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FCRLB (Fc receptor like B)

Identity

Alias_namesFCRLM2
Fc receptor-like and mucin-like 2
Fc receptor-like B
Alias_symbol (synonym)FLJ31052
FCRL2
FREB-2
FCRLY
Other aliasFcRY
HGNC (Hugo) FCRLB
LocusID (NCBI) 127943
Atlas_Id 56472
Location 1q23.3  [Link to chromosome band 1q23]
Location_base_pair Starts at 161691334 and ends at 161697933 bp from pter ( according to hg19-Feb_2009)

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)FCRLB   26431
Cards
Entrez_Gene (NCBI)FCRLB  127943  Fc receptor like B
AliasesFCRL2; FCRLM2; FCRLY; FREB-2; 
FcRY
GeneCards (Weizmann)FCRLB
Ensembl hg19 (Hinxton)ENSG00000162746 [Gene_View]  chr1:161691334-161697933 [Contig_View]  FCRLB [Vega]
Ensembl hg38 (Hinxton)ENSG00000162746 [Gene_View]  chr1:161691334-161697933 [Contig_View]  FCRLB [Vega]
ICGC DataPortalENSG00000162746
TCGA cBioPortalFCRLB
AceView (NCBI)FCRLB
Genatlas (Paris)FCRLB
WikiGenes127943
SOURCE (Princeton)FCRLB
Genetics Home Reference (NIH)FCRLB
Genomic and cartography
GoldenPath hg19 (UCSC)FCRLB  -     chr1:161691334-161697933 +  1q23.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)FCRLB  -     1q23.3   [Description]    (hg38-Dec_2013)
EnsemblFCRLB - 1q23.3 [CytoView hg19]  FCRLB - 1q23.3 [CytoView hg38]
Mapping of homologs : NCBIFCRLB [Mapview hg19]  FCRLB [Mapview hg38]
OMIM609251   
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)NM_001002901 NM_001288829 NM_001288830 NM_001288831 NM_001288832 NM_001320241
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FCRLB
Cluster EST : UnigeneHs.517422 [ NCBI ]
CGAP (NCI)Hs.517422
Alternative Splicing GalleryENSG00000162746
Gene ExpressionFCRLB [ NCBI-GEO ]   FCRLB [ EBI - ARRAY_EXPRESS ]   FCRLB [ SEEK ]   FCRLB [ MEM ]
Gene Expression Viewer (FireBrowse)FCRLB [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)127943
GTEX Portal (Tissue expression)FCRLB
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ6BAA4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ6BAA4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ6BAA4
Splice isoforms : SwissVarQ6BAA4
PhosPhoSitePlusQ6BAA4
Domaine pattern : Prosite (Expaxy)IG_LIKE (PS50835)   
Domains : Interpro (EBI)Ig-like_dom    Ig-like_fold    Ig_sub   
Domain families : Pfam (Sanger)Ig_2 (PF13895)   
Domain families : Pfam (NCBI)pfam13895   
Domain families : Smart (EMBL)IG (SM00409)  
Conserved Domain (NCBI)FCRLB
DMDM Disease mutations127943
Blocks (Seattle)FCRLB
SuperfamilyQ6BAA4
Human Protein AtlasENSG00000162746
Peptide AtlasQ6BAA4
HPRD08093
IPIIPI00457283   IPI00642052   IPI00061053   IPI00465241   IPI00658044   IPI00743560   
Protein Interaction databases
DIP (DOE-UCLA)Q6BAA4
IntAct (EBI)Q6BAA4
FunCoupENSG00000162746
BioGRIDFCRLB
STRING (EMBL)FCRLB
ZODIACFCRLB
Ontologies - Pathways
QuickGOQ6BAA4
Ontology : AmiGOcytoplasm  endoplasmic reticulum  negative regulation of immune response  
Ontology : EGO-EBIcytoplasm  endoplasmic reticulum  negative regulation of immune response  
NDEx NetworkFCRLB
Atlas of Cancer Signalling NetworkFCRLB
Wikipedia pathwaysFCRLB
Orthology - Evolution
OrthoDB127943
GeneTree (enSembl)ENSG00000162746
Phylogenetic Trees/Animal Genes : TreeFamFCRLB
HOVERGENQ6BAA4
HOGENOMQ6BAA4
Homologs : HomoloGeneFCRLB
Homology/Alignments : Family Browser (UCSC)FCRLB
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFCRLB [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FCRLB
dbVarFCRLB
ClinVarFCRLB
1000_GenomesFCRLB 
Exome Variant ServerFCRLB
ExAC (Exome Aggregation Consortium)FCRLB (select the gene name)
Genetic variants : HAPMAP127943
Genomic Variants (DGV)FCRLB [DGVbeta]
DECIPHER (Syndromes)1:161691334-161697933  ENSG00000162746
CONAN: Copy Number AnalysisFCRLB 
Mutations
ICGC Data PortalFCRLB 
TCGA Data PortalFCRLB 
Broad Tumor PortalFCRLB
OASIS PortalFCRLB [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICFCRLB  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDFCRLB
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 FCRLB
DgiDB (Drug Gene Interaction Database)FCRLB
DoCM (Curated mutations)FCRLB (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FCRLB (select a term)
intoGenFCRLB
Cancer3DFCRLB(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM609251   
Orphanet
MedgenFCRLB
Genetic Testing Registry FCRLB
NextProtQ6BAA4 [Medical]
TSGene127943
GENETestsFCRLB
Huge Navigator FCRLB [HugePedia]
snp3D : Map Gene to Disease127943
BioCentury BCIQFCRLB
ClinGenFCRLB
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD127943
Chemical/Pharm GKB GenePA162388195
Clinical trialFCRLB
Miscellaneous
canSAR (ICR)FCRLB (select the gene name)
Probes
Litterature
PubMed9 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFCRLB
EVEXFCRLB
GoPubMedFCRLB
iHOPFCRLB
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Thu Mar 30 15:01:07 CEST 2017

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