KEGG   Homo sapiens (human): 30000
Entry
30000             CDS       T01001                                 
Symbol
TNPO2, IDDHISD, IPO3, KPNB2B, TRN2
Name
(RefSeq) transportin 2
  KO
K18727  transportin-2
Organism
hsa  Homo sapiens (human)
Pathway
hsa03013  Nucleocytoplasmic transport
Disease
H02463  Syndromic intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09122 Translation
   03013 Nucleocytoplasmic transport
    30000 (TNPO2)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03019 Messenger RNA biogenesis [BR:hsa03019]
    30000 (TNPO2)
Messenger RNA biogenesis [BR:hsa03019]
 Eukaryotic type
  mRNA surveillance and transport factors
   Transport factors
    Ran-mediated transport factors
     30000 (TNPO2)
SSDB
Motif
Pfam: HEAT_EZ HEAT Arm HEAT_2 IBN_N Cnd1 Vac14_Fab1_bd PDS5 Adaptin_N MMS19_C UNC45-central SCD Dopey_N RTP1_C1 DUF2573
Other DBs
NCBI-GeneID: 30000
NCBI-ProteinID: NP_001129668
OMIM: 603002
HGNC: 19998
Ensembl: ENSG00000105576
UniProt: O14787 Q05D48
Position
19:complement(12699201..12723932)
AA seq 897 aa
MDWQPDEQGLQQVLQLLKDSQSPNTATQRIVQDKLKQLNQFPDFNNYLIFVLTRLKSEDE
PTRSLSGLILKNNVKAHYQSFPPPVADFIKQECLNNIGDASSLIRATIGILITTIASKGE
LQMWPELLPQLCNLLNSEDYNTCEGAFGALQKICEDSSELLDSDALNRPLNIMIPKFLQF
FKHCSPKIRSHAIACVNQFIMDRAQALMDNIDTFIEHLFALAVDDDPEVRKNVCRALVML
LEVRIDRLIPHMHSIIQYMLQRTQDHDENVALEACEFWLTLAEQPICKEVLASHLVQLIP
ILVNGMKYSEIDIILLKGDVEEDEAVPDSEQDIKPRFHKSRTVTLPHEAERPDGSEDAED
DDDDDALSDWNLRKCSAAALDVLANVFREELLPHLLPLLKGLLFHPEWVVKESGILVLGA
IAEGCMQGMVPYLPELIPHLIQCLSDKKALVRSIACWTLSRYAHWVVSQPPDMHLKPLMT
ELLKRILDGNKRVQEAACSAFATLEEEACTELVPYLSYILDTLVFAFGKYQHKNLLILYD
AIGTLADSVGHHLNQPEYIQKLMPPLIQKWNELKDEDKDLFPLLECLSSVATALQSGFLP
YCEPVYQRCVTLVQKTLAQAMMYTQHPEQYEAPDKDFMIVALDLLSGLAEGLGGHVEQLV
ARSNIMTLLFQCMQDSMPEVRQSSFALLGDLTKACFIHVKPCIAEFMPILGTNLNPEFIS
VCNNATWAIGEICMQMGAEMQPYVQMVLNNLVEIINRPNTPKTLLENTGRLTSPSAIPAI
TIGRLGYVCPQEVAPMLQQFIRPWCTSLRNIRDNEEKDSAFRGICMMIGVNPGGVVQDFI
FFCDAVASWVSPKDDLRDMFYKILHGFKDQVGEDNWQQFSEQFPPLLKERLAAFYGV
NT seq 2694 nt   +upstreamnt  +downstreamnt
atggactggcagccagacgagcagggcctgcagcaggtcctgcagctgctcaaagactca
cagtcgcccaacacagccactcagcgcatcgtgcaggataaactcaaacaactcaatcag
tttcctgacttcaacaactacctgattttcgtcctgaccagactcaagtcagaagatgag
ccaacgcgctctctcagtggcctcatcctcaagaacaacgtgaaggcacactatcagagc
ttcccaccccctgtggcagacttcatcaaacaggagtgtctcaacaacattggcgatgcc
tcctcgctcatccgagccaccattggcattctcatcaccaccatcgcttccaagggtgag
ctgcagatgtggcccgagctgctgccccagctctgcaacctgcttaactcggaggattac
aacacttgtgagggagcctttggagccctgcagaagatctgtgaagactcatcagagctt
ctggacagtgacgccctcaacaggcccctcaacatcatgatccccaagttcctgcagttc
ttcaagcactgcagtcccaagatccggtcccacgccatcgcctgcgtgaaccagttcatc
atggaccgggcccaggcgctgatggacaatattgacaccttcatcgagcacctatttgcc
