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C15orf32 (chromosome 15 putative open reading frame 32)

Identity

Alias (NCBI)-
HGNC (Hugo) C15orf32
HGNC Alias symbFLJ32831
LocusID (NCBI) 145858
Atlas_Id 60947
Location 15q26.1  [Link to chromosome band 15q26]
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
CLN3 (16p11.2) / C15orf32 (15q26.1)

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)C15orf32   26549
Cards
Entrez_Gene (NCBI)C15orf32    chromosome 15 putative open reading frame 32
Aliases
GeneCards (Weizmann)C15orf32
Ensembl hg19 (Hinxton)ENSG00000183643 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000183643 [Gene_View]  ENSG00000183643 [Sequence]  - [Contig_View]  C15orf32 [Vega]
ICGC DataPortalENSG00000183643
TCGA cBioPortalC15orf32
AceView (NCBI)C15orf32
Genatlas (Paris)C15orf32
SOURCE (Princeton)C15orf32
Genetics Home Reference (NIH)C15orf32
Genomic and cartography
GoldenPath hg38 (UCSC)C15orf32  -  
GoldenPath hg19 (UCSC)C15orf32  -  
GoldenPathC15orf32 - [CytoView hg19]  C15orf32 - [CytoView hg38]
ImmunoBaseENSG00000183643
Genome Data Viewer NCBIC15orf32 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AK057393 BC109252 BC109253
RefSeq transcript (Entrez)NM_001301106 NM_153040
Consensus coding sequences : CCDS (NCBI)C15orf32
Gene ExpressionC15orf32 [ NCBI-GEO ]   C15orf32 [ EBI - ARRAY_EXPRESS ]   C15orf32 [ SEEK ]   C15orf32 [ MEM ]
Gene Expression Viewer (FireBrowse)C15orf32 [ Firebrowse - Broad ]
GenevisibleExpression of C15orf32 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)145858
GTEX Portal (Tissue expression)C15orf32
Human Protein AtlasENSG00000183643-C15orf32 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ32M92   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ32M92  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ32M92
PhosPhoSitePlusQ32M92
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)C15orf32
SuperfamilyQ32M92
AlphaFold pdb e-kbQ32M92   
Human Protein Atlas [tissue]ENSG00000183643-C15orf32 [tissue]
HPRD08143
Protein Interaction databases
DIP (DOE-UCLA)Q32M92
IntAct (EBI)Q32M92
BioGRIDC15orf32
STRING (EMBL)C15orf32
ZODIACC15orf32
Ontologies - Pathways
QuickGOQ32M92
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkC15orf32
Atlas of Cancer Signalling NetworkC15orf32
Wikipedia pathwaysC15orf32
Orthology - Evolution
OrthoDB145858
GeneTree (enSembl)ENSG00000183643
Phylogenetic Trees/Animal Genes : TreeFamC15orf32
Homologs : HomoloGeneC15orf32
Homology/Alignments : Family Browser (UCSC)C15orf32
Gene fusions - Rearrangements
Fusion : QuiverC15orf32
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerC15orf32 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)C15orf32
dbVarC15orf32
ClinVarC15orf32
MonarchC15orf32
1000_GenomesC15orf32 
Exome Variant ServerC15orf32
GNOMAD BrowserENSG00000183643
Varsome BrowserC15orf32
ACMGC15orf32 variants
VarityQ32M92
Genomic Variants (DGV)C15orf32 [DGVbeta]
DECIPHERC15orf32 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisC15orf32 
Mutations
ICGC Data PortalC15orf32 
TCGA Data PortalC15orf32 
Broad Tumor PortalC15orf32
OASIS PortalC15orf32 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDC15orf32
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaC15orf32
DgiDB (Drug Gene Interaction Database)C15orf32
DoCM (Curated mutations)C15orf32
CIViC (Clinical Interpretations of Variants in Cancer)C15orf32
Cancer3DC15orf32
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETC15orf32
MedgenC15orf32
Genetic Testing Registry C15orf32
NextProtQ32M92 [Medical]
GENETestsC15orf32
Target ValidationC15orf32
Huge Navigator C15orf32 [HugePedia]
ClinGenC15orf32
Clinical trials, drugs, therapy
MyCancerGenomeC15orf32
Protein Interactions : CTDC15orf32
Pharm GKB GenePA142672268
PharosQ32M92
Clinical trialC15orf32
Miscellaneous
canSAR (ICR)C15orf32
HarmonizomeC15orf32
DataMed IndexC15orf32
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXC15orf32
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 : Mon Oct 4 15:43:50 CEST 2021

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