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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

SLAMF8 Gene

protein-coding   GIFtS: 44
GCID: GC01P159796

SLAM family member 8

 Explore 3 diseases affiliated with
SLAMF8 via our new
 Human Malady Compendium 
Biological research products
for SLAMF8
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Aliases
SLAM Family Member 81 2     B-Lymphocyte Activator Macrophage Expressed2 3
BLAME1 2 3 5     BCM-Like Membrane Protein2 3
CD3531 2     B Lymphocyte Activator Macrophage Expressed2
SBBI421 2     CD353 Antigen3

External Ids:    HGNC: 213911   Entrez Gene: 568332   Ensembl: ENSG000001587147   OMIM: 6066205   UniProtKB: Q9P0V83   

Export aliases for SLAMF8 gene to outside databases

Previous GC identifers: GC01P157013 GC01P156609 GC01P158063 GC01P131152


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for SLAMF8:
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 it may function during B cell lineage commitment. The gene is found in a region of chromosome 1
containing many CD2 genes. (provided by RefSeq, Jul 2008)

UniProtKB/Swiss-Prot: SLAF8_HUMAN, Q9P0V8
Function: May play a role in B-lineage commitment and/or modulation of signaling through the B-cell receptor

Gene Wiki entry for SLAMF8


(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000001.10  NC_018912.1  NT_004487.19  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the SLAMF8 gene promoter:
         Oct-B1   HOXA9   HOXA9B   Spz1   oct-B3   oct-B2   Meis-1b   POU2F1   POU2F1a   Meis-1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidSLAMF8 promoter sequence
   Search SABiosciences Chromatin IP Primers for SLAMF8

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat SLAMF8


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 1q23.2   Ensembl cytogenetic band:  1q23.2   HGNC cytogenetic band: 1q23.1

SLAMF8 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SLAMF8 gene location

GeneLoc information about chromosome 1         GeneLoc Exon Structure

GeneLoc location for GC01P159796:  view genomic region     (about GC identifiers)

Start:
159,796,479 bp from pter      End:
159,807,282 bp from pter
Size:
10,804 bases      Orientation:
plus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: SLAF8_HUMAN, Q9P0V8 (See protein sequence)
Recommended Name: SLAM family member 8 precursor  
Size: 285 amino acids; 31670 Da
Subcellular location: Membrane; Single-pass type I membrane protein
Secondary accessions: Q32MC6 Q5VU15
Alternative splicing: 2 isoforms:  Q9P0V8-1   Q9P0V8-2   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for SLAMF8: NX_Q9P0V8

SLAMF8 Protein expression data from MOPED and PaxDb:    About this image 

Estimated protein expression log10 (pmol).

REFSEQ proteins: NP_064510.1  
ENSEMBL proteins: 
 ENSP00000289707   ENSP00000357084  

Human Recombinant Protein Products: 
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Uscn Proteins for SLAMF8

Gene Ontology (GO): 1 cellular component term (GO ID links to tree view):    About this table

GO IDQualified GO termEvidencePubMed IDs
GO:0016021integral to membrane IEA--


SLAMF8 for ontologies           About GeneDecksing



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(According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
About This Section

SLAMF8 for domains           About GeneDecksing

2 InterPro domains/families:
 IPR007110 Ig-like_dom
 IPR015631 SLAM_fam_rcpts

Graphical View of Domain Structure for InterPro Entry Q9P0V8

ProtoNet protein and cluster: Q9P0V8

UniProtKB/Swiss-Prot: SLAF8_HUMAN, Q9P0V8
Similarity: Contains 1 Ig-like C2-type (immunoglobulin-like) domain


(According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
About This Section

Function Summary:

     UniProtKB/Swiss-Prot: SLAF8_HUMAN, Q9P0V8
Function: May play a role in B-lineage commitment and/or modulation of signaling through the B-cell receptor

miRNA
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SwitchGear 3'UTR luciferase reporter plasmidSLAMF8 3' UTR sequence
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Gene Ontology (GO): 1 molecular function term (GO ID links to tree view):    About this table

GO IDQualified GO termEvidencePubMed IDs
GO:0004872receptor activity IEA--


SLAMF8 for ontologies           About GeneDecksing


1 GenomeRNAi human phenotype for SLAMF8:
 Wnt reporter downregulated 

Animal Models:
     Mouse knock-out Slamf8tm1Lex for SLAMF8
     1 MGI mutant phenotype (inferred from 2 alleles(MGI details for Slamf8):
 immune system 

