KEGG   Homo sapiens (human): 10073
Entry
10073             CDS       T01001                                 
Symbol
SNUPN, KPNBL, LGMDR29, RNUT1, Snurportin1
Name
(RefSeq) snurportin 1
  KO
K13151  snurportin-1
Organism
hsa  Homo sapiens (human)
Pathway
hsa03013  Nucleocytoplasmic transport
Disease
H00593  Limb-girdle muscular dystrophy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09122 Translation
   03013 Nucleocytoplasmic transport
    10073 (SNUPN)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03041 Spliceosome [BR:hsa03041]
    10073 (SNUPN)
Spliceosome [BR:hsa03041]
 Other splicing related proteins
  Proteins involved in snRNP biogenesis
   Other proteins involved in snRNP biogenesis
    10073 (SNUPN)
SSDB
Motif
Pfam: SPN1_m3Gcap_bd Snurportin1 mRNA_cap_enzyme IBB
Other DBs
NCBI-GeneID: 10073
NCBI-ProteinID: NP_001036046
OMIM: 607902
HGNC: 14245
Ensembl: ENSG00000169371
UniProt: O95149
Structure
Position
15:complement(75598086..75626461)
AA seq 360 aa
MEELSQALASSFSVSQDLNSTAAPHPRLSQYKSKYSSLEQSERRRRLLELQKSKRLDYVN
HARRLAEDDWTGMESEEENKKDDEEMDIDTVKKLPKHYANQLMLSEWLIDVPSDLGQEWI
VVVCPVGKRALIVASRGSTSAYTKSGYCVNRFSSLLPGGNRRNSTAKDYTILDCIYNEVN
QTYYVLDVMCWRGHPFYDCQTDFRFYWMHSKLPEEEGLGEKTKLNPFKFVGLKNFPCTPE
SLCDVLSMDFPFEVDGLLFYHKQTHYSPGSTPLVGWLRPYMVSDVLGVAVPAGPLTTKPD
YAGHQLQQIMEHKKSQKEGMKEKLTHKASENGHYELEHLSTPKLKGSSHSPDHPGCLMEN
NT seq 1083 nt   +upstreamnt  +downstreamnt
atggaagagttgagtcaggccctggctagtagcttttctgtgtctcaagatctgaacagc
acagctgccccacacccccgcctatcccagtacaagtccaagtacagttccttggagcag
agtgagcgccgccggaggttactggaactgcagaaatccaagcggctggattatgtgaac
catgccagaagactggctgaagatgactggacagggatggagagtgaggaagaaaataag
aaagatgatgaagaaatggacattgacactgtcaagaagttaccaaaacactatgctaat
caattgatgctttctgagtggttaattgacgttccttcagatttggggcaggaatggatt
gtggtcgtgtgccctgttggaaaaagagcccttatcgtggcctccaggggttctaccagt
gcctacaccaagagtggctactgtgtcaacaggttttcttcacttctgccaggaggcaac
aggcgaaactcaacagcaaaagactacaccattctagattgcatttacaatgaggtaaac
cagacctactacgttctggatgtgatgtgctggcggggacaccctttttatgattgccag
actgatttccgattctactggatgcattcaaagttaccagaagaagaaggactgggagag
aaaaccaagcttaatccttttaaatttgtggggctaaagaacttcccttgcactcccgaa
agcctgtgtgatgtgctatctatggatttcccttttgaggtagatggacttctcttctac
cacaaacagacccactacagccccggaagcactcccttggtgggctggctgcgcccctac
atggtgtcagatgtccttggtgtagctgtgccggctggcccgctgaccaccaagccagac
tatgctgggcaccagctccagcagattatggagcacaagaagagccagaaggaaggcatg
aaggagaaactcacacacaaggcctctgagaatgggcactatgaattggagcacctgtct
actcccaagttgaagggttcttcccatagcccagaccaccctggatgcctcatggagaat
taa

  All links  
Disease (2)   
   OMIM (2)   
Gene (16)   
   RefGene (8)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (3)   
   OC (1)   
Protein sequence (5)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (3)   
DNA sequence (17)   
   RefSeq(nuc) (3)   
   GenBank (7)   
   EMBL (7)   
3D Structure (11)   
   PDB (11)   
Protein domain (4)   
   Pfam (4)   
All databases (55)   

Download RDF
DBGET integrated database retrieval system