Homo sapiens (human): 113130
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Entry
113130 CDS
T01001
Symbol
CDCA5, SORORIN
Name
(RefSeq) cell division cycle associated 5
KO
K17390
sororin
Organism
hsa
Homo sapiens (human)
Pathway
hsa04110
Cell cycle
hsa05206
MicroRNAs in cancer
Network
nt06512
Chromosome cohesion and segregation
Element
N01483
Cohesin acetylation
N01484
Establishment of cohesion
N01485
Cohesin dissociation in prophase
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09143 Cell growth and death
04110 Cell cycle
113130 (CDCA5)
09160 Human Diseases
09161 Cancer: overview
05206 MicroRNAs in cancer
113130 (CDCA5)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
113130 (CDCA5)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Sister chromatid cohesion proteins
Other sister chromatid cohesion factors
113130 (CDCA5)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Sororin
Motif
Other DBs
NCBI-GeneID:
113130
NCBI-ProteinID:
NP_542399
OMIM:
609374
HGNC:
14626
Ensembl:
ENSG00000146670
Pharos:
Q96FF9
(Tbio)
UniProt:
Q96FF9
LinkDB
All DBs
Position
11:complement(65061093..65084040)
Genome browser
AA seq
252 aa
AA seq
DB search
MSGRRTRSGGAAQRSGPRAPSPTKPLRRSQRKSGSELPSILPEIWPKTPSAAAVRKPIVL
KRIVAHAVEVPAVQSPRRSPRISFFLEKENEPPGRELTKEDLFKTHSVPATPTSTPVPNP
EAESSSKEGELDARDLEMSKKVRRSYSRLETLGSASTSTPGRRSCFGFEGLLGAEDLSGV
SPVVCSKLTEVPRVCAKPWAPDMTLPGISPPPEKQKRKKKKMPEILKTELDEWAAAMNAE
FEAAEQFDLLVE
NT seq
759 nt
NT seq
+upstream
nt +downstream
nt
atgtctgggaggcgaacgcggtccggaggagccgctcagcgctccgggccaagggcccca
tctcctactaagcctctgcggaggtcccagcggaaatcaggctctgaactcccgagcatc
ctccctgaaatctggccgaagacacccagtgcggctgcagtcagaaagcccatcgtctta
aagaggatcgtggcccatgctgtagaggtcccagctgtccaatcacctcgcaggagccct
aggatttcctttttcttggagaaagaaaacgagccccctggcagggagcttactaaggag
gaccttttcaagacacacagcgtccctgccacccccaccagcactcctgtgccgaaccct
gaggccgagtccagctccaaggaaggagagctggacgccagagacttggaaatgtctaag
aaagtcaggcgttcctacagccggctggagaccctgggctctgcctctacctccacccca
ggccgccggtcctgctttggcttcgaggggctgctgggggcagaagacttgtccggagtc
tcgccagtggtgtgctccaaactcaccgaggtccccagggtttgtgcaaagccctgggcc
ccagacatgactctccctggaatctccccaccacccgagaaacagaaacgtaagaagaag
aaaatgccagagatcttgaaaacggagctggatgagtgggctgcggccatgaatgccgag
tttgaagctgctgagcagtttgatctcctggttgaatga
Homo sapiens (human): 10664
Help
Entry
10664 CDS
T01001
Symbol
CTCF, CFAP108, FAP108, MRD21
Name
(RefSeq) CCCTC-binding factor
KO
K23195
transcriptional repressor CTCF
Organism
hsa
Homo sapiens (human)
Network
nt06512
Chromosome cohesion and segregation
Element
N01484
Establishment of cohesion
Disease
H00773
Autosomal dominant intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
10664 (CTCF)
03036 Chromosome and associated proteins [BR:
hsa03036
]
10664 (CTCF)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Zinc finger
Cys2His2 others
10664 (CTCF)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Chromatin remodeling factors
Other chromatin remodeling factors
10664 (CTCF)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
zf-H2C2_2
zf-C2H2
zf-C2H2_4
zf-H2C2_5
zf-C2H2_jaz
zf-met
zf-C2HE
zf-C2H2_6
zf-WIZ
Motif
Other DBs
NCBI-GeneID:
10664
NCBI-ProteinID:
NP_006556
OMIM:
604167
HGNC:
13723
Ensembl:
ENSG00000102974
Pharos:
