| Nomenclature |
HGNC (Hugo) | ZNF429 20817 |
| Cards |
Entrez_Gene (NCBI) | ZNF429 353088 zinc finger protein 429 |
Aliases | |
GeneCards (Weizmann) | ZNF429 |
Ensembl hg19 (Hinxton) | ENSG00000197013 [Gene_View] |
Ensembl hg38 (Hinxton) | ENSG00000197013 [Gene_View] chr19:21505552-21540667 [Contig_View] ZNF429 [Vega] |
ICGC DataPortal | ENSG00000197013 |
TCGA cBioPortal | ZNF429 |
AceView (NCBI) | ZNF429 |
Genatlas (Paris) | ZNF429 |
WikiGenes | 353088 |
SOURCE (Princeton) | ZNF429 |
Genetics Home Reference (NIH) | ZNF429 |
| Genomic and cartography |
GoldenPath hg38 (UCSC) | ZNF429 - chr19:21505552-21540667 + 19p12 [Description] (hg38-Dec_2013) |
GoldenPath hg19 (UCSC) | ZNF429 - 19p12 [Description] (hg19-Feb_2009) |
Ensembl | ZNF429 - 19p12 [CytoView hg19] ZNF429 - 19p12 [CytoView hg38] |
Mapping of homologs : NCBI | ZNF429 [Mapview hg19] ZNF429 [Mapview hg38] |
| Gene and transcription |
Genbank (Entrez) | AF325191 AK057495 AK308708 AY269786 BC156455 |
RefSeq transcript (Entrez) | NM_001001415 NM_001346912 NM_001346913 NM_001346914 NM_001346915 NM_001346916 |
RefSeq genomic (Entrez) | |
Consensus coding sequences : CCDS (NCBI) | ZNF429 |
Cluster EST : Unigene | Hs.709598 [ NCBI ] |
CGAP (NCI) | Hs.709598 |
Alternative Splicing Gallery | ENSG00000197013 |
Gene Expression | ZNF429 [ NCBI-GEO ] ZNF429 [ EBI - ARRAY_EXPRESS ]
ZNF429 [ SEEK ] ZNF429 [ MEM ] |
Gene Expression Viewer (FireBrowse) | ZNF429 [ Firebrowse - Broad ] |
SOURCE (Princeton) | Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60] |
Genevestigator | Expression in : [tissues]  [cell-lines]  [cancer]  [perturbations]   |
BioGPS (Tissue expression) | 353088 |
GTEX Portal (Tissue expression) | ZNF429 |
Human Protein Atlas | ENSG00000197013-ZNF429 [pathology] [cell] [tissue] |
| Protein : pattern, domain, 3D structure |
UniProt/SwissProt | Q86V71 [function] [subcellular_location] [family_and_domains] [pathology_and_biotech] [ptm_processing] [expression] [interaction] |
NextProt | Q86V71 [Sequence] [Exons] [Medical] [Publications] |
With graphics : InterPro | Q86V71 |
Splice isoforms : SwissVar | Q86V71 |
PhosPhoSitePlus | Q86V71 |
Domaine pattern : Prosite (Expaxy) | KRAB (PS50805) ZINC_FINGER_C2H2_1 (PS00028) ZINC_FINGER_C2H2_2 (PS50157) |
Domains : Interpro (EBI) | KRAB Znf_C2H2 Znf_C2H2-like Znf_C2H2/integrase_DNA-bd |
Domain families : Pfam (Sanger) | KRAB (PF01352) zf-C2H2 (PF00096) zf-C2H2_6 (PF13912) |
Domain families : Pfam (NCBI) | pfam01352 pfam00096 pfam13912 |
Domain families : Smart (EMBL) | KRAB (SM00349) ZnF_C2H2 (SM00355) |
Conserved Domain (NCBI) | ZNF429 |
DMDM Disease mutations | 353088 |
Blocks (Seattle) | ZNF429 |
Superfamily | Q86V71 |
Human Protein Atlas [tissue] | ENSG00000197013-ZNF429 [tissue] |
Peptide Atlas | Q86V71 |
HPRD | 18342 |
IPI | IPI00871958 |
| Protein Interaction databases |
DIP (DOE-UCLA) | Q86V71 |
