Homo sapiens (human): 5193 Help Entry 5193              CDS       T01001                                  Symbol PEX12, PAF-3, PBD3A Name (RefSeq) peroxisomal biogenesis factor 12   KO K13345   peroxin-12 Organism hsa  Homo sapiens (human) Pathway hsa04146   Peroxisome Disease H00177   Neonatal adrenoleukodystrophy H00205   Peroxisome biogenesis disorder H01342   Zellweger syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09141 Transport and catabolism    04146 Peroxisome     5193 (PEX12)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    04121 Ubiquitin system [BR:hsa04121]     5193 (PEX12) Ubiquitin system [BR:hsa04121]  Ubiquitin ligases (E3)   Single Ring-finger type E3    Peripheral membrane proteins     5193 (PEX12) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Pex2_Pex12 zf-C3HC4_2 zf-C3HC4_3 zf-C3HC4 zf-RING_2 DZR_2 Motif Other DBs NCBI-GeneID:  5193 NCBI-ProteinID:  NP_000277 OMIM:  601758 HGNC:  8854 Ensembl:  ENSG00000108733 UniProt:  O00623 LinkDB All DBs Position 17:complement(35574795..35578571) Genome browser AA seq 359 aa AA seqDB search MAEHGAHFTAASVADDQPSIFEVVAQDSLMTAVRPALQHVVKVLAESNPTHYGFLWRWFD EIFTLLDLLLQQHYLSRTSASFSENFYGLKRIVMGDTHKSQRLASAGLPKQQLWKSIMFL VLLPYLKVKLEKLVSSLREEDEYSIHPPSSRWKRFYRAFLAAYPFVNMAWEGWFLVQQLR YILGKAQHHSPLLRLAGVQLGRLTVQDIQALEHKPAKASMMQQPARSVSEKINSALKKAV GGVALSLSTGLSVGVFFLQFLDWWYSSENQETIKSLTALPTPPPPVHLDYNSDSPLLPKM KTVCPLCRKTRVNDTVLATSGYVFCYRCVFHYVRSHQACPITGYPTEVQHLIKLYSPEN NT seq 1080 nt NT seq  +upstreamnt  +downstreamnt atggctgagcacggggctcacttcacagctgcttctgtggccgatgaccagccatccatc tttgaggtggtagcacaggacagtttaatgacagcagtgagacccgctcttcagcatgtg gtcaaggttcttgcagaatcaaatcccacccactatggcttcttgtggaggtggtttgat gaaatctttactctgctagatcttctgctccagcaacattatctgtctagaaccagtgcc tcattttctgaaaacttttacggcttaaagagaattgtaatgggggacactcacaagtct cagagattggctagtgctggtctcccaaagcagcagctttggaaatctattatgttcctg gttcttcttccctatctgaaagtgaagctggagaagctggtttctagcctgagagaagag gatgaatattctattcatcccccttcttcccgctggaaacgattttacagagctttcctg gcagcctacccatttgtgaacatggcctgggaaggatggtttcttgtacaacaacttcga tacatcctaggaaaagctcagcatcactcaccactgctgaggctggctggagttcagcta ggtcgactgacagttcaggatatacaagctctggagcacaaaccagctaaggccagcatg atgcagcaaccagccaggagtgttagtgagaagataaactcagctctgaagaaagctgtt gggggtgttgccttatccctgtctactggcctttctgtgggtgtattcttcttgcagttc cttgactggtggtactcatctgaaaatcaagaaaccatcaagtcattgactgccctgcct actccaccaccacctgtacacctagactataactctgattctcccctcttacccaaaatg aagactgtgtgcccactgtgtcgtaaaacccgggtgaatgatactgttcttgccacctct ggctatgtgttttgttaccgctgtgtgtttcattatgtgaggagtcaccaagcttgtccc atcacaggttatccaacagaagtacaacatctgattaaactctactcccctgagaactga

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