Atlas of Genetics and Cytogenetics in Oncology and Haematology

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FAM99B (family with sequence similarity 99 member B)


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)


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



External links

HGNC (Hugo)FAM99B   32369
Entrez_Gene (NCBI)FAM99B    family with sequence similarity 99 member B
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
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]
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
Blocks (Seattle)FAM99B
Human Protein Atlas [tissue]ENSG00000205865-FAM99B [tissue]
Protein Interaction databases
Ontologies - Pathways
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
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 : Fri Jan 1 18:15:14 CET 2021

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