Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

C2orf57 (-)

Identity

Alias_symbol (synonym)MGC35154
Other alias-
HGNC (Hugo) -
LocusID (NCBI) 165100
Atlas_Id 61157
Location -  [Link to chromosome band ]
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
C2orf57 (2q37.1) / GABARAP (17p13.1)
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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)C2orf57  165100  -
Aliases
GeneCards (Weizmann)C2orf57
Ensembl hg19 (Hinxton)ENSG00000177673 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000177673 [Gene_View]  - [Contig_View]  C2orf57 [Vega]
ICGC DataPortalENSG00000177673
TCGA cBioPortalC2orf57
AceView (NCBI)C2orf57
Genatlas (Paris)C2orf57
WikiGenes165100
SOURCE (Princeton)C2orf57
Genetics Home Reference (NIH)C2orf57
Genomic and cartography
GoldenPath hg38 (UCSC)C2orf57  -  
GoldenPath hg19 (UCSC)C2orf57  -  
EnsemblC2orf57 - [CytoView hg19]  C2orf57 - [CytoView hg38]
Mapping of homologs : NCBIC2orf57 [Mapview hg19]  C2orf57 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)C2orf57
Alternative Splicing GalleryENSG00000177673
Gene ExpressionC2orf57 [ NCBI-GEO ]   C2orf57 [ EBI - ARRAY_EXPRESS ]   C2orf57 [ SEEK ]   C2orf57 [ MEM ]
Gene Expression Viewer (FireBrowse)C2orf57 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)165100
GTEX Portal (Tissue expression)C2orf57
Human Protein AtlasENSG00000177673-C2orf57 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)C2orf57
DMDM Disease mutations165100
Blocks (Seattle)C2orf57
Human Protein Atlas [tissue]ENSG00000177673-C2orf57 [tissue]
HPRD14602
Protein Interaction databases
FunCoupENSG00000177673
BioGRIDC2orf57
STRING (EMBL)C2orf57
ZODIACC2orf57
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease165100
BioCentury BCIQC2orf57
ClinGenC2orf57
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD165100
Clinical trialC2orf57
Miscellaneous
canSAR (ICR)C2orf57 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineC2orf57
EVEXC2orf57
GoPubMedC2orf57
iHOPC2orf57
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Nov 20 19:21:34 CET 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.