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FAM197Y7 (family with sequence similarity 197 Y-linked member 7)

Identity

Alias_namesFAM197Y7P
family with sequence similarity 197, Y-linked, member 7, pseudogene
family with sequence similarity 197 Y-linked member 7, pseudogene
Other alias
HGNC (Hugo) FAM197Y7
LocusID (NCBI) 105379269
Atlas_Id 79054
Location Yp11.2  [Link to chromosome band Yp11]
Location_base_pair Starts at 9349580 and ends at 9355182 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)FAM197Y7   37469
Cards
Entrez_Gene (NCBI)FAM197Y7  105379269  family with sequence similarity 197 Y-linked member 7
AliasesFAM197Y7P
GeneCards (Weizmann)FAM197Y7
Ensembl hg19 (Hinxton)ENSG00000228383 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000228383 [Gene_View]  chrY:9349580-9355182 [Contig_View]  FAM197Y7 [Vega]
ICGC DataPortalENSG00000228383
TCGA cBioPortalFAM197Y7
AceView (NCBI)FAM197Y7
Genatlas (Paris)FAM197Y7
WikiGenes105379269
SOURCE (Princeton)FAM197Y7
Genetics Home Reference (NIH)FAM197Y7
Genomic and cartography
GoldenPath hg38 (UCSC)FAM197Y7  -     chrY:9349580-9355182 -  Yp11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM197Y7  -     Yp11.2   [Description]    (hg19-Feb_2009)
EnsemblFAM197Y7 - Yp11.2 [CytoView hg19]  FAM197Y7 - Yp11.2 [CytoView hg38]
Mapping of homologs : NCBIFAM197Y7 [Mapview hg19]  FAM197Y7 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FAM197Y7
Alternative Splicing GalleryENSG00000228383
Gene ExpressionFAM197Y7 [ NCBI-GEO ]   FAM197Y7 [ EBI - ARRAY_EXPRESS ]   FAM197Y7 [ SEEK ]   FAM197Y7 [ MEM ]
Gene Expression Viewer (FireBrowse)FAM197Y7 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105379269
GTEX Portal (Tissue expression)FAM197Y7
Human Protein AtlasENSG00000228383-FAM197Y7 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM197Y7
DMDM Disease mutations105379269
Blocks (Seattle)FAM197Y7
Human Protein Atlas [tissue]ENSG00000228383-FAM197Y7 [tissue]
Protein Interaction databases
FunCoupENSG00000228383
BioGRIDFAM197Y7
STRING (EMBL)FAM197Y7
ZODIACFAM197Y7
Ontologies - Pathways
Huge Navigator FAM197Y7 [HugePedia]
snp3D : Map Gene to Disease105379269
BioCentury BCIQFAM197Y7
ClinGenFAM197Y7
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105379269
Clinical trialFAM197Y7
Miscellaneous
canSAR (ICR)FAM197Y7 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM197Y7
EVEXFAM197Y7
GoPubMedFAM197Y7
iHOPFAM197Y7
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Nov 21 14:01:05 CET 2017

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