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ADAL (adenosine deaminase like)

Identity

Other alias-
HGNC (Hugo) ADAL
LocusID (NCBI) 161823
Atlas_Id 53454
Location 15q15.3  [Link to chromosome band 15q15]
Location_base_pair Starts at 43330356 and ends at 43349417 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)ADAL   31853
Cards
Entrez_Gene (NCBI)ADAL  161823  adenosine deaminase like
Aliases
GeneCards (Weizmann)ADAL
Ensembl hg19 (Hinxton)ENSG00000168803 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000168803 [Gene_View]  chr15:43330356-43349417 [Contig_View]  ADAL [Vega]
ICGC DataPortalENSG00000168803
TCGA cBioPortalADAL
AceView (NCBI)ADAL
Genatlas (Paris)ADAL
WikiGenes161823
SOURCE (Princeton)ADAL
Genetics Home Reference (NIH)ADAL
Genomic and cartography
GoldenPath hg38 (UCSC)ADAL  -     chr15:43330356-43349417 +  15q15.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ADAL  -     15q15.3   [Description]    (hg19-Feb_2009)
EnsemblADAL - 15q15.3 [CytoView hg19]  ADAL - 15q15.3 [CytoView hg38]
Mapping of homologs : NCBIADAL [Mapview hg19]  ADAL [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK126583 AK298870 BC075857 BQ015642 BX647599
RefSeq transcript (Entrez)NM_001012969 NM_001159280 NM_001324364 NM_001324365 NM_001324366 NM_001324367 NM_001324368
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ADAL
Cluster EST : UnigeneHs.533913 [ NCBI ]
CGAP (NCI)Hs.533913
Alternative Splicing GalleryENSG00000168803
Gene ExpressionADAL [ NCBI-GEO ]   ADAL [ EBI - ARRAY_EXPRESS ]   ADAL [ SEEK ]   ADAL [ MEM ]
Gene Expression Viewer (FireBrowse)ADAL [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)161823
GTEX Portal (Tissue expression)ADAL
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ6DHV7   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ6DHV7  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ6DHV7
Splice isoforms : SwissVarQ6DHV7
PhosPhoSitePlusQ6DHV7
Domains : Interpro (EBI)A/AMP_deaminase_dom    Metal_Hydrolase   
Domain families : Pfam (Sanger)A_deaminase (PF00962)   
Domain families : Pfam (NCBI)pfam00962   
Conserved Domain (NCBI)ADAL
DMDM Disease mutations161823
Blocks (Seattle)ADAL
SuperfamilyQ6DHV7
Human Protein AtlasENSG00000168803
Peptide AtlasQ6DHV7
HPRD11779
IPIIPI00783550   IPI00238031   IPI00909141   
Protein Interaction databases
DIP (DOE-UCLA)Q6DHV7
IntAct (EBI)Q6DHV7
FunCoupENSG00000168803
BioGRIDADAL
STRING (EMBL)ADAL
ZODIACADAL
Ontologies - Pathways
QuickGOQ6DHV7
Ontology : AmiGOadenosine deaminase activity  cytosol  nucleotide metabolic process  drug metabolic process  purine-containing compound salvage  metal ion binding  
Ontology : EGO-EBIadenosine deaminase activity  cytosol  nucleotide metabolic process  drug metabolic process  purine-containing compound salvage  metal ion binding  
NDEx NetworkADAL
Atlas of Cancer Signalling NetworkADAL
Wikipedia pathwaysADAL
Orthology - Evolution
OrthoDB161823
GeneTree (enSembl)ENSG00000168803
Phylogenetic Trees/Animal Genes : TreeFamADAL
HOVERGENQ6DHV7
HOGENOMQ6DHV7
Homologs : HomoloGeneADAL
Homology/Alignments : Family Browser (UCSC)ADAL
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerADAL [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ADAL
dbVarADAL
ClinVarADAL
1000_GenomesADAL 
Exome Variant ServerADAL
ExAC (Exome Aggregation Consortium)ADAL (select the gene name)
Genetic variants : HAPMAP161823
Genomic Variants (DGV)ADAL [DGVbeta]
DECIPHERADAL [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisADAL 
Mutations
ICGC Data PortalADAL 
TCGA Data PortalADAL 
Broad Tumor PortalADAL
OASIS PortalADAL [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICADAL  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDADAL
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 ADAL
DgiDB (Drug Gene Interaction Database)ADAL
DoCM (Curated mutations)ADAL (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ADAL (select a term)
intoGenADAL
Cancer3DADAL(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenADAL
Genetic Testing Registry ADAL
NextProtQ6DHV7 [Medical]
TSGene161823
GENETestsADAL
Huge Navigator ADAL [HugePedia]
snp3D : Map Gene to Disease161823
BioCentury BCIQADAL
ClinGenADAL
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD161823
Chemical/Pharm GKB GenePA142672643
Clinical trialADAL
Miscellaneous
canSAR (ICR)ADAL (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineADAL
EVEXADAL
GoPubMedADAL
iHOPADAL
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Fri May 19 12:04:57 CEST 2017

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