPFLAENSAFPKMALQAKQD
GKKDVSHSSPVDLKIPQVRGMDLSWESRTGDQYSYSSLVMGSQTESALSKKLRAILPKQS
RKSMLDAGPDSWGSDAEQSTSGQPYPTSDQEGDPGSKQPRKKRGRYRQYNSEILEEAISV
VMSGKMSVSKAQSIYGIPHSTLEYKVKERLGTLKNPPKKKMKLMRSEGPDVSVKIELDPQ
GEAAQSANESKNE
NT seq 1302 nt   +upstreamnt  +downstreamnt
atgcagcgaatgatccaacaatttgctgctgaatatacctcaaaaaatagctctactcag
gaccccagccagcccaatagcacaaagaaccaaagcctgccgaaagcatctccagtcacc
acctctcccacggctgcaactactcagaaccctgtgctcagcaaacttctcatggctgac
caagactcacctctggaccttactgtcagaaagtctcagtcagaacctagcgaacaagac
ggtgtacttgatctgtccactaagaaaagtccatgtgctggcagcacttccctgagccac
tctccaggctgctccagtactcaagggaacgggcgacctgggagacccagccagtaccgc
ccagacggacttcggagtggtgatggggtacctccaagaagcttacaggatggaaccagg
gaaggttttggacactccacatcactcaaagttccactggctcgatccctgcagattagt
gaagaactactgagcagaaaccaattgtccacagctgccagccttgggccatctggatta
cagaatcatggacaacacttaatattatccagggaagcctcttgggcaaaaccacattac
gagttcaacctcagccgtatgaagttcaggggaaatggtgcactcagcaacatcagtgac
cttccttttcttgcagaaaactctgcctttccaaaaatggcacttcaagcaaaacaagat
ggaaaaaaggatgtgagccattcatctcctgtagatttaaagataccacaagttcgagga
atggatctttcttgggagtctcgcactggtgatcagtacagctatagctctttggtaatg
ggttcacaaacggagagcgcgcttagtaaaaaattaagggctattcttccaaaacaaagt
agaaaaagcatgttagatgctggacccgattcttggggctcagatgctgagcagtctacc
tctggacagccatatcccacatcggatcaagaaggagaccctggctccaagcagcctcgg
aagaaaagagggcgttacagacagtacaacagtgagatactggaggaagcaatctcagtg
gttatgagtggaaaaatgagtgtttccaaagctcagagtatttatgggattccccacagt
acactggagtacaaagtaaaggagaggctgggcactttgaaaaaccctccaaagaaaaag
atgaaattaatgaggtcggaggggccagatgtttctgtaaagattgaattagatccccag
ggagaggcagcacaaagtgcaaatgaatcaaaaaacgagtag

KEGG   Homo sapiens (human): 254251
Entry
254251            CDS       T01001                                 
Symbol
LCORL, MLR1
Name
(RefSeq) ligand dependent nuclear receptor corepressor like
Organism
hsa  Homo sapiens (human)
Network
nt06523  Epigenetic regulation by Polycomb complexes
  Element
N01577  Gene silencing by methylation of H3K27 and ubiquitination of H2AK119
SSDB
Motif
Pfam: HTH_psq
Other DBs
NCBI-GeneID: 254251
NCBI-ProteinID: NP_001159611
OMIM: 611799
HGNC: 30776
Ensembl: ENSG00000178177
UniProt: Q8N3X6
LinkDB
Position
4:complement(17841187..18021875)
AA seq 602 aa
MDKGRERMAAAAAAAAAAAAAAQCRSPRCAAERRGFRRELDSWRHRLMHCVGFESILEGL
YGPRLRRDLSLFEDCEPEELTDWSMDEKCSFCNLQREAVSDCIPSLDSSQSTPTEELSSQ
GQSNTDKIECQAENYLNALFRKKDLPQNCDPNIPLVAQELMKKMIRQFAIEYISKSGKTQ
ENRNGSIGPSIVCKSIQMNQAENSLQEEQEGPLDLTVNRMQEQNTQQGDGVLDLSTKKTS
IKSEESSICDPSSENSVAGRLHRNREDYVERSAEFADGLLSKALKDIQSGALDINKAGIL
YGIPQKTLLLHLEALPAGKPASFKNKTRDFHDSYSYKDSKETCAVLQKVALWARAQAERT
EKSKLNLLETSEIKFPTASTYLHQLTLQKMVTQFKEKNESLQYETSNPTVQLKIPQLRVS
SVSKSQPDGSGLLDVMYQVSKTSSVLEGSALQKLKNILPKQNKIECSGPVTHSSVDSYFL
HGDLSPLCLNSKNGTVDGTSENTEDGLDRKDSKQPRKKRGRYRQYDHEIMEEAIAMVMSG
KMSVSKAQGIYGVPHSTLEYKVKERSGTLKTPPKKKLRLPDTGLYNMTDSGTGSCKNSSK
PV
NT seq 1809 nt   +upstreamnt  +downstreamnt
