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HINT2 (histidine triad nucleotide binding protein 2)

Identity

Other aliasHIT-17
HGNC (Hugo) HINT2
LocusID (NCBI) 84681
Atlas_Id 53805
Location 9p13.3  [Link to chromosome band 9p13]
Location_base_pair Starts at 35812960 and ends at 35815045 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)HINT2   18344
Cards
Entrez_Gene (NCBI)HINT2  84681  histidine triad nucleotide binding protein 2
AliasesHIT-17
GeneCards (Weizmann)HINT2
Ensembl hg19 (Hinxton)ENSG00000137133 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000137133 [Gene_View]  chr9:35812960-35815045 [Contig_View]  HINT2 [Vega]
ICGC DataPortalENSG00000137133
TCGA cBioPortalHINT2
AceView (NCBI)HINT2
Genatlas (Paris)HINT2
WikiGenes84681
SOURCE (Princeton)HINT2
Genetics Home Reference (NIH)HINT2
Genomic and cartography
GoldenPath hg38 (UCSC)HINT2  -     chr9:35812960-35815045 -  9p13.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)HINT2  -     9p13.3   [Description]    (hg19-Feb_2009)
EnsemblHINT2 - 9p13.3 [CytoView hg19]  HINT2 - 9p13.3 [CytoView hg38]
Mapping of homologs : NCBIHINT2 [Mapview hg19]  HINT2 [Mapview hg38]
OMIM609997   
Gene and transcription
Genbank (Entrez)AF085236 AF356515 AF356875 AK222582 AK309795
RefSeq transcript (Entrez)NM_032593
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)HINT2
Cluster EST : UnigeneHs.70573 [ NCBI ]
CGAP (NCI)Hs.70573
Alternative Splicing GalleryENSG00000137133
Gene ExpressionHINT2 [ NCBI-GEO ]   HINT2 [ EBI - ARRAY_EXPRESS ]   HINT2 [ SEEK ]   HINT2 [ MEM ]
Gene Expression Viewer (FireBrowse)HINT2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)84681
GTEX Portal (Tissue expression)HINT2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9BX68   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9BX68  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9BX68
Splice isoforms : SwissVarQ9BX68
Catalytic activity : Enzyme3.-.-.- [ Enzyme-Expasy ]   3.-.-.-3.-.-.- [ IntEnz-EBI ]   3.-.-.- [ BRENDA ]   3.-.-.- [ KEGG ]   
PhosPhoSitePlusQ9BX68
Domaine pattern : Prosite (Expaxy)HIT_1 (PS00892)    HIT_2 (PS51084)   
Domains : Interpro (EBI)Histidine_triad_CS    Histidine_triad_HIT    HIT-like   
Domain families : Pfam (Sanger)HIT (PF01230)   
Domain families : Pfam (NCBI)pfam01230   
Conserved Domain (NCBI)HINT2
DMDM Disease mutations84681
Blocks (Seattle)HINT2
PDB (SRS)4INC    4INI    4NJX    4NJY    4NJZ    4NK0   
PDB (PDBSum)4INC    4INI    4NJX    4NJY    4NJZ    4NK0   
PDB (IMB)4INC    4INI    4NJX    4NJY    4NJZ    4NK0   
PDB (RSDB)4INC    4INI    4NJX    4NJY    4NJZ    4NK0   
Structural Biology KnowledgeBase4INC    4INI    4NJX    4NJY    4NJZ    4NK0   
SCOP (Structural Classification of Proteins)4INC    4INI    4NJX    4NJY    4NJZ    4NK0   
CATH (Classification of proteins structures)4INC    4INI    4NJX    4NJY    4NJZ    4NK0   
SuperfamilyQ9BX68
Human Protein AtlasENSG00000137133
Peptide AtlasQ9BX68
HPRD17106
IPIIPI00000335   
Protein Interaction databases
DIP (DOE-UCLA)Q9BX68
IntAct (EBI)Q9BX68
FunCoupENSG00000137133
BioGRIDHINT2
STRING (EMBL)HINT2
ZODIACHINT2
Ontologies - Pathways
QuickGOQ9BX68
Ontology : AmiGOnucleotide binding  nucleolus  mitochondrion  mitochondrion  steroid biosynthetic process  apoptotic process  hydrolase activity  multicellular organismal lipid catabolic process  negative regulation of peptidyl-lysine acetylation  
Ontology : EGO-EBInucleotide binding  nucleolus  mitochondrion  mitochondrion  steroid biosynthetic process  apoptotic process  hydrolase activity  multicellular organismal lipid catabolic process  negative regulation of peptidyl-lysine acetylation  
NDEx NetworkHINT2
Atlas of Cancer Signalling NetworkHINT2
Wikipedia pathwaysHINT2
Orthology - Evolution
OrthoDB84681
GeneTree (enSembl)ENSG00000137133
Phylogenetic Trees/Animal Genes : TreeFamHINT2
HOVERGENQ9BX68
HOGENOMQ9BX68
Homologs : HomoloGeneHINT2
Homology/Alignments : Family Browser (UCSC)HINT2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerHINT2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)HINT2
dbVarHINT2
ClinVarHINT2
1000_GenomesHINT2 
Exome Variant ServerHINT2
ExAC (Exome Aggregation Consortium)HINT2 (select the gene name)
Genetic variants : HAPMAP84681
Genomic Variants (DGV)HINT2 [DGVbeta]
DECIPHERHINT2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisHINT2 
Mutations
ICGC Data PortalHINT2 
TCGA Data PortalHINT2 
Broad Tumor PortalHINT2
OASIS PortalHINT2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICHINT2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDHINT2
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
LOVD (Leiden Open Variation Database)MSeqDR-LSDB Mitochondrial Disease Locus Specific Database
BioMutasearch HINT2
DgiDB (Drug Gene Interaction Database)HINT2
DoCM (Curated mutations)HINT2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)HINT2 (select a term)
intoGenHINT2
Cancer3DHINT2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM609997   
Orphanet
MedgenHINT2
Genetic Testing Registry HINT2
NextProtQ9BX68 [Medical]
TSGene84681
GENETestsHINT2
Target ValidationHINT2
Huge Navigator HINT2 [HugePedia]
snp3D : Map Gene to Disease84681
BioCentury BCIQHINT2
ClinGenHINT2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD84681
Chemical/Pharm GKB GenePA29287
Clinical trialHINT2
Miscellaneous
canSAR (ICR)HINT2 (select the gene name)
Probes
Litterature
PubMed14 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineHINT2
EVEXHINT2
GoPubMedHINT2
iHOPHINT2
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 19:11:30 CEST 2017

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