Homo sapiens (human): 5191 Help Entry 5191              CDS       T01001                                  Symbol PEX7, PBD9B, PTS2R, RCDP1, RD Name (RefSeq) peroxisomal biogenesis factor 7   KO K13341   peroxin-7 Organism hsa  Homo sapiens (human) Pathway hsa04146   Peroxisome Disease H00075   Refsum disease H00177   Neonatal adrenoleukodystrophy H00205   Peroxisome biogenesis disorder H00207   Rhizomelic chondrodysplasia punctata Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09141 Transport and catabolism    04146 Peroxisome     5191 (PEX7) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  WD40 WD40_CDC20-Fz WD40_Prp19 Beta-prop_RIG_2nd Beta-prop_EIPR1 Beta-prop_TEP1_2nd WD40_WDHD1_1st Beta-prop_EML_2 WDR55 Beta-prop_CAF1B_HIR1 EIF3I Beta-prop_TEP1_C WD40_MABP1-WDR62_2nd WD40_RFWD3 Beta-prop_WDR90_POC16_2nd Beta-prop_WDR75_1st Beta-prop_EML Beta-prop_SPT8 Beta-prop_WDR19_1st eIF2A NBCH_WD40 WDR90_beta-prop_4th MIOS_WD40 Beta-prop_DCAF4 Beta-prop_DCAF12 Beta-prop_SCAP Beta-prop_NUP159_NUP214 Beta-prop_WDR11_2nd K319L-like_PKD Motif Other DBs NCBI-GeneID:  5191 NCBI-ProteinID:  NP_000279 OMIM:  601757 HGNC:  8860 Ensembl:  ENSG00000112357 UniProt:  O00628 Q6FGN1 LinkDB All DBs Position 6:136822592..136913934 Genome browser AA seq 323 aa AA seqDB search MSAVCGGAARMLRTPGRHGYAAEFSPYLPGRLACATAQHYGIAGCGTLLILDPDEAGLRL FRSFDWNDGLFDVTWSENNEHVLITCSGDGSLQLWDTAKAAGPLQVYKEHAQEVYSVDWS QTRGEQLVVSGSWDQTVKLWDPTVGKSLCTFRGHESIIYSTIWSPHIPGCFASASGDQTL RIWDVKAAGVRIVIPAHQAEILSCDWCKYNENLLVTGAVDCSLRGWDLRNVRQPVFELLG HTYAIRRVKFSPFHASVLASCSYDFTVRFWNFSKPDSLLETVEHHTEFTCGLDFSLQSPT QVADCSWDETIKIYDPACLTIPA NT seq 972 nt NT seq  +upstreamnt  +downstreamnt atgagtgcggtgtgcggtggagcggcgcggatgctgcggacgccgggacgccacggctac gccgccgagttctccccgtacctgccgggccgcctggcctgcgccaccgcgcagcactac ggcatcgcgggctgtggaaccctactaatattggatccagatgaagctgggctaaggctt tttagaagctttgactggaatgatggtttgtttgatgtgacttggagtgagaacaacgaa catgtcctcatcacctgtagtggcgatggctcgctgcagctctgggacactgccaaagct gcagggccactgcaagtctataaagaacacgctcaggaggtgtatagtgttgattggagc caaaccagaggtgaacagcttgtggtgtctggctcatgggatcaaactgtcaaattgtgg gatccaactgttggaaagtctctgtgcacctttagaggccatgaaagtattatttatagc acaatctggtctccccacatccctggttgttttgcttcagcctcaggtgatcagactctg agaatatgggatgtgaaggcagcaggagtaagaatcgtgattcctgcacatcaggcagaa atcttgagttgtgactggtgtaaatacaatgagaatttgctggtgaccggggcggttgac tgtagtttgagaggctgggacttaaggaatgtacgacaaccagtgtttgaacttcttggt catacctatgctattaggagggtgaaattttcaccatttcatgcttctgtgctggcctct tgctcgtatgattttactgtaagattctggaacttttcaaagcctgactctcttcttgaa acagtggagcatcatacagagtttacttgtggtttagacttcagtcttcagagccccact caggtggctgactgttcttgggatgaaacaataaagatctatgaccctgcttgtcttact attcctgcttga

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