atggacaagggaagagagagaatggccgctgccgccgccgctgctgccgccgccgccgcc
gccgctcagtgccggagccctcggtgcgcggcggagagaagaggattccggcgggaactc
gactcttggcgccaccgcctcatgcactgtgtaggttttgagagtattttagaagggctt
tatggaccacggctacgaagagacctcagtttatttgaagactgtgaaccagaagagctg
actgactggtctatggatgaaaaatgttcattttgtaacctacagagagaagcagtcagt
gattgtataccatctcttgattcttcacagtcaacaccaacagaggagctatcatctcag
ggccagtccaacactgataagattgaatgccaagcagaaaattacctaaatgcactcttt
cgaaagaaagatcttcctcagaactgtgatcctaacattcccctagttgctcaggaatta
atgaaaaagatgatacgtcaatttgcgattgagtacatttcaaaaagtggtaaaactcaa
gagaatagaaatggttcaattggaccaagtatagtatgtaaaagtatccaaatgaatcaa
gcagaaaactcccttcaggaagagcaggaaggccccttagacctcactgtgaatcgaatg
caagaacaaaatactcagcaaggggatggagtgttagatctctctacaaagaaaaccagc
ataaaatctgaagagtcatccatatgtgatccttcttctgaaaattcagtggctgggaga
ctacacagaaacagagaggactatgtggaaagaagtgctgagtttgcagatggtttgctc
tcaaaagctttgaaagacattcagtctggagcactggacataaataaagcaggcatactt
tatggcatacctcaaaaaactttacttcttcacttagaagccttaccagcagggaagcct
gcatcttttaaaaacaaaactcgagatttccatgatagttattcatataaggacagtaaa
gaaacttgtgcagtgctgcaaaaagtagccttgtgggcaagagctcaagcagagcgcaca
gaaaaaagtaaactcaatctacttgaaacctcagaaataaaattcccaacagcttccact
tacctccatcagctaactctacagaaaatggtcactcagtttaaagaaaaaaatgaaagc
ctccaatatgaaacttcaaatcctactgtacagttaaaaattcctcagctacgagtaagt
tctgtctcaaaatcacaacctgatggttctggtctgttggatgttatgtatcaagtttcc
aaaacctcttcagtcctagaaggatcagctctccaaaaactgaaaaatatactccctaaa
cagaacaaaatagaatgttctgggcctgtaactcactcaagtgttgactcttactttcta
catggggacctctctcctttgtgtcttaattctaaaaatggaacagttgatggaacctct
gaaaatactgaagatggattagatcgaaaagacagtaagcagcccaggaaaaaacgtggc
cgctatcggcaatatgatcatgaaataatggaagaagctattgcaatggtaatgagcgga
aaaatgagtgtttccaaagcacaaggaatttatggggtacctcacagcactttagaatac
aaggtaaaagaaagatctggaacactgaagactcctccgaagaagaaactacgattacca
gacactgggttatataatatgacagattcagggactggcagctgcaaaaacagcagcaag
cctgtgtag

KEGG   Homo sapiens (human): 1487
Entry
1487              CDS       T01001                                 
Symbol
CTBP1, BARS, HADDTS
Name
(RefSeq) C-terminal binding protein 1
  KO
K04496  C-terminal binding protein [EC:1.1.1.428]
Organism
hsa  Homo sapiens (human)
Pathway
hsa04310  Wnt signaling pathway
hsa04330  Notch signaling pathway
hsa05200  Pathways in cancer
hsa05220  Chronic myeloid leukemia
Network
nt06523  Epigenetic regulation by Polycomb complexes
  Element
N01577  Gene silencing by methylation of H3K27 and ubiquitination of H2AK119
Disease
H01773  4p deletion syndrome
H02619  Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    1487 (CTBP1)
   04330 Notch signaling pathway
    1487 (CTBP1)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    1487 (CTBP1)
  09162 Cancer: specific types
   05220 Chronic myeloid leukemia
    1487 (CTBP1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    1487 (CTBP1)
Enzymes [BR:hsa01000]
 1. Oxidoreductases
  1.1  Acting on the CH-OH group of donors
