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FAM66E (family with sequence similarity 66 member E)

Identity

Alias_namesfamily with sequence similarity 66, member E
Other alias-
HGNC (Hugo) FAM66E
LocusID (NCBI) 100132103
Atlas_Id 63223
Location 8p23.1  [Link to chromosome band 8p23]
Location_base_pair Starts at 7955013 and ends at 8008755 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)FAM66E   18735
Cards
Entrez_Gene (NCBI)FAM66E  100132103  family with sequence similarity 66 member E
Aliases
GeneCards (Weizmann)FAM66E
Ensembl hg19 (Hinxton)ENSG00000225725 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000225725 [Gene_View]  chr8:7955013-8008755 [Contig_View]  FAM66E [Vega]
ICGC DataPortalENSG00000225725
TCGA cBioPortalFAM66E
AceView (NCBI)FAM66E
Genatlas (Paris)FAM66E
WikiGenes100132103
SOURCE (Princeton)FAM66E
Genetics Home Reference (NIH)FAM66E
Genomic and cartography
GoldenPath hg38 (UCSC)FAM66E  -     chr8:7955013-8008755 +  8p23.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM66E  -     8p23.1   [Description]    (hg19-Feb_2009)
EnsemblFAM66E - 8p23.1 [CytoView hg19]  FAM66E - 8p23.1 [CytoView hg38]
Mapping of homologs : NCBIFAM66E [Mapview hg19]  FAM66E [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FAM66E
Cluster EST : UnigeneHs.694680 [ NCBI ]
CGAP (NCI)Hs.694680
Alternative Splicing GalleryENSG00000225725
Gene ExpressionFAM66E [ NCBI-GEO ]   FAM66E [ EBI - ARRAY_EXPRESS ]   FAM66E [ SEEK ]   FAM66E [ MEM ]
Gene Expression Viewer (FireBrowse)FAM66E [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100132103
GTEX Portal (Tissue expression)FAM66E
Protein : pattern, domain, 3D structure
UniProt/SwissProtP0C841   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP0C841  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP0C841
Splice isoforms : SwissVarP0C841
PhosPhoSitePlusP0C841
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM66E
DMDM Disease mutations100132103
Blocks (Seattle)FAM66E
SuperfamilyP0C841
Human Protein AtlasENSG00000225725
Peptide AtlasP0C841
IPIIPI00902956   
Protein Interaction databases
DIP (DOE-UCLA)P0C841
IntAct (EBI)P0C841
FunCoupENSG00000225725
BioGRIDFAM66E
STRING (EMBL)FAM66E
ZODIACFAM66E
Ontologies - Pathways
QuickGOP0C841
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkFAM66E
Atlas of Cancer Signalling NetworkFAM66E
Wikipedia pathwaysFAM66E
Orthology - Evolution
OrthoDB100132103
GeneTree (enSembl)ENSG00000225725
Phylogenetic Trees/Animal Genes : TreeFamFAM66E
HOVERGENP0C841
HOGENOMP0C841
Homologs : HomoloGeneFAM66E
Homology/Alignments : Family Browser (UCSC)FAM66E
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFAM66E [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FAM66E
dbVarFAM66E
ClinVarFAM66E
1000_GenomesFAM66E 
Exome Variant ServerFAM66E
ExAC (Exome Aggregation Consortium)FAM66E (select the gene name)
Genetic variants : HAPMAP100132103
Genomic Variants (DGV)FAM66E [DGVbeta]
DECIPHERFAM66E [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisFAM66E 
Mutations
ICGC Data PortalFAM66E 
TCGA Data PortalFAM66E 
Broad Tumor PortalFAM66E
OASIS PortalFAM66E [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDFAM66E
BioMutasearch FAM66E
DgiDB (Drug Gene Interaction Database)FAM66E
DoCM (Curated mutations)FAM66E (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FAM66E (select a term)
intoGenFAM66E
Cancer3DFAM66E(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenFAM66E
Genetic Testing Registry FAM66E
NextProtP0C841 [Medical]
TSGene100132103
GENETestsFAM66E
Target ValidationFAM66E
Huge Navigator FAM66E [HugePedia]
snp3D : Map Gene to Disease100132103
BioCentury BCIQFAM66E
ClinGenFAM66E
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100132103
Chemical/Pharm GKB GenePA142671880
Clinical trialFAM66E
Miscellaneous
canSAR (ICR)FAM66E (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM66E
EVEXFAM66E
GoPubMedFAM66E
iHOPFAM66E
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 13:08:09 CEST 2017

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