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GFY (golgi associated olfactory signaling regulator)

Identity

Alias_symbol (synonym)Goofy
Other alias
HGNC (Hugo) GFY
LocusID (NCBI) 100507003
Atlas_Id 63762
Location 19q13.33  [Link to chromosome band 19q13]
Location_base_pair Starts at 49426431 and ends at 49428818 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)GFY   44663
Cards
Entrez_Gene (NCBI)GFY  100507003  golgi associated olfactory signaling regulator
AliasesGoofy
GeneCards (Weizmann)GFY
Ensembl hg19 (Hinxton)ENSG00000261949 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000261949 [Gene_View]  chr19:49426431-49428818 [Contig_View]  GFY [Vega]
ICGC DataPortalENSG00000261949
TCGA cBioPortalGFY
AceView (NCBI)GFY
Genatlas (Paris)GFY
WikiGenes100507003
SOURCE (Princeton)GFY
Genetics Home Reference (NIH)GFY
Genomic and cartography
GoldenPath hg38 (UCSC)GFY  -     chr19:49426431-49428818 +  19q13.33   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)GFY  -     19q13.33   [Description]    (hg19-Feb_2009)
EnsemblGFY - 19q13.33 [CytoView hg19]  GFY - 19q13.33 [CytoView hg38]
Mapping of homologs : NCBIGFY [Mapview hg19]  GFY [Mapview hg38]
Gene and transcription
Genbank (Entrez)DN930573
RefSeq transcript (Entrez)NM_001195256
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)GFY
Cluster EST : UnigeneHs.553831 [ NCBI ]
CGAP (NCI)Hs.553831
Alternative Splicing GalleryENSG00000261949
Gene ExpressionGFY [ NCBI-GEO ]   GFY [ EBI - ARRAY_EXPRESS ]   GFY [ SEEK ]   GFY [ MEM ]
Gene Expression Viewer (FireBrowse)GFY [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100507003
GTEX Portal (Tissue expression)GFY
Protein : pattern, domain, 3D structure
UniProt/SwissProtI3L273   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtI3L273  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProI3L273
Splice isoforms : SwissVarI3L273
PhosPhoSitePlusI3L273
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)GFY
DMDM Disease mutations100507003
Blocks (Seattle)GFY
SuperfamilyI3L273
Human Protein AtlasENSG00000261949
Peptide AtlasI3L273
Protein Interaction databases
DIP (DOE-UCLA)I3L273
IntAct (EBI)I3L273
FunCoupENSG00000261949
BioGRIDGFY
STRING (EMBL)GFY
ZODIACGFY
Ontologies - Pathways
QuickGOI3L273
Ontology : AmiGOsensory perception of smell  integral component of Golgi membrane  response to stimulus  protein localization to non-motile cilium  non-motile cilium assembly  
Ontology : EGO-EBIsensory perception of smell  integral component of Golgi membrane  response to stimulus  protein localization to non-motile cilium  non-motile cilium assembly  
NDEx NetworkGFY
Atlas of Cancer Signalling NetworkGFY
Wikipedia pathwaysGFY
Orthology - Evolution
OrthoDB100507003
GeneTree (enSembl)ENSG00000261949
Phylogenetic Trees/Animal Genes : TreeFamGFY
HOVERGENI3L273
HOGENOMI3L273
Homologs : HomoloGeneGFY
Homology/Alignments : Family Browser (UCSC)GFY
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerGFY [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)GFY
dbVarGFY
ClinVarGFY
1000_GenomesGFY 
Exome Variant ServerGFY
ExAC (Exome Aggregation Consortium)GFY (select the gene name)
Genetic variants : HAPMAP100507003
Genomic Variants (DGV)GFY [DGVbeta]
DECIPHERGFY [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisGFY 
Mutations
ICGC Data PortalGFY 
TCGA Data PortalGFY 
Broad Tumor PortalGFY
OASIS PortalGFY [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDGFY
BioMutasearch GFY
DgiDB (Drug Gene Interaction Database)GFY
DoCM (Curated mutations)GFY (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)GFY (select a term)
intoGenGFY
Cancer3DGFY(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenGFY
Genetic Testing Registry GFY
NextProtI3L273 [Medical]
TSGene100507003
GENETestsGFY
Target ValidationGFY
Huge Navigator GFY [HugePedia]
snp3D : Map Gene to Disease100507003
BioCentury BCIQGFY
ClinGenGFY
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100507003
Chemical/Pharm GKB GenePA166123689
Clinical trialGFY
Miscellaneous
canSAR (ICR)GFY (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineGFY
EVEXGFY
GoPubMedGFY
iHOPGFY
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Wed Jun 7 15:50:32 CEST 2017

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