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ZNF777 (zinc finger protein 777)

Identity

Alias_symbol (synonym)KIAA1285
Other alias-
HGNC (Hugo) ZNF777
LocusID (NCBI) 27153
Atlas_Id 76395
Location 7q36.1  [Link to chromosome band 7q36]
Location_base_pair Starts at 149128454 and ends at 149158053 bp from pter ( according to hg19-Feb_2009)

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)ZNF777   22213
Cards
Entrez_Gene (NCBI)ZNF777  27153  zinc finger protein 777
Aliases
GeneCards (Weizmann)ZNF777
Ensembl hg19 (Hinxton)ENSG00000196453 [Gene_View]  chr7:149128454-149158053 [Contig_View]  ZNF777 [Vega]
Ensembl hg38 (Hinxton)ENSG00000196453 [Gene_View]  chr7:149128454-149158053 [Contig_View]  ZNF777 [Vega]
ICGC DataPortalENSG00000196453
TCGA cBioPortalZNF777
AceView (NCBI)ZNF777
Genatlas (Paris)ZNF777
WikiGenes27153
SOURCE (Princeton)ZNF777
Genetics Home Reference (NIH)ZNF777
Genomic and cartography
GoldenPath hg19 (UCSC)ZNF777  -     chr7:149128454-149158053 -  7q36.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)ZNF777  -     7q36.1   [Description]    (hg38-Dec_2013)
EnsemblZNF777 - 7q36.1 [CytoView hg19]  ZNF777 - 7q36.1 [CytoView hg38]
Mapping of homologs : NCBIZNF777 [Mapview hg19]  ZNF777 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB033111 AK074515 AK075032 BC023985 BC105968
RefSeq transcript (Entrez)NM_015694
RefSeq genomic (Entrez)NC_000007 NC_018918 NT_007933 NW_004929333
Consensus coding sequences : CCDS (NCBI)ZNF777
Cluster EST : UnigeneHs.38512 [ NCBI ]
CGAP (NCI)Hs.38512
Alternative Splicing GalleryENSG00000196453
Gene ExpressionZNF777 [ NCBI-GEO ]   ZNF777 [ EBI - ARRAY_EXPRESS ]   ZNF777 [ SEEK ]   ZNF777 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF777 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)27153
GTEX Portal (Tissue expression)ZNF777
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9ULD5   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9ULD5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9ULD5
Splice isoforms : SwissVarQ9ULD5
PhosPhoSitePlusQ9ULD5
Domaine pattern : Prosite (Expaxy)KRAB (PS50805)    ZINC_FINGER_C2H2_1 (PS00028)    ZINC_FINGER_C2H2_2 (PS50157)   
Domains : Interpro (EBI)DUF3669_Znf    Krueppel-associated_box    Znf_C2H2    Znf_C2H2-like    Znf_C2H2/integrase_DNA-bd   
Domain families : Pfam (Sanger)DUF3669 (PF12417)    KRAB (PF01352)    zf-C2H2 (PF00096)   
Domain families : Pfam (NCBI)pfam12417    pfam01352    pfam00096   
Domain families : Smart (EMBL)KRAB (SM00349)  ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)ZNF777
DMDM Disease mutations27153
Blocks (Seattle)ZNF777
SuperfamilyQ9ULD5
Human Protein AtlasENSG00000196453
Peptide AtlasQ9ULD5
HPRD13849
IPIIPI00852944   IPI00401752   IPI00853640   IPI00181556   
Protein Interaction databases
DIP (DOE-UCLA)Q9ULD5
IntAct (EBI)Q9ULD5
FunCoupENSG00000196453
BioGRIDZNF777
STRING (EMBL)ZNF777
ZODIACZNF777
Ontologies - Pathways
QuickGOQ9ULD5
Ontology : AmiGOmolecular_function  DNA binding  cellular_component  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  biological_process  metal ion binding  
Ontology : EGO-EBImolecular_function  DNA binding  cellular_component  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  biological_process  metal ion binding  
NDEx NetworkZNF777
Atlas of Cancer Signalling NetworkZNF777
Wikipedia pathwaysZNF777
Orthology - Evolution
OrthoDB27153
GeneTree (enSembl)ENSG00000196453
Phylogenetic Trees/Animal Genes : TreeFamZNF777
HOVERGENQ9ULD5
HOGENOMQ9ULD5
Homologs : HomoloGeneZNF777
Homology/Alignments : Family Browser (UCSC)ZNF777
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF777 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF777
dbVarZNF777
ClinVarZNF777
1000_GenomesZNF777 
Exome Variant ServerZNF777
ExAC (Exome Aggregation Consortium)ZNF777 (select the gene name)
Genetic variants : HAPMAP27153
Genomic Variants (DGV)ZNF777 [DGVbeta]
DECIPHER (Syndromes)7:149128454-149158053  ENSG00000196453
CONAN: Copy Number AnalysisZNF777 
Mutations
ICGC Data PortalZNF777 
TCGA Data PortalZNF777 
Broad Tumor PortalZNF777
OASIS PortalZNF777 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF777  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDZNF777
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 ZNF777
DgiDB (Drug Gene Interaction Database)ZNF777
DoCM (Curated mutations)ZNF777 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF777 (select a term)
intoGenZNF777
Cancer3DZNF777(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenZNF777
Genetic Testing Registry ZNF777
NextProtQ9ULD5 [Medical]
TSGene27153
GENETestsZNF777
Huge Navigator ZNF777 [HugePedia]
snp3D : Map Gene to Disease27153
BioCentury BCIQZNF777
ClinGenZNF777
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD27153
Chemical/Pharm GKB GenePA162410383
Clinical trialZNF777
Miscellaneous
canSAR (ICR)ZNF777 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF777
EVEXZNF777
GoPubMedZNF777
iHOPZNF777
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:53:52 CET 2017

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