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TMEM211 (transmembrane protein 211)

Identity

Alias_symbol (synonym)bA9F11.1
Other alias
HGNC (Hugo) TMEM211
LocusID (NCBI) 255349
Atlas_Id 74876
Location 22q11.23  [Link to chromosome band 22q11]
Location_base_pair Starts at 24935241 and ends at 24939347 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)TMEM211   33725
Cards
Entrez_Gene (NCBI)TMEM211  255349  transmembrane protein 211
AliasesbA9F11.1
GeneCards (Weizmann)TMEM211
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr22:24935241-24939347 [Contig_View]  TMEM211 [Vega]
TCGA cBioPortalTMEM211
AceView (NCBI)TMEM211
Genatlas (Paris)TMEM211
WikiGenes255349
SOURCE (Princeton)TMEM211
Genetics Home Reference (NIH)TMEM211
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM211  -     chr22:24935241-24939347 -  22q11.23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM211  -     22q11.23   [Description]    (hg19-Feb_2009)
EnsemblTMEM211 - 22q11.23 [CytoView hg19]  TMEM211 - 22q11.23 [CytoView hg38]
Mapping of homologs : NCBITMEM211 [Mapview hg19]  TMEM211 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC130647 BC130649 CR456388 HQ258055
RefSeq transcript (Entrez)NM_001001663
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)TMEM211
Cluster EST : UnigeneHs.329040 [ NCBI ]
CGAP (NCI)Hs.329040
Gene ExpressionTMEM211 [ NCBI-GEO ]   TMEM211 [ EBI - ARRAY_EXPRESS ]   TMEM211 [ SEEK ]   TMEM211 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM211 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)255349
GTEX Portal (Tissue expression)TMEM211
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ6ICI0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ6ICI0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ6ICI0
Splice isoforms : SwissVarQ6ICI0
PhosPhoSitePlusQ6ICI0
Domains : Interpro (EBI)Lipome_HGMIC_fus_partner-like   
Domain families : Pfam (Sanger)L_HMGIC_fpl (PF10242)   
Domain families : Pfam (NCBI)pfam10242   
Conserved Domain (NCBI)TMEM211
DMDM Disease mutations255349
Blocks (Seattle)TMEM211
SuperfamilyQ6ICI0
Peptide AtlasQ6ICI0
HPRD17327
IPIIPI00419291   IPI00939452   
Protein Interaction databases
DIP (DOE-UCLA)Q6ICI0
IntAct (EBI)Q6ICI0
BioGRIDTMEM211
STRING (EMBL)TMEM211
ZODIACTMEM211
Ontologies - Pathways
QuickGOQ6ICI0
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkTMEM211
Atlas of Cancer Signalling NetworkTMEM211
Wikipedia pathwaysTMEM211
Orthology - Evolution
OrthoDB255349
Phylogenetic Trees/Animal Genes : TreeFamTMEM211
HOVERGENQ6ICI0
HOGENOMQ6ICI0
Homologs : HomoloGeneTMEM211
Homology/Alignments : Family Browser (UCSC)TMEM211
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM211 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM211
dbVarTMEM211
ClinVarTMEM211
1000_GenomesTMEM211 
Exome Variant ServerTMEM211
ExAC (Exome Aggregation Consortium)TMEM211 (select the gene name)
Genetic variants : HAPMAP255349
Genomic Variants (DGV)TMEM211 [DGVbeta]
DECIPHERTMEM211 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisTMEM211 
Mutations
ICGC Data PortalTMEM211 
TCGA Data PortalTMEM211 
Broad Tumor PortalTMEM211
OASIS PortalTMEM211 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICTMEM211  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDTMEM211
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch TMEM211
DgiDB (Drug Gene Interaction Database)TMEM211
DoCM (Curated mutations)TMEM211 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)TMEM211 (select a term)
intoGenTMEM211
Cancer3DTMEM211(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenTMEM211
Genetic Testing Registry TMEM211
NextProtQ6ICI0 [Medical]
TSGene255349
GENETestsTMEM211
Target ValidationTMEM211
Huge Navigator TMEM211 [HugePedia]
snp3D : Map Gene to Disease255349
BioCentury BCIQTMEM211
ClinGenTMEM211
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD255349
Chemical/Pharm GKB GenePA162406474
Clinical trialTMEM211
Miscellaneous
canSAR (ICR)TMEM211 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineTMEM211
EVEXTMEM211
GoPubMedTMEM211
iHOPTMEM211
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed May 31 15:46:07 CEST 2017

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