KEGG   Homo sapiens (human): 1155
Entry
1155              CDS       T01001                                 
Symbol
TBCB, CG22, CKAP1, CKAPI
Name
(RefSeq) tubulin-folding cofactor B isoform 1
  KO
K17262  tubulin-specific chaperone B
Organism
hsa  Homo sapiens (human)
Disease
H02397  Neurodevelopmental disorder with movement abnormalities or hypotonia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04812 Cytoskeleton proteins [BR:hsa04812]
    1155 (TBCB)
   04147 Exosome [BR:hsa04147]
    1155 (TBCB)
Cytoskeleton proteins [BR:hsa04812]
 Eukaryotic cytoskeleton proteins
  Microtubules
   Tubulin-binding proteins
    Others
     1155 (TBCB)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
   1155 (TBCB)
SSDB
Motif
Pfam: Ubiquitin_2 CAP_GLY RSV_NS2 OCRL_clath_bd DUF8537
Other DBs
NCBI-GeneID: 1155
NCBI-ProteinID: NP_001272
OMIM: 601303
HGNC: 1989
Ensembl: ENSP00000221855.3
UniProt: Q99426
Position
19:36114967..36125941
AA seq 244 aa
MEVTGVSAPTVTVFISSSLNTFRSEKRYSRSLTIAEFKCKLELLVGSPASCMELELYGVD
DKFYSKLDQEDALLGSYPVDDGCRIHVIDHSGARLGEYEDVSRVEKYTISQEAYDQRQDT
VRSFLKRSKLGRYNEEERAQQEAEAAQRLAEEKAQASSIPVGSRCEVRAAGQSPRRGTVM
YVGLTDFKPGYWIGVRYDEPLGKNDGSVNGKRYFECQAKYGAFVKPAVVTVGDFPEEDYG
LDEI
NT seq 735 nt   +upstreamnt  +downstreamnt
atggaggtgacgggggtgtcggcacccacggtgaccgttttcatcagcagctccctcaac
accttccgctccgagaagcgatacagccgcagcctcaccatcgctgagttcaagtgtaaa
ctggagttgctggtgggcagccctgcttcctgcatggaactggagctgtatggagttgac
gacaagttctacagcaagctggatcaagaggatgcgctcctgggctcctaccctgtagat
gacggctgccgcatccacgtcattgaccacagtggcgcccgccttggtgagtatgaggac
gtgtcccgggtggagaagtacacgatctcacaagaagcctacgaccagaggcaagacacg
gtccgctctttcctgaagcgcagcaagctcggccggtacaacgaggaggagcgggctcag
caggaggccgaggccgcccagcgcctggccgaggagaaggcccaggccagctccatcccc
gtgggcagccgctgtgaggtgcgggcggcgggacaatcccctcgccggggcaccgtcatg
tatgtaggtctcacagatttcaagcctggctactggattggtgtccgctatgatgagcca
ctggggaaaaatgatggcagtgtgaatgggaaacgctacttcgaatgccaggccaagtat
ggcgcctttgtcaagccagcagtcgtgacggtgggggacttcccggaggaggactacggg
ttggacgagatatga

  All links  
Disease (2)   
   OMIM (2)   
Gene (21)   
   RefGene (2)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (14)   
   OC (1)   
Protein sequence (4)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (25)   
   RefSeq(nuc) (3)   
   GenBank (11)   
   EMBL (11)   
Protein domain (5)   
   Pfam (5)   
All databases (57)   

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