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ZNF775 (zinc finger protein 775)

Identity

Alias_symbol (synonym)MGC33584
Other alias-
HGNC (Hugo) ZNF775
LocusID (NCBI) 285971
Atlas_Id 76393
Location 7q36.1  [Link to chromosome band 7q36]
Location_base_pair Starts at 150379317 and ends at 150398631 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)ZNF775   28501
Cards
Entrez_Gene (NCBI)ZNF775  285971  zinc finger protein 775
Aliases
GeneCards (Weizmann)ZNF775
Ensembl hg19 (Hinxton)ENSG00000196456 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000196456 [Gene_View]  chr7:150379317-150398631 [Contig_View]  ZNF775 [Vega]
ICGC DataPortalENSG00000196456
TCGA cBioPortalZNF775
AceView (NCBI)ZNF775
Genatlas (Paris)ZNF775
WikiGenes285971
SOURCE (Princeton)ZNF775
Genetics Home Reference (NIH)ZNF775
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF775  -     chr7:150379317-150398631 +  7q36.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF775  -     7q36.1   [Description]    (hg19-Feb_2009)
EnsemblZNF775 - 7q36.1 [CytoView hg19]  ZNF775 - 7q36.1 [CytoView hg38]
Mapping of homologs : NCBIZNF775 [Mapview hg19]  ZNF775 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AW402889 BC015152 BC038111 DB472309
RefSeq transcript (Entrez)NM_173680
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ZNF775
Cluster EST : UnigeneHs.655734 [ NCBI ]
CGAP (NCI)Hs.655734
Alternative Splicing GalleryENSG00000196456
Gene ExpressionZNF775 [ NCBI-GEO ]   ZNF775 [ EBI - ARRAY_EXPRESS ]   ZNF775 [ SEEK ]   ZNF775 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF775 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)285971
GTEX Portal (Tissue expression)ZNF775
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96BV0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96BV0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96BV0
Splice isoforms : SwissVarQ96BV0
PhosPhoSitePlusQ96BV0
Domaine pattern : Prosite (Expaxy)ZINC_FINGER_C2H2_1 (PS00028)    ZINC_FINGER_C2H2_2 (PS50157)   
Domains : Interpro (EBI)Znf_C2H2    Znf_C2H2-like    Znf_C2H2/integrase_DNA-bd   
Domain families : Pfam (Sanger)zf-C2H2 (PF00096)   
Domain families : Pfam (NCBI)pfam00096   
Domain families : Smart (EMBL)ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)ZNF775
DMDM Disease mutations285971
Blocks (Seattle)ZNF775
SuperfamilyQ96BV0
Human Protein AtlasENSG00000196456
Peptide AtlasQ96BV0
HPRD14567
IPIIPI00060265   IPI00947219   IPI00946740   
Protein Interaction databases
DIP (DOE-UCLA)Q96BV0
IntAct (EBI)Q96BV0
FunCoupENSG00000196456
BioGRIDZNF775
STRING (EMBL)ZNF775
ZODIACZNF775
Ontologies - Pathways
QuickGOQ96BV0
Ontology : AmiGODNA binding  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  metal ion binding  
Ontology : EGO-EBIDNA binding  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  metal ion binding  
NDEx NetworkZNF775
Atlas of Cancer Signalling NetworkZNF775
Wikipedia pathwaysZNF775
Orthology - Evolution
OrthoDB285971
GeneTree (enSembl)ENSG00000196456
Phylogenetic Trees/Animal Genes : TreeFamZNF775
HOVERGENQ96BV0
HOGENOMQ96BV0
Homologs : HomoloGeneZNF775
Homology/Alignments : Family Browser (UCSC)ZNF775
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF775 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF775
dbVarZNF775
ClinVarZNF775
1000_GenomesZNF775 
Exome Variant ServerZNF775
ExAC (Exome Aggregation Consortium)ZNF775 (select the gene name)
Genetic variants : HAPMAP285971
Genomic Variants (DGV)ZNF775 [DGVbeta]
DECIPHERZNF775 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF775 
Mutations
ICGC Data PortalZNF775 
TCGA Data PortalZNF775 
Broad Tumor PortalZNF775
OASIS PortalZNF775 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF775  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDZNF775
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 ZNF775
DgiDB (Drug Gene Interaction Database)ZNF775
DoCM (Curated mutations)ZNF775 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF775 (select a term)
intoGenZNF775
Cancer3DZNF775(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenZNF775
Genetic Testing Registry ZNF775
NextProtQ96BV0 [Medical]
TSGene285971
GENETestsZNF775
Target ValidationZNF775
Huge Navigator ZNF775 [HugePedia]
snp3D : Map Gene to Disease285971
BioCentury BCIQZNF775
ClinGenZNF775
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD285971
Chemical/Pharm GKB GenePA162410371
Clinical trialZNF775
Miscellaneous
canSAR (ICR)ZNF775 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF775
EVEXZNF775
GoPubMedZNF775
iHOPZNF775
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:45:19 CEST 2017

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