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INTS14 (integrator complex subunit 14)

Identity

Alias_namesC15orf44
VWA9
chromosome 15 open reading frame 44
von Willebrand factor A domain containing 9
Alias_symbol (synonym)DKFZP564O1664
Other alias
HGNC (Hugo) INTS14
LocusID (NCBI) 81556
Atlas_Id 79612
Location 15q22.31  [Link to chromosome band 15q22]
Location_base_pair Starts at 65578758 and ends at 65611289 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)INTS14   25372
Cards
Entrez_Gene (NCBI)INTS14  81556  integrator complex subunit 14
AliasesC15orf44; VWA9
GeneCards (Weizmann)INTS14
Ensembl hg19 (Hinxton)ENSG00000138614 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000138614 [Gene_View]  chr15:65578758-65611289 [Contig_View]  INTS14 [Vega]
ICGC DataPortalENSG00000138614
TCGA cBioPortalINTS14
AceView (NCBI)INTS14
Genatlas (Paris)INTS14
WikiGenes81556
SOURCE (Princeton)INTS14
Genetics Home Reference (NIH)INTS14
Genomic and cartography
GoldenPath hg38 (UCSC)INTS14  -     chr15:65578758-65611289 -  15q22.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)INTS14  -     15q22.31   [Description]    (hg19-Feb_2009)
EnsemblINTS14 - 15q22.31 [CytoView hg19]  INTS14 - 15q22.31 [CytoView hg38]
Mapping of homologs : NCBIINTS14 [Mapview hg19]  INTS14 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA745705 AK027475 AK293207 AK296134 AK301033
RefSeq transcript (Entrez)NM_001136043 NM_001207058 NM_001207059 NM_030800
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)INTS14
Cluster EST : UnigeneHs.6686 [ NCBI ]
CGAP (NCI)Hs.6686
Alternative Splicing GalleryENSG00000138614
Gene ExpressionINTS14 [ NCBI-GEO ]   INTS14 [ EBI - ARRAY_EXPRESS ]   INTS14 [ SEEK ]   INTS14 [ MEM ]
Gene Expression Viewer (FireBrowse)INTS14 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)81556
GTEX Portal (Tissue expression)INTS14
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96SY0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96SY0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96SY0
Splice isoforms : SwissVarQ96SY0
PhosPhoSitePlusQ96SY0
Domains : Interpro (EBI)VWF_A   
Domain families : Pfam (Sanger)VWA_2 (PF13519)   
Domain families : Pfam (NCBI)pfam13519   
Conserved Domain (NCBI)INTS14
DMDM Disease mutations81556
Blocks (Seattle)INTS14
SuperfamilyQ96SY0
Human Protein AtlasENSG00000138614
Peptide AtlasQ96SY0
IPIIPI00854811   IPI01018820   IPI00306017   IPI00914573   IPI00910192   IPI00984960   
Protein Interaction databases
DIP (DOE-UCLA)Q96SY0
IntAct (EBI)Q96SY0
FunCoupENSG00000138614
BioGRIDINTS14
STRING (EMBL)INTS14
ZODIACINTS14
Ontologies - Pathways
QuickGOQ96SY0
Ontology : AmiGOnucleoplasm  snRNA transcription from RNA polymerase II promoter  
Ontology : EGO-EBInucleoplasm  snRNA transcription from RNA polymerase II promoter  
NDEx NetworkINTS14
Atlas of Cancer Signalling NetworkINTS14
Wikipedia pathwaysINTS14
Orthology - Evolution
OrthoDB81556
GeneTree (enSembl)ENSG00000138614
Phylogenetic Trees/Animal Genes : TreeFamINTS14
HOVERGENQ96SY0
HOGENOMQ96SY0
Homologs : HomoloGeneINTS14
Homology/Alignments : Family Browser (UCSC)INTS14
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerINTS14 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)INTS14
dbVarINTS14
ClinVarINTS14
1000_GenomesINTS14 
Exome Variant ServerINTS14
ExAC (Exome Aggregation Consortium)INTS14 (select the gene name)
Genetic variants : HAPMAP81556
Genomic Variants (DGV)INTS14 [DGVbeta]
DECIPHERINTS14 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisINTS14 
Mutations
ICGC Data PortalINTS14 
TCGA Data PortalINTS14 
Broad Tumor PortalINTS14
OASIS PortalINTS14 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDINTS14
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 INTS14
DgiDB (Drug Gene Interaction Database)INTS14
DoCM (Curated mutations)INTS14 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)INTS14 (select a term)
intoGenINTS14
Cancer3DINTS14(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenINTS14
Genetic Testing Registry INTS14
NextProtQ96SY0 [Medical]
TSGene81556
GENETestsINTS14
Target ValidationINTS14
Huge Navigator INTS14 [HugePedia]
snp3D : Map Gene to Disease81556
BioCentury BCIQINTS14
ClinGenINTS14
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD81556
Chemical/Pharm GKB GenePA142672279
Clinical trialINTS14
Miscellaneous
canSAR (ICR)INTS14 (select the gene name)
Probes
Litterature
PubMed15 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineINTS14
EVEXINTS14
GoPubMedINTS14
iHOPINTS14
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 13:11:14 CEST 2017

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