Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   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

FAM86EP (family with sequence similarity 86, member A pseudogene)

Identity

Alias_namesfamily with sequence similarity 86, member E, pseudogene
Other alias-
HGNC (Hugo) FAM86EP
LocusID (NCBI) 348926
Atlas_Id 63264
Location 4p16.3  [Link to chromosome band 4p16]
Location_base_pair Starts at 3943487 and ends at 3957155 bp from pter ( according to hg19-Feb_2009)

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)FAM86EP   28017
Cards
Entrez_Gene (NCBI)FAM86EP  348926  family with sequence similarity 86, member A pseudogene
Aliases
GeneCards (Weizmann)FAM86EP
Ensembl hg19 (Hinxton)ENSG00000251669 [Gene_View]  chr4:3943487-3957155 [Contig_View]  FAM86EP [Vega]
Ensembl hg38 (Hinxton)ENSG00000251669 [Gene_View]  chr4:3943487-3957155 [Contig_View]  FAM86EP [Vega]
ICGC DataPortalENSG00000251669
TCGA cBioPortalFAM86EP
AceView (NCBI)FAM86EP
Genatlas (Paris)FAM86EP
WikiGenes348926
SOURCE (Princeton)FAM86EP
Genetics Home Reference (NIH)FAM86EP
Genomic and cartography
GoldenPath hg19 (UCSC)FAM86EP  -     chr4:3943487-3957155 -  4p16.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)FAM86EP  -     4p16.3   [Description]    (hg38-Dec_2013)
EnsemblFAM86EP - 4p16.3 [CytoView hg19]  FAM86EP - 4p16.3 [CytoView hg38]
Mapping of homologs : NCBIFAM86EP [Mapview hg19]  FAM86EP [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA421090 BC044637 BM718734 BU742387 CN271531
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000004 NC_018915 NT_006051 NW_004929314
Consensus coding sequences : CCDS (NCBI)FAM86EP
Cluster EST : UnigeneHs.591720 [ NCBI ]
CGAP (NCI)Hs.591720
Alternative Splicing GalleryENSG00000251669
Gene ExpressionFAM86EP [ NCBI-GEO ]   FAM86EP [ EBI - ARRAY_EXPRESS ]   FAM86EP [ SEEK ]   FAM86EP [ MEM ]
Gene Expression Viewer (FireBrowse)FAM86EP [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)348926
GTEX Portal (Tissue expression)FAM86EP
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM86EP
DMDM Disease mutations348926
Blocks (Seattle)FAM86EP
Human Protein AtlasENSG00000251669
IPIIPI00455597   
Protein Interaction databases
FunCoupENSG00000251669
BioGRIDFAM86EP
STRING (EMBL)FAM86EP
ZODIACFAM86EP
Ontologies - Pathways
Huge Navigator FAM86EP [HugePedia]
snp3D : Map Gene to Disease348926
BioCentury BCIQFAM86EP
ClinGenFAM86EP
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD348926
Clinical trialFAM86EP
Miscellaneous
canSAR (ICR)FAM86EP (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM86EP
EVEXFAM86EP
GoPubMedFAM86EP
iHOPFAM86EP
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 : Tue Mar 14 12:04:24 CET 2017

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

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.