Basic Information

CD36

Full name: CD36 molecule

Gene type: protein coding

HGNC ID: HGNC:1663

Gene location: 7q21.11

Gene resources

NCBI: https://www.ncbi.nlm.nih.gov/gene/948

Alliance of genome: https://www.alliancegenome.org/gene/HGNC:1663

MANE select: https://www.ncbi.nlm.nih.gov/gene/?term=NM_001001548.3

Protein resources

UniProt/Swiss-Prot: https://www.uniprot.org/uniprot/P16671

AlphaFold: https://alphafold.ebi.ac.uk/entry/P16671

MEME motif:

Clinical resources

OMIM: https://www.omim.org/entry/173510

dbVar: https://www.ncbi.nlm.nih.gov/dbvar?LinkName=gene_dbvar&from_uid=948

Pathway resources

KEGG pathway: https://www.genome.jp/pathway/hsa03320+948

Variant resources

Gene Disease type Variant type NCBI dbSNP Alleles Variant location
CD36 tAMD Intron Variant rs10499862 T>C chr7:80651984 (GRCh38.p13)
CD36 tAMD Intron Variant rs3173798 T>C chr7:80656534 (GRCh38.p13)
CD36 tAMD Intron Variant rs3211883 A>G / A>T chr7:80659727 (GRCh38.p13)
CD36 tAMD Intron Variant rs3173800 A>C / A>T chr7:80660605 (GRCh38.p13)
CD36 nAMD Intron Variant rs12531609 A>T chr7:80612263 (GRCh38.p13)
CD36 nAMD Intron Variant rs3211816 G>A chr7:80648674 (GRCh38.p13)
CD36 nAMD Intron Variant rs3211849 A>G / A>T chr7:80654007 (GRCh38.p13)
CD36 nAMD Intron Variant rs3211851 A>C / A>G chr7:80654141 (GRCh38.p13)
CD36 nAMD Intron Variant rs1054516 T>A / T>C chr7:80655626 (GRCh38.p13)
CD36 nAMD Intron Variant rs3211870 C>T chr7:80657893 (GRCh38.p13)
CD36 nAMD Intron Variant rs1358337 G>A chr7:80659069 (GRCh38.p13)
CD36 nAMD Intron Variant rs17154232 G>C chr7:80663725 (GRCh38.p13)
CD36 nAMD Intron Variant rs3211908 C>T chr7:80664600 (GRCh38.p13)
CD36 nAMD Intron Variant rs17154258 A>G chr7:80667614 (GRCh38.p13)
CD36 nAMD Intron Variant rs1527483 G>A chr7:80672184 (GRCh38.p13)
CD36 nAMD Intron Variant rs3211958 A>G / A>T chr7:80674756 (GRCh38.p13)
CD36 nAMD 3 Prime UTR Variant rs7755 G>A chr7:80676955 (GRCh38.p13)