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FSCB (fibrous sheath CABYR binding protein)

Identity

Alias_namesC14orf155
chromosome 14 open reading frame 155
Alias_symbol (synonym)DKFZP434F1017
Other alias
HGNC (Hugo) FSCB
LocusID (NCBI) 84075
Atlas_Id 63608
Location 14q21.2  [Link to chromosome band 14q21]
Location_base_pair Starts at 44504151 and ends at 44507296 bp from pter ( according to hg38-Dec_2013)

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)FSCB   20494
Cards
Entrez_Gene (NCBI)FSCB  84075  fibrous sheath CABYR binding protein
AliasesC14orf155
GeneCards (Weizmann)FSCB
Ensembl hg19 (Hinxton)ENSG00000189139 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000189139 [Gene_View]  chr14:44504151-44507296 [Contig_View]  FSCB [Vega]
ICGC DataPortalENSG00000189139
TCGA cBioPortalFSCB
AceView (NCBI)FSCB
Genatlas (Paris)FSCB
WikiGenes84075
SOURCE (Princeton)FSCB
Genetics Home Reference (NIH)FSCB
Genomic and cartography
GoldenPath hg38 (UCSC)FSCB  -     chr14:44504151-44507296 -  14q21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FSCB  -     14q21.2   [Description]    (hg19-Feb_2009)
EnsemblFSCB - 14q21.2 [CytoView hg19]  FSCB - 14q21.2 [CytoView hg38]
Mapping of homologs : NCBIFSCB [Mapview hg19]  FSCB [Mapview hg38]
OMIM611779   
Gene and transcription
Genbank (Entrez)AK124110 AK302615 AL136775 AM392986 BC039878
RefSeq transcript (Entrez)NM_032135
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FSCB
Cluster EST : UnigeneHs.307086 [ NCBI ]
CGAP (NCI)Hs.307086
Alternative Splicing GalleryENSG00000189139
Gene ExpressionFSCB [ NCBI-GEO ]   FSCB [ EBI - ARRAY_EXPRESS ]   FSCB [ SEEK ]   FSCB [ MEM ]
Gene Expression Viewer (FireBrowse)FSCB [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)84075
GTEX Portal (Tissue expression)FSCB
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5H9T9   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5H9T9  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5H9T9
Splice isoforms : SwissVarQ5H9T9
PhosPhoSitePlusQ5H9T9
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FSCB
DMDM Disease mutations84075
Blocks (Seattle)FSCB
SuperfamilyQ5H9T9
Human Protein AtlasENSG00000189139
Peptide AtlasQ5H9T9
HPRD12638
IPIIPI00922296   IPI01012559   
Protein Interaction databases
DIP (DOE-UCLA)Q5H9T9
IntAct (EBI)Q5H9T9
FunCoupENSG00000189139
BioGRIDFSCB
STRING (EMBL)FSCB
ZODIACFSCB
Ontologies - Pathways
QuickGOQ5H9T9
Ontology : AmiGOmotile cilium  
Ontology : EGO-EBImotile cilium  
NDEx NetworkFSCB
Atlas of Cancer Signalling NetworkFSCB
Wikipedia pathwaysFSCB
Orthology - Evolution
OrthoDB84075
GeneTree (enSembl)ENSG00000189139
Phylogenetic Trees/Animal Genes : TreeFamFSCB
HOVERGENQ5H9T9
HOGENOMQ5H9T9
Homologs : HomoloGeneFSCB
Homology/Alignments : Family Browser (UCSC)FSCB
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFSCB [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FSCB
dbVarFSCB
ClinVarFSCB
1000_GenomesFSCB 
Exome Variant ServerFSCB
ExAC (Exome Aggregation Consortium)FSCB (select the gene name)
Genetic variants : HAPMAP84075
Genomic Variants (DGV)FSCB [DGVbeta]
DECIPHERFSCB [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisFSCB 
Mutations
ICGC Data PortalFSCB 
TCGA Data PortalFSCB 
Broad Tumor PortalFSCB
OASIS PortalFSCB [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICFSCB  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDFSCB
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 FSCB
DgiDB (Drug Gene Interaction Database)FSCB
DoCM (Curated mutations)FSCB (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FSCB (select a term)
intoGenFSCB
Cancer3DFSCB(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM611779   
Orphanet
MedgenFSCB
Genetic Testing Registry FSCB
NextProtQ5H9T9 [Medical]
TSGene84075
GENETestsFSCB
Huge Navigator FSCB [HugePedia]
snp3D : Map Gene to Disease84075
BioCentury BCIQFSCB
ClinGenFSCB
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD84075
Chemical/Pharm GKB GenePA162389023
Clinical trialFSCB
Miscellaneous
canSAR (ICR)FSCB (select the gene name)
Probes
Litterature
PubMed9 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFSCB
EVEXFSCB
GoPubMedFSCB
iHOPFSCB
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Fri May 19 11:12:58 CEST 2017

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