KEGG   Homo sapiens (human): 57190
Entry
57190             CDS       T01001                                 
Symbol
SELENON, CFTD, CMYP3, MDRS1, RSMD1, RSS, SELN, SEPN1
Name
(RefSeq) selenoprotein N
  KO
K19874  selenoprotein N
Organism
hsa  Homo sapiens (human)
Disease
H00701  Congenital fiber type disproportion
H01310  Multi-minicore disease
H01810  Congenital myopathy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    57190 (SELENON)
Membrane trafficking [BR:hsa04131]
 Endoplasmic reticulum (ER) - Golgi transport
  Others
   Others
    57190 (SELENON)
SSDB
Motif
Pfam: EF-hand_6 EF-hand_1 RskA EF-hand_7 EF-hand_5
Other DBs
NCBI-GeneID: 57190
NCBI-ProteinID: NP_065184
OMIM: 606210
HGNC: 15999
Ensembl: ENSG00000162430
UniProt: Q9NZV5
Position
1:25800193..25818221
AA seq 590 aa
MGRARPGQRGPPSPGPAAQPPAPPRRRARSLALLGALLAAAAAAAVRVCARHAEAQAAAR
QELALKTLGTDGLFLFSSLDTDGDMYISPEEFKPIAEKLTGSCSVTQTGVQWCSHSSLQP
QLPWLNUSSCLSLLRSTPAASCEEEELPPDPSEETLTIEARFQPLLPETMTKSKDGFLGV
SRLALSGLRNWTAAASPSAVFATRHFQPFLPPPGQELGEPWWIIPSELSMFTGYLSNNRF
YPPPPKGKEVIIHRLLSMFHPRPFVKTRFAPQGAVACLTAISDFYYTVMFRIHAEFQLSE
PPDFPFWFSPAQFTGHIILSKDATHVRDFRLFVPNHRSLNVDMEWLYGASESSNMEVDIG
YIPQMELEATGPSVPSVILDEDGSMIDSHLPSGEPLQFVFEEIKWQQELSWEEAARRLEV
AMYPFKKVSYLPFTEAFDRAKAENKLVHSILLWGALDDQSCUGSGRTLRETVLESSPILT
LLNESFISTWSLVKELEELQNNQENSSHQKLAGLHLEKYSFPVEMMICLPNGTVVHHINA
NYFLDITSVKPEEIESNLFSFSSTFEDPSTATYMQFLKEGLRRGLPLLQP
NT seq 1773 nt   +upstreamnt  +downstreamnt
atgggccgggcccggccgggccaacgcgggccgcccagccccggccccgccgcgcagcct
cccgcgccaccgcgccgccgcgcccgttccctggcgctgctcggagccctgctggccgcc
gccgctgccgccgccgtccgggtctgcgcccgccacgccgaggcccaggcggccgcgcgg
caggaactggcgctgaagaccctggggacagatggcctttttctcttttcctccttggac
actgacggggatatgtacatcagccctgaggagttcaaacccattgctgagaagctaaca
gggtcttgttctgtcacccagactggagtgcagtggtgcagtcacagctcactgcagcct
caacttccctggctcaattgatcctcctgcctcagcctcctgaggtcaactcccgcggcc
agctgcgaggaggaggagttgccccctgaccctagcgaggagacgctcaccatagaagcc
cgattccagcctctgctcccggagaccatgaccaagagcaaagatggcttcctaggggtc
tcccgcctcgccctgtccggcctccgaaactggacagccgccgcctcaccaagtgcagtg
tttgccacccgccacttccagcccttccttcccccgccaggccaggagctgggtgagccc
tggtggatcatccccagtgagctgagcatgttcactggctacctgtccaacaaccgcttc
tatccaccgccgcccaagggcaaggaggtcatcatccaccggctcctgagcatgttccac
cctcggccctttgtgaagacccgctttgcccctcagggagctgtggcctgcctgactgcc
atcagcgacttctactacactgtgatgttccggatccatgccgagttccagctcagtgag
ccgcccgacttccccttttggttctcccctgctcagttcaccggccacatcatcctctcc
aaagacgccacccacgtccgcgacttccggctcttcgtgcccaaccacaggtctctgaat
gtggacatggagtggctttacggggccagtgaaagcagcaacatggaggtggacatcggc
tacataccccagatggagctggaggccacgggcccctctgtgccctccgtgatcctggat
gaggatggcagcatgatcgacagccacctgccttcaggggagcccctgcagtttgtgttt
gaggagatcaagtggcagcaggagctgagctgggaggaggctgcccggcgcctggaggtg
gccatgtaccccttcaagaaggtctcctacttgccgttcactgaggccttcgaccgagcc
aaggctgagaacaagctggtgcactcaatcctgctgtggggggccctggatgaccagtcc
tgctgaggttcagggcggactctccgggagactgtcctggaaagttcgcccatcctcacc
ctgctcaacgagagcttcatcagcacctggtccctggtgaaggagctggaggaactgcag
aacaaccaggagaactcgtcccaccagaagctggctggcctgcacctggagaagtacagc
ttccccgtggagatgatgatctgcctgcccaatggcaccgtggtccatcacatcaatgcc
aactacttcttggacatcacctccgtgaagcccgaggaaatcgagagcaatctcttcagc
ttctcatccacctttgaagacccgtccacggccacctacatgcagttcctgaaggaggga
ctccggcgtggcctgcccctcctccagccctag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (5)   
   KEGG DISEASE (3)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (24)   
   KEGG ORTHOLOGY (1)   
   RefGene (17)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (4)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (28)   
   RefSeq(nuc) (2)   
   GenBank (13)   
   EMBL (13)   
Protein domain (5)   
   Pfam (5)   
All databases (69)   

Download RDF
DBGET integrated database retrieval system