| Nomenclature |
|---|
| HGNC (Hugo) | ZNF146 12931 |
| Cards |
|---|
| Atlas | OZFID267 |
| Entrez_Gene (NCBI) | ZNF146 7705 zinc finger protein 146 |
| Aliases | OZF |
| GeneCards (Weizmann) | ZNF146 |
| Ensembl hg19 (Hinxton) | ENSG00000167635 [Gene_View] |
| Ensembl hg38 (Hinxton) | ENSG00000167635 [Gene_View] ENSG00000167635 [Sequence] chr19:36214602-36238773 [Contig_View] ZNF146 [Vega] |
| ICGC DataPortal | ENSG00000167635 |
| TCGA cBioPortal | ZNF146 |
| AceView (NCBI) | ZNF146 |
| Genatlas (Paris) | ZNF146 |
| WikiGenes | 7705 |
| SOURCE (Princeton) | ZNF146 |
| Genetics Home Reference (NIH) | ZNF146 |
| Genomic and cartography |
|---|
| GoldenPath hg38 (UCSC) | ZNF146 - chr19:36214602-36238773 + 19q13.12 [Description] (hg38-Dec_2013) |
| GoldenPath hg19 (UCSC) | ZNF146 - 19q13.12 [Description] (hg19-Feb_2009) |
| Ensembl | ZNF146 - 19q13.12 [CytoView hg19] ZNF146 - 19q13.12 [CytoView hg38] |
| Mapping of homologs : NCBI | ZNF146 [Mapview hg19] ZNF146 [Mapview hg38] |
| OMIM | 601505 |
| Gene and transcription |
|---|
| Genbank (Entrez) | AI039686 AK311486 AK313460 BC005154 BC065568 |
| RefSeq transcript (Entrez) | NM_001099638 NM_001099639 NM_007145 |
| RefSeq genomic (Entrez) | |
| Consensus coding sequences : CCDS (NCBI) | ZNF146 |
| Cluster EST : Unigene | Hs.643436 [ NCBI ] |
| CGAP (NCI) | Hs.643436 |
| Alternative Splicing Gallery | ENSG00000167635 |
| Gene Expression | ZNF146 [ NCBI-GEO ] ZNF146 [ EBI - ARRAY_EXPRESS ]
ZNF146 [ SEEK ] ZNF146 [ MEM ] |
| Gene Expression Viewer (FireBrowse) | ZNF146 [ Firebrowse - Broad ] |
| SOURCE (Princeton) | Expression in : [Datasets] [Normal Tissue Atlas] [carcinoma Classsification] [NCI60] |
| Genevestigator | Expression in : [tissues] [cell-lines] [cancer] [perturbations] |
| BioGPS (Tissue expression) | 7705 |
| GTEX Portal (Tissue expression) | ZNF146 |
| Human Protein Atlas | ENSG00000167635-ZNF146 [pathology] [cell] [tissue] |
| Protein : pattern, domain, 3D structure |
|---|
| UniProt/SwissProt | Q15072 [function] [subcellular_location] [family_and_domains] [pathology_and_biotech] [ptm_processing] [expression] [interaction] |
| NextProt | Q15072 [Sequence] [Exons] [Medical] [Publications] |
| With graphics : InterPro | Q15072 |
| Splice isoforms : SwissVar | Q15072 |
| PhosPhoSitePlus | Q15072 |
| Domaine pattern : Prosite (Expaxy) | ZINC_FINGER_C2H2_1 (PS00028) ZINC_FINGER_C2H2_2 (PS50157) |
| Domains : Interpro (EBI) | Znf_C2H2_sf Znf_C2H2_type |
| Domain families : Pfam (Sanger) | |
| Domain families : Pfam (NCBI) | |
| Domain families : Smart (EMBL) | ZnF_C2H2 (SM00355) |
| Conserved Domain (NCBI) | ZNF146 |
| DMDM Disease mutations | 7705 |
| Blocks (Seattle) | ZNF146 |
| Superfamily | Q15072 |
| Human Protein Atlas [tissue] | ENSG00000167635-ZNF146 [tissue] |
| Peptide Atlas | Q15072 |
| HPRD | 03296 |
| IPI | IPI00014305 |
| Protein Interaction databases |
|---|
| DIP (DOE-UCLA) | Q15072 |
| IntAct (EBI) | Q15072 |
| FunCoup | ENSG00000167635 |
| BioGRID | ZNF146 |
| STRING (EMBL) | ZNF146 |
| ZODIAC | ZNF146 |
| Ontologies - Pathways |
|---|
| QuickGO | Q15072 |
| Ontology : AmiGO | DNA-binding transcription factor activity, RNA polymerase II-specific DNA-binding transcription factor activity, RNA polymerase II-specific DNA binding nucleus nucleolus cytosol regulation of transcription, DNA-templated regulation of transcription by RNA polymerase II heparin binding zinc ion binding |
