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KIAA0895 (KIAA0895)

Identity

Other alias-
HGNC (Hugo) KIAA0895
LocusID (NCBI) 23366
Atlas_Id 64864
Location 7p14.2  [Link to chromosome band 7p14]
Location_base_pair Starts at 36324150 and ends at 36390125 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
HOXA3 (7p15.2) / KIAA0895 (7p14.2)ZNF503 (10q22.2) / KIAA0895 (7p14.2)

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)KIAA0895   22206
Cards
Entrez_Gene (NCBI)KIAA0895  23366  KIAA0895
Aliases
GeneCards (Weizmann)KIAA0895
Ensembl hg19 (Hinxton)ENSG00000164542 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000164542 [Gene_View]  chr7:36324150-36390125 [Contig_View]  KIAA0895 [Vega]
ICGC DataPortalENSG00000164542
TCGA cBioPortalKIAA0895
AceView (NCBI)KIAA0895
Genatlas (Paris)KIAA0895
WikiGenes23366
SOURCE (Princeton)KIAA0895
Genetics Home Reference (NIH)KIAA0895
Genomic and cartography
GoldenPath hg38 (UCSC)KIAA0895  -     chr7:36324150-36390125 -  7p14.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)KIAA0895  -     7p14.2   [Description]    (hg19-Feb_2009)
EnsemblKIAA0895 - 7p14.2 [CytoView hg19]  KIAA0895 - 7p14.2 [CytoView hg38]
Mapping of homologs : NCBIKIAA0895 [Mapview hg19]  KIAA0895 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB020702 AK293912 AK294686 AK302559 AK302632
RefSeq transcript (Entrez)NM_001100425 NM_001199706 NM_001199707 NM_001199708 NM_001300956 NM_015314
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)KIAA0895
Cluster EST : UnigeneHs.735371 [ NCBI ]
CGAP (NCI)Hs.735371
Alternative Splicing GalleryENSG00000164542
Gene ExpressionKIAA0895 [ NCBI-GEO ]   KIAA0895 [ EBI - ARRAY_EXPRESS ]   KIAA0895 [ SEEK ]   KIAA0895 [ MEM ]
Gene Expression Viewer (FireBrowse)KIAA0895 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)23366
GTEX Portal (Tissue expression)KIAA0895
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8NCT3   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8NCT3  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8NCT3
Splice isoforms : SwissVarQ8NCT3
PhosPhoSitePlusQ8NCT3
Domains : Interpro (EBI)DUF1704   
Domain families : Pfam (Sanger)DUF1704 (PF08014)   
Domain families : Pfam (NCBI)pfam08014   
Domain families : Smart (EMBL)DUF1704 (SM01154)  
Conserved Domain (NCBI)KIAA0895
DMDM Disease mutations23366
Blocks (Seattle)KIAA0895
SuperfamilyQ8NCT3
Human Protein AtlasENSG00000164542
Peptide AtlasQ8NCT3
HPRD17197
IPIIPI00184441   IPI00385117   IPI00927328   IPI00784547   IPI00926022   IPI00926818   IPI00926458   IPI00925825   IPI00926832   
Protein Interaction databases
DIP (DOE-UCLA)Q8NCT3
IntAct (EBI)Q8NCT3
FunCoupENSG00000164542
BioGRIDKIAA0895
STRING (EMBL)KIAA0895
ZODIACKIAA0895
Ontologies - Pathways
QuickGOQ8NCT3
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkKIAA0895
Atlas of Cancer Signalling NetworkKIAA0895
Wikipedia pathwaysKIAA0895
Orthology - Evolution
OrthoDB23366
GeneTree (enSembl)ENSG00000164542
Phylogenetic Trees/Animal Genes : TreeFamKIAA0895
HOVERGENQ8NCT3
HOGENOMQ8NCT3
Homologs : HomoloGeneKIAA0895
Homology/Alignments : Family Browser (UCSC)KIAA0895
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKIAA0895 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KIAA0895
dbVarKIAA0895
ClinVarKIAA0895
1000_GenomesKIAA0895 
Exome Variant ServerKIAA0895
ExAC (Exome Aggregation Consortium)KIAA0895 (select the gene name)
Genetic variants : HAPMAP23366
Genomic Variants (DGV)KIAA0895 [DGVbeta]
DECIPHERKIAA0895 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisKIAA0895 
Mutations
ICGC Data PortalKIAA0895 
TCGA Data PortalKIAA0895 
Broad Tumor PortalKIAA0895
OASIS PortalKIAA0895 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICKIAA0895  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDKIAA0895
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 KIAA0895
DgiDB (Drug Gene Interaction Database)KIAA0895
DoCM (Curated mutations)KIAA0895 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)KIAA0895 (select a term)
intoGenKIAA0895
Cancer3DKIAA0895(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenKIAA0895
Genetic Testing Registry KIAA0895
NextProtQ8NCT3 [Medical]
TSGene23366
GENETestsKIAA0895
Target ValidationKIAA0895
Huge Navigator KIAA0895 [HugePedia]
snp3D : Map Gene to Disease23366
BioCentury BCIQKIAA0895
ClinGenKIAA0895
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD23366
Chemical/Pharm GKB GenePA164721801
Clinical trialKIAA0895
Miscellaneous
canSAR (ICR)KIAA0895 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineKIAA0895
EVEXKIAA0895
GoPubMedKIAA0895
iHOPKIAA0895
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed Jun 7 15:54:25 CEST 2017

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