Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

C14orf144 (chromosome 14 open reading frame 144)

Identity

Other alias-
HGNC (Hugo) C14orf144
LocusID (NCBI) 145195
Atlas_Id 60931
Location 14q32.33  [Link to chromosome band 14q32]
Location_base_pair Starts at 104710546 and ends at 104712484 bp from pter ( according to hg19-Feb_2009)
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


External links

Nomenclature
HGNC (Hugo)C14orf144   20358
Cards
Entrez_Gene (NCBI)C14orf144  145195  chromosome 14 open reading frame 144
Aliases
GeneCards (Weizmann)C14orf144
Ensembl hg19 (Hinxton) [Gene_View]  chr14:104710546-104712484 [Contig_View]  C14orf144 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr14:104710546-104712484 [Contig_View]  C14orf144 [Vega]
TCGA cBioPortalC14orf144
AceView (NCBI)C14orf144
Genatlas (Paris)C14orf144
WikiGenes145195
SOURCE (Princeton)C14orf144
Genetics Home Reference (NIH)C14orf144
Genomic and cartography
GoldenPath hg19 (UCSC)C14orf144  -     chr14:104710546-104712484 +  14q32.33   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)C14orf144  -     14q32.33   [Description]    (hg38-Dec_2013)
EnsemblC14orf144 - 14q32.33 [CytoView hg19]  C14orf144 - 14q32.33 [CytoView hg38]
Mapping of homologs : NCBIC14orf144 [Mapview hg19]  C14orf144 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC007749
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000014 NT_026437
Consensus coding sequences : CCDS (NCBI)C14orf144
Cluster EST : UnigeneHs.679805 [ NCBI ]
CGAP (NCI)Hs.679805
Gene ExpressionC14orf144 [ NCBI-GEO ]   C14orf144 [ EBI - ARRAY_EXPRESS ]   C14orf144 [ SEEK ]   C14orf144 [ MEM ]
Gene Expression Viewer (FireBrowse)C14orf144 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)145195
GTEX Portal (Tissue expression)C14orf144
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96I85   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96I85  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96I85
Splice isoforms : SwissVarQ96I85
PhosPhoSitePlusQ96I85
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)C14orf144
DMDM Disease mutations145195
Blocks (Seattle)C14orf144
SuperfamilyQ96I85
Peptide AtlasQ96I85
IPIIPI00101680   IPI00917976   
Protein Interaction databases
DIP (DOE-UCLA)Q96I85
IntAct (EBI)Q96I85
BioGRIDC14orf144
STRING (EMBL)C14orf144
ZODIACC14orf144
Ontologies - Pathways
QuickGOQ96I85
Ontology : AmiGOextracellular region  
Ontology : EGO-EBIextracellular region  
NDEx NetworkC14orf144
Atlas of Cancer Signalling NetworkC14orf144
Wikipedia pathwaysC14orf144
Orthology - Evolution
OrthoDB145195
Phylogenetic Trees/Animal Genes : TreeFamC14orf144
HOVERGENQ96I85
HOGENOMQ96I85
Homologs : HomoloGeneC14orf144
Homology/Alignments : Family Browser (UCSC)C14orf144
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerC14orf144 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)C14orf144
dbVarC14orf144
ClinVarC14orf144
1000_GenomesC14orf144 
Exome Variant ServerC14orf144
ExAC (Exome Aggregation Consortium)C14orf144 (select the gene name)
Genetic variants : HAPMAP145195
Genomic Variants (DGV)C14orf144 [DGVbeta]
DECIPHER (Syndromes)14:104710546-104712484  
CONAN: Copy Number AnalysisC14orf144 
Mutations
ICGC Data PortalC14orf144 
TCGA Data PortalC14orf144 
Broad Tumor PortalC14orf144
OASIS PortalC14orf144 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICC14orf144  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDC14orf144
BioMutasearch C14orf144
DgiDB (Drug Gene Interaction Database)C14orf144
DoCM (Curated mutations)C14orf144 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)C14orf144 (select a term)
intoGenC14orf144
Cancer3DC14orf144(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenC14orf144
Genetic Testing Registry C14orf144
NextProtQ96I85 [Medical]
TSGene145195
GENETestsC14orf144
Huge Navigator C14orf144 [HugePedia]
snp3D : Map Gene to Disease145195
BioCentury BCIQC14orf144
ClinGenC14orf144
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD145195
Chemical/Pharm GKB GenePA134909645
Clinical trialC14orf144
Miscellaneous
canSAR (ICR)C14orf144 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineC14orf144
EVEXC14orf144
GoPubMedC14orf144
iHOPC14orf144
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Mar 14 11:56:29 CET 2017

Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.