SLAMF8 for phenotypes           About GeneDecksing


(Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
About This Section



Interactions:

    Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for SLAMF8

(Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
About This Section
Browse Small Molecules at EMD Millipore
Browse drugs & compounds from Enzo Life Sciences

Browse Tocris compounds for SLAMF8
Search CenterWatch for drugs/clinical trials and news about SLAMF8 / SLAF8 

(Secondary structures according to fRNAdb,
GenBank/EMBL/DDBJ Accessions according to
Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
RefSeq according to Entrez Gene,
DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
RNAi Products from EMD Millipore,
siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
About This Section

REFSEQ mRNAs for SLAMF8 gene: 
NM_020125.2  

Unigene Cluster for SLAMF8:

SLAM family member 8
Hs.438683  [show with all ESTs]
Unigene Representative Sequence: NM_020125
4 Ensembl transcripts including schematic representations, and UCSC links where relevant:
ENST00000289707(uc001fue.4) ENST00000368104 ENST00000471286 ENST00000497141


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hsa-miR-3164 hsa-miR-4311 hsa-miR-4254 hsa-miR-550a hsa-miR-3175 hsa-miR-371-5p hsa-miR-650 hsa-miR-199a-5p
SwitchGear 3'UTR luciferase reporter plasmidSLAMF8 3' UTR sequence
Inhib. RNA
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OriGene siRNA: SLAMF8
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Clone
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Primer
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Additional cDNA sequence: 

AF144235.1 AF146761.1 AK074669.1 BC109194.2 

11 DOTS entries:

DT.441784  DT.91708048  DT.121405823  DT.97815630  DT.97837392  DT.121405954  DT.100783193  DT.100777798 
DT.91708049  DT.100715115  DT.100777799 

24/78 AceView cDNA sequences (see all 78):

N79421 AW664177 BG230648 NM_020125 CD365198 CD368492 AA627522 BX118110 
CD367956 AF146761 CA307477 AI680659 AW662401 AA320408 BM725151 CA440043 
CO246344 AW206273 CA307285 N62522 AI298413 BU618114 AW952171 BF591200 

GeneLoc Exon Structure

3 Alternative Splicing Database (ASD) splice patterns (SP) for SLAMF8    About this scheme

ExUns: 1a · 1b · 1c ^ 2a · 2b ^ 3 ^ 4 ^ 5a · 5b
SP1:                                                      
SP2:                    -     -                           
SP3:                    -                                 


ECgene alternative splicing isoforms for SLAMF8

(RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
About This Section

SLAMF8 expression in normal human tissues (normalized intensities)
See probesets specificity/sensitivity at GeneAnnot
About this imageBioGPS
CGAP TAG: CAAAACTGGC

Microarray
RNAseq (Illumina Body Map)
(100×FPKM)½
SAGE (Serial Analysis of Gene Expression)

About this image
See SLAMF8 Protein Expression from SPIRE MOPED and PaxDB
Genevestigator expression for SLAMF8

SOURCE GeneReport for Unigene cluster: Hs.438683

UniProtKB/Swiss-Prot: SLAF8_HUMAN, Q9P0V8
Tissue specificity: Expressed in lymph node, spleen, thymus and bone marrow

    SABiosciences Custom PCR Arrays for SLAMF8
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In Situ
Assay Products:
 

 
Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SLAMF8

(Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
About This Section
  --

ENSEMBL Gene Tree for SLAMF8 (if available)
TreeFam Gene Tree for SLAMF8 (if available) 

(Paralogs according to 1HomoloGene,
2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
About This Section
  --

(SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
About This Section

10/287 NCBI SNPs in SLAMF8 are shown (see all 287    About this table
Genomic DataTranscription Related DataAllele Frequencies
SNP IDValidClinical
significance
Chr 1 posSequence#AA
Chg
TypeMore#Allele
freq
PopTotal
sample
More
----------
rs24944951,2
C,F,A,H,--159794514(+) GGGCTG/AAGCCT 1 -- us2k113Minor allele frequency- A:0.18NS EA NA WA CSA 660
rs1411300551,2
--159794551(+) CACCTA/GAGTAG 1 -- us2k10--------
rs25013431,2
C,F,A,H,--159794576(-) CATTCC/ATCAGG 1 -- us2k122Minor allele frequency- A:0.22EA NS NA WA CSA 2501
rs1427479121,2
--159794588(+) ATGACA/GGAATT 1 -- us2k10--------
rs1167856881,2
F,--159794635(+) TCTCCA/TCCCCC 1 -- us2k11Minor allele frequency- T:0.02WA 118
rs1445014941,2
--159794637(+) TCCACA/CCCCAT 1 -- us2k10--------
rs1831769511,2
--159794639(+) CACCCC/GCATGA 1 -- us2k10--------
rs1874471551,2
--159794655(+) AGCTTC/TCCAGT 1 -- us2k10--------
rs741247231,2
C,--159794675(+) TCCTCA/GGTACT 1 -- us2k14Minor allele frequency- G:0.11WA CSA 123
rs1926257761,2
--159794868(+) CCCAGA/TCCACC 1 -- us2k10--------

HapMap Linkage Disequilibrium report for SLAMF8 (159796479 - 159807282 bp)
Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
      Database of Genomic Variants (DGV) variations for SLAMF8: --

SABiosciences Cancer Mutation PCR Assays
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(in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
About This Section

SLAMF8 for disorders           About GeneDecksing

OMIM gene information: 606620    OMIM disorders: --

3 diseases for SLAMF8:    About MalaCards
dental caries    hepatitis b    hepatitis

Human Genome Epidemiology (HuGE) Navigator: SLAMF8 (1 document)

Export disorders for SLAMF8 gene to outside databases

(in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
About This Section

PubMed articles for SLAMF8 gene integrated from 9 sources:
(articles sorted by number of sources associating them with SLAMF8)
    Utopia: connect your pdf to the dynamic
world of online information

  1. Cloning, expression, and function of BLAME, a novel member of the CD2 family. (PubMed id 11313408)1, 2, 3 Kingsbury G.A....Villeval J.-L. (2001)
  2. The DNA sequence and biological annotation of human chromosome 1. (PubMed id 16710414)1, 2 Gregory S.G.... Bentley D.R. (2006)
  3. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1, 2 Gerhard D.S....Malek J. (2004)
  4. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
  5. Signal peptide prediction based on analysis of experimentally verified cleavage sites. (PubMed id 15340161)1, 2 Zhang Z. and Henzel W.J. (2004)
  6. Functional requirements for interactions between CD84 and Src homology 2 domain-containing proteins and their contribution to human T cell activation. (PubMed id 12928397)1, 9 Tangye S.G.... van de Weerdt B.C.M. (2003)
  7. New genetic associations detected in a host response study to hepatitis B vaccine. (PubMed id 20237496)1 Davila S....Seielstad M. (2010)
  8. Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. (PubMed id 16344560)1 Kimura K.... Sugano S. (2006)
  9. Signal sequence and keyword trap in silico for selection of full- length human cDNAs encoding secretion or membrane proteins from oligo- capped cDNA libraries. (PubMed id 16303743)1 Otsuki T....Isogai T. (2005)
  10. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. (PubMed id 12477932)1 Strausberg R.L....Marra M.A. (2002)

(in PubMed, OMIM, and NCBI Bookshelf)
About This Section
 ANDOR
Aliases
Free Text  

  Query String
PubMed
OMIM
NCBI Bookshelf
  (Note: In FireFox, select the above section and copy using Ctrl-C)

(According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
About This Section
Entrez Gene: 56833 HGNC: 21391 AceView: SLAMF8 Ensembl:ENSG00000158714 euGenes: HUgn56833
ECgene: SLAMF8 H-InvDB: SLAMF8

(According to HUGE)
About This Section
  --

(According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
About This Section
NameDescription
PharmGKB entry for SLAMF8 Pharmacogenomics, SNPs, Pathways

(Patent information from GeneIP,
Licensable technologies from WIS Yeda, Salk, Tufts,
IP news from LifeMap Sciences, Inc.)
About This Section
Patent Information for SLAMF8 gene:
Search GeneIP for patents involving SLAMF8

GeneCards and IP:
Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



(Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Uscn, Thermo Fisher Scientific, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript and LifeMap BioReagents, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences),
In Situ Hybridization Assays from
Advanced Cell Diagnostics
About This Section

 
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GeneCards Homepage - Last full update: 18 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 26 Apr 2013

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VWF
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von Willebrand factor
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