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ENKUR (enkurin, TRPC channel interacting protein)

Identity

Alias_namesC10orf63
chromosome 10 open reading frame 63
Alias_symbol (synonym)MGC26778
enkurin
CFAP106
Other alias
HGNC (Hugo) ENKUR
LocusID (NCBI) 219670
Atlas_Id 62833
Location 10p12.1  [Link to chromosome band 10p12]
Location_base_pair Starts at 24981979 and ends at 25062279 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
ARHGAP21 (10p12.1) / ENKUR (10p12.1)PSPC1 (13q12.11) / ENKUR (10p12.1)

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)ENKUR   28388
Cards
Entrez_Gene (NCBI)ENKUR  219670  enkurin, TRPC channel interacting protein
AliasesC10orf63; CFAP106
GeneCards (Weizmann)ENKUR
Ensembl hg19 (Hinxton)ENSG00000151023 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000151023 [Gene_View]  chr10:24981979-25062279 [Contig_View]  ENKUR [Vega]
ICGC DataPortalENSG00000151023
TCGA cBioPortalENKUR
AceView (NCBI)ENKUR
Genatlas (Paris)ENKUR
WikiGenes219670
SOURCE (Princeton)ENKUR
Genetics Home Reference (NIH)ENKUR
Genomic and cartography
GoldenPath hg38 (UCSC)ENKUR  -     chr10:24981979-25062279 -  10p12.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ENKUR  -     10p12.1   [Description]    (hg19-Feb_2009)
EnsemblENKUR - 10p12.1 [CytoView hg19]  ENKUR - 10p12.1 [CytoView hg38]
Mapping of homologs : NCBIENKUR [Mapview hg19]  ENKUR [Mapview hg38]
OMIM611025   
Gene and transcription
Genbank (Entrez)AK095021 AK292495 AY454125 BC026165 BM979174
RefSeq transcript (Entrez)NM_001270383 NM_145010
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ENKUR
Cluster EST : UnigeneHs.534486 [ NCBI ]
CGAP (NCI)Hs.534486
Alternative Splicing GalleryENSG00000151023
Gene ExpressionENKUR [ NCBI-GEO ]   ENKUR [ EBI - ARRAY_EXPRESS ]   ENKUR [ SEEK ]   ENKUR [ MEM ]
Gene Expression Viewer (FireBrowse)ENKUR [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)219670
GTEX Portal (Tissue expression)ENKUR
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8TC29   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8TC29  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8TC29
Splice isoforms : SwissVarQ8TC29
PhosPhoSitePlusQ8TC29
Domaine pattern : Prosite (Expaxy)ENKURIN (PS51665)   
Domains : Interpro (EBI)Enkur    Enkurin_dom   
Domain families : Pfam (Sanger)Enkurin (PF13864)   
Domain families : Pfam (NCBI)pfam13864   
Conserved Domain (NCBI)ENKUR
DMDM Disease mutations219670
Blocks (Seattle)ENKUR
SuperfamilyQ8TC29
Human Protein AtlasENSG00000151023
Peptide AtlasQ8TC29
HPRD12583
IPIIPI00152257   IPI00975556   IPI00643610   
Protein Interaction databases
DIP (DOE-UCLA)Q8TC29
IntAct (EBI)Q8TC29
FunCoupENSG00000151023
BioGRIDENKUR
STRING (EMBL)ENKUR
ZODIACENKUR
Ontologies - Pathways
QuickGOQ8TC29
Ontology : AmiGOacrosomal vesicle  calmodulin binding  SH3 domain binding  sperm principal piece  
Ontology : EGO-EBIacrosomal vesicle  calmodulin binding  SH3 domain binding  sperm principal piece  
NDEx NetworkENKUR
Atlas of Cancer Signalling NetworkENKUR
Wikipedia pathwaysENKUR
Orthology - Evolution
OrthoDB219670
GeneTree (enSembl)ENSG00000151023
Phylogenetic Trees/Animal Genes : TreeFamENKUR
HOVERGENQ8TC29
HOGENOMQ8TC29
Homologs : HomoloGeneENKUR
Homology/Alignments : Family Browser (UCSC)ENKUR
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerENKUR [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ENKUR
dbVarENKUR
ClinVarENKUR
1000_GenomesENKUR 
Exome Variant ServerENKUR
ExAC (Exome Aggregation Consortium)ENKUR (select the gene name)
Genetic variants : HAPMAP219670
Genomic Variants (DGV)ENKUR [DGVbeta]
DECIPHERENKUR [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisENKUR 
Mutations
ICGC Data PortalENKUR 
TCGA Data PortalENKUR 
Broad Tumor PortalENKUR
OASIS PortalENKUR [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICENKUR  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDENKUR
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch ENKUR
DgiDB (Drug Gene Interaction Database)ENKUR
DoCM (Curated mutations)ENKUR (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ENKUR (select a term)
intoGenENKUR
Cancer3DENKUR(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM611025   
Orphanet
MedgenENKUR
Genetic Testing Registry ENKUR
NextProtQ8TC29 [Medical]
TSGene219670
GENETestsENKUR
Target ValidationENKUR
Huge Navigator ENKUR [HugePedia]
snp3D : Map Gene to Disease219670
BioCentury BCIQENKUR
ClinGenENKUR
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD219670
Chemical/Pharm GKB GenePA165548526
Clinical trialENKUR
Miscellaneous
canSAR (ICR)ENKUR (select the gene name)
Probes
Litterature
PubMed6 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineENKUR
EVEXENKUR
GoPubMedENKUR
iHOPENKUR
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 13:07:06 CEST 2017

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