KEGG   Homo sapiens (human): 55213
Entry
55213             CDS       T01001                                 
Symbol
RCBTB1, CLLD7, CLLL7, GLP, RDEOA
Name
(RefSeq) RCC1 and BTB domain containing protein 1
  KO
K11494  RCC1 and BTB domain-containing protein
Organism
hsa  Homo sapiens (human)
Disease
H02289  Retinal dystrophy with or without extraocular anomalies
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    55213 (RCBTB1)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Chromosome condensation proteins
   Other regulators of chromosome condensation
    55213 (RCBTB1)
SSDB
Motif
Pfam: RCC1 RCC1_2 BTB BACK
Other DBs
NCBI-GeneID: 55213
NCBI-ProteinID: NP_060661
OMIM: 607867
HGNC: 18243
Ensembl: ENSG00000136144
UniProt: Q8NDN9 B3KR20
Position
13:complement(49531946..49585558)
AA seq 531 aa
MVDVGKWPIFTLLSPQEIASIRKACVFGTSASEALYVTDNDEVFVFGLNYSNCLGTGDNQ
STLVPKKLEGLCGKKIKSLSYGSGPHVLLSTEDGVVYAWGHNGYSQLGNGTTNQGIAPVQ
VCTNLLIKQVVEVACGSHHSMALAADGEVFAWGYNNCGQVGSGSTANQPTPRKVTNCLHI
KRVVGIACGQTSSMAVLDNGEVYGWGYNGNGQLGLGNNGNQLTPVRVAALHSVCVNQIVC
GYAHTLALTDEGLLYAWGANTYGQLGTGNKNNLLSPAHIMVEKERVVEIAACHSAHTSAA
KTQGGHVYMWGQCRGQSVILPHLTHFSCTDDVFACFATPAVSWRLLSVEHEDFLTVAESL
KKEFDSPETADLKFRIDGKYIHVHKAVLKIRCEHFRSMFQSYWNEDMKEVIEIDQFSYPV
YRAFLQYLYTDTVDLPPEDAIGLLDLATSYCENRLKKLCQHIIKRGITVENAFSLFSAAV
RYDAEDLEEFCFKFCINHLTEVTQTAAFWQMDGPLLKEFIAKASKCGAFKN
NT seq 1596 nt   +upstreamnt  +downstreamnt
atggtggatgtcggaaagtggcccatcttcactctactctcccctcaagagatcgcgtct
attcggaaggcgtgtgtcttcggcacctcagccagtgaagcactgtacgttactgacaat
gatgaggtctttgtatttggactgaactatagtaactgtctaggaactggagataaccag
agtacacttgtacccaaaaagctagaaggcttatgtggaaagaagattaaaagcctcagt
tacgggagtggaccacatgttcttctcagcaccgaagatggagtggtttatgcctggggc
cacaatggatatagccagcttgggaatgggacgaccaaccaaggcattgctcccgtccag
gtctgtaccaatctcttgatcaagcaagtggtggaagtagcttgtggctcacatcattca
atggctctggcagctgatggagaggtgtttgcttggggttataacaactgtggccaagtg
ggatcaggttctacagcaaatcaaccaactcctcgaaaagttacaaactgtttacatatt
aagagggtagttggcattgcctgtggtcagacttcatccatggctgttctggacaatggc
gaggtatatggctggggttacaatggcaacggtcagctgggcctgggaaacaatggcaac
cagctgacccctgtgagagtggcagctttgcacagcgtgtgtgtgaaccagattgtctgc
ggttacgcacatactctagcactaacagatgagggcttgctgtatgcctggggagctaac
acatatgggcagctgggaactggcaataaaaataacctgctaagcccagcacacatcatg
gtggagaaagaaagggtggtagagattgcagcctgtcactctgcccacacgtctgcagcc
aagacgcagggtgggcacgtgtacatgtggggccagtgccggggtcagtccgtgatcctc
ccgcacctcacccacttctcctgcaccgacgacgtgtttgcctgctttgccactcccgcc
gtctcgtggcgcctcctgtctgtggagcatgaagactttttaacagttgcagagtcactg
aagaaagaatttgatagtccagaaactgctgatctgaagtttcgaattgatggaaaatat
attcatgtccataaagctgttttgaaaatcaggtgtgagcattttcgatccatgttccag
tcgtattggaatgaagacatgaaggaagtgatagaaatcgatcagttttcttacccagtg
tatcgtgcctttctccagtacctctacacagacacagtcgacctgccgccagaagatgct
ataggtcttctggatttggcgacatcttactgtgaaaacagactgaaaaaactttgtcag
cacattatcaagagaggaattactgtggagaatgccttttcgctattctctgctgcagtc
agatatgatgcagaggatttagaagaattctgctttaagttttgcatcaatcatttgaca
gaagttacacagactgcagcattttggcaaatggatggccctctgctaaaggaattcatt
gctaaagccagtaaatgtggagcctttaagaactga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (14)   
   KEGG ORTHOLOGY (1)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (5)   
   OC (1)   
Protein sequence (21)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (18)   
DNA sequence (38)   
   RefSeq(nuc) (20)   
   GenBank (9)   
   EMBL (9)   
Protein domain (4)   
   Pfam (4)   
All databases (83)   

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