| Nomenclature |
HGNC (Hugo) | ZNF19 12981 |
| Cards |
Entrez_Gene (NCBI) | ZNF19 7567 zinc finger protein 19 |
Aliases | KOX12 |
GeneCards (Weizmann) | ZNF19 |
Ensembl hg19 (Hinxton) | ENSG00000157429 [Gene_View] |
Ensembl hg38 (Hinxton) | ENSG00000157429 [Gene_View]  ENSG00000157429 [Sequence] chr16:71474073-71489351 [Contig_View] ZNF19 [Vega] |
ICGC DataPortal | ENSG00000157429 |
TCGA cBioPortal | ZNF19 |
AceView (NCBI) | ZNF19 |
Genatlas (Paris) | ZNF19 |
WikiGenes | 7567 |
SOURCE (Princeton) | ZNF19 |
Genetics Home Reference (NIH) | ZNF19 |
| Genomic and cartography |
GoldenPath hg38 (UCSC) | ZNF19 - chr16:71474073-71489351 - 16q22.2 [Description] (hg38-Dec_2013) |
GoldenPath hg19 (UCSC) | ZNF19 - 16q22.2 [Description] (hg19-Feb_2009) |
Ensembl | ZNF19 - 16q22.2 [CytoView hg19] ZNF19 - 16q22.2 [CytoView hg38] |
Mapping of homologs : NCBI | ZNF19 [Mapview hg19] ZNF19 [Mapview hg38] |
OMIM | 194525 |
| Gene and transcription |
Genbank (Entrez) | AK055567 AK057330 AK292260 AK311003 AL834237 |
RefSeq transcript (Entrez) | NM_006961 |
RefSeq genomic (Entrez) | |
Consensus coding sequences : CCDS (NCBI) | ZNF19 |
Cluster EST : Unigene | Hs.660076 [ NCBI ] |
CGAP (NCI) | Hs.660076 |
Alternative Splicing Gallery | ENSG00000157429 |
Gene Expression | ZNF19 [ NCBI-GEO ] ZNF19 [ EBI - ARRAY_EXPRESS ]
ZNF19 [ SEEK ] ZNF19 [ MEM ] |
Gene Expression Viewer (FireBrowse) | ZNF19 [ Firebrowse - Broad ] |
SOURCE (Princeton) | Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60] |
Genevestigator | Expression in : [tissues]  [cell-lines]  [cancer]  [perturbations]   |
BioGPS (Tissue expression) | 7567 |
GTEX Portal (Tissue expression) | ZNF19 |
Human Protein Atlas | ENSG00000157429-ZNF19 [pathology] [cell] [tissue] |
| Protein : pattern, domain, 3D structure |
UniProt/SwissProt | P17023 [function] [subcellular_location] [family_and_domains] [pathology_and_biotech] [ptm_processing] [expression] [interaction] |
NextProt | P17023 [Sequence] [Exons] [Medical] [Publications] |
With graphics : InterPro | P17023 |
Splice isoforms : SwissVar | P17023 |
PhosPhoSitePlus | P17023 |
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) |
Domain families : Pfam (NCBI) | pfam01352 pfam00096 |
Domain families : Smart (EMBL) | KRAB (SM00349) ZnF_C2H2 (SM00355) |
Conserved Domain (NCBI) | ZNF19 |
DMDM Disease mutations | 7567 |
Blocks (Seattle) | ZNF19 |
Superfamily | P17023 |
Human Protein Atlas [tissue] | ENSG00000157429-ZNF19 [tissue] |
Peptide Atlas | P17023 |
HPRD | 01914 |
IPI | IPI00012358 IPI00643896 |
| Protein Interaction databases |
DIP (DOE-UCLA) | P17023 |
IntAct (EBI) | P17023 |
FunCoup | ENSG00000157429 |
BioGRID | ZNF19 |
STRING (EMBL) | ZNF19 |
ZODIAC | ZNF19 |
| Ontologies - Pathways |
QuickGO | P17023 |
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 | ZNF19 |
Atlas of Cancer Signalling Network | ZNF19 |
Wikipedia pathways | ZNF19 |
| Orthology - Evolution |
OrthoDB | 7567 |
GeneTree (enSembl) | ENSG00000157429 |
Phylogenetic Trees/Animal Genes : TreeFam | ZNF19 |
HOGENOM | P17023 |
Homologs : HomoloGene | ZNF19 |
Homology/Alignments : Family Browser (UCSC) | ZNF19 |
| Gene fusions - Rearrangements |
Fusion : Quiver | ZNF19 |
| Polymorphisms : SNP and Copy number variants |
NCBI Variation Viewer | ZNF19 [hg38] |
dbSNP Single Nucleotide Polymorphism (NCBI) | ZNF19 |
dbVar | ZNF19 |
ClinVar | ZNF19 |
1000_Genomes | ZNF19 |
Exome Variant Server | ZNF19 |
ExAC (Exome Aggregation Consortium) | ENSG00000157429 |
GNOMAD Browser | ENSG00000157429 |
Varsome Browser | ZNF19 |
Genetic variants : HAPMAP | 7567 |
Genomic Variants (DGV) | ZNF19 [DGVbeta] |
DECIPHER | ZNF19 [patients] [syndromes] [variants] [genes] |
CONAN: Copy Number Analysis | ZNF19 |
| Mutations |
ICGC Data Portal | ZNF19 |
TCGA Data Portal | ZNF19 |
Broad Tumor Portal | ZNF19 |
OASIS Portal | ZNF19 [ Somatic mutations - Copy number] |
Somatic Mutations in Cancer : COSMIC | ZNF19 [overview] [genome browser] [tissue] [distribution] |
Mutations and Diseases : HGMD | ZNF19 |
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 ZNF19 |
DgiDB (Drug Gene Interaction Database) | ZNF19 |
DoCM (Curated mutations) | ZNF19 (select the gene name) |
CIViC (Clinical Interpretations of Variants in Cancer) | ZNF19 (select a term) |
intoGen | ZNF19 |
Cancer3D | ZNF19(select the gene name) |
Impact of mutations | [PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser] |
| Diseases |
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OMIM | 194525 |
Orphanet | |
DisGeNET | ZNF19 |
Medgen | ZNF19 |
Genetic Testing Registry | ZNF19
|
NextProt | P17023 [Medical] |
TSGene | 7567 |
GENETests | ZNF19 |
Target Validation | ZNF19 |
Huge Navigator |
ZNF19 [HugePedia] |
snp3D : Map Gene to Disease | 7567 |
BioCentury BCIQ | ZNF19 |
ClinGen | ZNF19 |
| Clinical trials, drugs, therapy |
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Chemical/Protein Interactions : CTD | 7567 |
Chemical/Pharm GKB Gene | PA37562 |
Clinical trial | ZNF19 |
| Miscellaneous |
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canSAR (ICR) | ZNF19 (select the gene name) |
DataMed Index | ZNF19 |
| Probes |
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| Litterature |
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PubMed | 11 Pubmed reference(s) in Entrez |
GeneRIFs | Gene References Into Functions (Entrez) |
CoreMine | ZNF19 |
EVEX | ZNF19 |
GoPubMed | ZNF19 |
iHOP | ZNF19 |