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SLAMF9 (SLAM family member 9)

Identity

Alias_symbol (synonym)CD2F-10
CD84-H1
SF2001
Other aliasCD2F10
CD84H1
HGNC (Hugo) SLAMF9
LocusID (NCBI) 89886
Atlas_Id 73269
Location 1q23.2  [Link to chromosome band 1q23]
Location_base_pair Starts at 159951492 and ends at 159954254 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)		IGSF9 (1q23.2) / SLAMF9 (1q23.2)SLAMF9 (1q23.2) / ALG12 (22q13.33)

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 

External links

Nomenclature
HGNC (Hugo)SLAMF9   18430
Cards
Entrez_Gene (NCBI)SLAMF9  89886  SLAM family member 9
AliasesCD2F-10; CD2F10; CD84-H1; CD84H1; 
SF2001
GeneCards (Weizmann)SLAMF9
Ensembl hg19 (Hinxton)ENSG00000162723 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000162723 [Gene_View]  chr1:159951492-159954254 [Contig_View]  SLAMF9 [Vega]
ICGC DataPortalENSG00000162723
TCGA cBioPortalSLAMF9
AceView (NCBI)SLAMF9
Genatlas (Paris)SLAMF9
WikiGenes89886
SOURCE (Princeton)SLAMF9
Genetics Home Reference (NIH)SLAMF9
Genomic and cartography
GoldenPath hg38 (UCSC)SLAMF9  -     chr1:159951492-159954254 -  1q23.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SLAMF9  -     1q23.2   [Description]    (hg19-Feb_2009)
EnsemblSLAMF9 - 1q23.2 [CytoView hg19]  SLAMF9 - 1q23.2 [CytoView hg38]
Mapping of homologs : NCBISLAMF9 [Mapview hg19]  SLAMF9 [Mapview hg38]
OMIM608589   
Gene and transcription
Genbank (Entrez)AF275725 AY034613 AY358801 BC070213 BC074754
RefSeq transcript (Entrez)NM_001146172 NM_001146173 NM_033438
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SLAMF9
Cluster EST : UnigeneHs.661712 [ NCBI ]
CGAP (NCI)Hs.661712
Alternative Splicing GalleryENSG00000162723
Gene ExpressionSLAMF9 [ NCBI-GEO ]   SLAMF9 [ EBI - ARRAY_EXPRESS ]   SLAMF9 [ SEEK ]   SLAMF9 [ MEM ]
Gene Expression Viewer (FireBrowse)SLAMF9 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)89886
GTEX Portal (Tissue expression)SLAMF9
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96A28   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96A28  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96A28
Splice isoforms : SwissVarQ96A28
PhosPhoSitePlusQ96A28
Domaine pattern : Prosite (Expaxy)IG_LIKE (PS50835)   
Domains : Interpro (EBI)Ig-like_dom    Ig-like_fold   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SLAMF9
DMDM Disease mutations89886
Blocks (Seattle)SLAMF9
SuperfamilyQ96A28
Human Protein AtlasENSG00000162723
Peptide AtlasQ96A28
HPRD12263
IPIIPI00059190   IPI00647800   IPI00929126   
Protein Interaction databases
DIP (DOE-UCLA)Q96A28
IntAct (EBI)Q96A28
FunCoupENSG00000162723
BioGRIDSLAMF9
STRING (EMBL)SLAMF9
ZODIACSLAMF9
Ontologies - Pathways
QuickGOQ96A28
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkSLAMF9
Atlas of Cancer Signalling NetworkSLAMF9
Wikipedia pathwaysSLAMF9
Orthology - Evolution
OrthoDB89886
GeneTree (enSembl)ENSG00000162723
Phylogenetic Trees/Animal Genes : TreeFamSLAMF9
HOVERGENQ96A28
HOGENOMQ96A28
Homologs : HomoloGeneSLAMF9
Homology/Alignments : Family Browser (UCSC)SLAMF9
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerSLAMF9 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)SLAMF9
dbVarSLAMF9
ClinVarSLAMF9
1000_GenomesSLAMF9 
Exome Variant ServerSLAMF9
ExAC (Exome Aggregation Consortium)SLAMF9 (select the gene name)
Genetic variants : HAPMAP89886
Genomic Variants (DGV)SLAMF9 [DGVbeta]
DECIPHERSLAMF9 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisSLAMF9 
Mutations
ICGC Data PortalSLAMF9 
TCGA Data PortalSLAMF9 
Broad Tumor PortalSLAMF9
OASIS PortalSLAMF9 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICSLAMF9  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDSLAMF9
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch SLAMF9
DgiDB (Drug Gene Interaction Database)SLAMF9
DoCM (Curated mutations)SLAMF9 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)SLAMF9 (select a term)
intoGenSLAMF9
Cancer3DSLAMF9(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM608589   
Orphanet
MedgenSLAMF9
Genetic Testing Registry SLAMF9
NextProtQ96A28 [Medical]
TSGene89886
GENETestsSLAMF9
Target ValidationSLAMF9
Huge Navigator SLAMF9 [HugePedia]
snp3D : Map Gene to Disease89886
BioCentury BCIQSLAMF9
ClinGenSLAMF9
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD89886
Chemical/Pharm GKB GenePA134993219
Clinical trialSLAMF9
Miscellaneous
canSAR (ICR)SLAMF9 (select the gene name)
Probes
Litterature
PubMed8 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSLAMF9
EVEXSLAMF9
GoPubMedSLAMF9
iHOPSLAMF9
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed May 31 15:40:49 CEST 2017
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