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ARL14 (ADP ribosylation factor like GTPase 14)

Identity

Alias_namesARF7
ADP-ribosylation factor 7
ADP-ribosylation factor like GTPase 14
Alias_symbol (synonym)FLJ22595
Other alias
HGNC (Hugo) ARL14
LocusID (NCBI) 80117
Atlas_Id 60491
Location 3q25.33  [Link to chromosome band 3q25]
Location_base_pair Starts at 160677160 and ends at 160678447 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)ARL14   22974
Cards
Entrez_Gene (NCBI)ARL14  80117  ADP ribosylation factor like GTPase 14
AliasesARF7
GeneCards (Weizmann)ARL14
Ensembl hg19 (Hinxton)ENSG00000179674 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000179674 [Gene_View]  chr3:160677160-160678447 [Contig_View]  ARL14 [Vega]
ICGC DataPortalENSG00000179674
TCGA cBioPortalARL14
AceView (NCBI)ARL14
Genatlas (Paris)ARL14
WikiGenes80117
SOURCE (Princeton)ARL14
Genetics Home Reference (NIH)ARL14
Genomic and cartography
GoldenPath hg38 (UCSC)ARL14  -     chr3:160677160-160678447 +  3q25.33   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ARL14  -     3q25.33   [Description]    (hg19-Feb_2009)
EnsemblARL14 - 3q25.33 [CytoView hg19]  ARL14 - 3q25.33 [CytoView hg38]
Mapping of homologs : NCBIARL14 [Mapview hg19]  ARL14 [Mapview hg38]
OMIM614439   
Gene and transcription
Genbank (Entrez)AK026248 BC034354 BM760777 JF432865
RefSeq transcript (Entrez)NM_025047
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ARL14
Cluster EST : UnigeneHs.287702 [ NCBI ]
CGAP (NCI)Hs.287702
Alternative Splicing GalleryENSG00000179674
Gene ExpressionARL14 [ NCBI-GEO ]   ARL14 [ EBI - ARRAY_EXPRESS ]   ARL14 [ SEEK ]   ARL14 [ MEM ]
Gene Expression Viewer (FireBrowse)ARL14 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)80117
GTEX Portal (Tissue expression)ARL14
Human Protein AtlasENSG00000179674-ARL14 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8N4G2   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8N4G2  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8N4G2
Splice isoforms : SwissVarQ8N4G2
PhosPhoSitePlusQ8N4G2
Domaine pattern : Prosite (Expaxy)ARF (PS51417)   
Domains : Interpro (EBI)P-loop_NTPase    Small_GTP-bd_dom    Small_GTPase_ARF    Small_GTPase_ARF/SAR   
Domain families : Pfam (Sanger)Arf (PF00025)   
Domain families : Pfam (NCBI)pfam00025   
Conserved Domain (NCBI)ARL14
DMDM Disease mutations80117
Blocks (Seattle)ARL14
SuperfamilyQ8N4G2
Human Protein Atlas [tissue]ENSG00000179674-ARL14 [tissue]
Peptide AtlasQ8N4G2
HPRD07998
IPIIPI00296664   
Protein Interaction databases
DIP (DOE-UCLA)Q8N4G2
IntAct (EBI)Q8N4G2
FunCoupENSG00000179674
BioGRIDARL14
STRING (EMBL)ARL14
ZODIACARL14
Ontologies - Pathways
QuickGOQ8N4G2
Ontology : AmiGOprotein binding  GTP binding  small GTPase mediated signal transduction  cytoplasmic vesicle  
Ontology : EGO-EBIprotein binding  GTP binding  small GTPase mediated signal transduction  cytoplasmic vesicle  
NDEx NetworkARL14
Atlas of Cancer Signalling NetworkARL14
Wikipedia pathwaysARL14
Orthology - Evolution
OrthoDB80117
GeneTree (enSembl)ENSG00000179674
Phylogenetic Trees/Animal Genes : TreeFamARL14
HOVERGENQ8N4G2
HOGENOMQ8N4G2
Homologs : HomoloGeneARL14
Homology/Alignments : Family Browser (UCSC)ARL14
Gene fusions - Rearrangements
Fusion: Tumor Portal ARL14
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerARL14 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ARL14
dbVarARL14
ClinVarARL14
1000_GenomesARL14 
Exome Variant ServerARL14
ExAC (Exome Aggregation Consortium)ENSG00000179674
GNOMAD BrowserENSG00000179674
Genetic variants : HAPMAP80117
Genomic Variants (DGV)ARL14 [DGVbeta]
DECIPHERARL14 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisARL14 
Mutations
ICGC Data PortalARL14 
TCGA Data PortalARL14 
Broad Tumor PortalARL14
OASIS PortalARL14 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICARL14  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDARL14
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch ARL14
DgiDB (Drug Gene Interaction Database)ARL14
DoCM (Curated mutations)ARL14 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ARL14 (select a term)
intoGenARL14
Cancer3DARL14(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM614439   
Orphanet
MedgenARL14
Genetic Testing Registry ARL14
NextProtQ8N4G2 [Medical]
TSGene80117
GENETestsARL14
Target ValidationARL14
Huge Navigator ARL14 [HugePedia]
snp3D : Map Gene to Disease80117
BioCentury BCIQARL14
ClinGenARL14
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD80117
Chemical/Pharm GKB GenePA134971739
Clinical trialARL14
Miscellaneous
canSAR (ICR)ARL14 (select the gene name)
Probes
Litterature
PubMed10 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineARL14
EVEXARL14
GoPubMedARL14
iHOPARL14
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Thu Nov 9 11:38:14 CET 2017

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