Entity Details

Primary name CD151
Entity type gene
Source Source Link

Details

PrimaryID977
RefseqGeneNG_007478
SymbolCD151
NameCD151 molecule (Raph blood group)
Chromosome11
Location11p15.5
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1998-07-30
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsCD151_HUMAN

GO terms

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GOName
GO:0005178 integrin binding
GO:0005604 basement membrane
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0005925 focal adhesion
GO:0007155 cell adhesion
GO:0009986 cell surface
GO:0016020 membrane
GO:0016032 viral process
GO:0016477 cell migration
GO:0030199 collagen fibril organization
GO:0030335 positive regulation of cell migration
GO:0031581 hemidesmosome assembly
GO:0042098 T cell proliferation
GO:0044319 wound healing, spreading of cells
GO:0045807 positive regulation of endocytosis

Diseases

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Disease IDSourceNameDescription
609057 OMIMNephropathy with pretibial epidermolysis bullosa and deafness (NPEBD)A disorder characterized by the association of hereditary nephritis, epidermolysis bullosa, deafness, and beta-thalassemia minor. The disease is caused by variants affecting the gene represented in this entry.