ctggctgtggatgatgaccccgaggtgcggaagaatgtgtgccgtgccctggtgatgctt
ctggaagtgcggattgacaggctcatcccccacatgcacagcatcatccagtacatgctg
cagaggacccaggaccatgatgagaacgttgcccttgaggcctgtgagttctggctgacg
ctggccgagcagcccatctgcaaggaagtcctggcctcccatctggtccagttgatcccc
atcttggtgaatgggatgaagtactcggaaattgacatcatcctgctcaagggggatgtg
gaggaggatgaggctgtccccgacagtgagcaggacatcaagccacgcttccacaagtca
cgcacggtcacactgccccacgaggctgagcggcctgatggctccgaggacgcggaggat
gacgatgatgatgatgctctgtccgactggaatttgaggaagtgctcagcggctgcactg
gacgtcctcgccaatgtcttccgggaggaactgctgccccacctactcccactactcaaa
ggcctcctcttccaccccgagtgggtggtcaaggagtcgggcatcctggtgctgggcgcc
attgctgagggctgcatgcagggcatggtgccctacctgcctgagctgatcccgcacctg
atccagtgcctgtcggataagaaggccttggtccgctccatcgcctgctggacgctgagc
cgctatgcccactgggtggtcagccagccacccgacatgcacctcaagcccctgatgaca
gagctgctcaaacgcatcctggatggcaacaagagggtacaggaggcggcctgcagtgct
tttgccaccctggaggaagaggcctgcacggagctggtgccctacctcagctacatcctg
gacacccttgtctttgcctttgggaaataccagcacaagaacctgctcatcctctatgac
gccattggcaccctggccgactctgtaggccaccacctcaaccagccggaatacatccag
aagctgatgcccccactgatccagaagtggaatgagctcaaggacgaagacaaggacctc
ttccccctgctggagtgtctgtcatcggtggccaccgccctgcagagtggcttcctgcct
tactgtgagcccgtctaccagcgctgtgtcaccctggtgcagaagacactggctcaggcc
atgatgtacacccagcaccctgagcagtatgaggctcccgacaaggacttcatgatcgta
gcactggatctgctcagcggcctggccgagggcctgggtggtcacgtggagcagctggtg
gcccgcagcaacatcatgacattgctgttccagtgcatgcaggactcgatgcctgaggtc
cggcagagctcctttgccctcctgggagacctcaccaaagcctgcttcatccatgtcaag
ccctgtatcgccgagttcatgcccattctgggcaccaacctgaacccagagttcatctcc
gtctgcaacaacgccacctgggccattggtgaaatctgcatgcagatgggggcagagatg
cagccttatgtgcagatggtcctcaacaacctggtggaaatcattaaccgacccaacaca
cccaagacactgctggaaaacacaggtcgcctgacgagtccctctgccattccagccatc
accatcggccgcttgggctacgtgtgcccccaggaggtggcacccatgctgcagcagttc
atccggccttggtgcacgtccctcaggaacatcagggacaacgaggagaaggactcagcc
ttccgcggcatctgcatgatgatcggtgtcaacccggggggcgttgtgcaggactttatt
ttcttctgcgatgctgtagcctcctgggtgagcccgaaggatgaccttcgggacatgttt
tataagattctccacggcttcaaagaccaagttggggaagataactggcagcagttctct
gagcaattcccgccgctgctcaaggagaggctggcggctttctatggggtctag

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Ontology (2)   
   KEGG BRITE (2)   
Pathway (1)   
   KEGG PATHWAY (1)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (20)   
   KEGG ORTHOLOGY (1)   
   RefGene (11)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (3)   
   OC (1)   
Protein sequence (14)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (11)   
DNA sequence (49)   
   RefSeq(nuc) (17)   
   GenBank (16)   
   EMBL (16)   
Protein domain (15)   
   Pfam (15)   
All databases (105)   

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