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FAM197Y9 (family with sequence similarity 197 Y-linked member 9)

Identity

Alias_namesfamily with sequence similarity 197, Y-linked, member 9
Other alias-
HGNC (Hugo) FAM197Y9
LocusID (NCBI) 100132932
Atlas_Id 80008
Location Yp11.2  [Link to chromosome band Yp11]
Location_base_pair Starts at 6258333 and ends at 6263935 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)

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)FAM197Y9   37477
Cards
Entrez_Gene (NCBI)FAM197Y9  100132932  family with sequence similarity 197 Y-linked member 9
Aliases
GeneCards (Weizmann)FAM197Y9
Ensembl hg19 (Hinxton)ENSG00000234830 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000234830 [Gene_View]  chrY:6258333-6263935 [Contig_View]  FAM197Y9 [Vega]
ICGC DataPortalENSG00000234830
TCGA cBioPortalFAM197Y9
AceView (NCBI)FAM197Y9
Genatlas (Paris)FAM197Y9
WikiGenes100132932
SOURCE (Princeton)FAM197Y9
Genetics Home Reference (NIH)FAM197Y9
Genomic and cartography
GoldenPath hg38 (UCSC)FAM197Y9  -     chrY:6258333-6263935 -  Yp11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM197Y9  -     Yp11.2   [Description]    (hg19-Feb_2009)
EnsemblFAM197Y9 - Yp11.2 [CytoView hg19]  FAM197Y9 - Yp11.2 [CytoView hg38]
Mapping of homologs : NCBIFAM197Y9 [Mapview hg19]  FAM197Y9 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FAM197Y9
Alternative Splicing GalleryENSG00000234830
Gene ExpressionFAM197Y9 [ NCBI-GEO ]   FAM197Y9 [ EBI - ARRAY_EXPRESS ]   FAM197Y9 [ SEEK ]   FAM197Y9 [ MEM ]
Gene Expression Viewer (FireBrowse)FAM197Y9 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100132932
GTEX Portal (Tissue expression)FAM197Y9
Human Protein AtlasENSG00000234830-FAM197Y9 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM197Y9
DMDM Disease mutations100132932
Blocks (Seattle)FAM197Y9
Human Protein Atlas [tissue]ENSG00000234830-FAM197Y9 [tissue]
IPIIPI00888700   
Protein Interaction databases
FunCoupENSG00000234830
BioGRIDFAM197Y9
STRING (EMBL)FAM197Y9
ZODIACFAM197Y9
Ontologies - Pathways
Huge Navigator FAM197Y9 [HugePedia]
snp3D : Map Gene to Disease100132932
BioCentury BCIQFAM197Y9
ClinGenFAM197Y9
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100132932
Chemical/Pharm GKB GenePA165791416
Clinical trialFAM197Y9
Miscellaneous
canSAR (ICR)FAM197Y9 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM197Y9
EVEXFAM197Y9
GoPubMedFAM197Y9
iHOPFAM197Y9
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Nov 20 19:28:45 CET 2017

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