Homo sapiens (human): 5194 Help Entry 5194              CDS       T01001                                  Symbol PEX13, NALD, PBD11A, PBD11B, ZWS Name (RefSeq) peroxisomal biogenesis factor 13   KO K13344   peroxin-13 Organism hsa  Homo sapiens (human) Pathway hsa04146   Peroxisome Disease H00205   Peroxisome biogenesis disorder H01342   Zellweger syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09141 Transport and catabolism    04146 Peroxisome     5194 (PEX13) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Peroxin-13_N SH3_9 SH3_1 SH3_2 Motif Other DBs NCBI-GeneID:  5194 NCBI-ProteinID:  NP_002609 OMIM:  601789 HGNC:  8855 Ensembl:  ENSG00000162928 Pharos:  Q92968(Tbio) UniProt:  Q92968 Structure PDB LinkDB All DBs Position 2:61017720..61051990 Genome browser AA seq 403 aa AA seqDB search MASQPPPPPKPWETRRIPGAGPGPGPGPTFQSADLGPTLMTRPGQPALTRVPPPILPRPS QQTGSSSVNTFRPAYSSFSSGYGAYGNSFYGGYSPYSYGYNGLGYNRLRVDDLPPSRFVQ QAEESSRGAFQSIESIVHAFASVSMMMDATFSAVYNSFRAVLDVANHFSRLKIHFTKVFS AFALVRTIRYLYRRLQRMLGLRRGSENEDLWAESEGTVACLGAEDRAATSAKSWPIFLFF AVILGGPYLIWKLLSTHSDEVTDSINWASGEDDHVVARAEYDFAAVSEEEISFRAGDMLN LALKEQQPKVRGWLLASLDGQTTGLIPANYVKILGKRKGRKTVESSKVSKQQQSFTNPTL TKGATVADSLDEQEAAFESVFVETNKVPVAPDSIGKDGEKQDL NT seq 1212 nt NT seq  +upstreamnt  +downstreamnt atggcgtcccagccgccacctccccccaaaccctgggagacccgccgaattccgggagcc ggaccgggaccaggaccgggccccactttccaatctgctgatttgggtcctactttaatg acaagacctggacaaccagcacttaccagagtgcccccacctattcttccaaggccatca cagcagacaggaagtagcagtgtgaacacttttagacctgcttacagttcattttcttct ggatatggtgcctatggaaattcattttatggaggctatagtccttatagttatggatat aatgggctgggctacaaccgcctccgtgtagatgatcttccacccagtagatttgttcag caagctgaagaaagcagcaggggtgcatttcagtccattgaaagtattgtgcatgcattt gcctctgtcagtatgatgatggatgctaccttttcagctgtctataacagtttcagggct gtattggatgtagcaaatcacttttcccgattgaaaatacactttacaaaagtgttttca gcttttgcattggttaggactatacggtatctttacagacggctacagcggatgttaggt ttaagaagaggctctgagaatgaagacctctgggcagagagtgaaggaactgtggcatgc cttggtgctgaggaccgagcagctacctcagcaaaatcttggccaatattcttgttcttt gctgttatccttggtggtccttacctcatttggaaactattgtctactcacagtgatgaa gtaacagacagcatcaactgggcaagtggtgaggatgaccatgtagttgccagagcagaa tatgattttgctgccgtatctgaagaagaaatttctttccgggctggtgatatgctgaac ttagctctcaaagaacaacaacccaaagtgcgtggttggcttctggctagccttgatggc caaacaacaggacttatacctgcgaattatgtcaaaattcttggcaaaagaaaaggtagg aaaacggtggaatcaagtaaagtttccaagcagcaacaatcttttaccaacccaacacta actaaaggagccacggttgctgattctttggatgaacaggaagctgcctttgaatctgtt tttgttgaaactaataaggttccagttgcacctgattccattgggaaagatggagaaaag caagatctttga

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