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KIAA1614 (KIAA1614)

Identity

Other alias-
HGNC (Hugo) KIAA1614
LocusID (NCBI) 57710
Atlas_Id 64891
Location 1q25.3  [Link to chromosome band 1q25]
Location_base_pair Starts at 180913177 and ends at 180946103 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
UBAP2L (1q21.3) / KIAA1614 (1q25.3)

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)KIAA1614   29327
Cards
Entrez_Gene (NCBI)KIAA1614  57710  KIAA1614
Aliases
GeneCards (Weizmann)KIAA1614
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr1:180913177-180946103 [Contig_View]  KIAA1614 [Vega]
TCGA cBioPortalKIAA1614
AceView (NCBI)KIAA1614
Genatlas (Paris)KIAA1614
WikiGenes57710
SOURCE (Princeton)KIAA1614
Genetics Home Reference (NIH)KIAA1614
Genomic and cartography
GoldenPath hg38 (UCSC)KIAA1614  -     chr1:180913177-180946103 +  1q25.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)KIAA1614  -     1q25.3   [Description]    (hg19-Feb_2009)
EnsemblKIAA1614 - 1q25.3 [CytoView hg19]  KIAA1614 - 1q25.3 [CytoView hg38]
Mapping of homologs : NCBIKIAA1614 [Mapview hg19]  KIAA1614 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB046834 AK055739 AK090668 DA410555 DA807788
RefSeq transcript (Entrez)NM_020950
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)KIAA1614
Cluster EST : UnigeneHs.734816 [ NCBI ]
CGAP (NCI)Hs.734816
Gene ExpressionKIAA1614 [ NCBI-GEO ]   KIAA1614 [ EBI - ARRAY_EXPRESS ]   KIAA1614 [ SEEK ]   KIAA1614 [ MEM ]
Gene Expression Viewer (FireBrowse)KIAA1614 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)57710
GTEX Portal (Tissue expression)KIAA1614
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5VZ46   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5VZ46  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5VZ46
Splice isoforms : SwissVarQ5VZ46
PhosPhoSitePlusQ5VZ46
Domains : Interpro (EBI)DUF4685   
Domain families : Pfam (Sanger)DUF4685 (PF15737)   
Domain families : Pfam (NCBI)pfam15737   
Conserved Domain (NCBI)KIAA1614
DMDM Disease mutations57710
Blocks (Seattle)KIAA1614
SuperfamilyQ5VZ46
Peptide AtlasQ5VZ46
IPIIPI00288988   IPI00640946   
Protein Interaction databases
DIP (DOE-UCLA)Q5VZ46
IntAct (EBI)Q5VZ46
BioGRIDKIAA1614
STRING (EMBL)KIAA1614
ZODIACKIAA1614
Ontologies - Pathways
QuickGOQ5VZ46
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkKIAA1614
Atlas of Cancer Signalling NetworkKIAA1614
Wikipedia pathwaysKIAA1614
Orthology - Evolution
OrthoDB57710
Phylogenetic Trees/Animal Genes : TreeFamKIAA1614
HOVERGENQ5VZ46
HOGENOMQ5VZ46
Homologs : HomoloGeneKIAA1614
Homology/Alignments : Family Browser (UCSC)KIAA1614
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKIAA1614 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KIAA1614
dbVarKIAA1614
ClinVarKIAA1614
1000_GenomesKIAA1614 
Exome Variant ServerKIAA1614
ExAC (Exome Aggregation Consortium)KIAA1614 (select the gene name)
Genetic variants : HAPMAP57710
Genomic Variants (DGV)KIAA1614 [DGVbeta]
DECIPHERKIAA1614 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisKIAA1614 
Mutations
ICGC Data PortalKIAA1614 
TCGA Data PortalKIAA1614 
Broad Tumor PortalKIAA1614
OASIS PortalKIAA1614 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICKIAA1614  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDKIAA1614
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 KIAA1614
DgiDB (Drug Gene Interaction Database)KIAA1614
DoCM (Curated mutations)KIAA1614 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)KIAA1614 (select a term)
intoGenKIAA1614
Cancer3DKIAA1614(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenKIAA1614
Genetic Testing Registry KIAA1614
NextProtQ5VZ46 [Medical]
TSGene57710
GENETestsKIAA1614
Target ValidationKIAA1614
Huge Navigator KIAA1614 [HugePedia]
snp3D : Map Gene to Disease57710
BioCentury BCIQKIAA1614
ClinGenKIAA1614
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD57710
Chemical/Pharm GKB GenePA142671595
Clinical trialKIAA1614
Miscellaneous
canSAR (ICR)KIAA1614 (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineKIAA1614
EVEXKIAA1614
GoPubMedKIAA1614
iHOPKIAA1614
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 13:11:52 CEST 2017

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