Atlas of Genetics and Cytogenetics in Oncology and Haematology


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H1F0 (-)

Identity

Alias_namesH1(0)
H1-0
Alias_symbol (synonym)H10
Other alias-
HGNC (Hugo) -
LocusID (NCBI) 3005
Atlas_Id 45623
Location -  [Link to chromosome band ]
Location_base_pair Starts at 37805107 and ends at 37807436 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
C6orf1 (6p21.31) / H1F0 (22q13.1)H1F0 (22q13.1) / ACTB (7p22.1)H1F0 (22q13.1) / ADCY2 (5p15.31)
H1F0 (22q13.1) / AHSP (16p11.2)H1F0 (22q13.1) / C16orf46 (16q23.2)H1F0 (22q13.1) / H1F0 (22q13.1)
H1F0 (22q13.1) / KLF4 (9q31.2)H1F0 (22q13.1) / NINL (20p11.21)H1F0 (22q13.1) / SLC20A2 (8p11.21)

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

 


Other Solid tumors implicated (Data extracted from papers in the Atlas) [ 1 ]

Solid Tumors TT_t0722p22q13ID107511


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)H1F0  3005  -
Aliases
GeneCards (Weizmann)H1F0
Ensembl hg19 (Hinxton)ENSG00000189060 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000189060 [Gene_View]  ENSG00000189060 [Sequence]  chr22:37805107-37807436 [Contig_View]  H1F0 [Vega]
ICGC DataPortalENSG00000189060
TCGA cBioPortalH1F0
AceView (NCBI)H1F0
Genatlas (Paris)H1F0
WikiGenes3005
SOURCE (Princeton)H1F0
Genetics Home Reference (NIH)H1F0
Genomic and cartography
GoldenPath hg38 (UCSC)H1F0  -     chr22:37805107-37807436 +  -   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)H1F0  -     -   [Description]    (hg19-Feb_2009)
GoldenPathH1F0 - - [CytoView hg19]  H1F0 - - [CytoView hg38]
ImmunoBaseENSG00000189060
Mapping of homologs : NCBIH1F0 [Mapview hg19]  H1F0 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)H1F0
Alternative Splicing GalleryENSG00000189060
Gene ExpressionH1F0 [ NCBI-GEO ]   H1F0 [ EBI - ARRAY_EXPRESS ]   H1F0 [ SEEK ]   H1F0 [ MEM ]
Gene Expression Viewer (FireBrowse)H1F0 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)3005
GTEX Portal (Tissue expression)H1F0
Human Protein AtlasENSG00000189060-H1F0 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)H1F0
DMDM Disease mutations3005
Blocks (Seattle)H1F0
Human Protein Atlas [tissue]ENSG00000189060-H1F0 [tissue]
HPRD00819
IPIIPI00550239   IPI00979041   
Protein Interaction databases
FunCoupENSG00000189060
BioGRIDH1F0
STRING (EMBL)H1F0
ZODIACH1F0
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease3005
BioCentury BCIQH1F0
ClinGenH1F0
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD3005
Clinical trialH1F0
Miscellaneous
canSAR (ICR)H1F0 (select the gene name)
DataMed IndexH1F0
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineH1F0
EVEXH1F0
GoPubMedH1F0
iHOPH1F0
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 : Mon Aug 12 15:36:27 CEST 2019

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