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ARL14EPL (ADP-ribosylation factor-like 14 effector protein-like)

Identity

Alias_namesADP-ribosylation factor like GTPase 14 effector protein like
Other alias-
HGNC (Hugo) ARL14EPL
LocusID (NCBI) 644100
Atlas_Id 60493
Location 5q23.1  [Link to chromosome band 5q23]
Location_base_pair Starts at 115387163 and ends at 115394827 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)ARL14EPL   44201
Cards
Entrez_Gene (NCBI)ARL14EPL  644100  ADP-ribosylation factor-like 14 effector protein-like
Aliases
GeneCards (Weizmann)ARL14EPL
Ensembl hg19 (Hinxton) [Gene_View]  chr5:115387163-115394827 [Contig_View]  ARL14EPL [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr5:115387163-115394827 [Contig_View]  ARL14EPL [Vega]
TCGA cBioPortalARL14EPL
AceView (NCBI)ARL14EPL
Genatlas (Paris)ARL14EPL
WikiGenes644100
SOURCE (Princeton)ARL14EPL
Genetics Home Reference (NIH)ARL14EPL
Genomic and cartography
GoldenPath hg19 (UCSC)ARL14EPL  -     chr5:115387163-115394827 +  5q23.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)ARL14EPL  -     5q23.1   [Description]    (hg38-Dec_2013)
EnsemblARL14EPL - 5q23.1 [CytoView hg19]  ARL14EPL - 5q23.1 [CytoView hg38]
Mapping of homologs : NCBIARL14EPL [Mapview hg19]  ARL14EPL [Mapview hg38]
Gene and transcription
Genbank (Entrez)BF993117 DN930361 DN930362 DT932734
RefSeq transcript (Entrez)NM_001195581
RefSeq genomic (Entrez)NC_000005 NC_018916 NT_034772 NW_004929323
Consensus coding sequences : CCDS (NCBI)ARL14EPL
Cluster EST : UnigeneHs.730043 [ NCBI ]
CGAP (NCI)Hs.730043
Gene ExpressionARL14EPL [ NCBI-GEO ]   ARL14EPL [ EBI - ARRAY_EXPRESS ]   ARL14EPL [ SEEK ]   ARL14EPL [ MEM ]
Gene Expression Viewer (FireBrowse)ARL14EPL [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)644100
GTEX Portal (Tissue expression)ARL14EPL
Protein : pattern, domain, 3D structure
UniProt/SwissProtP0DKL9   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP0DKL9  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP0DKL9
Splice isoforms : SwissVarP0DKL9
PhosPhoSitePlusP0DKL9
Domains : Interpro (EBI)ARF7EP_C   
Domain families : Pfam (Sanger)ARF7EP_C (PF14949)   
Domain families : Pfam (NCBI)pfam14949   
Conserved Domain (NCBI)ARL14EPL
DMDM Disease mutations644100
Blocks (Seattle)ARL14EPL
SuperfamilyP0DKL9
Peptide AtlasP0DKL9
IPIIPI00977075   
Protein Interaction databases
DIP (DOE-UCLA)P0DKL9
IntAct (EBI)P0DKL9
BioGRIDARL14EPL
STRING (EMBL)ARL14EPL
ZODIACARL14EPL
Ontologies - Pathways
QuickGOP0DKL9
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkARL14EPL
Atlas of Cancer Signalling NetworkARL14EPL
Wikipedia pathwaysARL14EPL
Orthology - Evolution
OrthoDB644100
Phylogenetic Trees/Animal Genes : TreeFamARL14EPL
HOVERGENP0DKL9
HOGENOMP0DKL9
Homologs : HomoloGeneARL14EPL
Homology/Alignments : Family Browser (UCSC)ARL14EPL
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerARL14EPL [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ARL14EPL
dbVarARL14EPL
ClinVarARL14EPL
1000_GenomesARL14EPL 
Exome Variant ServerARL14EPL
ExAC (Exome Aggregation Consortium)ARL14EPL (select the gene name)
Genetic variants : HAPMAP644100
Genomic Variants (DGV)ARL14EPL [DGVbeta]
DECIPHER (Syndromes)5:115387163-115394827  
CONAN: Copy Number AnalysisARL14EPL 
Mutations
ICGC Data PortalARL14EPL 
TCGA Data PortalARL14EPL 
Broad Tumor PortalARL14EPL
OASIS PortalARL14EPL [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDARL14EPL
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 ARL14EPL
DgiDB (Drug Gene Interaction Database)ARL14EPL
DoCM (Curated mutations)ARL14EPL (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ARL14EPL (select a term)
intoGenARL14EPL
Cancer3DARL14EPL(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenARL14EPL
Genetic Testing Registry ARL14EPL
NextProtP0DKL9 [Medical]
TSGene644100
GENETestsARL14EPL
Huge Navigator ARL14EPL [HugePedia]
snp3D : Map Gene to Disease644100
BioCentury BCIQARL14EPL
ClinGenARL14EPL
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD644100
Clinical trialARL14EPL
Miscellaneous
canSAR (ICR)ARL14EPL (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineARL14EPL
EVEXARL14EPL
GoPubMedARL14EPL
iHOPARL14EPL
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 11:54:57 CET 2017

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