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C2orf76 (chromosome 2 open reading frame 76)

Identity

Alias (NCBI)AIM29
HGNC (Hugo) C2orf76
HGNC Alias symbMGC104437
LOC130355
AIM29
LocusID (NCBI) 130355
Atlas_Id 61166
Location 2q14.2  [Link to chromosome band 2q14]
Location_base_pair Starts at 119302217 and ends at 119366828 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)
LOC100507412 (-) / C2orf76 (2q14.2)

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)C2orf76   27017
Cards
Entrez_Gene (NCBI)C2orf76    chromosome 2 open reading frame 76
AliasesAIM29
GeneCards (Weizmann)C2orf76
Ensembl hg19 (Hinxton)ENSG00000186132 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000186132 [Gene_View]  ENSG00000186132 [Sequence]  chr2:119302217-119366828 [Contig_View]  C2orf76 [Vega]
ICGC DataPortalENSG00000186132
TCGA cBioPortalC2orf76
AceView (NCBI)C2orf76
Genatlas (Paris)C2orf76
SOURCE (Princeton)C2orf76
Genetics Home Reference (NIH)C2orf76
Genomic and cartography
GoldenPath hg38 (UCSC)C2orf76  -     chr2:119302217-119366828 -  2q14.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)C2orf76  -     2q14.2   [Description]    (hg19-Feb_2009)
GoldenPathC2orf76 - 2q14.2 [CytoView hg19]  C2orf76 - 2q14.2 [CytoView hg38]
ImmunoBaseENSG00000186132
Genome Data Viewer NCBIC2orf76 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AW015242 BC047365 BC062434 BC105805 BC126395
RefSeq transcript (Entrez)NM_001017927 NM_001322329 NM_001322330 NM_001322331 NM_001322332
Consensus coding sequences : CCDS (NCBI)C2orf76
Gene ExpressionC2orf76 [ NCBI-GEO ]   C2orf76 [ EBI - ARRAY_EXPRESS ]   C2orf76 [ SEEK ]   C2orf76 [ MEM ]
Gene Expression Viewer (FireBrowse)C2orf76 [ Firebrowse - Broad ]
GenevisibleExpression of C2orf76 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)130355
GTEX Portal (Tissue expression)C2orf76
Human Protein AtlasENSG00000186132-C2orf76 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ3KRA6   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ3KRA6  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ3KRA6
PhosPhoSitePlusQ3KRA6
Domains : Interpro (EBI)UPF0538   
Domain families : Pfam (Sanger)DUF2340 (PF10209)   
Domain families : Pfam (NCBI)pfam10209   
Conserved Domain (NCBI)C2orf76
SuperfamilyQ3KRA6
AlphaFold pdb e-kbQ3KRA6   
Human Protein Atlas [tissue]ENSG00000186132-C2orf76 [tissue]
HPRD18547
Protein Interaction databases
DIP (DOE-UCLA)Q3KRA6
IntAct (EBI)Q3KRA6
BioGRIDC2orf76
STRING (EMBL)C2orf76
ZODIACC2orf76
Ontologies - Pathways
QuickGOQ3KRA6
Ontology : AmiGOprotein binding  
Ontology : EGO-EBIprotein binding  
NDEx NetworkC2orf76
Atlas of Cancer Signalling NetworkC2orf76
Wikipedia pathwaysC2orf76
Orthology - Evolution
OrthoDB130355
GeneTree (enSembl)ENSG00000186132
Phylogenetic Trees/Animal Genes : TreeFamC2orf76
Homologs : HomoloGeneC2orf76
Homology/Alignments : Family Browser (UCSC)C2orf76
Gene fusions - Rearrangements
Fusion : QuiverC2orf76
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerC2orf76 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)C2orf76
dbVarC2orf76
ClinVarC2orf76
MonarchC2orf76
1000_GenomesC2orf76 
Exome Variant ServerC2orf76
GNOMAD BrowserENSG00000186132
Varsome BrowserC2orf76
ACMGC2orf76 variants
VarityQ3KRA6
Genomic Variants (DGV)C2orf76 [DGVbeta]
DECIPHERC2orf76 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisC2orf76 
Mutations
ICGC Data PortalC2orf76 
TCGA Data PortalC2orf76 
Broad Tumor PortalC2orf76
OASIS PortalC2orf76 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICC2orf76  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DC2orf76
Mutations and Diseases : HGMDC2orf76
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaC2orf76
DgiDB (Drug Gene Interaction Database)C2orf76
DoCM (Curated mutations)C2orf76
CIViC (Clinical Interpretations of Variants in Cancer)C2orf76
Cancer3DC2orf76
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETC2orf76
MedgenC2orf76
Genetic Testing Registry C2orf76
NextProtQ3KRA6 [Medical]
GENETestsC2orf76
Target ValidationC2orf76
Huge Navigator C2orf76 [HugePedia]
ClinGenC2orf76
Clinical trials, drugs, therapy
MyCancerGenomeC2orf76
Protein Interactions : CTDC2orf76
Pharm GKB GenePA162379558
PharosQ3KRA6
Clinical trialC2orf76
Miscellaneous
canSAR (ICR)C2orf76
HarmonizomeC2orf76
DataMed IndexC2orf76
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXC2orf76
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 15:44:15 CEST 2021

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