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FAM76B (family with sequence similarity 76 member B)

Identity

Alias_namesfamily with sequence similarity 76, member B
Alias_symbol (synonym)MGC33371
Other alias-
HGNC (Hugo) FAM76B
LocusID (NCBI) 143684
Atlas_Id 63244
Location 11q21  [Link to chromosome band 11q21]
Location_base_pair Starts at 95768942 and ends at 95789791 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)FAM76B   28492
Cards
Entrez_Gene (NCBI)FAM76B  143684  family with sequence similarity 76 member B
Aliases
GeneCards (Weizmann)FAM76B
Ensembl hg19 (Hinxton)ENSG00000077458 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000077458 [Gene_View]  chr11:95768942-95789791 [Contig_View]  FAM76B [Vega]
ICGC DataPortalENSG00000077458
TCGA cBioPortalFAM76B
AceView (NCBI)FAM76B
Genatlas (Paris)FAM76B
WikiGenes143684
SOURCE (Princeton)FAM76B
Genetics Home Reference (NIH)FAM76B
Genomic and cartography
GoldenPath hg38 (UCSC)FAM76B  -     chr11:95768942-95789791 -  11q21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM76B  -     11q21   [Description]    (hg19-Feb_2009)
EnsemblFAM76B - 11q21 [CytoView hg19]  FAM76B - 11q21 [CytoView hg38]
Mapping of homologs : NCBIFAM76B [Mapview hg19]  FAM76B [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI913200 AK021591 AK313727 AM392906 AW118814
RefSeq transcript (Entrez)NM_001330357 NM_144664
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FAM76B
Cluster EST : UnigeneHs.288304 [ NCBI ]
CGAP (NCI)Hs.288304
Alternative Splicing GalleryENSG00000077458
Gene ExpressionFAM76B [ NCBI-GEO ]   FAM76B [ EBI - ARRAY_EXPRESS ]   FAM76B [ SEEK ]   FAM76B [ MEM ]
Gene Expression Viewer (FireBrowse)FAM76B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)143684
GTEX Portal (Tissue expression)FAM76B
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5HYJ3   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5HYJ3  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5HYJ3
Splice isoforms : SwissVarQ5HYJ3
PhosPhoSitePlusQ5HYJ3
Domains : Interpro (EBI)FAM76    FAM76B   
Domain families : Pfam (Sanger)FAM76 (PF16046)   
Domain families : Pfam (NCBI)pfam16046   
Conserved Domain (NCBI)FAM76B
DMDM Disease mutations143684
Blocks (Seattle)FAM76B
SuperfamilyQ5HYJ3
Human Protein AtlasENSG00000077458
Peptide AtlasQ5HYJ3
HPRD11333
IPIIPI00552849   IPI00827638   IPI01014099   IPI01013639   IPI01011063   IPI01010167   
Protein Interaction databases
DIP (DOE-UCLA)Q5HYJ3
IntAct (EBI)Q5HYJ3
FunCoupENSG00000077458
BioGRIDFAM76B
STRING (EMBL)FAM76B
ZODIACFAM76B
Ontologies - Pathways
QuickGOQ5HYJ3
Ontology : AmiGOprotein binding  nuclear speck  
Ontology : EGO-EBIprotein binding  nuclear speck  
NDEx NetworkFAM76B
Atlas of Cancer Signalling NetworkFAM76B
Wikipedia pathwaysFAM76B
Orthology - Evolution
OrthoDB143684
GeneTree (enSembl)ENSG00000077458
Phylogenetic Trees/Animal Genes : TreeFamFAM76B
HOVERGENQ5HYJ3
HOGENOMQ5HYJ3
Homologs : HomoloGeneFAM76B
Homology/Alignments : Family Browser (UCSC)FAM76B
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFAM76B [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FAM76B
dbVarFAM76B
ClinVarFAM76B
1000_GenomesFAM76B 
Exome Variant ServerFAM76B
ExAC (Exome Aggregation Consortium)FAM76B (select the gene name)
Genetic variants : HAPMAP143684
Genomic Variants (DGV)FAM76B [DGVbeta]
DECIPHERFAM76B [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisFAM76B 
Mutations
ICGC Data PortalFAM76B 
TCGA Data PortalFAM76B 
Broad Tumor PortalFAM76B
OASIS PortalFAM76B [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICFAM76B  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDFAM76B
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 FAM76B
DgiDB (Drug Gene Interaction Database)FAM76B
DoCM (Curated mutations)FAM76B (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FAM76B (select a term)
intoGenFAM76B
Cancer3DFAM76B(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenFAM76B
Genetic Testing Registry FAM76B
NextProtQ5HYJ3 [Medical]
TSGene143684
GENETestsFAM76B
Target ValidationFAM76B
Huge Navigator FAM76B [HugePedia]
snp3D : Map Gene to Disease143684
BioCentury BCIQFAM76B
ClinGenFAM76B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD143684
Chemical/Pharm GKB GenePA142671838
Clinical trialFAM76B
Miscellaneous
canSAR (ICR)FAM76B (select the gene name)
Probes
Litterature
PubMed20 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM76B
EVEXFAM76B
GoPubMedFAM76B
iHOPFAM76B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:08:11 CEST 2017

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