KEGG   Homo sapiens (human): 8086
Entry
8086              CDS       T01001                                 
Symbol
AAAS, AAA, AAASb, ADRACALA, ADRACALIN, ALADIN, GL003
Name
(RefSeq) aladin WD repeat nucleoporin
  KO
K14320  aladin
Organism
hsa  Homo sapiens (human)
Pathway
hsa03013  Nucleocytoplasmic transport
Disease
H00257  Achalasia Addisonianism Alacrima syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09122 Translation
   03013 Nucleocytoplasmic transport
    8086 (AAAS)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03019 Messenger RNA biogenesis [BR:hsa03019]
    8086 (AAAS)
Messenger RNA biogenesis [BR:hsa03019]
 Eukaryotic type
  mRNA surveillance and transport factors
   Transport factors
    Nuclear pore complex
     8086 (AAAS)
SSDB
Motif
Pfam: WD40_WDHD1_1st WD40 ANAPC4_WD40 WD40_CDC20-Fz WD40_Prp19 Beta-prop_EML_2 Beta-prop_RIG_2nd Beta-prop_WDR19_1st Beta-prop_IFT140_1st PD40 Beta-prop_CAF1B_HIR1 WDR90_beta-prop_4th DUF5789
Other DBs
NCBI-GeneID: 8086
NCBI-ProteinID: NP_056480
OMIM: 605378
HGNC: 13666
Ensembl: ENSG00000094914
UniProt: Q9NRG9
Structure
Position
12:complement(53307460..53321610)
AA seq 546 aa
MCSLGLFPPPPPRGQVTLYEHNNELVTGSSYESPPPDFRGQWINLPVLQLTKDPLKTPGR
LDHGTRTAFIHHREQVWKRCINIWRDVGLFGVLNEIANSEEEVFEWVKTASGWALALCRW
ASSLHGSLFPHLSLRSEDLIAEFAQVTNWSSCCLRVFAWHPHTNKFAVALLDDSVRVYNA
SSTIVPSLKHRLQRNVASLAWKPLSASVLAVACQSCILIWTLDPTSLSTRPSSGCAQVLS
HPGHTPVTSLAWAPSGGRLLSASPVDAAIRVWDVSTETCVPLPWFRGGGVTNLLWSPDGS
KILATTPSAVFRVWEAQMWTCERWPTLSGRCQTGCWSPDGSRLLFTVLGEPLIYSLSFPE
RCGEGKGCVGGAKSATIVADLSETTIQTPDGEERLGGEAHSMVWDPSGERLAVLMKGKPR
VQDGKPVILLFRTRNSPVFELLPCGIIQGEPGAQPQLITFHPSFNKGALLSVGWSTGRIA
HIPLYFVNAQFPRFSPVLGRAQEPPAGGGGSIHDLPLFTETSPTSAPWDPLPGPPPVLPH
SPHSHL
NT seq 1641 nt   +upstreamnt  +downstreamnt
atgtgctctctggggttgttccctcctccaccgcctcggggtcaagtcaccctatatgag
cacaataacgagctggtgacgggcagtagctatgagagcccgccccccgacttccggggc
cagtggatcaatcttcctgtcctacaactgacaaaggatcccctaaagacccctggaagg
ctggaccatggcacaagaactgccttcatccatcaccgggagcaagtgtggaagagatgc
atcaacatttggcgtgatgtgggcctttttggggtgctaaatgaaattgcaaactcagaa
gaagaggtgtttgagtgggtgaagacggcatccggctgggccctggcactctgtcgatgg
gcctcttccctccatgggtccctgttcccccatctgtctctcaggagcgaagatctgatc
gctgaatttgcccaagtcacaaattggtccagctgctgcttgcgtgtctttgcatggcac
ccccacaccaacaagtttgcagtggccctgctagatgactcagtccgtgtgtataatgcc
agcagcaccatagtcccctccctgaagcaccggctgcagcgaaatgtggcgtctctggcc
tggaagccccttagtgcctctgtcttggctgtggcctgccagagctgcattcttatctgg
accctggaccctacctccttgtctacccgaccctcttctggctgtgcccaagtgctgtct
caccctgggcatacacctgttaccagcttggcctgggcccccagtggggggcggctgctc
tcagcttcacccgtggatgctgctatccgggtatgggatgtctcaacagagacctgtgtc
ccccttccctggttccgaggaggtggggtgaccaacctgctctggtccccagacggcagc
aaaatcctggctaccactccttcagctgtctttcgagtctgggaggcccagatgtggact
tgtgagaggtggcctactctatcagggcgctgtcagactggctgctggagcccagatggc
agccgactgctgttcactgtattgggagagccactgatttactccctgtcttttccagaa
cgttgtggtgagggaaaggggtgcgttggaggtgcaaagtcagcaacgattgtggcagat
ctgtctgagacaacaatacagacaccagatggtgaggagaggcttgggggagaggctcac
tccatggtctgggaccccagtggggaacgtctggctgtgcttatgaaaggaaagccaagg
gtacaggatggtaaaccagtcatcctcctttttcgcactcgaaacagccctgtgtttgag
ctccttccctgtggcattatccagggggagccaggagcccagccccagctcatcactttc
catccttccttcaacaaaggggccctgctcagtgtgggctggtccacaggccgaattgcc
cacatcccgctgtactttgtcaatgcccagtttccacgttttagcccagtgcttgggcgg
gcccaggaaccccctgctgggggtggaggctctattcatgacctgcccctctttactgag
acatccccaacctctgccccttgggaccctctcccagggccaccacctgttctgccccac
tccccacattcccacctctaa

  All links  
Disease (2)   
   OMIM (2)   
Gene (15)   
   RefGene (6)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (4)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (26)   
   RefSeq(nuc) (2)   
   GenBank (12)   
   EMBL (12)   
3D Structure (4)   
   PDB (4)   
Protein domain (13)   
   Pfam (13)   
All databases (64)   

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