Atlas of Genetics and Cytogenetics in Oncology and Haematology


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FAM99B (family with sequence similarity 99 member B)

Identity

Alias (NCBI)-
HGNC (Hugo) FAM99B
HGNC Alias symbDKFZp781M09150
HGNC Previous namefamily with sequence similarity 99, member B
 family with sequence similarity 99, member B (non-protein coding)
 family with sequence similarity 99 member B (non-protein coding)
LocusID (NCBI) 100132464
Atlas_Id 58132
Location 11p15.5  [Link to chromosome band 11p15]
Location_base_pair Starts at 1665597 and ends at 1667457 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)FAM99B   32369
Cards
Entrez_Gene (NCBI)FAM99B  100132464  family with sequence similarity 99 member B
Aliases
GeneCards (Weizmann)FAM99B
Ensembl hg19 (Hinxton)ENSG00000205865 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000205865 [Gene_View]  ENSG00000205865 [Sequence]  chr11:1665597-1667457 [Contig_View]  FAM99B [Vega]
ICGC DataPortalENSG00000205865
TCGA cBioPortalFAM99B
AceView (NCBI)FAM99B
Genatlas (Paris)FAM99B
WikiGenes100132464
SOURCE (Princeton)FAM99B
Genetics Home Reference (NIH)FAM99B
Genomic and cartography
GoldenPath hg38 (UCSC)FAM99B  -     chr11:1665597-1667457 +  11p15.5   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM99B  -     11p15.5   [Description]    (hg19-Feb_2009)
GoldenPathFAM99B - 11p15.5 [CytoView hg19]  FAM99B - 11p15.5 [CytoView hg38]
ImmunoBaseENSG00000205865
genome Data Viewer NCBIFAM99B [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000011 NT_187584 NT_187657
Consensus coding sequences : CCDS (NCBI)FAM99B
Alternative Splicing GalleryENSG00000205865
Gene ExpressionFAM99B [ NCBI-GEO ]   FAM99B [ EBI - ARRAY_EXPRESS ]   FAM99B [ SEEK ]   FAM99B [ MEM ]
Gene Expression Viewer (FireBrowse)FAM99B [ Firebrowse - Broad ]
GenevisibleExpression of FAM99B in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100132464
GTEX Portal (Tissue expression)FAM99B
Human Protein AtlasENSG00000205865-FAM99B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM99B
DMDM Disease mutations100132464
Blocks (Seattle)FAM99B
Human Protein Atlas [tissue]ENSG00000205865-FAM99B [tissue]
Protein Interaction databases
FunCoupENSG00000205865
BioGRIDFAM99B
STRING (EMBL)FAM99B
ZODIACFAM99B
Ontologies - Pathways
Huge Navigator FAM99B [HugePedia]
snp3D : Map Gene to Disease100132464
BioCentury BCIQFAM99B
ClinGenFAM99B
Clinical trials, drugs, therapy
Protein Interactions : CTD100132464
Pharm GKB GenePA142671781
Clinical trialFAM99B
Miscellaneous
canSAR (ICR)FAM99B (select the gene name)
HarmonizomeFAM99B
DataMed IndexFAM99B
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM99B
EVEXFAM99B
GoPubMedFAM99B
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 14 14:10:56 CEST 2020

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