Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
948
Gene name Gene Name - the full gene name approved by the HGNC.
CD36 molecule (CD36 blood group)
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CD36
Synonyms (NCBI Gene) Gene synonyms aliases
BDPLT10, CHDS7, FAT, GP3B, GP4, GPIV, PASIV, SCARB3
Disease Acronyms (UniProt) Disease acronyms from UniProt database
CHDS7
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q21.11
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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.
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 factor Regulation Reference
PPARA Unknown 16713233;20110263
PPARG Activation 11795270
PPARG Unknown 15104237;17322100
RUNX3 Repression 16887969
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II 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
GO:0001954 Process Positive regulation of cell-matrix adhesion IDA 17416590
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
173510 1663 ENSG00000135218
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Platelet-type bleeding disorder platelet-type bleeding disorder 10 GenCC
Dementia Dementia GWAS
Mental Depression Mental Depression GWAS
Associations from Text Mining
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