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GAB4 (GRB2 associated binding protein family member 4)

Identity

Alias_namesGRB2-associated binding protein family, member 4
Other alias-
HGNC (Hugo) GAB4
LocusID (NCBI) 128954
Atlas_Id 63642
Location 22q11.1  [Link to chromosome band 22q11]
Location_base_pair Starts at 16961936 and ends at 17008222 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)GAB4   18325
Cards
Entrez_Gene (NCBI)GAB4  128954  GRB2 associated binding protein family member 4
Aliases
GeneCards (Weizmann)GAB4
Ensembl hg19 (Hinxton)ENSG00000215568 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000215568 [Gene_View]  chr22:16961936-17008222 [Contig_View]  GAB4 [Vega]
ICGC DataPortalENSG00000215568
TCGA cBioPortalGAB4
AceView (NCBI)GAB4
Genatlas (Paris)GAB4
WikiGenes128954
SOURCE (Princeton)GAB4
Genetics Home Reference (NIH)GAB4
Genomic and cartography
GoldenPath hg38 (UCSC)GAB4  -     chr22:16961936-17008222 -  22q11.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)GAB4  -     22q11.1   [Description]    (hg19-Feb_2009)
EnsemblGAB4 - 22q11.1 [CytoView hg19]  GAB4 - 22q11.1 [CytoView hg38]
Mapping of homologs : NCBIGAB4 [Mapview hg19]  GAB4 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB076978 AK057252
RefSeq transcript (Entrez)NM_001037814
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)GAB4
Cluster EST : UnigeneHs.434113 [ NCBI ]
CGAP (NCI)Hs.434113
Alternative Splicing GalleryENSG00000215568
Gene ExpressionGAB4 [ NCBI-GEO ]   GAB4 [ EBI - ARRAY_EXPRESS ]   GAB4 [ SEEK ]   GAB4 [ MEM ]
Gene Expression Viewer (FireBrowse)GAB4 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)128954
GTEX Portal (Tissue expression)GAB4
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ2WGN9   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ2WGN9  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ2WGN9
Splice isoforms : SwissVarQ2WGN9
PhosPhoSitePlusQ2WGN9
Domaine pattern : Prosite (Expaxy)PH_DOMAIN (PS50003)   
Domains : Interpro (EBI)PH_dom-like    PH_domain   
Domain families : Pfam (Sanger)PH (PF00169)   
Domain families : Pfam (NCBI)pfam00169   
Domain families : Smart (EMBL)PH (SM00233)  
Conserved Domain (NCBI)GAB4
DMDM Disease mutations128954
Blocks (Seattle)GAB4
SuperfamilyQ2WGN9
Human Protein AtlasENSG00000215568
Peptide AtlasQ2WGN9
IPIIPI00413295   IPI00983415   
Protein Interaction databases
DIP (DOE-UCLA)Q2WGN9
IntAct (EBI)Q2WGN9
FunCoupENSG00000215568
BioGRIDGAB4
STRING (EMBL)GAB4
ZODIACGAB4
Ontologies - Pathways
QuickGOQ2WGN9
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkGAB4
Atlas of Cancer Signalling NetworkGAB4
Wikipedia pathwaysGAB4
Orthology - Evolution
OrthoDB128954
GeneTree (enSembl)ENSG00000215568
Phylogenetic Trees/Animal Genes : TreeFamGAB4
HOVERGENQ2WGN9
HOGENOMQ2WGN9
Homologs : HomoloGeneGAB4
Homology/Alignments : Family Browser (UCSC)GAB4
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerGAB4 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)GAB4
dbVarGAB4
ClinVarGAB4
1000_GenomesGAB4 
Exome Variant ServerGAB4
ExAC (Exome Aggregation Consortium)GAB4 (select the gene name)
Genetic variants : HAPMAP128954
Genomic Variants (DGV)GAB4 [DGVbeta]
DECIPHERGAB4 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisGAB4 
Mutations
ICGC Data PortalGAB4 
TCGA Data PortalGAB4 
Broad Tumor PortalGAB4
OASIS PortalGAB4 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICGAB4  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDGAB4
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 GAB4
DgiDB (Drug Gene Interaction Database)GAB4
DoCM (Curated mutations)GAB4 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)GAB4 (select a term)
intoGenGAB4
Cancer3DGAB4(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenGAB4
Genetic Testing Registry GAB4
NextProtQ2WGN9 [Medical]
TSGene128954
GENETestsGAB4
Target ValidationGAB4
Huge Navigator GAB4 [HugePedia]
snp3D : Map Gene to Disease128954
BioCentury BCIQGAB4
ClinGenGAB4
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD128954
Chemical/Pharm GKB GenePA134933290
Clinical trialGAB4
Miscellaneous
canSAR (ICR)GAB4 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineGAB4
EVEXGAB4
GoPubMedGAB4
iHOPGAB4
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 13:09:03 CEST 2017

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