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ENKUR (enkurin, TRPC channel interacting protein)

Identity

Alias (NCBI)C10orf63
CFAP106
HGNC (Hugo) ENKUR
HGNC Alias symbMGC26778
enkurin
CFAP106
HGNC Previous nameC10orf63
HGNC Previous namechromosome 10 open reading frame 63
LocusID (NCBI) 219670
Atlas_Id 57978
Location 10p12.1  [Link to chromosome band 10p12]
Location_base_pair Starts at 24981986 and ends at 25016158 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)
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    enkurin, TRPC channel interacting protein
AliasesC10orf63; CFAP106
GeneCards (Weizmann)ENKUR
Ensembl hg19 (Hinxton)ENSG00000151023 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000151023 [Gene_View]  ENSG00000151023 [Sequence]  chr10:24981986-25016158 [Contig_View]  ENKUR [Vega]
ICGC DataPortalENSG00000151023
TCGA cBioPortalENKUR
AceView (NCBI)ENKUR
Genatlas (Paris)ENKUR
SOURCE (Princeton)ENKUR
Genetics Home Reference (NIH)ENKUR
Genomic and cartography
GoldenPath hg38 (UCSC)ENKUR  -     chr10:24981986-25016158 -  10p12.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ENKUR  -     10p12.1   [Description]    (hg19-Feb_2009)
GoldenPathENKUR - 10p12.1 [CytoView hg19]  ENKUR - 10p12.1 [CytoView hg38]
ImmunoBaseENSG00000151023
Genome Data Viewer NCBIENKUR [Mapview hg19]  
OMIM611025   
Gene and transcription
Genbank (Entrez)AK095021 AK292495 AY454125 BC026165 BM979174
RefSeq transcript (Entrez)NM_001270383 NM_145010
Consensus coding sequences : CCDS (NCBI)ENKUR
Gene ExpressionENKUR [ NCBI-GEO ]   ENKUR [ EBI - ARRAY_EXPRESS ]   ENKUR [ SEEK ]   ENKUR [ MEM ]
Gene Expression Viewer (FireBrowse)ENKUR [ Firebrowse - Broad ]
GenevisibleExpression of ENKUR in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)219670
GTEX Portal (Tissue expression)ENKUR
Human Protein AtlasENSG00000151023-ENKUR [pathology]   [cell]   [tissue]
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
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
SuperfamilyQ8TC29
AlphaFold pdb e-kbQ8TC29   
Human Protein Atlas [tissue]ENSG00000151023-ENKUR [tissue]
Protein Interaction databases
DIP (DOE-UCLA)Q8TC29
IntAct (EBI)Q8TC29
BioGRIDENKUR
STRING (EMBL)ENKUR
ZODIACENKUR
Ontologies - Pathways
QuickGOQ8TC29
Ontology : AmiGOacrosomal vesicle  protein binding  calmodulin binding  SH3 domain binding  flagellated sperm motility  establishment of left/right asymmetry  sperm principal piece  9+0 motile cilium  9+2 motile cilium  
Ontology : EGO-EBIacrosomal vesicle  protein binding  calmodulin binding  SH3 domain binding  flagellated sperm motility  establishment of left/right asymmetry  sperm principal piece  9+0 motile cilium  9+2 motile cilium  
NDEx NetworkENKUR
Atlas of Cancer Signalling NetworkENKUR
Wikipedia pathwaysENKUR
Orthology - Evolution
OrthoDB219670
GeneTree (enSembl)ENSG00000151023
Phylogenetic Trees/Animal Genes : TreeFamENKUR
Homologs : HomoloGeneENKUR
Homology/Alignments : Family Browser (UCSC)ENKUR
Gene fusions - Rearrangements
Fusion : QuiverENKUR
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerENKUR [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ENKUR
dbVarENKUR
ClinVarENKUR
MonarchENKUR
1000_GenomesENKUR 
Exome Variant ServerENKUR
GNOMAD BrowserENSG00000151023
Varsome BrowserENKUR
ACMGENKUR variants
VarityQ8TC29
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]  
Somatic Mutations in Cancer : COSMIC3DENKUR
Mutations and Diseases : HGMDENKUR
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaENKUR
DgiDB (Drug Gene Interaction Database)ENKUR
DoCM (Curated mutations)ENKUR
CIViC (Clinical Interpretations of Variants in Cancer)ENKUR
Cancer3DENKUR
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM611025   
Orphanet
DisGeNETENKUR
MedgenENKUR
Genetic Testing Registry ENKUR
NextProtQ8TC29 [Medical]
GENETestsENKUR
Target ValidationENKUR
Huge Navigator ENKUR [HugePedia]
ClinGenENKUR
Clinical trials, drugs, therapy
MyCancerGenomeENKUR
Protein Interactions : CTDENKUR
Pharm GKB GenePA165548526
PharosQ8TC29
Clinical trialENKUR
Miscellaneous
canSAR (ICR)ENKUR
HarmonizomeENKUR
DataMed IndexENKUR
Probes
Litterature
PubMed16 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXENKUR
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 15:08:11 CEST 2021
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