| Nomenclature |
HGNC (Hugo) | ZNF623 29084 |
| Cards |
Entrez_Gene (NCBI) | ZNF623 9831 zinc finger protein 623 |
Aliases | |
GeneCards (Weizmann) | ZNF623 |
Ensembl hg19 (Hinxton) | [Gene_View] |
Ensembl hg38 (Hinxton) | [Gene_View] chr8:143636162-143653730 [Contig_View] ZNF623 [Vega] |
TCGA cBioPortal | ZNF623 |
AceView (NCBI) | ZNF623 |
Genatlas (Paris) | ZNF623 |
WikiGenes | 9831 |
SOURCE (Princeton) | ZNF623 |
Genetics Home Reference (NIH) | ZNF623 |
| Genomic and cartography |
GoldenPath hg38 (UCSC) | ZNF623 - chr8:143636162-143653730 + 8q24.3 [Description] (hg38-Dec_2013) |
GoldenPath hg19 (UCSC) | ZNF623 - 8q24.3 [Description] (hg19-Feb_2009) |
Ensembl | ZNF623 - 8q24.3 [CytoView hg19] ZNF623 - 8q24.3 [CytoView hg38] |
Mapping of homologs : NCBI | ZNF623 [Mapview hg19] ZNF623 [Mapview hg38] |
| Gene and transcription |
Genbank (Entrez) | AB014528 AK294695 AW161801 BC067516 BC067517 |
RefSeq transcript (Entrez) | NM_001082480 NM_001261843 NM_014789 |
RefSeq genomic (Entrez) | NC_000008 NC_018919 NT_187571 |
Consensus coding sequences : CCDS (NCBI) | ZNF623 |
Cluster EST : Unigene | Hs.745418 [ NCBI ] |
CGAP (NCI) | Hs.745418 |
Gene Expression | ZNF623 [ NCBI-GEO ] ZNF623 [ EBI - ARRAY_EXPRESS ]
ZNF623 [ SEEK ] ZNF623 [ MEM ] |
Gene Expression Viewer (FireBrowse) | ZNF623 [ Firebrowse - Broad ] |
SOURCE (Princeton) | Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60] |
Genevestigator | Expression in : [tissues]  [cell-lines]  [cancer]  [perturbations]   |
BioGPS (Tissue expression) | 9831 |
GTEX Portal (Tissue expression) | ZNF623 |
| Protein : pattern, domain, 3D structure |
UniProt/SwissProt | O75123 [function] [subcellular_location] [family_and_domains] [pathology_and_biotech] [ptm_processing] [expression] [interaction] |
NextProt | O75123 [Sequence] [Exons] [Medical] [Publications] |
With graphics : InterPro | O75123 |
Splice isoforms : SwissVar | O75123 |
PhosPhoSitePlus | O75123 |
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) | ZNF623 |
DMDM Disease mutations | 9831 |
Blocks (Seattle) | ZNF623 |
Superfamily | O75123 |
Peptide Atlas | O75123 |
HPRD | 18358 |
IPI | IPI00006466 IPI00908573 IPI00829987 |
| Protein Interaction databases |
DIP (DOE-UCLA) | O75123 |
IntAct (EBI) | O75123 |
BioGRID | ZNF623 |
STRING (EMBL) | ZNF623 |
ZODIAC | ZNF623 |
| Ontologies - Pathways |
QuickGO | O75123 |
Ontology : AmiGO | DNA binding transcription factor activity, sequence-specific DNA binding nucleus transcription, DNA-templated regulation of transcription, DNA-templated metal ion binding |
Ontology : EGO-EBI | DNA binding transcription factor activity, sequence-specific DNA binding nucleus transcription, DNA-templated regulation of transcription, DNA-templated metal ion binding |
NDEx Network | ZNF623 |
Atlas of Cancer Signalling Network | ZNF623 |
Wikipedia pathways | ZNF623 |
| Orthology - Evolution |
OrthoDB | 9831 |
Phylogenetic Trees/Animal Genes : TreeFam | ZNF623 |
HOVERGEN | O75123 |
HOGENOM | O75123 |
Homologs : HomoloGene | ZNF623 |
Homology/Alignments : Family Browser (UCSC) | ZNF623 |
| Gene fusions - Rearrangements |
Fusion : Quiver | ZNF623 |
| Polymorphisms : SNP and Copy number variants |
NCBI Variation Viewer | ZNF623 [hg38] |
dbSNP Single Nucleotide Polymorphism (NCBI) | ZNF623 |
dbVar | ZNF623 |
ClinVar | ZNF623 |
1000_Genomes | ZNF623 |
Exome Variant Server | ZNF623 |
Genetic variants : HAPMAP | 9831 |
Genomic Variants (DGV) | ZNF623 [DGVbeta] |
DECIPHER | ZNF623 [patients] [syndromes] [variants] [genes] |
CONAN: Copy Number Analysis | ZNF623 |
| Mutations |
ICGC Data Portal | ZNF623 |
TCGA Data Portal | ZNF623 |
Broad Tumor Portal | ZNF623 |
OASIS Portal | ZNF623 [ Somatic mutations - Copy number] |
Somatic Mutations in Cancer : COSMIC | ZNF623 [overview] [genome browser] [tissue] [distribution] |
Mutations and Diseases : HGMD | ZNF623 |
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 |
BioMuta | search ZNF623 |
DgiDB (Drug Gene Interaction Database) | ZNF623 |
DoCM (Curated mutations) | ZNF623 (select the gene name) |
CIViC (Clinical Interpretations of Variants in Cancer) | ZNF623 (select a term) |
intoGen | ZNF623 |
Cancer3D | ZNF623(select the gene name) |
Impact of mutations | [PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser] |
| Diseases |
---|
OMIM | |
Orphanet | |
DisGeNET | ZNF623 |
Medgen | ZNF623 |
Genetic Testing Registry | ZNF623
|
NextProt | O75123 [Medical] |
TSGene | 9831 |
GENETests | ZNF623 |
Target Validation | ZNF623 |
Huge Navigator |
ZNF623 [HugePedia] |
snp3D : Map Gene to Disease | 9831 |
BioCentury BCIQ | ZNF623 |
ClinGen | ZNF623 |
| Clinical trials, drugs, therapy |
---|
Chemical/Protein Interactions : CTD | 9831 |
Chemical/Pharm GKB Gene | PA134969295 |
Clinical trial | ZNF623 |
| Miscellaneous |
---|
canSAR (ICR) | ZNF623 (select the gene name) |
| Probes |
---|
| Litterature |
---|
PubMed | 7 Pubmed reference(s) in Entrez |
GeneRIFs | Gene References Into Functions (Entrez) |
CoreMine | ZNF623 |
EVEX | ZNF623 |
GoPubMed | ZNF623 |
iHOP | ZNF623 |