Gene Gene information from NCBI Gene database.
Entrez ID 728
Gene name Complement C5a receptor 1
Gene symbol C5AR1
Synonyms (NCBI Gene)
C5AC5ARC5R1CD88
Chromosome 19
Chromosome location 19q13.32
miRNA miRNA information provided by mirtarbase database.
84
miRTarBase ID miRNA Experiments Reference
MIRT019124 hsa-miR-335-5p Microarray 18185580
MIRT030190 hsa-miR-26b-5p Microarray 19088304
MIRT848590 hsa-miR-1262 CLIP-seq
MIRT848591 hsa-miR-1343 CLIP-seq
MIRT848592 hsa-miR-3179 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
55
GO ID Ontology Definition Evidence Reference
GO:0001774 Process Microglial cell activation IEA
GO:0001774 Process Microglial cell activation ISS
GO:0002430 Process Complement receptor mediated signaling pathway IBA
GO:0002430 Process Complement receptor mediated signaling pathway IDA 37169960
GO:0002682 Process Regulation of immune system process IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
113995 1338 ENSG00000197405
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P21730
Protein name C5a anaphylatoxin chemotactic receptor 1 (C5a anaphylatoxin chemotactic receptor) (C5a-R) (C5aR) (CD antigen CD88)
Protein function Receptor for the chemotactic and inflammatory peptide anaphylatoxin C5a (PubMed:10636859, PubMed:15153520, PubMed:1847994, PubMed:29300009, PubMed:7622471, PubMed:8182049, PubMed:9553099). The ligand interacts with at least two sites on the rece
PDB 2K3U , 5O9H , 6C1Q , 6C1R , 7Y64 , 7Y65 , 7Y66 , 7Y67 , 8GO8 , 8GOO , 8HK5 , 8I0N , 8I0Z , 8IA2 , 8JZP , 8JZZ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 54 300 7 transmembrane receptor (rhodopsin family) Family
Sequence
Sequence length 350
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
7
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
C5AR1-related disorder Uncertain significance; Likely benign rs750171124, rs774370669, rs2514890152, rs2514890878, rs750580655, rs948785923, rs117536261 RCV003410140
RCV003414480
RCV003400234
RCV003902239
RCV003949844
RCV003957187
RCV003950394
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Abortion Spontaneous Stimulate 24802103
Acute Kidney Injury Stimulate 30451738
Alzheimer Disease Associate 23394121, 30403186
Alzheimer Disease Stimulate 37679689
Alzheimer Disease 15 Associate 23394121
AMR Syndrome Associate 38128610
Amyotrophic Lateral Sclerosis Associate 33216044
Anaphylaxis Associate 16301808
Anti Neutrophil Cytoplasmic Antibody Associated Vasculitis Associate 22691190
Antiphospholipid Syndrome Associate 16982920