KEGG   Homo sapiens (human): 10483
Entry
10483             CDS       T01001                                 
Symbol
SEC23B, CDA-II, CDAII, CDAN2, CWS7, HEMPAS, hSec23B
Name
(RefSeq) SEC23 homolog B, COPII coat complex component
  KO
K14006  protein transport protein SEC23
Organism
hsa  Homo sapiens (human)
Pathway
hsa04141  Protein processing in endoplasmic reticulum
Network
nt06180  Pathogenic Escherichia coli
  Element
N01289  COPII vesicle formation
Disease
H00917  Congenital dyserythropoietic anemia
H01222  Cowden syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09123 Folding, sorting and degradation
   04141 Protein processing in endoplasmic reticulum
    10483 (SEC23B)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    10483 (SEC23B)
Membrane trafficking [BR:hsa04131]
 Endoplasmic reticulum (ER) - Golgi transport
  Forward pathways
   Coat protein complex II (COP-II)
    10483 (SEC23B)
SSDB
Motif
Pfam: Sec23_trunk Sec23_helical Sec23_BS Gelsolin zf-Sec23_Sec24
Other DBs
NCBI-GeneID: 10483
NCBI-ProteinID: NP_001166216
OMIM: 610512
HGNC: 10702
Ensembl: ENSG00000101310
UniProt: Q15437
Position
20:18507548..18561415
AA seq 767 aa
MATYLEFIQQNEERDGVRFSWNVWPSSRLEATRMVVPLACLLTPLKERPDLPPVQYEPVL
CSRPTCKAVLNPLCQVDYRAKLWACNFCFQRNQFPPAYGGISEVNQPAELMPQFSTIEYV
IQRGAQSPLIFLYVVDTCLEEDDLQALKESLQMSLSLLPPDALVGLITFGRMVQVHELSC
EGISKSYVFRGTKDLTAKQIQDMLGLTKPAMPMQQARPAQPQEHPFASSRFLQPVHKIDM
NLTDLLGELQRDPWPVTQGKRPLRSTGVALSIAVGLLEGTFPNTGARIMLFTGGPPTQGP
GMVVGDELKIPIRSWHDIEKDNARFMKKATKHYEMLANRTAANGHCIDIYACALDQTGLL
EMKCCANLTGGYMVMGDSFNTSLFKQTFQRIFTKDFNGDFRMAFGATLDVKTSRELKIAG
AIGPCVSLNVKGPCVSENELGVGGTSQWKICGLDPTSTLGIYFEVVNQHNTPIPQGGRGA
IQFVTHYQHSSTQRRIRVTTIARNWADVQSQLRHIEAAFDQEAAAVLMARLGVFRAESEE
GPDVLRWLDRQLIRLCQKFGQYNKEDPTSFRLSDSFSLYPQFMFHLRRSPFLQVFNNSPD
ESSYYRHHFARQDLTQSLIMIQPILYSYSFHGPPEPVLLDSSSILADRILLMDTFFQIVI
YLGETIAQWRKAGYQDMPEYENFKHLLQAPLDDAQEILQARFPMPRYINTEHGGSQARFL
LSKVNPSQTHNNLYAWGQETGAPILTDDVSLQVFMDHLKKLAVSSAC
NT seq 2304 nt   +upstreamnt  +downstreamnt
atggcgacatacctggagttcatccagcagaatgaagaacgggatggtgtgcgttttagt
tggaacgtgtggccttccagccggctggaggctacaagaatggttgtacccctggcttgt
ctccttactcctttgaaagaacgtccagacctacctcctgtacaatatgaacctgtgctt
tgcagcaggccaacttgtaaagctgttctcaacccactttgtcaggttgattatcgagca
aaactttgggcctgtaatttctgttttcaaagaaatcagtttcctccagcttatggaggc
atatctgaggtgaatcaacctgccgaattgatgccccagttttctacaattgagtacgtg
atacagcgaggtgctcagtcccctctgatctttctctatgtggttgacacatgcctggag
gaagatgaccttcaagcactcaaagagtccctgcagatgtccctgagtcttcttcctcca
gatgctctggtgggtctgatcacatttggaaggatggtgcaggttcatgagctaagctgt
gaaggaatctccaaaagttatgtcttccgagggaccaaggatttaactgcaaagcaaata
caggatatgttgggcctgaccaagccagccatgcccatgcagcaagcacgacctgcacaa
ccacaggagcacccttttgcttcaagcagatttctgcagcctgttcacaagattgatatg
aacctcactgatcttcttggggagctacagagggacccatggccagtaactcaggggaag
agacctttgcgatccactggtgtggctttgtccattgctgttggcttgctggagggcact
tttccaaacacaggagccaggatcatgctgtttactggaggtccccctacccaagggcct
ggcatggtggttggagatgaattaaagattcctattcgttcttggcatgatattgagaaa
gataatgcacgattcatgaaaaaggcaaccaagcactatgagatgcttgctaatcgaaca
gctgcaaatggtcactgcattgatatttatgcttgtgcccttgatcaaactggacttttg
gagatgaagtgttgtgcaaatcttactggaggctacatggtaatgggagattctttcaac
acttctctcttcaagcagacattccaaagaatctttactaaagattttaatggagatttc
cgaatggcatttggtgctactttggacgtaaagacctctcgggaactgaagattgcagga
gccattggtccatgcgtatctctgaatgtgaaaggaccgtgtgtgtcagaaaatgagctt
ggtgttggtggcacgagtcagtggaaaatctgtggcctagatcctacatctacacttggc
atctattttgaagttgtcaatcagcacaacaccccgatcccccaaggaggcagaggagcc
atccagtttgtcacgcattatcagcactccagcacccagagacgcatccgcgtgaccacc
atcgcccgaaattgggcagatgtacagagtcagctcaggcacatagaagcagcatttgac
caggaggctgcggcagtgttgatggcacggcttggggtgttccgagcggagtcagaggag
gggcccgatgtgctccggtggctggaccgacaactcatccgactgtgtcaaaagtttgga
cagtataacaaagaagaccccacttcttttaggttatcagattccttttctctatatcct
cagtttatgttccatctgagaagatctccatttcttcaagtgtttaacaacagtcctgat
gagtcgtcatattacagacatcattttgcccggcaggacctgacccagtccctcatcatg
atccagcccattctctactcttactcctttcatgggccaccagagccagtactcttggat
agcagcagcattctagctgacagaattttgctgatggatactttctttcaaattgtcatt
tatcttggtgagaccatagcccagtggcgtaaagctggctaccaggacatgcccgagtat
gaaaacttcaagcaccttctgcaggcaccactggatgatgctcaagaaattctgcaagca
cgcttcccgatgccacgttacatcaacacggagcatggaggcagtcaggctcgattcctt
ttgtccaaagtgaacccatctcagacacacaataacctgtatgcttggggacaggaaact
ggagcacccatcctaactgatgatgttagcctgcaggtgttcatggaccatttgaagaag
ctggctgtctccagtgcctgttaa

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Ontology (2)   
   KEGG BRITE (2)   
Pathway (1)   
   KEGG PATHWAY (1)   
Network (2)   
   KEGG NETWORK (2)   
Disease (5)   
   KEGG DISEASE (2)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (18)   
   KEGG ORTHOLOGY (1)   
   RefGene (6)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (6)   
   OC (1)   
Protein sequence (7)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (5)   
DNA sequence (45)   
   RefSeq(nuc) (5)   
   GenBank (20)   
   EMBL (20)   
Protein domain (5)   
   Pfam (5)   
All databases (86)   

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