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KIAA0087 (KIAA0087)

Identity

Other alias-
HGNC (Hugo) KIAA0087
LocusID (NCBI) 9808
Atlas_Id 64848
Location 7p15.2  [Link to chromosome band 7p15]
Location_base_pair Starts at 26575432 and ends at 26578237 bp from pter ( according to hg19-Feb_2009)

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)KIAA0087   22191
Cards
Entrez_Gene (NCBI)KIAA0087  9808  KIAA0087
Aliases
GeneCards (Weizmann)KIAA0087
Ensembl hg19 (Hinxton)ENSG00000122548 [Gene_View]  chr7:26575432-26578237 [Contig_View]  KIAA0087 [Vega]
Ensembl hg38 (Hinxton)ENSG00000122548 [Gene_View]  chr7:26575432-26578237 [Contig_View]  KIAA0087 [Vega]
ICGC DataPortalENSG00000122548
TCGA cBioPortalKIAA0087
AceView (NCBI)KIAA0087
Genatlas (Paris)KIAA0087
WikiGenes9808
SOURCE (Princeton)KIAA0087
Genetics Home Reference (NIH)KIAA0087
Genomic and cartography
GoldenPath hg19 (UCSC)KIAA0087  -     chr7:26575432-26578237 -  7p15.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)KIAA0087  -     7p15.2   [Description]    (hg38-Dec_2013)
EnsemblKIAA0087 - 7p15.2 [CytoView hg19]  KIAA0087 - 7p15.2 [CytoView hg38]
Mapping of homologs : NCBIKIAA0087 [Mapview hg19]  KIAA0087 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC128257 D42038 DB147006
RefSeq transcript (Entrez)NM_014769
RefSeq genomic (Entrez)NC_000007 NC_018918 NT_007819 NW_004929329
Consensus coding sequences : CCDS (NCBI)KIAA0087
Cluster EST : UnigeneHs.69749 [ NCBI ]
CGAP (NCI)Hs.69749
Alternative Splicing GalleryENSG00000122548
Gene ExpressionKIAA0087 [ NCBI-GEO ]   KIAA0087 [ EBI - ARRAY_EXPRESS ]   KIAA0087 [ SEEK ]   KIAA0087 [ MEM ]
Gene Expression Viewer (FireBrowse)KIAA0087 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)9808
GTEX Portal (Tissue expression)KIAA0087
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ14695   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ14695  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ14695
Splice isoforms : SwissVarQ14695
PhosPhoSitePlusQ14695
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)KIAA0087
DMDM Disease mutations9808
Blocks (Seattle)KIAA0087
SuperfamilyQ14695
Human Protein AtlasENSG00000122548
Peptide AtlasQ14695
IPIIPI00032390   
Protein Interaction databases
DIP (DOE-UCLA)Q14695
IntAct (EBI)Q14695
FunCoupENSG00000122548
BioGRIDKIAA0087
STRING (EMBL)KIAA0087
ZODIACKIAA0087
Ontologies - Pathways
QuickGOQ14695
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkKIAA0087
Atlas of Cancer Signalling NetworkKIAA0087
Wikipedia pathwaysKIAA0087
Orthology - Evolution
OrthoDB9808
GeneTree (enSembl)ENSG00000122548
Phylogenetic Trees/Animal Genes : TreeFamKIAA0087
HOVERGENQ14695
HOGENOMQ14695
Homologs : HomoloGeneKIAA0087
Homology/Alignments : Family Browser (UCSC)KIAA0087
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKIAA0087 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KIAA0087
dbVarKIAA0087
ClinVarKIAA0087
1000_GenomesKIAA0087 
Exome Variant ServerKIAA0087
ExAC (Exome Aggregation Consortium)KIAA0087 (select the gene name)
Genetic variants : HAPMAP9808
Genomic Variants (DGV)KIAA0087 [DGVbeta]
DECIPHER (Syndromes)7:26575432-26578237  ENSG00000122548
CONAN: Copy Number AnalysisKIAA0087 
Mutations
ICGC Data PortalKIAA0087 
TCGA Data PortalKIAA0087 
Broad Tumor PortalKIAA0087
OASIS PortalKIAA0087 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDKIAA0087
BioMutasearch KIAA0087
DgiDB (Drug Gene Interaction Database)KIAA0087
DoCM (Curated mutations)KIAA0087 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)KIAA0087 (select a term)
intoGenKIAA0087
Cancer3DKIAA0087(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenKIAA0087
Genetic Testing Registry KIAA0087
NextProtQ14695 [Medical]
TSGene9808
GENETestsKIAA0087
Huge Navigator KIAA0087 [HugePedia]
snp3D : Map Gene to Disease9808
BioCentury BCIQKIAA0087
ClinGenKIAA0087
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD9808
Chemical/Pharm GKB GenePA162392815
Clinical trialKIAA0087
Miscellaneous
canSAR (ICR)KIAA0087 (select the gene name)
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineKIAA0087
EVEXKIAA0087
GoPubMedKIAA0087
iHOPKIAA0087
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Mar 14 12:09:39 CET 2017

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