Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
8862
Gene name Gene Name - the full gene name approved by the HGNC.
Apelin
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
APLN
Synonyms (NCBI Gene) Gene synonyms aliases
APEL, XNPEP2
Chromosome Chromosome number
X
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Xq26.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a peptide that functions as an endogenous ligand for the G-protein coupled apelin receptor. The encoded preproprotein is proteolytically processed into biologically active C-terminal peptide fragments. These peptide fragments activate di
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT047924 hsa-miR-30c-5p CLASH 23622248
MIRT046134 hsa-miR-30b-5p CLASH 23622248
MIRT573091 hsa-miR-6729-3p PAR-CLIP 20371350
MIRT573092 hsa-miR-4286 PAR-CLIP 20371350
MIRT573090 hsa-miR-361-3p PAR-CLIP 20371350
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001525 Process Angiogenesis IEA
GO:0002026 Process Regulation of the force of heart contraction IEA
GO:0005102 Function Signaling receptor binding TAS 9792798
GO:0005179 Function Hormone activity IMP 28137936
GO:0005576 Component Extracellular region IDA 28137936
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
300297 16665 ENSG00000171388
Protein
UniProt ID Q9ULZ1
Protein name Apelin (APJ endogenous ligand) [Cleaved into: Apelin-36; Apelin-31; Apelin-28; Apelin-13]
Protein function Peptide hormone that functions as endogenous ligand for the G-protein-coupled apelin receptor (APLNR/APJ), that plays a role in cadiovascular homeostasis (PubMed:10525157, PubMed:22810587, PubMed:35817871, PubMed:38428423). Functions as a balanc
PDB 8XQE , 8XQF , 8XZG , 8XZH , 8XZJ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15360 Apelin 23 77 APJ endogenous ligand Family
Tissue specificity TISSUE SPECIFICITY: Expressed in the brain with highest levels in the frontal cortex, thalamus, hypothalamus and midbrain (PubMed:10617103). Secreted by the mammary gland into the colostrum and the milk. {ECO:0000269|PubMed:10617103}.
Sequence
Sequence length 77
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Neuroactive ligand-receptor interaction
Apelin signaling pathway
  Peptide ligand-binding receptors
G alpha (i) signalling events
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Heart failure Heart Failure, Diastolic 29556499 ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Acute Coronary Syndrome Associate 28902642
Adenocarcinoma Stimulate 36591713
Adenocarcinoma of Lung Stimulate 24374773
Albuminuria Associate 35748053
Alcohol Related Disorders Associate 25918383
Alzheimer Disease Associate 31816601
Anemia Sickle Cell Associate 25486928
Angina Stable Inhibit 19015606
Angina Stable Associate 33881940
Arrhythmias Cardiac Associate 29721104