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FUZ (fuzzy planar cell polarity protein)

Identity

Alias_namesfuzzy homolog (Drosophila)
Alias_symbol (synonym)FLJ22688
Fy
Other aliasFY
NTD
HGNC (Hugo) FUZ
LocusID (NCBI) 80199
Atlas_Id 56211
Location 19q13.33  [Link to chromosome band 19q13]
Location_base_pair Starts at 49806866 and ends at 49813310 bp from pter ( according to hg38-Dec_2013)

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)FUZ   26219
Cards
Entrez_Gene (NCBI)FUZ  80199  fuzzy planar cell polarity protein
AliasesFY; NTD
GeneCards (Weizmann)FUZ
Ensembl hg19 (Hinxton)ENSG00000010361 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000010361 [Gene_View]  chr19:49806866-49813310 [Contig_View]  FUZ [Vega]
ICGC DataPortalENSG00000010361
TCGA cBioPortalFUZ
AceView (NCBI)FUZ
Genatlas (Paris)FUZ
WikiGenes80199
SOURCE (Princeton)FUZ
Genetics Home Reference (NIH)FUZ
Genomic and cartography
GoldenPath hg38 (UCSC)FUZ  -     chr19:49806866-49813310 -  19q13.33   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FUZ  -     19q13.33   [Description]    (hg19-Feb_2009)
EnsemblFUZ - 19q13.33 [CytoView hg19]  FUZ - 19q13.33 [CytoView hg38]
Mapping of homologs : NCBIFUZ [Mapview hg19]  FUZ [Mapview hg38]
OMIM182940   610622   
Gene and transcription
Genbank (Entrez)AK026341 AK057964 AK295072 AK315445 BC004445
RefSeq transcript (Entrez)NM_001171937 NM_025129
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FUZ
Cluster EST : UnigeneHs.288800 [ NCBI ]
CGAP (NCI)Hs.288800
Alternative Splicing GalleryENSG00000010361
Gene ExpressionFUZ [ NCBI-GEO ]   FUZ [ EBI - ARRAY_EXPRESS ]   FUZ [ SEEK ]   FUZ [ MEM ]
Gene Expression Viewer (FireBrowse)FUZ [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)80199
GTEX Portal (Tissue expression)FUZ
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9BT04   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9BT04  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9BT04
Splice isoforms : SwissVarQ9BT04
PhosPhoSitePlusQ9BT04
Domains : Interpro (EBI)Fuzzy   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FUZ
DMDM Disease mutations80199
Blocks (Seattle)FUZ
SuperfamilyQ9BT04
Human Protein AtlasENSG00000010361
Peptide AtlasQ9BT04
HPRD08662
IPIIPI00018580   IPI00879241   IPI00645475   IPI00909021   IPI00978886   IPI00984903   IPI00976124   IPI00974181   IPI00976902   
Protein Interaction databases
DIP (DOE-UCLA)Q9BT04
IntAct (EBI)Q9BT04
FunCoupENSG00000010361
BioGRIDFUZ
STRING (EMBL)FUZ
ZODIACFUZ
Ontologies - Pathways
QuickGOQ9BT04
Ontology : AmiGOestablishment of planar polarity  neural tube closure  neural tube closure  hair follicle development  protein binding  cytoplasm  cytoskeleton  negative regulation of cell proliferation  regulation of smoothened signaling pathway  embryonic body morphogenesis  protein transport  negative regulation of cell migration  cell projection  positive regulation of cilium assembly  embryonic skeletal system morphogenesis  cilium assembly  extracellular exosome  negative regulation of canonical Wnt signaling pathway  negative regulation of neural crest formation  non-motile cilium assembly  negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation  
Ontology : EGO-EBIestablishment of planar polarity  neural tube closure  neural tube closure  hair follicle development  protein binding  cytoplasm  cytoskeleton  negative regulation of cell proliferation  regulation of smoothened signaling pathway  embryonic body morphogenesis  protein transport  negative regulation of cell migration  cell projection  positive regulation of cilium assembly  embryonic skeletal system morphogenesis  cilium assembly  extracellular exosome  negative regulation of canonical Wnt signaling pathway  negative regulation of neural crest formation  non-motile cilium assembly  negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation  
NDEx NetworkFUZ
Atlas of Cancer Signalling NetworkFUZ
Wikipedia pathwaysFUZ
Orthology - Evolution
OrthoDB80199
GeneTree (enSembl)ENSG00000010361
Phylogenetic Trees/Animal Genes : TreeFamFUZ
HOVERGENQ9BT04
HOGENOMQ9BT04
Homologs : HomoloGeneFUZ
Homology/Alignments : Family Browser (UCSC)FUZ
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFUZ [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FUZ
dbVarFUZ
ClinVarFUZ
1000_GenomesFUZ 
Exome Variant ServerFUZ
ExAC (Exome Aggregation Consortium)FUZ (select the gene name)
Genetic variants : HAPMAP80199
Genomic Variants (DGV)FUZ [DGVbeta]
DECIPHERFUZ [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisFUZ 
Mutations
ICGC Data PortalFUZ 
TCGA Data PortalFUZ 
Broad Tumor PortalFUZ
OASIS PortalFUZ [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICFUZ  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDFUZ
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
BioMutasearch FUZ
DgiDB (Drug Gene Interaction Database)FUZ
DoCM (Curated mutations)FUZ (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FUZ (select a term)
intoGenFUZ
Cancer3DFUZ(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM182940    610622   
Orphanet875    946    20199    20198    20197    20196    20195    20194    20192    20188    20189    20190    20191    20187   
MedgenFUZ
Genetic Testing Registry FUZ
NextProtQ9BT04 [Medical]
TSGene80199
GENETestsFUZ
Target ValidationFUZ
Huge Navigator FUZ [HugePedia]
snp3D : Map Gene to Disease80199
BioCentury BCIQFUZ
ClinGenFUZ
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD80199
Chemical/Pharm GKB GenePA145148782
Clinical trialFUZ
Miscellaneous
canSAR (ICR)FUZ (select the gene name)
Probes
Litterature
PubMed9 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFUZ
EVEXFUZ
GoPubMedFUZ
iHOPFUZ
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 25 19:09:07 CEST 2017

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