Atlas of Genetics and Cytogenetics in Oncology and Haematology


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C14orf28 (chromosome 14 open reading frame 28)

Identity

Alias_symbol (synonym)DRIP-1
Other aliasDRIP1
c14_5270
HGNC (Hugo) C14orf28
LocusID (NCBI) 122525
Atlas_Id 60939
Location 14q21.2  [Link to chromosome band 14q21]
Location_base_pair Starts at 44897304 and ends at 44907257 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)C14orf28   19834
Cards
Entrez_Gene (NCBI)C14orf28  122525  chromosome 14 open reading frame 28
AliasesDRIP-1; DRIP1; c14_5270
GeneCards (Weizmann)C14orf28
Ensembl hg19 (Hinxton)ENSG00000179476 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000179476 [Gene_View]  chr14:44897304-44907257 [Contig_View]  C14orf28 [Vega]
ICGC DataPortalENSG00000179476
TCGA cBioPortalC14orf28
AceView (NCBI)C14orf28
Genatlas (Paris)C14orf28
WikiGenes122525
SOURCE (Princeton)C14orf28
Genetics Home Reference (NIH)C14orf28
Genomic and cartography
GoldenPath hg38 (UCSC)C14orf28  -     chr14:44897304-44907257 +  14q21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)C14orf28  -     14q21.2   [Description]    (hg19-Feb_2009)
EnsemblC14orf28 - 14q21.2 [CytoView hg19]  C14orf28 - 14q21.2 [CytoView hg38]
Mapping of homologs : NCBIC14orf28 [Mapview hg19]  C14orf28 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF250395 AK126985 BC030258 BC105030 BC105032
RefSeq transcript (Entrez)NM_001017923
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)C14orf28
Cluster EST : UnigeneHs.82098 [ NCBI ]
CGAP (NCI)Hs.82098
Alternative Splicing GalleryENSG00000179476
Gene ExpressionC14orf28 [ NCBI-GEO ]   C14orf28 [ EBI - ARRAY_EXPRESS ]   C14orf28 [ SEEK ]   C14orf28 [ MEM ]
Gene Expression Viewer (FireBrowse)C14orf28 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)122525
GTEX Portal (Tissue expression)C14orf28
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ4W4Y0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ4W4Y0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ4W4Y0
Splice isoforms : SwissVarQ4W4Y0
PhosPhoSitePlusQ4W4Y0
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)C14orf28
DMDM Disease mutations122525
Blocks (Seattle)C14orf28
SuperfamilyQ4W4Y0
Human Protein AtlasENSG00000179476
Peptide AtlasQ4W4Y0
HPRD18544
IPIIPI00043479   IPI01024853   
Protein Interaction databases
DIP (DOE-UCLA)Q4W4Y0
IntAct (EBI)Q4W4Y0
FunCoupENSG00000179476
BioGRIDC14orf28
STRING (EMBL)C14orf28
ZODIACC14orf28
Ontologies - Pathways
QuickGOQ4W4Y0
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkC14orf28
Atlas of Cancer Signalling NetworkC14orf28
Wikipedia pathwaysC14orf28
Orthology - Evolution
OrthoDB122525
GeneTree (enSembl)ENSG00000179476
Phylogenetic Trees/Animal Genes : TreeFamC14orf28
HOVERGENQ4W4Y0
HOGENOMQ4W4Y0
Homologs : HomoloGeneC14orf28
Homology/Alignments : Family Browser (UCSC)C14orf28
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerC14orf28 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)C14orf28
dbVarC14orf28
ClinVarC14orf28
1000_GenomesC14orf28 
Exome Variant ServerC14orf28
ExAC (Exome Aggregation Consortium)C14orf28 (select the gene name)
Genetic variants : HAPMAP122525
Genomic Variants (DGV)C14orf28 [DGVbeta]
DECIPHERC14orf28 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisC14orf28 
Mutations
ICGC Data PortalC14orf28 
TCGA Data PortalC14orf28 
Broad Tumor PortalC14orf28
OASIS PortalC14orf28 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICC14orf28  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDC14orf28
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch C14orf28
DgiDB (Drug Gene Interaction Database)C14orf28
DoCM (Curated mutations)C14orf28 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)C14orf28 (select a term)
intoGenC14orf28
Cancer3DC14orf28(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenC14orf28
Genetic Testing Registry C14orf28
NextProtQ4W4Y0 [Medical]
TSGene122525
GENETestsC14orf28
Target ValidationC14orf28
Huge Navigator C14orf28 [HugePedia]
snp3D : Map Gene to Disease122525
BioCentury BCIQC14orf28
ClinGenC14orf28
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD122525
Chemical/Pharm GKB GenePA134923136
Clinical trialC14orf28
Miscellaneous
canSAR (ICR)C14orf28 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineC14orf28
EVEXC14orf28
GoPubMedC14orf28
iHOPC14orf28
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 13:02:46 CEST 2017

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