Atlas of Genetics and Cytogenetics in Oncology and Haematology

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KIAA1614 (KIAA1614)

Identity

Alias (NCBI)-
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 2017)		Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
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    KIAA1614
Aliases
GeneCards (Weizmann)KIAA1614
Ensembl hg19 (Hinxton)ENSG00000135835 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000135835 [Gene_View]  ENSG00000135835 [Sequence]  chr1:180913177-180946103 [Contig_View]  KIAA1614 [Vega]
ICGC DataPortalENSG00000135835
TCGA cBioPortalKIAA1614
AceView (NCBI)KIAA1614
Genatlas (Paris)KIAA1614
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)
GoldenPathKIAA1614 - 1q25.3 [CytoView hg19]  KIAA1614 - 1q25.3 [CytoView hg38]
ImmunoBaseENSG00000135835
genome Data Viewer NCBIKIAA1614 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AB046834 AK055739 AK090668 DA410555 DA807788
RefSeq transcript (Entrez)NM_020950
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)KIAA1614
Alternative Splicing GalleryENSG00000135835
Gene ExpressionKIAA1614 [ NCBI-GEO ]   KIAA1614 [ EBI - ARRAY_EXPRESS ]   KIAA1614 [ SEEK ]   KIAA1614 [ MEM ]
Gene Expression Viewer (FireBrowse)KIAA1614 [ Firebrowse - Broad ]
GenevisibleExpression of KIAA1614 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)57710
GTEX Portal (Tissue expression)KIAA1614
Human Protein AtlasENSG00000135835-KIAA1614 [pathology]   [cell]   [tissue]
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
Blocks (Seattle)KIAA1614
SuperfamilyQ5VZ46
Human Protein Atlas [tissue]ENSG00000135835-KIAA1614 [tissue]
Peptide AtlasQ5VZ46
IPIIPI00288988   IPI00640946   
Protein Interaction databases
DIP (DOE-UCLA)Q5VZ46
IntAct (EBI)Q5VZ46
BioGRIDKIAA1614
STRING (EMBL)KIAA1614
ZODIACKIAA1614
Ontologies - Pathways
QuickGOQ5VZ46
Ontology : AmiGOprotein kinase C binding  nucleus  cell cortex  centrosome cycle  establishment or maintenance of cell polarity  apical plasma membrane  Rho GTPase binding  regulation of cellular localization  
Ontology : EGO-EBIprotein kinase C binding  nucleus  cell cortex  centrosome cycle  establishment or maintenance of cell polarity  apical plasma membrane  Rho GTPase binding  regulation of cellular localization  
NDEx NetworkKIAA1614
Atlas of Cancer Signalling NetworkKIAA1614
Wikipedia pathwaysKIAA1614
Orthology - Evolution
OrthoDB57710
GeneTree (enSembl)ENSG00000135835
Phylogenetic Trees/Animal Genes : TreeFamKIAA1614
HOGENOMQ5VZ46
Homologs : HomoloGeneKIAA1614
Homology/Alignments : Family Browser (UCSC)KIAA1614
Gene fusions - Rearrangements
Fusion : QuiverKIAA1614
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKIAA1614 [hg38]
dbVarKIAA1614
ClinVarKIAA1614
MonarchKIAA1614
1000_GenomesKIAA1614 
Exome Variant ServerKIAA1614
GNOMAD BrowserENSG00000135835
Varsome BrowserKIAA1614
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]  
Somatic Mutations in Cancer : COSMIC3DKIAA1614
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] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETKIAA1614
MedgenKIAA1614
Genetic Testing Registry KIAA1614
NextProtQ5VZ46 [Medical]
GENETestsKIAA1614
Target ValidationKIAA1614
Huge Navigator KIAA1614 [HugePedia]
ClinGenKIAA1614
Clinical trials, drugs, therapy
MyCancerGenomeKIAA1614
Protein Interactions : CTD
Pharm GKB GenePA142671595
Clinical trialKIAA1614
Miscellaneous
canSAR (ICR)KIAA1614 (select the gene name)
HarmonizomeKIAA1614
DataMed IndexKIAA1614
Probes
Litterature
PubMed6 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineKIAA1614
EVEXKIAA1614
GoPubMedKIAA1614
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Sat Dec 5 16:58:43 CET 2020
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