Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
975
Gene name Gene Name - the full gene name approved by the HGNC.
CD81 molecule
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CD81
Synonyms (NCBI Gene) Gene synonyms aliases
CVID6, S5.7, TAPA1, TSPAN28
Disease Acronyms (UniProt) Disease acronyms from UniProt database
CVID6
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11p15.5
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs587776775 G>A Pathogenic Splice donor variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT020808 hsa-miR-155-5p Proteomics 18668040
MIRT052151 hsa-let-7b-5p CLASH 23622248
MIRT039120 hsa-miR-769-3p CLASH 23622248
MIRT038125 hsa-miR-423-5p CLASH 23622248
MIRT052737 hsa-miR-1260b CLASH 23622248
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000187 Process Activation of MAPK activity IDA 14676841
GO:0001618 Function Virus receptor activity IMP 20375010
GO:0001771 Process Immunological synapse formation IMP 23858057
GO:0001772 Component Immunological synapse IDA 21930792, 23858057
GO:0002455 Process Humoral immune response mediated by circulating immunoglobulin IMP 20237408
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
186845 1701 ENSG00000110651
Protein
UniProt ID P60033
Protein name CD81 antigen (26 kDa cell surface protein TAPA-1) (Target of the antiproliferative antibody 1) (Tetraspanin-28) (Tspan-28) (CD antigen CD81)
Protein function Structural component of specialized membrane microdomains known as tetraspanin-enriched microdomains (TERMs), which act as platforms for receptor clustering and signaling. Essential for trafficking and compartmentalization of CD19 receptor on th
PDB 1G8Q , 1IV5 , 3X0E , 5DFV , 5DFW , 5M2C , 5M33 , 5M3D , 5M3T , 5M4R , 5TCX , 6EJG , 6EJM , 6EK2 , 6U9S , 7JIC
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00335 Tetraspanin 10 229 Tetraspanin family Family
Tissue specificity TISSUE SPECIFICITY: Expressed on B cells (at protein level) (PubMed:20237408). Expressed in hepatocytes (at protein level) (PubMed:12483205). Expressed in monocytes/macrophages (at protein level) (PubMed:12796480). Expressed on both naive and memory CD4-p
Sequence
Sequence length 236
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Virion - Hepatitis viruses
B cell receptor signaling pathway
Malaria
Hepatitis C
  Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell
Regulation of Complement cascade
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Anemia Anemia, Hemolytic rs118204044, rs118204045, rs118204046, rs121918330, rs869320719, rs869312029, rs121918332, rs869320724, rs767094129, rs786205058, rs786205059, rs137853119, rs137853120, rs137853121, rs1384933966
View all (89 more)
Bronchiectasis Bronchiectasis rs121908758, rs121908811, rs76649725, rs267606722, rs121909008, rs387906360, rs387906361, rs80034486, rs74767530, rs121908776, rs121909012, rs77646904, rs121908754, rs121909015, rs121909016
View all (214 more)
Common variable immunodeficiency Common Variable Immunodeficiency, Acquired Hypogammaglobulinemia, IMMUNODEFICIENCY, COMMON VARIABLE, 6, Common variable immunodeficiency rs72553883, rs121908379, rs104894650, rs587776775, rs398122863, rs398122864, rs397514332, rs397514331, rs727502786, rs727502787, rs72553882, rs869320688, rs869320689, rs869320754, rs773694113
View all (35 more)
21970952, 27250108
Diabetes mellitus Diabetes Mellitus, Non-Insulin-Dependent rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
View all (293 more)
28254843
Unknown
Disease term Disease name Evidence References Source
Otitis media Chronic otitis media ClinVar
Common Variable Immunodeficiency common variable immunodeficiency GenCC
Diabetes Diabetes GWAS
Breast Cancer Breast Cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Adenomatous Polyposis Coli Associate 24462038
Anemia Sickle Cell Associate 23762099
Apical Hypertrophic Cardiomyopathy Stimulate 35328555
Arthritis Rheumatoid Associate 36826611
Astrocytoma Associate 24650279
Autoimmune Diseases Associate 11985527
Breast Neoplasms Associate 22791584, 30117494, 35157300, 35579189
Burkitt Lymphoma Associate 28509416, 9737661
Carcinoma Hepatocellular Associate 22577054, 29577937, 32322956
Carcinoma Hepatocellular Inhibit 32350244