KEGG   Homo sapiens (human): 50515
Entry
50515             CDS       T01001                                 
Symbol
CHST11, C4ST, C4ST-1, C4ST1, HSA269537, OCBMD
Name
(RefSeq) carbohydrate sulfotransferase 11
  KO
K01017  chondroitin 4-sulfotransferase 11 [EC:2.8.2.5]
Organism
hsa  Homo sapiens (human)
Pathway
hsa00532  Glycosaminoglycan biosynthesis - chondroitin sulfate / dermatan sulfate
Disease
H02801  Osteochondrodysplasia, brachydactyly, and overlapping malformed digits
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09100 Metabolism
  09107 Glycan biosynthesis and metabolism
   00532 Glycosaminoglycan biosynthesis - chondroitin sulfate / dermatan sulfate
    50515 (CHST11)
 09180 Brite Hierarchies
  09181 Protein families: metabolism
   01003 Glycosyltransferases [BR:hsa01003]
    50515 (CHST11)
Enzymes [BR:hsa01000]
 2. Transferases
  2.8  Transferring sulfur-containing groups
   2.8.2  Sulfotransferases
    2.8.2.5  chondroitin 4-sulfotransferase
     50515 (CHST11)
Glycosyltransferases [BR:hsa01003]
 Unclassified
  Sulfotransferases
   50515 (CHST11)
SSDB
Motif
Pfam: Sulfotransfer_2
Other DBs
NCBI-GeneID: 50515
NCBI-ProteinID: NP_060883
OMIM: 610128
HGNC: 17422
Ensembl: ENSG00000171310
UniProt: Q9NPF2
Position
12:104456948..104762014
AA seq 352 aa
MKPALLEVMRMNRICRMVLATCLGSFILVIFYFQSMLHPVMRRNPFGVDICCRKGSRSPL
QELYNPIQLELSNTAVLHQMRRDQVTDTCRANSATSRKRRVLTPNDLKHLVVDEDHELIY
CYVPKVACTNWKRLMMVLTGRGKYSDPMEIPANEAHVSANLKTLNQYSIPEINHRLKSYM
KFLFVREPFERLVSAYRNKFTQKYNISFHKRYGTKIIKRQRKNATQEALRKGDDVKFEEF
VAYLIDPHTQREEPFNEHWQTVYSLCHPCHIHYDLVGKYETLEEDSNYVLQLAGVGSYLK
FPTYAKSTRTTDEMTTEFFQNISSEHQTQLYEVYKLDFLMFNYSVPSYLKLE
NT seq 1059 nt   +upstreamnt  +downstreamnt
atgaagccagcgctgctggaagtgatgaggatgaacagaatctgccggatggtgctggcc
acttgcttgggatcctttatcctggtcatcttctatttccaaagtatgttgcacccagtc
atgcggaggaatccctttggtgtggacatctgctgccggaaggggtcccgaagccccctg
caggaactctacaacccaatccagctggagctctcaaacactgctgtcctgcaccagatg
cggcgggaccaggtgacagacacgtgccgagccaacagcgccacaagccgtaagcggagg
gtgctgacccccaacgacctgaagcacttggtggtggatgaggaccacgagctcatctac
tgctacgtgcccaaggtggcctgcaccaactggaagcggctcatgatggtcctgaccggg
cgggggaagtacagcgaccccatggagatcccggccaacgaggcacacgtctccgccaac
ctgaagaccctgaaccagtacagcatcccagaaatcaaccaccgcttgaaaagctacatg
aagttcctgtttgtccgggagcccttcgagaggctagtgtccgcctaccgcaacaagttc
acccagaagtacaacatctccttccacaagcggtacggcaccaagatcatcaaacgccag
cggaagaacgccacccaggaggccctgcgcaaaggggacgatgtcaaattcgaggagttt
gtggcctatctcatcgacccacacacccagcgggaggagcctttcaacgaacactggcaa
accgtctactcactctgccatccctgccacatccactatgacctcgtgggcaagtacgag
acactggaagaggattctaattacgtcctgcagctggcaggagtgggcagctacctgaag
ttccccacctatgcaaagtctacgagaactactgatgaaatgaccacagaattcttccag
aacatcagctcagagcaccaaacgcagctgtacgaagtctacaaactcgattttttaatg
ttcaattactcagtgccaagctacctgaaattggaataa

  All links  
Disease (2)   
   OMIM (2)   
Gene (13)   
   RefGene (6)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
Protein sequence (8)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (6)   
DNA sequence (36)   
   RefSeq(nuc) (6)   
   GenBank (15)   
   EMBL (15)   
Protein domain (1)   
   Pfam (1)   
All databases (60)   

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