   1.1.1  With NAD+ or NADP+ as acceptor
    1.1.1.428  4-methylthio 2-oxobutanoate reductase (NADH)
     1487 (CTBP1)
Membrane trafficking [BR:hsa04131]
 Endocytosis
  Macropinocytosis
   Others
    1487 (CTBP1)
SSDB
Motif
Pfam: 2-Hacid_dh_C 2-Hacid_dh NAD_binding_2 XdhC_C RS_preATP-grasp-like F420_oxidored
Other DBs
NCBI-GeneID: 1487
NCBI-ProteinID: NP_001319
OMIM: 602618
HGNC: 2494
Ensembl: ENSG00000159692
UniProt: Q13363 X5D8Y5
Structure
LinkDB
Position
4:complement(1211445..1250355)
AA seq 440 aa
MGSSHLLNKGLPLGVRPPIMNGPLHPRPLVALLDGRDCTVEMPILKDVATVAFCDAQSTQ
EIHEKVLNEAVGALMYHTITLTREDLEKFKALRIIVRIGSGFDNIDIKSAGDLGIAVCNV
PAASVEETADSTLCHILNLYRRATWLHQALREGTRVQSVEQIREVASGAARIRGETLGII
GLGRVGQAVALRAKAFGFNVLFYDPYLSDGVERALGLQRVSTLQDLLFHSDCVTLHCGLN
EHNHHLINDFTVKQMRQGAFLVNTARGGLVDEKALAQALKEGRIRGAALDVHESEPFSFS
QGPLKDAPNLICTPHAAWYSEQASIEMREEAAREIRRAITGRIPDSLKNCVNKDHLTAAT
HWASMDPAVVHPELNGAAYRYPPGVVGVAPTGIPAAVEGIVPSAMSLSHGLPPVAHPPHA
PSPGQTVKPEADRDHASDQL
NT seq 1323 nt   +upstreamnt  +downstreamnt
atgggcagctcgcacttgctcaacaagggcctgccgcttggcgtccgacctccgatcatg
aacgggcccctgcacccgcggcccctggtggcattgctggatggccgggactgcacagtg
gagatgcccatcctgaaggacgtggccactgtggccttctgcgacgcgcagtccacgcag
gagatccatgagaaggtcctgaacgaggctgtgggggccctgatgtaccacaccatcact
ctcaccagggaggacctggagaagttcaaagccctccgcatcatcgtccggattggcagt
ggttttgacaacatcgacatcaagtcggccggggatttaggcattgccgtctgcaacgtg
cccgcggcgtctgtggaggagacggccgactcgacgctgtgccacatcctgaacctgtac
cggcgggccacctggctgcaccaggcgctgcgggagggcacacgagtccagagcgtcgag
cagatccgcgaggtggcgtccggcgctgccaggatccgcggggagaccttgggcatcatc
ggacttggtcgcgtggggcaggcagtggcgctgcgggccaaggccttcggcttcaacgtg
ctcttctacgacccttacttgtcggatggcgtggagcgggcgctggggctgcagcgtgtc
agcaccctgcaggacctgctcttccacagcgactgcgtgaccctgcactgcggcctcaac
gagcacaaccaccacctcatcaacgacttcaccgtcaagcagatgagacaaggggccttc
ctggtgaacacagcccggggtggcctggtggatgagaaggcgctggcccaggccctgaag
gagggccggatccgcggcgcggccctggatgtgcacgagtcggaacccttcagctttagc
cagggccctctgaaggatgcacccaacctcatctgcaccccccatgctgcatggtacagc
gagcaggcatccatcgagatgcgagaggaggcggcacgggagatccgcagagccatcaca
ggccggatcccagacagcctgaagaactgtgtcaacaaggaccatctgacagccgccacc
cactgggccagcatggaccccgccgtcgtgcaccctgagctcaatggggctgcctatagg
taccctccgggcgtggtgggcgtggcccccactggcatcccagctgctgtggaaggtatc
gtccccagcgccatgtccctgtcccacggcctgccccctgtggcccacccgccccacgcc
ccttctcctggccaaaccgtcaagcccgaggcggatagagaccacgccagtgaccagttg
tag

KEGG   Homo sapiens (human): 1488
Entry
1488              CDS       T01001                                 
Symbol
CTBP2
Name
(RefSeq) C-terminal binding protein 2
  KO
K04496  C-terminal binding protein [EC:1.1.1.428]
Organism
hsa  Homo sapiens (human)
Pathway
hsa04310  Wnt signaling pathway
hsa04330  Notch signaling pathway
hsa05200  Pathways in cancer
hsa05220  Chronic myeloid leukemia
Network
nt06523  Epigenetic regulation by Polycomb complexes
  Element
