Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

FAM66B (family with sequence similarity 66 member B)

Identity

Alias_namesfamily with sequence similarity 66, member B
Other aliasFAM66E
HGNC (Hugo) FAM66B
LocusID (NCBI) 100128890
Atlas_Id 63220
Location 8p23.1  [Link to chromosome band 8p23]
Location_base_pair Starts at 7301611 and ends at 7355354 bp from pter ( according to hg38-Dec_2013)

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)FAM66B   28890
Cards
Entrez_Gene (NCBI)FAM66B  100128890  family with sequence similarity 66 member B
AliasesFAM66E
GeneCards (Weizmann)FAM66B
Ensembl hg19 (Hinxton)ENSG00000215374 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000215374 [Gene_View]  chr8:7301611-7355354 [Contig_View]  FAM66B [Vega]
ICGC DataPortalENSG00000215374
TCGA cBioPortalFAM66B
AceView (NCBI)FAM66B
Genatlas (Paris)FAM66B
WikiGenes100128890
SOURCE (Princeton)FAM66B
Genetics Home Reference (NIH)FAM66B
Genomic and cartography
GoldenPath hg38 (UCSC)FAM66B  -     chr8:7301611-7355354 -  8p23.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM66B  -     8p23.1   [Description]    (hg19-Feb_2009)
EnsemblFAM66B - 8p23.1 [CytoView hg19]  FAM66B - 8p23.1 [CytoView hg38]
Mapping of homologs : NCBIFAM66B [Mapview hg19]  FAM66B [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK302471
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FAM66B
Cluster EST : UnigeneHs.694680 [ NCBI ]
CGAP (NCI)Hs.694680
Alternative Splicing GalleryENSG00000215374
Gene ExpressionFAM66B [ NCBI-GEO ]   FAM66B [ EBI - ARRAY_EXPRESS ]   FAM66B [ SEEK ]   FAM66B [ MEM ]
Gene Expression Viewer (FireBrowse)FAM66B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100128890
GTEX Portal (Tissue expression)FAM66B
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM66B
DMDM Disease mutations100128890
Blocks (Seattle)FAM66B
Human Protein AtlasENSG00000215374
Protein Interaction databases
FunCoupENSG00000215374
BioGRIDFAM66B
STRING (EMBL)FAM66B
ZODIACFAM66B
Ontologies - Pathways
Huge Navigator FAM66B [HugePedia]
snp3D : Map Gene to Disease100128890
BioCentury BCIQFAM66B
ClinGenFAM66B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100128890
Chemical/Pharm GKB GenePA142671877
Clinical trialFAM66B
Miscellaneous
canSAR (ICR)FAM66B (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM66B
EVEXFAM66B
GoPubMedFAM66B
iHOPFAM66B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Sep 18 13:08:08 CEST 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.