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KIAA0895L (KIAA0895 like)

Identity

Alias_symbol (synonym)LOC653319
Other alias-
HGNC (Hugo) KIAA0895L
LocusID (NCBI) 653319
Atlas_Id 64865
Location 16q22.1  [Link to chromosome band 16q22]
Location_base_pair Starts at 67175602 and ends at 67183980 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
KIAA0895L (16q22.1) / VAV2 (9q34.2)

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)KIAA0895L   34408
Cards
Entrez_Gene (NCBI)KIAA0895L  653319  KIAA0895 like
Aliases
GeneCards (Weizmann)KIAA0895L
Ensembl hg19 (Hinxton)ENSG00000196123 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000196123 [Gene_View]  chr16:67175602-67183980 [Contig_View]  KIAA0895L [Vega]
ICGC DataPortalENSG00000196123
TCGA cBioPortalKIAA0895L
AceView (NCBI)KIAA0895L
Genatlas (Paris)KIAA0895L
WikiGenes653319
SOURCE (Princeton)KIAA0895L
Genetics Home Reference (NIH)KIAA0895L
Genomic and cartography
GoldenPath hg38 (UCSC)KIAA0895L  -     chr16:67175602-67183980 -  16q22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)KIAA0895L  -     16q22.1   [Description]    (hg19-Feb_2009)
EnsemblKIAA0895L - 16q22.1 [CytoView hg19]  KIAA0895L - 16q22.1 [CytoView hg38]
Mapping of homologs : NCBIKIAA0895L [Mapview hg19]  KIAA0895L [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK092303 AK094787 AK096855 AL834156 BC007594
RefSeq transcript (Entrez)NM_001040715
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)KIAA0895L
Cluster EST : UnigeneHs.651201 [ NCBI ]
CGAP (NCI)Hs.651201
Alternative Splicing GalleryENSG00000196123
Gene ExpressionKIAA0895L [ NCBI-GEO ]   KIAA0895L [ EBI - ARRAY_EXPRESS ]   KIAA0895L [ SEEK ]   KIAA0895L [ MEM ]
Gene Expression Viewer (FireBrowse)KIAA0895L [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)653319
GTEX Portal (Tissue expression)KIAA0895L
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ68EN5   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ68EN5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ68EN5
Splice isoforms : SwissVarQ68EN5
PhosPhoSitePlusQ68EN5
Domains : Interpro (EBI)DUF1704   
Domain families : Pfam (Sanger)DUF1704 (PF08014)   
Domain families : Pfam (NCBI)pfam08014   
Domain families : Smart (EMBL)DUF1704 (SM01154)  
Conserved Domain (NCBI)KIAA0895L
DMDM Disease mutations653319
Blocks (Seattle)KIAA0895L
SuperfamilyQ68EN5
Human Protein AtlasENSG00000196123
Peptide AtlasQ68EN5
IPIIPI00795583   IPI00645300   IPI00385803   
Protein Interaction databases
DIP (DOE-UCLA)Q68EN5
IntAct (EBI)Q68EN5
FunCoupENSG00000196123
BioGRIDKIAA0895L
STRING (EMBL)KIAA0895L
ZODIACKIAA0895L
Ontologies - Pathways
QuickGOQ68EN5
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkKIAA0895L
Atlas of Cancer Signalling NetworkKIAA0895L
Wikipedia pathwaysKIAA0895L
Orthology - Evolution
OrthoDB653319
GeneTree (enSembl)ENSG00000196123
Phylogenetic Trees/Animal Genes : TreeFamKIAA0895L
HOVERGENQ68EN5
HOGENOMQ68EN5
Homologs : HomoloGeneKIAA0895L
Homology/Alignments : Family Browser (UCSC)KIAA0895L
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKIAA0895L [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KIAA0895L
dbVarKIAA0895L
ClinVarKIAA0895L
1000_GenomesKIAA0895L 
Exome Variant ServerKIAA0895L
ExAC (Exome Aggregation Consortium)KIAA0895L (select the gene name)
Genetic variants : HAPMAP653319
Genomic Variants (DGV)KIAA0895L [DGVbeta]
DECIPHERKIAA0895L [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisKIAA0895L 
Mutations
ICGC Data PortalKIAA0895L 
TCGA Data PortalKIAA0895L 
Broad Tumor PortalKIAA0895L
OASIS PortalKIAA0895L [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICKIAA0895L  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDKIAA0895L
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 KIAA0895L
DgiDB (Drug Gene Interaction Database)KIAA0895L
DoCM (Curated mutations)KIAA0895L (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)KIAA0895L (select a term)
intoGenKIAA0895L
Cancer3DKIAA0895L(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenKIAA0895L
Genetic Testing Registry KIAA0895L
NextProtQ68EN5 [Medical]
TSGene653319
GENETestsKIAA0895L
Target ValidationKIAA0895L
Huge Navigator KIAA0895L [HugePedia]
snp3D : Map Gene to Disease653319
BioCentury BCIQKIAA0895L
ClinGenKIAA0895L
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD653319
Chemical/Pharm GKB GenePA164721818
Clinical trialKIAA0895L
Miscellaneous
canSAR (ICR)KIAA0895L (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineKIAA0895L
EVEXKIAA0895L
GoPubMedKIAA0895L
iHOPKIAA0895L
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 13:11:48 CEST 2017

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