Homo sapiens (human): 348995 Help Entry 348995            CDS       T01001                                  Symbol NUP43, bA350J20.1, p42 Name (RefSeq) nucleoporin 43   KO K14305   nuclear pore complex protein Nup43 Organism hsa  Homo sapiens (human) Pathway hsa03013   Nucleocytoplasmic transport hsa05014   Amyotrophic lateral sclerosis Network nt06464  Amyotrophic lateral sclerosis   Element N01152   Nuclear export of mRNA N01153   Mutation-caused aberrant GLE1 to nuclear export of mRNA Brite KEGG Orthology (KO) [BR:hsa00001]  09120 Genetic Information Processing   09122 Translation    03013 Nucleocytoplasmic transport     348995 (NUP43)  09160 Human Diseases   09164 Neurodegenerative disease    05014 Amyotrophic lateral sclerosis     348995 (NUP43)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03019 Messenger RNA biogenesis [BR:hsa03019]     348995 (NUP43)    03036 Chromosome and associated proteins [BR:hsa03036]     348995 (NUP43) Messenger RNA biogenesis [BR:hsa03019]  Eukaryotic type   mRNA surveillance and transport factors    Transport factors     Nuclear pore complex      348995 (NUP43) Chromosome and associated proteins [BR:hsa03036]  Eukaryotic type   Centrosome formation proteins    Spindle formation proteins     348995 (NUP43) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  WDR55 WD40_Prp19 WD40_CDC20-Fz WD40 Beta-prop_EIPR1 Beta-prop_EML_2 Beta-prop_EML WD40_WDHD1_1st Beta-prop_TEP1_2nd Beta-prop_SCAP Beta-prop_WDR75_1st Beta-prop_WDR90_POC16_2nd WD40_MABP1-WDR62_2nd Beta-prop_RIG_2nd WD_LRWD1 WD40_MABP1-WDR62_1st EIF3I Beta-prop_SPT8 KNTC1_N Motif Other DBs NCBI-GeneID:  348995 NCBI-ProteinID:  NP_942590 OMIM:  608141 HGNC:  21182 Ensembl:  ENSG00000120253 UniProt:  Q8NFH3 Q8TEA6 Structure PDBPDBj LinkDB All DBs Position 6:complement(149724315..149749358) Genome browser AA seq 380 aa AA seqDB search MEEIYAKFVSQKISKTRWRPLPPGSLQTAETFATGSWDNEENYISLWSIGDFGNLDSDGG FEGDHQLLCDIRHHGDVMDLQFFDQERIVAASSTGCVTVFLHHPNNQTLSVNQQWTTAHY HTGPGSPSYSSAPCTGVVCNNPEIVTVGEDGRINLFRADHKEAVRTIDNADSSTLHAVTF LRTPEILTVNSIGQLKIWDFRQQGNEPSQILSLTGDRVPLHCVDRHPNQQHVVATGGQDG MLSIWDVRQGTMPVSLLKAHEAEMWEVHFHPSNPEHLFTCSEDGSLWHWDASTDVPEKSS LFHQGGRSSTFLSHSISNQANVHQSVISSWLSTDPAKDRIEITSLLPSRSLSVNTLDVLG PCLVCGTDAEAIYVTRHLFS NT seq 1143 nt NT seq  +upstreamnt  +downstreamnt atggaggaaatttatgcgaagtttgtgtcccagaaaatcagcaaaacccgctggcgaccg ctgcctccgggaagtttacagaccgcggagacgttcgctacaggatcttgggacaatgag gaaaattatatttcactgtggtctattggagattttggaaacttggactctgatggaggg tttgaaggagaccatcagttattgtgtgatatcagacaccatggtgatgtaatggattta cagttttttgaccaggaaagaattgtcgctgcttcatcaacaggatgtgtaacagttttc cttcaccatccaaataaccagactctgtcagtcaaccagcagtggactacagctcactac cacacaggccctggcagtccttcctatagcagtgcaccatgtacaggtgttgtgtgcaac aacccagaaatcgttacagttggagaggatggtcgaataaatctcttcagagctgatcac aaggaagctgtaagaaccatagacaatgcagatagtagtacactccatgctgtaaccttt cttcgaactcctgagattcttactgtaaattcaattggacagttgaaaatatgggatttc agacaacaaggaaatgagccttctcagatattgtcactgactggtgaccgagtgccactc cactgtgttgatagacatcccaaccaacagcatgttgtagctactggtggccaagatgga atgttgagtatttgggatgttagacaaggtactatgcctgtatctctgctgaaggctcat gaagctgaaatgtgggaagttcactttcacccatccaacccagaacatctttttacctgc tctgaagatggatccctctggcactgggatgcttccacagatgtacctgaaaagtcgtca ctctttcaccaaggaggaagaagcagtacttttttgtctcatagcattagtaaccaagct aatgttcaccagtctgtcattagctcctggctcagcactgatcctgcaaaagaccgaatt gaaatcacaagcttacttcccagtaggtctctgtctgtgaacactttggatgttttaggt ccttgtcttgtttgtggaaccgatgcagaagcaatttatgttactagacatcttttttcg tag

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