Gene Gene information from NCBI Gene database.
Entrez ID 56833
Gene name SLAM family member 8
Gene symbol SLAMF8
Synonyms (NCBI Gene)
BLAMECD353SBBI42
Chromosome 1
Chromosome location 1q23.2
Summary This gene encodes a member of the CD2 family of cell surface proteins involved in lymphocyte activation. These proteins are characterized by Ig domains. This protein is expressed in lymphoid tissues, and studies of a similar protein in mouse suggest that
miRNA miRNA information provided by mirtarbase database.
97
miRTarBase ID miRNA Experiments Reference
MIRT1351521 hsa-miR-1183 CLIP-seq
MIRT1351522 hsa-miR-1193 CLIP-seq
MIRT1351523 hsa-miR-1207-5p CLIP-seq
MIRT1351524 hsa-miR-145 CLIP-seq
MIRT1351525 hsa-miR-146a CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0002232 Process Leukocyte chemotaxis involved in inflammatory response ISS
GO:0002336 Process B-1 B cell lineage commitment ISS 11313408
GO:0005515 Function Protein binding IPI 32296183, 33961781
GO:0006955 Process Immune response IBA
GO:0009986 Component Cell surface NAS 11313408
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
606620 21391 ENSG00000158714
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9P0V8
Protein name SLAM family member 8 (B-lymphocyte activator macrophage expressed) (BCM-like membrane protein) (CD antigen CD353)
Protein function May play a role in B-lineage commitment and/or modulation of signaling through the B-cell receptor.
Family and domains
Tissue specificity TISSUE SPECIFICITY: Expressed in lymph node, spleen, thymus and bone marrow. {ECO:0000269|PubMed:11313408}.
Sequence
MVMRPLWSLLLWEALLPITVTGAQVLSKVGGSVLLVAARPPGFQVREAIWRSLWPSEELL
ATFFRGSLETLYHSRFLGRAQLHSNLSLELGPLESGDSGNFSVLMVDTRGQPWTQTLQLK
VYDAVPRPVVQVFIAVERDAQPSKTCQVFLSCWAPNISEITYSWRRETTMDFGMEPHSLF
TDGQVLSISLGPGDRDVAYSCIVSNPVSWDLATVTPWDSCHHEAAPGKASYKDVLLVVVP
VSLLLMLVTLFSAWHWCPCSGKKKKDVHADRVGPETENPLVQDLP
Sequence length 285
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
2
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Clear cell carcinoma of kidney Uncertain significance rs367765736 RCV005939199
Sarcoma Uncertain significance rs367765736 RCV005939200
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Arthritis Rheumatoid Associate 35506438
Carotid Stenosis Associate 36304068
Glioma Associate 30105842
Immune System Diseases Associate 30105842
Inflammation Associate 30105842
Lymphoma Large Cell Anaplastic Associate 32054954
Neoplasms Stimulate 30105842
Neoplasms Associate 38017548
Prostatic Neoplasms Associate 38017548
Stomach Neoplasms Stimulate 30873760