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

FAM21EP (family with sequence similarity 21, member A pseudogene)

Identity

Alias_namesfamily with sequence similarity 21, member E, pseudogene
Alias_symbol (synonym)FLJ31813
Other alias-
HGNC (Hugo) FAM21EP
LocusID (NCBI) 100421577
Atlas_Id 63150
Location 10q11.23  [Link to chromosome band 10q11]
Location_base_pair Starts at 50021182 and ends at 50067803 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)FAM21EP   45010
Cards
Entrez_Gene (NCBI)FAM21EP  100421577  family with sequence similarity 21, member A pseudogene
Aliases
GeneCards (Weizmann)FAM21EP
Ensembl hg19 (Hinxton)ENSG00000235618 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000235618 [Gene_View]  chr10:50021182-50067803 [Contig_View]  FAM21EP [Vega]
ICGC DataPortalENSG00000235618
TCGA cBioPortalFAM21EP
AceView (NCBI)FAM21EP
Genatlas (Paris)FAM21EP
WikiGenes100421577
SOURCE (Princeton)FAM21EP
Genetics Home Reference (NIH)FAM21EP
Genomic and cartography
GoldenPath hg38 (UCSC)FAM21EP  -     chr10:50021182-50067803 -  10q11.23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FAM21EP  -     10q11.23   [Description]    (hg19-Feb_2009)
EnsemblFAM21EP - 10q11.23 [CytoView hg19]  FAM21EP - 10q11.23 [CytoView hg38]
Mapping of homologs : NCBIFAM21EP [Mapview hg19]  FAM21EP [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK056375
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FAM21EP
Cluster EST : UnigeneHs.712902 [ NCBI ]
CGAP (NCI)Hs.712902
Alternative Splicing GalleryENSG00000235618
Gene ExpressionFAM21EP [ NCBI-GEO ]   FAM21EP [ EBI - ARRAY_EXPRESS ]   FAM21EP [ SEEK ]   FAM21EP [ MEM ]
Gene Expression Viewer (FireBrowse)FAM21EP [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100421577
GTEX Portal (Tissue expression)FAM21EP
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FAM21EP
DMDM Disease mutations100421577
Blocks (Seattle)FAM21EP
Human Protein AtlasENSG00000235618
Protein Interaction databases
FunCoupENSG00000235618
BioGRIDFAM21EP
STRING (EMBL)FAM21EP
ZODIACFAM21EP
Ontologies - Pathways
Huge Navigator FAM21EP [HugePedia]
snp3D : Map Gene to Disease100421577
BioCentury BCIQFAM21EP
ClinGenFAM21EP
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100421577
Clinical trialFAM21EP
Miscellaneous
canSAR (ICR)FAM21EP (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFAM21EP
EVEXFAM21EP
GoPubMedFAM21EP
iHOPFAM21EP
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 13:07:55 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.