KEGG   Homo sapiens (human): 116519
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]
 09150 Organismal Systems
  09152 Endocrine system
   03320 PPAR signaling pathway
    116519 (APOA5)
 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)
SSDB
Motif
Pfam: Apolipoprotein YtxH Exonuc_VII_L DUF4456 BAG6
Other DBs
NCBI-GeneID: 116519
NCBI-ProteinID: NP_001160070
OMIM: 606368
HGNC: 17288
Ensembl: ENSG00000110243
UniProt: Q6Q788 A0A0B4RUS7
Position
11:complement(116789367..116792420)
AA seq 366 aa
MASMAAVLTWALALLSAFSATQARKGFWDYFSQTSGDKGRVEQIHQQKMAREPATLKDSL
EQDLNNMNKFLEKLRPLSGSEAPRLPQDPVGMRRQLQEELEEVKARLQPYMAEAHELVGW
NLEGLRQQLKPYTMDLMEQVALRVQELQEQLRVVGEDTKAQLLGGVDEAWALLQGLQSRV
VHHTGRFKELFHPYAESLVSGIGRHVQELHRSVAPHAPASPARLSRCVQVLSRKLTLKAK
ALHARIQQNLDQLREELSRAFAGTGTEEGAGPDPQMLSEEVRQRLQAFRQDTYLQIAAFT
RAIDQETEEVQQQLAPPPPGHSAFAPEFQQTDSGKVLSKLQARLDDLWEDITHSLHDQGH
SHLGDP
NT seq 1101 nt   +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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Ontology (2)   
   KEGG BRITE (2)   
Pathway (1)   
   KEGG PATHWAY (1)   
Disease (7)   
   KEGG DISEASE (4)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (10)   
   KEGG ORTHOLOGY (1)   
   RefGene (4)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (6)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (3)   
DNA sequence (23)   
   RefSeq(nuc) (3)   
   GenBank (10)   
   EMBL (10)   
Protein domain (5)   
   Pfam (5)   
All databases (55)   

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