IntAct (EBI) | Q86V71 |
FunCoup | ENSG00000197013 |
BioGRID | ZNF429 |
STRING (EMBL) | ZNF429 |
ZODIAC | ZNF429 |
| Ontologies - Pathways |
QuickGO | Q86V71 |
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 | ZNF429 |
Atlas of Cancer Signalling Network | ZNF429 |
Wikipedia pathways | ZNF429 |
| Orthology - Evolution |
OrthoDB | 353088 |
GeneTree (enSembl) | ENSG00000197013 |
Phylogenetic Trees/Animal Genes : TreeFam | ZNF429 |
HOVERGEN | Q86V71 |
HOGENOM | Q86V71 |
Homologs : HomoloGene | ZNF429 |
Homology/Alignments : Family Browser (UCSC) | ZNF429 |
| Gene fusions - Rearrangements |
Fusion : Quiver | ZNF429 |
| Polymorphisms : SNP and Copy number variants |
NCBI Variation Viewer | ZNF429 [hg38] |
dbSNP Single Nucleotide Polymorphism (NCBI) | ZNF429 |
dbVar | ZNF429 |
ClinVar | ZNF429 |
1000_Genomes | ZNF429 |
Exome Variant Server | ZNF429 |
ExAC (Exome Aggregation Consortium) | ENSG00000197013 |
GNOMAD Browser | ENSG00000197013 |
Genetic variants : HAPMAP | 353088 |
Genomic Variants (DGV) | ZNF429 [DGVbeta] |
DECIPHER | ZNF429 [patients] [syndromes] [variants] [genes] |
CONAN: Copy Number Analysis | ZNF429 |
| Mutations |
ICGC Data Portal | ZNF429 |
TCGA Data Portal | ZNF429 |
Broad Tumor Portal | ZNF429 |
OASIS Portal | ZNF429 [ Somatic mutations - Copy number] |
Somatic Mutations in Cancer : COSMIC | ZNF429 [overview] [genome browser] [tissue] [distribution] |
Mutations and Diseases : HGMD | ZNF429 |
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 ZNF429 |
DgiDB (Drug Gene Interaction Database) | ZNF429 |
DoCM (Curated mutations) | ZNF429 (select the gene name) |
CIViC (Clinical Interpretations of Variants in Cancer) | ZNF429 (select a term) |
intoGen | ZNF429 |
Cancer3D | ZNF429(select the gene name) |
Impact of mutations | [PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser] |
| Diseases |
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OMIM | |
Orphanet | |
DisGeNET | ZNF429 |
Medgen | ZNF429 |
Genetic Testing Registry | ZNF429
|
NextProt | Q86V71 [Medical] |
TSGene | 353088 |
GENETests | ZNF429 |
Target Validation | ZNF429 |
Huge Navigator |
ZNF429 [HugePedia] |
snp3D : Map Gene to Disease | 353088 |
BioCentury BCIQ | ZNF429 |
ClinGen | ZNF429 |
| Clinical trials, drugs, therapy |
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Chemical/Protein Interactions : CTD | 353088 |
Chemical/Pharm GKB Gene | PA134910790 |
Clinical trial | ZNF429 |
| Miscellaneous |
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canSAR (ICR) | ZNF429 (select the gene name) |
| Probes |
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| Litterature |
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PubMed | 5 Pubmed reference(s) in Entrez |
GeneRIFs | Gene References Into Functions (Entrez) |
CoreMine | ZNF429 |
EVEX | ZNF429 |
GoPubMed | ZNF429 |
iHOP | ZNF429 |