Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
56833
Gene name Gene Name - the full gene name approved by the HGNC.
SLAM family member 8
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLAMF8
Synonyms (NCBI Gene) Gene synonyms aliases
BLAME, CD353, SBBI42
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q23.2
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
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
GO:0009986 Component Cell surface NAS 11313408
GO:0010760 Process Negative regulation of macrophage chemotaxis ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606620 21391 ENSG00000158714
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Inflammatory bowel disease Inflammatory Bowel Diseases rs137853579, rs137853580, rs121909601, rs149491038, rs368287711, rs387907326, rs587777338, rs758439420, rs1329427406, rs1264862631, rs1192830343, rs1373354533, rs1419560997, rs1591263883, rs1989014468 28067908
Unknown
Disease term Disease name Evidence References Source
Crohn disease Crohn Disease 28067908 ClinVar
Crohn Disease Crohn Disease GWAS
Inflammatory Bowel Disease Inflammatory Bowel Disease GWAS
Associations from Text Mining
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