Gene Gene information from NCBI Gene database.
Entrez ID 187
Gene name Apelin receptor
Gene symbol APLNR
Synonyms (NCBI Gene)
AGTRL1APJAPJRHG11
Chromosome 11
Chromosome location 11q12.1
Summary This gene encodes a member of the G protein-coupled receptor gene family. The encoded protein is related to the angiotensin receptor, but is actually an apelin receptor that inhibits adenylate cyclase activity and plays a counter-regulatory role against t
miRNA miRNA information provided by mirtarbase database.
56
miRTarBase ID miRNA Experiments Reference
MIRT051137 hsa-miR-16-5p CLASH 23622248
MIRT047418 hsa-miR-10b-5p CLASH 23622248
MIRT732441 hsa-miR-483-3p Luciferase reporter assayqRT-PCRWestern blotting 33436040
MIRT734203 hsa-miR-424-5p ELISALuciferase reporter assayqRT-PCRWestern blotting 32774725
MIRT734203 hsa-miR-424-5p ELISALuciferase reporter assayqRT-PCRWestern blotting 32774725
Transcription factors Transcription factors information provided by TRRUST V2 database.
1
Transcription factor Regulation Reference
SP1 Activation 17309882
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
73
GO ID Ontology Definition Evidence Reference
GO:0001525 Process Angiogenesis IEA
GO:0001568 Process Blood vessel development IBA
GO:0001570 Process Vasculogenesis IEA
GO:0001570 Process Vasculogenesis ISS
GO:0001944 Process Vasculature development IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
600052 339 ENSG00000134817
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P35414
Protein name Apelin receptor (Angiotensin receptor-like 1) (G-protein coupled receptor APJ) (G-protein coupled receptor HG11)
Protein function G protein-coupled receptor for peptide hormones apelin (APLN) and apelin receptor early endogenous ligand (APELA/ELA), that plays a role in the regulation of normal cardiovascular function and fluid homeostasis (PubMed:11090199, PubMed:22810587,
PDB 2LOT , 2LOU , 2LOV , 2LOW , 5VBL , 6KNM , 7SUS , 7W0L , 7W0M , 7W0N , 7W0O , 7W0P , 8XQE , 8XQF , 8XQI , 8XQJ , 8XZF , 8XZG , 8XZH , 8XZI , 8XZJ , 8Z74 , 8Z7J
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 45 309 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Expressed in heart, brain, kidney, stomach, spleen, thymus, lung, ovary, small intestine and colon, adipose tissues and pancreas (PubMed:25639753, PubMed:8294032). Expressed in glial cells, astrocytes and neuronal subpopulations (PubMe
Sequence
Sequence length 380
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 associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
7
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GOUT GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INSOMNIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Alzheimer Disease Alzheimer disease Pubtator 34443478 Associate
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Arteriosclerosis Arteriosclerosis BEFREE 19680269, 25438973, 27825851, 29691838
★☆☆☆☆
Found in Text Mining only
Atherosclerosis Atherosclerosis BEFREE 19680269, 25438973, 27825851, 29691838
★☆☆☆☆
Found in Text Mining only
Atherosclerosis Atherosclerosis Pubtator 20649580 Associate
★☆☆☆☆
Found in Text Mining only
Atrial Fibrillation Atrial Fibrillation BEFREE 25438973, 30278567, 30518720
★☆☆☆☆
Found in Text Mining only
Atrial Fibrillation Atrial fibrillation Pubtator 30518720 Inhibit
★☆☆☆☆
Found in Text Mining only
Brain Infarction Brain Infarction BEFREE 17309882
★☆☆☆☆
Found in Text Mining only
Brain Infarction Brain Infarction LHGDN 17309882
★☆☆☆☆
Found in Text Mining only
Brain Neoplasms Brain Neoplasms BEFREE 17412318
★☆☆☆☆
Found in Text Mining only
Brain Neoplasms Brain Neoplasms LHGDN 17412318
★☆☆☆☆
Found in Text Mining only