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FER1L6-AS2 (FER1L6 antisense RNA 2)

Identity

Alias_namesC8orf78
chromosome 8 open reading frame 78
FER1L6 antisense RNA 2 (non-protein coding)
Alias_symbol (synonym)FLJ32770
Other alias
HGNC (Hugo) FER1L6-AS2
LocusID (NCBI) 157376
Atlas_Id 78137
Location 8q24.13  [Link to chromosome band 8q24]

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)FER1L6-AS2   26534
Cards
Entrez_Gene (NCBI)FER1L6-AS2  157376  FER1L6 antisense RNA 2
AliasesC8orf78
GeneCards (Weizmann)FER1L6-AS2
Ensembl hg19 (Hinxton)ENSG00000253868 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000253868 [Gene_View]  - [Contig_View]  FER1L6-AS2 [Vega]
ICGC DataPortalENSG00000253868
TCGA cBioPortalFER1L6-AS2
AceView (NCBI)FER1L6-AS2
Genatlas (Paris)FER1L6-AS2
WikiGenes157376
SOURCE (Princeton)FER1L6-AS2
Genetics Home Reference (NIH)FER1L6-AS2
Genomic and cartography
GoldenPath hg38 (UCSC)FER1L6-AS2  -  
GoldenPath hg19 (UCSC)FER1L6-AS2  -  
EnsemblFER1L6-AS2 - [CytoView hg19]  FER1L6-AS2 - [CytoView hg38]
Mapping of homologs : NCBIFER1L6-AS2 [Mapview hg19]  FER1L6-AS2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI425048 AK057332 BC101502 BC101506
RefSeq transcript (Entrez)NM_182525
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FER1L6-AS2
Cluster EST : UnigeneHs.662360 [ NCBI ]
CGAP (NCI)Hs.662360
Alternative Splicing GalleryENSG00000253868
Gene ExpressionFER1L6-AS2 [ NCBI-GEO ]   FER1L6-AS2 [ EBI - ARRAY_EXPRESS ]   FER1L6-AS2 [ SEEK ]   FER1L6-AS2 [ MEM ]
Gene Expression Viewer (FireBrowse)FER1L6-AS2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)157376
GTEX Portal (Tissue expression)FER1L6-AS2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96M78   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96M78  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96M78
Splice isoforms : SwissVarQ96M78
PhosPhoSitePlusQ96M78
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FER1L6-AS2
DMDM Disease mutations157376
Blocks (Seattle)FER1L6-AS2
SuperfamilyQ96M78
Human Protein AtlasENSG00000253868
Peptide AtlasQ96M78
HPRD08138
IPIIPI00307503   
Protein Interaction databases
DIP (DOE-UCLA)Q96M78
IntAct (EBI)Q96M78
FunCoupENSG00000253868
BioGRIDFER1L6-AS2
STRING (EMBL)FER1L6-AS2
ZODIACFER1L6-AS2
Ontologies - Pathways
QuickGOQ96M78
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkFER1L6-AS2
Atlas of Cancer Signalling NetworkFER1L6-AS2
Wikipedia pathwaysFER1L6-AS2
Orthology - Evolution
OrthoDB157376
GeneTree (enSembl)ENSG00000253868
Phylogenetic Trees/Animal Genes : TreeFamFER1L6-AS2
HOVERGENQ96M78
HOGENOMQ96M78
Homologs : HomoloGeneFER1L6-AS2
Homology/Alignments : Family Browser (UCSC)FER1L6-AS2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFER1L6-AS2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FER1L6-AS2
dbVarFER1L6-AS2
ClinVarFER1L6-AS2
1000_GenomesFER1L6-AS2 
Exome Variant ServerFER1L6-AS2
ExAC (Exome Aggregation Consortium)FER1L6-AS2 (select the gene name)
Genetic variants : HAPMAP157376
Genomic Variants (DGV)FER1L6-AS2 [DGVbeta]
DECIPHERFER1L6-AS2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisFER1L6-AS2 
Mutations
ICGC Data PortalFER1L6-AS2 
TCGA Data PortalFER1L6-AS2 
Broad Tumor PortalFER1L6-AS2
OASIS PortalFER1L6-AS2 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDFER1L6-AS2
BioMutasearch FER1L6-AS2
DgiDB (Drug Gene Interaction Database)FER1L6-AS2
DoCM (Curated mutations)FER1L6-AS2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FER1L6-AS2 (select a term)
intoGenFER1L6-AS2
Cancer3DFER1L6-AS2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenFER1L6-AS2
Genetic Testing Registry FER1L6-AS2
NextProtQ96M78 [Medical]
TSGene157376
GENETestsFER1L6-AS2
Target ValidationFER1L6-AS2
Huge Navigator FER1L6-AS2 [HugePedia]
snp3D : Map Gene to Disease157376
BioCentury BCIQFER1L6-AS2
ClinGenFER1L6-AS2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD157376
Chemical/Pharm GKB GenePA143485342
Clinical trialFER1L6-AS2
Miscellaneous
canSAR (ICR)FER1L6-AS2 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFER1L6-AS2
EVEXFER1L6-AS2
GoPubMedFER1L6-AS2
iHOPFER1L6-AS2
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 13:08:26 CEST 2017

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