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ANKRD63 (ankyrin repeat domain 63)

Identity

Other alias-
HGNC (Hugo) ANKRD63
LocusID (NCBI) 100131244
Atlas_Id 60365
Location 15q15.1  [Link to chromosome band 15q15]
Location_base_pair Starts at 40278372 and ends at 40282586 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)ANKRD63   40027
Cards
Entrez_Gene (NCBI)ANKRD63  100131244  ankyrin repeat domain 63
Aliases
GeneCards (Weizmann)ANKRD63
Ensembl hg19 (Hinxton)ENSG00000230778 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000230778 [Gene_View]  chr15:40278372-40282586 [Contig_View]  ANKRD63 [Vega]
ICGC DataPortalENSG00000230778
TCGA cBioPortalANKRD63
AceView (NCBI)ANKRD63
Genatlas (Paris)ANKRD63
WikiGenes100131244
SOURCE (Princeton)ANKRD63
Genetics Home Reference (NIH)ANKRD63
Genomic and cartography
GoldenPath hg38 (UCSC)ANKRD63  -     chr15:40278372-40282586 -  15q15.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ANKRD63  -     15q15.1   [Description]    (hg19-Feb_2009)
EnsemblANKRD63 - 15q15.1 [CytoView hg19]  ANKRD63 - 15q15.1 [CytoView hg38]
Mapping of homologs : NCBIANKRD63 [Mapview hg19]  ANKRD63 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BF940541 HY318958
RefSeq transcript (Entrez)NM_001190479
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ANKRD63
Cluster EST : UnigeneHs.711376 [ NCBI ]
CGAP (NCI)Hs.711376
Alternative Splicing GalleryENSG00000230778
Gene ExpressionANKRD63 [ NCBI-GEO ]   ANKRD63 [ EBI - ARRAY_EXPRESS ]   ANKRD63 [ SEEK ]   ANKRD63 [ MEM ]
Gene Expression Viewer (FireBrowse)ANKRD63 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100131244
GTEX Portal (Tissue expression)ANKRD63
Protein : pattern, domain, 3D structure
UniProt/SwissProtC9JTQ0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtC9JTQ0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProC9JTQ0
Splice isoforms : SwissVarC9JTQ0
PhosPhoSitePlusC9JTQ0
Domaine pattern : Prosite (Expaxy)ANK_REP_REGION (PS50297)    ANK_REPEAT (PS50088)   
Domains : Interpro (EBI)Ankyrin_rpt    Ankyrin_rpt-contain_dom   
Domain families : Pfam (Sanger)Ank_2 (PF12796)   
Domain families : Pfam (NCBI)pfam12796   
Domain families : Smart (EMBL)ANK (SM00248)  
Conserved Domain (NCBI)ANKRD63
DMDM Disease mutations100131244
Blocks (Seattle)ANKRD63
SuperfamilyC9JTQ0
Human Protein AtlasENSG00000230778
Peptide AtlasC9JTQ0
IPIIPI00888968   
Protein Interaction databases
DIP (DOE-UCLA)C9JTQ0
IntAct (EBI)C9JTQ0
FunCoupENSG00000230778
BioGRIDANKRD63
STRING (EMBL)ANKRD63
ZODIACANKRD63
Ontologies - Pathways
QuickGOC9JTQ0
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkANKRD63
Atlas of Cancer Signalling NetworkANKRD63
Wikipedia pathwaysANKRD63
Orthology - Evolution
OrthoDB100131244
GeneTree (enSembl)ENSG00000230778
Phylogenetic Trees/Animal Genes : TreeFamANKRD63
HOVERGENC9JTQ0
HOGENOMC9JTQ0
Homologs : HomoloGeneANKRD63
Homology/Alignments : Family Browser (UCSC)ANKRD63
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerANKRD63 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ANKRD63
dbVarANKRD63
ClinVarANKRD63
1000_GenomesANKRD63 
Exome Variant ServerANKRD63
ExAC (Exome Aggregation Consortium)ANKRD63 (select the gene name)
Genetic variants : HAPMAP100131244
Genomic Variants (DGV)ANKRD63 [DGVbeta]
DECIPHERANKRD63 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisANKRD63 
Mutations
ICGC Data PortalANKRD63 
TCGA Data PortalANKRD63 
Broad Tumor PortalANKRD63
OASIS PortalANKRD63 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICANKRD63  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDANKRD63
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 ANKRD63
DgiDB (Drug Gene Interaction Database)ANKRD63
DoCM (Curated mutations)ANKRD63 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ANKRD63 (select a term)
intoGenANKRD63
Cancer3DANKRD63(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenANKRD63
Genetic Testing Registry ANKRD63
NextProtC9JTQ0 [Medical]
TSGene100131244
GENETestsANKRD63
Target ValidationANKRD63
Huge Navigator ANKRD63 [HugePedia]
snp3D : Map Gene to Disease100131244
BioCentury BCIQANKRD63
ClinGenANKRD63
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100131244
Chemical/Pharm GKB GenePA166049049
Clinical trialANKRD63
Miscellaneous
canSAR (ICR)ANKRD63 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineANKRD63
EVEXANKRD63
GoPubMedANKRD63
iHOPANKRD63
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 13:01:27 CEST 2017

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