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ZNF691 (zinc finger protein 691)

Identity

Alias_symbol (synonym)Zfp691
Other alias
HGNC (Hugo) ZNF691
LocusID (NCBI) 51058
Atlas_Id 76335
Location 1p34.2  [Link to chromosome band 1p34]
Location_base_pair Starts at 43312244 and ends at 43318146 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
SLCO4A1 (20q13.33) / ZNF691 (1p34.2)ZNF691 (1p34.2) / GNS (12q14.3)

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)ZNF691   28028
Cards
Entrez_Gene (NCBI)ZNF691  51058  zinc finger protein 691
AliasesZfp691
GeneCards (Weizmann)ZNF691
Ensembl hg19 (Hinxton)ENSG00000164011 [Gene_View]  chr1:43312244-43318146 [Contig_View]  ZNF691 [Vega]
Ensembl hg38 (Hinxton)ENSG00000164011 [Gene_View]  chr1:43312244-43318146 [Contig_View]  ZNF691 [Vega]
ICGC DataPortalENSG00000164011
TCGA cBioPortalZNF691
AceView (NCBI)ZNF691
Genatlas (Paris)ZNF691
WikiGenes51058
SOURCE (Princeton)ZNF691
Genetics Home Reference (NIH)ZNF691
Genomic and cartography
GoldenPath hg19 (UCSC)ZNF691  -     chr1:43312244-43318146 +  1p34.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)ZNF691  -     1p34.2   [Description]    (hg38-Dec_2013)
EnsemblZNF691 - 1p34.2 [CytoView hg19]  ZNF691 - 1p34.2 [CytoView hg38]
Mapping of homologs : NCBIZNF691 [Mapview hg19]  ZNF691 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF131739 AK000938 AK296201 BC000157 BM741761
RefSeq transcript (Entrez)NM_001242739 NM_015911
RefSeq genomic (Entrez)NC_000001 NC_018912 NT_032977 NW_004929290
Consensus coding sequences : CCDS (NCBI)ZNF691
Cluster EST : UnigeneHs.745530 [ NCBI ]
CGAP (NCI)Hs.745530
Alternative Splicing GalleryENSG00000164011
Gene ExpressionZNF691 [ NCBI-GEO ]   ZNF691 [ EBI - ARRAY_EXPRESS ]   ZNF691 [ SEEK ]   ZNF691 [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF691 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)51058
GTEX Portal (Tissue expression)ZNF691
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5VV52   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5VV52  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5VV52
Splice isoforms : SwissVarQ5VV52
PhosPhoSitePlusQ5VV52
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)ZNF691
DMDM Disease mutations51058
Blocks (Seattle)ZNF691
SuperfamilyQ5VV52
Human Protein AtlasENSG00000164011
Peptide AtlasQ5VV52
HPRD14229
IPIIPI00395807   IPI00301583   IPI00642841   IPI00478751   
Protein Interaction databases
DIP (DOE-UCLA)Q5VV52
IntAct (EBI)Q5VV52
FunCoupENSG00000164011
BioGRIDZNF691
STRING (EMBL)ZNF691
ZODIACZNF691
Ontologies - Pathways
QuickGOQ5VV52
Ontology : AmiGODNA binding  nucleus  metal ion binding  
Ontology : EGO-EBIDNA binding  nucleus  metal ion binding  
NDEx NetworkZNF691
Atlas of Cancer Signalling NetworkZNF691
Wikipedia pathwaysZNF691
Orthology - Evolution
OrthoDB51058
GeneTree (enSembl)ENSG00000164011
Phylogenetic Trees/Animal Genes : TreeFamZNF691
HOVERGENQ5VV52
HOGENOMQ5VV52
Homologs : HomoloGeneZNF691
Homology/Alignments : Family Browser (UCSC)ZNF691
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF691 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF691
dbVarZNF691
ClinVarZNF691
1000_GenomesZNF691 
Exome Variant ServerZNF691
ExAC (Exome Aggregation Consortium)ZNF691 (select the gene name)
Genetic variants : HAPMAP51058
Genomic Variants (DGV)ZNF691 [DGVbeta]
DECIPHER (Syndromes)1:43312244-43318146  ENSG00000164011
CONAN: Copy Number AnalysisZNF691 
Mutations
ICGC Data PortalZNF691 
TCGA Data PortalZNF691 
Broad Tumor PortalZNF691
OASIS PortalZNF691 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICZNF691  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDZNF691
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch ZNF691
DgiDB (Drug Gene Interaction Database)ZNF691
DoCM (Curated mutations)ZNF691 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF691 (select a term)
intoGenZNF691
Cancer3DZNF691(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenZNF691
Genetic Testing Registry ZNF691
NextProtQ5VV52 [Medical]
TSGene51058
GENETestsZNF691
Huge Navigator ZNF691 [HugePedia]
snp3D : Map Gene to Disease51058
BioCentury BCIQZNF691
ClinGenZNF691
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD51058
Chemical/Pharm GKB GenePA142670490
Clinical trialZNF691
Miscellaneous
canSAR (ICR)ZNF691 (select the gene name)
Probes
Litterature
PubMed9 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF691
EVEXZNF691
GoPubMedZNF691
iHOPZNF691
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 12:53:40 CET 2017

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