| 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] |
Genevestigator | 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 |
Fusion : Quiver | ZNF818P |
| 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 |
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 |
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OMIM | |
Orphanet | |
DisGeNET | ZNF818P |
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 |
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Chemical/Protein Interactions : CTD | 390963 |
Clinical trial | ZNF818P |
| Miscellaneous |
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canSAR (ICR) | ZNF818P (select the gene name) |
| Probes |
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| Litterature |
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PubMed | 1 Pubmed reference(s) in Entrez |
GeneRIFs | Gene References Into Functions (Entrez) |
CoreMine | ZNF818P |
EVEX | ZNF818P |
GoPubMed | ZNF818P |
iHOP | ZNF818P |