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ZNF767P (zinc finger family member 767, pseudogene)

Identity

Alias_namesZNF767
zinc finger family member 767
Alias_symbol (synonym)FLJ12700
Other alias
HGNC (Hugo) ZNF767P
LocusID (NCBI) 79970
Atlas_Id 76385
Location 7q36.1  [Link to chromosome band 7q36]
Location_base_pair Starts at 149547154 and ends at 149624727 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
ZNF767P (7q36.1) / FAAH2 (Xp11.21)

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)ZNF767P   21884
Cards
Entrez_Gene (NCBI)ZNF767P  79970  zinc finger family member 767, pseudogene
AliasesZNF767
GeneCards (Weizmann)ZNF767P
Ensembl hg19 (Hinxton)ENSG00000133624 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000133624 [Gene_View]  chr7:149547154-149624727 [Contig_View]  ZNF767P [Vega]
ICGC DataPortalENSG00000133624
TCGA cBioPortalZNF767P
AceView (NCBI)ZNF767P
Genatlas (Paris)ZNF767P
WikiGenes79970
SOURCE (Princeton)ZNF767P
Genetics Home Reference (NIH)ZNF767P
Genomic and cartography
GoldenPath hg38 (UCSC)ZNF767P  -     chr7:149547154-149624727 -  7q36.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ZNF767P  -     7q36.1   [Description]    (hg19-Feb_2009)
EnsemblZNF767P - 7q36.1 [CytoView hg19]  ZNF767P - 7q36.1 [CytoView hg38]
Mapping of homologs : NCBIZNF767P [Mapview hg19]  ZNF767P [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK022762 AK124860 AK295771 AY359125 BC047675
RefSeq transcript (Entrez)NM_024910
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ZNF767P
Cluster EST : UnigeneHs.520785 [ NCBI ]
CGAP (NCI)Hs.520785
Alternative Splicing GalleryENSG00000133624
Gene ExpressionZNF767P [ NCBI-GEO ]   ZNF767P [ EBI - ARRAY_EXPRESS ]   ZNF767P [ SEEK ]   ZNF767P [ MEM ]
Gene Expression Viewer (FireBrowse)ZNF767P [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)79970
GTEX Portal (Tissue expression)ZNF767P
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ75MW2   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ75MW2  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ75MW2
Splice isoforms : SwissVarQ75MW2
PhosPhoSitePlusQ75MW2
Domains : Interpro (EBI)DUF3669_Znf   
Domain families : Pfam (Sanger)DUF3669 (PF12417)   
Domain families : Pfam (NCBI)pfam12417   
Conserved Domain (NCBI)ZNF767P
DMDM Disease mutations79970
Blocks (Seattle)ZNF767P
SuperfamilyQ75MW2
Human Protein AtlasENSG00000133624
Peptide AtlasQ75MW2
HPRD07791
IPIIPI00016544   IPI01020923   IPI00981329   IPI00432060   
Protein Interaction databases
DIP (DOE-UCLA)Q75MW2
IntAct (EBI)Q75MW2
FunCoupENSG00000133624
BioGRIDZNF767P
STRING (EMBL)ZNF767P
ZODIACZNF767P
Ontologies - Pathways
QuickGOQ75MW2
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkZNF767P
Atlas of Cancer Signalling NetworkZNF767P
Wikipedia pathwaysZNF767P
Orthology - Evolution
OrthoDB79970
GeneTree (enSembl)ENSG00000133624
Phylogenetic Trees/Animal Genes : TreeFamZNF767P
HOVERGENQ75MW2
HOGENOMQ75MW2
Homologs : HomoloGeneZNF767P
Homology/Alignments : Family Browser (UCSC)ZNF767P
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerZNF767P [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ZNF767P
dbVarZNF767P
ClinVarZNF767P
1000_GenomesZNF767P 
Exome Variant ServerZNF767P
ExAC (Exome Aggregation Consortium)ZNF767P (select the gene name)
Genetic variants : HAPMAP79970
Genomic Variants (DGV)ZNF767P [DGVbeta]
DECIPHERZNF767P [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisZNF767P 
Mutations
ICGC Data PortalZNF767P 
TCGA Data PortalZNF767P 
Broad Tumor PortalZNF767P
OASIS PortalZNF767P [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDZNF767P
BioMutasearch ZNF767P
DgiDB (Drug Gene Interaction Database)ZNF767P
DoCM (Curated mutations)ZNF767P (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ZNF767P (select a term)
intoGenZNF767P
Cancer3DZNF767P(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenZNF767P
Genetic Testing Registry ZNF767P
NextProtQ75MW2 [Medical]
TSGene79970
GENETestsZNF767P
Target ValidationZNF767P
Huge Navigator ZNF767P [HugePedia]
snp3D : Map Gene to Disease79970
BioCentury BCIQZNF767P
ClinGenZNF767P
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD79970
Chemical/Pharm GKB GenePA162410326
Clinical trialZNF767P
Miscellaneous
canSAR (ICR)ZNF767P (select the gene name)
Probes
Litterature
PubMed10 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineZNF767P
EVEXZNF767P
GoPubMedZNF767P
iHOPZNF767P
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:45:18 CEST 2017

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