| Ontology : EGO-EBI | DNA-binding transcription factor activity, RNA polymerase II-specific DNA-binding transcription factor activity, RNA polymerase II-specific DNA binding nucleus nucleolus cytosol regulation of transcription, DNA-templated regulation of transcription by RNA polymerase II heparin binding zinc ion binding |
| NDEx Network | ZNF146 |
| Atlas of Cancer Signalling Network | ZNF146 |
| Wikipedia pathways | ZNF146 |
| Orthology - Evolution |
|---|
| OrthoDB | 7705 |
| GeneTree (enSembl) | ENSG00000167635 |
| Phylogenetic Trees/Animal Genes : TreeFam | ZNF146 |
| HOGENOM | Q15072 |
| Homologs : HomoloGene | ZNF146 |
| Homology/Alignments : Family Browser (UCSC) | ZNF146 |
| Gene fusions - Rearrangements |
|---|
| Fusion : Mitelman | ZNF146/NCAM2 [19q13.12/21q21.1] |
| Fusion Portal | ZNF146 19q13.12 AD000671.1 LGG |
| Fusion Portal | ZNF146 19q13.12 NCAM2 21q21.1 LUAD |
| Fusion : Quiver | ZNF146 |
| Polymorphisms : SNP and Copy number variants |
|---|
| NCBI Variation Viewer | ZNF146 [hg38] |
| dbSNP Single Nucleotide Polymorphism (NCBI) | ZNF146 |
| dbVar | ZNF146 |
| ClinVar | ZNF146 |
| 1000_Genomes | ZNF146 |
| Exome Variant Server | ZNF146 |
| ExAC (Exome Aggregation Consortium) | ENSG00000167635 |
| GNOMAD Browser | ENSG00000167635 |
| Varsome Browser | ZNF146 |
| Genetic variants : HAPMAP | 7705 |
| Genomic Variants (DGV) | ZNF146 [DGVbeta] |
| DECIPHER | ZNF146 [patients] [syndromes] [variants] [genes] |
| CONAN: Copy Number Analysis | ZNF146 |
| Mutations |
|---|
| ICGC Data Portal | ZNF146 |
| TCGA Data Portal | ZNF146 |
| Broad Tumor Portal | ZNF146 |
| OASIS Portal | ZNF146 [ Somatic mutations - Copy number] |
| Somatic Mutations in Cancer : COSMIC | ZNF146 [overview] [genome browser] [tissue] [distribution] |
| Mutations and Diseases : HGMD | ZNF146 |
| 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 ZNF146 |
| DgiDB (Drug Gene Interaction Database) | ZNF146 |
| DoCM (Curated mutations) | ZNF146 (select the gene name) |
| CIViC (Clinical Interpretations of Variants in Cancer) | ZNF146 (select a term) |
| intoGen | ZNF146 |
| NCG5 (London) | ZNF146 |
| Cancer3D | ZNF146(select the gene name) |
| Impact of mutations | [PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser] |
| Diseases |
|---|
| OMIM | 601505 |
| Orphanet | |
| DisGeNET | ZNF146 |
| Medgen | ZNF146 |
| Genetic Testing Registry | ZNF146
|
| NextProt | Q15072 [Medical] |
| TSGene | 7705 |
| GENETests | ZNF146 |
| Target Validation | ZNF146 |
| Huge Navigator |
ZNF146 [HugePedia] |
| snp3D : Map Gene to Disease | 7705 |
| BioCentury BCIQ | ZNF146 |
| ClinGen | ZNF146 |
| Clinical trials, drugs, therapy |
|---|
| Chemical/Protein Interactions : CTD | 7705 |
| Chemical/Pharm GKB Gene | PA37518 |
| Clinical trial | ZNF146 |
| Miscellaneous |
|---|
| canSAR (ICR) | ZNF146 (select the gene name) |
| DataMed Index | ZNF146 |
| Probes |
|---|
| Litterature |
|---|
| PubMed | 23 Pubmed reference(s) in Entrez |
| GeneRIFs | Gene References Into Functions (Entrez) |
| CoreMine | ZNF146 |
| EVEX | ZNF146 |
| GoPubMed | ZNF146 |
| iHOP | ZNF146 |
