| Nomenclature |
|---|
| HGNC (Hugo) | ZNF818P 33265 |
| Cards |
|---|
| Entrez_Gene (NCBI) | ZNF818P 390963 zinc finger protein 818, pseudogene |
| Aliases | ZNF818 |
| GeneCards (Weizmann) | ZNF818P |
| Ensembl hg19 (Hinxton) | [Gene_View] |
| Ensembl hg38 (Hinxton) | [Gene_View] chr19:53212975-53216095 [Contig_View] ZNF818P [Vega] |
| TCGA cBioPortal | ZNF818P |
| AceView (NCBI) | ZNF818P |
| Genatlas (Paris) | ZNF818P |
| WikiGenes | 390963 |
| SOURCE (Princeton) | ZNF818P |
| Genetics Home Reference (NIH) | ZNF818P |
| Genomic and cartography |
|---|
| GoldenPath hg38 (UCSC) | ZNF818P - chr19:53212975-53216095 + 19q13.42 [Description] (hg38-Dec_2013) |
| GoldenPath hg19 (UCSC) | ZNF818P - 19q13.42 [Description] (hg19-Feb_2009) |
| Ensembl | ZNF818P - 19q13.42 [CytoView hg19] ZNF818P - 19q13.42 [CytoView hg38] |
| Mapping of homologs : NCBI | ZNF818P [Mapview hg19] ZNF818P [Mapview hg38] |
| Gene and transcription |
|---|
| Genbank (Entrez) | AK128250 BF908632 BG759674 GD137562 |
| RefSeq transcript (Entrez) | NM_001001675 |
| RefSeq genomic (Entrez) | |
| Consensus coding sequences : CCDS (NCBI) | ZNF818P |
| Cluster EST : Unigene | Hs.444446 [ NCBI ] |
| CGAP (NCI) | Hs.444446 |
| Gene Expression | ZNF818P [ NCBI-GEO ] ZNF818P [ EBI - ARRAY_EXPRESS ]
ZNF818P [ SEEK ] ZNF818P [ MEM ] |
| Gene Expression Viewer (FireBrowse) | ZNF818P [ Firebrowse - Broad ] |
| SOURCE (Princeton) | Expression in : [Datasets] [Normal Tissue Atlas] [carcinoma Classsification] [NCI60] |
| Genevisible | Expression in : [tissues] [cell-lines] [cancer] [perturbations] |
| BioGPS (Tissue expression) | 390963 |
| GTEX Portal (Tissue expression) | ZNF818P |
| Protein : pattern, domain, 3D structure |
|---|
| UniProt/SwissProt | Q6ZRF7 [function] [subcellular_location] [family_and_domains] [pathology_and_biotech] [ptm_processing] [expression] [interaction] |
| NextProt | Q6ZRF7 [Sequence] [Exons] [Medical] [Publications] |
| With graphics : InterPro | Q6ZRF7 |
| Splice isoforms : SwissVar | Q6ZRF7 |
| PhosPhoSitePlus | Q6ZRF7 |
| 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) | |
| Domain families : Pfam (NCBI) | |
| Domain families : Smart (EMBL) | ZnF_C2H2 (SM00355) |
| Conserved Domain (NCBI) | ZNF818P |
| DMDM Disease mutations | 390963 |
| Blocks (Seattle) | ZNF818P |
| Superfamily | Q6ZRF7 |
| Peptide Atlas | Q6ZRF7 |
| HPRD | 13537 |
| IPI | IPI00874023 |
| Protein Interaction databases |
|---|
| DIP (DOE-UCLA) | Q6ZRF7 |
| IntAct (EBI) | Q6ZRF7 |
| BioGRID | ZNF818P |
| STRING (EMBL) | ZNF818P |
| ZODIAC | ZNF818P |
| Ontologies - Pathways |
|---|
| QuickGO | Q6ZRF7 |
| 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 | ZNF818P |
| Atlas of Cancer Signalling Network | ZNF818P |
| Wikipedia pathways | ZNF818P |
| Orthology - Evolution |
|---|
| OrthoDB | 390963 |
| Phylogenetic Trees/Animal Genes : TreeFam | ZNF818P |
| HOVERGEN | Q6ZRF7 |
| HOGENOM | Q6ZRF7 |
| Homologs : HomoloGene | ZNF818P |
| Homology/Alignments : Family Browser (UCSC) | ZNF818P |
| Gene fusions - Rearrangements |
|---|
| Polymorphisms : SNP and Copy number variants |
|---|
| NCBI Variation Viewer | ZNF818P [hg38] |
| dbSNP Single Nucleotide Polymorphism (NCBI) | ZNF818P |
| dbVar | ZNF818P |
| ClinVar | ZNF818P |
| 1000_Genomes | ZNF818P |
| Exome Variant Server | ZNF818P |
| ExAC (Exome Aggregation Consortium) | ZNF818P (select the gene name) |
| Genetic variants : HAPMAP | 390963 |
| Genomic Variants (DGV) | ZNF818P [DGVbeta] |
| DECIPHER | ZNF818P [patients] [syndromes] [variants] [genes] |
| CONAN: Copy Number Analysis | ZNF818P |
| Mutations |
|---|
| ICGC Data Portal | ZNF818P |
| TCGA Data Portal | ZNF818P |
| Broad Tumor Portal | ZNF818P |
| OASIS Portal | ZNF818P [ Somatic mutations - Copy number] |
| Mutations and Diseases : HGMD | ZNF818P |
| BioMuta | search ZNF818P |
| DgiDB (Drug Gene Interaction Database) | ZNF818P |
| DoCM (Curated mutations) | ZNF818P (select the gene name) |
| CIViC (Clinical Interpretations of Variants in Cancer) | ZNF818P (select a term) |
| intoGen | ZNF818P |
| Cancer3D | ZNF818P(select the gene name) |
| Impact of mutations | [PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser] |
| Diseases |
|---|
| OMIM | |
| Orphanet | |
| Medgen | ZNF818P |
| Genetic Testing Registry | ZNF818P
|
| NextProt | Q6ZRF7 [Medical] |
| TSGene | 390963 |
| GENETests | ZNF818P |
| Target Validation | ZNF818P |
| Huge Navigator |
ZNF818P [HugePedia] |
| snp3D : Map Gene to Disease | 390963 |
| BioCentury BCIQ | ZNF818P |
| ClinGen | ZNF818P |
| Clinical trials, drugs, therapy |
|---|
| Chemical/Protein Interactions : CTD | 390963 |
| Clinical trial | ZNF818P |
| Miscellaneous |
|---|
| canSAR (ICR) | ZNF818P (select the gene name) |
| Probes |
|---|
| Litterature |
|---|
| PubMed | 1 Pubmed reference(s) in Entrez |
| GeneRIFs | Gene References Into Functions (Entrez) |
| CoreMine | ZNF818P |
| EVEX | ZNF818P |
| GoPubMed | ZNF818P |
| iHOP | ZNF818P |
