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TMEM211 (transmembrane protein 211)

Identity

Alias (NCBI)bA9F11.1
HGNC (Hugo) TMEM211
HGNC Alias symbbA9F11.1
LocusID (NCBI) 255349
Atlas_Id 74876
Location 22q11.23  [Link to chromosome band 22q11]
Location_base_pair Starts at 24934954 and ends at 24946695 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)

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    transmembrane protein 211
AliasesbA9F11.1
GeneCards (Weizmann)TMEM211
Ensembl hg19 (Hinxton)ENSG00000206069 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000206069 [Gene_View]  ENSG00000206069 [Sequence]  chr22:24934954-24946695 [Contig_View]  TMEM211 [Vega]
ICGC DataPortalENSG00000206069
TCGA cBioPortalTMEM211
AceView (NCBI)TMEM211
Genatlas (Paris)TMEM211
SOURCE (Princeton)TMEM211
Genetics Home Reference (NIH)TMEM211
Genomic and cartography
GoldenPath hg38 (UCSC)TMEM211  -     chr22:24934954-24946695 -  22q11.23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)TMEM211  -     22q11.23   [Description]    (hg19-Feb_2009)
GoldenPathTMEM211 - 22q11.23 [CytoView hg19]  TMEM211 - 22q11.23 [CytoView hg38]
ImmunoBaseENSG00000206069
Genome Data Viewer NCBITMEM211 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)BC130647 BC130649 BG222046 BU584904 CR456388
RefSeq transcript (Entrez)NM_001001663 NM_001388199
Consensus coding sequences : CCDS (NCBI)TMEM211
Gene ExpressionTMEM211 [ NCBI-GEO ]   TMEM211 [ EBI - ARRAY_EXPRESS ]   TMEM211 [ SEEK ]   TMEM211 [ MEM ]
Gene Expression Viewer (FireBrowse)TMEM211 [ Firebrowse - Broad ]
GenevisibleExpression of TMEM211 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)255349
GTEX Portal (Tissue expression)TMEM211
Human Protein AtlasENSG00000206069-TMEM211 [pathology]   [cell]   [tissue]
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
PhosPhoSitePlusQ6ICI0
Domains : Interpro (EBI)LHFPL   
Domain families : Pfam (Sanger)L_HMGIC_fpl (PF10242)   
Domain families : Pfam (NCBI)pfam10242   
Conserved Domain (NCBI)TMEM211
SuperfamilyQ6ICI0
AlphaFold pdb e-kbQ6ICI0   
Human Protein Atlas [tissue]ENSG00000206069-TMEM211 [tissue]
HPRD17327
Protein Interaction databases
DIP (DOE-UCLA)Q6ICI0
IntAct (EBI)Q6ICI0
BioGRIDTMEM211
STRING (EMBL)TMEM211
ZODIACTMEM211
Ontologies - Pathways
QuickGOQ6ICI0
Ontology : AmiGOmembrane  integral component of membrane  
Ontology : EGO-EBImembrane  integral component of membrane  
NDEx NetworkTMEM211
Atlas of Cancer Signalling NetworkTMEM211
Wikipedia pathwaysTMEM211
Orthology - Evolution
OrthoDB255349
GeneTree (enSembl)ENSG00000206069
Phylogenetic Trees/Animal Genes : TreeFamTMEM211
Homologs : HomoloGeneTMEM211
Homology/Alignments : Family Browser (UCSC)TMEM211
Gene fusions - Rearrangements
Fusion : QuiverTMEM211
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerTMEM211 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)TMEM211
dbVarTMEM211
ClinVarTMEM211
MonarchTMEM211
1000_GenomesTMEM211 
Exome Variant ServerTMEM211
GNOMAD BrowserENSG00000206069
Varsome BrowserTMEM211
ACMGTMEM211 variants
VarityQ6ICI0
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]  
Somatic Mutations in Cancer : COSMIC3DTMEM211
Mutations and Diseases : HGMDTMEM211
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaTMEM211
DgiDB (Drug Gene Interaction Database)TMEM211
DoCM (Curated mutations)TMEM211
CIViC (Clinical Interpretations of Variants in Cancer)TMEM211
Cancer3DTMEM211
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETTMEM211
MedgenTMEM211
Genetic Testing Registry TMEM211
NextProtQ6ICI0 [Medical]
GENETestsTMEM211
Target ValidationTMEM211
Huge Navigator TMEM211 [HugePedia]
ClinGenTMEM211
Clinical trials, drugs, therapy
MyCancerGenomeTMEM211
Protein Interactions : CTDTMEM211
Pharm GKB GenePA162406474
PharosQ6ICI0
Clinical trialTMEM211
Miscellaneous
canSAR (ICR)TMEM211
HarmonizomeTMEM211
DataMed IndexTMEM211
Probes
Litterature
PubMed6 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXTMEM211
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 16:26:00 CEST 2021

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