P49711
(Tbio)
UniProt:
P49711
Structure
PDB
LinkDB
All DBs
Position
16:67562526..67639185
Genome browser
AA seq
727 aa
AA seq
DB search
MEGDAVEAIVEESETFIKGKERKTYQRRREGGQEEDACHLPQNQTDGGEVVQDVNSSVQM
VMMEQLDPTLLQMKTEVMEGTVAPEAEAAVDDTQIITLQVVNMEEQPINIGELQLVQVPV
PVTVPVATTSVEELQGAYENEVSKEGLAESEPMICHTLPLPEGFQVVKVGANGEVETLEQ
GELPPQEDPSWQKDPDYQPPAKKTKKTKKSKLRYTEEGKDVDVSVYDFEEEQQEGLLSEV
NAEKVVGNMKPPKPTKIKKKGVKKTFQCELCSYTCPRRSNLDRHMKSHTDERPHKCHLCG
RAFRTVTLLRNHLNTHTGTRPHKCPDCDMAFVTSGELVRHRRYKHTHEKPFKCSMCDYAS
VEVSKLKRHIRSHTGERPFQCSLCSYASRDTYKLKRHMRTHSGEKPYECYICHARFTQSG
TMKMHILQKHTENVAKFHCPHCDTVIARKSDLGVHLRKQHSYIEQGKKCRYCDAVFHERY
ALIQHQKSHKNEKRFKCDQCDYACRQERHMIMHKRTHTGEKPYACSHCDKTFRQKQLLDM
HFKRYHDPNFVPAAFVCSKCGKTFTRRNTMARHADNCAGPDGVEGENGGETKKSKRGRKR
KMRSKKEDSSDSENAEPDLDDNEDEEEPAVEIEPEPEPQPVTPAPPPAKKRRGRPPGRTN
QPKQNQPTAIIQVEDQNTGAIENIIVEVKKEPDAEPAEGEEEEAQPAATDAPNGDLTPEM
ILSMMDR
NT seq
2184 nt
NT seq
+upstream
nt +downstream
nt
atggaaggtgatgcagtcgaagccattgtggaggagtccgaaacttttattaaaggaaag
gagagaaagacttaccagagacgccgggaagggggccaggaagaagatgcctgccactta
ccccagaaccagacggatgggggtgaggtggtccaggatgtcaacagcagtgtacagatg
gtgatgatggaacagctggaccccacccttcttcagatgaagactgaagtaatggagggc
acagtggctccagaagcagaggctgctgtggacgatacccagattataactttacaggtt
gtaaatatggaggaacagcccataaacataggagaacttcagcttgttcaagtacctgtt
cctgtgactgtacctgttgctaccacttcagtagaagaacttcagggggcttatgaaaat
gaagtgtctaaagagggccttgcggaaagtgaacccatgatatgccacaccctacctttg
cctgaagggtttcaggtggttaaagtgggggccaatggagaggtggagacactagaacaa
ggggaacttccaccccaggaagatcctagttggcaaaaagacccagactatcagccacca
gccaaaaaaacaaagaaaaccaaaaagagcaaactgcgttatacagaggagggcaaagat
gtagatgtgtctgtctacgattttgaggaagaacagcaggagggtctgctatcagaggtt
aatgcagagaaagtggttggtaatatgaagcctccaaagccaacaaaaattaaaaagaaa
ggtgtaaagaagacattccagtgtgagctttgcagttacacgtgtccacggcgttcaaat
ttggatcgtcacatgaaaagccacactgatgagagaccacacaagtgccatctctgtggc
agggcattcagaacagtcaccctcctgaggaatcaccttaacacacacacaggtactcgt
cctcacaagtgcccagactgcgacatggcctttgtgaccagtggagaattggttcggcat
cgtcgttacaaacacacccacgagaagccattcaagtgttccatgtgcgattacgccagt
gtagaagtcagcaaattaaaacgtcacattcgctctcatactggagagcgtccgtttcag
tgcagtttgtgcagttatgccagcagggacacatacaagctgaaaaggcacatgagaacc
cattcaggggaaaagccttatgaatgttatatttgtcatgctcggtttacccaaagtggt
accatgaagatgcacattttacagaagcacacagaaaatgtggccaaatttcactgtccc
cactgtgacacagtcatagcccgaaaaagtgatttgggtgtccacttgcgaaagcagcat
tcctatattgagcaaggcaagaaatgccgttactgtgatgctgtgtttcatgagcgctat
gccctcatccagcatcagaagtcacacaagaatgagaagcgctttaagtgtgaccagtgt
gattacgcttgtagacaggagaggcacatgatcatgcacaagcgcacccacaccggggag
aagccttacgcctgcagccactgcgataagaccttccgccagaagcagcttctcgacatg
cacttcaagcgctatcacgaccccaacttcgtccctgcggcttttgtctgttctaagtgt
gggaaaacatttacacgtcggaataccatggcaagacatgctgataattgtgctggccca
gatggcgtagagggggaaaatggaggagaaacgaagaagagtaaacgtggaagaaaaaga
aagatgcgctctaagaaagaagattcctctgacagtgaaaatgctgaaccagatctggac
gacaatgaggatgaggaggagcctgccgtagaaattgaacctgagccagagcctcagcct
gtgaccccagccccaccacccgccaagaagcggagaggacgaccccctggcagaaccaac
cagcccaaacagaaccagccaacagctatcattcaggttgaagaccagaatacaggtgca
attgagaacattatagttgaagtaaaaaaagagccagatgctgagcccgcagagggagag
gaagaggaggcccagccagctgccacagatgcccccaacggagacctcacgcccgagatg
atcctcagcatgatggaccggtga
DBGET
integrated database retrieval system