Homo sapiens (human): 335 Help Entry 335               CDS       T01001                                  Symbol APOA1, AMYLD3, HPALP2, apo(a) Name (RefSeq) apolipoprotein A1   KO K08757   apolipoprotein A-I Organism hsa  Homo sapiens (human) Pathway hsa03320   PPAR signaling pathway hsa04975   Fat digestion and absorption hsa04977   Vitamin digestion and absorption hsa04979   Cholesterol metabolism hsa05143   African trypanosomiasis hsa05417   Lipid and atherosclerosis Disease H00845   Familial amyloidosis H00930   Hypoalphalipoproteinemia H02505   Atherosclerosis Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09152 Endocrine system    03320 PPAR signaling pathway     335 (APOA1)   09154 Digestive system    04975 Fat digestion and absorption     335 (APOA1)    04979 Cholesterol metabolism     335 (APOA1)    04977 Vitamin digestion and absorption     335 (APOA1)  09160 Human Diseases   09174 Infectious disease: parasitic    05143 African trypanosomiasis     335 (APOA1)   09166 Cardiovascular disease    05417 Lipid and atherosclerosis     335 (APOA1)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04147 Exosome [BR:hsa04147]     335 (APOA1) Exosome [BR:hsa04147]  Exosomal proteins   Exosomal proteins of other cancer cells    335 (APOA1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Apolipoprotein Exonuc_VII_L ApoLp-III DHC_N1 CCDC90-like DUF948 DUF4455 Gp58 ORC3_ins DUF4015 PIN_8 OmpH FUT8_N_cat DUF1664 DUF4456 DUF2894 Sec10_N NNH6 PnpCD_PnpD_N BshC KMP11 Borrelia_REV LMP DksA_N FlgN Motif Other DBs NCBI-GeneID:  335 NCBI-ProteinID:  NP_000030 OMIM:  107680 HGNC:  600 Ensembl:  ENSG00000118137 UniProt:  P02647 A0A024R3E3 Structure PDB LinkDB All DBs Position 11:complement(116835751..116837622) Genome browser AA seq 267 aa AA seqDB search MKAAVLTLAVLFLTGSQARHFWQQDEPPQSPWDRVKDLATVYVDVLKDSGRDYVSQFEGS ALGKQLNLKLLDNWDSVTSTFSKLREQLGPVTQEFWDNLEKETEGLRQEMSKDLEEVKAK VQPYLDDFQKKWQEEMELYRQKVEPLRAELQEGARQKLHELQEKLSPLGEEMRDRARAHV DALRTHLAPYSDELRQRLAARLEALKENGGARLAEYHAKATEHLSTLSEKAKPALEDLRQ GLLPVLESFKVSFLSALEEYTKKLNTQ NT seq 804 nt NT seq  +upstreamnt  +downstreamnt atgaaagctgcggtgctgaccttggccgtgctcttcctgacggggagccaggctcggcat ttctggcagcaagatgaacccccccagagcccctgggatcgagtgaaggacctggccact gtgtacgtggatgtgctcaaagacagcggcagagactatgtgtcccagtttgaaggctcc gccttgggaaaacagctaaacctaaagctccttgacaactgggacagcgtgacctccacc ttcagcaagctgcgcgaacagctcggccctgtgacccaggagttctgggataacctggaa aaggagacagagggcctgaggcaggagatgagcaaggatctggaggaggtgaaggccaag gtgcagccctacctggacgacttccagaagaagtggcaggaggagatggagctctaccgc cagaaggtggagccgctgcgcgcagagctccaagagggcgcgcgccagaagctgcacgag ctgcaagagaagctgagcccactgggcgaggagatgcgcgaccgcgcgcgcgcccatgtg gacgcgctgcgcacgcatctggccccctacagcgacgagctgcgccagcgcttggccgcg cgccttgaggctctcaaggagaacggcggcgccagactggccgagtaccacgccaaggcc accgagcatctgagcacgctcagcgagaaggccaagcccgcgctcgaggacctccgccaa ggcctgctgcccgtgctggagagcttcaaggtcagcttcctgagcgctctcgaggagtac actaagaagctcaacacccagtga

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