Homo sapiens (human): 116519 Help Entry 116519            CDS       T01001                                  Symbol APOA5, APOAV, RAP3 Name (RefSeq) apolipoprotein A5   KO K09025   apolipoprotein A-V Organism hsa  Homo sapiens (human) Pathway hsa03320   PPAR signaling pathway Disease H00157   Hyperlipoproteinemia, type V H01635   Hyperlipidemia H01637   Hypertriglyceridemia H01784   Primary hyperchylomicronemia Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:hsa00536]     116519 (APOA5) Glycosaminoglycan binding proteins [BR:hsa00536]  Heparan sulfate / Heparin   Others    116519 (APOA5) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Apolipoprotein YtxH Exonuc_VII_L DUF4456 BAG6 Motif Other DBs NCBI-GeneID:  116519 NCBI-ProteinID:  NP_001160070 OMIM:  606368 HGNC:  17288 Ensembl:  ENSG00000110243 UniProt:  Q6Q788 A0A0B4RUS7 LinkDB All DBs Position 11:complement(116789367..116792420) Genome browser AA seq 366 aa AA seqDB search MASMAAVLTWALALLSAFSATQARKGFWDYFSQTSGDKGRVEQIHQQKMAREPATLKDSL EQDLNNMNKFLEKLRPLSGSEAPRLPQDPVGMRRQLQEELEEVKARLQPYMAEAHELVGW NLEGLRQQLKPYTMDLMEQVALRVQELQEQLRVVGEDTKAQLLGGVDEAWALLQGLQSRV VHHTGRFKELFHPYAESLVSGIGRHVQELHRSVAPHAPASPARLSRCVQVLSRKLTLKAK ALHARIQQNLDQLREELSRAFAGTGTEEGAGPDPQMLSEEVRQRLQAFRQDTYLQIAAFT RAIDQETEEVQQQLAPPPPGHSAFAPEFQQTDSGKVLSKLQARLDDLWEDITHSLHDQGH SHLGDP NT seq 1101 nt NT seq  +upstreamnt  +downstreamnt atggcaagcatggctgccgtgctcacctgggctctggctcttctttcagcgttttcggcc acccaggcacggaaaggcttctgggactacttcagccagaccagcggggacaaaggcagg gtggagcagatccatcagcagaagatggctcgcgagcccgcgaccctgaaagacagcctt gagcaagacctcaacaatatgaacaagttcctggaaaagctgaggcctctgagtgggagc gaggctcctcggctcccacaggacccggtgggcatgcggcggcagctgcaggaggagttg gaggaggtgaaggctcgcctccagccctacatggcagaggcgcacgagctggtgggctgg aatttggagggcttgcggcagcaactgaagccctacacgatggatctgatggagcaggtg gccctgcgcgtgcaggagctgcaggagcagttgcgcgtggtgggggaagacaccaaggcc cagttgctggggggcgtggacgaggcttgggctttgctgcagggactgcagagccgcgtg gtgcaccacaccggccgcttcaaagagctcttccacccatacgccgagagcctggtgagc ggcatcgggcgccacgtgcaggagctgcaccgcagtgtggctccgcacgcccccgccagc cccgcgcgcctcagtcgctgcgtgcaggtgctctcccggaagctcacgctcaaggccaag gccctgcacgcacgcatccagcagaacctggaccagctgcgcgaagagctcagcagagcc tttgcaggcactgggactgaggaaggggccggcccggacccccagatgctctccgaggag gtgcgccagcgacttcaggctttccgccaggacacctacctgcagatagctgccttcact cgcgccatcgaccaggagactgaggaggtccagcagcagctggcgccacctccaccaggc cacagtgccttcgccccagagtttcaacaaacagacagtggcaaggttctgagcaagctg caggcccgtctggatgacctgtgggaagacatcactcacagccttcatgaccagggccac agccatctgggggacccctga

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