KEGG   Homo sapiens (human): 1212
Entry
1212              CDS       T01001                                 
Symbol
CLTB, LCB
Name
(RefSeq) clathrin light chain B
  KO
K04645  clathrin light chain B
Organism
hsa  Homo sapiens (human)
Pathway
hsa04142  Lysosome
hsa04144  Endocytosis
hsa04721  Synaptic vesicle cycle
hsa04961  Endocrine and other factor-regulated calcium reabsorption
hsa05016  Huntington disease
hsa05100  Bacterial invasion of epithelial cells
Network
nt06515  Regulation of kinetochore-microtubule interactions
  Element
N01547  Kinetochore fiber organization
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09141 Transport and catabolism
   04144 Endocytosis
    1212 (CLTB)
   04142 Lysosome
    1212 (CLTB)
 09150 Organismal Systems
  09155 Excretory system
   04961 Endocrine and other factor-regulated calcium reabsorption
    1212 (CLTB)
  09156 Nervous system
   04721 Synaptic vesicle cycle
    1212 (CLTB)
 09160 Human Diseases
  09171 Infectious disease: bacterial
   05100 Bacterial invasion of epithelial cells
    1212 (CLTB)
  09164 Neurodegenerative disease
   05016 Huntington disease
    1212 (CLTB)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    1212 (CLTB)
Membrane trafficking [BR:hsa04131]
 Endocytosis
  Clathrin-mediated endocytosis
   Clathrin
    1212 (CLTB)
SSDB
Motif
Pfam: Clathrin_lg_ch bDLD3 POP1_C
Other DBs
NCBI-GeneID: 1212
NCBI-ProteinID: NP_009028
OMIM: 118970
HGNC: 2091
Ensembl: ENSG00000175416
UniProt: P09497
Position
5:complement(176392455..176416569)
AA seq 229 aa
MADDFGFFSSSESGAPEAAEEDPAAAFLAQQESEIAGIENDEGFGAPAGSHAAPAQPGPT
SGAGSEDMGTTVNGDVFQEANGPADGYAAIAQADRLTQEPESIRKWREEQRKRLQELDAA
SKVTEQEWREKAKKDLEEWNQRQSEQVEKNKINNRIADKAFYQQPDADIIGYVASEEAFV
KESKEETPGTEWEKVAQLCDFNPKSSKQCKDVSRLRSVLMSLKQTPLSR
NT seq 690 nt   +upstreamnt  +downstreamnt
atggctgatgactttggcttcttctcgtcgtcggagagcggtgccccggaggcggcggag
gaggacccggcggccgccttcctggcccagcaggagagcgagattgcaggcatagagaac
gacgagggcttcggggcacctgccggcagccatgcggcccccgcgcagccgggccccacg
agtggggctggttctgaggacatggggaccacagtcaatggagatgtgtttcaggaggcc
aacggtcctgctgatggctacgcagccattgcccaggctgacaggctgacccaggagcct
gagagcatccgcaagtggcgagaggagcagaggaaacggctgcaagagctggatgctgca
tctaaggtcacggaacaggaatggcgggagaaggccaagaaggacctggaggagtggaac
cagcgccagagtgaacaagtagagaagaacaagatcaacaaccggatcgctgacaaagca
ttctaccagcagccagatgctgatatcatcggctacgtggcatccgaggaggctttcgtg
aaggaatccaaggaggagaccccaggcacagagtgggagaaggtggcccagctatgtgac
ttcaaccccaagagcagcaagcagtgcaaagatgtgtcccgcctgcgctcggtgctcatg
tccctgaagcagacgccactgtcccgctag

  All links  
Disease (1)   
   OMIM (1)   
Gene (17)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (12)   
   OC (1)   
Protein sequence (10)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (8)   
DNA sequence (30)   
   RefSeq(nuc) (10)   
   GenBank (10)   
   EMBL (10)   
Protein domain (3)   
   Pfam (3)   
All databases (61)   

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