Gene Gene information from NCBI Gene database.
Entrez ID 948
Gene name CD36 molecule (CD36 blood group)
Gene symbol CD36
Synonyms (NCBI Gene)
BDPLT10CHDS7FATGP3BGP4GPIVPASIVSCARB3
Chromosome 7
Chromosome location 7q21.11
Summary The protein encoded by this gene is the fourth major glycoprotein of the platelet surface and serves as a receptor for thrombospondin in platelets and various cell lines. Since thrombospondins are widely distributed proteins involved in a variety of adhes
SNPs SNP information provided by dbSNP.
20
SNP ID Visualize variation Clinical significance Consequence
rs1049673 C>G,T Risk-factor 3 prime UTR variant, genic downstream transcript variant
rs1527483 G>A Risk-factor Intron variant
rs1761667 G>A Risk-factor Genic upstream transcript variant, intron variant
rs1984112 A>C,G,T Risk-factor Genic upstream transcript variant, intron variant
rs3211893 T>A,C,G Likely-pathogenic Splice donor variant
miRNA miRNA information provided by mirtarbase database.
293
miRTarBase ID miRNA Experiments Reference
MIRT018933 hsa-miR-335-5p Microarray 18185580
MIRT021050 hsa-miR-155-5p Proteomics;Other 20584899
MIRT030109 hsa-miR-26b-5p Microarray 19088304
MIRT609641 hsa-miR-8485 HITS-CLIP 23313552
MIRT616399 hsa-miR-8064 HITS-CLIP 23313552
Transcription factors Transcription factors information provided by TRRUST V2 database.
4
Transcription factor Regulation Reference
PPARA Unknown 16713233;20110263
PPARG Activation 11795270
PPARG Unknown 15104237;17322100
RUNX3 Repression 16887969
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
179
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IEA
GO:0000165 Process MAPK cascade IEA
GO:0001540 Function Amyloid-beta binding IC 20037584
GO:0001540 Function Amyloid-beta binding IDA 29518356
GO:0001540 Function Amyloid-beta binding TAS 20037584
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
173510 1663 ENSG00000135218
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P16671
Protein name Platelet glycoprotein 4 (Fatty acid translocase) (FAT) (Glycoprotein IIIb) (GPIIIB) (Leukocyte differentiation antigen CD36) (PAS IV) (PAS-4) (Platelet collagen receptor) (Platelet glycoprotein IV) (GPIV) (Thrombospondin receptor) (CD antigen CD36)
Protein function Multifunctional glycoprotein that acts as a receptor for a broad range of ligands. Ligands can be of proteinaceous nature like thrombospondin, fibronectin, collagen or amyloid-beta as well as of lipidic nature such as oxidized low-density lipopr
PDB 5LGD
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01130 CD36 14 463 CD36 family Family
Sequence
Sequence length 472
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
216
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
CD36-related disorder Likely pathogenic; Pathogenic rs748431584, rs753754773, rs2535905306, rs550565800, rs375042355, rs1451278617, rs775734577, rs772709798, rs753791074, rs2535739173, rs148051111, rs148910227 RCV003324407
RCV004741075
RCV004550744
RCV003330584
RCV004552511
RCV004554095
RCV004550603
RCV004550918
RCV004548763
RCV004551039
RCV004551576
RCV004549857
Coronary heart disease, susceptibility to, 7 Likely pathogenic; Pathogenic rs775478465, rs572295823, rs148051111, rs3211901 RCV004796600
RCV002503831
RCV000477879
RCV005047030
Inherited bleeding disorder, platelet-type Likely pathogenic rs201765331 RCV004017735
Malaria, susceptibility to Likely pathogenic; Pathogenic rs775478465, rs572295823, rs148051111, rs766920034, rs3211901 RCV004796600
RCV002503831
RCV000477879
RCV000714683
RCV005047030
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
- no classification for the single variant rs1984112, rs1049673 -
Acute myeloid leukemia Benign; Uncertain significance rs1527483, rs780361615 RCV005898537
RCV005913978
Cervical cancer Uncertain significance rs375587618 RCV005939103
Clear cell carcinoma of kidney Uncertain significance rs371153088 RCV005914004
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Acute Coronary Syndrome Associate 35666553
Adrenal Hyperplasia Congenital Associate 36583008
Alzheimer Disease Associate 30235742, 35768560
Anemia hypochromic microcytic Associate 19359777
Anodontia Associate 31185924
Arterial Occlusive Diseases Associate 27869039
Asthma Associate 40450010
Atherosclerosis Associate 12419963
Blood Platelet Disorders Associate 30721642
Carcinoma Hepatocellular Associate 26424075