N01577  Gene silencing by methylation of H3K27 and ubiquitination of H2AK119
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    1488 (CTBP2)
   04330 Notch signaling pathway
    1488 (CTBP2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    1488 (CTBP2)
  09162 Cancer: specific types
   05220 Chronic myeloid leukemia
    1488 (CTBP2)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    1488 (CTBP2)
Enzymes [BR:hsa01000]
 1. Oxidoreductases
  1.1  Acting on the CH-OH group of donors
   1.1.1  With NAD+ or NADP+ as acceptor
    1.1.1.428  4-methylthio 2-oxobutanoate reductase (NADH)
     1488 (CTBP2)
Membrane trafficking [BR:hsa04131]
 Endocytosis
  Macropinocytosis
   Others
    1488 (CTBP2)
SSDB
Motif
Pfam: 2-Hacid_dh_C 2-Hacid_dh NAD_binding_2
Other DBs
NCBI-GeneID: 1488
NCBI-ProteinID: NP_001077383
OMIM: 602619
HGNC: 2495
Ensembl: ENSG00000175029
UniProt: P56545
Structure
LinkDB
Position
10:complement(124984317..125162463)
AA seq 445 aa
MALVDKHKVKRQRLDRICEGIRPQIMNGPLHPRPLVALLDGRDCTVEMPILKDLATVAFC
DAQSTQEIHEKVLNEAVGAMMYHTITLTREDLEKFKALRVIVRIGSGYDNVDIKAAGELG
IAVCNIPSAAVEETADSTICHILNLYRRNTWLYQALREGTRVQSVEQIREVASGAARIRG
ETLGLIGFGRTGQAVAVRAKAFGFSVIFYDPYLQDGIERSLGVQRVYTLQDLLYQSDCVS
LHCNLNEHNHHLINDFTIKQMRQGAFLVNAARGGLVDEKALAQALKEGRIRGAALDVHES
EPFSFAQGPLKDAPNLICTPHTAWYSEQASLEMREAAATEIRRAITGRIPESLRNCVNKE
FFVTSAPWSVIDQQAIHPELNGATYRYPPGIVGVAPGGLPAAMEGIIPGGIPVTHNLPTV
AHPSQAPSPNQPTKHGDNREHPNEQ
NT seq 1338 nt   +upstreamnt  +downstreamnt
atggcccttgtggataagcacaaagtcaagagacagcgattggacagaatttgtgaaggt
atccgcccccagatcatgaacggccccctgcacccccgccccctggtggcgctgctggac
ggccgcgactgcactgtggagatgcccatcctgaaggacctggccactgtggccttctgt
gacgcgcagtcgacgcaggaaatccacgagaaggttctaaacgaagccgtgggcgccatg
atgtaccacaccatcaccctcaccagggaggacctggagaagttcaaggccctgagagtg
atcgtgcggataggcagtggctatgacaacgtggacatcaaggctgccggcgagctcgga
attgccgtgtgcaacatcccgtctgcagccgtggaagagacagcggactctaccatctgc
cacatcctcaacctgtaccggaggaacacgtggctgtaccaggcactgcgggaaggcacg
cgggttcagagcgtggagcagatccgcgaggtggcctcgggagcggcccgcatccgtggg
gagacgctgggcctcattggctttggtcgcacggggcaggcggttgcagttcgagccaag
gcctttggattcagcgtcatattttatgacccctacttgcaggatgggatcgagcggtcc
ctgggcgtgcagagggtctacaccctgcaggatttgctgtatcagagcgactgcgtctcc
ttgcactgcaatctcaacgaacataaccaccacctcatcaatgactttaccataaagcag
atgaggcagggagcattccttgtgaacgcagcccgtggcggcctggtggacgagaaagcc
ttagcacaagccctcaaggagggcaggatacgaggggcagccctcgacgtgcatgagtca
gagcccttcagctttgctcagggtccgttgaaagatgccccgaatctcatctgcactcct
cacactgcctggtacagtgagcaggcgtcactggagatgagggaggcagctgccaccgag
atccgccgagccatcacaggtcgcatcccagaaagcttaagaaattgtgtgaacaaggaa
ttctttgtcacatcagcgccttggtcagtaatagaccagcaagcaattcatcctgagctc
aatggtgccacatacagatatccgccaggcatcgtgggtgtggctccaggaggacttcct
gcagccatggaagggatcatccctggaggcatcccagtgactcacaacctcccgacagtg
gcacatccttcccaagcgccctctcccaaccagcccacaaaacacggggacaatcgagag
caccccaacgagcaatag

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