Atlas of Genetics and Cytogenetics in Oncology and Haematology

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ANO9 (anoctamin 9)

Identity

Alias_namesTP53I5
TMEM16J
tumor protein p53 inducible protein 5
transmembrane protein 16J
Alias_symbol (synonym)PIG5
Other alias
HGNC (Hugo) ANO9
LocusID (NCBI) 338440
Atlas_Id 42671
Location 11p15.5  [Link to chromosome band 11p15]
Location_base_pair Starts at 417930 and ends at 442011 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)		Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
ANO9 (11p15.5) / ANO9 (11p15.5)ANO9 (11p15.5) / DEAF1 (11p15.5)ANO9 (11p15.5) / TFAP4 (16p13.3)
ANO9 11p15.5 / DEAF1 11p15.5

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

 

Other Solid tumors implicated (Data extracted from papers in the Atlas) [ 2 ]

Solid Tumors TT_t1111p15p15ID100504 TT_t1111p15p15ID100515

External links

Nomenclature
HGNC (Hugo)ANO9   20679
Cards
Entrez_Gene (NCBI)ANO9  338440  anoctamin 9
AliasesPIG5; TMEM16J; TP53I5
GeneCards (Weizmann)ANO9
Ensembl hg19 (Hinxton)ENSG00000185101 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000185101 [Gene_View]  ENSG00000185101 [Sequence]  chr11:417930-442011 [Contig_View]  ANO9 [Vega]
ICGC DataPortalENSG00000185101
TCGA cBioPortalANO9
AceView (NCBI)ANO9
Genatlas (Paris)ANO9
WikiGenes338440
SOURCE (Princeton)ANO9
Genetics Home Reference (NIH)ANO9
Genomic and cartography
GoldenPath hg38 (UCSC)ANO9  -     chr11:417930-442011 -  11p15.5   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ANO9  -     11p15.5   [Description]    (hg19-Feb_2009)
GoldenPathANO9 - 11p15.5 [CytoView hg19]  ANO9 - 11p15.5 [CytoView hg38]
ImmunoBaseENSG00000185101
Mapping of homologs : NCBIANO9 [Mapview hg19]  ANO9 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI986229 AK026923 AK074088 AK096874 AK303642
RefSeq transcript (Entrez)NM_001012302 NM_001347882
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ANO9
Cluster EST : UnigeneHs.501622 [ NCBI ]
CGAP (NCI)Hs.501622
Alternative Splicing GalleryENSG00000185101
Gene ExpressionANO9 [ NCBI-GEO ]   ANO9 [ EBI - ARRAY_EXPRESS ]   ANO9 [ SEEK ]   ANO9 [ MEM ]
Gene Expression Viewer (FireBrowse)ANO9 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)338440
GTEX Portal (Tissue expression)ANO9
Human Protein AtlasENSG00000185101-ANO9 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtA1A5B4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtA1A5B4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProA1A5B4
Splice isoforms : SwissVarA1A5B4
PhosPhoSitePlusA1A5B4
Domains : Interpro (EBI)Anoctamin    Anoctamin-9   
Domain families : Pfam (Sanger)Anoctamin (PF04547)   
Domain families : Pfam (NCBI)pfam04547   
Conserved Domain (NCBI)ANO9
DMDM Disease mutations338440
Blocks (Seattle)ANO9
SuperfamilyA1A5B4
Human Protein Atlas [tissue]ENSG00000185101-ANO9 [tissue]
Peptide AtlasA1A5B4
HPRD18214
IPIIPI00152780   IPI00922125   IPI00922523   
Protein Interaction databases
DIP (DOE-UCLA)A1A5B4
IntAct (EBI)A1A5B4
FunCoupENSG00000185101
BioGRIDANO9
STRING (EMBL)ANO9
ZODIACANO9
Ontologies - Pathways
QuickGOA1A5B4
Ontology : AmiGOintracellular calcium activated chloride channel activity  intracellular calcium activated chloride channel activity  protein binding  plasma membrane  plasma membrane  chloride transport  integral component of membrane  phospholipid scramblase activity  ion transmembrane transport  calcium activated phosphatidylserine scrambling  calcium activated phosphatidylcholine scrambling  calcium activated galactosylceramide scrambling  negative regulation of intracellular calcium activated chloride channel activity  
Ontology : EGO-EBIintracellular calcium activated chloride channel activity  intracellular calcium activated chloride channel activity  protein binding  plasma membrane  plasma membrane  chloride transport  integral component of membrane  phospholipid scramblase activity  ion transmembrane transport  calcium activated phosphatidylserine scrambling  calcium activated phosphatidylcholine scrambling  calcium activated galactosylceramide scrambling  negative regulation of intracellular calcium activated chloride channel activity  
NDEx NetworkANO9
Atlas of Cancer Signalling NetworkANO9
Wikipedia pathwaysANO9
Orthology - Evolution
OrthoDB338440
GeneTree (enSembl)ENSG00000185101
Phylogenetic Trees/Animal Genes : TreeFamANO9
HOGENOMA1A5B4
Homologs : HomoloGeneANO9
Homology/Alignments : Family Browser (UCSC)ANO9
Gene fusions - Rearrangements
Fusion : MitelmanANO9/DEAF1 [11p15.5/11p15.5]  
Fusion PortalANO9 11p15.5 DEAF1 11p15.5 BRCA
Fusion : QuiverANO9
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerANO9 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ANO9
dbVarANO9
ClinVarANO9
1000_GenomesANO9 
Exome Variant ServerANO9
ExAC (Exome Aggregation Consortium)ENSG00000185101
GNOMAD BrowserENSG00000185101
Varsome BrowserANO9
Genetic variants : HAPMAP338440
Genomic Variants (DGV)ANO9 [DGVbeta]
DECIPHERANO9 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisANO9 
Mutations
ICGC Data PortalANO9 
TCGA Data PortalANO9 
Broad Tumor PortalANO9
OASIS PortalANO9 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICANO9  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DANO9
Mutations and Diseases : HGMDANO9
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 ANO9
DgiDB (Drug Gene Interaction Database)ANO9
DoCM (Curated mutations)ANO9 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ANO9 (select a term)
intoGenANO9
Cancer3DANO9(select the gene name)
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETANO9
MedgenANO9
Genetic Testing Registry ANO9
NextProtA1A5B4 [Medical]
TSGene338440
GENETestsANO9
Target ValidationANO9
Huge Navigator ANO9 [HugePedia]
snp3D : Map Gene to Disease338440
BioCentury BCIQANO9
ClinGenANO9
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD338440
Chemical/Pharm GKB GenePA164715791
Clinical trialANO9
Miscellaneous
canSAR (ICR)ANO9 (select the gene name)
DataMed IndexANO9
Probes
Litterature
PubMed19 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineANO9
EVEXANO9
GoPubMedANO9
iHOPANO9
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Feb 3 14:47:18 CET 2020
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