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HAUS2 (HAUS augmin like complex subunit 2)

Identity

Alias_namesC15orf25
CEP27
chromosome 15 open reading frame 25
centrosomal protein 27kDa
Alias_symbol (synonym)FLJ10460
HsT17025
Other alias
HGNC (Hugo) HAUS2
LocusID (NCBI) 55142
Atlas_Id 64174
Location 15q15.2  [Link to chromosome band 15q15]
Location_base_pair Starts at 42548813 and ends at 42569992 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)		HAUS2 (15q15.2) / HAUS2 (15q15.2)

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)HAUS2   25530
Cards
Entrez_Gene (NCBI)HAUS2  55142  HAUS augmin like complex subunit 2
AliasesC15orf25; CEP27; HsT17025
GeneCards (Weizmann)HAUS2
Ensembl hg19 (Hinxton)ENSG00000137814 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000137814 [Gene_View]  chr15:42548813-42569992 [Contig_View]  HAUS2 [Vega]
ICGC DataPortalENSG00000137814
TCGA cBioPortalHAUS2
AceView (NCBI)HAUS2
Genatlas (Paris)HAUS2
WikiGenes55142
SOURCE (Princeton)HAUS2
Genetics Home Reference (NIH)HAUS2
Genomic and cartography
GoldenPath hg38 (UCSC)HAUS2  -     chr15:42548813-42569992 +  15q15.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)HAUS2  -     15q15.2   [Description]    (hg19-Feb_2009)
EnsemblHAUS2 - 15q15.2 [CytoView hg19]  HAUS2 - 15q15.2 [CytoView hg38]
Mapping of homologs : NCBIHAUS2 [Mapview hg19]  HAUS2 [Mapview hg38]
OMIM613429   
Gene and transcription
Genbank (Entrez)AI368236 AK001322 AK022939 BC010903 DA923763
RefSeq transcript (Entrez)NM_001130447 NM_001323629 NM_001323630 NM_001323631 NM_001323632 NM_018097
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)HAUS2
Cluster EST : UnigeneHs.14347 [ NCBI ]
CGAP (NCI)Hs.14347
Alternative Splicing GalleryENSG00000137814
Gene ExpressionHAUS2 [ NCBI-GEO ]   HAUS2 [ EBI - ARRAY_EXPRESS ]   HAUS2 [ SEEK ]   HAUS2 [ MEM ]
Gene Expression Viewer (FireBrowse)HAUS2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)55142
GTEX Portal (Tissue expression)HAUS2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9NVX0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9NVX0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9NVX0
Splice isoforms : SwissVarQ9NVX0
PhosPhoSitePlusQ9NVX0
Domains : Interpro (EBI)HAUS2    HAUS2_metazoa   
Domain families : Pfam (Sanger)HAUS2 (PF15003)   
Domain families : Pfam (NCBI)pfam15003   
Conserved Domain (NCBI)HAUS2
DMDM Disease mutations55142
Blocks (Seattle)HAUS2
SuperfamilyQ9NVX0
Human Protein AtlasENSG00000137814
Peptide AtlasQ9NVX0
HPRD07675
IPIIPI00018198   IPI00515011   IPI01008924   
Protein Interaction databases
DIP (DOE-UCLA)Q9NVX0
IntAct (EBI)Q9NVX0
FunCoupENSG00000137814
BioGRIDHAUS2
STRING (EMBL)HAUS2
ZODIACHAUS2
Ontologies - Pathways
QuickGOQ9NVX0
Ontology : AmiGOG2/M transition of mitotic cell cycle  molecular_function  centrosome  cytosol  spindle microtubule  centrosome cycle  spindle assembly  cell division  HAUS complex  ciliary basal body docking  
Ontology : EGO-EBIG2/M transition of mitotic cell cycle  molecular_function  centrosome  cytosol  spindle microtubule  centrosome cycle  spindle assembly  cell division  HAUS complex  ciliary basal body docking  
NDEx NetworkHAUS2
Atlas of Cancer Signalling NetworkHAUS2
Wikipedia pathwaysHAUS2
Orthology - Evolution
OrthoDB55142
GeneTree (enSembl)ENSG00000137814
Phylogenetic Trees/Animal Genes : TreeFamHAUS2
HOVERGENQ9NVX0
HOGENOMQ9NVX0
Homologs : HomoloGeneHAUS2
Homology/Alignments : Family Browser (UCSC)HAUS2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerHAUS2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)HAUS2
dbVarHAUS2
ClinVarHAUS2
1000_GenomesHAUS2 
Exome Variant ServerHAUS2
ExAC (Exome Aggregation Consortium)HAUS2 (select the gene name)
Genetic variants : HAPMAP55142
Genomic Variants (DGV)HAUS2 [DGVbeta]
DECIPHERHAUS2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisHAUS2 
Mutations
ICGC Data PortalHAUS2 
TCGA Data PortalHAUS2 
Broad Tumor PortalHAUS2
OASIS PortalHAUS2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICHAUS2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDHAUS2
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 HAUS2
DgiDB (Drug Gene Interaction Database)HAUS2
DoCM (Curated mutations)HAUS2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)HAUS2 (select a term)
intoGenHAUS2
Cancer3DHAUS2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM613429   
Orphanet
MedgenHAUS2
Genetic Testing Registry HAUS2
NextProtQ9NVX0 [Medical]
TSGene55142
GENETestsHAUS2
Target ValidationHAUS2
Huge Navigator HAUS2 [HugePedia]
snp3D : Map Gene to Disease55142
BioCentury BCIQHAUS2
ClinGenHAUS2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD55142
Chemical/Pharm GKB GenePA165479051
Clinical trialHAUS2
Miscellaneous
canSAR (ICR)HAUS2 (select the gene name)
Probes
Litterature
PubMed27 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineHAUS2
EVEXHAUS2
GoPubMedHAUS2
iHOPHAUS2
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 13:10:14 CEST 2017
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