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ANHX (anomalous homeobox)

Identity

Other alias-
HGNC (Hugo) ANHX
LocusID (NCBI) 647589
Atlas_Id 60297
Location 12q24.33  [Link to chromosome band 12q24]
Location_base_pair Starts at 133218312 and ends at 133235836 bp from pter ( according to hg38-Dec_2013)

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)ANHX   40024
Cards
Entrez_Gene (NCBI)ANHX  647589  anomalous homeobox
Aliases
GeneCards (Weizmann)ANHX
Ensembl hg19 (Hinxton)ENSG00000227059 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000227059 [Gene_View]  chr12:133218312-133235836 [Contig_View]  ANHX [Vega]
ICGC DataPortalENSG00000227059
TCGA cBioPortalANHX
AceView (NCBI)ANHX
Genatlas (Paris)ANHX
WikiGenes647589
SOURCE (Princeton)ANHX
Genetics Home Reference (NIH)ANHX
Genomic and cartography
GoldenPath hg38 (UCSC)ANHX  -     chr12:133218312-133235836 -  12q24.33   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ANHX  -     12q24.33   [Description]    (hg19-Feb_2009)
EnsemblANHX - 12q24.33 [CytoView hg19]  ANHX - 12q24.33 [CytoView hg38]
Mapping of homologs : NCBIANHX [Mapview hg19]  ANHX [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK057223 DB032853
RefSeq transcript (Entrez)NM_001191054
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ANHX
Cluster EST : UnigeneHs.703008 [ NCBI ]
CGAP (NCI)Hs.703008
Alternative Splicing GalleryENSG00000227059
Gene ExpressionANHX [ NCBI-GEO ]   ANHX [ EBI - ARRAY_EXPRESS ]   ANHX [ SEEK ]   ANHX [ MEM ]
Gene Expression Viewer (FireBrowse)ANHX [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)647589
GTEX Portal (Tissue expression)ANHX
Protein : pattern, domain, 3D structure
UniProt/SwissProtE9PGG2   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtE9PGG2  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProE9PGG2
Splice isoforms : SwissVarE9PGG2
PhosPhoSitePlusE9PGG2
Domaine pattern : Prosite (Expaxy)HOMEOBOX_1 (PS00027)    HOMEOBOX_2 (PS50071)   
Domains : Interpro (EBI)Homeobox-like    Homeobox_CS    Homeobox_dom    SIX1_SD   
Domain families : Pfam (Sanger)Homeobox (PF00046)    SIX1_SD (PF16878)   
Domain families : Pfam (NCBI)pfam00046    pfam16878   
Domain families : Smart (EMBL)HOX (SM00389)  
Conserved Domain (NCBI)ANHX
DMDM Disease mutations647589
Blocks (Seattle)ANHX
SuperfamilyE9PGG2
Human Protein AtlasENSG00000227059
Peptide AtlasE9PGG2
IPIIPI00387132   
Protein Interaction databases
DIP (DOE-UCLA)E9PGG2
IntAct (EBI)E9PGG2
FunCoupENSG00000227059
BioGRIDANHX
STRING (EMBL)ANHX
ZODIACANHX
Ontologies - Pathways
QuickGOE9PGG2
Ontology : AmiGOnucleus  regulation of transcription, DNA-templated  sequence-specific DNA binding  
Ontology : EGO-EBInucleus  regulation of transcription, DNA-templated  sequence-specific DNA binding  
NDEx NetworkANHX
Atlas of Cancer Signalling NetworkANHX
Wikipedia pathwaysANHX
Orthology - Evolution
OrthoDB647589
GeneTree (enSembl)ENSG00000227059
Phylogenetic Trees/Animal Genes : TreeFamANHX
HOVERGENE9PGG2
HOGENOME9PGG2
Homologs : HomoloGeneANHX
Homology/Alignments : Family Browser (UCSC)ANHX
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerANHX [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ANHX
dbVarANHX
ClinVarANHX
1000_GenomesANHX 
Exome Variant ServerANHX
ExAC (Exome Aggregation Consortium)ANHX (select the gene name)
Genetic variants : HAPMAP647589
Genomic Variants (DGV)ANHX [DGVbeta]
DECIPHERANHX [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisANHX 
Mutations
ICGC Data PortalANHX 
TCGA Data PortalANHX 
Broad Tumor PortalANHX
OASIS PortalANHX [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICANHX  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDANHX
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 ANHX
DgiDB (Drug Gene Interaction Database)ANHX
DoCM (Curated mutations)ANHX (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ANHX (select a term)
intoGenANHX
Cancer3DANHX(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenANHX
Genetic Testing Registry ANHX
NextProtE9PGG2 [Medical]
TSGene647589
GENETestsANHX
Target ValidationANHX
Huge Navigator ANHX [HugePedia]
snp3D : Map Gene to Disease647589
BioCentury BCIQANHX
ClinGenANHX
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD647589
Chemical/Pharm GKB GenePA166049047
Clinical trialANHX
Miscellaneous
canSAR (ICR)ANHX (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineANHX
EVEXANHX
GoPubMedANHX
iHOPANHX
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 13:01:16 CEST 2017

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