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C7orf77 (chromosome 7 open reading frame 77)

Identity

Other alias-
HGNC (Hugo) C7orf77
LocusID (NCBI) 154872
Atlas_Id 76648
Location 7q31.33  [Link to chromosome band 7q31]
Location_base_pair Starts at 124777292 and ends at 124790810 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)C7orf77   51256
Cards
Entrez_Gene (NCBI)C7orf77  154872  chromosome 7 open reading frame 77
Aliases
GeneCards (Weizmann)C7orf77
Ensembl hg19 (Hinxton)ENSG00000275356 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000275356 [Gene_View]  chr7:124777292-124790810 [Contig_View]  C7orf77 [Vega]
ICGC DataPortalENSG00000275356
TCGA cBioPortalC7orf77
AceView (NCBI)C7orf77
Genatlas (Paris)C7orf77
WikiGenes154872
SOURCE (Princeton)C7orf77
Genetics Home Reference (NIH)C7orf77
Genomic and cartography
GoldenPath hg38 (UCSC)C7orf77  -     chr7:124777292-124790810 -  7q31.33   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)C7orf77  -     7q31.33   [Description]    (hg19-Feb_2009)
EnsemblC7orf77 - 7q31.33 [CytoView hg19]  C7orf77 - 7q31.33 [CytoView hg38]
Mapping of homologs : NCBIC7orf77 [Mapview hg19]  C7orf77 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC130600 BC130604
RefSeq transcript (Entrez)NM_001024603
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)C7orf77
Cluster EST : UnigeneHs.444163 [ NCBI ]
CGAP (NCI)Hs.444163
Alternative Splicing GalleryENSG00000275356
Gene ExpressionC7orf77 [ NCBI-GEO ]   C7orf77 [ EBI - ARRAY_EXPRESS ]   C7orf77 [ SEEK ]   C7orf77 [ MEM ]
Gene Expression Viewer (FireBrowse)C7orf77 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)154872
GTEX Portal (Tissue expression)C7orf77
Protein : pattern, domain, 3D structure
UniProt/SwissProtA4D0Y5   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtA4D0Y5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProA4D0Y5
Splice isoforms : SwissVarA4D0Y5
PhosPhoSitePlusA4D0Y5
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)C7orf77
DMDM Disease mutations154872
Blocks (Seattle)C7orf77
SuperfamilyA4D0Y5
Human Protein AtlasENSG00000275356
Peptide AtlasA4D0Y5
HPRD18562
IPIIPI00081562   
Protein Interaction databases
DIP (DOE-UCLA)A4D0Y5
IntAct (EBI)A4D0Y5
FunCoupENSG00000275356
BioGRIDC7orf77
STRING (EMBL)C7orf77
ZODIACC7orf77
Ontologies - Pathways
QuickGOA4D0Y5
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkC7orf77
Atlas of Cancer Signalling NetworkC7orf77
Wikipedia pathwaysC7orf77
Orthology - Evolution
OrthoDB154872
GeneTree (enSembl)ENSG00000275356
Phylogenetic Trees/Animal Genes : TreeFamC7orf77
HOVERGENA4D0Y5
HOGENOMA4D0Y5
Homologs : HomoloGeneC7orf77
Homology/Alignments : Family Browser (UCSC)C7orf77
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerC7orf77 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)C7orf77
dbVarC7orf77
ClinVarC7orf77
1000_GenomesC7orf77 
Exome Variant ServerC7orf77
ExAC (Exome Aggregation Consortium)C7orf77 (select the gene name)
Genetic variants : HAPMAP154872
Genomic Variants (DGV)C7orf77 [DGVbeta]
DECIPHERC7orf77 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisC7orf77 
Mutations
ICGC Data PortalC7orf77 
TCGA Data PortalC7orf77 
Broad Tumor PortalC7orf77
OASIS PortalC7orf77 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDC7orf77
BioMutasearch C7orf77
DgiDB (Drug Gene Interaction Database)C7orf77
DoCM (Curated mutations)C7orf77 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)C7orf77 (select a term)
intoGenC7orf77
Cancer3DC7orf77(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenC7orf77
Genetic Testing Registry C7orf77
NextProtA4D0Y5 [Medical]
TSGene154872
GENETestsC7orf77
Target ValidationC7orf77
Huge Navigator C7orf77 [HugePedia]
snp3D : Map Gene to Disease154872
BioCentury BCIQC7orf77
ClinGenC7orf77
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD154872
Clinical trialC7orf77
Miscellaneous
canSAR (ICR)C7orf77 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineC7orf77
EVEXC7orf77
GoPubMedC7orf77
iHOPC7orf77
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 : Wed Jun 7 15:41:34 CEST 2017

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